From 2014.igem.org

(Difference between revisions)

Latest revision as of 21:10, 16 October 2014

Notebook: June

02.06.2014

13.56 Making glycerine stocks of the following strains

Aim: Storage of strains

Dh5α piGEM010 (p003 + Tag 21)
Dh5α piGEM015 (p004 + Tag 23)
Dh5α piGEM014 (p003 + Tag 22)
Dh5α piGEM008 (p002 + Tag 22)
Dh5α piGEM007 (p002 + Tag 21)
Dh5α piGEM011 (p003 + Tag 22)
Dh5α piGEM012 (p003 + Tag 23)

13.57 Mini Prep of cultures inoculated on Friday 30.05.14 containing the nose plasmids

piGEM010 = 22ng/µl
piGEM013 = 46 ng/µl
piGEM 009 = 13 ng/µl

low concentration: new transformation to obtain more plasmid DNA
Strain: new competent E. coli XL1-blue

15.50 Miniprep of pMAD-fla-cup1-1 for miniprep

The miniprep was performed according to the miniprep protocol.

Concentration 40 ng/µL
low concentration: new transformation to gain more plasmid DNA should be done
Strain: new competent E. coli XL1-blue

13.58 Bacillus Trafo with all Nose Plasmids containing one/no Degradation Tag

Aim: Create Bacillus subtilis strain 3610 containing the following plasmids: piGEM002 to 004 and piGEM007 to 016

Add 5µl plasmid DNA and incubate for 30 min at 37°C, LB plate with 5 ng/µL Cm (prepared freshly)

13.59 Inoculation of Bacillus subtilis wildtype (3610), gfp and silver nose

Aim: perform MTA to test the Ag concentrations where cells are still viable, since 1 mM until 10 µM were too high and the cells died

Starting from 1 mM, eight serial dilutions have been prepared

14.38 Purification of PheA-Arc1p-C-1x

Aim: Purify PheA-Arc1p-C-1x in three steps

The resuspended cells from 14.37 were lysed using a french press. The lysate was incubated on ice with 5 µg/mL DNAseA and RNAseI for 10 min and centrifuged (27000 rpm, 45 min, 4 °C) to pellet cell debris. The supernatant was filtered (0.45 µm) and PheA-Arc1p-C-1x purified from the cleared solution by NiNTA affinity chromatography. The combined elution fractions containing crude PheA-Arc1p-C-1x were concentrated to a volume of 2 mL and further purified using an anion exchange column to get rid of possible tRNA contaminations. Finally the buffer was changed to dialysis buffer and the protein concentrated and stored at -80 °C in aliquods for further use.

18.1 Tumor Terminator - Dilution of Plasmid

Aim: Creating a stock solution

We received the synthetized DARPin-gene in a pEC-A2 vector with SpeI restriction sites at the 5' - and 3' -site with an amount of 2,7 µg plasmid per tube.

A stock solution was created by adding 27 µl water to the tube.

Concentration of stock solution = 100 ng/µl

A 1:10 dilution was created by using 1 µl of stock solution adding 9µL of water to an end concentration of 10ng/µl.

Concentration of stock dilution = 10 ng/µl.

18.2 Transformation of E.coli XL1-Blue with pEX-A2-DARPin

Aim: Transformation of E.coli XL1-Blue with pEX-A2-DARPin for amplification of the plasmid.

1µl of the 1:10 dilution was used for transformation of E. Coli XL1-Blue

03.06.2014

18.3 Miniprep of pEX-A2-DARPin from E.coli XL1-Blue

Aim: Receiving a higher amount of plasmid for further experiments.

3 x 6ml LB-Amp were inoculated with clones from the successful transformed plate (18.2) and incubated at 37°C overnight.

13.60 Microtiter plate assay with wildtype, gfp strain 186 and silver nose

Aim: perform MTA to test the Ag concentrations where cells are still viable, since 1mM until 10 µM was too high and the cells died

Starting from 1 mM 8 dilutions have been prepared.
In the beginning Minimalmedium S750 has been prepared with 0.5‰ Xylose
In the wells the following mix was added to a total volume of 150 µl:
135µl of MM (90‰) and Silver solution (10‰)
15µl of cells
Finally 70 µl are added to avoid evaporation of the medium

Incubation for appr. 24 hours at 37°C shaking (Viktor AG Waldminghaus)

No positive GFP signal could be detected for the B. subtilis strain with the possible Ag sensitive promoter. The strain was restreaked onto a LB-Cm plate and he did not grow, which proved it to be a wrong strain, which has not been transformed successfully.

13.61 Checking Bacillus Trafo with all Nose Plasmids containing one/no Degradation Tag

Every transformation plate showed a huge growth of bacillus without single colonies. After one day of incubation this seems to be an unrealistic growth, which is why we planned to repeat the transformation after checking the growth of the Bacillus subtilis wildtype 3610 on LB-CM plate with 5 µg/ml chloramphenicol.

13.62 Checking Bacillus Trafo Wildtype 3610

Aim: check if wildtype has a resistance against chloramphenicol or if the plates are faulty

Bacillus subtilis Wildtype 3610 was plated on LB-chloramphenicol plate with 5 µg/ml chloramphenicol and incubated overnight at 37°C.

15.51 Making selection plates for clean deletions - integration of pMAD-construct into Bacillus subtilis chromosome

Aim: For the integration of the constructs we cloned into pMAD many steps of a special selection are necessary.

Antibiotics and chemicals:

Erythromycin 4 mg/ml
Lincomycin 25mg/ml
X-Gal 100mg/ml

For MLS selection plates erythromycin with 1 mg/ml were needed. Therefore the 4 mg/ml stock solution was diluted 1:4 by mixing 400 µl eryhtromycin with 1200 µl of 70% ethanol.

3 types of plates were made:

1. MLS selectin: 800 mL LB agar + 800 µl eryhtromycin + 800 µl lincomycin
2. MLS X-Gal: 800 mL LB agar + 800 µl eryhtromycin + 800 µl lincomycin + 800 µl X-Gal
3. X-Gal: 800 mL LB agar + 800 µL X-Gal

04.06.2014

18.4 Miniprep of pEX-A2-DARPin from E.coli XL1-Blue

Plasmid pEX-A2 + DARPinEc1	Concentration after prep (ng/µl)
Clone 1	398,7
Clone 2	340
Clone 3	309

15.52 Sequencing of pMAD-fla-cup1-1

Aim: Checking the correct insertion of the metallothionein-domain into the hag-flank construct

Making a pre-mix for Eurofins MWG prepairing the sequencing. Primers from Florian Altegoer were used:

Flo83- Hag11_fw 1:10 with 1µl primer and 9µl water
Flo86- Hag12_rv 1:10 with 1µl primer and 9µl water

	Pre-mix 1 (µL)	Pre-mix 2 (µL)
piGEM-016 pMAD-cup1-1 40ng/µL	10	10
Flo83- Hag11_fw	2	-
Flo86- Hag12_rv	-	2
Total Volume	12	12

Label	Pre-mix 1	Primer
AGB0023375	Pre-mix 1	Flo83 – Hag11_fw
AGB0023374	Pre-mix 1	Flo86 - Hag12_rv

13.62 Checking Bacillus Trafo Wildtype 3610

Aim: check if wildtype has a resistance against chloramphenicol or if the plates are not effective/ made wrong

Result: Bacillus subtilis Wildtype 3610 grew on the chloramphenicol plate which shows us that there has to be a mistake in making the LB-chloramphenicol plates or the WT has a resistance.

New plates were made with new chloramphenicol-stocks with 25 mg/ml and 5 mg/ml.

3 aliquots of competent B.s. WT3610 were plated on new LB-chloramphenicol plates and incubated at 37°C.

18.5 SpeI restriction pEX-A2-DARPin & pMAD-hag-flank (piGEM-005)

Aim: Receiving iGEM-005 as linearized vector for cloning the DARPin gene with SpeI sites into pMAD-fla (iGEM-005)

Restriction	pEX-A2-DARPin digest (µl)	pMAD-Hag-Flank digest (µl)	Spe1-Mastermix
pEX-A2+DARPin (398 µg/µL)	15 = ca. 6µg	-	-
pMAD-Fla (114 µg/µL)	-	10= ca. 1,14 µg	-
SpeI	-	-	1,5
CutSmart-Buffer (10x)	-	-	2
H2O	-	-	16,5
Mastermix	5	10	-
Total	20	20	20

Incubation at 37°C for 2h and heat shock at 81°C for 5 min. After that the pMAD-hag-flank-construct was purified with the OMEGA gel extraction kit according to the protocol.

c(digested piGEM-005)= 4 ng/µl

13.62 Checking Bacillus Trafo Wildtype 3610

Aim: check if wildtype has a resistance against chloramphenicol or if the plates are not effective/ made wrong

Result: Bacillus subtilis Wildtype 3610 grew on the chloramphenicol plate. We have already repeated making plates so it might be that the WT has got a resistance while making it competent. A new WT was plated on 2 chloramphenicol plates with 5 µg/mL (old and new one) and 2x LB plates from gly stocks.

Incubation at 37°C overnight.

05.06.2014

14.39 Creating PheA-Arc1p-C-0x

Aim: Using Round-the-horn mutagenesis to create PheA-Arc1p-C-0x-pET28a

The PCR with 5' phosphorylated TG_0xGSSG FP und TG_0xGSSG RP should generate the 7491 bp fragment for ligation from the methylated template PheA-Arc1p-C-8x-pET28a from 14.5.

The used Primer concentration was 1 µM, the concentration of the template was 1 ng/µL and we used a hot start to avoid unspecific annealing of primers.

Content	Volume [µL]
Water	29.5
5x GC Buffer	10
DMSO	2.5
TG_0xGSSG FP	2.5
TG_0xGSSG RP	2.5
PheA-Arc1p-C-8x-pET28a	1
dNTPs	1
Phusion-Polymerase	1
Total Volume	50

Step	Temperature [°C]	Time [min:sec]
1	98	2:00
2	add Polymerase
3	98	0:10
4	67.5	0:30
5	72	4:00
6	go to 3	32x
7	72	10:00
8	4	hold

The amplified fragment was purified on an agarose gel on which it showed the correct size. The extracted linear template was then digested to degrade the original unmutated plasmid using DpnI.

Content	Volume [µL]
10x CutSmart Buffer	3.6
Plasmid	30
DpnI	3
Total Volume	36.6

The reaction mixture was incubated at 37 °C and 300 rpm for 1 h and afterwards heated to 80 °C for 20 min.

In order to create the circular plasmid 100 ng of the linear template were mixed with 1 µL 10x T4-Ligasebuffer, 1 µL T4-Ligase and water to give a total volume of 10 µL. This mixture was incubated for 9 h at 16 °C. The resulting plasmid was dialysed with water to decrease the salt concentration for the following transformation of E. coli Top10 electrocompetent cells with the plasmid.

06.06.2014

19. Crystallization of flagellin

In order to crystallize flagellin with a domain it is necessary to produce the protein by E. coli in a high concentration. For that aim the Fla-construct will be amplified out of pET24d which includes a domain. For elimination of the flanks a PCR has to be performed which just amplifies hag with domain and creates NcoI and BamHI restriction sites. After purification and digest with Nco/Bam the fragment can be ligated into digested pET24d . After transformation the production can be induced by IPTG.

19.1 Elimination of flanks from fla-construct including cup1-1 from pET24d

Aim: Preparation for using pET24d as expression vector for flagellin

The flagellin construct was amplified with specifically designed primers (95 and 54 from Florian Altegoer), which allow the amplification of the construct with cup1-1 without flanks (just Hag) including NcoI & BamHI restriction sites.
Template dilution 1:10:
1 µL pET24d-cup1-1 was mixed with 9 µL to an 1:10 dilution of 16,3 ng/µL
Primer dilution 1:10:
The primers were diluted 1:10 by mixing 10 µL of primers with 90 µL millipore water each.

Mix [µl]	reaction with phusion	reaction with Q5 mastermix
pET24d-cup1-1 1:10 dilution	1	1
Primer 54Flo	1	1
Primer 56Flo	1	1
Phusion	1	-
Phusion Buffer 5x	10	-
dNTP Mix	1	-
Water	35	22
Q5 Mastermix	-	25
Total Volume	50	20

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	2 min
5	Go To 2	30x
6	72	4min
7	8	infinite

The PCR was run over night.

19.2 Restriction digest of pET24d with NcoI and BamHI

Aim: Creating Nco/Bam restriction sites in pET24d for cloning PCR fragments amplified with primers flo56 and flo54 which contain these sites as well.

Isolated pET24d was cut with NcoI and BamHI in order to create restriction sites for ligating the Flagellin/ Hag-Domain fragments into the vector. The Hag-fragments which were amplified via PCR with primers flo54 and 56 contain NcoI/ BamHI restriction sites for that purpose as well.

Component	Volume [µl]
pET24d (148 ng/µL)	7
CutSmart 10x	2
NcoI	0,5
BamHI	0,5
Water	10
Total Volume	20

Incubation for 1 hour at 37°C and heat shocked at 80°C.

15.52 Miniprep of different plasmids

Aim: Receiving more plasmid DNA for further experiments

Colonies were picked from plates and 8ml LB with necessary antibiotics each inoculated, followed by incubation at 37°C overnight.

Clones were picked from plates with plasmids:

pET24d-Fla-Cup1-1 (piGEM-006)
pMAD-Hag-Flank (piGEM-005)
pMAD-Hag-Flank -Cup1-1 (piGEM-016)
pEX-A2+DARPin (piGEM-017)

07.062014

15.53 Sequencing pMAD-fla-cup1-1

The sequencing showed the correct insertion of the cup-1-1 gene into the hag-flank construct but contained a stop codon, which was not removed by the used reverse primer. Unfortunately we used primers for amplification of the whole cup1-1 gene and not just for the truncated gene coding for the metallothionein domain only. Therefore new primers had to be designed an the Gibson assembly for integration of the metallothionein domain into pMAD and pET24d has to be repeated.

18.6 gel extraction & purification of DARPin gene

Aim: Receiving DARPin gene with SpeI sites for ligation into linearized piGEM-005

The with SpeI digested pEX-A2 was purified via electrophoresis with an 1% agarose gel in order to divide pEX-A2 backbone and the DARPin gene (489 bp). The digest attempt was splitted and loaded into two pockets to be sure not to overload the gel. The correct bands were cut out and the DNA fragment was rescued according to the protocol of our OMEGA gel extraction kit.

Expected bands:
DARPin gene: 489 bp
pEX-A2 backbone: 1961bp
The concentration after gel extraction: 9 ng/µl

18.7 Ligation of DARPin gene and linearized piGEM-005

Aim: Ligation of DARPin- (from 18.6) into Spe1 digested piGEM-005 from 18.5 for integration of the DARPin-Flagellin construct into Bacillus subtilis chromosome

The DARPin gene with SpeI sites was used as insert for the ligation into linearized pMAD (from 18.5) which contains the designed restriction site. The ligation attempt was done twofold and calculated by the Ligation Calculator from the iGEM-Team Texas in 2011:

Component	Volume [µl]
Insert (DARPin, c= 9 ng/µL)	2
Vector (piGEM-005, c=4ng/µL)	10
Ligase-Buffer 10x	2
T4 Ligase	1
Milipore water	5
Total Volume	20

Incubation was performed overnight at room temperature.

13.63 checking Bacillus WT 3610 growth on 5µg/µL CM

Aim: check if wildtype has a resistance against chloramphenicol (CM)

Result: Bacillus subtilis Wildtype 3610 grew on the CM plate.

In order to make out if a selection is possible WT3610 was plated out from an LB plate (13.62) on 25 ng/ µL CM to check were the threshold of CM for B. subtilis is.

Incubation at 30°C over two days.

08.06.2014

18.8 new SpeI restriction of DARPin-gene in pEX-A2 & pMAD-hag-flank (piGEM-005)

Aim: Receiving new insert and vector in case of an unsuccessful ligation for further attempts.

Restriction	pEX-A2-DARPin digest (µl)	pMAD-Hag-Flank digest (µl)	SpeI-Mastermix
pEX-A2+DARPin (398 µg/µL)	10 = ca. 4µg	-	-
pMAD-Fla (150 µg/µL)	-	7= ca. 1 µg	-
SpeI	-	-	1
CutSmart-Buffer (10x)	-	-	2,5
Water	-	-	21,5
Mastermix	10	13	-
Total Volume	20	20	25

Incubation was performed for 2 h at 37°C and heat inactivated at 80°C for 5 minutes.

18.9 Transformation of ligation from 18.7

The whole 20µL attempt from the ligations were used to transform E.Coli XL1-Blue, which were plated on LB-Amp plates. Additionally a negative control was created by transforming E.Coli XL1-Blue with 1 µL SpeI cut piGEM-005 as well.

18.10 Gel extraction for isolation of DARPin gene out of pEX-A2

Aim: Receiving new insert in case of an unsuccessful ligation for further attempts like in 18.6

The SpeI digested pEX-A2 was purified via electrophoresis with an 1% agarose gel like in 18.6. The correct bands were cut out and the DNA fragment was purified according to the protocol of our OMEGA gel extraction kit.

Expected bands:
DARPin gene: 489 bp
pEX-A2 backbone: 1961bp
The concentration after gel extraction: 10 ng/µl

09.06.2014

18.12 Checking transformation of overnight ligation from 18.7

Plate	Amount of colonies
Negative control	6
Ligation attempt 1	7
Ligation attempt 2	0

18.13 Checking success of ligation via cPCR

Aim: A cPCR with the primers 54 and 56 shows the success of ligation by amplification of the Hag-construct.

In order to check the positive insertion of the DARPin gene into pMAD a PCR amplification with primers 54 and 56 for the flagellin should generate an ca. 1500 bp fragment on the gel. Negative clones would just show a 1000 bp band because of the amplification of the Hag-SpeI site construct. The picked clones were transferred on a new LB-amp plate.

Mix	Master-Mix for 7 attempts (µL)	Mix for PCR attempt (µL)
Colony	-	part of a colony
Primer Flo 54	3,5	-
Primer Flo 56	3,5	-
Phusion	7	-
Phusion Buffer 5x	28	-
dNTP Mix	3,5	-
Water	94,5	-
Mastermix	-	20
Total Volume	140	20

Expected bands:
Hag-DARPin-construct: ca. 1500 bp

The gel shows bands at 1000 which means that the clones contain just relegated pMAD vector and are all negative. The ligation had to be repeated.

18.14 Dephosphorylation of linearized piGEM-005

Aim: Dephosphorylation of 5'-end with antarctic phosphatase in order to decrease the religation of the linearized piGEM-005 from 18.8

The cut SpeI cut piGEM-005 was dephosporylated at the 5'-end with antarctic phosphatase to prevent the vector from relegation.

Component	Volume [µl]
Vector (piGEM-005, c=148 ng/µL)	20 (=ca. 2 µg)
Antarctic phos.-Buffer 10x	3
Antarctic phosphatase	1
Milipore Water	6
Total Volume	30

The sample was incubated for 1 h at 37°C at heat inactivated at 70°C for 10 minutes.

18. new ligation of linearized/ dephosphorylized piGEM-005 & DARPin gene

Aim: Dephosphorylation piGEM-005 was ligated with extracted DARPin gene again

Because of the negative colony PCR from 18.13 a new ligation with dephosphorylized piGEM-005 from 18.14 and new extracted DARPin gene from 18.10 was performed in 2 attempts.

Component	Volume [µl]
Insert (DARPin, c= 10 ng/µL)	12,4
Vector (piGEM-005, c= 148 ng/µL)	4,6
Ligase-Buffer 10x	2
T4 Ligase	1
Milipore Water	5
Total Volume	20

Incubation 3h at room temperature

18.16 Transformation of overnight ligation from 18.15

The whole 20 µL reaction of the ligations (18.15) were used to transform E. coli XL1-Blue and plated on LB-Amp plates. Additionally a negative control was created by transforming E.Coli XL1-Blue with 1µL SpeI digested piGEM-005 as well.

13.64 checking Bacillus WT 3610 growth on 5, 10 & 15 µg/µL CM

Aim: check if wildtype has a resistance against CM

Result: Bacillus subtilis Wildtype 3610 did not grow on the 25 ng/µl CM plate

In order to check at which concentration CM Bacillus cannot survive he was plated out from an LB plate on LB-CM plates with different CM concentrations (5, 10, 15 ng/mL).

Incubation at 30°C over night.

10.06.2014

18.17 Checking Transformation of ligation from 18.16

Plate	Amount of colonies
Negative control	1
Ligation attempt 1	2
Ligation attempt 2	>80

18.18 Checking success of ligation via cPCR

Aim: A cPCR with the primers 54 and 56 shows the success of ligation by amplification of the Hag-construct.

In order to check the positive insertion of the DARPin gene into pMAD a PCR amplification with primers 54 and 56 for the flagellin should generate an ca. 1500 bp fragment on the gel. Negative clones would show still just a 1000 bp band because of the amplification of the Hag-Spe1 site construct. The picked clones were transferred on a new LB-amp plate. 12 clones were picked.

Mix	Master-Mix for 14 attempts (µL)	Mix for PCR attempt (µL)
Colony	-	part of a colony
Primer Flo 54	7	-
Primer Flo 56	7	-
Phusion	14	-
Phusion Buffer 5x	56	-
dNTP Mix	7	-
Water	189	-
Mastermix	-	20
Total Volume	280	20

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	1min 45sec
4	72	1 min
5	Go To 2	30x
6	72	4min
7	8	infinite

Expected bands:
Hag-DARPin-construct: ca. 1500 bp

Clone 1, 2, 3, 4, 5, 7, 9, 11 and 12 were the positive clones at 1500 bp.

14.40 Overnight culture

Aim: Amplify Plasmid in an overnight culture

Six clones of the transformed E. coli Top10 cells from 14.39 were picked and used to inoculate overnight cultures (6 x 5 mL).

18.19 Miniprep of positive clones

Aim: In order to check the orientation of the insert in the vector of the positive clones minipreps were inoculated for further experiments

Because of the ligation via two SpeI sites, the chance is 50:50 that the clones contain the pMAD-Hag-Flank-DARPin construct in the right orientation (Startcodon on the Hag1-site). For test digests a higher amount of plasmid is needed, which is achieved by inoculation of minipreps.

The clones were used to inoculate 7 mL LB-Amp and incubated at 37°C over night.

13.64 checking Bacillus subtilis WT 3610 growth on 25 & 35 µg/µL CM

Aim: check if wildtype has a resistance against CM

Result: Bacillus subtilis Wildtype 3610 grew on the 5, 10 & 15µg/µl LB-CM plate.

We saw that the Bacillus grew on almost every CM concentrations except 25 µg/µL. So we transformed competent WT3610 with Nose plasmid piGEM-003 as a positive control and plated them out on LB-CM with 25 µg/µL and 35 µg/µL.

Additionally, competent wildtype 3610 cells were transformed with piGEM-004 and plated out on LB-CM with 5, 10 and 15 µg/mL CM to check, if these cells can be selected better.

Incubation at 30°C for 2 days.

11.06.2014

18.19 Miniprep of positive clones

The concentration of the isolated plasmids was between 100 and 150 ng/µL.

18.20 Test digest with EcoRV

Aim: Checking the right orientation of the insert in the isolated plasmids

The plasmids from the positive clones were digested with EcoRV so that specific fragments emerge when cutting into the DARPin gene and the vector backbone.

Component	Volume [µl]	Mastermix for 10 attempts [µl]
Plasmid of clone	2 (ca. 200ng)	-
Cutsmart 10x	-	8
EcoRV	-	1
Millipore water	-	71
Mastermix	8	-
Total Volume	10	80

Right orientation: 7900 – 1570 – 2500 – 55
Wrong orientation: 7900 – 1170 – 2500 – 460

Clone 1, 2, 3, 4, 7, 9 and 11 have the right orientation.

