Team:Paris Saclay/Notebook/July/29

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{{Team:Paris_Saclay/notebook_header}}
=Tuesday 29th July=
=Tuesday 29th July=
-
 
==Lab Work==
==Lab Work==
-
 
+
===The frame coli Odor free===
-
===A - The frame===
+
-
 
+
====PCR====
====PCR====
''by Romain''
''by Romain''
-
StrainS used: E. coli MG1655Z1 and E. coli MG1655, and oligonucleotides used: FTR-Apra-F and FTR-Apra-R.
+
Strains used: E. coli MG1655Z1 and E. coli MG1655, and oligonucleotides used: FTR-Apra-F and FTR-Apra-R.
-
Protocol:
+
'''Protocol'''
 +
 
 +
Add into a PCR tube the following:
 +
 
 +
{| class="wikitable centre" width="50%"
 +
|+
 +
|-
 +
! scope=col | Component
 +
! scope=col | For a total volume of 50μl
 +
|-
 +
|H<sub>2</sub>O
 +
|27.25μl
 +
|-
 +
| Green GoTaq buffer 5X
 +
| 10μl
 +
|-
 +
| dNTPs
 +
| 1μl
 +
|-
 +
| FTR-Apra-F
 +
| 2μl
 +
|-
 +
| FTR-Apra-R
 +
| 2μl
 +
|-
 +
| DMSO
 +
| 1.5μl
 +
|-
 +
| MgCl<sub>2</sub>
 +
| 4μl
 +
|-
 +
| Bacterial culture
 +
| 2μl
 +
|-
 +
| Green GoTaq enzyme
 +
| 0.25μl
 +
|}
 +
 
 +
Tube was placed in PCR machine with the following parameters.
 +
 
 +
{| class="wikitable centre" width="80%"
 +
|+
 +
|-
 +
! scope=col | Cycle step
 +
! scope=col | Temperature
 +
! scope=col | Time
 +
! scope=col | Cycle
 +
|-
 +
| width="25%" |
 +
Initial denaturation
 +
| width="25%" |
 +
95°C
 +
| width="25%" |
 +
5 min
 +
| width="25%" |
 +
1
 +
|-
 +
| Denaturation
 +
| 95°C
 +
| 30 s
 +
| 30
 +
|-
 +
| Annealing
 +
| 60°C
 +
| 30 s
 +
| 30
 +
|-
 +
| Extension
 +
| 72°C
 +
| 2 min
 +
| 30
 +
|-
 +
| Final extension
 +
| 72°C
 +
| 5 min
 +
| 1
 +
|-
 +
| Final extension
 +
| 12°C
 +
| hold
 +
| 1
 +
|}
-
*218µl of H20 MilliQ
+
The different bacterial cultures in each tubes:
-
*80µl GoTaq buffer 5X
+
-
*16µl oligonucleotide FTR-Apra-F (10mM)
+
-
*16µl oligonucleotide FTR-Apra-R (10mM)
+
-
*12µl DMSO 10mM
+
-
*32µl MgCl2 (25mM)
+
-
*8µl dNTP (10mM)
+
-
*2µl of GoTaq enzyme
+
-
*2µl of different bacterial cultures in each tubes:
+
#Tube 1: MG1655Z1 10I
#Tube 1: MG1655Z1 10I
Line 30: Line 101:
#Tube 7: MG1655Z1 10I positive control with plasmid
#Tube 7: MG1655Z1 10I positive control with plasmid
-
====Electrophoresis====
+
Results of the PCR: The electrophoresis revealed nothing
-
''by Fabio & Romain''
+
-
'''Members there''':
+
New PCR with different enyme.
-
* Instructors and advisors: Alice, Solenne and Sylvie.
+
-
* Students: Arnaud, Fabio, Romain, Sean and Terry.
+
-
===C - Lemon scent===
+
Strains used: MG1655 and MG1655Z1, and oligonucleotides used: FTR-Apra-F and FTR-Apra-R.
 +
 
 +
'''Protocol'''
 +
 
 +
Add into a PCR tube the following:
 +
 
 +
{| class="wikitable centre" width="50%"
 +
|+
 +
|-
 +
! scope=col | Component
 +
! scope=col | For a total volume of 50μl
 +
|-
 +
|H<sub>2</sub>O
 +
|37.25μl
 +
|-
 +
| DreamTaq buffer 10X
 +
| 5μl
 +
|-
 +
| dNTPs
 +
| 1μl
 +
|-
 +
| FTR-Apra-F
 +
| 1μl
 +
|-
 +
| FTR-Apra-R
 +
| 1μl
 +
|-
 +
| DMSO
 +
| 2.5μl
 +
|-
 +
| Bacterial culture
 +
| 2μl
 +
|-
 +
| DreamTaq enzyme
 +
| 0.25μl
 +
|}
 +
 
