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Latest revision as of 19:28, 16 October 2014

Notebook: May

01.05.2014

15.16 Purification of Restriction Digest from 30.04.14

Purifying the samples from the 30.04.2014 with gel extraction kit (QIAquick Gel Extraction Kit) according to the protocol.

Fragment	Concentration [ng/µl]
pMAD Digest 1	21
pMAD Digest 2	19
Hag-Flank Construct 1 Digest	16,9
Hag-Flank Construct 2 Digest	17,6
Hag-Flank Construct 3 Digest	11,3

15.17 Ligation of purified pMAD and Constructs

The ligation is carried out with the purified pMAD digest and the hag-flank-construct digest from 15.16 in order to transform the ligation mix into E.Coli DH5α. For the ligation was the following calculator used: UT Dallas

Mix [µl]	Control 1	Control 2	Construct 1.1	Construct 1.2	Construct 2.1	Construct 2.2	Construct 3.1	Construct 3.2
Plasmid (pMAD digest 1)	1	-	4,5	-	4,7	-	3	-
Plasmid (pMAD digest 2)	-	1	-	5	-	5	-	3,3
Insert (construct)	-	-	5	5	5	4,8	5	5
T Ligase	1	1	1	1	1	1	1	1
T4 Ligase Buffer 10x	2	2	2	2	2	2	2	2
H2O	16	16	7,5	7	7,3	7,2	9	8,7
Total Volume	20	20	20	20	20	20	20	20

Incubation for 1,5 h at room temperature.

15.18 Transformation of E.coli DH5α

Transformation of E.coli DH5α with the ligation attempt.
10µl of each the attempts were used to transform 50 µl of competent E. coli DH5α in order to test the success of the ligation and raising colonies for inoculating a mini prep.

15.19 PCR with primers

To have enough of the construct for further works, a new PCR (as described before) was done overnight.

02.05.2014

13.36 Miniprep of pMA12 from Yeast

Aim: Isolate the plasmid from yeast.

The yeast was washed from the plate with 2 ml of A. dest. After centrifugation at 11000 rpm for 1 min the supernatant was discarded and 500 µl of Solution 1 of the Omega plasmid prep kit was added. The yeast was vortexed for 5 min after addition of a few glas balls. After that the miniprep was carried out according to the protocol (Omega). (c = 134.5 ng/µl)

13.377 Transformation of E.coli DH5α with the isolated pMA12

Aim: Transform E.coli with the isolated plasmid to increase the amount of plasmid.

E. coli DH5Alpha cells were transformed with 10µl of the isolated plasmid pMa12. They were incubated at room temperature over the weekend.

15.20 Purification of Fragments

Purification of the fragments from 01.05.14. The PCR-products were separated on a 1% agarose-gel.

Results

The fragment with the correct size was excised from the gel and purified with the Gel Extraction Kit (QIAquick Gel Extraction Kit)(c = 6.6 ng/µl; c2 = 5.8 ng/µl).

05.05.2014

13.38 Inoculation of Miniprep Cultures

Aim: Pick clones to check for the correct plasmids.

15 colonies of the transformed E.coli DH5α were picked and incubated in 6 ml LB-Amp at 37°C overnight.

15.21 Ligation of the hag/flank and pET24d both cut with BamHI and NcoI followed by Transformation of E. coli

The ligation with pMAD was not successful so it was decided to clone the hag/flank-construct first into pET24d. The ligation was done after using the ligation calculator: UT Dallas

[µl]	Fragment 1	Fragment 2	Fragment 3
pET24d	2,9	3,1	2
Fragment	10	10	10
T4-Ligase-Buffer (10x)	2	2	2
T4 Ligase	1	1	1
H20	4,1	3,9	5
Total	20	20	20

The ligation was incubated at RT for about 2 hours followed by a transformation of E. coli DH5α. The transformed cells were plated out on LB-Kan and incubated at 37°C over night.

06.05.2014

13.39 Miniprep of the 15 Cultures and Restriction with NcoI

Aim: isolate the plasmid from the picked clones and check for restriction sites of NcoI.

The plasmids were isolated according to the protocol "Miniprep (Plasmid DNA Miniprep Kit II, Omega)".

Clone	Concentration (ng/µl)
1	570,2
2	735,5
3	671,9
4	642,6
5	660,9
6	688
7	982,6
8	637,4
9	635,4
10	1306,6
11	523,9
12	554,4
13	501,3
14	825
15	771,2

The isolated plasmids were digested with NcoI for 1h 20 min and further analyzed on a 1% agarose gel.

Results

Restriction of the isolated pMa12 with NcoI; the lanes contain the digested pMa12 in the order of the picked clones 1 - 15; clone 9 was negative; the lanes between the restrictions and the marker contain the isolated pMAD but it appears to be empty.
The most clones contained a plasmid that has only one NcoI restriction site. The expected size of the pMa12 should be around 6.6 kb. All fragments are of the expected size.

13.40 Restriction of pMa12 (isolated from Clone 10) with SacI and NcoI

Aim: create fitting ends to anneal the promotor oligos.

The isolated pMa12 of clone 10 was used for a restriction with SacI-HF and NcoI. The restriction leads to fitting ends for the designed oligos which are the promoters we are about to test: PargJ and PykuO. The restriction is incubated at RT over night.

Restriction	Volume [µl]
pMA12 from clone 10	2
NcoI	1
SacI-HF	1
CutSmart Buffer (10x)	2
H2O	14
Total	20

15.21 Inoculation of the DH5α and Miniprep of pET24d_hag/flank

Aim: amplifying and isolation of pET24d_hag/flank.

On the plates with the transformands of yesterday were only three colonies. Each 6 ml LB-Kan were inoculated with the colonies and incubated at 27°C for around 9 h. After growth of the bacteria the plasmids were isolated with the Omega Plasmid Prep Kit.

07.05.2014

15.22 Restriction of 3 isolated plasmids (6.5.14) with NcoI and BamHI

Aim: Test whether the isolated plasmid contains the 2 kb insert (hag-flank construct).

[µl]	Clone 1	Clone 2	Clone 3
Plasmid (500ng)	10	5	5
Water	8	12	12
CutSmart Buffer (10x)	2	2	3
NcoI	0,5	0,5	0,5
BamHI	0,5	0,5	0,5

Restriction for 45 min at 37°C.
Agarose-gel (1%) to compare the cut and uncut plasmid.

Agarose gel with control (uncut) and 3 cut clones of pEt24d containing the hag-flank construct, fragments are of expected size.

13.41 Purification of overnight digested plasmid pMa12 (3 inserts, only 1 NcoI restriction site) by gel-elution.

Aim: purify plasmid to clone annealed oligos for the promoter sequences into the plasmid.

Concentration: 3ng/µl

13.42 Annealing of Oligos

Aim: create promotor sequences in plasmid piGEM001

[µl]	Reaction 1	Reaction 2
Oligos	iGEM012/iGEM013 10µl/10µl	iGEM014/iGEM015 10µl/10µl
Water	80	80
Total	100	100

Heat up at 98°C for a few minutes. Let it cool down until room temperature

13.43 Ligation of the annealed oligos into digested piGEM001

Aim: Create plasmid with the corresponding promoter sequences for Ag/Cu

[µl]	Reaction (Ag)	Reaction (Cu)
Plasmid (3ng/µl)	5,5	5,5
Water	15	15
Buffer (Ligation Buffer 10x)	2,5	2,5
Oligo-Mix	12/13	14/15
T4-DNA-Ligase	1	1

10µl of the ligation reaction will be transformed into chemically competent E.coli DH5α as described before.

13.44 Over night restriction of pMA12 to obtain more digested plasmid (clone 10)

See 06.05.2014

Restriction	Volume [µl]
pMA12 from clone 10	2
NcoI	1
SacI-HF	1
CutSmart Buffer (10x)	2
H2O	14
Total	20

08.05.2014

13.43 Repeat Transformation for AG/Cu Promoters

No colonies on the plates, repeat ligation and transformation with new digested plasmid.
Concentration plasmid: 17 ng/µl
Ligation: 1.5µl of plasmid used
Tranformation: as usual

1. Sequencing

Label	Description	Primer
AFD001881	piGEM001	T7
AFD001882	piGEM001	T7 Turn
AFD001883	piGEM001	Hag revers (Flo)
AFD001884	piGEM002	TW 260 (Daniel)

Plasmids have to be prepared in a concentration between 50-100 ng/µl in a total volume of 10 to 15µl.
2µl Primers have been added to the premixes, Sample 881 and 882 will be sequenced with primers already present at the company (mwg eurofins).

09.05.2014

13.43 Repeat Transformation for AG/Cu Promotors

No colonies on the plates
Repeat annealing of oligos
Step 1:

Amount [µl]
1	Oligo 1
1	Oligo 2
5	Ligase Buffer
1	PNK
42	Water

Incubation at 37°C for 30 min
Step 2:
Heat up water in microwave until boiling, add the tubes with primer mix
let it cool down to room temperature
Step 3:
1:100 dilution
Step 4: Ligation

Amount [µl]
3	Plasmid (17,6ng/µl)
2	Annealed Oligos (1:100)
1	Ligase
2	Ligase Buffer
12	Water

Step 5: Transformation
Incubation at room temperature over two days.
Step 6: Results
Hag Flank construct digestion with SpeI was positive.

10.05.2014

13.43 Repeated Transformation for AG/Cu Promoters

No colonies

15.23 PCR for amplification of flagellin-constructs out of pet24-fla-Construct from 05.05.14

Aim: Amplification of the flagellin-constructs from the pET24-fla-plasmid as a template was done in order to make a restriction digest with SpeI. This showed, which clone contained the successfully synthesized construct with SpeI restriction site because of the Strep-Tag from sequencing.

Mix [µl]	Pet24fla1	Pet24fla2	Pet24fla3
Temp. - pet24fla cone 1 (lig1 05.05.14)	0,5	-	-
Temp. - pet24fla cone 2 (lig2 05.05.14)	-	0,5	-
Temp. - pet24fla cone 3 (lig3 05.05.14)	-	-	0,5
Primer iGEM-89flo	1	1	1
Primer iGEM-89flo	1	1	1
Q5-Buffer 5x	10	10	10
Phusion-Polymerase	0,5	0,5	0,5
Water	37	37	37
Total Volume	50	50	50

PCR protocol for "PCR Q5 elongation for 2kb fragments".

Step	Temperature °C	Time
1	95	3 min
2	95	30 sec
3	55	30 sec
4	72	2,5 min
5	Go To 2	35x
6	72	5min
7	4	Infinite

Result: PCR not successful - no band at 2,2kb

15.24 Transformation of E.coli DH5α with pET24-fla-Construct from 05.05.14

Aim: Amplification plasmid for further experiments.

3 aliquots competent E.Coli DH5α were transformed with 1µll of the purified plasmid pet24-fla construct from 05.05.14 from 3 different clones (lig 1-3) each
After regeneration the cells were plated on LB-canamycin plates and incubated at room temperature until Monday

15.25 New PCR for amplification of flagellin-constructs out of pET24-fla-Construct from 05.05.14

Aim: Amplification of the fragment for further experiments with pet24-fla from 15.21 as template. The prior PCR was not successful.

Mix [µl]	Pet24fla1	Pet24fla2	Pet24fla3
Temp. – pet24fla cone 1 (lig1 05.05.14)	0,5	-	-
Temp. – pet24fla cone 2 (lig2 05.05.14)	-	0,5	-
Temp. – pet24fla cone 3 (lig3 05.05.14)	-	-	0,5
Primer iGEM-89flo	1	1	1
Primer iGEM-89flo	1	1	1
Q5-Mastermix	25	25	25
Water	22,5	22,5	22,5
Total Volume	50	50	50

Q5 PCR

Step	Temperature °C	Time
1	95	3 min
2	95	30 sec
3	55	30 sec
4	72	1 min
5	Go To 2	35x
6	72	5min
7	4	Infinite

11.05.2014

13.43 Repeat Transformation for AG/Cu Promotors

No colonies

15.25 New PCR for ampl. of flagellin-constructs out of pet24-fla-Construct from 05.05.14

Results:

PCR result from the amplification of the fla-construct out of the pET24d. The gel shows that the three clones contain a construct in the pet24d vector. The fragment is about 2,2kb.

15.26 Gel Extraction of PCR Products

Aim: purification of constructs from gel as a preparation for the restriction digest with spe1. The digest will show which clone contains the construct with the replaced strap-tag.

Gel extraction was performed according to the gel extraction kit by Omega.

Extracted PCR product	Concentration [ng/µl]
clone 1	80,2
clone 2	88,2
clone 3	93,9

15.27 Restriction Digest of PCR Products from with SpeI

Aim: The digest with Spe1 will show, which clone contains the fla-construct with replaced StrepTag by a SpeI restriction site

[µl]	Mastermix with NcoI - for 4 attempts	Attempt 1-3 SpeI (20kU/ml)
DNA	-	Ca. 85ng/µl ca. 1µg → 12µl
Spe1	1	-
Master-Mix	-	3
Cutsmart (10x)	6	-
H2O	5	-
Total Volume	12	15
Loading Dye 6x	-	2,5/attempt

Incubation for 60min at 37°C
Heat shock for 2min at 80°C

Results:

The digestion of the PCR amplified construct shows 3 bands. The 2,2kb band is the uncut construct whereby the smaller bands are the two fragments as a result of the SpeI cut. The constructs in the pET24d still contain the right SpeI restriction site.

15.28 Transformation of E.coli DH5α with pET24-fla-Construct from 05.05.14

Colonies were grown on every plate → successful transformation

15.29 Inoculation for Miniprep of Transformed E.Coli DH5α with pet24-fla-Construct from 10.05.14

Aim: Amplification of transformed plasmid for miniprep in order to receive more plasmid for further experiments

3x6ml LB + 6µl canamycin each were inoculated with 1 colony of plate 1-3 from 10.05.14. The plates were incubated over night at 37°C

12.05.2014

15.30 Miniprep of Transformed E.coli DH5α with pET24-fla-Construct from 11.05.14

Aim: Isolation of plasmid in order to obtain more plasmid for further experiments

15.31 PCR of Construct with pET24d as Template from Miniprep 11.05.14

Aim: Amplification of the plasmid from clone 2 for further experiments

Mix [µl]	Pet24fla2
Temp. - pet24fla clone 2 (lig2 11.05.14)	0,5
Primer iGEM-89flo	1
Primer iGEM-89flo	1
Q5-Mastermix	25
Water	22,5
Total Volume	50

The PCR was performed according to the "PCRQ5" protocol.

Step	Temperature °C	Time
1	95	3 min
2	95	30 sec
3	55	30 sec
4	72	1 min
5	Go To 2	35x
6	72	5min
7	4	Infinite

The PCR-products were separated on a 1 % agarose gel. The bands of 2.2 kb were cut out and a gel extraction was carried out (c = 100 ng/µl) according to the "Gel Extraction (QIAquick Gel Extraction Kit)" protocol.

15.32 Restriction of the PCR-Fragment with BamHI and NcoI

Aim: Creating corresponding ends for ligation into pMAD

Restriction	Volume [µl]
PCR-product hag/flank (100 ng/µl)	5
NcoI-HF	1
BamHI-HF	1
CutSmart-Buffer (10x)	2
H2O	11
Total Volume	20

The restriction is incubated at RT overnight.

13.44 Phosphorylation and Annealing of Promoter-Oligos

Aim: phosphorylation of single stranded oligos with subsequent annealing for cloning into pMa12

For ligation to occur at least one of the DNA ends (insert or vector) should contain a 5' phosphate. Primers are usually supplied non-phosphorylated; therefore, the oligos or PCR product will not contain a 5' phosphate. The digestion of DNA with a restriction enzyme will always produce a 5´ phosphate. A DNA fragment can be phosphorylated by incubation with T4 Polynucleotide Kinase in T4-ligase-buffer which already contains the necessary ATP in an appropriate amount (1 mM):

Phosphorylation [µl]	P(argJ)	P(ykuO)
iGEM-012	1	-
iGEM-013	1	-
iGEM-014	-	1
iGEM-015	-	1
T4-ligase buffer	5	5
T4 PNK	1	1
H2O	42	42
Total Volume	50	50

The reaction was done in a PCR cycler with a subsequent heat inactivation of the PNK and annealing reaction (protocol: "Annealing with PNK Inactivation")

14.24 Transformation of BL21 cells

Aim: Transform E. coli BL21(DE3) with PheA-Arc1p-C-2x-pET28a

40 µL E. coli BL21(DE3) electrocompetent cells were transformed with 1 ng of the previously purified plasmid PheA-Arc1p-C-2x-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.

13.05.2014

14.25 Overnight culture

Aim: Inoculate Overnight culture of PheA-Arc1p-C-2x-pET28a

5 mL of LB-Kan⁵⁰ medium were inoculated with a clone from 14.24 bearing the PheA-Arc1p-C-2x-pET28a plasmid.

15.33 Miniprep and Restriction of pMAD with BamHI and NcoI

Aim: isolate pMAD and create linearized vector with corresponding ends for ligation with the construct

The plasmid pMAD was isolated and digested with the restriction enzymes BamHI and NcoI to create fitting ends for the ligation with the digested PCR-fragment.

Restriction	Volume [µl]
pMAD (174.9 ng/µl)	2
NcoI-HF	1
BamHI-HF	1
CutSmart-Buffer (10x)	2
H2O	14
Total Volume	20

The restriction was incubated at 37°C for 1h.

15.34 Ligation of digested pMAD with the digested hag/flank-Construct and trafo

Aim: link the fragment with the vector and trafo of DH5α

The ligation of pMAD and the digested PCR-fragment was done according to the previous mentioned ligation calculator.

Ligation	Volume [µl]
pMAD	5
Hag/flank-construct	10
T4 Ligase Buffer (10x)	2
T4 DNA-Ligase	1
H2O	2
Total Volume	20

The ligation was incubated at RT for 1.5 h. After that E. coli DH5α were transformed with the ligation mix and plated out onto LB-Amp plates which were incubated at 37°C overnight.

13.45 Ligation of Annealed Oligos with digested pMa12-Construct and Trafo of E. coli DH5Alpha

Aim: clone the promoter sequences in front of the gfp

A ligation of the SacI and NcoI digested pMa12-construct with the annealed oligos was carried out. The annealed oligos (iGEM-012/013 c = 762.3 ng/µl and iGEM-014/015 c = 825.5 ng/µl) were diluted up to 10-2. 10 ng of the insert and 100 ng of the vector were used for the ligation.