20.1 inoculation of preculture from Bacillus subtilis WT 3610

Aim: Preparation of for mainculture the next day

2 x 6 mL of LB were inoculated with Bacillus subtilis WT3610 from an LB plate and incubated at 37°C overnight.

14.41 Preparation of plasmids

Aim: Purify the amplified plasmids from overnight cultures

The plasmids were purified from the overnight cultures created in 14.40 using Sigma GenElute Plasmid Miniprep Kit following the included protocol. The plasmids were eluted using 45 µL water.

12.06.2014

18.21 PCR with pMAD-Hag-Flank-DARPin (piGEM-019) and piGEM-005

Aim: Amplification of Hag-SpeI-construct and Hag-DARPin construct with NcoI/BamHI sites for cloning into pET24d → crystallization of domains.

The templates (piGEM-005, prepped pasmid from clone 7 & 12 ) were diluted 1:10. piGEM-005 should function as a negative control. Clone 12 was picked in case the second orientation could be used for different experiments. 5 µL PCR product + 1 µL loading dye were analysed on an 1% agarose gel.

Mix	Volume
Template 1:10	1
Primer Flo 54	1
Primer Flo 56	1
Phusion DNA-polymerase	1
Phusion Buffer 5x	10
dNTP Mix	1
Water	35
Total Volume	50

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	1min 45sec
4	72	2 min
5	Go To 2	30x
6	72	4min
7	8	infinite

Expected bands:
clone 7 & 12 PCR product at ca. 1500bp – piGEM-005 PCR product at 1kb

14.42 Transformation of BL21 cells

Aim: Transform E. coli BL21(DE3) with PheA-Arc1p-C-0x-pET28a

40 µL E. coli BL21(DE3) electrocompetent cells were transformed with 1 ng of the previously purified plasmid PheA-Arc1p-C-0x-pET28a from two different clones, incubated for 1 h at 37 °C and plated out on LB-Kan⁵⁰ plates that were incubated overnight at 37 °C.

18.22 restriction digest of Hag PCR fragments from 18.21 with NcoI/BamHI

Aim: creating restriction sites for cloning into pET24d cut with NcoI/BamHI

The PCR products from 18.21 were digested with NcoI and BamHI to create restriction sites in order to ligate the fragments into NcoI/BamHI cut pET24d.

Component	Volume [µl]
PCR products	45
Cutsmart 10x	5,2
NcoI	1
BamHI	1
Water	2,8
Total Volume	52

Incubation for 2 hours at 37°C with heat shock at 80°C.

18.23 Ligation of pET24d and Hag PCR fragments from 18.22 cut with NcoI/BamHI

Aim: cloning inserts into pET24d for crystallization

The NcoI/BamHI digested flagellin PCR products from 18.22 (from clone 7 and piGEM-005) were ligated with NcoI/BamHI digested pET24d.

Component	Pet-Hag attempt (µL)	Pet-Hag-DARPin attempt (µL)
Insert (PCR fragments , c= ca. 400 ng/µL)	2	2
Vector (pet24d, c= 50ng/µL)	5	5
Ligase-Buffer 10x	2	2
T4 Ligase	1	1
Millipore Water	10	10
Total Volume	20	20

Incubation over night at room temperature.

20.2 Transformation of competent Bacillus subtilis

Aim: transformation of Bacillus subtilis WT3610 with piGEM005 and piGEM018

100 µL of overnight culture were added to 10 mL of MNGE-Medium and incubated to an OD₆₀₀ of 1,1-1,3 at 37°C which could take 4-5 hours.

After reaching an OD of 1,1-1,3 2 x 400 µL of the culture were transformed with 1,5 µg piGEM-005 and -018. After one hour incubation at 37°C 100 µL expression mix were added and incubated for one hour as well.

In the end the 500 µL sample was plated out on MLS-X-Gal plates and incubated at 30 °C until colonies could be seen.

13.06.2014

18.24 Transformation of ligation

Aim: checking success of ligation and amplification of ligated construct

The whole 20 µL attempt was used to transform E. coli X1-Blue, plated out on LB-Can plates and incubated at 37°C overnight.

18.25 Miniprep of pMAD-Hag-Flank-DARPin (piGEM-018)

Aim: increase amount of plasmid for work and storage

2 x 6 mL of LB-Amp were inoculated with a colony from a piGEM-018 transformation plate and incubated at 37°C overnight.

18.26 Sequencing of constructs

Aim: checking the right insertion into the plasmids

pMAD-Hag-Flank-DARPin was sent in form of a premix with primers for sequencing. 10 µL with 50-100 ng/µL were mixed with 2 µL of primers for sequencing according to the following scheme:

Premix	Label-Nr.	Construct	Primer
1	391	pMAD-Hag-Flank-DARPin	Flo54 (Hag-F-Nco)
2	392	pMAD-Hag-Flank-DARPin	Flo56 (Hag-R-Bam)

13.65 Checking growth of Bacillus subtilis WT3610

Aim: check which WT can be used for selection with Nose plasmids

Competent 3610 were transformed with piGEM-002, -003 and -004 by incubating the aliquots with 5 µL plasmid for 30 min at 37°C. After half an hour the whole sample was plated out on LB-Cm (5 ng/µL).

Incubation at 30°C for 2 days.

14.06.2014

18.27 miniprep of plasmids from 18.25

Aim: isolation of plasmids

The miniprep of pMAD-Hag-Flank-DARPin was done according to the protocol of the OMEGA DNA kit.

18.28 pET24d digest with Nco/Bam

Aim: preparing vector for new ligation attempts

Because of the unsuccessful ligation from 18.23 new vector (pET24d) was digested with NcoI and BamHI according to the following scheme:

Component	Volume [µl]
pET24d (148 ng/µL)	15
Cutsmart 10x	3
NcoI	0,5
BamHI	0,5
Water	6
Total Volume	30

Incubation at 37°C for 2h.

18.29 PstI digestion of PCR fragments from piGEM-018 with Hag-primers

Aim: check if the correct inserts are used for ligation

The DARPin-Hag constructs contain a PstI restriction site which could be used to check if the DARPin gene was inserted into the Hag-construct correctly again. For that purpose PCR products based on piGEM-018 from clone 7 and 12 (right and wrong orientation) as a template were digested with PstI.

PCR products from clone 7: 658 bp and 781 bp fragment.

PCR products from clone 12: 1000bp and 429 bp fragments.

Component	Volume [µl]
PCR fragment (350 ng/µL)	3
Cutsmart 10x	1
PstI	0,5
Water	5,5
Total Volume	10

Incubation at 37°C for 2h.

18.30 PCR amplification of DARPin-Hag and Hag fragment

Aim: amplification of DARPin-Hag fragments for repeating the ligation

piGEM-018 & -005 were used as template for a PCR with the primers 54flo and 56flo. The products could be used for further cloning after NcoI/BamHI digest.

Mix	Volume
Template (piGEM-005 & -018)	1
Primer Flo 54	1
Primer Flo 56	1
Phusion	1
Phusion Buffer 5x	10
dNTP Mix	1
Water	35
Total Volume	50

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	1min 45sec
4	72	2 min
5	Go To 2	30x
6	72	4min
7	8	infinite

The fragments were analysed on an 1% agarose gel.

15.54 new PCR amplification of cup1-1

Aim: amplification of cup1-1 domain for Gibson assembly with pMAD

The cup1-1 domain was amplified via PCR with new primers iGEM-024 and -025. The fragment should be ca. 160 bp.

Mix	Volume
Template (cup1-1 gene)	1
Primer iGEM-024	1
Primer iGEM-025	1
Phusion DNA-polymerase	1
Phusion Buffer 5x	10
dNTP Mix	1
Water	35
Total Volume	50

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	30 sec
5	Go To 2	30x
6	72	4min
7	8	infinite

According to the gel analysis the amplification was successful.

15.06.2014

20.3 Overnight culture of positive clones

Aim: transformation of Bacillus subtilis WT3610 with plasmid

Colonies grew on the transformand plates (piGEM-005 & - 018). The blue/ white screening showed positive transformed blue clones. Three clones per plate were picked and used for inoculation of LB-MLS (4 mL LB, 4 µL lincomycin, 4 µL erythromycin). Incubation was carried out over night at 30°C with the six cultures.

16.06.2014

14.43 Overnight culture

Aim: Inoculate Overnight culture of PheA-Arc1p-C-0x-pET28a

5 mL of LB-Kan⁵⁰ medium were inoculated with a clone from 14.42 bearing the PheA-Arc1p-C-0x-pET28a plasmid.

17.06.2014

20.3 First temperature shift

Aim: integration of pMAD-Insert into Bacillus chromosome via flanks

The 6 overnight cultures were used to inoculate 10 mL LB MLS, which were incubated until the culture obtained an OD of 0,1. The cultures were incubated at 30°C for 2h.

Subsequently, the temperature was shifted to 42°C for 6h.

After the heat shock dilutions from 10^-4 to 10^-6 of each culture were plated out on MLS-X-Gal so that 18 plates could be incubated overnight at 42°C.

15.54 Gibson-assembly with PCR amplified cup1-1 and SpeI digested piGEM-005

Aim: insertion of cup1-1 into piGEM-005

The cup1-1 domain was amplified via PCR with new primers iGEM-024 and -025. Vector and template were diluted to a concentration under 75 ng/µL. Spe1 cut piGEM-005 was used from the cloning experiments with DARPin.

PCR fragment cup1-1 (464 ng/µL) dilution 1:10

SpeI digested pIGEM-005 (148 ng/µL) dilution 1:2

Component	Volume [µl]
Gibson-Mix	15
Insert (cup1-1 58 ng/µL)	1,3
piGEM-005	1
Water	2,7
Total Volume	20

The mix was incubated 5 min at room temperature and then for 1h at 50°C.

In the end the whole mix was transformed into E.Coli XL1-Blue and plated out on LB-Amp. Incubation was done overnight at 37°C.

14.44 Test Expression

Aim: Test the expression of PheA-Arc1p-C-0x

Using the preculture from 14.43 60 mL of LB-Kan⁵⁰ medium were inoculated with 600 µL of the preculture and incubated at 37 °C and 220 rpm until OD₆₀₀ reached 0.5. The culture was cooled down to 18 °C and the protein production was induced with 12 µL of 500 mM IPTG. Over night the culture was incubated at 18 °C and 220 rpm. Afterwards the cell culture was centrifuged (17000 rpm, 20 min, 4 °C), the pellet resuspended in 3 mL buffer A and stored at -20 °C. A glycerolstock of the strain containing the PheA-Arc1p-C-0x-pET28a plasmid was stored at -80 °C.

18.06.2014

20.4 Second temperature shift

Aim: flip out of the pMAD backbone

One blue colony per diluted clone was used to inoculate 4 mL LB. The 6 cultures were incubated at 30°C for 6h and afterwards for 3h at 42°C.

Dilutions from 10^-4 to 10^-4 were plated out on 18 X-Gal plates without MLS selection. The positive clones should not contain the resistance inside the backbone as well as the galactosidase, resulting in normal colored colonies. The plates were incubated at 42°C overnight.

15.54 Checking Gibson assembly plate piGEM-005-cup1-1

Aim: insertion of cup1-1 into piGEM-005

Unfortunately the plate was empty: no colonies. The vector was digested again in order to repeat the assembly.

15.55 restriction digest of piGEM-005 with SpeI

Aim: linearizing plasmid for repeating the Gibson assembly

In order to repeat the Gibson assembly the piGEM-005 was cut with SpeI again.

Component	Volume [µl]
piGEM-005 (108 ng/µL)	10
Cutsmart 10x	2
SpeI	0,5
Water	7,5
Total Volume	20

Incubation 1h at 37°C with following heat shock at 80°C

19.06.2014

20.5 Selection of positive clones

Aim: check the correct excision of the pMAD backbone

One white clone was picked from the dilution plates and transferred on a X-Gal Plate as well as on a MLS plate so that 18 clones were tested for the right integration of the insert although flipping out the pMAD backbone.

The plates were incubated at 42°C over night.

15.56 new Gibson-assembly with cup1-1 and SpeI digested piGEM-005

Aim: insertion of cup1-1 into piGEM-005

As insert cup1-1 PCR product from 15.55 and SpeI digested piGEM-005 from 15.55 were used for a new Gibson assembly.

PCR fragment cup1-1 (464 ng/µL)

SpeI digested pIGEM-005 (53 ng/µL)

Component	Volume [µl]
Gibson-Mix	15
Insert (cup1-1 58 ng/µL)	2,5
piGEM-005	2,5
Total Volume	20

The mix was incubated 5 min at room temperature and then for 1h at 50°C.

In the end the whole mix was used to transform E. coli XL1-Blue and plated out on LB-Amp. Incubation was done overnight at 37°C.

20.06.2014

20.5 selection of positive clones

Aim: checking the correct flip out of the pMAD backbone

The white colonies grew on the X-Gal Master plates but not on MLS plates so the transformation seemed to be successful. The Backbone with the MLS resistance flipped out of the genome.

20.6a cPCR with checked clones

Aim: checking integration of constructs Hag-Spe and Hag-Spe-DARPin into B. s. genome

No clone was growing on MLS plates so the picked clones seemed to be positive. In order to check the correct integration of the domain constructs, a cPCR with the picked clones on the X-Gal plates was done. The 18 picked B.subtilis clones were cooked in 10 µL PBS for 5 min at 95°C.

Mix	Master-Mix for 18 attempts (µL)	Mix for PCR attempt (µL)
Colony (picked clones 1-9 from Flagellin/-DARPin B.s. plates)	-	Part of a cooked colony
Primer Flo54 Hag-fw	9	-
Primer Flo56 Hag-rv	9	-
Phusion	18	-
Phusion Buffer 5x	72	-
dNTP Mix	9	-
Water	237	-
DMSO	6	-
Mastermix	-	20
Total Volume	100	360

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	1 min 45 sec
4	72	2 min
5	Go To 2	30x
6	72	4min
7	8	infinite

The gel showed no bands. The PCR had to be repeated.

15.57 Miniprep of clones from Gibson assembly from 15.56

Aim: increase the amount of plasmid for further experiments

4 x 5 mL of LB-Amp was were inoculated with a picked colony from a transformation plate with XL1-Blue containing the Gibson-assembly product from 15.56.

Incubation at 37°C overnight.

21.06.2014

15.58 cPCR with colonies from Gibson-assembly of piGEM-005 + cup1-1 plate

Aim: checking correct insertion of cup1-1

In order to check the correct insertion of the cup1-1 domain into the Hag-Flank-construct in pMAD a cPCR with primers iGEM-025 (Cup1-1 rv) and Flo89 (pMAD-flank1-BamHI fw) was performed. The picked colonies were the same which were used to inoculate minipreps from 15.57. The fragment was supposed to have approx. 1250 bp.

Mix	Master-Mix for 5 attempts (µL)	Mix for PCR attempt (µL)
Colony (picked clones 1-4 for miniprep)	-	Part of a colony
Primer Flo89	2,5	-
Primer piGEM-025	2,5	-
Phusion DNA-polymerase	2,5	-
Phusion Buffer 5x	20	-
dNTP Mix	2,5	-
Water	70	-
Mastermix	-	20
Total Volume	100	20

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	1 min 30 sec
5	Go To 2	30x
6	72	4min
7	8	infinite

The analysis via 1% agarose gel eletrophoresis showed now bands. The plasmids of all four clones were isolated to use them as template.

15.59 PCR with isolated plasmid from Gibson piGEM-005 + cup1-1 plate

Aim: checking correct insertion of cup1-1

This time the isolated plasmid DNA from the picked six clones was used as a template with different primer pairs. First of all the PCR reactions were performed with primers Flo89 and Flo90 in order to receive the whole Hag-Flank-Cup1-1 construct with ca. 2100 bp length. As negative control also piGEM-005 was used as template producing a 2000kb fragment. Because of the small difference, all six reactions were also performed with the primers Flo89 and iGEM-025 (cup1-1 rv) in order to check the insertion of cup1-1 directly with a fragment of 1268 bp.

Mix	Master-Mix 1 for 5 reactions (µL)	Master-Mix 2 for 5 reactions (µL)	Mix 1 for PCR reactions (µL)	Mix 2for PCR reactions (µL)
Plasmid DNA from clone 1-4/ piGEM-005	-	-	1	-
Primer Flo89	2,5	2,5	-	-
Primer Flo90	2,5	-	-	-
Primer piGEM-025	-	2,5	-	-
Phusion DNA-polymerase	2,5	2,5	-	-
Phusion Buffer 5x	20	20	-	-
dNTP-mix	2,5	2,5	-	-
Water	70	70	-	-
Master-Mix 1/ 2	-	-	20	20
Total Volume	100	100	20	20

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	20 sec
5	Go To 2	30x
6	72	4min
7	8	infinite

The gel analysis shows that all 4 clones seem to be positive. An amplification of the cup1-1 fragment with the plasmid DNA as template could proof that.

20.6b Repeated cPCR with checked clones

Aim: checking integration of constructs Hag-SpeI and Hag-SpeI-DARPin into B. s. genome

Because of the unsuccessful cPCR before, the PCR was repeated. The 18 picked B.subtilis clones were cooked in 30 µL PBS for 10 min at 95°C.

Mix	Master-Mix for 18 attempts (µL)	Mix for PCR attempt (µL)
Colony (picked clones 1-9 from Flagellin/-DARPin B.s. plates)	-	Part of a cooked colony
Primer Flo54 Hag-fw	9	-
Primer Flo56 Hag-rv	9	-
Phusion DNA-polymerase	18	-
Phusion Buffer 5x	72	-
dNTP Mix	9	-
Water	237	-
DMSO	6	-
Mastermix	-	20
Total Volume	100	360

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	1 min 45 sec
4	72	2 min
5	Go To 2	30x
6	72	4min
7	8	infinite

All nine clones with piGEM-005 seem to be positive. Clone 1, 3, 7, 8 and 9 of transformed piGEM-018.1 might be positive as well as clone 2-6 from piGEM-018.2. The sequencing of the PCR products should tell us if the insertion was successful.

22.06.2014

18.31 PCR amplification of DARPin-Hag and Hag fragment

Aim: amplification of DARPin-Hag fragments for repeating the ligation

piGEM-018 & -005 were used as template for a PCR with the primers Flo 54 and Flo 56. The products could be used for further cloning after NcoI/BamHI digest.

Content	Volume [µl]
Template (piGEM-005 & -018)	1
Primer Flo 54	1
Primer Flo 56	1
Phusion	1
Phusion Buffer 5x	10
dNTP Mix	1
Water	35
Total Volume	50

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	1 min 45 sec
5	Go To 2	30x
6	72	4min
7	8	infinite

18.32 cPCR with new clones

Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pET24d

More clones from each plate were picked to analyse them via cPCR with the primers flo54 and flo56 (Hag-fw and Hag-rv). The result should be a ca. 1kb fragment for correct pET24d-Hag containing clones and a 1,5 kb fragment for pET24d-Hag-DARPin containing clones.

Content	Volume (µL)	MM for 14 attempts (µL
Colony (8-15 from pet-Hag,7-14 from pet-Hag-DARPin)	1 colony	-
Primer Flo 54	-	7
Primer Flo 56	-	7
Phusion DNA-polymerase	-	7
Phusion Buffer 5x	-	56
dNTP Mix	-	7
Water	-	196
Mastermix	20	-
Total Volume	20	280

Step	Temperature °C	Time
1	98	10 min
2	98	30 sec
3	55	30 sec
4	72	1 min 45 sec
5	Go To 2	35x
6	72	4min
7	8	infinite

Clone 1 from each pET24d-Hag-SpeI and pET24d-Hag-DARPin clones was positive and were digested with NcoI/BamI to check them again.

18.33 pET24d digest with NcoI/BamHI

Aim: preparing vector for new ligation attempts

Because of the low amount of right clones, new vector (pET24d) was digested with NcoI and BamHI according to the following scheme:

Component	Volume (µL)
pET24d (50 ng/µL)	20
CutSmart 10x	3
NcoI	0,5
BamHI	0,5
Water	6
Total Volume	30

Incubation at 37°C for 2 hours with heat shock in the end at 80°C

Endconcentration: 32 ng/µL

18.34 Restriction digest of Hag PCR fragments from 18.31 with NcoI/BamHI

Aim: creating restriction sites for cloning into pet24d cut with NcoI/BamHI

The PCR products from 18.31 were digested with NcoI andBamHI to create restriction sites in order to ligate the fragments into NcoI/BamHI digested pet24d in case of negative clones refering to the cPCR from 18.x

Component	PCR Hag-fragment (µL)	PCR Hag-DARPin fragment (µL)
PCR products	45	45
Cutsmart 10x	5,2	5,2
NcoI	0,5	0,5
BamHI	0,5	0,5
Water	3,8	3,8
Total Volume	52	52

Incubation for 2h at 37°C with heat shock at 80°C.

Endconcentration:
digested Hag-fragment 260 ng/µL
digested Hag-fragment 268 ng/µL

15.60 PCR pMAD-Hag-Flank-cup1-1 (piGEM-016)

Aim: checking success of Gibson assembly with pMAD-Hag-Flank and cup1-1

Using the plasmids as template the cup1-1 fragment at 160 bp should be visible on the agarose gel. As positive control PCR products from the cup1-1 amplification used for the Gibson Assembly into piGEM-005 were applied to the gel as well.

Content	Volume (µL)	MM for 5 attempts (µL)
Template (Plasmid from clone 1-4)	0,5	-
Primer iGEM-024	-	2,5
Primer iGEM-025	-	2,5
Phusion DNA-polymerase	-	2,5
Phusion Buffer 5x	-	20
dNTP Mix	-	2,5
Water	-	70
Mastermix	19,5	-
Total Volume	20	100

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	20 sec
5	Go To 2	35x
6	72	4min
7	8	infinite

The bands under the 200 bp mark indicate the positive insertion of cup1-1 into piGEM-005. The plasmid has to be sequenced and is named iGEM-016.

18.35 Test digest with NcoI/BamHI - Checking insertion of Hag/-DARPin into pet24d

Aim: proving insertion of Hag/-DARPin fragment into pET24d

The plasmids are digested with NcoI and BamHI. In case of a correct insertion the pET24d backbone and the insert should be seen on the gel at 5300 bp and 1000/ 1500 bp. As control pET24d-Hag-Flank (piGEM-001) is used to check the mastermix.

Component	Volume (µl)	Mastermix
2x Plasmid from clone 6	5	-
CutSmart 10x	-	5
NcoI	-	0,5
BamHI	-	0,5
Water	-	19
Total Volume	10	25

The used marker was the GeneRuler 1 kb DNA ladder. The lower fragment of the digested pET24d-Hag was too big (2 kb) and pET24d-Hag-DARPin seemed only to be linearized with the exception of two very thin bands below the linear plasmid, which were all of the wrong size.

18.36 ligation of pET24d and PCR Hag/ Hag-DARPin fragments cut NcoI/BamHI

Aim: ligation of construct with pET24d for overproduction of flagellin and crystallization

The NcoI/BamHI digested flagellin PCR products from 18.22 (from clone 7 and piGEM-005) were ligated with NcoI/BamHI digested pET24d.

Component	pET24d-Hag reaction (µL)	pET24d-Hag-DARPin raction (µL)
Insert (PCR fragments) (ca. 260 ng/µL)	2	2
Vector (pET24d, c= 50ng/µL)	5	5
Ligase-Buffer 10x	2	2
T4 Ligase	1	10
Millipore Water	10	10
Total Volume	20	20

The reactions were prepared in double and were incubated at room temperature. One reaction was incubated for 1 hour followed by transformation of E. coli XL1-Blue and the second one over night.