 +
Tube was placed in PCR machine with the following parameters.
 +
 
 +
{| class="wikitable centre" width="80%"
 +
|+
 +
|-
 +
! scope=col | Cycle step
 +
! scope=col | Temperature
 +
! scope=col | Time
 +
! scope=col | Cycle
 +
|-
 +
| width="25%" |
 +
Initial denaturation
 +
| width="25%" |
 +
95°C
 +
| width="25%" |
 +
5 min
 +
| width="25%" |
 +
1
 +
|-
 +
| Denaturation
 +
| 95°C
 +
| 30 s
 +
| 30
 +
|-
 +
| Annealing
 +
| 60°C
 +
| 30 s
 +
| 30
 +
|-
 +
| Extension
 +
| 72°C
 +
| 2 min
 +
| 30
 +
|-
 +
| Final extension
 +
| 72°C
 +
| 5 min
 +
| 1
 +
|-
 +
| Final extension
 +
| 12°C
 +
| hold
 +
| 1
 +
|}
 +
 
 +
#Tube 1: MG1655Z1 10I
 +
#Tube 2: MG1655 100II
 +
#Tube 3: MG1655 50I
 +
#Tube 4: MG1655 100I
 +
#Tube 5: MG1655Z1 10II
 +
#Tube 6: MG1655 50II
 +
#Tube 7: MG1655Z1 10I positive control with plasmid
 +
 
 +
Results of the PCR: The electrophoresis revealed successfully the DNA!
 +
 
 +
===Salicylate Inducible Suppressing System===
 +
====Digestion====
 +
''by Fabio''
 +
 
 +
After the experiments done [https://2014.igem.org/Team:Paris_Saclay/Notebook/July/28#C_-_Salicylate_Inducible_Suppressing_System yesterday], we are sure to manipulate the right plasmid from both BioBricks and also that we have a good concentration of them. Now it's time to start the [http://parts.igem.org/Help:Assembly/3A_Assembly Assembly procedure] in order to concatenate both BioBricks.
 +
 
 +
* BioBrick '''BBa_J61051''' (Salicylate promoter + NahR) as '''Part A'''
 +
* BioBrick '''BBa_K228001''' (RNA suppressor) as '''Part B'''
 +
 
 +
The enzymes used were:
 +
 
 +
* '''EcoRI''' and '''SpeI''' for '''BBa_J61051'''
 +
* '''PstI''' and '''XbaI''' for '''BBa_K228001'''
 +
 
 +
<font color="#F00">TODO: Illustration of the process</font>
 +
 
 +
[https://2014.igem.org/Team:Paris_Saclay/Protocols/BioBrick_Assembly#Digest_reaction BioBrick Assembly - Digest Reaction Protocol]
 +
 
 +
====Segregate Process by Electrophoresis====
 +
[[File:LU000107a.jpg|right|300px]]
 +
[[File:RL007744.jpg|right|300px]]
 +
''by Fabio''
 +
 
 +
First we tested both products of the digestions in order to verify the success of the reaction (''Process A''), which remained for 25 minutes in 100V. Once the sizes of the digestion's products confirmed, we did the ''Process B'' (1 hour in 100V) in order to segregate a good amount of DNA to the next step.
 +
 
 +
'''''Process A'''''
 +
# BBa_J61051
 +
# BBa_K228001
 +
 
 +
'''''Process B'''''
 +
# BBa_J61051 ''strains from the bottom band of '''process A'''''
 +
 
 +
'''Results:'''
 +
*'''A''' #1: Success, we can clearly see the vector and the core of the BioBrick after the digestion.
 +
*'''A''' #2: Success, the digested BioBrick was cut one time and has the expected size.
 +
*'''B''': Success, we have a very good concentration of the BBa_J61051's core.
 +
 
 +
[https://2014.igem.org/Team:Paris_Saclay/Protocols/BioBrick_Assembly#Segregate_process BioBrick Assembly - Segregate Process Protocol]
 +
 
 +
===Lemon scent===
 +
====Transformation of electrocompetent cells====
 +
''by Arnaud & Terry''
 +
 
 +
Strain used: DY330. Plasmid used: pJBEI-6409 (code for enzymes to produce limonene from glucose in E. coli)
 +
 
 +
Make 2 électroporations in cold electroporation cuvettes:
 +
 
 +
*A control cuvette(without DNA): 50µl of DY330.
 +
*A second cuvette: 50µl of DY330 culture + 1µl of pJBEI-6409 plasmid.
 +
 
 +
Electroporation : 2500V, 132W, 40µF.
 +
 
 +
After that, add 1ml of cold LB in each cuvette and transfer in 2 tubes to incubate during 1 to 2h at 30°C.
 +
 
 +
Spread on 4 dishes LB + Cm:
 +
 
 +
*100µl of control (without plasmid)
 +
*50µl of transformed DY330 with pJBEI-6409
 +
*100µl of transformed DY330 with pJBEI-6409
 +
*The rest of transformed DY330 with pJBEI-6409 (concentrate in approximately 150µl)
 +
 