Ligation [µl]	P(argJ)-pMa12-construct	P(ykuO)-pMa12-construct
iGEM-012/013 (7.6 ng/µl)	1,5	-
iGEM-014/015 (8.3 ng/µl)	-	1,5
T4-ligase-buffer (10x)	2	2
T4-Ligase	1	1
H2O	15,5	15,5
Total Volume	20	20

The ligation was incubated at RT for 2h. The E. coli DH5Alpha were transformed afterwards with the whole ligation mix and plated on LB-Amp, which were incubated at 37°C overnight.

14.05.2014

14.26 Test Expression

Aim: Test the expression of PheA-Arc1p-C-2x

Using the preculture from 14.25 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. A glycerolstock of the strain containing the PheA-Arc1p-C-2x-pET28a plasmid was stored at -80 °C.

15.35 Inoculation Miniprep and Restriction of pMAD with BamHI and NcoI

Aim: the ligation from 15.34 was not successful. Inoculation of pMAD for miniprep in order to have more plasmid for further experiments.
Additionally we create linearized vector with corresponding ends for ligation with the construct with rest from 13.05.14.

The plasmid pMAD from 13.05.14 (ca. 25µl) and digested with the restriction enzymes BamHI and NcoI to create fitting ends for the ligation with the digested PCR-fragment. The digest was performed in 2 Eppis with 12,5µl plasmid each.

Restriction [µl]	Mastermix	Volume
pMAD (174.9 ng/µl)	-	12,5
Mastermix	-	7,5
NcoI-HF	1	-
BamHI-HF	1	-
CutSmart-Buffer (10x)	4	-
H2O	9	-
Total Volume	15	20

The restriction was incubated at 37°C for 2h.

15.36 Transformation of pET24d-clone2 into E.Coli DH5α

Aim: raising colonies for further minipreps of successful construct containing clone

The plasmid pET24d with the fla construct from clone 2 was transformed into E.Coli DH5α and plated on LB-canamycin. Incubation overnight at 37°C.

13.37 Inoculation for Miniprep of E.Coli DH5α with pET24d-fla Construct Clone2

Aim: raising colonies for further minipreps of successful construct containing clone2

One clone with plasmid pET24d with the fla construct was used for inoculation of LB-medium. Incubation overnight at 37°C

13.46 Transformation of Nose-Plasmid from Clone 10 into E.Coli DH5α

Aim: raising colonies for miniprep of new Nose-plasmid for further experiments

The plasmid pMA12+Nose-Construct from clone 10 was transformed into E.Coli DH5α and plated on LB-AMP. Incubation overnight at 37°C

13.37 Ligation of digested pMAD from 14.05.14 with the digested hag/flank-construct

Aim: link the fragment with the vector

The ligation of pMAD and the digested PCR-fragment was done according to the previous ligation calculator.

Ligation	Volume [µl]
pMAD	5
Hag/flank-construct	20
T4-Ligase-Buffer (10x)	3
T4-DNA-Ligase	1
H2O	1
Total Volume	30

Incubation overnight at room temperature.

13.47 Restriction and purification of piGEM002 (Nose) and following ligation and transformation

Aim: create more plasmid for further experiments, 2 digests were performed to get a high amount of plasmid (pooled during purification)
concentration= 44 ng/µl

Restriction	Volume [µl]
pMa12 from clone 10	1,5
NcoI	1
SacI-HF	1
CutSmart-Buffer (10x)	2
H2O	14,5
Total Volume	20

One ligation was performed for 1h and transformed into chemocompetent cells, the second ligation was performed over night in case no colonies grow on the trafo plates.

Ligation Mix	Volume [µl]
Buffer	2
Water	14,5
Plasmid	1,5
Primer Mix (1:100)	1
Ligase	1

Transformation:
thaw on ice: 5 min
add DNA, keep on ice: 5 min
heat shock in water bath at 37°C: 45 sec
put back on ice and add 1 ml LB
recovery for LB: 20 min

17.1 Inoculate Bacillus Strains

Aim: have bacillus strains to work with in MTA and make competent cells

Wildtype on LB plate and in LB liquid without an antibiotic.
Bacillus subtilis strain 186 on plates containing xylose (Incubation overnight).

15.05.2014

17.2 Make Competent Cells

Aim: making Bacillus subtilis cells competent for transformation

Inoculate Bacillus wildtype strain in SPC medium.

Time	OD570
13:30	5,7
14:00	6,2
15:45	6,6
16:30	7
17:00	7,2
	→ new media Incubation for 1,5h

Aliquot and thaw in liquid nitrogen. Store at -80°C.

14.27 Purification of test expression

Aim: Purify PheA-Arc1p-C-2x on a small scale

The cell culture from 14.26 was centrifuged (17000 rpm, 20 min, 4 °C) and the pellet resuspended in 3 mL buffer A. Lysozyme was added 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 14.26 and incubated at 37 °C and 220 rpm over night.

15.38 Transformation of ligated pMAD and the digested hag/flank-Construct

Aim: produce cells that contain the ligated plasmid

Chemically competent cells from Daniel were transformed with the 20µl ligation-mix, 20µl of the cells were transformed with 1µl pMad uncut (control).
Protocol: see yesterday

15.39 PCR for amplification of Hag-Flank-construct in pET24d and following restriction

After plasmid isolation a PCR was run to amplify the hag-Flank-construct, afterwards it will be digested with SpeI to find a clone with pure product (no tag but only SpeI restriction site).

PCR Mix	Volume [µl]
Q5-Mastermix	88
Water	110
Primer 89	5,5
Primer 90	5,5
Template	1

Gel foto after amplification of hag flank insert from 10 clones: all positive.
Whole insert has been digested for 1h with SpeI in a 20µl reaction mix
17.5µl insert, 2µl buffer and 1µl ligase

Gel foto after restriction of the 2.2 kb fragment with SpeI (expected sizes appear on the gel) no undigested bands= only fragments with the restriction site are in

13.48 Colony PCR after transformation

Aim: find out which colonies contain the right plasmid

Pick a colony from the trafo plate, streak it on a new plate and dip in the PCR Premix

[µl]	Amount Ag	Amount Cu
Q5-Mastermix	8	8
Water	10	10
TW 260	1	1
Primer 12	1	-
Primer 14	-	1

17.3 First Plate Reader Measurement with Bacillus subtilis wildtype and strain 186 containing a gfp

Aim: Test for differences between the two strains and first check if experiment works at all

Both strains grew best in LB medium like expected, a clearly better growth was shown by the wildtype in the minimal medium compared to the gfp bearing strain.

The fluorescence is shown in dependence of the culture growth in order to relativise the fluorescence signal. Like expected, the wt exhibited no fluorescence in both media. The fluorescence of the gfp strain was higher in the minimal medium with xylose, than without xylose.

16.05.2014

15.40 Colony PCR with colonies from 16.05.14

Aim: test the success of ligation from pMAD & Hag-Flank-Construct

A PCR ran with 5 picked clones from 16.05.14 and primers Flo89 and 90 for amplification of inserted construct

	Attempt [µl]
Colony	1 colony
Q5-Mastermix	10
Water	8
Primer Flo89	1
Primer Flo90	1

Results

Test if insert in pMad has the right size of about 2000 bp → not precise repeat on Monday

15.41 Inoculation of colonies E. coli pMad plus hag-flank-Insert

Aim: grow cells that contain the mentioned plasmid and subsequently isolation of the plasmid for further work

Inoculate 5 clones in LB liquid and incubation over the weekend at room temperature

14.28 Expression of PheA-Arc1p-C-2x

Aim: Express PheA-Arc1p-C-2x for further use

10 x 500 mL LB-Kan⁵⁰ medium were inoculated with 5 mL of the overnight culture prepared in 14.27 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.

19.05.2014

15.42 Test restriction of pMad-hag-flank and Test PCR

Aim: determine whether the plasmid contains the right insert

Restriction: concentration of plasmid after isolation between 20 and 30 ng/µl

	Volume [µl]
Buffer / Water	27
Template	10
NcoI	0,5
BamHI	0,5

Results

Test restriction of pMad with hag flank insert did not show a clear result (last band is a different sample)

	Amount [µl]
Q5-Mastermix	10
Primer 89	1
Primer 90	1
Template	1
Water	7

Results

The PCR showed the expected fragment of the hag-flank construct with a size of approx. 2 kb.

17.4 Bacillus Trafo with Nose Plasmids

5µl DNA were added to 100µl cells, 30 min incubation at 37°C and plated on LB-Cm.

14.29 Purification of PheA-Arc1p-C-2x

Aim: Purify PheA-Arc1p-C-2x in three steps

The resuspended cells from 14.28 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-2x purified from the cleared solution by NiNTA affinity chromatography. The combined elution fractions containing crude PheA-Arc1p-C-2x 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.

20.05.2014

14.30 Creating PheA-Arc1p-C-1x

Aim: Using Round-the-horn mutagenesis to create PheA-Arc1p-C-1x-pET28a

The PCR with 5' phosphorylated TG_1xGSSG FP und TG_0xGSSG RP should generate the 7509 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_1xGSSG 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.

15.43 PCR to Amplify Cup 1 from Yeast gDNA

Aim: create the DNA fragment cup1 (metallothionein) for insertion into the flagellin (Gibson assembly with pMad by cutting the plasmid with SpeI at the created restriction site)

	Amount [µl]
Q5-Mix	20
Primer 89	1
Primer 90	1
Template	1
Water	17

The Purple 2-log ladder was used as a marker. The amplified cup1 could be seen as a 204 bp fragment on the gel.

17.5 Bacillus Trafo with Nose Plasmids

No colonies → new trafo
New LB-chloramphenicol plates for Bacillus (only 5µg/ml instead of 25µg/ml)

21.05.2014

15.44 Restriction pMad with SpeI

Aim: Create a linearized plasmid for following Gibson assembly with cup1

	Volume [µl]
Buffer	2,5
Plasmid	20
SpeI	1
Water	-

Concentration of plasmid after purification only 7 ng/µl

14.31 Overnight culture

Aim: Amplify Plasmid in an overnight culture

Six clones of the transformed E. coli Top10 cells from 14.30 were picked and used to inoculate overnight cultures (6 x 5 mL).

15.45 Gibson Assembly of digested pMad-fla and cup 1 and Transformation into E.Coli XL1-Blue

Aim: create a flagellin that contains the metallothinein cup1

[µl]	Control	With Insert
Gibson Mix	15	15
Plasmid (7ng/µl)	5	5
Insert	-	1
Water	1	-

A part of the aliquot was plated on LB-tet for inoculation of colonies for competent XL1-Blue.

22.05.2014

17.6 MTA Bacillus Nose Ag

Transformation from 20.5.14: one colony on the Ag Nose plate
Inoculation of shaking culture in the morning together with the wildtype and the gfp strain in LB liquid without antibiotics

Inoculate 96 well plate in the afternoon 15:00

Prepare Cu and Ag solutions to test different concentrations in MTA and see if the Ag nose responds to Ag and also if it is specific for Ag and does not respond to Cu

Ag and Cu in stock solution of 10 mM have been prepared
Added (Concentration): 11 mM, 100µM and 10µM
Cells: Ag Nose mutant, wildtype (AG GM) and gfp

The MTA showed no significant increase of fluorescence. The bacteria had difficulties in growth, thus it seemed that the metal ion concentrations were too high.

17.7 Digestion of piGEM002 and the nose plasmids for Ag/Cu

Aim: Linearize the plasmids with SpeI to built in the instability tags (25µl mix)

[µl]	piGem 002 clone 7	Nose plasmid 003/004	Amount
Template ~10µg	15	20	15
SpeI	1	1	1
CutSmart-Buffer	2,5	2,5	2,5
Water	6,5	1,5	6,5

Incubation at room temperature over night.

14.32 Preparation of plasmids

Aim: Purify the amplified plasmids from overnight cultures

The plasmids were purified from the overnight cultures created in 14.31 using Sigma GenElute Plasmid Miniprep Kit following the included protocol. The plasmids were eluted using 45 µL water.

23.05.2014

17.7 Create Instability Tags for gfp in the Nose Plasmids

Aim: GFP is a stable protein, which would accumulate and distort the results if not degraded, instability tags of different strength cause the degradation and therefore cause quantitative results

First step: Linearize the following plasmids: piGEM 002 without promoter as well as the plasmids containing the silver and copper sensitive promoters
Second step: PCR to anneal the oligos 20+21, 20+22 and 20+23

	Volume [µl]
Primer A	5
Primer B	5
Phusion	0,25
dNTPs	0,25
Buffer	5
Water	34,5
Cycle	3

Afterwards clean up with kit (all three mixes were carried out in a duplicate, 1 each was frozen away at minus 20)

Third step: Yeast transformation
9 Reactions (3 plasmids and 3 instability (ssrA-)tags)

100 ng plasmid plus 1µl of primer mix were filled to 14µl and added to the yeast transformation mix and subsequently transformed into yeast.

26.05.2014

15.46 Restriction of pMAD-fla with SpeI, Gibson-Assembly with cup1-1 and transformation of E. coli DH5α

Aim: insert cup1-1 into the hag/flank-construct

To insert the metallothionein gene cup1-1 into the hag/flank-construct the pMAD-fla was digested with SpeI to linearize it.

Restriction	Volume [µl]
pMAD-fla (330 ng/µl)	4
SpeI	1
CutSmart Buffer (10x)	1
H2O	6
Total Volume	10

The restriction was carried out at 37°C for 1h.
The restriction was cleaned with a DNA Gel Ex Kit (c = 40 ng/µl). 4µl (160 ng) of this digested plasmid were mixed with 1 µl of the cup1-1 fragment (9.6 ng/µl). These 5 µl were inserted into the prepared 15 µl Gibson-mix. The reaction was incubated at RT for 1 min and then at 50°C for 1 hour. An extra Gibson-reaction was carried out as a control with just the linearized pMAD without the cup1-1.
E. coli DH5α cells were transformed with the Gibson reactions and plated out on LB-Amp. They were incubated at 37°C over night.

15.47 Colony-PCR of E. coli XLI-Blue pMAD-fla + cup1-1 from 21.05.14 and 23.05.14

Aim: check for correct insertion of cup1-1 into the hag/flank-construct

Since a Gibson-Assembly with the same aim was carried out last week, the colonies were checked by a colony PCR with the primers for cup1-1 iGEM-018 and iGEM-019. One colony was picked from the plate from 23rd May and three were taken from the plate from 21st May. The latter was contaminated with Bacillus colonies. For this reason E. coli was picked and streaked out onto a new plate on Friday the 23rd May. The consequence is a plate with just one clone, what is the reason, that only one colony was picked from this plate.

Mix	Volume [µl]
E. coli XLI-Blue pMAD-fla+cup1-1	part of a colony
Primer iGEM-018	0,5
Primer iGEM-019	0,5
Q5-Mastermix	10
Water	9
Total Volume	20

A part of each colony was transferred onto a new LB-Amp plate, which was incubated at 37°C overnight.

Result

The expected fragment in size of the cup1 could be amplified from the template, which indicates a positive result.

14.33 Transformation of BL21 cells

Aim: Transform E. coli BL21(DE3) with PheA-Arc1p-C-1x-pET28a

40 µL E. coli BL21(DE3) electrocompetent cells were transformed with 1 ng of the previously purified plasmid PheA-Arc1p-C-1x-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.

13.49 PlasmidPprep from Yeast and Transformation of E. coli DH5Alpha

Aim: increase the amount of plasmid in E. coli for further experiments with the degradation tags

The gfp in piGEM002, piGEM002-Ag (and piGEM002-Cu was tagged with different degradation tags by yeast recombination. The plasmids have been isolated from yeast.

E. coli DH5α cells were transformed with 15 µl of each isolated plasmid and plated out on LB-Amp. They were incubated at 37°C over night.

Gly-Stocks - Making of -stocks for long time storage of bacteria strains
For long time freezer storage of bacteria, they have to be treated with glycerine to prevent the crystallization and damaging of the cells. For this reason 2 ml of LB with the respective antibiotic were inoculated with the bacteria, which were meant to be stored and were incubated at 37°C overnight.

Strains that are to be stored:

E. coli XLI-Blue pMAD-fla (piGEM-005)
E. coli XLI-Blue pMa12-construct (piGEM-002)
E. coli XLI-Blue pMa12-Cu (piGEM-004)
E. coli XLI-Blue pMa12-Ag (piGEM-003)
E. coli BL21(DE3) pLysS

27.05.2014

14.34 Overnight culture

Aim: Inoculate Overnight culture of PheA-Arc1p-C-1x-pET28a

5 mL of LB-Kan⁵⁰ medium were inoculated with a clone from 14.33 bearing the PheA-Arc1p-C-1x-pET28a plasmid.

15.48 Restriction of pET24d-fla with SpeI and Gibson-Assembly with cup1-1

Aim: linearize pET24d-fla and insert cup1-1 into pET24d-fla

Since the colony-PCR (26.05.14) was negative and the Gibson-Assembly of linearized pMAD-fla with cup1-1 showed no results the pET24d-fla construct was linearized with SpeI.

Restriction	Volume [µl]
pET24d-fla (98.8 ng/µl)	8
SpeI	1
CutSmart-Buffer (10x)	2
H2O	9
Total Volume	20

The restriction was incubated at 37°C for 1 h.

The restriction mix was purified with the Gel Ex Kit. The yield was too low (c = 3.1 ng/µl) to use it for a Gibson-Assembly, so the rest of the pET24d-fla was digested with SpeI.

Restriction	Volume [µl]
pET24d-fla (98.8 ng/µl)	18,5
SpeI	1
CutSmart-Buffer (10x)	2,5
H2O	3
Total Volume	25

The restriction was incubated at 37°C for 1h.

The restriction mix was purified with the Gel Ex Kit (c = 20.1 ng/µl), which was enough for the Gibson-Assembly. 4µl (80 ng) of this digested plasmid were mixed with 1 µl of the cup1-1 fragment (9.6 ng/µl). These 5 µl were inserted into the prepared 15µl Gibson-mix. The reaction was incubated at RT for 1 min and then at 50°C for 1 h. An extra Gibson-reaction was carried out as a control with just the linearized pET24d-fla without the cup1-1.

Competent E. coli XLI-Blue were transformed with the whole Gibson-reactions. They were plated on LB-Kan an incubated at 37°C overnight.

13.50 Colony-PCR of the E. colis Containing the Degradation tagged Constructs

Aim: check for correct tagging of gfp with the respective degradation tag

The transformation with the degradation tag-constructs were successful nearly in all cases except the pMa12-Ag-21. The transformation was repeated, the plate was incubated at 37°C over night.
Four colonies of every plate have been picked, transferred to new LB-Amp plates and were subsequently used for the colony-PCR. The Master Mix was portioned in aliquots of 20 µl per PCR-cup and inoculated with the respective colony.