18.37 Repetition of PCR with 3 clones of pET24d-Hag and pET24d-Hag-DARPin ligation

Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pET24d

3 clones from ligation plates with pET-Hag and pET-Hag-DARPin were resuspended in 30 µL PBS and cooked at 95 °C for 10 min. After that procedure 1 µL of this suspension was used as PCR template.

Content	Volume (µL)	MM for 7 reactions (µL)
Template ( 1µL cooked suspension) (8-10 from pET-Hag, 7-9 from pET-Hag-DARPin)	1	-
Primer Flo 54	-	3,5
Primer Flo 56	-	3,5
Phusion DNA-polymerase	-	3,5
Phusion Buffer 5x	-	28
dNTP-mix	-	3,5
Water	-	98
Mastermix	19	-
Total Volume	20	140

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	1 min 45 sec
5	Go To 2	35x
6	72	4min
7	8	infinite

Run over night

Transformation

Plasmid	Concentration (ng/µL)	Antibiotic	Cells	Volume (µL)
pET24d	148	Can	DH5α	1
piGEM-018	160	Amp	DH5α	0,5
piGEM-014	350	Amp	DH5α	0,5
Gibson pMAD-cup1-1 clone 4	60	Amp	DH5α	1
pET-Hag attempt from 18.36	-	Can	XL1-Blue	20
pET-Hag-DARPin attempt from 18.36	-	Can	XL1-Blue	20
Control pET24d cut NcoI/BamHI	32	Can	XL1-Blue	1

23.06.2014

14.45 Purification of test expression

Aim: Purify PheA-Arc1p-C-0x on a small scale

Lysozyme was added to the cell suspension from 14.44 to a final concentration of 1 mg/mL and incubated on ice for 30 min. Afterwards the cells were lysed using ultra sound (2x 18 pulses, 30 s on ice inbetween). To clear the suspension of cell debris it was centrifuged (13000 rpm, 15 min, 4 °C). The supernatant was purified using QIAGEN Ni-NTA Spin Columns. An SDS-PAGE gel showed that the protein is produced and can be purified using Ni affinity chromatography.

60 mL LB-Kan⁵⁰ medium was inoculated from the glycerolstock prepared in 14.44 and incubated at 37 °C and 220 rpm over night.

Sequencing of constructs from 23.06.2014

Premix	Label-Nr.	Construct	Primer
1	AGB0023402	piGEM-018 (pMAD-DARPin)	Flo54 (Hag-F-Nco)
2	AGB0023403	piGEM-018 (pMAD-DARPin)	Flo56 (Hag-R-Bam)
3	AGB0023404	pMAD-Hag-Flank-cup1-1	Flo54 (Hag-F-Nco)
4	AGB0023405	pMAD-Hag-Flank-cup1-1	Flo56 (Hag-R-Bam)
5	AGB0023406	piGEM-002 (Nose plasmid)	TW259

18.37 Repetition of PCR with 3 clones of pET24d-Hag and pET24d-Hag-DARPin ligation

Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pET24d

Gel electrophoresis:

The gel shows negative bands in case of the Hag-DARPin clones. The PCR for Hag 8 and 9 did not work although we cooked the clones in PBS. The transformation efficiency seemed to be very low, so clones from the new ligation attempts should be analysed.

18.38 Ligation checking success of transformed ligation attempts

On every plate grew a high amount of colonies. 6 clones of each plate were picked for inoculation of minipreps and for cPCR after cooking with PBS. The clones were transferred to another LB-Can plate.

18.39 cPCR with picked clones from 18.38 ligation attempt transformation

Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pET24d

For checking the insertion of the Hag/-DARPin into pET24d the clones from the transformation plate were transferred to another LB-Can plate and cooked for 10 min in 30 µL PBS at 95°C. At the same time the colonies were used to inoculate LB-Can for minipreps.

Content	Volume (µL)	MM for 14 attempts (µL)
Template ( 1µL cooked suspension) (1-6 from pet-Hag, 1-6 from pet-Hag-DARPin)	1	-
Primer Flo 54	-	7
Primer Flo 56	-	7
Phusion DNA-polymerase	-	7
Phusion Buffer 5x	-	198
dNTP-mix	-	7
Water	-	98
Mastermix	19	-
Total Volume	20	280

Step	Temperature °C	Time
1	98	5 min
2	98	30 sec
3	55	30 sec
4	72	1 min 45 sec
5	Go To 2	35x
6	72	4min
7	8	infinite

Run over night

24.06.2014

14.46 Expression of PheA-Arc1p-C-0x

Aim: Express PheA-Arc1p-C-0x for further use

10 x 500 mL LB-Kan⁵⁰ medium were inoculated with 5 mL of the overnight culture prepared in 14.45 and incubated at 37 °C and 220 rpm until OD₆₀₀ reached 0.5. The flasks were cooled to 18 °C and protein production was induced by adding 100 µL 500 mM IPTG. The cultures were incubated over night at 18 °C and 220 rpm. Afterwards the cells were collected by centrifugation (6000 rpm, 20 min, 4 °C), resuspended in buffer A and stored at -20 °C until further use.

25.06.2014

Sequencing results of constructs from 23.06.2014

Premix	Label-Nr.	Construct	Result
1	AGB0023402	piGEM-018 (pMAD-DARPin)	Correct insertion of DARPin
2	AGB0023403	piGEM-018 (pMAD-DARPin)	Did not work
3	AGB0023404	pMAD-Hag-Flank-cup1-1	Correct insertion, point mutation refers to bad sequencing
4	AGB0023405	pMAD-Hag-Flank-cup1-1	Did not work
5	AGB0023406	piGEM-002 (Nose plasmid)	Correct insertion of the CM resistance

18.39 Gel cPCR with picked clones from 18.38 ligation attempt transformation

Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pET24d

Gel electrophoresis: no bands except for the controls were seen. The PCR has to be repeated with more colony in the PCR tubes or the prepped plasmids

18.40 Test digest with NcoI/BamHI of isolated plasmids from picked colonies

Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pET24d

The picked clones from the ligation attempts 18.38 were isolated. In order to check the insertion of the Hag/ Hag-DARPin domain the plasmids were digested with NcoI/BamHI so that the gel should show the insert of 1 or 1,5 bp length and the pET24d backbone at 5300 bp. Because of an unavailable marker as a control the PCR amplified inserts which were used for the ligation will run with the gel as well. piGEM-001 will also be cut NcoI/BamHI in order to receive a marker band for the pET24d backbone.

Component	Volume (µL)	Mastermix for 8 attempts
Plasmid (ca. 45 ng/µL	5	-
Cutsmart 10x	-	4
NcoI	-	0,5
BamHI	-	0,5
Water	-	35
Mastermix	5	-
Total Volume	10	40

The gel shows that the digested clones were all negative. The ligation had to be performed again.

20.6 Purification of cPCR samples with Gel extraction kit

Aim: purification of samples for sequencing

Purified samples:
clone 3 & 5 from transformed piGEM-005
clone 3 & 9 from transformed piGEM-018

Clone	Concentration (ng/µl)
Hag 3	10
Hag 5	14
Hag-DARPin 3	9
Hag-DARPin 9	9

26.06.2014

20.7 PCR with purified cPCR samples from 20.6

Aim: PCR amplification of purified cPCR samples

The concentration of the cPCR samples after purification was too low for sequencing. Therefore the cPCR samples have to be amplified with PCR again.

Content	Volume (µL)	MM for 6 attempts (µL)
Purified cPCR product from 20.6 (3 & 5 from pet-Hag, 3 & 9 from pet-Hag-DARPin)	1	-
Primer Flo 54	-	6
Primer Flo 56	-	6
Phusion DNA-polymerase	-	6
Phusion Buffer 5x	-	6
dNTP-mix	-	60
Water	-	216
Mastermix	19	-
Total Volume	20	300

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	1 min 45 sec
5	Go To 2	35x
6	72	4min
7	8	infinite

20.8 Sequencing of purified cPCR samples from pMAD transformation

Premix	Label-Nr.	Construct	Primer
1	AGB0023407	Hag-SpeI in B. subtilis genome clone 3	Hag-Nco-fw
2	AGB0023408	Hag-SpeI in B. subtilis genome clone 5	Hag-Nco-fw
3	AGB0023409	Hag-SpeI-DARPin in B. subtilis genome clone3	Hag-Nco-fw
4	AGB0023410	Hag-SpeI-DARPin in B. subtilis genome clone 9	Hag-Nco-fw

18.41 New ligation of pET24d and PCR Hag/ Hag-DARPin fragments cut NcoI/BamHI transformation

Aim: ligation of construct with pET24d for overproduction of flagellin and crystallization

The cut pET24d NcoI/BamHI which was used for the previous ligations was not purified and contained an 1 kb insert. For a new clean ligation the reaction was repeated with digested pET24d. The NcoI/BamHI digested flagellin PCR products (from clone 7 and piGEM-005) were ligated with NcoI/BamHI digested pET24d.

The reactions were carried out in double and were incubated 1h at room temperature. Finally they were used to transform E. coli XL1-Blue after inactivation at 65°C for 10 min. The attempts 1.1 and 2.1 were incubated over night at room temperature. 1 µL of digested vector was used for a transformation as a negative control in order to check the amount of religants.

Component	pET-Hag attempt (µL) – 1 & 1.1	pET-Hag-DARPin attempt (µL) 2& 2.1
Insert (PCR fragments) (ca. 260 ng/µL)	3	3
Vector (pET24d, c= 86ng/µL)	5	5
Ligase-Buffer 10x	2	2
T4 Ligase	1	1
Millipore water	9	9
Total Volume	20	20

27.06.2014

18.42 Miniprep of ligation clones

The ligation between pET24d and the Hag-/Hag-DARPin fragments which were both cut NcoI/BamHI was successful. The ligation plates showed over 20 clones each. However, on the negative control grew a few clones as well, which were very small and sticking together. In order to analyse the insert of the clones, 5 clones per ligation plate 1 and 2 were used to inoculate minipreps in 5 mL LB-Can. For the Ligation 1 pET-Hag clones 1-5 were picked, as well as clones 6-10 from Plate Ligation 2 pET-Hag-DARPin.

The cultures were inoculated over night at 37°C.

28.06.2014

18.42 Miniprep of ligation clones

Construct	Clone	Concentration (ng/µL)
pET24d-Hag	1	50
pET24d-Hag	2	87
pET24d-Hag	3	65
pET24d-Hag-DARPin	6	83
pET24d-Hag-DARPin	7	59

18.43 cPCR of clones from 18.41

Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pET24d

Plasmid from isolated clones from each plate were analysed via cPCR with the primers flo54 and flo56 (Hag-fw and Hag-rv). The result should be a ca. 1kb fragment for correct pET24d-Hag containing clones and a 1,5 kb fragment for pET24d-Hag-DARPin containing clones.

Content	Volume (µL)	MM for 6 attempts (µL)
Picked clones from 18.42 (1-3 pET24d-Hag, 6-7 from pET24d-Hag-DARPin)	0,5	-
Primer Flo 54	-	3
Primer Flo 56	-	3
Phusion DNA-polymerase	-	3
Phusion Buffer 5x	-	6
dNTP-mix	-	24
Water	-	81
Mastermix	19,5	-
Total Volume	20	120

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	1 min 45 sec
5	Go To 2	30x
6	72	4min
7	8	infinite

The samples can be seen on the gel under 18.44. The PCR for the Hag-fragment in pET24d seemed to be positive (PCR.H1 - H3), as well as for the Hag-DARPin fragment (PCR.D7)

18.44 test digest with NcoI/BamHI - Checking insertion of Hag/-DARPin into pET24d

Aim: proving insertion of Hag/-DARPin fragment into pET24d

The plasmids were digested with NcoI and BamHI. In case of a correct insertion the pet24d backbone and the insert should be seen on the gel at 5300 bp and 1000/ 1500 bp. As control pET24d-Hag-Flank (piGEM-001) is used to check the mastermix.

Component	Volume (µL)	Mastermix(6 attempts)
Plasmid from clone ( pET24d-Hag 1-3, pET24d-Hag-DARPin 6 & 7)	5	-
Cutsmart 10x	-	3
NcoI	-	0,5
BamHI	-	0,5
Water	-	26
Total Volume	10	30

20.9 Gel Purification of amplified cPCR products

Aim: Purification for more efficient sequencing

The PCR product of the amplification of cPCR products was not pure considering different bands on the gel next to the right one. In order to prevent sequencing mistakes the PCR attempts were purified via gel extraction of the 1,5 kb band in case of the Hag-DARPin construct.

20.10 PCR with purified Hag-DARPin cPCR products for sequencing

Aim: amplification of purified Hag-DARPin fragment for sequencing

The purified cPCR product from 20.9 has to be amplified again in order to get a higher concentration for sequencing.

Content	Volume (µL)	MM for 2 attempts (µL)
Purified PCR product from 20.x (Hag-/ Hag-DARPin fragment)	1-2	-
Primer Flo 54	-	1
Primer Flo 56	-	1
Phusion DNA-polymerase	-	1
Phusion Buffer 5x	-	2
dNTP-mix	-	20
Water	-	75
Mastermix	19	-
Total Volume	20	100

Step	Temperature °C	Time
1	98	5 min
2	98	30 sec
3	55	30 sec
4	72	1 min 45 sec
5	Go To 2	35x
6	72	4min
7	8	infinite

18.45 SpeI digest of pET24d-Hag (piGEM-019)

Aim: linearizing pET24d-Hag with SpeI site for a Gibson assembly with Cup1-1

Component	Volume (µL)
piGEM-016 (ng/µL)	17
CutSmart 10x	2
SpeI	0,5
Water	0,5
Total Volume	20

Incubation 1 h at 37°C with following heat inactivation at 80°C

18.46 Gibson assembly with linearized pET24d-Hag (piGEM-019) and cup1-1

Aim: Insertion of cup1-1 domain into pET24d-Hag construct for crystallization

As insert cup1-1 PCR product from 15.55 and SpeI digested piGEM-016 from 18.44 were used for a new Gibson assembly.
PCR fragment cup1-1 (464 ng/µL)
SpeI digested pIGEM-005 ( ng/µL)

Component	Volume (µl)
Gibson-mix	15
Insert (cup1-1 464 ng/µL)	2,5
piGEM-019	2,5
Total Volume	20

The mix was incubated 5 min at room temperature and then for 1h at 50°C.

In the end the whole mix was used to transform E. coli XL1-Blue, which were plated out on LB-Amp. Incubation was done over night at 37°C.

29.06.2014

18.47 cPCR of Gibson assembly clones of pET24d-Hag (piGEM-019) and cup1-1

Aim: screening clones for right insert

In order to screen the clones for the right insertion of cup1-1 four clones were picked from the LB-Can plate and transferred onto a LB-Can plate. Additionally the clones were used for inoculation of minipreps and also cooked in 50 µL dest. Water for 10 min at 95°C. The lysate was used as template.

The PCR with Flo54 and iGEM-025 should generate a 785 bp fragment and the one with iGEM-024 and -025 the 164bp cup domain fragment.

Content	Volume (µL)	MM 1 for 5 attempts (µL)	MM 2 for 5 attempts (µL)
Cooked lysate solution from clones 1-4	3	-
Primer Flo 54	-	2,5	-
Primer iGEM-024	-	-	2,5
Primer iGEM-025	-	-	2,5
dNTP-mix	-	2,5	2,5
Phusion DNA-polymerase	-	5	5
Phusion Buffer 5x	-	20	20
Water	-	67,5	67,5
Mastermix	17	-	-
Total Volume	20	100	100

Step	Temperature °C	Time
1	98	10 min
2	98	30 sec
3	55	30 sec
4	72	1 min 45 sec
5	Go To 2	35x
6	72	4min
7	8	infinite

The PCR showed no bands. Nevertheless, colonies were used to inoculate cultures for minipreps so that the isolated plasmid can be further analysed for the insert.

30.06.2014

Sequencing

Premix	Label-Nr.	Construct	Primers
1	AGB0023411	pET24d-Hag-SpeI construct cl. 2	Hag-Nco-fw
2	AGB0023412	pET24d-Hag-DARPin construct cl. 7	Hag-Nco-fw

18.48a Miniprep of plasmids from Gibson assembly clones with pET24d-Hag (piGEM-019) and cup1-1

Aim: isolation of Plasmid DNA for further experiments

Construct	Clone	Concentration (ng/µL)
pET24d-Hag-Cup1-1	1	122
pET24d-Hag-Cup1-1	2	85
pET24d-Hag-Cup1-1	3	172
pET24d-Hag-Cup1-1	4	116

18.48b PCR of isolated plasmids from Gibson assembly clones (pET24d-Hag (piGEM-019) and cup1-1)

Aim: screening clones for right insert

The isolated plasmid 1:10 diluted from the picked clones 1-4 were used as PCR template.

The PCR with Flo54 and iGEM-025 should generate a 785 bp fragment and the one with iGEM-024 and -025 the 164bp domain fragment.

Content	Volume (µL)	MM 1 for 5 attempts (µL)	MM 2 for 5 attempts (µL)
Cooked lysate solution from clones 1-4 (1:10)	3	-
Primer Flo 54	-	2,5	-
Primer iGEM-024	-	-	2,5
Primer iGEM-025	-	2,5	2,5
dNTP-mix	-	2,5	2,5
Phusion	-	5	5
Phusion Buffer 5x	-	20	20
Water	-	67,5	67,5
Mastermix	17	-	-
Total Volume	20	100	100

Step	Temperature °C	Time
1	98	3 min
2	98	30 sec
3	55	30 sec
4	72	1 min 45 sec
5	Go To 2	35x
6	72	4min
7	8	infinite

No bands could be observed on the gel. The PCR was repeated with Q5 mastermix to exclude the disfunction of the polymerase.

20.9 Inoculation of a preculture from Bacillus subtilis WT 3610

Aim: Preparation for a mainculture the for the next day

2 x 6 mL of LB were inoculated with Bacillus subtilis WT3610 from an LB plate and incubated at 37°C over night.

14.47 Purification of PheA-Arc1p-C-0x

Aim: Purify PheA-Arc1p-C-0x in three steps

The resuspended cells from 14.46 were lysed using a french press. The lysate was incubated on ice with 5 µg/mL DNAseA and RNAseI for 10 min and centrifuged (27000 rpm, 45 min, 4 °C) to pellet cell debris. The supernatant was filtered (0.45 µm) and PheA-Arc1p-C-0x purified from the cleared solution by NiNTA affinity chromatography. The combined elution fractions containing crude PheA-Arc1p-C-0x were concentrated to a volume of 2 mL and further purified using an anion exchange column to get rid of possible tRNA contaminations. Finally the buffer was changed to dialysis buffer and the protein concentrated and stored at -80 °C in aliquods for further use.