MasterMix for 33 reactions	Volume [µl]
E. coli DH5Alpha with construct	part of a colony
AG TW 260	16
AG TW 316	16
Q5-Mastermix	165
Water	133
Total Volume	330

Step	Temperature °C	Time
1	95	5 min
2	95	20 sec
3	55	20 sec
4	72	20 sec
5	Go To 2	35x
6	72	5min
7	4	Infinite

Colony-PCR of E. coli with the degradation-tag constructs

The bands slightly higher than 200 bp indicated a positive clone. Positive constructs are available: 002-21, Cu-23, Ag-22 and Cu-22.

Gly-Stocks - Making of glycerin-stocks for long time storage of bacteria strains

1 ml of the bacteria which were inoculated yesterday (26.05.2014) were transferred to new, sterile 1.5 ml Eppendorf-cups. 600 µl of 50% glycerin were added and the cells were frozen and stored at -80°C in the freezer.

18.1 Making competent E. coli XLI-Blue with RbCl: Inoculation of LB-Tet with E.Coli XL1-Blue as a preculture

9 ml LB-Tetracycline (1:1000) were inoculated with E. coli XLI-Blue cells as a preculture. They were incubated at 37°C overnight.

28.05.2014

18.2 Inoculating E.Coli XL1-Blue main culture

93 mL of LB-tet were added to 7 mL of preculture for inculation of main culture. The main culture was incubated at 37°C until an OD of 0,5.

18.3 Preparing Transformation Buffer TBF1 and TBF2

TBF1 recipe

TBF2 recipe

for 50ml

potassium acetate	0,15g
MnCl2 x 4H2O
1M RbCl	5 ml
1m CaCl2	0,5 ml
87% glycerine	8,6 ml
A.dest	35,9 ml
autoclave or sterile filtration

for 250 ml

1M NaMOPS (pH7)	2,5 ml
1M CaCl2 x 2H2O	8,75 ml
1M RbCl2	2,5 ml
87% glycerine	43,75 ml
A.dest	192,5 ml
adjust pH7
store at 4°C in the dark
sterile filtration

18.4 Preparing E.Coli XL1-Blue

Grow 100 ml E.coli culture to OD600=0,5
Put on ice for 10 min
Centrifuge 2x 50 ml for 10 min at 3000 rpm and 4°C
Wash pellets in 10 ml TFB1 (10 min; 3000 rpm; 4°C)
Resuspend pellets in 2ml TFB2
Pipett 200µl aliquots in precooled 1,5 ml tubes
store at -80°C

14.35 Test Expression

Aim: Test the expression of PheA-Arc1p-C-1x

Using the preculture from 14.34 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. A glycerolstock of the strain containing the PheA-Arc1p-C-1x-pET28a plasmid was stored at -80 °C.

15.49 Colony-PCR with transformed E. coli XLI-Blue including pET24d-fla-cup1-1

Aim: testing the success of insertion of cup1-1 into pET24d-fla

6 clones were picked from transformation plate and a colony PCR was ran with primers iGEM-018 & - 019. The result should be a band at 240 bp in case of a positive clone.

[µl]	Mastermix	Mix for PCR attempts
E. coli XLI-Blue pet24d-fla+cup1-1		part of a colony
Primer iGEM-018	3,5	-
Primer iGEM-019	3,5	-
Q5-Masterix	70	-
Water	63	-
Master-Mix	-	20
Total Volume	140

Step	Temperature °C	Time
1	95	1 min
2	95	20 sec
3	55	20 sec
4	72	20 sec
5	Go To 2	35x
6	72	5min
7	4	Infinite

The expected band of approx. 240 bp could be seen in every sample, more or less clearly

13.51 Colony-PCR of the E. coli containing the degradation tagged constructs

Aim: check for correct tagging of gfp with the respective degradation tag

The Colony-PCR was repeated with pMa12-Ag-21 after successful transformation.
Four colonies have been picked, transferred to new LB-Amp plates and were subsequently used for the colony-PCR.
The Master Mix was portioned in aliquots of 20 µl per PCR-cup and inoculated with the respective colony.

[µl]	Master-Mix for attempts	Mix for PCR attempt
E. coli DH5α with Ag21	-	part of a colony
AG TW 260	2,5	-
AG TW 316	2,5	-
Q5-Mastermix	50	-
Water	45	-
Master-Mix	-	20
Total Volume	100	20

Colony-PCR of E. coli containing the degradation-tag construct Ag-21

In an additional reaction the colony-PCRs of the negative clones (gel 28.05.14) were repeated with more picked clones per construct. This time 8 colonies of each negative construct were picked, transferred to another LB-Amp-plate and used for the PCR-reaction. Four times eight reactions were carried out, a master mix was prepared for 33 reactions.

[µl]	Master-Mix for 33 reactions	Mix for one PCR reaction
Part of a colony	-	1
AG TW 260	8	0,25
AG TW 316	8	0,25
Q5-Mastermix	330	10
Water	314	9,5
Master-Mix	-	20
Total Volume	660	20

Step	Temperature °C	Time
1	95	3 min
2	95	20 sec
3	55	20 sec
4	72	20 sec
5	Go To 2	35x
6	72	5min
7	4	Infinite

E. coli containing the degradation-tag constructs

Positive clones could be obtained with the Ag-23 and the 002-22 constructs (approx. 250 bp).

18.5 Transformation test with E.Coli XL1-Blue and pMAD (fla)

E.Coli XL1-Blue were transformed with 1µl pMAD (189 ng/µl). Another aliquod was transformed with pMAD-fla.
In comparison E.Coli DH5α were transformed the same way.

29.05.2014

18.5 Transformation Test with E.Coli XL1-Blue and pMAD (fla)

Every transformation was successful. The higher number of colonies on the pMAD-transformation plate shows a higher transformation efficiency compared with DH5α.

18.6 Inoculation for Miniprep and Glycerin stock of pMAD-fla

Aim: In order to save pMAD and pMAD-fla for further experiments and storage, minipreps and glycerine stocks have to be inoculated

For minipreps 2 x 6 ml of LB-Amp were inoculated with one colony from the pMAD XL1-Blue-transformation plate. Additionally 3 x 6 ml of LB-Amp were inoculated with one colony from the pMAD-fla XL1-Blue-Transformation plate.
Furthermore 2 x 2 mL LB-Amp were inoculated with a clone from pMAD-fla XL1-Blue-Transformation plate for glycerine stocks.
Every attempt was incubated at 37°C overnight.

13.52 Colony-PCR of the E. coli containing the degradation tagged constructs

Aim: check for correct tagging of gfp with the respective degradation tag

The Colony-PCR was repeated with 002-Cu21 and 002-23.
Four colonies have been picked, transferred to new LB-Amp plates and were subsequently used for the colony-PCR.
The Master Mix was portioned in aliquots of 20 µl per PCR-cup and inoculated with the respective colony.

[µl]	Master-Mix for 18 attempts	Mix for PCR attempt 002-23.1-8	Mix for PCR attempt 002-Cu21.1-8
E. coli DH5α with 002-23	-	part of a colony	-
E. coli DH5α with Cu21	-	-	part of a colony
AG TW 260	9	-	-
AG TW 316	9	-	-
Phusion DNA-polymerase	3,6	-	-
Q5-Buffer 5x	72	-	-
dNTP-Mix	5	-	-
Water	261,4	-	-
Master-Mix	-	20	20
Total Volume	360	20	20

Step	Temperature °C	Time
1	95	3 min
2	95	20 sec
3	55	20 sec
4	72	20 sec
5	Go To 2	35x
6	72	5min
7	4	Infinite

14.36 Purification of test expression

Aim: Purify PheA-Arc1p-C-1x on a small scale

The cell culture from 14.35 was centrifuged (17000 rpm, 20 min, 4 °C) and the pellet resuspended in 3 mL buffer A. Lysozyme was added 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 14.35 and incubated at 37 °C and 220 rpm over night.

15.53 Inoculation of Minipreps from Nose-Tag-Plasmids

Aim: isolate the plasmid to tansform Bacillus for further plate reader assays

6 mL LB-Amp were inoculated with different colonies cotaining the following plasmid-constructs:

002-21
002-22
002-Cu-23
002-Ag-23
002-Cu-22
002-Ag-22

Incubation over night at 37°C

30.05.2014

14.37 Expression of PheA-Arc1p-C-1x

Aim: Express PheA-Arc1p-C-1x for further use

10 x 500 mL LB-Kan⁵⁰ medium were inoculated with 5 mL of the overnight culture prepared in 14.36 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.

18.7 Miniprep of E.Coli XL1-Blue with pMAD and pMAD-fla

Plasmid	Concentration after prep (ng/µL)
pMAD	114 & 108
pMAD-fla (iGEM-005)	114, 128 & 142

Plasmids were frozen away at -20°C

13.54 Minipreps of Nose-Tag-plasmids

Plasmid	Concentration after prep (ng/µl)
002-21	368
002-22	401
002-Cu-22	425
002-Cu-23	427
002-Ag-22	806
002-Cu-23	402

13.55 Inoculation of Minipreps with Ag-21

The positive clone 3 from the colony PCR (28.05.14) was used to inoculate 6 ml LB-Amp for a miniprep in order to receive the plasmid for transforming Bacillus subtilis.
Incubation at room temperature over two days.

15.49 Inoculation of pMAD-fla-cup1-1 for Miniprep

Aim: inoculation for miniprep in order to receive plasmid for bacillus-trafo

6 mL LB-Amp were inoculated with the positive clone 1 from the Gibson assembly with cup1-1 of the transformed E. coli XL1-Blue from 26.05.14. After isolation of the plasmid Bacillus Subtilis. can be transformed.
Incubation at room temperature over two days.

13.54 Transformation of Bacillus with isolated plasmids

Aim: Creation of Bacillus strains with the following plasmids:

BS piGEM002 + DT22
BS piGEM 011 (002 AG + DT22)
BS piGEM 012 (002 AG + DT23)
BS piGEM 014 (002 Cu + DT22)
BS piGEM 002 (Nose)
BS piGEM 003 (Nose Ag)
BS piGEM 004 (Nose Cu)

13.55 Colony-PCR of the E. coli containing the degradation tagged constructs

Aim: check for correct tagging of gfp with the respective degradation tag

Phusion and Q5 Buffer did not work out so the PCR was repeated with Q5 Mastermix.
PCR performed with 002-Cu21 and 002-23
Positive clones for both tags (approx. 250 bp) have subsequently been inoculated in LB-Amp and incubated at room temperature over two days.