@@ Line 15: / Line 15: @@
 </h2>
 <fieldset class="exp13">
-     <legend><a name="exp13.56">13.56 Make Gly Stocks of the following strains </a></legend>
+     <legend><a name="exp13.56">13.56 Making glycerine stocks of the following strains </a></legend>
 	<div class="aim">
-		<p>Aim: Have gly stocks</p>
+		<p>Aim: Storage of strains</p>
      </div>
      <div class="exp-contest">
      	<ul class="list">
-        	<li>Dh5a pRSII426 –hGRa</li>
+             <li>Dh5&alpha; piGEM010 (p003 + Tag 21)</li>
-             <li>Dh5a piGEM010 (p003 + Tag 21)</li>
+             <li>Dh5&alpha; piGEM015 (p004 + Tag 23)</li>
-             <li>Dh5a piGEM015 (p004 + Tag 23)</li>
+             <li>Dh5&alpha; piGEM014 (p003 + Tag 22)</li>
-             <li>Dh5a piGEM014 (p003 + Tag 22)</li>
+             <li>Dh5&alpha; piGEM008 (p002 + Tag 22)</li>
-             <li>Dh5a piGEM008 (p002 + Tag 22)</li>
+             <li>Dh5&alpha; piGEM007 (p002 + Tag 21)</li>
-             <li>Dh5a piGEM007 (p002 + Tag 21)</li>
+             <li>Dh5&alpha; piGEM011 (p003 + Tag 22)</li>
-             <li>Dh5a piGEM011 (p003 + Tag 22)</li>
+             <li>Dh5&alpha; piGEM012 (p003 + Tag 23)</li>
-             <li>Dh5a piGEM012 (p003 + Tag 23)</li>
          </ul>
      </div>
 </fieldset>
 <fieldset class="exp13">
-     <legend><a name="exp13.57">13.57 Mini Prep of  cultures inoculated on Friday 30.5. Nose Plasmids</a></legend>
+     <legend><a name="exp13.57">13.57 Mini Prep of  cultures inoculated on Friday 30.05.14 containing the nose plasmids</a></legend>
      <div class="exp-content">
      	<ul class="list">
@@ Line 40: / Line 39: @@
              <li>piGEM 009 = 13 ng/&micro;l</li>
          </ul>
-         <p>low concentration: new transformation to gain more plasmid DNA<br />
+         <p>low concentration: new transformation to obtain more plasmid DNA<br />
 		Strain: new competent <em>E. coli</em> XL1-blue</p>
      </div>
@@ Line 47: / Line 46: @@
      <legend><a name="exp15.50">15.50 Miniprep of pMAD-fla-cup1-1  for miniprep</a></legend>
      <div class="exp-content">
-     <p>The miniprep was performed accoding to the miniprep protocol.</p>
+     <p>The miniprep was performed according to the miniprep protocol.</p>
      <p>Concentration 40 ng/&micro;L<br />
      low concentration: new transformation to gain more plasmid DNA should be done<br  />
@@ Line 56: / Line 55: @@
      <legend><a name="exp13.58">13.58 Bacillus Trafo with all Nose Plasmids containing one/no Degradation Tag</a></legend>
      <div class="aim">
-     <p>Aim:  Create Bacillus subtilis strain 3610 containing the following plasmids: piGEM002 to 004 and piGEM007 to 016</p>
+     <p>Aim:  Create <i>Bacillus subtilis</i> strain 3610 containing the following plasmids: piGEM002 to 004 and piGEM007 to 016</p>
      </div>
      <div class="exp-content">
@@ Line 63: / Line 62: @@
 </fieldset>
 <fieldset class="exp13">
-     <legend><a name="exp13.59">13.59 Inoculation of <em>Bacillus subtilis</em> wildtype (3610), gfp (186) and silver nose</a></legend>
+     <legend><a name="exp13.59">13.59 Inoculation of <em>Bacillus subtilis</em> wildtype (3610), <i>gfp</i> and silver nose</a></legend>
      	<div class="aim">
-         <p>Aim: Aim: MTA tomorrow to check out what concentrations of Ag+ are still okay for the cells to survive, since 1mM until 10&micro;M was too high and the cells died</p>
+         <p>Aim: perform MTA to test the Ag concentrations where cells are still viable, since 1 mM until 10 &micro;M were too high and the cells died</p>
          </div>
          <div class="exp-content">
-         <p>Starting from 1 mM 8 dilutions have been prepared</p>
+         <p>Starting from 1 mM, eight serial dilutions have been prepared</p>
          </div>
 </fieldset>
@@ Line 95: / Line 94: @@
          <div class="exp-content">
         <img src="https://static.igem.org/mediawiki/2014/0/0e/MR_2014-06-02_plasmidmap.png" width="50%" />
-        <p>We received the synthetized DARPin-gene in a pEC-A2 vector with spe1 restriction sites at the 5’- and 3’-site at an amount of 2,7&micro;g plasmid in the tube.</p>
+        <p>We received the synthetized DARPin-gene in a pEC-A2 vector with <i>Spe</i>I restriction sites at the 5' - and 3' -site with an amount of 2,7 &micro;g plasmid per tube.</p>
-        <p>A stock solution was created by adding 27&micro;l water to the tube.</p>
+        <p>A stock solution was created by adding 27 &micro;l water to the tube.</p>
         <p>Concentration of stock solution = 100 ng/&micro;l</p>
-        <p>A 1:10 dilution was created by using 1&micro;l of stock solution adding 9µL of water to an end concentration of 10ng/&micro;l.</p>
+        <p>A 1:10 dilution was created by using 1 &micro;l of stock solution adding 9&micro;L of water to an end concentration of 10ng/&micro;l.</p>
         <p>Concentration of stock dilution = 10 ng/&micro;l.</p>
          </div>
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.2">18.2 Transformation of DARPin-gene in plasmid into <em>E.Coli</em> XL1-Blue</a></legend>
+     <legend><a name="exp18.2">18.2 Transformation of <em>E.coli</em> XL1-Blue with pEX-A2-DARPin</a></legend>
      	<div class="aim">
-         <p>Aim: Transforming pEX-A2 plasmid with DARPin-gene into E.Coli for amplification of the Gene.</p>
+         <p>Aim: Transformation of <em>E.coli</em> XL1-Blue with pEX-A2-DARPin for amplification of the plasmid.</p>
          </div>
          <div class="exp-content">
-        <p>1&micro;l of the 1:10 stock dilution were used for transformation of <em>E. Coli</em> XL1-Blue</p>
+        <p>1&micro;l of the 1:10 dilution was used for transformation of <em>E. Coli</em> XL1-Blue</p>
          </div>
 </fieldset>
@@ Line 120: / Line 119: @@
 </h2>
 <fieldset class="exp18">
-     <legend><a name="exp18.3">18.3 Miniprep of DARPin-gene in plasmid in <em>E.Coli</em> XL1-Blue</a></legend>
+     <legend><a name="exp18.3">18.3 Miniprep of pEX-A2-DARPin from <em>E.coli</em> XL1-Blue</a></legend>
      <div class="aim">
      <p>Aim: Receiving a higher amount of plasmid for further experiments.</p>
      </div>
      <div class="exp-content">
-     <p>3 x6ml LB-Amp were inoculated with clones from the successful transformed plate (18.2) and incubated at 37&deg;C overnight.</p>
+     <p>3 x 6ml LB-Amp were inoculated with clones from the successful transformed plate (18.2) and incubated at 37&deg;C overnight.</p>
      </div>
 </fieldset>
@@ Line 131: / Line 130: @@
      <legend><a name="exp13.60">13.60 Microtiter plate assay with wildtype, gfp strain 186 and silver nose</a></legend>
      <div class="aim">
-     <p>Aim: MTA tomorrow to check out what concentrations of Ag+ are still okay for the cells to survive, since 1mM until 10 &micro;M was too high and the cells died</p>
+     <p>Aim: perform MTA to test the Ag concentrations where cells are still viable, since 1mM until 10 &micro;M was too high and the cells died</p>
      </div>
      <div class="exp-content">
      <p>Starting from 1 mM 8 dilutions have been prepared.<br />In the beginning Minimalmedium S750 has been prepared with 0.5&permil; Xylose<br />In the wells the following mix was added to a total volume of 150 &micro;l:<br />135&micro;l of MM (90&permil;) and Silver solution (10&permil;)<br />15&micro;l of cells<br />Finally 70 &micro;l are added to avoid evaporation of the medium</p>
-     <p>Incubation for appr. 24h at 37&deg;C shaking (Viktor AG Waldminghaus)</p>
+     <p>Incubation for appr. 24 hours at 37&deg;C shaking (Viktor AG Waldminghaus)</p>
+	<br />
+	<p>No positive GFP signal could be detected for the <i>B. subtilis</i> strain with the possible Ag sensitive promoter. The strain was restreaked onto a LB-Cm plate and he did not grow, which proved it to be a wrong strain, which has not been transformed successfully.</p>
      </div>
 </fieldset>
@@ Line 141: / Line 142: @@
      <legend><a name="exp13.61">13.61 Checking Bacillus Trafo with all Nose Plasmids containing one/no Degradation Tag</a></legend>
      <div class="exp-content">
-     <p>Every transformation plate showed a huge growth of bacillus without single colonies. After one day of incubation this seems to be an unrealistic growth which is why we plan to repeat the transformation after checking the growth of the <em>Bacillus subtilis</em> Wildtype 3610 on LB-CM plate with 5 &micro;g/ml CM.</p>
+     <p>Every transformation plate showed a huge growth of bacillus without single colonies. After one day of incubation this seems to be an unrealistic growth, which is why we planned to repeat the transformation after checking the growth of the <em>Bacillus subtilis</em> wildtype 3610 on LB-CM plate with 5 &micro;g/ml chloramphenicol.</p>
      </div>
 </fieldset>
@@ Line 147: / Line 148: @@
      <legend><a name="exp13.62a">13.62 Checking Bacillus Trafo Wildtype 3610</a></legend>
      <div class="aim">
-     <p>Aim: check if wildtype has a resistance against CM or if the plates are not effective/ made wrong</p>
+     <p>Aim: check if wildtype has a resistance against chloramphenicol or if the plates are faulty</p>
      </div>
      <div class="exp-content">
-     <p>Bacillus subtilis Wildtype 3610 was plated on LB-CM plate with 5 &micro;g/ml CM and incubated overnight at 37&deg;C.</p>
+     <p><i>Bacillus subtilis</i> Wildtype 3610 was plated on LB-chloramphenicol plate with 5 &micro;g/ml chloramphenicol and incubated overnight at 37&deg;C.</p>
      </div>
 </fieldset>
 <fieldset class="exp15">
-     <legend><a name="exp15.51">15.51 Making selection plates for clean deletions – integration of pMAD-construct into Bacillus subtilis chromosome</a></legend>
+     <legend><a name="exp15.51">15.51 Making selection plates for clean deletions - integration of pMAD-construct into <i>Bacillus subtilis</i> chromosome</a></legend>
      <div class="aim">
-     <p>Aim: For the integration of the constructs we cloned into pMAD many steps of a special selection are necessary.  For the protocoll we received from Florian Altegoer MLS and MLS X-gal plates have to be used.</p>
+     <p>Aim: For the integration of the constructs we cloned into pMAD many steps of a special selection are necessary.</p>
      </div>
      <div class="exp-content">
@@ Line 165: / Line 166: @@
      <li>X-Gal 100mg/ml</li>
      </ul>
-     <p>For MLS selection plates Erythromycin with 1mg/ml were needed. Therefore the 4 mg/mL stock solution was diluted 1:4 by mixing 400 &micro;l Eryhtomycin with 1200 &micro;l of 70&deg; ethanol.</p>
+     <p>For MLS selection plates erythromycin with 1 mg/ml were needed. Therefore the 4 mg/ml stock solution was diluted 1:4 by mixing 400 &micro;l eryhtromycin with 1200 &micro;l of 70% ethanol.</p>
      <p>3 types of plates were made:</p>
      <ul class="list">
-     <li>1.	MLS selectin: 800 mL LB agar + 800 &micro;l Eryhtromycin + 800 &micro;l Lincomycin</li>
+     <li>1.	MLS selectin: 800 mL LB agar + 800 &micro;l eryhtromycin + 800 &micro;l lincomycin</li>
-     <li>2.	MLS X-Gal: 800 mL LB agar + 800 &micro;l Eryhtromycin + 800 &micro;l Lincomycin + 800 &micro;l X-Gal</li>
+     <li>2.	MLS X-Gal: 800 mL LB agar + 800 &micro;l eryhtromycin + 800 &micro;l lincomycin + 800 &micro;l X-Gal</li>
-     <li>3. X-Gal: 800 mL LB agar + 800 µL X-Gal
+     <li>3. X-Gal: 800 mL LB agar + 800 &micro;L X-Gal
      </ul>
-    <p>About 120 plates were stored at the 4&deg;C room at AG Graumann labs.</p>
      </div>
 </fieldset>
@@ Line 184: / Line 184: @@
 </h2>
 <fieldset class="exp18">
-     <legend><a name="exp18.4">18.4 Miniprep of DARPin-gene in plasmid in <em>E.Coli</em> XL1-Blue</a></legend>
+     <legend><a name="exp18.4">18.4 Miniprep of pEX-A2-DARPin from <em>E.coli</em> XL1-Blue</a></legend>
      <div class="exp-content">
      <table width="100%" border="1">
@@ Line 207: / Line 207: @@
 </fieldset>
 <fieldset class="exp15">
-     <legend><a name="exp15.52">15.52 Sequencing pMAD-fla-cup1-1</a></legend>
+     <legend><a name="exp15.52">15.52 Sequencing of pMAD-fla-cup1-1</a></legend>
      <div class="aim">
-     <p>Aim: Checking the correct insertion of the metallothionein-domain into the hag –flank construct</p>
+     <p>Aim: Checking the correct insertion of the metallothionein-domain into the hag-flank construct</p>
      </div>
      <div class="exp-content">
@@ Line 267: / Line 267: @@
      <legend><a name="exp13.62b">13.62 Checking Bacillus Trafo Wildtype 3610</a></legend>
      <div class="aim">
-     <p>Aim: check if wildtype has a resistance against CM or if the plates are not effective/ made wrong</p>
+     <p>Aim: check if wildtype has a resistance against chloramphenicol or if the plates are not effective/ made wrong</p>
      </div>
      <div class="results">
-     <p>Result: Bacillus subtilis Wildtype 3610 grew on the CM plate which shows us that there has to be a mistake in making the LB-CM plates or the WT has a resistance.</p>
+     <p>Result: <i>Bacillus subtilis</i> Wildtype 3610 grew on the chloramphenicol plate which shows us that there has to be a mistake in making the LB-chloramphenicol plates or the WT has a resistance.</p>
      </div>
      <div class="exp-content">
-     <p>In order to exclude the false making of plates new ones were made with new CM-stocks with 25 mg/ml and 5 mg/ml.</p>
+     <p>New plates were made with new chloramphenicol-stocks with 25 mg/ml and 5 mg/ml.</p>
-     <p>3 aliquots of competent <em>B.s.</em> WT3610 were plated on new LB-CM plates and incubated at 37&deg;C.</p>
+     <p>3 aliquots of competent <em>B.s.</em> WT3610 were plated on new LB-chloramphenicol plates and incubated at 37&deg;C.</p>
      </div>
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.5">18.5 Spe1 restriction of DARPin-gene in pEX-A2 & pMAD-hag-flank (piGEM-005)</a></legend>
+     <legend><a name="exp18.5">18.5 <i>Spe</i>I restriction pEX-A2-DARPin & pMAD-hag-flank (piGEM-005)</a></legend>
      <div class="aim">
-     <p>Aim: Receiving iGEM-005 as linearized vector for cloning the DARPin gene with Spe1 sites into pMAD-fla (iGEM-005) </p>
+     <p>Aim: Receiving iGEM-005 as linearized vector for cloning the DARPin gene with <i>Spe</i>I sites into pMAD-fla (iGEM-005) </p>
      </div>
      <div class="exp-content">
@@ Line 333: / Line 333: @@
        </tr>
      </table>
-     <p>Incubation at 37&deg;C for 2h and heat shock at 81&deg;C for 5 min. After that the pMAD-Hag-Flank-Construct was purified with the OMEGA gel extraction kit according to the protocol.</p>
+     <p>Incubation at 37&deg;C for 2h and heat shock at 81&deg;C for 5 min. After that the pMAD-hag-flank-construct was purified with the OMEGA gel extraction kit according to the protocol.</p>
      <p>c(digested piGEM-005)= 4 ng/&micro;l</p>
      </div>
@@ Line 340: / Line 340: @@
      <legend><a name="exp13.62c">13.62 Checking Bacillus Trafo Wildtype 3610</a></legend>
      <div class="aim">
-     <p>Aim: check if wildtype has a resistance against CM or if the plates are not effective/ made wrong</p>
+     <p>Aim: check if wildtype has a resistance against chloramphenicol or if the plates are not effective/ made wrong</p>
      </div>
      <div class="exp-content">
-     <p>Result: Bacillus subtilis Wildtype 3610 grew on the CM plate. We have already repeated making plates so it might be that the WT has got a resistance while making it competent. New WT from Florian Altegoer was plated on 2 CM plates with 5µg/µL (old and new one) and 2x LB plates from gly stocks.</p>
+     <p>Result: <i>Bacillus subtilis</i> Wildtype 3610 grew on the chloramphenicol plate. We have already repeated making plates so it might be that the WT has got a resistance while making it competent. A new WT was plated on 2 chloramphenicol plates with 5 &micro;g/mL (old and new one) and 2x LB plates from gly stocks.</p>
      <p>Incubation at 37&deg;C overnight.</p>
      </div>
 </fieldset>
+</div/
+<!-- 05.06.14 -->
+<div class="notebooky-entry">
+<h2 class="title">
+	<a name="05.06.2014">05.06.2014</a>
+</h2>
@@ Line 473: / Line 481: @@
 </table>
 <p>The reaction mixture was incubated at 37 &deg;C and 300 rpm for 1 h and afterwards heated to 80 &deg;C for 20 min.</p>
-<p>In order to create the circular plasmid 100 ng of the linear template were mixed with 1 &micro;L 10x T4-Ligasebuffer,  1 &micro;L T4-Ligase and water to give a total volume of 10 &micro;L. This mixture was incubated for 9 h at 16 &deg;C. The resulting plasmid was dialysed with water to decrease the salt concentration for the following transformation of E. coli Top10 electrocompetent cells with the plasmid.</p>
+<p>In order to create the circular plasmid 100 ng of the linear template were mixed with 1 &micro;L 10x T4-Ligasebuffer,  1 &micro;L T4-Ligase and water to give a total volume of 10 &micro;L. This mixture was incubated for 9 h at 16 &deg;C. The resulting plasmid was dialysed with water to decrease the salt concentration for the following transformation of <i>E. coli</i> Top10 electrocompetent cells with the plasmid.</p>
      </div>
 </fieldset>
@@ Line 491: / Line 499: @@
      <legend><a name="exp19">19. Crystallization of flagellin</a></legend>
      <div class="concent">
-     <p>In order to cristallize flagellin with a domain it is necessary to produce the protein by E.Coli in a high concentration.  For that aim the Fla-construct will be amplificated out of pet24d which includes a domain. For elimination of the flanks a PCR has to be perfomed which just amplificates Hag with Domain and creates Nco1 and BamH1 restriction sites. After purification and digest with Nco/Bam the fragment can be ligated into Nco/Bam digested pet24d . After transformation the synthesis can be induced by IPTG.</p>
+     <p>In order to crystallize flagellin with a domain it is necessary to produce the protein by <i>E. coli</i> in a high concentration.  For that aim the Fla-construct will be amplified out of pET24d which includes a domain. For elimination of the flanks a PCR has to be performed which just amplifies hag with domain and creates <i>Nco</i>I and <i>Bam</i>HI restriction sites. After purification and digest with <i>Nco</i>/<i>Bam</i> the fragment can be ligated into digested pET24d . After transformation the production can be induced by IPTG.</p>
      </div>
 </fieldset>
 <fieldset class="exp19">
-     <legend><a name="exp19.1">19.1 Eliminiation of flanks from Fla-construct including cup1-1out of pet24d</a></legend>
+     <legend><a name="exp19.1">19.1 Elimination of flanks from fla-construct including <i>cup</i>1-1 from pET24d</a></legend>
      <div class="aim">
-     <p>Aim: Preparation for using pet24d as expression vector for flagellin</p>
+     <p>Aim: Preparation for using pET24d as expression vector for flagellin</p>
      </div>
      <div class="exp-content">
-     <p>The flagellin construct was  amplificated with Primer 95 and 54 from Florian Altegoer which allow the  amplification of the construct with cup1-1 without flanks (just Hag) including  Nco1 &amp; BamH1 restriction sites.<br />
+     <p>The flagellin construct was  amplified with specifically designed primers (95 and 54 from Florian Altegoer), which allow the  amplification of the construct with <i>cup</i>1-1 without flanks (just Hag) including  <i>Nco</i>I &amp; <i>Bam</i>HI restriction sites.<br />
        Template dilution 1:10:<br />
-&micro;L pet24d-cup1-1 was mixed with  9 &micro;L to an 1:10 dilution of 16,3 ng/&micro;L<br />
+&micro;L pET24d-<i>cup</i>1-1 was mixed with  9 &micro;L to an 1:10 dilution of 16,3 ng/&micro;L<br />
        Primer dilution 1:10:<br />
-       Primers 95 &amp; 54 from Florian  Altegoer were diluted 1:10 by mixing 10&micro;L of primers with 90&micro;L milipore water  each.</p>
+       The primers were diluted 1:10 by mixing 10 &micro;L of primers with 90 &micro;L millipore water  each.</p>
 	  <table width="100%" border="1">
        <tr>
          <th scope="col">Mix [&micro;l]</th>
-         <th scope="col">1 attempt with phusion</th>
+         <th scope="col">reaction with phusion</th>
-         <th scope="col">One attempt with Q5 mastermix</th>
+         <th scope="col">reaction with Q5 mastermix</th>
        </tr>
        <tr>
-         <th scope="row">Pet24d-cup1-1<br />1:10 dilution</th>
+         <th scope="row">pET24d-<i>cup</i>1-1<br />1:10 dilution</th>
          <td>1</td>
          <td>1</td>
@@ Line 600: / Line 608: @@
    </tr>
 </table>
-	<p>PCR was run overnight.</p>
+	<p>The PCR was run over night.</p>
      </div>
 </fieldset>
 <fieldset class="exp19">
-     <legend><a name="exp19.2">19.2 Restriction digest of pet24d with Nco1 and BamH1</a></legend>
+     <legend><a name="exp19.2">19.2 Restriction digest of pET24d with <i>Nco</i>I and <i>Bam</i>HI</a></legend>
      <div class="aim">
-     <p>Aim: Creating Nco/ Bam restriction sites in pet24d for cloning PCR fragments amplified with primers flo56 and flo54 which contain Nco/Bam sites as well.</p>
+     <p>Aim: Creating Nco/Bam restriction sites in pET24d for cloning PCR fragments amplified with primers flo56 and flo54 which contain these sites as well.</p>
      </div>
      <div class="exp-content">
-     <p>Prepped pet24d was cut with Nco1 and BamH1 in order to create restriction sites for ligating the Flagellin/ Hag-Domain fragments into the vector. The Hag-fragments which were amplified via PCR with primers flo54 and 56 contain Nco1/ BamH1 restriction sites for that purpose as well.</p>
+     <p>Isolated pET24d was cut with <i>Nco</i>I and <i>Bam</i>HI in order to create restriction sites for ligating the Flagellin/ Hag-Domain fragments into the vector. The Hag-fragments which were amplified via PCR with primers flo54 and 56 contain <i>Nco</i>I/ <i>Bam</i>HI restriction sites for that purpose as well.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 616: / Line 624: @@
    </tr>
    <tr>
-     <th scope="row">Pet24d (148 ng/&micro;L)</th>
+     <th scope="row">pET24d (148 ng/&micro;L)</th>
      <td>7</td>
    </tr>
    <tr>
-     <th scope="row">Cutsmart 10x</th>
+     <th scope="row">CutSmart 10x</th>
      <td>2</td>
    </tr>
    <tr>
-     <th scope="row">Nco1</th>
+     <th scope="row"><i>Nco</i>I</th>
      <td>0,5</td>
    </tr>
    <tr>
-     <th scope="row">BamH1</th>
+     <th scope="row"><i>Bam</i>HI</th>
      <td>0,5</td>