@@ Line 17: / Line 17: @@
      <legend><a name="exp15.16">15.16 Purification of Restriction Digest from 30.04.14</a></legend>
      <div class="exp-content">
-     <p>Purifying the attempts from the 30.04.2014 with gel extraction kit (QIAquick Gel Extraction Kit) according to the protocol.</p>
+     <p>Purifying the samples from the 30.04.2014 with gel extraction kit (QIAquick Gel Extraction Kit) according to the protocol.</p>
      <table width="100%" border="1">
    <tr>
      <th scope="col">Fragment</th>
-     <th scope="col">Concentration [ng/µl]</th>
+     <th scope="col">Concentration [ng/&micro;l]</th>
    </tr>
    <tr>
@@ Line 49: / Line 49: @@
      <legend><a name="exp15.17">15.17 Ligation of purified pMAD and Constructs</a></legend>
      <div class="exp-content">
-     <p>The ligation is carried out with the purified pMAD digest  and the hag-flank-construct digest from  in order to transform the ligation mix into<em> E.Coli</em> DH5Alpha.
+     <p>The ligation is carried out with the purified pMAD digest and the hag-flank-construct digest from 15.16 in order to transform the ligation mix into<em> E.Coli</em> DH5&alpha;.
 For the ligation was the following calculator used: <a href="https://2011.igem.org/Team:UT_Dallas/ligation">UT Dallas</a></p>
 <table width="100%" border="1">
    <tr>
-     <th scope="col">Mix [µl]</th>
+     <th scope="col">Mix [&micro;l]</th>
      <th scope="col">Control 1</th>
      <th scope="col">Control 2</th>
@@ Line 141: / Line 141: @@
    </tr>
 </table>
-	<p>Incubation for 1,5h at room temperature.</p>
+	<p>Incubation for 1,5 h at room temperature.</p>
      </div>
 </fieldset>
 <fieldset class="exp15">
-     <legend><a name="exp15.18">15.18 Transformation of <em>E.coli</em> DH5Alpha</a></legend>
+     <legend><a name="exp15.18">15.18 Transformation of <em>E.coli</em> DH5&alpha;</a></legend>
      <div class="">
-     <p>Transformation of <em>E.coli</em> DH5Alpha with the ligation attempt.<br>
+     <p>Transformation of <em>E.coli</em> DH5&alpha; with the ligation attempt.<br>
-&micro;l of each the attempts was transformed into 50µL of competent<em> E. coli </em>DH5Alpha in order to test the success of the ligation and raising colonies for inoculating a mini prep. </p>
+&micro;l of each the attempts were used to transform 50 &micro;l of competent<em> E. coli </em>DH5&alpha; in order to test the success of the ligation and raising colonies for inoculating a mini prep. </p>
      </div>
 </fieldset>
@@ Line 171: / Line 171: @@
      </div>
      <div class="exp-content">
-     <p>The yeast was washed from the plate with 2 ml of A. dest. After centrifugation at 11000 rpm for 1 min the supernatant was discarded and 500 µl of Solution 1 of the Omega plasmid prep kit was added. The yeast was vortexed for 5 min after addition of a few glas balls. After that the miniprep was carried out according to the protocol (Omega). (c = 134.5 ng/µl)</p>
+     <p>The yeast was washed from the plate with 2 ml of A. dest. After centrifugation at 11000 rpm for 1 min the supernatant was discarded and 500 &micro;l of Solution 1 of the Omega plasmid prep kit was added. The yeast was vortexed for 5 min after addition of a few glas balls. After that the miniprep was carried out according to the protocol (Omega). (c = 134.5 ng/&micro;l)</p>
      </div>
 </fieldset>
 <fieldset class="exp13">
-     <legend><a name="exp13.37">13.377 Transformation of <em>E.coli</em> DH5Alpha with the prepped pMA12</a></legend>
+     <legend><a name="exp13.37">13.377 Transformation of <em>E.coli</em> DH5&alpha; with the isolated pMA12</a></legend>
      <div class="aim">
-     <p>Aim: Transform <em>E.coli</em> with the prepped plasmid to increase the amount of plasmid.</p>
+     <p>Aim: Transform <em>E.coli</em> with the isolated plasmid to increase the amount of plasmid.</p>
      </div>
      <div class="exp-content">
-     <p><em>E. coli</em> DH5Alpha cells were transformed with 10µl of the prepped plasmid pMa12. They were incubated at room temperature over the weekend.</p>
+     <p><em>E. coli</em> DH5Alpha cells were transformed with 10&micro;l of the isolated plasmid pMa12. They were incubated at room temperature over the weekend.</p>
      </div>
 </fieldset>
@@ Line 186: / Line 186: @@
      <legend><a name="exp15.20">15.20 Purification of Fragments</a></legend>
      <div class="exp-content">
-     <p>Purification of the fragments from the 01.05.14. The PCR-products were separated on a 1% agarose-gel.</p>
+     <p>Purification of the fragments from 01.05.14. The PCR-products were separated on a 1% agarose-gel.</p>
      </div>
      <div class="results">
@@ Line 199: / Line 199: @@
 <div class="notebooky-entry">
 <h2 class="title">
-	<a name="12.04.2014">12.04.2014</a>
+	<a name="05.05.2014">05.05.2014</a>
 </h2>
 <fieldset class="exp13">
@@ Line 207: / Line 207: @@
      </div>
      <div class="exp-content">
-     <p>15 colonies of the transformed <em>E.coli</em> DH5Alpha were picked and incubated in 6 ml LB-Amp at 37&deg;C overnight.</p>
+     <p>15 colonies of the transformed <em>E.coli</em> DH5&alpha; were picked and incubated in 6 ml LB-Amp at 37&deg;C overnight.</p>
      </div>
 </fieldset>
 <fieldset class="exp15">
-     <legend><a name="exp15.21">15.21 Ligation of the hag/flank and pET24d both cut with BamHI and NcoI followed by Transformation of <em>E. coli</em></a></legend>
+     <legend><a name="exp15.21">15.21 Ligation of the hag/flank and pET24d both cut with <i>Bam</i>HI and <i>Nco</i>I followed by Transformation of <em>E. coli</em></a></legend>
      <div class="exp-content">
      <p>The ligation with pMAD was not successful so it was decided to clone the hag/flank-construct first into pET24d. The ligation was done after using the ligation calculator: <a href="https://2011.igem.org/Team:UT_Dallas/ligation" target="_blank">UT Dallas</a></p>
@@ Line 258: / Line 258: @@
    </tr>
 </table>
-	<p>The ligation was incubated at RT for about 2h followed by a transformation of <em>E. coli</em> DH5Alpha. The transformed cells were plated out on LB-Kan and incubated at 37&deg;C over night.</p>
+	<p>The ligation was incubated at RT for about 2 hours followed by a transformation of <em>E. coli</em> DH5&alpha;. The transformed cells were plated out on LB-Kan and incubated at 37&deg;C over night.</p>
      </div>
 </fieldset>
@@ Line 270: / Line 270: @@
 </h2>
 <fieldset class="exp13">
-     <legend><a name="exp13.39">13.39 Miniprep of the 15 Cultures and Restriction with NcoI</a></legend>
+     <legend><a name="exp13.39">13.39 Miniprep of the 15 Cultures and Restriction with <i>Nco</i>I</a></legend>
      <div class="aim">
-     <p>Aim: isolate the plasmid from the picked clones and check for restriction sites of NcoI.</p>
+     <p>Aim: isolate the plasmid from the picked clones and check for restriction sites of <i>Nco</i>I.</p>
      </div>
      <div class="exp-content">
@@ Line 342: / Line 342: @@
    </tr>
 </table>
-	<p>The prepped plasmids were restricted with NcoI for 1h 20min and further analyzed on a 1% agarose gel.</p>
+	<p>The isolated plasmids were digested with <i>Nco</i>I for 1h 20 min and further analyzed on a 1% agarose gel.</p>
      </div>
      <div class="results">
      <h3>Results</h3>
      <img src="https://static.igem.org/mediawiki/2014/5/5e/MR_2014-05-06_NcoI.PNG" width="30%" />
-     <p><strong>Figure: restriction of the prepped pMa12 with NcoI; the lanes contain the restricted pMa12 in the order of the picked clones 1 – 15; clone 9 was negative; the lanes between the restrictions and the marker contain the prepped pMAD but it appears to be empty.</strong><br />
+     <p>Restriction of the isolated pMa12 with <i>Nco</i>I; the lanes contain the digested pMa12 in the order of the picked clones 1 - 15; clone 9 was negative; the lanes between the restrictions and the marker contain the isolated pMAD but it appears to be empty.<br />
-       The most clones contained a plasmid that has only one NcoI restriction site. The expected size of the pMa12 should be around 6.6 kb. All fragments are of the expected size.</p>
+       The most clones contained a plasmid that has only one <i>Nco</i>I restriction site. The expected size of the pMa12 should be around 6.6 kb. All fragments are of the expected size.</p>
      </div>
 </fieldset>
 <fieldset class="exp13">
-     <legend><a name="exp13.40">13.40 Restriction of pMa12 (prepped from Clone 10) with SacI and NcoI</a></legend>
+     <legend><a name="exp13.40">13.40 Restriction of pMa12 (isolated from Clone 10) with <i>Sac</i>I and <i>Nco</i>I</a></legend>
 	<div class="aim">
      <p>Aim: create fitting ends to anneal the promotor oligos.</p>
      </div>
      <div class="exp-content">
-     <p>The isolated pMa12 of clone 10 was used for a restriction with SacI-HF and NcoI. The restriction leads to fitting ends for the designed oligos which are the promoters we are about to test: PargJ and PykuO. The restriction is incubated at RT over night.</p>
+     <p>The isolated pMa12 of clone 10 was used for a restriction with <i>Sac</i>I-HF and <i>Nco</i>I. The restriction leads to fitting ends for the designed oligos which are the promoters we are about to test: PargJ and PykuO. The restriction is incubated at RT over night.</p>
      <table width="100%" border="1">
    <tr>
      <th scope="col">Restriction</th>
-     <th scope="col">Volume [µl]</th>
+     <th scope="col">Volume [&micro;l]</th>
    </tr>
    <tr>
@@ Line 368: / Line 368: @@
    </tr>
    <tr>
-     <th scope="row">NcoI</th>
+     <th scope="row"><i>Nco</i>I</th>
      <td>1</td>
    </tr>
    <tr>
-     <th scope="row">SacI-HF</th>
+     <th scope="row"><i>Sac</i>I-HF</th>
      <td>1</td>
    </tr>
@@ Line 391: / Line 391: @@
 </fieldset>
 <fieldset class="exp15">
-     <legend><a name="exp15.21">15.21 Inoculation of the DH5Alpha and Miniprep of pET24d_hag/flank</a></legend>
+     <legend><a name="exp15.21">15.21 Inoculation of the DH5&alpha; and Miniprep of pET24d_hag/flank</a></legend>
      <div class="aim">
      <p>Aim: amplifying and isolation of pET24d_hag/flank.</p>
@@ Line 408: / Line 408: @@
 </h2>
 <fieldset class="exp15">
-     <legend><a name="exp15.22">15.22 Restriction of 3 prepped plasmids (6.5.14) with NcoI and BamHI</a></legend>
+     <legend><a name="exp15.22">15.22 Restriction of 3 isolated plasmids (6.5.14) with <i>Nco</i>I and <i>Bam</i>HI</a></legend>
      <div class="aim">
-     <p>Aim: Test whether the prepped plasmid contains the 2 kb insert (hag-flank construct).</p>
+     <p>Aim: Test whether the isolated plasmid contains the 2 kb insert (hag-flank construct).</p>
      </div>
      <div class="exp-content">
      <table width="100%" border="1">
    <tr>
-     <th scope="col">[µl]</th>
+     <th scope="col">[&micro;l]</th>
      <th scope="col">Clone 1</th>
      <th scope="col">Clone 2</th>
@@ Line 439: / Line 439: @@
    </tr>
    <tr>
-     <th scope="row">NcoI</th>
+     <th scope="row"><i>Nco</i>I</th>
      <td>0,5</td>
      <td>0,5</td>
@@ Line 445: / Line 445: @@
    </tr>
    <tr>
-     <th scope="row">BamHI</th>
+     <th scope="row"><i>Bam</i>HI</th>
      <td>0,5</td>
      <td>0,5</td>
@@ Line 456: / Line 456: @@
      <div class="results">
      <img src="https://static.igem.org/mediawiki/2014/e/e0/MR_2014-05-07_NcoI_BamHI.png" width="30%" />
-     <p>Figure: Agarose gel with control (uncut) and 3 cut clones of pEt24d containing the hag-flank construct, fragments are of expected size.</p>
+     <p>Agarose gel with control (uncut) and 3 cut clones of pEt24d containing the hag-flank construct, fragments are of expected size.</p>
      </div>
 </fieldset>
 <fieldset class="exp13">
-     <legend><a name="exp13.41">13.41 Clean up of overnight digested plasmid pMa12 (3 inserts, only 1 NcoI resriction site) by gel-elution.</a></legend>
+     <legend><a name="exp13.41">13.41 Purification of overnight digested plasmid pMa12 (3 inserts, only 1 <i>Nco</i>I restriction site) by gel-elution.</a></legend>
      <div class="aim">
-     <p>Aim: purify plasmid to clone annealed oligos for the promotor sequences into the plasmid.</p>
+     <p>Aim: purify plasmid to clone annealed oligos for the promoter sequences into the plasmid.</p>
      </div>
      <div class="exp-content">
@@ Line 483: / Line 483: @@
      <th scope="row">Oligos</th>
      <td>iGEM012/iGEM013<br />
-µl/10µl</td>
+&micro;l/10&micro;l</td>
      <td>iGEM014/iGEM015<br />
-µl/10µl</td>
+&micro;l/10&micro;l</td>
    </tr>
    <tr>
@@ Line 502: / Line 502: @@
 </fieldset>
 <fieldset class="exp13">
-     <legend><a name="exp13.43">13.43 Ligation of the annealed oligos into restricted iGEM001</a></legend>
+     <legend><a name="exp13.43">13.43 Ligation of the annealed oligos into digested piGEM001</a></legend>
      <div class="aim">
-     <p>Aim: Create plasmid with the corresponding promotor sequences for Ag/Cu</p>
+     <p>Aim: Create plasmid with the corresponding promoter sequences for Ag/Cu</p>
      </div>
      <div class="exp-content">
      <table width="100%" border="1">
    <tr>
-     <th scope="col">[µl]</th>
+     <th scope="col">[&micro;l]</th>
      <th scope="col">Reaction (Ag)</th>
      <th scope="col">Reaction (Cu)</th>
    </tr>
    <tr>
-     <th scope="row">Plasmid (3ng/µl)</th>
+     <th scope="row">Plasmid (3ng/&micro;l)</th>
      <td>5,5</td>
      <td>5,5</td>
@@ Line 539: / Line 539: @@
    </tr>
 </table>
-	<p>10&micro;l of the ligation reaction will be transformed into chemically competent <em>E.coli</em> DH5Alpha als described before.</p>
+	<p>10&micro;l of the ligation reaction will be transformed into chemically competent <em>E.coli</em> DH5&alpha; as described before.</p>
      </div>
 </fieldset>
 <fieldset class="exp13">
-     <legend><a name="exp13.44">13.44 Over night restriction of pMA12 to get more of the cut plasmid (clone 10)</a></legend>
+     <legend><a name="exp13.44">13.44 Over night restriction of pMA12 to obtain more digested plasmid (clone 10)</a></legend>
      <div class="exp-content">
      <p>See 06.05.2014</p>
@@ Line 549: / Line 549: @@
    <tr>
      <th scope="col">Restriction</th>
-     <th scope="col">Volume [µl]</th>
+     <th scope="col">Volume [&micro;l]</th>
    </tr>
    <tr>
@@ Line 556: / Line 556: @@
    </tr>
    <tr>
-     <th scope="row">NcoI</th>
+     <th scope="row"><i>Nco</i>I</th>
      <td>1</td>
    </tr>
    <tr>
-     <th scope="row">SacI-HF</th>
+     <th scope="row"><i>Sac</i>I-HF</th>
      <td>1</td>
    </tr>
@@ Line 587: / Line 587: @@
 </h2>
 <fieldset class="exp13">
-     <legend><a name="exp13.43a">13.43 Repeat Transformation for AG/Cu Promotors</a></legend>
+     <legend><a name="exp13.43a">13.43 Repeat Transformation for AG/Cu Promoters</a></legend>
      <div class="exp-content">
      <p>No colonies on the plates, repeat ligation and transformation with new digested plasmid.<br />
@@ Line 665: / Line 665: @@
    </tr>
 </table>
-	<p> Incubation at 37°C for 30 min<br />
+	<p> Incubation at 37&deg;C for 30 min<br />
      Step 2:<br />
-     Heat up water in microwave until boiling, add the eppis bis primer mix<br />
+     Heat up water in microwave until boiling, add the tubes with primer mix<br />
-     let it cool down to roomtempertur (over lunch)<br />
+     let it cool down to room temperature<br />
      Step 3:<br />
 :100 dilution<br />
@@ Line 699: / Line 699: @@
    </tr>
 </table>
-	<p>Step 5: Tranformation<br />
+	<p>Step 5: Transformation<br />
-	Incubation at room temperature over the weekend.<br />
+	Incubation at room temperature over two days.<br />
      Step 6: Results<br />
-     Hag Flank construct digestion with speI was positive.</p>
+     Hag Flank construct digestion with <i>Spe</i>I was positive.</p>
      </div>
 </fieldset>
@@ Line 714: / Line 714: @@
 </h2>
 <fieldset class="exp13">
-     <legend><a name="exp13.43c">13.43 Repeat Transformation for AG/Cu Promotors</a></legend>
+     <legend><a name="exp13.43c">13.43 Repeated Transformation for AG/Cu Promoters</a></legend>
      <p>No colonies</p>
 </fieldset>
@@ Line 720: / Line 720: @@
      <legend><a name="exp15.23">15.23 PCR for amplification of flagellin-constructs out of pet24-fla-Construct from 05.05.14</a></legend>
 	<div class="aim">
-     <p>Aim: Amplification of the flagellin-constructs from the pet24-fla-plasmid as a template is done in order to make a restriction digest with spe1. This will show which clone contains the successfully synthetized construct with spe1 restriction site because of the Strep-Tag from sequencing.</p>
+     <p>Aim: Amplification of the flagellin-constructs from the pET24-fla-plasmid as a template was done in order to make a restriction digest with <i>Spe</i>I. This showed, which clone contained the successfully synthesized construct with <i>Spe</i>I restriction site because of the Strep-Tag from sequencing.</p>
      </div>
      <div class="exp-content">
@@ Line 731: / Line 731: @@
    </tr>
    <tr>
-     <th scope="row">Temp.  – pet24fla cone 1 (lig1 05.05.14)</th>
+     <th scope="row">Temp. - pet24fla cone 1 (lig1 05.05.14)</th>
      <td>0,5</td>
      <td>-</td>
@@ Line 737: / Line 737: @@
    </tr>
    <tr>
-     <th scope="row">Temp.  – pet24fla cone 2 (lig2 05.05.14)</th>
+     <th scope="row">Temp. - pet24fla cone 2 (lig2 05.05.14)</th>
      <td>-</td>
      <td>0,5</td>
@@ Line 743: / Line 743: @@
    </tr>
    <tr>
-     <th scope="row">Temp.  – pet24fla cone 3 (lig3 05.05.14)</th>
+     <th scope="row">Temp. - pet24fla cone 3 (lig3 05.05.14)</th>
      <td>-</td>
      <td>-</td>
@@ Line 767: / Line 767: @@
    </tr>
    <tr>
-     <th scope="row">Phusion-Polymase</th>
+     <th scope="row">Phusion-Polymerase</th>
      <td>0,5</td>
      <td>0,5</td>
@@ Line 829: / Line 829: @@
 </table>
 <br />
-     <table width="100%" border="1">
+	<img src="https://static.igem.org/mediawiki/2014/0/04/MR_20140510_PCRpET24fla.jpg" width="20%" />
-  <tr>
+	<br />
-    <th width="17%" scope="col">Step</th>
+     <p>Result: PCR not successful - no band at 2,2kb</p>