    </tr>
@@ Line 640: / Line 648: @@
    </tr>
 </table>
-	<p>Incubation for 1h at 37&deg;C and heat shocked at 80&deg;C.</p>
+	<p>Incubation for 1 hour at 37&deg;C and heat shocked at 80&deg;C.</p>
      </div>
 </fieldset>
@@ Line 652: / Line 660: @@
      <p>Clones were picked from plates with plasmids:</p>
      <ul class="list">
-       <li>Pet24d-Fla-Cup1-1 (piGEM-006)</li>
+       <li>pET24d-Fla-Cup1-1 (piGEM-006)</li>
        <li>pMAD-Hag-Flank (piGEM-005)</li>
        <li>pMAD-Hag-Flank -Cup1-1 (piGEM-016)</li>
@@ Line 670: / Line 678: @@
      <legend><a name="exp15.53">15.53 Sequencing pMAD-fla-cup1-1 </a></legend>
      <div class="exp-content">
-     <p>The sequencing showed the correct insertion of the cup-1-1 gene into the hag-flank construct but contained a stop codon which was not removed by the used reverse primer. Unfortunately we used primers for amplification of the whole cup1-1 gene and not just for the truncated gene coding  for the metallothionein domain only. Therefore new primers had to be designed an the gibson assembly for integration of the metallothionein domain into pMAD and pet24d has to be repeated.</p>
+     <p>The sequencing showed the correct insertion of the cup-1-1 gene into the hag-flank construct but contained a stop codon, which was not removed by the used reverse primer. Unfortunately we used primers for amplification of the whole cup1-1 gene and not just for the truncated gene coding  for the metallothionein domain only. Therefore new primers had to be designed an the Gibson assembly for integration of the metallothionein domain into pMAD and pET24d has to be repeated.</p>
      </div>
 </fieldset>
@@ Line 676: / Line 684: @@
      <legend><a name="exp18.6">18.6 gel extraction & purification of DARPin gene </a></legend>
      <div class="aim">
-     <p>Aim: Receiving DARPin gene with spe1 sites for ligation into linearized piGEM-005</p>
+     <p>Aim: Receiving DARPin gene with <i>Spe</i>I sites for ligation into linearized piGEM-005</p>
      </div>
      <div class="exp-content">
-     <p>The with Spe1 digested pEX-A2 was purified via electrophoresis with an 1% agarose gel in order to divide pEX-A2 backbone and the DARPin gene (489 bp). The digest attempt was splitted and loaded into two pockets to be sure not to overload the gel. The correct bands were cut out and the DNA fragment was rescued according to the protocol of our OMEGA gel extraction kit.</p>
+     <p>The with <i>Spe</i>I digested pEX-A2 was purified via electrophoresis with an 1% agarose gel in order to divide pEX-A2 backbone and the DARPin gene (489 bp). The digest attempt was splitted and loaded into two pockets to be sure not to overload the gel. The correct bands were cut out and the DNA fragment was rescued according to the protocol of our OMEGA gel extraction kit.</p>
      <img src="https://static.igem.org/mediawiki/2014/a/a0/MR_2014-06-07_DARPin.jpg" width="20%"/>
      <p>Expected bands:<br />
@@ Line 690: / Line 698: @@
      <legend><a name="exp18.7">18.7 Ligation of DARPin gene and linearized piGEM-005</a></legend>
      <div class="aim">
-     <p>Aim: Ligation of DARPin- (from 18.6) into Spe1 cut piGEM-005 from 18.5 for integration of the DARPin-Flagellin construct into Bacillus subtilis chromosome</p>
+     <p>Aim: Ligation of DARPin- (from 18.6) into <i>Spe</i>1 digested piGEM-005 from 18.5 for integration of the DARPin-Flagellin construct into <i>Bacillus subtilis</i> chromosome</p>
      </div>
      <div class="exp-content">
-     <p>The DARPin gene with Spe1 sites was used as insert for the ligation into linearized pMAD (from 18.5) which contains the designed Spe1 site. The ligation attempt was done twofold and calculated by the Ligation Calculator from the iGEM-Team Texas in 2011:</p>
+     <p>The DARPin gene with <i>Spe</i>I sites was used as insert for the ligation into linearized pMAD (from 18.5) which contains the designed restriction site. The ligation attempt was done twofold and calculated by the Ligation Calculator from the iGEM-Team Texas in 2011:</p>
      <table width="100%" border="1">
    <tr>
@@ Line 730: / Line 738: @@
      <legend><a name="exp13.63">13.63 checking Bacillus WT 3610  growth on 5&micro;g/&micro;L CM</a></legend>
      <div class="aim">
-     <p>Aim: check if wildtype has a resistance against CM </p>
+     <p>Aim: check if wildtype has a resistance against chloramphenicol (CM) </p>
      </div>
      <div class="exp-content">
      <p>Result: <em>Bacillus subtilis</em> Wildtype 3610 grew on the CM plate.</p>
-     <p>In order to make out if a selection is possible WT3610 was plated out  from an LB plate (13.62)&nbsp; on 25 ng/ &micro;L CM  to check were Bacillus CM threshold is.</p>
+     <p>In order to make out if a selection is possible WT3610 was plated out  from an LB plate (13.62)&nbsp; on 25 ng/ &micro;L CM  to check were the threshold of CM for <i>B. subtilis</i> is.</p>
-     <p>Incubation at 30&deg;C over the weekend.</p>
+     <p>Incubation at 30&deg;C over two days.</p>
 	</div>
 </fieldset>
@@ Line 747: / Line 755: @@
 </h2>
 <fieldset class="exp18">
-     <legend><a name="exp18.8">18.8 new Spe1 restriction of DARPin-gene in pEX-A2 & pMAD-hag-flank (piGEM-005)</a></legend>
+     <legend><a name="exp18.8">18.8 new <i>Spe</i>I restriction of DARPin-gene in pEX-A2 & pMAD-hag-flank (piGEM-005)</a></legend>
      <div class="aim">
      <p>Aim: Receiving new insert and vector in case of an unsuccessful ligation for further attempts. </p>
@@ Line 757: / Line 765: @@
      <th scope="col">pEX-A2-DARPin digest (&micro;l)</th>
      <th scope="col">pMAD-Hag-Flank digest (&micro;l)</th>
-     <th scope="col">Spe1-Mastermix</th>
+     <th scope="col"><i>Spe</i>I-Mastermix</th>
    </tr>
    <tr>
@@ Line 772: / Line 780: @@
    </tr>
    <tr>
-     <th scope="row">SpeI</th>
+     <th scope="row"><i>Spe</i>I</th>
      <td>-</td>
      <td>-</td>
@@ Line 802: / Line 810: @@
    </tr>
 </table>
-	<p>Incubation was performed for 2h at 37&deg;C and heat inactivated at 80&deg;C for  5 minutes.</p>
+	<p>Incubation was performed for 2 h at 37&deg;C and heat inactivated at 80&deg;C for  5 minutes.</p>
 	</div>
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.9">18.9 Transformation of overnight ligation from 18.7</a></legend>
+     <legend><a name="exp18.9">18.9 Transformation of ligation from 18.7</a></legend>
      <div class="exp-content">
-     <p>The whole 20&micro;L attempt from the  overnight ligations were transformed into <em>E.Coli  XL1-Blue</em> and plated on LB-Amp plates.&nbsp;  Additionally a negative control was created by transforming 1&micro;L Spe1 cut  piGEM-005 into <em>E.Coli XL1-Blue </em>as  well.</p>
+     <p>The whole 20&micro;L attempt from the ligations were used to transform <em>E.Coli  XL1-Blue</em>, which were plated on LB-Amp plates.&nbsp;  Additionally a negative control was created by transforming <em>E.Coli XL1-Blue </em> with 1 &micro;L <i>Spe</i>I cut  piGEM-005 as  well.</p>
 	</div>
 </fieldset>
@@ Line 817: / Line 825: @@
      </div>
      <div class="exp-content">
-     <p>The with Spe1 digested pEX-A2 was  purified via electrophoresis with an 1% agarose gel like in 18.6. The band correct bands were cut out and the DNA fragment was rescued according to the  protocol of our OMEGA gel extraction kit.</p>
+     <p>The <i>Spe</i>I digested pEX-A2 was purified via electrophoresis with an 1% agarose gel like in 18.6. The correct bands were cut out and the DNA fragment was purified according to the  protocol of our OMEGA gel extraction kit.</p>
      <img src="https://static.igem.org/mediawiki/2014/1/16/MR_2014-06-08_Darpin.jpg" width="20%" />
      <p>Expected bands:<br />
@@ Line 834: / Line 842: @@
 </h2>
 <fieldset class="exp18">
-     <legend><a name="exp18.12">18.12 Checking Transformation of overnight ligation from 18.7 </a></legend>
+     <legend><a name="exp18.12">18.12 Checking transformation of overnight ligation from 18.7 </a></legend>
      <div class="exp-content">
      <table width="100%" border="1">
@@ Line 862: / Line 870: @@
      </div>
      <div class="exp-content">
-       <p>In order to check the positive  insertion of the DARPin gene into pMAD a PCR amplification with primers 54 and  56 for the flagellin should generate an ca. 1500 bp fragment on the gel.  Negative clones would show still just a 1000 bp band because of the  amplification of the Hag-Spe1 site construct. The picked  clones were transferred on a new LB-amp plate.</p>
+       <p>In order to check the positive  insertion of the DARPin gene into pMAD a PCR amplification with primers 54 and  56 for the flagellin should generate an ca. 1500 bp fragment on the gel.  Negative clones would just show a 1000 bp band because of the  amplification of the Hag-<i>Spe</i>I site construct. The picked  clones were transferred on a new LB-amp plate.</p>
        <table width="100%" border="1">
    <tr>
@@ Line 925: / Line 933: @@
      <legend><a name="exp18.14">18.14 Dephosphorylation of linearized piGEM-005</a></legend>
      <div class="aim">
-     <p>Aim: Dephosphorylation of 5’-end with antarctic phosphatase in order to decrease the religation of the linearized piGEM-005 from 18.8</p>
+     <p>Aim: Dephosphorylation of 5'-end with antarctic phosphatase in order to decrease the religation of the linearized piGEM-005 from 18.8</p>
      </div>
      <div class="exp-content">
-     <p>The cut Spe1 cut piGEM-005 was dephosporylated at the 5’-end with Antarctic phosphatase to prevent the vector from relegation.</p>
+     <p>The cut <i>Spe</i>I cut piGEM-005 was dephosporylated at the 5'-end with antarctic phosphatase to prevent the vector from relegation.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 955: / Line 963: @@
    </tr>
 </table>
-     <p>The sample was incubated for 1h at 37&deg;C at heat inactivated at 70&deg;C for  10minutes.</p>
+     <p>The sample was incubated for 1 h at 37&deg;C at heat inactivated at 70&deg;C for  10 minutes.</p>
      </div>
 </fieldset>
@@ Line 1,001: / Line 1,009: @@
      <legend><a name="exp18.16">18.16 Transformation of overnight ligation from 18.15</a></legend>
      <div class="exp-content">
-     <p>The whole 20&micro;L attempt from the  ligations (18.15) were transformed into <em>E.Coli  XL1-Blue</em> and plated on LB-Amp plates.&nbsp;  Additionally a negative control was created by transforming 1&micro;L Spe1 cut  piGEM-005 into <em>E.Coli XL1-Blue </em>as  well.</p>
+     <p>The whole 20 &micro;L reaction of the ligations (18.15) were used to transform <em>E. coli</em>  XL1-Blue and plated on LB-Amp plates.&nbsp;  Additionally a negative control was created by transforming <em>E.Coli XL1-Blue </em> with 1&micro;L <i>Spe</i>I digested  piGEM-005 as  well.</p>
 	</div>
 </fieldset>
@@ Line 1,010: / Line 1,018: @@
      </div>
      <div class="exp-content">
-     <p>Result: <em>Bacillus subtilis</em> Wildtype 3610 did not grow on the 25 ng/µLCM plate</p>
+     <p>Result: <em>Bacillus subtilis</em> Wildtype 3610 did not grow on the 25 ng/&micro;l CM plate</p>
      <p>In order to check at which concentration CM Bacillus cannot survive he  was plated out from an LB plate on LB-CM plates with different CM  concentrations (5, 10, 15 ng/mL).</p>
      <p>Incubation at 30&deg;C over night.</p>
@@ Line 1,164: / Line 1,172: @@
      </div>
      <div class="exp-content">
-     <p>Six clones of the transformed Top10 cells from 14.39 were picked and used to inoculate overnight cultures (6 x 5 mL).</p>
+     <p>Six clones of the transformed <i>E. coli</i> Top10 cells from 14.39 were picked and used to inoculate overnight cultures (6 x 5 mL).</p>
      </div>
 </fieldset>
@@ Line 1,174: / Line 1,182: @@
      <legend><a name="exp18.9">18.19 Miniprep of positive clones</a></legend>
      <div class="aim">
-     <p>Aim: In order to check the orientation of the positive clones minipreps were inoculated for further experiments</p>
+     <p>Aim: In order to check the orientation of the insert in the vector of the positive clones minipreps were inoculated for further experiments</p>
      </div>
      <div class="exp-content">
-     <p>Because of the ligation via 2  Spe1 sites the chance is 50:50 that the clones contain the  pMAD-Hag-Flank-DARPin construct in the right orientation (Startcodon on the  Hag1-site). For test digests the plasmids have to be amplified by minipreps. </p>
+     <p>Because of the ligation via two  <i>Spe</i>I sites, the chance is 50:50 that the clones contain the  pMAD-Hag-Flank-DARPin construct in the right orientation (Startcodon on the  Hag1-site). For test digests a higher amount of plasmid is needed, which is achieved by inoculation of minipreps.</p>
-     <p>The clones were used to inoculate  7 mL LB-Amp and incubated at 37&deg;C Overnight.</p>
+     <p>The clones were used to inoculate  7 mL LB-Amp and incubated at 37&deg;C over night.</p>
 </div>
 </fieldset>
 <fieldset class="exp13">
-     <legend><a name="exp13.64">13.64 checking Bacillus WT 3610 growth on 25 & 35 &micro;g/&micro;L CM</a></legend>
+     <legend><a name="exp13.64">13.64 checking <i>Bacillus subtilis</i> WT 3610 growth on 25 & 35 &micro;g/&micro;L CM</a></legend>
      <div class="aim">
      <p>Aim: check if wildtype has a resistance against CM </p>
      </div>
      <div class="exp-content">
-     <p>Result: Bacillus subtilis Wildtype 3610 grew on the 5, 10 & 15&micro;g//&micro;l LB-CM plate.</p>
+     <p>Result: <i>Bacillus subtilis</i> Wildtype 3610 grew on the 5, 10 & 15&micro;g/&micro;l LB-CM plate.</p>
-     <p>We saw that Bacillus grew on almost every CM concentration except 25  &micro;g/&micro;L. So we transformed competent WT3610 with Nose plasmid piGEM-003 as a  positive control and plated them out on LB-CM with 25 &micro;g/&micro;L and 35 &micro;g/&micro;L from  Daniel Schindler.</p>
+     <p>We saw that the Bacillus grew on almost every CM concentrations except 25  &micro;g/&micro;L. So we transformed competent WT3610 with Nose plasmid piGEM-003 as a  positive control and plated them out on LB-CM with 25 &micro;g/&micro;L and 35 &micro;g/&micro;L.</p>
-     <p>Additionally WT from Felix Dempwolff which was made competent was also  transformed with piGEM-004 was plated out on LB-CM with 5, 10 and 15 &micro;g/mL CM  to check if these cells can be selected better. </p>
+     <p>Additionally, competent wildtype  3610 cells were transformed with piGEM-004 and plated out on LB-CM with 5, 10 and 15 &micro;g/mL CM  to check, if these cells can be selected better. </p>
      <p>Incubation at 30&deg;C for 2 days.</p>
 </div>
@@ Line 1,204: / Line 1,212: @@
      <legend><a name="exp18.19">18.19 Miniprep of positive clones</a></legend>
      <div class="exp-content">
-     <p>The concentration of the prepped plasmids was between 100 and 150 ng/&micro;L.</p>
+     <p>The concentration of the isolated plasmids was between 100 and 150 ng/&micro;L.</p>
      </div>
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.20">18.20 Test digest with EcoRV </a></legend>
+     <legend><a name="exp18.20">18.20 Test digest with <i>Eco</i>RV </a></legend>
      <div class="aim">
-     <p>Aim: Checking the right orientation of the prepped plasmids</p>
+     <p>Aim: Checking the right orientation of the insert in the isolated plasmids</p>
      </div>
      <div classs="exp-content">
-     <p>The plasmids from the positive clones were digested with EcoRV so that specific fragments emerge when cutting into the DARPin gene and the vector backbone.</p>
+     <p>The plasmids from the positive clones were digested with <i>Eco</i>RV so that specific fragments emerge when cutting into the DARPin gene and the vector backbone.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 1,231: / Line 1,239: @@
    </tr>
    <tr>
-     <th scope="row">EcoRV</th>
+     <th scope="row"><i>Eco</i>RV</th>
      <td>-</td>
      <td>1</td>
    </tr>
    <tr>
-     <th scope="row">Milipore water</th>
+     <th scope="row">Millipore water</th>
      <td>-</td>
      <td>71</td>
@@ Line 1,256: / Line 1,264: @@
        <p>Clone 1, 2, 3, 4, 7, 9 and 11 have the right orientation.</p>
 </div>
+</fieldset>
+<fieldset class="exp20">
+    <legend><a name="exp20.1">20.1 inoculation of preculture from <i>Bacillus subtilis</i> WT 3610</a></legend>
+    <div class="aim">
+    <p>Aim: Preparation of for mainculture the next day</p>
+	</div>
+    <div class="exp-content">
+	<p>2 x 6 mL of LB were inoculated with <i>Bacillus subtilis</i> WT3610 from an LB plate and incubated at 37°C overnight.</p>
+	</div>
 </fieldset>
@@ Line 1,285: / Line 1,302: @@
      <legend><a name="exp18.21">18.21 PCR with pMAD-Hag-Flank-DARPin (piGEM-019) and piGEM-005</a></legend>
      <div class="aim">
-     <p>Aim: Amplification  of Hag-Spe1-construct and Hag-DARPin construct with Nco1/BamH1 sites for  cloning into pet24d &rarr; crystallization of domains.</p>
+     <p>Aim: Amplification  of Hag-<i>Spe</i>I-construct and Hag-DARPin construct with <i>Nco</i>I/<i>Bam</i>HI sites for  cloning into pET24d &rarr; crystallization of domains.</p>
 	</div>
      <div class="exp-content">
@@ Line 1,307: / Line 1,324: @@
      </tr>
    <tr>
-     <th scope="row">Phusion</th>
+     <th scope="row">Phusion DNA-polymerase</th>
      <td>1</td>
      </tr>
@@ Line 1,393: / Line 1,410: @@
 <fieldset class="exp18">
-     <legend><a name="exp18.22">18.22 restriction digest of Hag PCR fragments from 18.21 with Nco1/ BamH1</a></legend>
+     <legend><a name="exp18.22">18.22 restriction digest of Hag PCR fragments from 18.21 with <i>Nco</i>I/<i>Bam</i>HI</a></legend>
      <div class="aim">
-     <p>Aim: creating restriction sites for cloning into pet24d cut with Nco/Bam</p>
+     <p>Aim: creating restriction sites for cloning into pET24d cut with <i>Nco</i>I/<i>Bam</i>HI</p>
      </div>
      <div class="exp-content">
-     <p>The PCR  products from 18.21 were digested with Nco1 and BamH1 to create restriction  sites in order to ligate the fragments into Nco/Bam cut pet24d.</p>
+     <p>The PCR  products from 18.21 were digested with <i>Nco</i>I and <i>Bam</i>HI to create restriction  sites in order to ligate the fragments into <i>Nco</i>I/<i>Bam</i>HI cut pET24d.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 1,413: / Line 1,430: @@
    </tr>
    <tr>
-     <th scope="row">Nco1</th>
+     <th scope="row"><i>Nco</i>I</th>
      <td>1</td>
    </tr>
    <tr>
-     <th scope="row">BamH1</th>
+     <th scope="row"><i>Bam</i>HI</th>
      <td>1</td>
    </tr>
@@ Line 1,429: / Line 1,446: @@
    </tr>
 </table>
-	<p>&nbsp;Incubation for 2h at 37&deg;C with heat shock at  80&deg;C.</p>
+	<p>&nbsp;Incubation for 2 hours at 37&deg;C with heat shock at 80&deg;C.</p>
 </div>
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.23">18.23 Ligation of pet24d and Hag PCR fragments from 18.22 cut with Nco/Bam</a></legend>
+     <legend><a name="exp18.23">18.23 Ligation of pET24d and Hag PCR fragments from 18.22 cut with <i>Nco</i>I/<i>Bam</i>HI</a></legend>
      <div class="aim">
-     <p>Aim: cloning inserts into pet24d for crystallization</p>
+     <p>Aim: cloning inserts into pET24d for crystallization</p>
      </div>
      <div class="exp-content">
-     <p>The Nco/cut Flagellin PCR products from 18.22 (from clone 7 and piGEM-005) were ligated with Nco1 and BamH1 cut pet24d. </p>
+     <p>The <i>Nco</i>I/<i>Bam</i>HI digested flagellin PCR products from 18.22 (from clone 7 and piGEM-005) were ligated with <i>Nco</i>I/<i>Bam</i>HI digested pET24d. </p>
      <table width="100%" border="1">
    <tr>
@@ Line 1,466: / Line 1,483: @@
    </tr>
    <tr>
-     <th scope="row">Milipore Water</th>
+     <th scope="row">Millipore Water</th>
      <td>10</td>
      <td>10</td>
@@ Line 1,476: / Line 1,493: @@
    </tr>
 </table>
-	<p>Incubation overnight at room temperature.</p>
+	<p>Incubation over night at room temperature.</p>
      </div>
 </fieldset>
@@ Line 1,482: / Line 1,499: @@
      <legend><a name="exp20.2">20.2 Transformation of competent <em>Bacillus subtilis</em></a></legend>
      <div class="aim">
-     <p>Aim: transformation of plasmid into Bacillus subtilis WT3610</p>
+     <p>Aim: transformation of <i>Bacillus subtilis</i> WT3610 with piGEM005 and piGEM018</p>
      </div>
      <div class="exp-content">
-     <p>100 &micro;L  of overnight culture were added to 10 mL of MNGE-Medium and incubated till an  OD of 1,1-1,3 at 37&deg;C which could take 4-5h.</p>
+     <p>100 &micro;L  of overnight culture were added to 10 mL of MNGE-Medium and incubated to an  OD<sub>600</sub> of 1,1-1,3 at 37&deg;C which could take 4-5 hours.</p>
-     <p>After  reaching OD of 1,1-1,3 2 x 400 &micro;L of the culture were transformed with 1,5 &micro;g  piGEM-005 and -018. After 1h incubation at 37&deg;C 100 &micro;L Expression mix were  added and incubated for 1h as well.</p>
+     <p>After  reaching an OD of 1,1-1,3 2 x 400 &micro;L of the culture were transformed with 1,5 &micro;g  piGEM-005 and -018. After one hour incubation at 37&deg;C 100 &micro;L expression mix were  added and incubated for one hour as well.</p>
-     <p>In the  end the 500 &micro;L attempt was plated out on MLS-X-Gal plates and incubated at 30  &deg;C overnight until colonies could be seen. </p>
+     <p>In the  end the 500 &micro;L sample was plated out on MLS-X-Gal plates and incubated at 30  &deg;C until colonies could be seen. </p>
 </div>
 </fieldset>
@@ Line 1,499: / Line 1,516: @@
 </h2>
 <fieldset class="exp18">
-     <legend><a name="exp18.24">18.24 Transformation of overnight ligation</a></legend>
+     <legend><a name="exp18.24">18.24 Transformation of ligation</a></legend>
      <div class="aim">
      <p>Aim: checking success of ligation and amplification of ligated construct</p>
      </div>
      <div class="exp-content">
-     <p>The  whole 20&micro;L attempt was transformed into E.Coli X1-Blue, plated out on LB-Can  plates and incubated at 37&deg;C overnight.</p>
+     <p>The  whole 20 &micro;L attempt was used to transform <i>E. coli</i> X1-Blue, plated out on LB-Can  plates and incubated at 37&deg;C overnight.</p>
 </div>
 </fieldset>
@@ Line 1,510: / Line 1,527: @@
      <legend><a name="exp18.25">18.25 Miniprep of pMAD-Hag-Flank-DARPin (piGEM-018)</a></legend>
      <div class="aim">
-     <p>Aim: Amplification of plasmids for work and storage</p>
+     <p>Aim: increase amount of plasmid for work and storage</p>
      </div>
      <div class="exp-content">
-     <p>2x 6 mL of LB-Amp were inoculated  with a colony from apiGEM-018 transformation plate and incubated at 37&deg;C  overnight. </p>
+     <p>2 x 6 mL of LB-Amp were inoculated  with a colony from a piGEM-018 transformation plate and incubated at 37&deg;C  overnight. </p>
 </div>
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.26">18.26 sequencing of constructs</a></legend>
+     <legend><a name="exp18.26">18.26 Sequencing of constructs</a></legend>
      <div class="aim">
      <p>Aim: checking the right insertion into the plasmids</p>
      </div>
      <div class="exp-content">
-     <p>pMAD-Hag-Flank-DARPin and the  hormone receptor clone 1 were given away in form of a premix with primers for  sequencing. 10 &micro;L with 50-100 ng/&micro;L were mixed with 2 &micro;L of primers for  sequencing according to the following scheme:</p>
+     <p>pMAD-Hag-Flank-DARPin was sent in form of a premix with primers for sequencing. 10 &micro;L with 50-100 ng/&micro;L were mixed with 2 &micro;L of primers for  sequencing according to the following scheme:</p>
      <table width="100%" border="1">
    <tr>
@@ Line 1,541: / Line 1,558: @@
      <td>pMAD-Hag-Flank-DARPin</td>
      <td>Flo56 (Hag-R-Bam)</td>
-  </tr>
-  <tr>
-    <th scope="row">3</th>
-    <td>393</td>
-    <td>pRSGII426+receptor  gene</td>
-    <td>TW248</td>
-  </tr>
-  <tr>
-    <th scope="row">4</th>
-    <td>394</td>
-    <td>pRSGII426+receptor  gene</td>
-    <td>TW249</td>
    </tr>
 </table>
@@ Line 1,558: / Line 1,563: @@
 </fieldset>
 <fieldset class="exp13">
-     <legend><a name="exp13.65">13.65 checking Bacillus WT from Felix Dempwolff growth</a></legend>
+     <legend><a name="exp13.65">13.65 Checking growth of <i>Bacillus subtilis</i> WT3610</a></legend>
      <div class="aim">
-     <p>Aim: check which WT can used for selection with Nose plasmids</p>
+     <p>Aim: check which WT can be used for selection with Nose plasmids</p>
      </div>
      <div class="exp-content">
      <p></p>
-     <p>Competent WT from Felix Dempwolff was transformed with piGEM-002, -003  and -004 by incubating the aliquods with 5 &micro;L plasmid for 30 min at 37&deg;C. After  half an hour the whole attempt was plated out on LB-Cm (5 ng/&micro;L). </p>
+     <p>Competent 3610 were transformed with piGEM-002, -003  and -004 by incubating the aliquots with 5 &micro;L plasmid for 30 min at 37&deg;C. After  half an hour the whole sample was plated out on LB-Cm (5 ng/&micro;L). </p>
      <p>Incubation at 30&deg;C for 2 days.</p>
 </div>
@@ Line 1,577: / Line 1,582: @@
 </h2>
 <fieldset class="exp18">
-     <legend><a name="exp18.27">18.27 miniprep of inoculated plasmids from 18.25</a></legend>
+     <legend><a name="exp18.27">18.27 miniprep of plasmids from 18.25</a></legend>
      <div class="aim">
      <p>Aim: isolation of plasmids</p>
@@ Line 1,586: / Line 1,591: @@
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.28">18.28 pet24d digest with Nco/Bam</a></legend>
+     <legend><a name="exp18.28">18.28 pET24d digest with Nco/Bam</a></legend>
      <div class="aim">
      <p>Aim: preparing vector for new ligation attempts</p>
      </div>
      <div class="exp-content">
-     <p>Because of the unsuccessful ligation from 18.23 new vector (pet24d) was cut with Nco1 and BamH1 according to the following scheme: </p>
+     <p>Because of the unsuccessful ligation from 18.23 new vector (pET24d) was digested with <i>Nco</i>I and <i>Bam</i>HI according to the following scheme: </p>
         <table width="100%" border="1">
    <tr>
@@ Line 1,598: / Line 1,603: @@
    </tr>
    <tr>
-     <th scope="row">Pet24d (148 ng/&micro;L)</th>
+     <th scope="row">pET24d (148 ng/&micro;L)</th>
      <td>15</td>
    </tr>
@@ Line 1,606: / Line 1,611: @@
    </tr>
    <tr>
-     <th scope="row">Nco1</th>
+     <th scope="row"><i>Nco</i>I</th>
      <td>0,5</td>
    </tr>
    <tr>
-     <th scope="row">BamH1</th>
+     <th scope="row"><i>Bam</i>HI</th>
      <td>0,5</td>
    </tr>
@@ Line 1,626: / Line 1,631: @@
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.29">18.29 Pst1 digest of PCR fragments from piGEM-018 with Hag-primers</a></legend>
+     <legend><a name="exp18.29">18.29 <i>Pst</i>I digestion of PCR fragments from piGEM-018 with Hag-primers</a></legend>
      <div class="aim">
-     <p>Aim: checking if the correct inserts are used for ligation </p>
+     <p>Aim: check if the correct inserts are used for ligation </p>
      </div>
      <div class="exp-content">
-     <p>The DARPin-Hag  constructs contain a Pst1 restriction site which could be used to check if the  DARPin gene was inserted into the Hag-construct correctly again. For that  purpose PCR products based on piGEM-018 from clone 7 and 12 (right and wrong  orientation) as a template were cut with Pst1. </p>
+     <p>The DARPin-Hag  constructs contain a <i>Pst</i>I restriction site which could be used to check if the  DARPin gene was inserted into the Hag-construct correctly again. For that  purpose PCR products based on piGEM-018 from clone 7 and 12 (right and wrong  orientation) as a template were digested with <i>Pst</i>I. </p>
      <p>PCR  products from clone 7: 658 bp and 781 bp fragment.</p>
-     <p>&nbsp;PCR products from clone 12:1000bp and 429 bp  fragments.</p>
+     <p>&nbsp;PCR products from clone 12: 1000bp and 429 bp  fragments.</p>
       <table width="100%" border="1">
    <tr>
@@ Line 1,648: / Line 1,653: @@
    </tr>
    <tr>
-     <th scope="row">Pst1</th>
+     <th scope="row"><i>Pst</i>I</th>
      <td>0,5</td>
    </tr>
@@ Line 1,670: / Line 1,675: @@
      </div>
      <div class="exp-content">
-     <p>piGEM-018 & -005 were used as template for a PCR with the primers from Florian Altegoer 54 and 56. The products could be used for further cloning after Nco/Bam digest.</p>
+     <p>piGEM-018 & -005 were used as template for a PCR with the primers  54flo and 56flo. The products could be used for further cloning after <i>Nco</i>I/<i>Bam</i>HI digest.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 1,759: / Line 1,764: @@
      <legend><a name="exp15.54">15.54 new PCR amplification of cup1-1</a></legend>
      <div class="aim">
-     <p>Aim: amplification of cup1-1 domain for Gibson assembly into pMAD</p>
+     <p>Aim: amplification of cup1-1 domain for Gibson assembly with pMAD</p>
      </div>
      <div class="exp-content">
@@ Line 1,781: / Line 1,786: @@
      </tr>
    <tr>
-     <th scope="row">Phusion</th>
+     <th scope="row">Phusion DNA-polymerase</th>
      <td>1</td>
      </tr>
@@ Line 1,844: / Line 1,849: @@
    </tr>
 </table>
+<br />
 	<img src="https://static.igem.org/mediawiki/2014/e/e2/MR_2014-06-14_cup1-1.jpg" width="10%" />
-	<p>Referring to the gel analysis the amplification was successful.</p>
+	<br />
+	<p>According to the gel analysis the amplification was successful.</p>
      </div>
 </fieldset>
@@ Line 1,857: / Line 1,864: @@
 </h2>
 <fieldset class="ex20">
-     <legend><a name="exp20.3a">20.3 Overnight culture of blue clones</a></legend>
+     <legend><a name="exp20.3a">20.3 Overnight culture of positive clones</a></legend>
      <div class="aim">
-     <p>Aim: transformation of plasmid into Bacillus subtilis WT3610</p>
+     <p>Aim: transformation of <i>Bacillus subtilis</i> WT3610 with plasmid</p>
      </div>
      <div class="exp-content">
-     <p>Colonies  were grown on the plates with transformed piGEM-005 &amp; - 018. The blue/  white screening showed positive transformed blue clones.&nbsp; 3 clones of different morphology per plate  were picked and used for inoculation of LB-MLS (4 mL LB, 4 &micro;L Lincomycin, 4 &micro;L  Erythromycin). Incubation was carried out overnight at 30&deg;C with the 6  cultures.<strong> </strong></p>
+     <p>Colonies grew on the transformand plates (piGEM-005 &amp; - 018). The blue/  white screening showed positive transformed blue clones.&nbsp; Three clones per plate were picked and used for inoculation of LB-MLS (4 mL LB, 4 &micro;L lincomycin, 4 &micro;L  erythromycin). Incubation was carried out over night at 30&deg;C with the six cultures.</p>
 </div>
 </fieldset>
@@ Line 1,902: / Line 1,909: @@
      </div>
      <div class="exp-content">
-     <p>The 6  overnight cultures were used to inoculate 10 mL LB MLS until&nbsp; the culture obtained an OD of 0,1. The  cultures were incubated at 30&deg;C for 2h.</p>
+     <p>The 6  overnight cultures were used to inoculate 10 mL LB MLS, which were incubated until the culture obtained an OD of 0,1. The  cultures were incubated at 30&deg;C for 2h.</p>
-     <p>Then  the temperature was shifted to 42&deg;C for 6h.</p>
+     <p>Subsequently, the temperature was shifted to 42&deg;C for 6h.</p>
-     <p>After  the heat shock dilutions from 10-4 to 10-6 of each culture  were plated out on MLS-X-Gal so that 18 plates could be incubated overnight at  42&deg;C.</p>
+     <p>After  the heat shock dilutions from 10<sup>-4</sup> to 10<sup>-6</sup> of each culture  were plated out on MLS-X-Gal so that 18 plates could be incubated overnight at  42&deg;C.</p>
 </div>
 </fieldset>
 <fieldset class="exp15">
-     <legend><a name="exp15.54">15.54 Gibson-assebmly with  PCR amplificated cup1-1 and spe1 cut piGEM-005</a></legend>
+     <legend><a name="exp15.54">15.54 Gibson-assembly with  PCR amplified <i>cup</i>1-1 and <i>Spe</i>I digested piGEM-005</a></legend>
      <div class="aim">
-     <p>Aim: insertion of cup1-1 into piGEM-005</p>
+     <p>Aim: insertion of <i>cup</i>1-1 into piGEM-005</p>
      </div>
      <div class="exp-content">
-     <p>The cup1-1 domain was amplified via PCR with new primers iGEM-024 and  -025. Vector and template were diluted to a concentration under 75 ng/&micro;L. Spe1  cut piGEM-005 was used from the cloning experiments with DARPin.</p>
+     <p>The <i>cup</i>1-1 domain was amplified via PCR with new primers iGEM-024 and  -025. Vector and template were diluted to a concentration under 75 ng/&micro;L. Spe1  cut piGEM-005 was used from the cloning experiments with DARPin.</p>
-     <p>PCR fragment cup1-1 (464 ng/&micro;L) dilution 1:10</p>
+     <p>PCR fragment <i>cup</i>1-1 (464 ng/&micro;L) dilution 1:10</p>
-     <p>Spe1 cut pIGEM-005 (148 ng/&micro;L) dilution 1:2</p>
+     <p><i>Spe</i>I digested pIGEM-005 (148 ng/&micro;L) dilution 1:2</p>
      <table width="100%" border="1">
    <tr>
@@ Line 1,926: / Line 1,933: @@
    </tr>
    <tr>
-     <th scope="row">Insert (cup1-1 58 ng/&micro;L)</th>
+     <th scope="row">Insert (<i>cup</i>1-1 58 ng/&micro;L)</th>
      <td>1,3</td>
    </tr>
@@ Line 1,978: / Line 1,985: @@
      <div class="exp-content">
      <p>One  blue colony per diluted clone was used to inoculate 4 mL LB. The 6 cultures  were incubated at 30&deg;C for 6h and afterwards for 3h at 42&deg;C.</p>
-     <p>Dilutions  from 10-4&shy; to 10-6 were plated out on 18 X-Gal plates  WITHOUT MLS selection. The positive clones should not contain the resistance  inside the backbone as well as the galactosidase. The plates were incubated at  42&deg;C overnight.</p>
+     <p>Dilutions  from 10<sup>-4</sup> to 10<sup>-4</sup> were plated out on 18 X-Gal plates  without MLS selection. The positive clones should not contain the resistance  inside the backbone as well as the galactosidase, resulting in normal colored colonies. The plates were incubated at  42&deg;C overnight.</p>
 </div>
 </fieldset>
@@ Line 1,987: / Line 1,994: @@
      </div>
      <div class="exp-content">
-     <p>Unfortunately the plate was empty, no colonies. The vector was cut newly in order to repeat the assembly.</p>
+     <p>Unfortunately the plate was empty: no colonies. The vector was digested again in order to repeat the assembly.</p>
      </div>
 </fieldset>
 <fieldset class="exp15">
-     <legend><a name="exp15.55">15.55 restriction digest of piGEM-005 with spe1</a></legend>
+     <legend><a name="exp15.55">15.55 restriction digest of piGEM-005 with <i>Spe</i>I</a></legend>
      <div class="aim">
      <p>Aim: linearizing plasmid for repeating the Gibson assembly</p>
      </div>
      <div class="exp-content">
-     <p>In order to repeat the Gibson assembly the piGEM-005 was cut with spe1 freshly.</p>
+     <p>In order to repeat the Gibson assembly the piGEM-005 was cut with <i>Spe</i>I again.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 2,011: / Line 2,018: @@
    </tr>
    <tr>
-     <th scope="row">Spe1</th>
+     <th scope="row"><i>Spe</i>I</th>
      <td>0,5</td>
    </tr>
@@ Line 2,023: / Line 2,030: @@
    </tr>
 </table>
+<br />
 	<p>Incubation 1h  at 37&deg;C with following heat shock at 80&deg;C</p>
 </div>
@@ Line 2,035: / Line 2,043: @@
 </h2>
 <fieldset class="exp20">
-     <legend><a name="exp20.5">20.5 selection of positive clones</a></legend>
+     <legend><a name="exp20.5">20.5 Selection of positive clones</a></legend>
      <div class="aim">
-     <p>Aim: checking the correct flip out of the pMAD backbone</p>
+     <p>Aim: check the correct excision of the pMAD backbone</p>
      </div>
      <div class="exp-content">
-     <p>From  the dilution plates was one WHITE clone picked and transferred on a Master  X-Gal Plate as well as on a MLS plate so that 18 clones were proven for the  right integration of the insert although flipping out the pMAD backbone.</p>
+     <p>One white clone was picked from the dilution plates and transferred on a X-Gal Plate as well as on a MLS plate so that 18 clones were tested for the  right integration of the insert although flipping out the pMAD backbone.</p>
-     <p>The  plates were incubated at 42&deg;C overnight.</p>
+     <p>The  plates were incubated at 42&deg;C over night.</p>
 </div>
 </fieldset>
 <fieldset class="exp15">
-     <legend><a name="exp15.56">15.56 new Gibson-assembly with  cup1-1 and spe1 cut piGEM-005</a></legend>
+     <legend><a name="exp15.56">15.56 new Gibson-assembly with  cup1-1 and <i>Spe</i>I digested piGEM-005</a></legend>
      <div class="aim">
      <p>Aim: insertion of cup1-1 into piGEM-005</p>
      </div>
      <div class="exp-content">
-     <p>As insert cup1-1 PCR product from 15.55 and Spe1 cut piGEM-005 from  15.55 were used for a new Gibson assembly.</p>
+     <p>As insert cup1-1 PCR product from 15.55 and <i>Spe</i>I digested piGEM-005 from  15.55 were used for a new Gibson assembly.</p>
 <p>PCR fragment cup1-1 (464 ng/&micro;L)</p>
-     <p>Spe1 cut pIGEM-005 (53 ng/&micro;L) </p>
+     <p><i>Spe</i>I digested pIGEM-005 (53 ng/&micro;L) </p>
      <table width="100%" border="1">
    <tr>
@@ Line 2,076: / Line 2,084: @@
 </table>
 	<p>The mix was incubated 5 min at room temperature and then for 1h at 50&deg;C.</p>
-<p>In the end the whole mix was transformed into E.Coli XL1-Blue and plated  out on LB-Amp. Incubation was done overnight at 37&deg;C.</p>
+<p>In the end the whole mix was used to transform  <i>E. coli</i> XL1-Blue and plated  out on LB-Amp. Incubation was done overnight at 37&deg;C.</p>
 </div>
 </fieldset>
@@ Line 2,093: / Line 2,101: @@
      </div>
      <div class="exp-content">
-     <p>The white colonies  grew on the X-Gal Master plates but not on MLS plates so the transformation  seemed to be successful. The Backbone with the MLS resistance flipped out of  the genome</p>
+     <p>The white colonies  grew on the X-Gal Master plates but not on MLS plates so the transformation  seemed to be successful. The Backbone with the MLS resistance flipped out of  the genome.</p>
      </div>
 </fieldset>
 <fieldset class="exp20">
-     <legend><a name="exp20.6">20. 6 cPCR with checked clones</a></legend>
+     <legend><a name="exp20.6a">20.6a cPCR with checked clones</a></legend>
      <div class="aim">
      <p>Aim: checking integration of constructs Hag-Spe and Hag-Spe-DARPin into B. s. genome</p>
      </div>
      <div class="exp-content">
-     <p>No  clone was growing on MLS plates so the picked clones seemed to be positive. In  order to check the correct integration of the domain constructs a cPCR with the  picked clones on the X-Gal plates was done. The picked 18 B.s. clones were  cooked in 10 &micro;L PBS for 5 min at 95&deg;C.</p>
+     <p>No  clone was growing on MLS plates so the picked clones seemed to be positive. In  order to check the correct integration of the domain constructs, a cPCR with the picked clones on the X-Gal plates was done. The 18 picked <i>B.subtilis</i> clones were  cooked in 10 &micro;L PBS for 5 min at 95&deg;C.</p>
           <table width="100%" border="1">
            <tr>
@@ Line 2,209: / Line 2,217: @@
      <legend><a name="exp15.57">15.57 Miniprep of clones from Gibson assembly from 15.56</a></legend>
      <div class="aim">
-     <p>Aim: Plasmid amplification for further experiments</p>
+     <p>Aim: increase the amount of plasmid for further experiments</p>
      </div>
      <div class="exp-content">
-     <p>4x 5 mL of LB-Amp was were  inoculated with a picked colony from a transformation plate with XL1-Blue  containing the Gibson-Assembly product from 15.56.</p>
+     <p>4 x 5 mL of LB-Amp was were  inoculated with a picked colony from a transformation plate with XL1-Blue  containing the Gibson-assembly product from 15.56.</p>
      <p>Incubation at 37&deg;C overnight.</p>
 </div>
@@ Line 2,225: / Line 2,233: @@
 </h2>
 <fieldset class="exp15">
-     <legend><a name="exp15.58">15.58 cPCR with colonies from Gibson piGEM-005 + cup1-1 plate</a></legend>
+     <legend><a name="exp15.58">15.58 cPCR with colonies from Gibson-assembly of piGEM-005 + cup1-1 plate</a></legend>
      <div class="aim">
      <p>Aim: checking correct insertion of cup1-1</p>
      </div>
      <div class="exp-content">
-     <p>In order to check the correct  insertion of the cup1-1 domain into the Hag-Flank-construct in pMAD a cPCR with  primers iGEM-025 (Cup1-1 rv) and Flo89 (pMAD-flank1-Bamh1 fw) was performed. The picked colonies were the same which wre  used to inoculate minipreps from 15.57. The fragment was supposed to e ca. 1250  bp. </p>
+     <p>In order to check the correct  insertion of the cup1-1 domain into the Hag-Flank-construct in pMAD a cPCR with  primers iGEM-025 (Cup1-1 rv) and Flo89 (pMAD-flank1-<i>Bam</i>HI fw) was performed. The picked colonies were the same which were used to inoculate minipreps from 15.57. The fragment was supposed to have approx. 1250  bp. </p>
      <table width="100%" border="1">
            <tr>
@@ Line 2,253: / Line 2,261: @@
          </tr>
            <tr>
-             <th scope="row">Phusion</th>
+             <th scope="row">Phusion DNA-polymerase</th>
              <td>2,5</td>
              <td>-</td>
@@ Line 2,326: / Line 2,334: @@
            </tr>
          </table>
-         <p>The analysis via 1% agarose gel eletrophoresis showed now bands. All 4 picked clones were prepped to use the plasmid as template.</p>
+         <p>The analysis via 1% agarose gel eletrophoresis showed now bands. The plasmids of all four clones were isolated to use them as template.</p>
 	</div>
 </fieldset>
 <fieldset class="exp15">
-     <legend><a name="exp15.59">15.59 PCR with prepped plasmid from Gibson piGEM-005 + cup1-1 plate</a></legend>
+     <legend><a name="exp15.59">15.59 PCR with isolated plasmid from Gibson piGEM-005 + cup1-1 plate</a></legend>
      <div class="aim">
      <p>Aim: checking correct insertion of cup1-1</p>
      </div>
      <div class="exp-content">
-     <p>This  time the prepped plasmid DNA from the picked 6clones was used as a template  with different primer pairs. First of all tie PCR attempts were performed with  primers Flo89 and Flo90 in order to receive the whole Hag-Flank-Cup1-1  construct with ca. 2100 bp length. As negative control also piGEM-005 was used  as template producing a 2000kb fragment. Because of the small difference all 6  attempts were also driven with the primers Flo89 and iGEM-025 (cup1-1 rv) in  order to check the insertion of cup1-1 directly with a fragment of 1268 bp.</p>
+     <p>This  time the isolated plasmid DNA from the picked six clones was used as a template  with different primer pairs. First of all the PCR reactions were performed with  primers Flo89 and Flo90 in order to receive the whole Hag-Flank-Cup1-1  construct with ca. 2100 bp length. As negative control also piGEM-005 was used  as template producing a 2000kb fragment. Because of the small difference, all six reactions were also performed with the primers Flo89 and iGEM-025 (cup1-1 rv) in  order to check the insertion of cup1-1 directly with a fragment of 1268 bp.</p>
      <table width="100%" border="1">
        <tr>
          <th scope="col">Mix</th>
-         <th scope="col"><strong>Master-Mix 1 for&nbsp;  5 attempts (&micro;L)</strong></th>
+         <th scope="col"><strong>Master-Mix 1 for&nbsp;  5 reactions (&micro;L)</strong></th>
-         <th scope="col"><strong>Master-Mix 2 for&nbsp;  5 attempts (&micro;L)</strong></th>
+         <th scope="col"><strong>Master-Mix 2 for&nbsp;  5 reactions (&micro;L)</strong></th>
-         <th scope="col"><strong>Mix 1 for PCR attempt (&micro;L)</strong></th>
+         <th scope="col"><strong>Mix 1 for PCR reactions (&micro;L)</strong></th>
-         <th scope="col"><strong>Mix 2for PCR attempt (&micro;L)</strong></th>
+         <th scope="col"><strong>Mix 2for PCR reactions (&micro;L)</strong></th>
        </tr>
        <tr>
@@ Line 2,373: / Line 2,381: @@
        </tr>
        <tr>
-         <th scope="row">Phusion</th>
+         <th scope="row">Phusion DNA-polymerase</th>
          <td>2,5</td>
          <td>2,5</td>
@@ Line 2,459: / Line 2,467: @@
          </table>
          <br />
-         <img src="https://static.igem.org/mediawiki/2014/6/61/MR_2014-06-21_piGEM-005_cup1-1.jpg" width="20%" />
+         <img src="https://static.igem.org/mediawiki/2014/6/61/MR_2014-06-21_piGEM-005_cup1-1.jpg" width="30%" />
-         <p>The gel analysis shows that all 4 clones seem to be positive. By amplification of the cup1-1 fragment with the plasmid DNA as template could proof that.</p>
+         <p>The gel analysis shows that all 4 clones seem to be positive. An amplification of the cup1-1 fragment with the plasmid DNA as template could proof that.</p>