-    <th width="58%" scope="col">Temperature &deg;C</th>
-    <th width="25%" scope="col">Time</th>
-  </tr>
-  <tr>
-    <th scope="row">1</th>
-    <td>95</td>
-    <td>3 min</td>
-  </tr>
-  <tr>
-    <th scope="row">2</th>
-    <td>95</td>
-    <td>30 sec</td>
-  </tr>
-  <tr>
-    <th scope="row">3</th>
-    <td>55</td>
-    <td>30 sec</td>
-  </tr>
-  <tr>
-    <th scope="row">4</th>
-    <td>72</td>
-    <td>2,5 min</td>
-  </tr>
-  <tr>
-    <th scope="row">5</th>
-    <td>Go To 2</td>
-    <td>35x</td>
-  </tr>
-  <tr>
-    <th scope="row">6</th>
-    <td>72</td>
-    <td>5min</td>
-  </tr>
-  <tr>
-    <th scope="row">7</th>
-    <td>4</td>
-    <td>Infinite</td>
-  </tr>
-</table>
-     <p>Result: PCR not successfull – no band at 2,2kb</p>
      </div>
 </fieldset>
 <fieldset class="exp15">
-     <legend><a name="exp15.24">15.24 Transformation of <em>E.coli</em> DH5Alpha with pet24-fla-Construct from 05.05.14</a></legend>
+     <legend><a name="exp15.24">15.24 Transformation of <em>E.coli</em> DH5&alpha; with pET24-fla-Construct from 05.05.14</a></legend>
 	<div class="aim">
      <p>Aim: Amplification plasmid for further experiments.</p>
@@ Line 881: / Line 841: @@
      <div class="exp-content">
      <ul class="list">
-     <li>3 aliquots competent E.Coli DH5Alpha were transformed with 1&micro;ll of the purified plasmid  pet24-fla construct from 05.05.14 from 3 different clones (lig 1-3) each</li>
+     <li>3 aliquots competent E.Coli DH5&alpha; were transformed with 1&micro;ll of the purified plasmid  pet24-fla construct from 05.05.14 from 3 different clones (lig 1-3) each</li>
      <li>After regeneration the cells were plated on LB-canamycin plates and incubated at room temperature until Monday</li>
      </ul>
@@ Line 887: / Line 847: @@
 </fieldset>
 <fieldset class="exp15">
-     <legend><a name="exp15.25a">15.25 New PCR for ampl. of flagellin-constructs out of pet24-fla-Construct from 05.05.14</a></legend>
+     <legend><a name="exp15.25a">15.25 New PCR for amplification of flagellin-constructs out of pET24-fla-Construct from 05.05.14</a></legend>
 	<div class="exp-content">
      <p>Aim: Amplification of the fragment for further experiments with pet24-fla from 15.21 as template. The prior PCR was not successful.</p>
@@ Line 1,012: / Line 972: @@
      <h3>Results:</h3>
      <img src="https://static.igem.org/mediawiki/2014/7/7a/MR_2014-05-11_pet24-fla.jpg" width="30%" />
-     <p><strong>Figure: PCR result from the amplification of the fla-construct out of the pet24d. The gel shows that the 3 clones contain a construct in the pet24d vector. The fragment is about 2,2kb.</strong></p>
+     <p>PCR result from the amplification of the fla-construct out of the pET24d. The gel shows that the three clones contain a construct in the pet24d vector. The fragment is about 2,2kb.</p>
      </div>
 </fieldset>
@@ Line 1,043: / Line 1,003: @@
 </fieldset>
 <fieldset class="exp15">
-     <legend><a name="exp15.27">15.27 Restriction Digest of PCR Products from with Spe1</a></legend>
+     <legend><a name="exp15.27">15.27 Restriction Digest of PCR Products from with <i>Spe</i>I</a></legend>
      <div class="aim">
-     <p>Aim: The digest with spe1 will show which clone contains the fla-construct with replaced STRAP-Tag by a spe1 restriction site</p>
+     <p>Aim: The digest with <i>Spe</i>1 will show, which clone contains the fla-construct with replaced StrepTag by a <i>Spe</i>I restriction site</p>
      </div>
      <div class="exp-content">
@@ Line 1,051: / Line 1,011: @@
    <tr>
      <th scope="col">[&micro;l]</th>
-     <th scope="col">Mastermix with NcoI - for 4 attempts</th>
+     <th scope="col">Mastermix with <i>Nco</i>I - for 4 attempts</th>
-     <th scope="col">Attempt 1-3 Spe1 (20kU/ml)</th>
+     <th scope="col">Attempt 1-3 <i>Spe</i>I (20kU/ml)</th>
    </tr>
    <tr>
@@ Line 1,095: / Line 1,055: @@
      <h3>Results:</h3>
      <img src="https://static.igem.org/mediawiki/2014/7/7f/MR_2014_05_11_Spe1.jpg" width="30%">
-     <p><strong>Figure: The spe1 digest of the pcr amplified construct shows 3 bands. The 2,2kb band is the uncut construct whereby the smaller bands are the two fragments as a result of the spe1 cut. The constructs in the pet24d still contain the right spe1 restriction site.</strong></p>
+     <p>The digestion of the PCR amplified construct shows 3 bands. The 2,2kb band is the uncut construct whereby the smaller bands are the two fragments as a result of the <i>Spe</i>I cut. The constructs in the pET24d still contain the right <i>Spe</i>I restriction site.</p>
      </div>
 </fieldset>
 <fieldset class="exp15">
-     <legend><a name="exp15.28">15.28 Transformation of <em>E.coli</em> DH5Alpha with pet24-fla-Construct from 05.05.14</a></legend>
+     <legend><a name="exp15.28">15.28 Transformation of <em>E.coli</em> DH5&alpha; with pET24-fla-Construct from 05.05.14</a></legend>
 	<div class="exp-content">
      <p>Colonies were grown on every plate &rarr; successful transformation</p>
@@ Line 1,105: / Line 1,065: @@
 </fieldset>
 <fieldset class="exp15">
-     <legend><a name="exp15.29">15.29 Inoculation for Miniprep of Transformed <em>E.Coli</em> DH5Alpha with pet24-fla-Construct from 10.05.14</a></legend>
+     <legend><a name="exp15.29">15.29 Inoculation for Miniprep of Transformed <em>E.Coli</em> DH5&alpha; with pet24-fla-Construct from 10.05.14</a></legend>
      <div class="aim">
-     <p>Aim: Amplication of transformed plasmid for miniprep in order to receive more plasmid for further experiments</p>
+     <p>Aim: Amplification of transformed plasmid for miniprep in order to receive more plasmid for further experiments</p>
      </div>
      <div class="exp-content">
-     <p>3x6ml LB + 6&micro;l canamycin each were inoculated with 1 colony of plate 1-3 from 10.05.14. The plates were incubated overnight at 37&deg;C</p>
+     <p>3x6ml LB + 6&micro;l canamycin each were inoculated with 1 colony of plate 1-3 from 10.05.14. The plates were incubated over night at 37&deg;C</p>
      </div>
 </fieldset>
@@ Line 1,122: / Line 1,082: @@
 </h2>
 <fieldset class="exp15">
-     <legend><a name="exp15.30">15.30 Miniprep of Transformed <em>E.coli</em> DH5Alpha  with pET24-fla-Construct from 11.05.14</a></legend>
+     <legend><a name="exp15.30">15.30 Miniprep of Transformed <em>E.coli</em> DH5&alpha;  with pET24-fla-Construct from 11.05.14</a></legend>
 	<div classs="aim">
-     <p>Aim: Prep of transformed plasmid in order to receive more plasmid    for further experiments</p>
+     <p>Aim: Isolation of plasmid in order to obtain more plasmid for further experiments</p>
      </div>
 </fieldset>
@@ Line 1,130: / Line 1,090: @@
      <legend><a name="exp15.31">15.31 PCR of Construct with pET24d as Template from Miniprep 11.05.14</a></legend>
      <div class="aim">
-     <p>Aim: Amplification of clone 2 for further experiments</p>
+     <p>Aim: Amplification of the plasmid from clone 2 for further experiments</p>
      </div>
      <div class="exp-content">
@@ Line 1,139: / Line 1,099: @@
    </tr>
    <tr>
-     <th scope="row">Temp.  – pet24fla clone 2 (lig2 11.05.14)</th>
+     <th scope="row">Temp. - pet24fla clone 2 (lig2 11.05.14)</th>
      <td>0,5</td>
    </tr>
@@ Line 1,210: / Line 1,170: @@
 </fieldset>
 <fieldset class="exp15">
-     <legend><a name="exp15.32">15.32 Restriction of the PCR-Fragment with BamHI and NcoI</a></legend>
+     <legend><a name="exp15.32">15.32 Restriction of the PCR-Fragment with <i>Bam</i>HI and <i>Nco</i>I</a></legend>
      <div class="aim">
      <p>Aim: Creating corresponding ends for ligation into pMAD</p>
@@ Line 1,225: / Line 1,185: @@
    </tr>
    <tr>
-     <th scope="row">NcoI-HF</th>
+     <th scope="row"><i>Nco</i>I-HF</th>
      <td>1</td>
    </tr>
    <tr>
-     <th scope="row">BamHI-HF</th>
+     <th scope="row"><i>Bam</i>HI-HF</th>
      <td>1</td>
    </tr>
@@ Line 1,251: / Line 1,211: @@
      <legend><a name="exp13.44">13.44 Phosphorylation and Annealing of Promoter-Oligos</a></legend>
      <div class="aim">
-     <p>Aim: phosphorylation of singlestand oligos with subsequent annealing for cloning into pMa12</p>
+     <p>Aim: phosphorylation of single stranded oligos with subsequent annealing for cloning into pMa12</p>
      </div>
      <div class="exp-content">
-     <p>For ligation to occur at least one of the DNA ends (insert or vector) should contain a 5´ phosphate. Primers are usually supplied non-phosphorylated; therefore, the oligos or PCR product will not contain a 5´ phosphate. The digestion of DNA with a restriction enzyme will always produce a 5´ phosphate. A DNA fragment can be phosphorylated by incubation with T4 Polynucleotide Kinase in T4-ligase-buffer which already contains the necessary ATP in an appropriate amount (1 mM):</p>
+     <p>For ligation to occur at least one of the DNA ends (insert or vector) should contain a 5' phosphate. Primers are usually supplied non-phosphorylated; therefore, the oligos or PCR product will not contain a 5' phosphate. The digestion of DNA with a restriction enzyme will always produce a 5´ phosphate. A DNA fragment can be phosphorylated by incubation with T4 Polynucleotide Kinase in T4-ligase-buffer which already contains the necessary ATP in an appropriate amount (1 mM):</p>
      <table width="100%" border="1">
    <tr>
@@ Line 1,306: / Line 1,266: @@
 </fieldset>
 </div>
+<!-- ROMAN -->
+<fieldset class="exp14">
+ <legend><a name="exp14.24">14.24 Transformation of BL21 cells</a></legend>
+    <div class="aim">
+    <p>Aim: Transform E. coli BL21(DE3) with PheA-Arc1p-C-2x-pET28a</p>
+    </div>
+    <div class="exp-content">
+    <p>40 &micro;L E. coli BL21(DE3) electrocompetent cells were transformed with 1 ng of the previously purified plasmid PheA-Arc1p-C-2x-pET28a from two different clones, incubated for 1 h at 37 &deg;C and plated out on LB-Kan<sup>50</sup> plates that were incubated overnight at 37 &deg;C.</p>
+    </div>
+</fieldset>
+<!-- ROMAN -->
 <!-- 13.05.14 -->
@@ Line 1,313: / Line 1,289: @@
 	<a name="13.05.2014">13.05.2014</a>
 </h2>
+<!-- ROMAN -->
+<fieldset class="exp14">
+ <legend><a name="exp14.25">14.25 Overnight culture</a></legend>
+    <div class="aim">
+    <p>Aim: Inoculate Overnight culture of PheA-Arc1p-C-2x-pET28a</p>
+    </div>
+    <div class="exp-content">
+    <p>5 mL of LB-Kan<sup>50</sup> medium were inoculated with a clone from 14.24 bearing the PheA-Arc1p-C-2x-pET28a plasmid.</p>
+    </div>
+</fieldset>
+<!-- ROMAN -->
 <fieldset class="exp15">
-     <legend><a name="exp15.33">15.33 Miniprep and Restriction of pMAD with BamHI and NnoI</a></legend>
+     <legend><a name="exp15.33">15.33 Miniprep and Restriction of pMAD with <i>Bam</i>HI and <i>Nco</i>I</a></legend>
      <div class="aim">
      <p>Aim: isolate pMAD and create linearized vector with corresponding ends for ligation with the construct</p>
      </div>
      <div class="exp-content">
-     <p>The plasmid pMAD was isolated and restricted with the restriction enzymes BamHI and NcoI to create fitting ends for the ligation with the restricted PCR-fragment.</p>
+     <p>The plasmid pMAD was isolated and digested with the restriction enzymes <i>Bam</i>HI and <i>Nco</i>I to create fitting ends for the ligation with the digested PCR-fragment.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 1,330: / Line 1,321: @@
    </tr>
    <tr>
-     <th scope="row">NcoI-HF</th>
+     <th scope="row"><i>Nco</i>I-HF</th>
      <td>1</td>
    </tr>
    <tr>
-     <th scope="row">BamHI-HF</th>
+     <th scope="row"><i>Bam</i>HI-HF</th>
      <td>1</td>
    </tr>
@@ Line 1,354: / Line 1,345: @@
 </fieldset>
 <fieldset class="exp15">
-     <legend><a name="exp15.34">15.34 Ligation of Restricted pMAD with the Restricted hag/flank-Construct and Trafo</a></legend>
+     <legend><a name="exp15.34">15.34 Ligation of digested pMAD with the digested hag/flank-Construct and trafo</a></legend>
      <div class="aim">
-     <p>Aim: link the fragment with the vector and trafo of DH5Alpha</p>
+     <p>Aim: link the fragment with the vector and trafo of DH5&alpha;</p>
      </div>
      <div class="exp-content">
-     <p>The ligation of pMAD and the restricted PCR-fragment was done according to the previous mentioned ligation calculator.</p>
+     <p>The ligation of pMAD and the digested PCR-fragment was done according to the previous mentioned ligation calculator.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 1,390: / Line 1,381: @@
    </tr>
 </table>
-	<p>The ligation was incubated at RT for 1.5 h. After that <em>E. coli</em> DH5Alpha were transformed with the ligation mix and plated out onto LB-Amp plates which were incubated at 37&deg;C overnight.</p>
+	<p>The ligation was incubated at RT for 1.5 h. After that <em>E. coli</em> DH5&alpha; were transformed with the ligation mix and plated out onto LB-Amp plates which were incubated at 37&deg;C overnight.</p>
      </div>
 </fieldset>
 <fieldset class="exp13">
-     <legend><a name="exp13.45">13.45 Ligation of Annealed Oligos with Restricted pMa12-Construct and Trafo of <em>E. coli</em> DH5Alpha</a></legend>
+     <legend><a name="exp13.45">13.45 Ligation of Annealed Oligos with digested pMa12-Construct and Trafo of <em>E. coli</em> DH5Alpha</a></legend>
      <div class="aim">
      <p>Aim: clone the promoter sequences in front of the gfp</p>
      </div>
      <div class="exp-content">
-     <p>A ligation of the SacI and NcoI restricted pMa12-construct with the annealed oligos was carried out. The annealed oligos (iGEM-012/013 c = 762.3 ng/&micro;l and iGEM-014/015 c = 825.5 ng/&micro;l) were diluted up to 10-2. 10ng of the insert and 100ng of the vector were used for the ligation.</p>
+     <p>A ligation of the <i>Sac</i>I and <i>Nco</i>I digested pMa12-construct with the annealed oligos was carried out. The annealed oligos (iGEM-012/013 c = 762.3 ng/&micro;l and iGEM-014/015 c = 825.5 ng/&micro;l) were diluted up to 10-2. 10 ng of the insert and 100 ng of the vector were used for the ligation.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 1,448: / Line 1,439: @@
 	<a name="14.05.2014">14.05.2014</a>
 </h2>
+<!-- ROMAN -->
+<fieldset class="exp14">
+ <legend><a name="exp14.26">14.26 Test Expression</a></legend>
+    <div class="aim">
+    <p>Aim: Test the expression of PheA-Arc1p-C-2x</p>
+    </div>
+    <div class="exp-content">
+    <p>Using the preculture from 14.25 60 mL of LB-Kan<sup>50</sup> medium were inoculated with 600 &micro;L of the preculture and incubated at 37 &deg;C and 220 rpm until OD<sub>600</sub> reached 0.5. The culture was cooled down to 18 &deg;C and the protein production was induced with 12 &micro;L of 500 mM IPTG. Over night the culture was incubated at 18 &deg;C and 220 rpm. A glycerolstock of the strain containing the PheA-Arc1p-C-2x-pET28a plasmid was stored at -80 &deg;C.</p>
+    </div>
+</fieldset>
+<!-- ROMAN -->
 <fieldset class="exp15">
-     <legend><a name="exp15.35">15.35 Inoculation Miniprep and Restriction of pMAD with BamHI and NcoI</a></legend>
+     <legend><a name="exp15.35">15.35 Inoculation Miniprep and Restriction of pMAD with <i>Bam</i>HI and <i>Nco</i>I</a></legend>
      <div class="aim">
      <p>Aim: the ligation from 15.34 was not successful. Inoculation of pMAD for miniprep in order to have more plasmid for further experiments.<br />
@@ Line 1,455: / Line 1,463: @@
      </div>
      <div class="exp-content">
-     <p>The plasmid pMAD from 13.05.14 (ca. 25&micro;l) and restricted with the restriction enzymes BamHI and NcoI to create fitting ends for the ligation with the restricted PCR-fragment. The digest was performed in 2 Eppis with 12,5&micro;l plasmid each.</p>
+     <p>The plasmid pMAD from 13.05.14 (ca. 25&micro;l) and digested with the restriction enzymes <i>Bam</i>HI and <i>Nco</i>I to create fitting ends for the ligation with the digested PCR-fragment. The digest was performed in 2 Eppis with 12,5&micro;l plasmid each.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 1,502: / Line 1,510: @@
 </fieldset>
 <fieldset class="exp15">
-     <legend><a name="exp15.36">15.36 Transformation of pet24d-clone2 into <em>E.Coli</em> DH5Alpha</a></legend>
+     <legend><a name="exp15.36">15.36 Transformation of pET24d-clone2 into <em>E.Coli</em> DH5&alpha;</a></legend>
      <div class="aim">
      <p>Aim: raising colonies for further minipreps of successful construct containing clone</p>
      </div>
      <div class="exp-content">
-     <p>The plasmid pet24d with the fla construct from clone 2 was transformed into <em>E.Coli</em> DH5Alpha and plated on LB-Canamycin. Incubation overnight at 37&deg;C.</p>
+     <p>The plasmid pET24d with the fla construct from clone 2 was transformed into <em>E.Coli</em> DH5&alpha; and plated on LB-canamycin. Incubation overnight at 37&deg;C.</p>
      </div>
 </fieldset>
 <fieldset class="exp15">
-     <legend><a name="exp15.37a">13.37 Inoculation for Miniprep of <em>E.Coli</em> DH5Alpha with pet24d-fla Construct Clone2</a></legend>
+     <legend><a name="exp15.37a">13.37 Inoculation for Miniprep of <em>E.Coli</em> DH5&alpha; with pET24d-fla Construct Clone2</a></legend>
      <div class="aim">
      <p>Aim: raising colonies for further minipreps of successful construct containing clone2</p>
      </div>
      <div class="exp-content">
-     <p>One clone with plasmid pet24d with the fla construct was used for inoculation of LB-medium. Incubation overnight at 37&deg;C</p>
+     <p>One clone with plasmid pET24d with the fla construct was used for inoculation of LB-medium. Incubation overnight at 37&deg;C</p>
      </div>
 </fieldset>
 <fieldset class="exp13">
-     <legend><a name="exp13.46">13.46 Transformation of Nose-Plasmid from Clone 10 into <em>E.Coli</em> DH5Alpha</a></legend>
+     <legend><a name="exp13.46">13.46 Transformation of Nose-Plasmid from Clone 10 into <em>E.Coli</em> DH5&alpha;</a></legend>
 	<div class="aim">
      <p>Aim: raising colonies for miniprep of new Nose-plasmid for further experiments</p>
      </div>