 </div>
 </fieldset>
 <fieldset class="exp20">
-     <legend><a name="exp20.6a">20. 6 repeating cPCR with checked clones</a></legend>
+     <legend><a name="exp20.6a">20.6b Repeated cPCR with checked clones</a></legend>
      <div class="aim">
-     <p>Aim: checking integration of constructs Hag-Spe and Hag-Spe-DARPin into B. s. genome</p>
+     <p>Aim: checking integration of constructs Hag-<i>Spe</i>I and Hag-<i>Spe</i>I-DARPin into B. s. genome</p>
      </div>
      <div class="exp-content">
-     <p>Because  of the unsuccessful cPCR before the PCR was repeated. The picked 18 B.s. clones  were cooked in 30 &micro;L PBS for 10 min at 95&deg;C.</p>
+     <p>Because  of the unsuccessful cPCR before, the PCR was repeated. The 18 picked <i>B.subtilis</i> clones  were cooked in 30 &micro;L PBS for 10 min at 95&deg;C.</p>
              <table width="100%" border="1">
            <tr>
@@ Line 2,492: / Line 2,500: @@
              </tr>
            <tr>
-             <th scope="row">Phusion</th>
+             <th scope="row">Phusion DNA-polymerase</th>
              <td>18</td>
              <td>-</td>
@@ Line 2,571: / Line 2,579: @@
          </table>
          <br />
-         <img src="https://static.igem.org/mediawiki/2014/1/18/MR_2014-06-21_darpin.jpg" width="30%" />
+         <img src="https://static.igem.org/mediawiki/2014/1/18/MR_2014-06-21_darpin.jpg" width="40%" />
-</div>
+		<br />
-</fieldset>
+		<p>All nine clones with piGEM-005 seem to be positive. Clone 1, 3, 7, 8 and  9 of transformed piGEM-018.1 might be positive as well as clone 2-6 from  piGEM-018.2. The sequencing of the PCR products should tell us if the insertion  was successful.</p>
-<fieldset class="exp20">
+	</div>
-    <legend><a name="exp20.6b">20. 6 repeating cPCR with checked clones</a></legend>
-    <div class="exp-content">
-    <p>The clones with piGEM-005 seem to be positive all 9. Clone 1, 3, 7, 8 and  9 of transformed piGEM-018.1 might be positive as well as clone 2-6 from  piGEM-018.2. The sequencing of the PCR products should tell us if the insertion  was successful.</p>
-</div>
 </fieldset>
 </div>
@@ Line 2,594: / Line 2,598: @@
      </div>
      <div class="exp-content">
-     <p>piGEM-018  &amp; -005 were used as template for a PCR with the primers from Florian  Altegoer 54 and 56. The products could be used for further cloning after  Nco/Bam digest. </p>
+     <p>piGEM-018  &amp; -005 were used as template for a PCR with the primers Flo 54 and Flo 56. The products could be used for further cloning after  <i>Nco</i>I/<i>Bam</i>HI digest. </p>
      <table width="100%" border="1">
    <tr>
@@ Line 2,681: / Line 2,685: @@
      <legend><a name="exp18.32">18.32 cPCR with new clones</a></legend>
      <div class="aim">
-     <p>Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pet24d</p>
+     <p>Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pET24d</p>
      </div>
      <div class="exp-content">
-     <p>more clones from each  plate were picked to analyse them via cPCR with the primers flo54 and flo56  (Hag-fw and Hag-rv). The result should be a ca. 1kb fragment for correct  pet24d-Hag containing clones and a 1,5 kb fragment for pet24d-Hag-DARPin  containing clones.</p>
+     <p>More clones from each  plate were picked to analyse them via cPCR with the primers flo54 and flo56  (Hag-fw and Hag-rv). The result should be a ca. 1kb fragment for correct  pET24d-Hag containing clones and a 1,5 kb fragment for pET24d-Hag-DARPin  containing clones.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 2,708: / Line 2,712: @@
    </tr>
    <tr>
-     <th scope="row">Phusion</th>
+     <th scope="row">Phusion DNA-polymerase</th>
      <td>-</td>
      <td>7</td>
@@ Line 2,748: / Line 2,752: @@
              <th scope="row">1</th>
              <td>98</td>
-             <td>3 min</td>
+             <td>10 min</td>
            </tr>
            <tr>
@@ Line 2,768: / Line 2,772: @@
              <th scope="row">5</th>
              <td>Go To 2</td>
-             <td>30x</td>
+             <td>35x</td>
            </tr>
            <tr>
@@ Line 2,781: / Line 2,785: @@
            </tr>
          </table>
+		<br />
+		<img src="https://static.igem.org/mediawiki/2014/b/bf/MR_20140622_PCR_DARPin-Hag_Hag-fragment.png" width="40%" />
+		<br />
+		<p>Clone 1 from each pET24d-Hag-<i>Spe</i>I and pET24d-Hag-DARPin clones was positive and were digested with <i>Nco</i>I/<i>Bam</i>I to check them again.</p>
      </div>
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.33">18.33 pet24d digest with Nco/Bam</a></legend>
+     <legend><a name="exp18.33">18.33 pET24d digest with <i>Nco</i>I/<i>Bam</i>HI</a></legend>
      <div class="aim">
      <p>Aim: preparing vector for new ligation attempts</p>
      </div>
      <div class="exp-content">
-     <p>Because  of the low amount of right clones new vector (pet24d) was cut with Nco1 and  BamH1 according to the following scheme:</p>
+     <p>Because  of the low amount of right clones, new vector (pET24d) was digested with <i>Nco</i>I and <i>Bam</i>HI according to the following scheme:</p>
      <table width="100%" border="1">
    <tr>
@@ Line 2,796: / Line 2,804: @@
    </tr>
    <tr>
-     <th scope="row">Pet24d (50 ng/&micro;L)</th>
+     <th scope="row">pET24d (50 ng/&micro;L)</th>
      <td>20</td>
    </tr>
    <tr>
-     <th scope="row">Cutsmart 10x</th>
+     <th scope="row">CutSmart 10x</th>
      <td>3</td>
    </tr>
    <tr>
-     <th scope="row">Nco1</th>
+     <th scope="row"><i>Nco</i>I</th>
      <td>0,5</td>
    </tr>
    <tr>
-     <th scope="row">BamH1</th>
+     <th scope="row"><i>Bam</i>HI</th>
      <td>0,5</td>
    </tr>
@@ Line 2,820: / Line 2,828: @@
    </tr>
 </table>
-	<p>Incubation at 37°C for 2h with heat shock in the end at 80&deg;C</p>
+	<p>Incubation at 37&deg;C for 2 hours with heat shock in the end at 80&deg;C</p>
 	<p>Endconcentration:  32 ng/&micro;L</p>
 </div>
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.34">18.34 restriction digest of Hag PCR fragments from 18.31 with Nco1/ BamH1</a></legend>
+     <legend><a name="exp18.34">18.34 Restriction digest of Hag PCR fragments from 18.31 with <i>Nco</i>I/<i>Bam</i>HI</a></legend>
      <div class="aim">
-     <p>Aim: creating restriction sites for cloning into pet24d cut with Nco/Bam</p>
+     <p>Aim: creating restriction sites for cloning into pet24d cut with <i>Nco</i>I/<i>Bam</i>HI</p>
      </div>
      <div class="exp-content">
-     <p>The PCR products from 18.x were digested with Nco1 and BamH1 to create restriction sites in order to ligate the fragments into Nco/Bam cut pet24d in case of negative clones refering to the cPCR from 18.x</p>
+     <p>The PCR products from 18.31 were digested with <i>Nco</i>I and<i>Bam</i>HI to create restriction sites in order to ligate the fragments into <i>Nco</i>I/<i>Bam</i>HI digested pet24d in case of negative clones refering to the cPCR from 18.x</p>
      <table width="100%" border="1">
    <tr>
@@ Line 2,848: / Line 2,856: @@
    </tr>
    <tr>
-     <th scope="row">Nco1</th>
+     <th scope="row"><i>Nco</i>I</th>
      <td>0,5</td>
      <td>0,5</td>
    </tr>
    <tr>
-     <th scope="row">BamH1</th>
+     <th scope="row"><i>Bam</i>HI</th>
      <td>0,5</td>
      <td>0,5</td>
@@ Line 2,881: / Line 2,889: @@
      </div>
      <div class="exp-content">
-     <p>Using  the plasmids as template the cup1-1 fragment at 160 bp should be visible on the  agarose gel. As positive control PCR products from the cup1-1 amplification  used for the Gibson Assembly into piGEM-005 were applicated on the gel as well. </p>
+     <p>Using  the plasmids as template the cup1-1 fragment at 160 bp should be visible on the  agarose gel. As positive control PCR products from the cup1-1 amplification  used for the Gibson Assembly into piGEM-005 were applied to the gel as well. </p>
      <table width="100%" border="1">
    <tr>
@@ Line 2,904: / Line 2,912: @@
    </tr>
    <tr>
-     <th scope="row">Phusion</th>
+     <th scope="row">Phusion DNA-polymerase</th>
      <td>-</td>
      <td>2,5</td>
@@ Line 2,964: / Line 2,972: @@
              <th scope="row">5</th>
              <td>Go To 2</td>
-             <td>30x</td>
+             <td>35x</td>
            </tr>
            <tr>
@@ Line 2,983: / Line 2,991: @@
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.35">18.35 test digest with Nco/Bam – Checking insertion of Hag/-DARPin into pet24d</a></legend>
+     <legend><a name="exp18.35">18.35 Test digest with <i>Nco</i>I/<i>Bam</i>HI - Checking insertion of Hag/-DARPin into pet24d</a></legend>
      <div class="aim">
-     <p>Aim: proving insertion of Hag/-DARPin fragment into pet24d</p>
+     <p>Aim: proving insertion of Hag/-DARPin fragment into pET24d</p>
      </div>
      <div class="exp-content">
-     <p>The  plasmids are digested with Nco1 and BamH1. In case of a correct insertion the  pet24d backbone and the insert should be seen on the gel at 5300 bp and 1000/  1500 bp. As control Pet24d-Hag-Flank (piGEM-001) is used to check the  mastermix.</p>
+     <p>The  plasmids are digested with <i>Nco</i>I and <i>Bam</i>HI. In case of a correct insertion the  pET24d backbone and the insert should be seen on the gel at 5300 bp and 1000/  1500 bp. As control pET24d-Hag-Flank (piGEM-001) is used to check the  mastermix.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 3,001: / Line 3,009: @@
    </tr>
    <tr>
-     <th scope="row">Cutsmart 10x</th>
+     <th scope="row">CutSmart 10x</th>
      <td>-</td>
      <td>5</td>
    </tr>
    <tr>
-     <th scope="row">Nco1</th>
+     <th scope="row"><i>Nco</i>I</th>
      <td>-</td>
      <td>0,5</td>
    </tr>
    <tr>
-     <th scope="row">BamH1</th>
+     <th scope="row"><i>Bam</i>HI</th>
      <td>-</td>
      <td>0,5</td>
@@ Line 3,026: / Line 3,034: @@
    </tr>
 </table>
+<br />
+<img src="https://static.igem.org/mediawiki/2014/5/51/MR_20140622_pET24d-Hag_pET24d-Hag-DARPin_NcoI_BamHI.png" width="20%" />
+<br />
+<p>The used marker was the GeneRuler 1 kb DNA ladder. The lower fragment of the digested pET24d-Hag was too big (2 kb) and pET24d-Hag-DARPin seemed only to be linearized with the exception of two very thin bands below the linear plasmid, which were all of the wrong size.</p>
 </div>
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.36">18.36 ligation of pet24d  and PCR Hag/ Hag-DARPin fragments cut Nco/Bam</a></legend>
+     <legend><a name="exp18.36">18.36 ligation of pET24d  and PCR Hag/ Hag-DARPin fragments cut <i>Nco</i>I/<i>Bam</i>HI</a></legend>
      <div class="aim">
-     <p>Aim: ligation of construct with pet24d for overproduction of flagellin and crystallization</p>
+     <p>Aim: ligation of construct with pET24d for overproduction of flagellin and crystallization</p>
      </div>
      <div class="exp-content">
-     <p>The  Nco/cut Flagellin PCR products from 18.x (from clone 7 and piGEM-005) were  ligated with Nco1 and BamH1 cut pet24d. </p>
+     <p>The  <i>Nco</i>I/<i>Bam</i>HI digested flagellin PCR products from 18.22 (from clone 7 and piGEM-005) were  ligated with <i>Nco</i>I/<i>Bam</i>HI digested pET24d.</p>
      <table width="100%" border="1">
    <tr>
      <th scope="col">Component</th>
-     <th scope="col">Pet-Hag attempt (&micro;L) </th>
+     <th scope="col">pET24d-Hag reaction (&micro;L) </th>
-     <th scope="col">Pet-Hag-DARPin attempt (&micro;L)</th>
+     <th scope="col">pET24d-Hag-DARPin raction (&micro;L)</th>
    </tr>
    <tr>
@@ Line 3,047: / Line 3,059: @@
    </tr>
    <tr>
-     <th scope="row">Vector (pet24d, c= 50ng/&micro;L)</th>
+     <th scope="row">Vector (pET24d, c= 50ng/&micro;L)</th>
      <td>5</td>
      <td>5</td>
@@ Line 3,062: / Line 3,074: @@
    </tr>
    <tr>
-     <th scope="row">Milipore Water</th>
+     <th scope="row">Millipore Water</th>
      <td>10</td>
      <td>10</td>
@@ Line 3,072: / Line 3,084: @@
    </tr>
 </table>
-	<p>The attempts were carried out in double and incubated at room  temperature -One attempt for 1h&nbsp; followed  by transformation into <em>E.Coli XL1-Blue </em>and  the second one overnight.</p>
+	<p>The reactions were prepared in double and were incubated at room  temperature. One reaction was incubated for 1 hour followed  by transformation of <em>E. coli</em> XL1-Blue and  the second one over night.</p>
 </div>
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.37a">18.37 repetition of PCR with 3 clones of Pet-Hag and Pet-Hag-DARPin ligation</a></legend>
+     <legend><a name="exp18.37a">18.37 Repetition of PCR with 3 clones of pET24d-Hag and pET24d-Hag-DARPin ligation</a></legend>
      <div clacc="aim">
-     <p>Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pet24d</p>
+     <p>Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pET24d</p>
      </div>
      <div class="exp-content">
-     <p>3  clones from ligation plates with pet-Hag and pet-Hag-DARPin were resuspended in  30 &micro;L PBS and cooked at 95 &deg;C for 10min. After that procedure 1 &micro;L of this  suspenion was used as PCR template.</p>
+     <p>3  clones from ligation plates with pET-Hag and pET-Hag-DARPin were resuspended in  30 &micro;L PBS and cooked at 95 &deg;C for 10 min. After that procedure 1 &micro;L of this  suspension was used as PCR template.</p>
      <table width="100%" border="1">
    <tr>
      <th scope="col">Content</th>
      <th scope="col">Volume (&micro;L)</th>
-     <th scope="col">MM for 7 attempts (&micro;L)</th>
+     <th scope="col">MM for 7 reactions (&micro;L)</th>
    </tr>
    <tr>
      <th scope="row">Template ( 1&micro;L cooked suspension)<br />
-&nbsp;(8-10 from pet-Hag, 7-9 from pet-Hag-DARPin)</th>
+&nbsp;(8-10 from pET-Hag, 7-9 from pET-Hag-DARPin)</th>
      <td>1</td>
      <td>-</td>
@@ Line 3,105: / Line 3,117: @@
    </tr>
    <tr>
-     <th scope="row">Phusion</th>
+     <th scope="row">Phusion DNA-polymerase</th>
      <td>-</td>
      <td>3,5</td>
@@ Line 3,165: / Line 3,177: @@
              <th scope="row">5</th>
              <td>Go To 2</td>
-             <td>30x</td>
+             <td>35x</td>
            </tr>
            <tr>
@@ Line 3,178: / Line 3,190: @@
            </tr>
          </table>
-         <p>Run overnight</p>
+         <p>Run over night</p>
 </div>
 </fieldset>
@@ Line 3,193: / Line 3,205: @@
    </tr>
    <tr>
-     <th scope="row">Pet24d</th>
+     <th scope="row">pET24d</th>
      <td>148</td>
      <td>Can</td>
@@ Line 3,221: / Line 3,233: @@
    </tr>
    <tr>
-     <th scope="row">Pet-Hag attempt from 18.36</th>
+     <th scope="row">pET-Hag attempt from 18.36</th>
      <td>-</td>
      <td>Can</td>
@@ Line 3,228: / Line 3,240: @@
    </tr>
    <tr>
-     <th scope="row">Pet-Hag-DARPin attempt from 18.36</th>
+     <th scope="row">pET-Hag-DARPin attempt from 18.36</th>
      <td>-</td>
      <td>Can</td>
@@ Line 3,235: / Line 3,247: @@
    </tr>
    <tr>
-     <th scope="row">Control pet24d cut Nco/Bam</th>
+     <th scope="row">Control pET24d cut <i>Nco</i>I/<i>Bam</i>HI</th>
      <td>32</td>
      <td>Can</td>
@@ Line 3,314: / Line 3,326: @@
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.37b">18.37 repetition of PCR with 3 clones of Pet-Hag and Pet-Hag-DARPin ligation</a></legend>
+     <legend><a name="exp18.37b">18.37 Repetition of PCR with 3 clones of pET24d-Hag and pET24d-Hag-DARPin ligation</a></legend>
      <div class="aim">
-     <p>Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pet24d</p>
+     <p>Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pET24d</p>
      </div>
      <div class="exp-content">
      <p>Gel electrophoresis:</p>
      <img src="https://static.igem.org/mediawiki/2014/8/80/MR_2014-06-23_18.37.jpg" width="30%" />
-     <p>The gel shows negative bands in case of the Hag-DARPin clones. The PCR for Hag 8 and 9 did not work although we cooked the clones with PBS. The transformation efficiency seemed to be very low so clones from the new ligation attempts should be analysed.</p>
+     <p>The gel shows negative bands in case of the Hag-DARPin clones. The PCR for Hag 8 and 9 did not work although we cooked the clones in PBS. The transformation efficiency seemed to be very low, so clones from the new ligation attempts should be analysed.</p>
      </div>
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.38">18.38 ligation checking success of transformed ligation attempts</a></legend>
+     <legend><a name="exp18.38">18.38 Ligation checking success of transformed ligation attempts</a></legend>
      <div class="exp-content">
      <p>On every plate grew a high amount of colonies. 6 clones of each plate were picked for inoculation of minipreps and for cPCR after cooking with PBS. The clones were transferred to another LB-Can plate.</p>
@@ Line 3,333: / Line 3,345: @@
      <legend><a name="exp18.39">18.39 cPCR with picked clones from 18.38 ligation attempt transformation</a></legend>
      <div class="aim">
-     <p>Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pet24d</p>
+     <p>Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pET24d</p>
      </div>
      <div class="exp-content">
-     <p>For  checking the insertion of the Hag/-DARPin into pet24 the clones from the  transformation plate were transferred to another LB-Can plate&nbsp; and cooked for 10 min in 30&micro;L PBS at 95&deg;C. At  the same time the colonies were used to inoculate LB-Can for minipreps.</p>
+     <p>For  checking the insertion of the Hag/-DARPin into pET24d the clones from the  transformation plate were transferred to another LB-Can plate&nbsp; and cooked for 10 min in 30 &micro;L PBS at 95&deg;C. At  the same time the colonies were used to inoculate LB-Can for minipreps.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 3,360: / Line 3,372: @@
    </tr>
    <tr>
-     <th scope="row">Phusion</th>
+     <th scope="row">Phusion DNA-polymerase</th>
      <td>-</td>
      <td>7</td>
@@ Line 3,400: / Line 3,412: @@
              <th scope="row">1</th>
              <td>98</td>
-             <td>3 min</td>
+             <td>5 min</td>
            </tr>
            <tr>
@@ Line 3,420: / Line 3,432: @@
              <th scope="row">5</th>
              <td>Go To 2</td>
-             <td>30x</td>
+             <td>35x</td>
            </tr>
            <tr>
@@ Line 3,433: / Line 3,445: @@
            </tr>
          </table>
-         <p>Run overnight</p>
+         <p>Run over night</p>
 </div>
 </fieldset>
@@ Line 3,514: / Line 3,526: @@
      <legend><a name="exp18.39">18.39 Gel cPCR with picked clones from 18.38 ligation attempt transformation</a></legend>
      <div class="aim">
-     <p>Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pet24d</p>
+     <p>Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pET24d</p>
      </div>
      <div class="exp-content">
@@ Line 3,521: / Line 3,533: @@
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.40">18.40 test digest with Nco/Bam of prepped plasmids from picked colonies</a></legend>
+     <legend><a name="exp18.40">18.40 Test digest with <i>Nco</i>I/<i>Bam</i>HI of isolated plasmids from picked colonies</a></legend>
      <div class="aim">
-     <p>Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pet24d</p>
+     <p>Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pET24d</p>
      </div>
      <div class="exp-content">
-     <p>The picked clones from the ligation attempts 18.38 were prepped. In  order to check the insertion of the Hag/ Hag-DARPin domain the plasmids were  digested with Nco1/ BamH1 so that the gel should show the insert of 1 or 1,5 bp  length and the pet24d backbone at 5300 bp. Because of an unavailable marker as  a control the PCR amplified inserts which were used for the ligation will  run&nbsp; with the gel as well. piGEM-001 will  also be cut Nco/Bam in order to receive a marker band for the pet24d backbone.</p>
+     <p>The picked clones from the ligation attempts 18.38 were isolated. In  order to check the insertion of the Hag/ Hag-DARPin domain the plasmids were  digested with <i>Nco</i>I/<i>Bam</i>HI so that the gel should show the insert of 1 or 1,5 bp  length and the pET24d backbone at 5300 bp. Because of an unavailable marker as  a control the PCR amplified inserts which were used for the ligation will  run&nbsp; with the gel as well. piGEM-001 will  also be cut <i>Nco</i>I/<i>Bam</i>HI in order to receive a marker band for the pET24d backbone.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 3,544: / Line 3,556: @@
    </tr>
    <tr>
-     <th scope="row">NcoI</th>
+     <th scope="row"><i>Nco</i>I</th>
      <td>-</td>
      <td>0,5</td>
    </tr>
    <tr>
-     <th scope="row">BamH1</th>
+     <th scope="row"><i>Bam</i>HI</th>
      <td>-</td>
      <td>0,5</td>
@@ Line 3,569: / Line 3,581: @@
    </tr>
 </table>
+<br />
+<img src="https://static.igem.org/mediawiki/2014/1/13/MR_20140625_pET24d-Hag_pET24d-Hag-DARPin_NcoI_BamHI_test_digest.png" width="20%" />
+<br />
+<p>The gel shows that the digested clones were all negative. The ligation had to be performed again.</p>
 </div>
 </fieldset>
@@ Line 3,613: / Line 3,629: @@
 </h2>
 <fieldset class="exp20">
-     <legend><a name="exp20.7">20.7 PCR with purified cPCR samples from 20.x</a></legend>
+     <legend><a name="exp20.7">20.7 PCR with purified cPCR samples from 20.6</a></legend>
      <div class="aim">
      <p>Aim: PCR amplification of purified cPCR samples</p>
@@ Line 3,626: / Line 3,642: @@
    </tr>
    <tr>
-     <th scope="row">Purified cPCR product from 20.x<br />
+     <th scope="row">Purified cPCR product from 20.6<br />
 &nbsp;(3 &amp; 5 from pet-Hag, 3 &amp; 9 from  pet-Hag-DARPin)</th>
      <td>1</td>
@@ Line 3,642: / Line 3,658: @@
    </tr>
    <tr>
-     <th scope="row">Phusion</th>
+     <th scope="row">Phusion DNA-polymerase</th>
      <td>-</td>
      <td>6</td>
@@ Line 3,702: / Line 3,718: @@
              <th scope="row">5</th>
              <td>Go To 2</td>
-             <td>30x</td>
+             <td>35x</td>
            </tr>
            <tr>
@@ Line 3,730: / Line 3,746: @@
      <th scope="row">1</th>
      <td>AGB0023<strong>407</strong></td>
-     <td>Hag-Spe1 in B.s.  genome clone 3</td>
+     <td>Hag-<i>Spe</i>I in <i>B. subtilis</i>  genome clone 3</td>
      <td>Hag-Nco-fw</td>
    </tr>
@@ Line 3,736: / Line 3,752: @@