      <div class="exp-content">
-     <p>The plasmid pMA12+Nose-Construct from clone 10 was transformed into <em>E.Coli</em> DH5Alpha and plated on LB-AMP. Incubation overnight at 37&deg;C</p>
+     <p>The plasmid pMA12+Nose-Construct from clone 10 was transformed into <em>E.Coli</em> DH5&alpha; and plated on LB-AMP. Incubation overnight at 37&deg;C</p>
      </div>
 </fieldset>
 <fieldset class="exp15">
-     <legend><a name="exp15.37b">13.37 Ligation of Restricted pMAD from 14.05.14 with the Restricted hag/flank-Construct</a></legend>
+     <legend><a name="exp15.37b">13.37 Ligation of digested pMAD from 14.05.14 with the digested hag/flank-construct</a></legend>
 	<div class="aim">
      <p>Aim: link the fragment with the vector</p>
      </div>
      <div class="exp-content">
-     <p>The ligation of pMAD and the restricted PCR-fragment was done according to the previous ligation calculator.</p>
+     <p>The ligation of pMAD and the digested PCR-fragment was done according to the previous ligation calculator.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 1,569: / Line 1,577: @@
 </fieldset>
 <fieldset class="exp13">
-     <legend><a name="exp13.47">13.47 Restriction and Clean-up of piGEM002 (Nose) and Following Ligation and Tranformation</a></legend>
+     <legend><a name="exp13.47">13.47 Restriction and purification of piGEM002 (Nose) and following ligation and transformation</a></legend>
      <div class"aim">
-     <p>Aim: create more plasmid for further experiments, 2 digests were performed to get a high amount of plasmid (in the end pooled in the clean up)<br />
+     <p>Aim: create more plasmid for further experiments, 2 digests were performed to get a high amount of plasmid (pooled during purification)<br />
 concentration= 44 ng/&micro;l</p>
 	<table width="100%" border="1">
@@ Line 1,583: / Line 1,591: @@
    </tr>
    <tr>
-     <th scope="row">NcoI</th>
+     <th scope="row"><i>Nco</i>I</th>
      <td>1</td>
    </tr>
    <tr>
-     <th scope="row">SacI-HF</th>
+     <th scope="row"><i>Sac</i>I-HF</th>
      <td>1</td>
    </tr>
@@ Line 1,603: / Line 1,611: @@
    </tr>
 </table>
-	<p>One ligation was performed for 1h and transformed into chemocompetent cells from Daniel, the second ligation was performed over night in case no colonies grow on the trafo plates.</p>
+	<p>One ligation was performed for 1h and transformed into chemocompetent cells, the second ligation was performed over night in case no colonies grow on the trafo plates.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 1,631: / Line 1,639: @@
 </table>
      </div>
-     <p>Transformation with daniels cells:<br />
+     <p>Transformation:<br />
      thaw on ice: 5 min<br />
      add DNA, keep on ice: 5 min<br />
@@ Line 1,639: / Line 1,647: @@
 </fieldset>
 <fieldset class="exp17">
-     <legend><a name="exp17.1">17.1 Innoculate Bacillus Strains</a></legend>
+     <legend><a name="exp17.1">17.1 Inoculate Bacillus Strains</a></legend>
      <div class="aim">
      <p>Aim: have bacillus strains to work with in MTA and make competent cells</p>
      </div>
      <div class="exp-content">
-     <p>Wildtype on LB plate and in LB liquid without an antibiotic.<br />Bacillus strain 186 on plates containing xylose (Incubation overnight).</p>
+     <p>Wildtype on LB plate and in LB liquid without an antibiotic.<br /><i>Bacillus subtilis</i> strain 186 on plates containing xylose (Incubation overnight).</p>
      </div>
 </fieldset>
@@ Line 1,658: / Line 1,666: @@
      <legend><a name="exp17.2">17.2 Make Competent Cells</a></legend>
      <div class="aim">
-     <p>Aim: make competent cells bacillus cells for transforming into bacillus</p>
+     <p>Aim: making <i>Bacillus subtilis</i> cells competent for transformation</p>
      </div>
      <div class="exp-content">
-     <p>Innoculate Bacillus wildtype strain in SPC medium.</p>
+     <p>Inoculate Bacillus wildtype strain in SPC medium.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 1,695: / Line 1,703: @@
      </div>
 </fieldset>
+<!-- ROMAN -->
+<fieldset class="exp14">
+ <legend><a name="exp14.27">14.27 Purification of test expression</a></legend>
+    <div class="aim">
+    <p>Aim: Purify PheA-Arc1p-C-2x on a small scale</p>
+    </div>
+    <div class="exp-content">
+    <p>The cell culture from 14.26 was centrifuged (17000 rpm, 20 min, 4 &deg;C) and the pellet resuspended in 3 mL buffer A. Lysozyme was added 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 &deg;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.</p>
+    <p>60 mL LB-Kan<sup>50</sup> medium was inoculated from the glycerolstock prepared in 14.26 and incubated at 37 &deg;C and 220 rpm over night.</p>
+    </div>
+</fieldset>
+<!-- ROMAN -->
 <fieldset class="exp15">
-     <legend><a name="exp15.38">15.38 Transformation of Ligated pMAD and the Restricted hag/flank-Construct</a></legend>
+     <legend><a name="exp15.38">15.38 Transformation of ligated pMAD and the digested hag/flank-Construct</a></legend>
      <div class="aim">
      <p>Aim: produce cells that contain the ligated plasmid</p>
@@ Line 1,705: / Line 1,731: @@
 </fieldset>
 <fieldset class="exp15">
-     <legend><a name="exp15.39">15.39 PCR for Amplification of Hag-Flank-Construct in pet24d and Following Restriction</a></legend>
+     <legend><a name="exp15.39">15.39 PCR for amplification of Hag-Flank-construct in pET24d and following restriction</a></legend>
 	<div class="aim">
-     <p>After plasmid prep pcr was run to amplify the hag-Flank-construct, afterwards it will be digested with SpeI to find a clone with pure pruduct (no tag but only SpeI restriction site).</p>
+     <p>After plasmid isolation a PCR was run to amplify the hag-Flank-construct, afterwards it will be digested with <i>Spe</i>I to find a clone with pure product (no tag but only <i>Spe</i>I restriction site).</p>
      </div>
      <div class="exp-content">
@@ Line 1,739: / Line 1,765: @@
      <div class="results">
      <img src="https://static.igem.org/mediawiki/2014/5/53/MR_2014-05-15_Hag-Flank-Construct.png" width="30%" />
-     <p><strong>Figure: gel foto after amplification of hag flank insert from 10 clones: all positive.<br />
+     <p>Gel foto after amplification of hag flank insert from 10 clones: all positive.<br />
 Whole insert has been digested for 1h with SpeI in a 20&micro;l reaction mix<br />
-.5&micro;l insert, 2&micro;l buffer and 1&micro;l ligase</strong></p>
+.5&micro;l insert, 2&micro;l buffer and 1&micro;l ligase</p>
 	<img src="https://static.igem.org/mediawiki/2014/a/a8/MR_2014-05-15_Hag-Flank-Construct2.png" width="30%"  />
-     <p><strong>Figure: gel foto after restriction of the 2.2 kb fragment with spe I (expected sizes appear on the gel) no undigested bands= only fragments with the restriction site are in</strong></p>
+     <p>Gel foto after restriction of the 2.2 kb fragment with <i>Spe</i>I (expected sizes appear on the gel) no undigested bands= only fragments with the restriction site are in</p>
      </div>
 </fieldset>
 <fieldset class="exp13">
-     <legend><a name="exp13.48">13.48 Colony PCR after Transformation</a></legend>
+     <legend><a name="exp13.48">13.48 Colony PCR after transformation</a></legend>
      <div class="aim">
      <p>Aim: find out which colonies contain the right plasmid</p>
      </div>
      <div class="exp-content">
-     <p>Dip in a colony on the trafo plate, streak it on a new plate and dip in the PCR Premix</p>
+     <p>Pick a colony from the trafo plate, streak it on a new plate and dip in the PCR Premix</p>
      <table width="100%" border="1">
    <tr>
@@ Line 1,788: / Line 1,814: @@
 </fieldset>
 <fieldset class="exp17">
-     <legend><a name="exp17.3">17.3 First Plate Reader Measurement with Bacillus Wildtype and Strain 186 (gfp)</a></legend>
+     <legend><a name="exp17.3">17.3 First Plate Reader Measurement with <i>Bacillus subtilis</i> wildtype and strain 186 containing a <i>gfp</i></a></legend>
      <div class="aim">
      <p>Aim: Test for differences between the two strains and first check if experiment works at all</p>
      </div>
+	<br />
+	<img src="https://static.igem.org/mediawiki/2014/3/3b/MR_20140520_MTA_growth_Bsubtilis_wt_gfp_MM_LB.jpg" width="40%" />
+	<br />
+	<img src="https://static.igem.org/mediawiki/2014/0/09/MR_20140520_MTA_fluorescence_bsubtilis_wt_gfp_MM_xyl_LB.jpg" width="40%" />
+	<br />
+	<p>Both strains grew best in LB medium like expected, a clearly better growth was shown by the wildtype in the minimal medium compared to the <i>gfp</i> bearing strain.</p>
+	<p>The fluorescence is shown in dependence of the culture growth in order to relativise the fluorescence signal. Like expected, the wt exhibited no fluorescence in both media. The fluorescence of the <i>gfp</i> strain was higher in the minimal medium with xylose, than without xylose.</p>
 </fieldset>
 </div>
@@ Line 1,802: / Line 1,835: @@
 </h2>
 <fieldset class="exp15">
-    <legend><a name="exp15.38b">15.38 Transformation of Ligated pMAD and the Restricted hag/flank-Construct</a></legend>
+     <legend><a name="exp15.40">15.40 Colony PCR with colonies from 16.05.14</a></legend>
-    <div class="results">
-    <p>Successful</p>
-    </div>
-</fieldset>
-<fieldset class="exp15">
-     <legend><a name="exp15.40">15.40 Colony PCR with Colonies from 16.05.14</a></legend>
      <div class="aim">
      <p>Aim: test the success of ligation from pMAD & Hag-Flank-Construct</p>
      </div>
      <div class="exp-content">
-     <p>A PCR ran with 5 picked clones from 16.05.14 and Primers Flo89 and 90 for amplification of inserted construct</p>
+     <p>A PCR ran with 5 picked clones from 16.05.14 and primers Flo89 and 90 for amplification of inserted construct</p>
      <table width="100%" border="1">
    <tr>
@@ Line 1,844: / Line 1,871: @@
      <h3>Results</h3>
      <img src="https://static.igem.org/mediawiki/2014/3/35/MR_2014-05-16_colony_PCR.png" width="30%" />
-     <p><strong>Figure: Test if insert in pMad has the right size of about 2000 bp &rarr; not precise repeat on Monday</strong></p>
+     <p>Test if insert in pMad has the right size of about 2000 bp &rarr; not precise repeat on Monday</p>
      </div>
 </fieldset>
 <fieldset class="exp15">
-     <legend><a name="exp15.41">15.41 Innoculation of Colonies pMad plus hag-flank-Insert</a></legend>
+     <legend><a name="exp15.41">15.41 Inoculation of colonies <i>E. coli</i> pMad plus hag-flank-Insert</a></legend>
      <div class="aim">
-     <p>Aim: grow cells that contain the mentioned plasmid and subsequently prep that plasmid for further work</p>
+     <p>Aim: grow cells that contain the mentioned plasmid and subsequently isolation of the plasmid for further work</p>
      </div>
      <div class="exp-content">
-     <p>Innoculate 5 clones in LB liquid and incubation over the weekend at room temperature</p>
+     <p>Inoculate 5 clones in LB liquid and incubation over the weekend at room temperature</p>
      </div>
 </fieldset>
+<!-- ROMAN -->
+<fieldset class="exp14">
+ <legend><a name="exp14.28">14.28 Expression of PheA-Arc1p-C-2x</a></legend>
+    <div class="aim">
+    <p>Aim: Express PheA-Arc1p-C-2x for further use</p>
+    </div>
+    <div class="exp-content">
+    <p>10 x 500 mL LB-Kan<sup>50</sup> medium were inoculated with 5 mL of the overnight culture prepared in 14.27 and incubated at 37 &deg;C and 220 rpm until OD<sub>600</sub> reached 0.5. The flasks were cooled to 18 &deg;C and protein production was induced by adding 100 &micro;L 500 mM IPTG. The cultures were incubated over night at 18 &deg;C and 220 rpm. Afterwards the cells were collected by centrifugation (6000 rpm, 20 min, 4 &deg;C), resuspended in buffer A and stored at -20 &deg;C until further use.</p>
+    </div>
+</fieldset>
+<!-- ROMAN -->
 </div>
@@ Line 1,865: / Line 1,907: @@
 </h2>
 <fieldset class="exp15">
-     <legend><a name="exp15.42">15.42 Test Restriction of pMad-hag-flank and Test PCR</a></legend>
+     <legend><a name="exp15.42">15.42 Test restriction of pMad-hag-flank and Test PCR</a></legend>
      <div class="aim">
      <p>Aim: determine whether the plasmid contains the right insert</p>
      </div>
      <div class="exp-content">
-     <p>Restriction: Concentration of plasmid after prep between 20 and 30 ng/&micro;l</p>
+     <p>Restriction: concentration of plasmid after isolation between 20 and 30 ng/&micro;l</p>
      <table width="100%" border="1">
    <tr>
@@ Line 1,885: / Line 1,927: @@
    </tr>
    <tr>
-     <th scope="row">NcoI</th>
+     <th scope="row"><i>Nco</i>I</th>
      <td>0,5</td>
    </tr>
    <tr>
-     <th scope="row">BamHI</th>
+     <th scope="row"><i>Bam</i>HI</th>
      <td>0,5</td>
    </tr>
@@ Line 1,897: / Line 1,939: @@
      <h3>Results</h3>
      <img src="https://static.igem.org/mediawiki/2014/7/70/MR_2014-05-19_pMAD-hag-flank.png" width="30%" />
-     <p><strong>Figure: Testrestriction of pMad with hag flank insert did not bring a clear result (last band belongs to Flo)</strong></p>
+     <p>Test restriction of pMad with hag flank insert did not show a clear result (last band is a different sample)</p>
      </div>
      <div class="exp-content">
@@ Line 1,930: / Line 1,972: @@
      <h3>Results</h3>
      <img src="https://static.igem.org/mediawiki/2014/e/e1/MR_2014-05-19_pMAD-hag-flank2.png" width="30%" />
-     </div>
+     <br />
+	<p>The PCR showed the expected fragment of the hag-flank construct with a size of approx. 2 kb.</p>
+	</div>
 </fieldset>
 <fieldset class="exp17">
      <legend><a name="exp17.4">17.4 Bacillus Trafo with Nose Plasmids</a></legend>
      <div class="exp-content">
-     <p>Bacillus Trafo: rf. Diploma thesis from Dr. Felix Dempwolff<br />
+     <p>5&micro;l DNA were added to 100&micro;l cells, 30 min incubation at 37&deg;C and plated on LB-Cm.</p>
-&micro;l DNA were added to 100&micro;l cells, 30 min incubation at 37&deg;C and plated on LB-Cm.</p>
 	</div>
 </fieldset>
+<!-- ROMAN -->
+<fieldset class="exp14">
+ <legend><a name="exp14.29">14.29 Purification of PheA-Arc1p-C-2x</a></legend>
+    <div class="aim">
+    <p>Aim: Purify PheA-Arc1p-C-2x in three steps</p>
+    </div>
+    <div class="exp-content">
+    <p>The resuspended cells from 14.28 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-2x purified from the cleared solution by NiNTA affinity chromatography. The combined elution fractions containing crude PheA-Arc1p-C-2x 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>
@@ Line 1,947: / Line 2,005: @@
 	<a name="20.05.2014">20.05.2014</a>
 </h2>
+<!-- ROMAN -->
+<fieldset class="exp14">
+ <legend><a name="exp14.30">14.30 Creating PheA-Arc1p-C-1x</a></legend>
+    <div class="aim">
+    <p>Aim: Using Round-the-horn mutagenesis to create PheA-Arc1p-C-1x-pET28a</p>
+    </div>
+    <div class="exp-content">
+    The PCR with 5' phosphorylated TG_1xGSSG FP und TG_0xGSSG RP should generate the 7509 bp fragment for ligation from the methylated template PheA-Arc1p-C-8x-pET28a from 14.5.</p>
+    <p>The used Primer concentration was 1
+    &micro;M, the concentration of the template was 1 ng/&micro;L and we used a hot start to avoid unspecific annealing of primers.</p>
+    <table width="100%" border="1">
+  <tr>
+    <th scope="col">Content</th>
+    <th scope="col">Volume [&micro;L]</th>
+  </tr>
+  <tr>
+    <th scope="row">Water</th>
+    <td>29.5</td>
+  </tr>
+  <tr>
+    <th scope="row">5x GC Buffer</th>
+    <td>10</td>
+  </tr>
+  <tr>
+    <th scope="row">DMSO</th>
+    <td>2.5</td>
+  </tr>
+  <tr>
+    <th scope="row">TG_1xGSSG FP</th>
+    <td>2.5</td>
+  </tr>
+  <tr>
+    <th scope="row">TG_0xGSSG RP</th>
+    <td>2.5</td>
+  </tr>
+  <tr>
+    <th scope="row">PheA-Arc1p-C-8x-pET28a</th>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">dNTPs</th>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Phusion-Polymerase</th>
+    <td>1</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>50</td>
+  </tr>
+</table><br />
+<table width="100%" border="1">
+  <tr>
+    <th scope="col">Step</th>
+    <th scope="col">Temperature [&deg;C]</th>
+    <th scope="col">Time [min:sec]</th>
+  </tr>
+  <tr>
+    <th scope="row">1</th>
+    <td>98</td>
+    <td>2:00</td>
+  </tr>
+  <tr>
+    <th scope="row">2</th>
+    <td>add Polymerase</td>
+    <td>&nbsp;</td>
+  </tr>
+  <tr>
+    <th scope="row">3</th>
+    <td>98</td>
+    <td>0:10</td>
+  </tr>
+  <tr>
+    <th scope="row">4</th>
+    <td>67.5</td>
+    <td>0:30</td>
+  </tr>
+  <tr>
+    <th scope="row">5</th>
+    <td>72</td>
+    <td>4:00</td>
+  </tr>
+  <tr>
+    <th scope="row">6</th>
+    <td>go to 3</td>
+    <td>32x</td>
+  </tr>
+  <tr>
+    <th scope="row">7</th>
+    <td>72</td>
+    <td>10:00</td>
+  </tr>
+  <tr>
+    <th scope="row">8</th>
+    <td>4</td>
+    <td>hold</td>
+  </tr>
+</table>
+<p>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.</p>
+<table width="100%" border="1">
+  <tr>
+    <th scope="col">Content</th>
+    <th scope="col">Volume [&micro;L]</th>
+  </tr>
+  <tr>
+    <th scope="row">10x CutSmart Buffer</th>
+    <td>3.6</td>
+  </tr>
+  <tr>
+    <th scope="row">Plasmid</th>
+    <td>30</td>
+  </tr>
+  <tr>
+    <th scope="row">DpnI</th>
+    <td>3</td>
+  </tr>
+  <tr>
+    <th scope="row">Total Volume</th>
+    <td>36.6</td>
+  </tr>
+</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>
+    </div>
+</fieldset>
+<!-- ROMAN -->
 <fieldset class="exp15">
      <legend><a name="exp15.43">15.43 PCR to Amplify Cup 1 from Yeast gDNA</a></legend>
      <div class="aim">
-     <p>Aim: create the DNA fragment cup 1 (metallothionein to insert it into the flagellin (Gib-son assembly in pMad by cutting the plasmid with SpeI at the created restriction site)</p>
+     <p>Aim: create the DNA fragment <i>cup</i>1 (metallothionein) for insertion into the flagellin (Gibson assembly with pMad by cutting the plasmid with <i>Spe</i>I at the created restriction site)</p>
      </div>
      <div class="exp-content">
@@ Line 1,982: / Line 2,173: @@
      <div class="results">
      <img src="https://static.igem.org/mediawiki/2014/4/46/MR_2014-05-20_Cup1.png" width="30%" />
-     </div>
+     <p>The Purple 2-log ladder was used as a marker. The amplified cup1 could be seen as a 204 bp fragment on the gel.</p>
+	</div>
 </fieldset>
 <fieldset class="exp17">
      <legend><a name="exp17.5">17.5 Bacillus Trafo with Nose Plasmids</a></legend>
      <div class="exp-content">
-     <p>No colonies &rarr; new trafo<br />New LB Cm plates for Bacillus (only 5&micro;g/ml instead of 25&micro;g/ml)</p>
+     <p>No colonies &rarr; new trafo<br />New LB-chloramphenicol plates for Bacillus (only 5&micro;g/ml instead of 25&micro;g/ml)</p>
      </div>
 </fieldset>
@@ Line 1,999: / Line 2,191: @@
 </h2>
 <fieldset class="exp15">
-     <legend><a name="exp15.44">15.44 Restriction pMad with SpeI</a></legend>
+     <legend><a name="exp15.44">15.44 Restriction pMad with <i>Spe</i>I</a></legend>
      <div class="aim">
-     <p>Aim: Create a linearized plasmid for following gibson assembly with Cup1</p>
+     <p>Aim: Create a linearized plasmid for following Gibson assembly with <i>cup</i>1</p>
      </div>
      <div class="exp-content">
@@ Line 2,026: / Line 2,218: @@
    </tr>
 </table>
-	<p>Concentration of plasmid after clean up only 7 ng/&micro;l</p>
+	<p>Concentration of plasmid after purification only 7 ng/&micro;l</p>
      </div>
 </fieldset>
+<!-- ROMAN -->
+<fieldset class="exp14">
+ <legend><a name="exp14.31">14.31 Overnight culture</a></legend>
+    <div class="aim">
+    <p>Aim: Amplify Plasmid in an overnight culture</p>
+    </div>
+    <div class="exp-content">
+    <p>Six clones of the transformed <i>E. coli</i> Top10 cells from 14.30 were picked and used to inoculate overnight cultures (6 x 5 mL).</p>
+    </div>
+</fieldset>
+<!-- ROMAN -->
 <fieldset class="exp15">
-     <legend><a name="exp15.45">15.45 Gibson Assembly of Restricted pMad-fla and cup 1 and Transformation into <em>E.Coli</em> XL1-Blue</a></legend>
+     <legend><a name="exp15.45">15.45 Gibson Assembly of digested pMad-fla and cup 1 and Transformation into <em>E.Coli</em> XL1-Blue</a></legend>
      <div class="aim">
      <p>Aim: create a flagellin that contains the metallothinein cup1</p>
@@ Line 2,076: / Line 2,285: @@
      <legend><a name="exp17.6">17.6 MTA Bacillus Nose Ag </a></legend>
      <div class="exp-content">
-     <p>Tranformation from 20.5.14: one colony on the Ag Nose plate<br />
+     <p>Transformation from 20.5.14: one colony on the Ag Nose plate<br />
-     Innoculate shaking culture in the morning together with the wildtype and the gfp strain (186) in LB liquid without antibiotics</p>
+     Inoculation of shaking culture in the morning together with the wildtype and the <i>gfp</i> strain in LB liquid without antibiotics</p>
-     <p>Inocculate 96 well plate in the afternoon 15:00</p>
+     <p>Inoculate 96 well plate in the afternoon 15:00</p>
-     <p>Prepate Cu and Ag solutions to test different concentrations in MTA and see if the Ag nose responds to Ag and also if it is specific for Ag and does not respond to Cu</p>
+     <p>Prepare Cu and Ag solutions to test different concentrations in MTA and see if the Ag nose responds to Ag and also if it is specific for Ag and does not respond to Cu</p>
      <p>Ag and Cu in stock solution of 10 mM have been prepared<br />
      Added (Concentration): 11 mM, 100&micro;M and 10&micro;M<br />
-     Cells: Ag Nose mutant, wildtype (AG GM) and gfp (186)</p>
+     Cells: Ag Nose mutant, wildtype (AG GM) and <i>gfp</i></p>
+	<br />
+	<p>The MTA showed no significant increase of fluorescence. The bacteria had difficulties in growth, thus it seemed that the metal ion concentrations were too high.</p>
      </div>
 </fieldset>
 <fieldset class="exp17">
-     <legend><a name="exp17.7a">17.7 Overnight Restriction piGEM 002 and the  Nose Plasmide for Ag/Cu</a></legend>
+     <legend><a name="exp17.7a">17.7 Digestion of piGEM002 and the nose plasmids for Ag/Cu</a></legend>
      <div class="aim">
-     <p>Aim: Linearize the plasmids with SpeI to built in the instability tags (25&micro;l mix)</p>
+     <p>Aim: Linearize the plasmids with <i>Spe</i>I to built in the instability tags (25&micro;l mix)</p>
      </div>
      <div class="exp-content">
@@ Line 2,101: / Line 2,312: @@
    </tr>
    <tr>
-     <th scope="row"><strong>Template ≈10&micro;g</strong></th>
+     <th scope="row"><strong>Template ~10&micro;g</strong></th>
      <td>15</td>
      <td>20</td>
@@ Line 2,125: / Line 2,336: @@
    </tr>
 </table>
-	<p>Incubation at room temperature</p>
+	<p>Incubation at room temperature over night.</p>
      </div>
 </fieldset>
+<!-- ROMAN -->
+<fieldset class="exp14">
+ <legend><a name="exp14.32">14.32 Preparation of plasmids</a></legend>
+    <div class="aim">
+    <p>Aim: Purify the amplified plasmids from overnight cultures</p>
+    </div>
+    <div class="exp-content">
+    <p>The plasmids were purified from the overnight cultures created in 14.31 using Sigma GenElute Plasmid Miniprep Kit following the included protocol. The plasmids were eluted using 45 &micro;L water.</p>
+    </div>
+</fieldset>
+<!-- ROMAN -->
 </div>
@@ Line 2,139: / Line 2,367: @@
      <legend><a name="exp17.7b">17.7 Create Instability Tags for gfp in the Nose Plasmids</a></legend>
      <div class="aim">
-     <p>Aim: Gfp is a stable protein which would accumulate and wrong the results if not digested, instability tags of different strength cause the degradation and therefore cause quantitative results</p>
+     <p>Aim: GFP is a stable protein, which would accumulate and distort the results if not degraded, instability tags of different strength cause the degradation and therefore cause quantitative results</p>
      </div>
      <div class="exp-content">
-     <p>First step: Linearize the following plasmids: piGEM 002 without promotor as well as the plasmids containing the Silver and copper promotor<br />
+     <p>First step: Linearize the following plasmids: piGEM 002 without promoter as well as the plasmids containing the silver and copper sensitive promoters<br />
-Second step: PCR to anneal the oligos 20+21, 20+22 and 20+23</p>
+		Second step: PCR to anneal the oligos 20+21, 20+22 and 20+23</p>
 	<table width="100%" border="1">
    <tr>
@@ Line 2,180: / Line 2,408: @@
 	<p>Afterwards clean up with kit (all three mixes were carried out in a duplicate, 1 each was frozen away at minus 20)</p>
 	<p>Third step: Yeast transformation<br />
-Reactions (3 plasmids and 3 instability tags)</p>
+Reactions (3 plasmids and 3 instability (ssrA-)tags)</p>
-ng plasmid plus 1&micro;l of primer mix were filled to 14&micro;ll and added to the yeast transformation mix and subsequently transformed into yeast.</p>
+ng plasmid plus 1&micro;l of primer mix were filled to 14&micro;l and added to the yeast transformation mix and subsequently transformed into yeast.</p>
      </div>
 </fieldset>
@@ Line 2,193: / Line 2,421: @@
 </h2>
 <fieldset class="exp15">
-     <legend><a name="exp15.46">15.46 Restriction of pMAD-fla with SpeI, Gibson-Assembly with cup1-1 and Transformation of <em>E. coli</em> DH5Alpha</a></legend>
+     <legend><a name="exp15.46">15.46 Restriction of pMAD-fla with <i>Spe</i>I, Gibson-Assembly with <i>cup</i>1-1 and transformation of <em>E. coli</em> DH5&alpha;</a></legend>
      <div class="aim">
      <p>Aim: insert cup1-1 into the hag/flank-construct</p>
      </div>
      <div class="exp-content">
-     <p>To insert the metallothionein gene cup1-1 into the hag/flank-construct the pMAD-fla was restricted with SpeI to linearize it.</p>
+     <p>To insert the metallothionein gene <i>cup</i>1-1 into the hag/flank-construct the pMAD-fla was digested with <i>Spe</i>I to linearize it.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 2,226: / Line 2,454: @@
 </table>
 	<p>The restriction was carried out at 37&deg;C for 1h.<br />
-     The restriction was cleaned with a DNA Gel Ex Kit (c = 40 ng/&micro;l). 4&micro;l (160 ng) of this restricted plasmid were mixed with 1&micro;l of the cup1-1 fragment (9.6 ng/&micro;l). These 5&micro;l were inserted into the prepared 15&micro;l Gibson-mix. The reaction was incubated at RT for 1 min and then at 50&deg;C for 1h. An extra Gibson-reaction was carried out as a control with just the linearized pMAD without the cup1-1.<br />
+     The restriction was cleaned with a DNA Gel Ex Kit (c = 40 ng/&micro;l). 4&micro;l (160 ng) of this digested plasmid were mixed with 1 &micro;l of the cup1-1 fragment (9.6 ng/&micro;l). These 5 &micro;l were inserted into the prepared 15 &micro;l Gibson-mix. The reaction was incubated at RT for 1 min and then at 50&deg;C for 1 hour. An extra Gibson-reaction was carried out as a control with just the linearized pMAD without the <i>cup</i>1-1.<br />
-     <em>E. coli</em> DH5Alpha cells were transformed with the Gibson reactions and plated out on LB-Amp. They were incubated at 37&deg;C over night.</p>
+     <em>E. coli</em> DH5&alpha; cells were transformed with the Gibson reactions and plated out on LB-Amp. They were incubated at 37&deg;C over night.</p>
      </div>
 </fieldset>
 <fieldset class="exp15">
-     <legend><a name="exp15.47">15.47 Colony-PCR of <em>E. coli</em> XLI-Blue pMAD-fla + cup1-1 from 21.05.14 and 23.05.14</a></legend>
+     <legend><a name="exp15.47">15.47 Colony-PCR of <em>E. coli</em> XLI-Blue pMAD-fla + <i>cup</i>1-1 from 21.05.14 and 23.05.14</a></legend>
      <div class="aim">
-     <p>Aim: check for correct insertion of cup1-1 into the hag/flank-construct</p>
+     <p>Aim: check for correct insertion of <i>cup</i>1-1 into the hag/flank-construct</p>
      </div>
      <div class="exp-content">
-     <p>Since a Gibson-Assembly with the same aim was carried out last week, the colonies were checked by a colony PCR with the primers for cup1-1 iGEM-018 and iGEM-019. One colony was picked from the plate from 23rd May and three were taken from the plate from 21st May. The latter was contaminated with Bacillus colonies. For this reason <em>E. coli</em> was picked and streaked out onto a new plate on Friday the 23rd May. The consequence is a plate with just one clone, what is the reason, that only one colony was picked from this plate.</p>
+     <p>Since a Gibson-Assembly with the same aim was carried out last week, the colonies were checked by a colony PCR with the primers for <i>cup</i>1-1 iGEM-018 and iGEM-019. One colony was picked from the plate from 23rd May and three were taken from the plate from 21st May. The latter was contaminated with Bacillus colonies. For this reason <em>E. coli</em> was picked and streaked out onto a new plate on Friday the 23rd May. The consequence is a plate with just one clone, what is the reason, that only one colony was picked from this plate.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 2,271: / Line 2,499: @@
      <div class="result">
      <h3>Result</h3>
+	<img src="https://static.igem.org/mediawiki/2014/f/fc/MR_20140526_colonyPCR_pMAD-fla-cup1.jpg" width="20%" />
+	<br />
+	<p>The expected fragment in size of the <i>cup</i>1 could be amplified from the template, which indicates a positive result.</p>
      </div>
 </fieldset>
+<!-- ROMAN -->
+<fieldset class="exp14">
+ <legend><a name="exp14.33">14.33 Transformation of BL21 cells</a></legend>
+    <div class="aim">
+    <p>Aim: Transform E. coli BL21(DE3) with PheA-Arc1p-C-1x-pET28a</p>
+    </div>
+    <div class="exp-content">
+    <p>40 &micro;L E. coli BL21(DE3) electrocompetent cells were transformed with 1 ng of the previously purified plasmid PheA-Arc1p-C-1x-pET28a from two different clones, incubated for 1 h at 37 &deg;C and plated out on LB-Kan<sup>50</sup> plates that were incubated overnight at 37 &deg;C.</p>
+    </div>
+</fieldset>
+<!-- ROMAN -->
 <fieldset class="exp13">
      <legend><a name="exp13.49">13.49 PlasmidPprep from Yeast and Transformation of <em>E. coli</em> DH5Alpha</a></legend>
@@ Line 2,279: / Line 2,527: @@
      </div>
      <div class="exp-content">
-     <p>The gfp in piGEM002, piGEM002-Ag (and piGEM002-Cu was tagged with different degradation tags by yeast recombination. The plasmids have been prepped form yeast.</p>
+     <p>The <i>gfp</i> in piGEM002, piGEM002-Ag (and piGEM002-Cu was tagged with different degradation tags by yeast recombination. The plasmids have been isolated from yeast.</p>
-    <table width="100%" border="1">
+	<p><em>E. coli</em> DH5&alpha; cells were transformed with 15 &micro;l of each isolated plasmid and plated out on LB-Amp. They were incubated at 37&deg;C over night.</p>
-  <tr>
-    <th scope="col">Clone</th>
-    <th scope="col">Concentration (ng/&micro;l)</th>
-  </tr>
-  <tr>
-    <th scope="row">002-21</th>
-    <td>&nbsp;</td>
-  </tr>
-  <tr>
-    <th scope="row">002-22</th>
-    <td>&nbsp;</td>
-  </tr>
-  <tr>
-    <th scope="row">002-23</th>
-    <td>&nbsp;</td>
-  </tr>
-  <tr>
-    <th scope="row">002-Ag-21</th>
-    <td>&nbsp;</td>
-  </tr>
-  <tr>
-    <th scope="row">002-Ag-22</th>
-    <td>&nbsp;</td>
-  </tr>
-  <tr>
-    <th scope="row">002-Ag-23</th>
-    <td>&nbsp;</td>
-  </tr>
-  <tr>
-    <th scope="row">002-Cu-21</th>
-    <td>&nbsp;</td>
-  </tr>
-  <tr>
-    <th scope="row">002-Cu-22</th>
-    <td>&nbsp;</td>
-  </tr>
-  <tr>
-    <th scope="row">002-Cu-23</th>
-    <td>&nbsp;</td>
-  </tr>
-</table>
-	<p><em>E. coli</em> DH5Alpha cells were transformed with 15&micro;l of each prepped plasmid and plated out on LB-Amp. They were incubated at 37&deg;C over night.</p>
      <p>Gly-Stocks - Making of -stocks for long time storage of bacteria strains<br />
-     For long time freezer storage of bacteria, they have to be treated with glycerin to prevent the crystallization and damaging of the cells. For this reason 2ml of LB with the respective antibiotic were inoculated with the bacteria which were to be stored and were incubated at 37&deg;C overnight.</p>
+     For long time freezer storage of bacteria, they have to be treated with glycerine to prevent the crystallization and damaging of the cells. For this reason 2 ml of LB with the respective antibiotic were inoculated with the bacteria, which were meant to be stored and were incubated at 37&deg;C overnight.</p>
      <p>Strains that are to be stored:
      <ul class="strains">
@@ Line 2,343: / Line 2,549: @@
 	<a name="27.05.2014">27.05.2014</a>
 </h2>
+<!-- ROMAN -->
+<fieldset class="exp14">
+ <legend><a name="exp14.34">14.34 Overnight culture</a></legend>
+    <div class="aim">
+    <p>Aim: Inoculate Overnight culture of PheA-Arc1p-C-1x-pET28a</p>
+    </div>
+    <div class="exp-content">
+    <p>5 mL of LB-Kan<sup>50</sup> medium were inoculated with a clone from 14.33 bearing the PheA-Arc1p-C-1x-pET28a plasmid.</p>
+    </div>
+</fieldset>
+<!-- ROMAN -->
 <fieldset class="exp15">
-     <legend><a name="exp15.48">15.48 Restriction of pET24d-fla with SpeI and Gibson-Assembly with cup1-1</a></legend>
+     <legend><a name="exp15.48">15.48 Restriction of pET24d-fla with <i>Spe</i>I and Gibson-Assembly with <i>cup</i>1-1</a></legend>
      <div class="aim">
-     <p>Aim: linearize pET24d-fla and insert cup1-1 into pET24d-fla</p>
+     <p>Aim: linearize pET24d-fla and insert <i>cup</i>1-1 into pET24d-fla</p>
      </div>
      <div class="exp-content">
-     <p>Since the colony-PCR (26.05.14) was negative and the Gibson-Assembly of linearized pMAD-fla with cup1-1 showed no results the pET24d-fla construct was linearized with SpeI.</p>
+     <p>Since the colony-PCR (26.05.14) was negative and the Gibson-Assembly of linearized pMAD-fla with <i>cup</i>1-1 showed no results the pET24d-fla construct was linearized with <i>Spe</i>I.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 2,376: / Line 2,599: @@
    </tr>
 </table>
-	<p>The restriction was incubated at 37&deg;C for 1h.</p>
+	<p>The restriction was incubated at 37&deg;C for 1 h.</p>
-     <p>The restriction mix was purified with the Gel Ex Kit. The yield was too low (c = 3.1 ng/&micro;l) to use it for a Gibson-Assembly, so the rest of the pET24d-fla was restricted with SpeI.</p>
+     <p>The restriction mix was purified with the Gel Ex Kit. The yield was too low (c = 3.1 ng/&micro;l) to use it for a Gibson-Assembly, so the rest of the pET24d-fla was digested with <i>Spe</i>I.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 2,405: / Line 2,628: @@
 </table>
 	<p>The restriction was incubated at 37&deg;C for 1h.</p>
-     <p>The restriction mix was purified with the Gel Ex Kit (c = 20.1 ng/&micro;l), which was enough for the Gibson-Assembly. 4&micro;l (80 ng) of this restricted plasmid were mixed with 1 µl of the cup1-1 fragment (9.6 ng/&micro;l). These 5 µl were inserted into the prepared 15&micro;l Gibson-mix. The reaction was incubated at RT for 1 min and then at 50&deg;C for 1 h. An extra Gibson-reaction was carried out as a control with just the linearized pET24d-fla without the cup1-1.</p>
+     <p>The restriction mix was purified with the Gel Ex Kit (c = 20.1 ng/&micro;l), which was enough for the Gibson-Assembly. 4&micro;l (80 ng) of this digested plasmid were mixed with 1 µl of the cup1-1 fragment (9.6 ng/&micro;l). These 5 &micro;l were inserted into the prepared 15&micro;l Gibson-mix. The reaction was incubated at RT for 1 min and then at 50&deg;C for 1 h. An extra Gibson-reaction was carried out as a control with just the linearized pET24d-fla without the <i>cup</i>1-1.</p>
-     <p>Competent <em>E. coli</em> XLI-Blue from Daniel were transformed with the whole Gibson-reactions. They were plated on LB-Kan an incubated at 37&deg;C overnight.</p>
+     <p>Competent <em>E. coli</em> XLI-Blue were transformed with the whole Gibson-reactions. They were plated on LB-Kan an incubated at 37&deg;C overnight.</p>
      </div>
 </fieldset>
@@ Line 2,412: / Line 2,635: @@
      <legend><a name="exp13.50">13.50 Colony-PCR of the <em>E. colis</em> Containing the Degradation tagged Constructs</a></legend>
      <div class="aim">
-     <p>Aim: check for correct tagging of gfp with the respective degradation tag</p>