      <th scope="row">2</th>
      <td>AGB0023<strong>408</strong></td>
-     <td>Hag-Spe1 in B.s.  genome clone 5</td>
+     <td>Hag-<i>Spe</i>I in <i>B. subtilis</i>  genome clone 5</td>
      <td>Hag-Nco-fw</td>
    </tr>
@@ Line 3,742: / Line 3,758: @@
      <th scope="row">3</th>
      <td>AGB0023<strong>409</strong></td>
-     <td>Hag-Spe1-DARPin  in B.s. genome clone 3</td>
+     <td>Hag-<i>Spe</i>I-DARPin in <i>B. subtilis</i>  genome clone3</td>
      <td>Hag-Nco-fw</td>
    </tr>
@@ Line 3,748: / Line 3,764: @@
      <th scope="row">4</th>
      <td>AGB0023<strong>410</strong></td>
-     <td>Hag-Spe1-DARPin  in B.s. genome clone 9</td>
+     <td>Hag-<i>Spe</i>I-DARPin in <i>B. subtilis</i>  genome clone 9</td>
      <td>Hag-Nco-fw</td>
    </tr>
@@ Line 3,755: / Line 3,771: @@
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.41">18.41 new ligation of pet24d  and PCR Hag/ Hag-DARPin fragments cut Nco/Bam transformation</a></legend>
+     <legend><a name="exp18.41">18.41 New ligation of pET24d  and PCR Hag/ Hag-DARPin fragments cut <i>Nco</i>I/<i>Bam</i>HI transformation</a></legend>
      <div class="aim">
-     <p>Aim: ligation of construct with pet24d for overproduction of flagellin and crystallization</p>
+     <p>Aim: ligation of construct with pET24d for overproduction of flagellin and crystallization</p>
      </div>
      <div class="exp-content">
-     <p>The cut  pet24d Nco/Bam which was used for the previous ligations was not purified and  contained an 1 kb insert. For a new cealn ligation the attempt was repreated  with pet24d cut by Carina Knauer .The Nco/cut Flagellin PCR products (from  clone 7 and piGEM-005) were ligated with Nco1 and BamH1 cut pet24d. </p>
+     <p>The cut  pET24d <i>Nco</i>I/<i>Bam</i>HI which was used for the previous ligations was not purified and  contained an 1 kb insert. For a new clean ligation the reaction was repeated  with digested pET24d. The <i>Nco</i>I/<i>Bam</i>HI digested flagellin PCR products (from  clone 7 and piGEM-005) were ligated with <i>Nco</i>I/<i>Bam</i>HI digested pET24d.</p>
-     <p>The  attempts were carried out in double. The attempts 1 &amp; 2 were incubated 1h  at room temperature and finally transformed into E. Coli XL1-Blue after  inactivation at 65 for 10 min. The attempts 1.1 and 2.1 were incubated  overnight at room temperature. 1 &micro;L of cut vector was transformed as a negative  control in order to check the amount of religants.</p>
+     <p>The  reactions were carried out in double and were incubated 1h  at room temperature. Finally they were used to transform  <i>E. coli</i> XL1-Blue after  inactivation at 65&deg;C for 10 min. The attempts 1.1 and 2.1 were incubated  over night at room temperature. 1 &micro;L of digested vector was used for a transformation as a negative  control in order to check the amount of religants.</p>
      <table width="100%" border="1">
    <tr>
      <th scope="col">Component</th>
-     <th scope="col">Pet-Hag attempt (&micro;L) &ndash; 1 &amp; 1.1</th>
+     <th scope="col">pET-Hag attempt (&micro;L) &ndash; 1 &amp; 1.1</th>
-     <th scope="col">Pet-Hag-DARPin attempt (&micro;L) 2&amp; 2.1</th>
+     <th scope="col">pET-Hag-DARPin attempt (&micro;L) 2&amp; 2.1</th>
    </tr>
    <tr>
@@ Line 3,774: / Line 3,790: @@
    </tr>
    <tr>
-     <th scope="row">Vector (pet24d, c= 86ng/&micro;L)</th>
+     <th scope="row">Vector (pET24d, c= 86ng/&micro;L)</th>
      <td>5</td>
      <td>5</td>
@@ Line 3,812: / Line 3,828: @@
      <legend><a name="exp18.42">18.42 Miniprep of ligation clones</a></legend>
      <div class="exp-content">
-     <p>The  ligation between pet24d and the Hag-/Hag-DARPin fragments which were both cut  Nco/Bam was successful. The ligation plates showed over 20 clones each whereby  on the negative control&nbsp; grew a few clones  as well which were very small and sticking together. Bad plate out might be the  reason for that. In order to analyse the insert of the clones 5 clones per  ligation plate 1 and 2 were used to inoculate minipreps in 5 mL LB-Can. For the  Ligation 1 Pet-Hag clones 1-5 were picked, as well as clones 6-10 from Plate  Ligation 2 Pet-Hag-DARPin. </p>
+     <p>The  ligation between pET24d and the Hag-/Hag-DARPin fragments which were both cut  <i>Nco</i>I/<i>Bam</i>HI was successful. The ligation plates showed over 20 clones each. However, on the negative control&nbsp; grew a few clones  as well, which were very small and sticking together. In order to analyse the insert of the clones, 5 clones per  ligation plate 1 and 2 were used to inoculate minipreps in 5 mL LB-Can. For the  Ligation 1 pET-Hag clones 1-5 were picked, as well as clones 6-10 from Plate  Ligation 2 pET-Hag-DARPin. </p>
-     <p>The  cultures were inoculated overnight at 37&deg;C.</p>
+     <p>The  cultures were inoculated over night at 37&deg;C.</p>
 </div>
 </fieldset>
@@ Line 3,834: / Line 3,850: @@
    </tr>
    <tr>
-     <th scope="row">Pet-Hag</th>
+     <th scope="row">pET24d-Hag</th>
      <td>1</td>
      <td>50</td>
    </tr>
    <tr>
-     <th scope="row">Pet-Hag</th>
+     <th scope="row">pET24d-Hag</th>
      <td>2</td>
      <td>87</td>
    </tr>
    <tr>
-     <th scope="row">Pet-Hag</th>
+     <th scope="row">pET24d-Hag</th>
      <td>3</td>
      <td>65</td>
    </tr>
    <tr>
-     <th scope="row">Pet-Hag-DARPin</th>
+     <th scope="row">pET24d-Hag-DARPin</th>
      <td>6</td>
      <td>83</td>
    </tr>
    <tr>
-     <th scope="row">Pet-Hag-DARPin</th>
+     <th scope="row">pET24d-Hag-DARPin</th>
      <td>7</td>
      <td>59</td>
@@ Line 3,862: / Line 3,878: @@
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.43">18.43 cPCR of clones from 18.42</a></legend>
+     <legend><a name="exp18.43">18.43 cPCR of clones from 18.41</a></legend>
      <div class="aim">
-     <p>Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pet24d</p>
+     <p>Aim: checking picked clones for correct Hag/ Hag-DARPin insert in pET24d</p>
      </div>
      <div class="exp-content">
-     <p>Plasmid  from prepped clones from each plate were analysed via cPCR with the primers flo54  and flo56 (Hag-fw and Hag-rv). The result should be a ca. 1kb fragment for  correct pet24d-Hag containing clones and a 1,5 kb fragment for  pet24d-Hag-DARPin containing clones.</p>
+     <p>Plasmid  from isolated clones from each plate were analysed via cPCR with the primers flo54  and flo56 (Hag-fw and Hag-rv). The result should be a ca. 1kb fragment for  correct pET24d-Hag containing clones and a 1,5 kb fragment for  pET24d-Hag-DARPin containing clones.</p>
          <table width="100%" border="1">
    <tr>
@@ Line 3,875: / Line 3,891: @@
    </tr>
    <tr>
-     <th scope="row">Picked clones from 18.42<br />(1-3pet-Hag, 6-7 from pet-Hag-DARPin)</th>
+     <th scope="row">Picked clones from 18.42<br />(1-3 pET24d-Hag, 6-7 from pET24d-Hag-DARPin)</th>
      <td>0,5</td>
      <td>-</td>
@@ Line 3,890: / Line 3,906: @@
    </tr>
    <tr>
-     <th scope="row">Phusion</th>
+     <th scope="row">Phusion DNA-polymerase</th>
      <td>-</td>
      <td>3</td>
@@ Line 3,963: / Line 3,979: @@
            </tr>
          </table>
+		<br />
+		<p>The samples can be seen on the gel under 18.44. The PCR for the Hag-fragment in pET24d seemed to be positive (PCR.H1 - H3), as well as for the Hag-DARPin fragment (PCR.D7) </p>
 </div>
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.44">18.44 test digest with Nco/Bam – Checking insertion of Hag/-DARPin into pet24d</a></legend>
+     <legend><a name="exp18.44">18.44 test digest with <i>Nco</i>I/<i>Bam</i>HI - Checking insertion of Hag/-DARPin into pET24d</a></legend>
      <div class="aim">
-     <p>Aim: proving insertion of Hag/-DARPin fragment into pet24d</p>
+     <p>Aim: proving insertion of Hag/-DARPin fragment into pET24d</p>
      </div>
      <div class="exp-content">
-     <p>The plasmids were digested with Nco1 and BamH1. In case of a correct insertion the pet24d backbone and the insert should be seen on the gel at 5300 bp and 1000/ 1500 bp. As control Pet24d-Hag-Flank (piGEM-001) is used to check the mastermix.</p>
+     <p>The plasmids were digested with <i>Nco</i>I and <i>Bam</i>HI. In case of a correct insertion the pet24d backbone and the insert should be seen on the gel at 5300 bp and 1000/ 1500 bp. As control pET24d-Hag-Flank (piGEM-001) is used to check the mastermix.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 3,980: / Line 3,998: @@
    <tr>
      <th scope="row">Plasmid from clone <br />
-       ( Pet-Hag 1-3, Pet-Hag-DARPin 6 & 7)</th>
+       ( pET24d-Hag 1-3, pET24d-Hag-DARPin 6 & 7)</th>
      <td>5</td>
      <td>-</td>
@@ Line 3,990: / Line 4,008: @@
    </tr>
    <tr>
-     <th scope="row">NcoI</th>
+     <th scope="row"><i>Nco</i>I</th>
      <td>-</td>
      <td>0,5</td>
    </tr>
    <tr>
-     <th scope="row">BamHI</th>
+     <th scope="row"><i>Bam</i>HI</th>
      <td>-</td>
      <td>0,5</td>
@@ Line 4,020: / Line 4,038: @@
      </div>
      <div class="exp-content">
-     <p>The PCR product of the  amplification of cPCR products was not pure considering different bands on the  gel next to the right one. In order to exclude sequencing mistakes the PCR  attempts were purified via gel extraction of the 1,5 kb band in case of the  Hag-DARPin construct.</p>
+     <p>The PCR product of the  amplification of cPCR products was not pure considering different bands on the  gel next to the right one. In order to prevent sequencing mistakes the PCR  attempts were purified via gel extraction of the 1,5 kb band in case of the  Hag-DARPin construct.</p>
 </div>
 </fieldset>
 <fieldset class="exp20">
-     <legend><a name="exp20.8">20.8  PCR with Gel Purified Hag-DARPin cPCR products for sequencing</a></legend>
+     <legend><a name="exp20.10">20.10  PCR with purified Hag-DARPin cPCR products for sequencing</a></legend>
      <div class="aim">
      <p>Aim: amplification of purified Hag-DARPin fragment for sequencing</p>
      </div>
      <div class="exp-content">
-     <p>The purified cPCR product from 20.x has to be amplified again in order to get a higher concentration for sequencing. </p>
+     <p>The purified cPCR product from 20.9 has to be amplified again in order to get a higher concentration for sequencing. </p>
              <table width="100%" border="1">
    <tr>
@@ Line 4,052: / Line 4,070: @@
    </tr>
    <tr>
-     <th scope="row">Phusion</th>
+     <th scope="row">Phusion DNA-polymerase</th>
      <td>-</td>
      <td>1</td>
@@ Line 4,092: / Line 4,110: @@
              <th scope="row">1</th>
              <td>98</td>
-             <td>3 min</td>
+             <td>5 min</td>
            </tr>
            <tr>
@@ Line 4,125: / Line 4,143: @@
            </tr>
          </table>
-    </div>
-</fieldset>
-<fieldset class="exp">
-    <legend><a name="exp_4">Transformation</a></legend>
-    <div class="exp-content">
-        <table width="100%" border="1">
-  <tr>
-    <th scope="col">Plasmid</th>
-    <th scope="col">Concentration (ng/&micro;L)</th>
-    <th scope="col">Antibiotic</th>
-    <th scope="col">Cells</th>
-    <th scope="col">Volume (&micro;L)</th>
-  </tr>
-  <tr>
-    <th scope="row">Pet-Hag clone 2</th>
-    <td>87</td>
-    <td>Can</td>
-    <td>DH5&alpha;</td>
-    <td>1</td>
-  </tr>
-  <tr>
-    <th scope="row">Pet-Hag clone 3</th>
-    <td>65</td>
-    <td>Can</td>
-    <td>DH5&alpha;</td>
-    <td>1</td>
-  </tr>
-  <tr>
-    <th scope="row">Pet-Hag-DARPin clone 7</th>
-    <td>59</td>
-    <td>Can</td>
-    <td>DH5&alpha;</td>
-    <td>1</td>
-  </tr>
-  <tr>
-    <th scope="row">Gibson Pet-Hag-Cup1-1</th>
-    <td>-</td>
-    <td>Can</td>
-    <td>DH5&alpha;</td>
-    <td>20</td>
-  </tr>
-</table>
      </div>
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.45">18.45 Spe1  digest of Pet-Hag (piGEM-019)</a></legend>
+     <legend><a name="exp18.45">18.45 <i>Spe</i>I  digest of pET24d-Hag (piGEM-019)</a></legend>
      <div class="aim">
-     <p>Aim: linearizing Pet24d-Hag with Spe1 site for a Gibson assembly with Cup1-1</p>
+     <p>Aim: linearizing pET24d-Hag with <i>Spe</i>I site for a Gibson assembly with Cup1-1</p>
      </div>
      <div class="exp-content">
@@ Line 4,185: / Line 4,161: @@
    </tr>
    <tr>
-     <th scope="row">Cutsmart 10x</th>
+     <th scope="row">CutSmart 10x</th>
      <td>2</td>
    </tr>
    <tr>
-     <th scope="row">Spe1</th>
+     <th scope="row"><i>Spe</i>I</th>
      <td>0,5</td>
    </tr>
@@ Line 4,201: / Line 4,177: @@
    </tr>
 </table>
-	<p>Incubation 1h  at 37&deg;C with following heat shock at 80&deg;C</p>
+	<p>Incubation 1 h  at 37&deg;C with following heat inactivation at 80&deg;C</p>
 </div>
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.46">18.46 Gibson assembly with linearized Pet-Hag (piGEM-019) and Cup1-1</a></legend>
+     <legend><a name="exp18.46">18.46 Gibson assembly with linearized pET24d-Hag (piGEM-019) and cup1-1</a></legend>
      <div class="aim">
-     <p>Aim: Insertion of Cup1-1 domain into Pet-Hag construct for crystallization</p>
+     <p>Aim: Insertion of cup1-1 domain into pET24d-Hag construct for crystallization</p>
      </div>
      <div class="exp-content">
-     <p>As insert cup1-1 PCR product from 15.55 and Spe1 cut piGEM-016 from 18.44 were used for a new Gibson assembly.<br />
+     <p>As insert cup1-1 PCR product from 15.55 and <i>Spe</i>I digested piGEM-016 from 18.44 were used for a new Gibson assembly.<br />
        PCR fragment cup1-1 (464 ng/&micro;L)    <br />
-       Spe1 cut pIGEM-005 ( ng/&micro;L)    </p>
+       <i>Spe</i>I digested pIGEM-005 ( ng/&micro;L)    </p>
        <table width="100%" border="1">
    <tr>
@@ Line 4,236: / Line 4,212: @@
 </table>
 	<p>The mix was incubated 5 min at room temperature and then for 1h at 50&deg;C.</p>
-	<p>In the end the whole mix was transformed into E.Coli XL1-Blue and plated  out on LB-Amp. Incubation was done overnight at 37&deg;C.</p>
+	<p>In the end the whole mix was used to transform <i>E. coli</i> XL1-Blue, which were plated  out on LB-Amp. Incubation was done over night at 37&deg;C.</p>
 </div>
 </fieldset>
@@ Line 4,248: / Line 4,224: @@
 </h2>
 <fieldset class="exp18">
-     <legend><a name="exp18.47">18.47 cPCR of Gibson assembly lones of Pet-Hag (piGEM-019) and Cup1-1</a></legend>
+     <legend><a name="exp18.47">18.47 cPCR of Gibson assembly clones of pET24d-Hag (piGEM-019) and cup1-1</a></legend>
      <div class="aim">
      <p>Aim: screening clones for right insert</p>
      </div>
      <div class="exp-content">
-     <p>In order to screen the clones for  the right insertion of cup1-1 4 clones were picked from the LB-Can plate and  transferred to a LB-Can Master plate. Additionally the clones were used for  inoculation of minipreps and also cooked in 50 &micro;L dest. Water for 10 min at  95&deg;C. The lysate was used as template.</p>
+     <p>In order to screen the clones for  the right insertion of cup1-1 four clones were picked from the LB-Can plate and  transferred onto a LB-Can plate. Additionally the clones were used for  inoculation of minipreps and also cooked in 50 &micro;L dest. Water for 10 min at  95&deg;C. The lysate was used as template.</p>
-     <p>The PCR with Flo54 and iGEM-025  should generate a 785 bp fragment and the one with iGEM-024 and -025 the 164bp  domain fragment.</p>
+     <p>The PCR with Flo54 and iGEM-025  should generate a 785 bp fragment and the one with iGEM-024 and -025 the 164bp cup domain fragment.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 4,293: / Line 4,269: @@
    </tr>
    <tr>
-     <th scope="row">Phusion</th>
+     <th scope="row">Phusion DNA-polymerase</th>
      <td>-</td>
      <td>5</td>
@@ Line 4,333: / Line 4,309: @@
              <th scope="row">1</th>
              <td>98</td>
-             <td>3 min</td>
+             <td>10 min</td>
            </tr>
            <tr>
@@ Line 4,366: / Line 4,342: @@
            </tr>
          </table>
-         <p>The PCR showed no bands. The  colonies were used for minipreps so that the isolated plasmid can the used for  analysis of the insert.</p>
+         <p>The PCR showed no bands. Nevertheless, colonies were used to inoculate cultures for minipreps so that the isolated plasmid can be further analysed for the insert.</p>
 </div>
 </fieldset>
@@ Line 4,377: / Line 4,353: @@
 	<a name="30.06.2014">30.06.2014</a>
 </h2>
+<fieldset class="exp">
+    <legend><a name="exp_5">Sequencing</a></legend>
+    <div class="exp-content">
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Premix</th>
+    <th scope="col">Label-Nr.</th>
+    <th scope="col">Construct</th>
+    <th scope="col">Primers</th>
+  </tr>
+  <tr>
+    <th scope="row">1</th>
+    <td>AGB0023<strong>411</strong></td>
+    <td>pET24d-Hag-<i>Spe</i>I  construct cl. 2</td>
+    <td>Hag-Nco-fw</td>
+  </tr>
+  <tr>
+    <th scope="row">2</th>
+    <td>AGB0023<strong>412</strong></td>
+    <td>pET24d-Hag-DARPin  construct cl. 7</td>
+    <td>Hag-Nco-fw</td>
+  </tr>
+</table>
+    </div>
+</fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.48">18.48 miniprep of clones from Gibson assembly with Pet-Hag (piGEM-019) and Cup1-1</a></legend>
+     <legend><a name="exp18.48a">18.48a Miniprep of plasmids from Gibson assembly clones with pET24d-Hag (piGEM-019) and cup1-1</a></legend>
      <div class="aim">
      <p>Aim: isolation of Plasmid DNA for further experiments</p>
@@ Line 4,390: / Line 4,391: @@
    </tr>
    <tr>
-     <th scope="row">Pet-Hag-Cup1-1</th>
+     <th scope="row">pET24d-Hag-Cup1-1</th>
      <td>1</td>
      <td>122</td>
    </tr>
    <tr>
-     <th scope="row">Pet-Hag-Cup1-1</th>
+     <th scope="row">pET24d-Hag-Cup1-1</th>
      <td>2</td>
      <td>85</td>
    </tr>
    <tr>
-     <th scope="row">Pet-Hag-Cup1-1</th>
+     <th scope="row">pET24d-Hag-Cup1-1</th>
      <td>3</td>
      <td>172</td>
    </tr>
    <tr>
-     <th scope="row">Pet-Hag-Cup1-1</th>
+     <th scope="row">pET24d-Hag-Cup1-1</th>
      <td>4</td>
      <td>116</td>
-  </tr>
-</table>
-    </div>
-</fieldset>
-<!-- ROMAN -->
-<fieldset class="exp14">
- <legend><a name="exp14.47">14.47 Purification of PheA-Arc1p-C-0x</a></legend>
-    <div class="aim">
-    <p>Aim: Purify PheA-Arc1p-C-0x in three steps</p>
-    </div>
-    <div class="exp-content">
-    <p>The resuspended cells from 14.46 were lysed using a french press. The lysate was incubated on ice with 5 &micro;g/mL DNAseA and RNAseI for 10 min and centrifuged (27000 rpm, 45 min, 4 &deg;C) to pellet cell debris. The supernatant was filtered (0.45 &micro;m) and PheA-Arc1p-C-0x purified from the cleared solution by NiNTA affinity chromatography. The combined elution fractions containing crude PheA-Arc1p-C-0x were concentrated to a volume of 2 mL and further purified using an anion exchange column to get rid of possible tRNA contaminations. Finally the buffer was changed to dialysis buffer and the protein concentrated and stored at -80 &deg;C in aliquods for further use.</p>
-    </div>
-</fieldset>
-<!-- ROMAN -->
-<fieldset class="exp">
-    <legend><a name="exp_5">Sequencing</a></legend>
-    <div class="exp-content">
-    <table width="100%" border="1">
-  <tr>
-    <th scope="col">Premix</th>
-    <th scope="col">Label-Nr.</th>
-    <th scope="col">Construct</th>
-    <th scope="col">Primers</th>
-  </tr>
-  <tr>
-    <th scope="row">1</th>
-    <td>AGB0023<strong>411</strong></td>
-    <td>Pet24d-Hag-Spe1  construct cl. 2</td>
-    <td>Hag-Nco-fw</td>
-  </tr>
-  <tr>
-    <th scope="row">2</th>
-    <td>AGB0023<strong>412</strong></td>
-    <td>Pet24d-Hag-DARPin  construct cl. 7</td>
-    <td>Hag-Nco-fw</td>
    </tr>
 </table>
@@ Line 4,455: / Line 4,414: @@
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.48">18.48 PCR of prepped Gibson assembly clones ( Pet-Hag (piGEM-019) and Cup1-1)</a></legend>
+     <legend><a name="exp18.48b">18.48b PCR of isolated plasmids from Gibson assembly clones (pET24d-Hag (piGEM-019) and cup1-1)</a></legend>
      <div class="aim">
      <p>Aim: screening clones for right insert</p>
@@ Line 4,573: / Line 4,532: @@
            </tr>
          </table>
-         <p>No bands were shown on the gel. The PCR was repeated with Q5 mastermix to exclude the disfunction of the polymerase.</p>
+         <p>No bands could be observed on the gel. The PCR was repeated with Q5 mastermix to exclude the disfunction of the polymerase.</p>
 </div>
 </fieldset>
 <fieldset class="exp20">
-     <legend><a name="exp20.9">20.9 inoculation of preculture from Bacillus WT 3610</a></legend>
+     <legend><a name="exp20.9">20.9 Inoculation of a preculture from <i>Bacillus subtilis</i> WT 3610</a></legend>
      <div class="aim">
-     <p>Aim:Preparation of for mainculture the next day</p>
+     <p>Aim: Preparation for a mainculture the for the next day</p>
      </div>
      <div class="exp-content">
-     <p>2x6 mL of LB were inoculated with  Bacillus WT3610 from an LB plate and incubated at 37&deg;C overnight.</p>
+     <p>2 x 6 mL of LB were inoculated with  <i>Bacillus subtilis</i> WT3610 from an LB plate and incubated at 37&deg;C over night.</p>
 </div>
 </fieldset>
+<!-- ROMAN -->
+<fieldset class="exp14">
+ <legend><a name="exp14.47">14.47 Purification of PheA-Arc1p-C-0x</a></legend>
+    <div class="aim">
+    <p>Aim: Purify PheA-Arc1p-C-0x in three steps</p>
+    </div>
+    <div class="exp-content">
+    <p>The resuspended cells from 14.46 were lysed using a french press. The lysate was incubated on ice with 5 &micro;g/mL DNAseA and RNAseI for 10 min and centrifuged (27000 rpm, 45 min, 4 &deg;C) to pellet cell debris. The supernatant was filtered (0.45 &micro;m) and PheA-Arc1p-C-0x purified from the cleared solution by NiNTA affinity chromatography. The combined elution fractions containing crude PheA-Arc1p-C-0x were concentrated to a volume of 2 mL and further purified using an anion exchange column to get rid of possible tRNA contaminations. Finally the buffer was changed to dialysis buffer and the protein concentrated and stored at -80 &deg;C in aliquods for further use.</p>
+    </div>
+</fieldset>
+<!-- ROMAN -->
 </div>
 </html>
 {{Team:Marburg/Template:End}}

Team:Marburg:Project:Notebook:June

From 2014.igem.org

Latest revision as of 21:10, 16 October 2014

Notebook: June