+     <p>Aim: check for correct tagging of <i>gfp</i> with the respective degradation tag</p>
      </div>
      <div class="exp-content">
-     <p>The transformation with the tag-constructs were nearly in all cases successful except the pMa12-Ag-21. The transformation was repeated, the plate was incubated at 37&deg;C over night. <br />
+     <p>The transformation with the degradation tag-constructs were successful nearly in all cases except the pMa12-Ag-21. The transformation was repeated, the plate was incubated at 37&deg;C over night. <br />
 Four colonies of every plate have been picked, transferred to new LB-Amp plates and were subsequently used for the colony-PCR.
-The Master Mix was portioned in aliquots of 20&micro;l per PCR-cup and inoculated with the respective colony.</p>
+The Master Mix was portioned in aliquots of 20 &micro;l per PCR-cup and inoculated with the respective colony.</p>
 	<table width="100%" border="1">
    <tr>
@@ Line 2,495: / Line 2,718: @@
      <img src="https://static.igem.org/mediawiki/2014/b/b6/MR_2014-05-27_colony_PCR1.jpg" width="30%" />
      <img src="https://static.igem.org/mediawiki/2014/9/9d/MR_2014-05-27_colony_PCR2.jpg" width="30%" />
-     <p><strong>Figures : Colony-PCR of E. coli with the degradation-tag constructs</strong></p>
+     <p>Colony-PCR of E. coli with the degradation-tag constructs</p>
      <p>The bands slightly higher than 200 bp indicated a positive clone. Positive constructs are available: 002-21, Cu-23, Ag-22 and Cu-22.</p>
      </div>
      <div class="exp-content">
      <p>Gly-Stocks - Making of glycerin-stocks for long time storage of bacteria strains</p>
-     <p>1 ml of the bacteria which were inoculated yesterday (26.05.2014) were transferred to new, sterile 1.5 ml Eppendorf-cups. 600&micro;l of 50% glycerin were added and the cells were frozen and stored at -80&deg;C in the freezer.</p>
+     <p>1 ml of the bacteria which were inoculated yesterday (26.05.2014) were transferred to new, sterile 1.5 ml Eppendorf-cups. 600 &micro;l of 50% glycerin were added and the cells were frozen and stored at -80&deg;C in the freezer.</p>
      </div>
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.1">18.1 Making competent <em>E. coli</em> XLI-Blue with RbC: Inoculating LB-Tet with <em>E.Coli</em> XL1-Blue as preculture</a></legend>
+     <legend><a name="exp18.1">18.1 Making competent <em>E. coli</em> XLI-Blue with RbCl: Inoculation of LB-Tet with <em>E.Coli</em> XL1-Blue as a preculture</a></legend>
      <div class="exp-content">
      <p>9 ml LB-Tetracycline (1:1000) were inoculated with <em>E. coli</em> XLI-Blue cells as a preculture. They were incubated at 37&deg;C overnight.</p>
@@ Line 2,542: / Line 2,765: @@
        </tr>
        <tr>
-         <td>Kaliumacetat</td>
+         <td>potassium acetate</td>
          <td>0,15g</td>
        </tr>
@@ Line 2,550: / Line 2,773: @@
        </tr>
        <tr>
-         <td>1M RbCl2</td>
+         <td>1M RbCl</td>
          <td>5 ml</td>
        </tr>
@@ Line 2,558: / Line 2,781: @@
        </tr>
        <tr>
-         <td>87% Glycerin</td>
+         <td>87% glycerine</td>
          <td>8,6 ml</td>
        </tr>
@@ Line 2,596: / Line 2,819: @@
        </tr>
        <tr>
-         <td>87% Glycerin</td>
+         <td>87% glycerine</td>
          <td>43,75 ml</td>
        </tr>
@@ Line 2,624: / Line 2,847: @@
      <div class="exp-content">
      <ul class="list">
-     <li>Grow 100ml <em>E.coli</em> culture to OD600=0,5</li>
+     <li>Grow 100 ml <em>E.coli</em> culture to OD600=0,5</li>
      <li>Put on  ice for 10 min </li>
      <li>Centrifuge  2x 50 ml for 10 min at 3000 rpm and 4&deg;C </li>
@@ Line 2,630: / Line 2,853: @@
      <li>Resuspend  pellets in 2ml TFB2 </li>
      <li>Pipett  200&micro;l aliquots in precooled 1,5 ml tubes</li>
-     <li>store  at  -80&micro;C </li>
+     <li>store  at  -80&deg;C </li>
      </ul>
      </div>
 </fieldset>
+<!-- ROMAN -->
+<fieldset class="exp14">
+ <legend><a name="exp14.35">14.35 Test Expression</a></legend>
+    <div class="aim">
+    <p>Aim: Test the expression of PheA-Arc1p-C-1x</p>
+    </div>
+    <div class="exp-content">
+    <p>Using the preculture from 14.34 60 mL of LB-Kan<sup>50</sup> medium were inoculated with 600 &micro;L of the preculture and incubated at 37 &deg;C and 220 rpm until OD<sub>600</sub> reached 0.5. The culture was cooled down to 18 &deg;C and the protein production was induced with 12 &micro;L of 500 mM IPTG. Over night the culture was incubated at 18 &deg;C and 220 rpm. A glycerolstock of the strain containing the PheA-Arc1p-C-1x-pET28a plasmid was stored at -80 &deg;C.</p>
+    </div>
+</fieldset>
+<!-- ROMAN -->
 <fieldset class="exp15">
-     <legend><a name="exp15.49a">15.49 Colony-PCR with transformed <em>E. coli</em> XLI-Blue including pet24d-Fla-Cup1-1</a></legend>
+     <legend><a name="exp15.49a">15.49 Colony-PCR with transformed <em>E. coli</em> XLI-Blue including pET24d-fla-cup1-1</a></legend>
 	<div class="aim">
-     <p>Aim: testing the squccess of insertion of cup1-1 into pet24d-fla </p>
+     <p>Aim: testing the success of insertion of <i>cup</i>1-1 into pET24d-fla </p>
      </div>
      <div class="exp-content">
@@ Line 2,726: / Line 2,966: @@
    </tr>
 </table>
+<br />
+<img src="https://static.igem.org/mediawiki/2014/8/87/MR_20140528_colonyPCR_pMAD-fla-cup1_isolated_from_XLIBlue.jpg" width="20%" />
+<br />
+<p>The expected band of approx. 240 bp could be seen in every sample, more or less clearly</p>
      </div>
 </fieldset>
 <fieldset class="exp13">
-     <legend><a name="exp13.51">13.51 Colony-PCR of the <em>E. colis</em> Containing the Degradation Tagged Constructs</a></legend>
+     <legend><a name="exp13.51">13.51 Colony-PCR of the <em>E. coli</em> containing the degradation tagged constructs</a></legend>
 	<div class="aim">
-     <p>Aim: check for correct tagging of gfp with the respective degradation tag</p>
+     <p>Aim: check for correct tagging of <i>gfp</i> with the respective degradation tag</p>
      </div>
      <div class="exp-content">
      <p>The Colony-PCR was repeated with pMa12-Ag-21 after successful transformation.<br />
 Four colonies have been picked, transferred to new LB-Amp plates and were subsequently used for the colony-PCR.<br />
-The Master Mix was portioned in aliquots of 20 µl per PCR-cup and inoculated with the respective colony.</p>
+The Master Mix was portioned in aliquots of 20 &micro;l per PCR-cup and inoculated with the respective colony.</p>
 	<table width="100%" border="1">
    <tr>
@@ Line 2,744: / Line 2,988: @@
    </tr>
    <tr>
-     <th scope="row"><em>E. coli</em> DH5α with Ag21</th>
+     <th scope="row"><em>E. coli</em> DH5&alpha; with Ag21</th>
      <td>-</td>
      <td>part of a colony</td>
@@ Line 2,782: / Line 3,026: @@
      <div class="results">
      <img src="https://static.igem.org/mediawiki/2014/f/fb/MR_2014-05-27_colony_PCR.jpg" width="30%" />
-     <p><strong>Figure : Colony-PCR of <em>E. coli</em> containing the degradation-tag construct Ag-21</strong></p>
+     <p>Colony-PCR of <em>E. coli</em> containing the degradation-tag construct Ag-21</p>
      </div>
      <div class="exp-content">
@@ Line 2,814: / Line 3,058: @@
    <tr>
      <th scope="row">Water</th>
-     <td>315</td>
+     <td>314</td>
      <td>9,5</td>
    </tr>
@@ Line 2,838: / Line 3,082: @@
      <th scope="row">1</th>
      <td>95</td>
-     <td>5 min</td>
+     <td>3 min</td>
    </tr>
    <tr>
@@ Line 2,875: / Line 3,119: @@
      <img src="https://static.igem.org/mediawiki/2014/6/6f/MR_2014-05-28_PCR2.jpg" width="30%" />
      <img src="https://static.igem.org/mediawiki/2014/5/52/MR_2014-05-28_PCR3.jpg" width="30%" />
-     <p><strong>Figures : Colony-PCR with E. coli containing the degradation-tag constructs</strong></p>
+     <p><Colony-PCR with <i>E. coli</i> containing the degradation-tag constructs</strong></p>
-     <p>Positive clones could be obtained with the Ag-23 and the 002-22 constructs.</p>
+     <p>Positive clones could be obtained with the Ag-23 and the 002-22 constructs (approx. 250 bp).</p>
      </div>
 </fieldset>
@@ Line 2,883: / Line 3,127: @@
      <div class="exp-content">
      <p><em>E.Coli</em> XL1-Blue were transformed with 1&micro;l pMAD (189 ng/&micro;l). Another aliquod was transformed with pMAD-fla.<br />
-In comparison <em>E.Coli</em> DH5Alpha were transformed the same way.</p>
+In comparison <em>E.Coli</em> DH5&alpha; were transformed the same way.</p>
 	</div>
 </fieldset>
@@ Line 2,897: / Line 3,141: @@
      <legend><a name="exp18.5b">18.5 Transformation Test with <em>E.Coli</em> XL1-Blue and pMAD (fla)</a></legend>
      <div class="exp-content">
-     <p>Every transformation was successful. The higher number of colonies on the pMAD-transformation plate shows a higher transformation efficiency compared with DH5Alpha.</p>
+     <p>Every transformation was successful. The higher number of colonies on the pMAD-transformation plate shows a higher transformation efficiency compared with DH5&alpha;.</p>
      </div>
 </fieldset>
 <fieldset class="exp18">
-     <legend><a name="exp18.6">18.6 Inoculation for Miniprep and Glycerin Storing of pMAD-fla</a></legend>
+     <legend><a name="exp18.6">18.6 Inoculation for Miniprep and Glycerin stock of pMAD-fla</a></legend>
      <div class="aim">
-     <p>Aim: In order to save pMAD and pMAD-fla for further experiments and storage minipreps and glycerin stocks have to be inoculated</p>
+     <p>Aim: In order to save pMAD and pMAD-fla for further experiments and storage, minipreps and glycerine stocks have to be inoculated</p>
      </div>
      <div class="exp-content">
-         <p>For minipreps 2x6ml of LB-Amp were inoculated with one colony from the pMAD XL1-Blue-Transformation plate. Additionally 3x6ml of LB-Amp were inoculated with one colony from the pMAD-fla XL1-Blue-Transformation plate. <br />
+         <p>For minipreps 2 x 6 ml of LB-Amp were inoculated with one colony from the pMAD XL1-Blue-transformation plate. Additionally 3 x 6 ml of LB-Amp were inoculated with one colony from the pMAD-fla XL1-Blue-Transformation plate. <br />
-     Furthermore 2x 2 mL LB-Amp were inoculated with a clone from pMAD-fla XL1-Blue-Transformation plate for glycerin storage.<br />
+     Furthermore 2 x 2 mL LB-Amp were inoculated with a clone from pMAD-fla XL1-Blue-Transformation plate for glycerine stocks.<br />
-     Every attempt was incubated at 37°C overnight.</div>
+     Every attempt was incubated at 37&deg;C overnight.</div>
 </fieldset>
 <fieldset class="exp13">
-     <legend><a name="exp13.52">13.52 Colony-PCR of the E. colis containing the degradation tagged constructs</a></legend>
+     <legend><a name="exp13.52">13.52 Colony-PCR of the <i>E. coli</i> containing the degradation tagged constructs</a></legend>
      <div class="aim">
-     <p>Aim: check for correct tagging of gfp with the respective degradation tag</p>
+     <p>Aim: check for correct tagging of <i>gfp</i> with the respective degradation tag</p>
      </div>
      <div class="exp-content">
      <p>The Colony-PCR was repeated with 002-Cu21 and 002-23.<br />
      Four colonies have been picked, transferred to new LB-Amp plates and were subsequently used for the colony-PCR.<br />
-     The Master Mix was portioned in aliquots of 20 µl per PCR-cup and inoculated with the respective colony.</p>
+     The Master Mix was portioned in aliquots of 20 &micro;l per PCR-cup and inoculated with the respective colony.</p>
      <table width="100%" border="1">
    <tr>
@@ Line 2,927: / Line 3,171: @@
    </tr>
    <tr>
-     <th scope="row"><em>E. coli</em> DH5α with 002-23</th>
+     <th scope="row"><em>E. coli</em> DH5&alpha; with 002-23</th>
      <td>-</td>
      <td>part of a colony</td>
@@ Line 2,933: / Line 3,177: @@
    </tr>
    <tr>
-     <th scope="row"><em>E. coli</em> DH5α with Cu21</th>
+     <th scope="row"><em>E. coli</em> DH5&alpha; with Cu21</th>
      <td>-</td>
      <td>-</td>
@@ Line 2,951: / Line 3,195: @@
    </tr>
    <tr>
-     <th scope="row">Phusion</th>
+     <th scope="row">Phusion DNA-polymerase</th>
      <td>3,6</td>
      <td>-</td>
@@ Line 2,997: / Line 3,241: @@
      <th scope="row">1</th>
      <td>95</td>
-     <td>5 min</td>
+     <td>3 min</td>
    </tr>
    <tr>
@@ Line 3,032: / Line 3,276: @@
 	</div>
 </fieldset>
+<!-- ROMAN -->
+<fieldset class="exp14">
+ <legend><a name="exp14.36">14.36 Purification of test expression</a></legend>
+    <div class="aim">
+    <p>Aim: Purify PheA-Arc1p-C-1x on a small scale</p>
+    </div>
+    <div class="exp-content">
+    <p>The cell culture from 14.35 was centrifuged (17000 rpm, 20 min, 4 &deg;C) and the pellet resuspended in 3 mL buffer A. Lysozyme was added 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 &deg;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.</p>
+    <p>60 mL LB-Kan<sup>50</sup> medium was inoculated from the glycerolstock prepared in 14.35 and incubated at 37 &deg;C and 220 rpm over night.</p>
+    </div>
+</fieldset>
+<!-- ROMAN -->
 <fieldset class="exp13">
      <legend><a name="exp13.53">15.53 Inoculation of Minipreps from Nose-Tag-Plasmids</a></legend>
      <div class="aim">
-     <p>Aim: miniprep for isolation of plasmids in order to transform them into bacillus for plate reader assays</p>
+     <p>Aim: isolate the plasmid to tansform Bacillus for further plate reader assays</p>
      </div>
      <div class="exp-content">
@@ Line 3,047: / Line 3,309: @@
      <li>002-Ag-22</li>
      </ul>
-     <p>Incubation Overnight at 37&deg;C</p>
+     <p>Incubation over night at 37&deg;C</p>
      </div>
 </fieldset>
@@ Line 3,058: / Line 3,320: @@
 	<a name="30.05.2014">30.05.2014</a>
 </h2>
+<!-- ROMAN -->
+<fieldset class="exp14">
+ <legend><a name="exp14.37">14.37 Expression of PheA-Arc1p-C-1x</a></legend>
+    <div class="aim">
+    <p>Aim: Express PheA-Arc1p-C-1x for further use</p>
+    </div>
+    <div class="exp-content">
+    <p>10 x 500 mL LB-Kan<sup>50</sup> medium were inoculated with 5 mL of the overnight culture prepared in 14.36 and incubated at 37 &deg;C and 220 rpm until OD<sub>600</sub> reached 0.5. The flasks were cooled to 18 &deg;C and protein production was induced by adding 100 &micro;L 500 mM IPTG. The cultures were incubated over night at 18 &deg;C and 220 rpm. Afterwards the cells were collected by centrifugation (6000 rpm, 20 min, 4 &deg;C), resuspended in buffer A and stored at -20 &deg;C until further use.</p>
+    </div>
+</fieldset>
+<!-- ROMAN -->
 <fieldset class="exp18">
      <legend><a name="exp18.7">18.7 Miniprep of <em>E.Coli</em> XL1-Blue with pMAD and pMAD-fla</a></legend>
@@ Line 3,079: / Line 3,358: @@
 </fieldset>
 <fieldset class="exp13">
-     <legend><a name="exp13.54">13.54 Minipreps from Nose-Tag-Plasmids</a></legend>
+     <legend><a name="exp13.54">13.54 Minipreps of Nose-Tag-plasmids</a></legend>
      <div class="exp-content">
      <table width="100%" border="1">
@@ Line 3,116: / Line 3,395: @@
      <legend><a name="exp13.55">13.55 Inoculation of Minipreps with Ag-21</a></legend>
      <div class="exp-content">
-     <p>The positive clone 3 from the colony PCR (28.05.14) was used to inoculate 6 ml LB-Amp for a miniprep in order to receive the plasmid for transforming it into <em>Bacillus subtilis</em>.<br />
+     <p>The positive clone 3 from the colony PCR (28.05.14) was used to inoculate 6 ml LB-Amp for a miniprep in order to receive the plasmid for transforming <em>Bacillus subtilis</em>.<br />
-       Incubation at room temperature over the weekend.</p>
+       Incubation at room temperature over two days.</p>
      </div>
 </fieldset>
@@ Line 3,126: / Line 3,405: @@
      </div>
      <div class="exp-content">
-     <p>6 mL LB-Amp were inoculated with  the positive clone 1 from the Gibson assembly with cup1-1 transformed into  E.Coli XL1-Blue from 26.05.14. After miniprep the plasmid can be transformed into <em>Bacillus Subtilis.</em><br />Incubation at room temperature over the weekend.</p>
+     <p>6 mL LB-Amp were inoculated with  the positive clone 1 from the Gibson assembly with <i>cup</i>1-1 of the transformed <i>E. coli</i> XL1-Blue from 26.05.14. After isolation of the plasmid <em>Bacillus Subtilis.</em> can be transformed.<br />Incubation at room temperature over two days.</p>
 </div>
 </fieldset>
 <fieldset class="exp13">
-     <legend><a name="exp13.54b">13.54 Transformation of Bacillus with Plasmids</a></legend>
+     <legend><a name="exp13.54b">13.54 Transformation of Bacillus with isolated plasmids</a></legend>
      <div class="aim">
-     <p>Aim: Create Bacillus strains with the following plasmids:</p>
+     <p>Aim: Creation of Bacillus strains with the following plasmids:</p>
      </div>
      <div class="exp-content">
@@ Line 3,147: / Line 3,426: @@
 </fieldset>
 <fieldset class="exp13">
-     <legend><a name="exp13.55b">13.55 Colony-PCR of the <em>E. colis</em> Containing the Degradation Tagged Constructs</a></legend>
+     <legend><a name="exp13.55b">13.55 Colony-PCR of the <em>E. coli</em> containing the degradation tagged constructs</a></legend>
      <div class="aim">
-     <p>Aim: check for correct tagging of gfp with the respective degradation tag</p>
+     <p>Aim: check for correct tagging of <i>gfp</i> with the respective degradation tag</p>
      </div>
      <div class="exp-content">
      <p>Phusion and Q5 Buffer did not work out so the PCR was repeated with Q5 Mastermix.<br />
 	PCR performed with 002-Cu21 and 002-23<br />
-	Result: Positive clones for both Tags have subsequently been inoculated in LB-Amp and incubated at room temperature over the weekend.</p>
+	Positive clones for both tags (approx. 250 bp) have subsequently been inoculated in LB-Amp and incubated at room temperature over two days.</p>
      </div>
      <div class="results">

Team:Marburg:Project:Notebook:May

From 2014.igem.org

Latest revision as of 19:28, 16 October 2014

Notebook: May

Results

Results

1. Sequencing

Results:

Results:

Results

Results

Results

Result