 +
Incubate for the weekend at 30°C.
====PCR of BBa_K762100====
====PCR of BBa_K762100====
Line 78: Line 299:
|}
|}
-
[https://2014.igem.org/Team:Paris_Saclay/Notebook Back to the calendar]
+
Tube was placed in PCR machine with the following parameters.
 +
 
 +
{| class="wikitable centre" width="80%"
 +
|+
 +
|-
 +
! scope=col | Cycle step
 +
! scope=col | Temperature
 +
! scope=col | Time
 +
! scope=col | Cycle
 +
|-
 +
| width="25%" |
 +
Initial denaturation
 +
| width="25%" |
 +
98°C
 +
| width="25%" |
 +
1 min
 +
| width="25%" |
 +
1
 +
|-
 +
| Denaturation
 +
| 98°C
 +
| 15 s
 +
| 25 - 30
 +
|-
 +
| Annealing
 +
| 55°C
 +
| variable
 +
| 25 - 30
 +
|-
 +
| Extension
 +
| 72°C
 +
| 45 s
 +
| 25-30
 +
|-
 +
| Final extension
 +
| 72°C
 +
| 10 min
 +
| 1
 +
|-
 +
| Final extension
 +
| 8°C
 +
| hold
 +
| 1
 +
|}
 +
 
 +
 
 +
==Photo of the Day==
 +
[[File:Paris Saclay 29_july.jpg|600px|center]]
 +
 
 +
'''Members there''':
 +
* Instructors and advisors: Alice, Solenne and Sylvie.
 +
* Students: Arnaud, Fabio, Romain, Sean and Terry.
 +
{{Team:Paris_Saclay/notebook_footer}}

Latest revision as of 15:44, 14 October 2014

Contents

Tuesday 29th July

Lab Work

The frame coli Odor free

PCR

by Romain

Strains used: E. coli MG1655Z1 and E. coli MG1655, and oligonucleotides used: FTR-Apra-F and FTR-Apra-R.

Protocol

Add into a PCR tube the following:

Component For a total volume of 50μl
H2O 27.25μl
Green GoTaq buffer 5X 10μl
dNTPs 1μl
FTR-Apra-F 2μl
FTR-Apra-R 2μl
DMSO 1.5μl
MgCl2 4μl
Bacterial culture 2μl
Green GoTaq enzyme 0.25μl

Tube was placed in PCR machine with the following parameters.

Cycle step Temperature Time Cycle

Initial denaturation

95°C

5 min

1

Denaturation 95°C 30 s 30
Annealing 60°C 30 s 30
Extension 72°C 2 min 30
Final extension 72°C 5 min 1
Final extension 12°C hold 1

The different bacterial cultures in each tubes:

  1. Tube 1: MG1655Z1 10I
  2. Tube 2: MG1655 100II
  3. Tube 3: MG1655 50I
  4. Tube 4: MG1655 100I
  5. Tube 5: MG1655Z1 10II
  6. Tube 6: MG1655 50II
  7. Tube 7: MG1655Z1 10I positive control with plasmid

Results of the PCR: The electrophoresis revealed nothing

New PCR with different enyme.

Strains used: MG1655 and MG1655Z1, and oligonucleotides used: FTR-Apra-F and FTR-Apra-R.

Protocol

Add into a PCR tube the following:

Component For a total volume of 50μl
H2O 37.25μl
DreamTaq buffer 10X 5μl
dNTPs 1μl
FTR-Apra-F 1μl
FTR-Apra-R 1μl
DMSO 2.5μl
Bacterial culture 2μl
DreamTaq enzyme 0.25μl

Tube was placed in PCR machine with the following parameters.

Cycle step Temperature Time Cycle

Initial denaturation

95°C

5 min

1

Denaturation 95°C 30 s 30
Annealing 60°C 30 s 30
Extension 72°C 2 min 30
Final extension 72°C 5 min 1
Final extension 12°C hold 1
  1. Tube 1: MG1655Z1 10I
  2. Tube 2: MG1655 100II
  3. Tube 3: MG1655 50I
  4. Tube 4: MG1655 100I
  5. Tube 5: MG1655Z1 10II
  6. Tube 6: MG1655 50II
  7. Tube 7: MG1655Z1 10I positive control with plasmid

Results of the PCR: The electrophoresis revealed successfully the DNA!

Salicylate Inducible Suppressing System

Digestion

by Fabio

After the experiments done yesterday, we are sure to manipulate the right plasmid from both BioBricks and also that we have a good concentration of them. Now it's time to start the [http://parts.igem.org/Help:Assembly/3A_Assembly Assembly procedure] in order to concatenate both BioBricks.

  • BioBrick BBa_J61051 (Salicylate promoter + NahR) as Part A
  • BioBrick BBa_K228001 (RNA suppressor) as Part B

The enzymes used were:

  • EcoRI and SpeI for BBa_J61051
  • PstI and XbaI for BBa_K228001

TODO: Illustration of the process

BioBrick Assembly - Digest Reaction Protocol

Segregate Process by Electrophoresis

LU000107a.jpg
RL007744.jpg

by Fabio

First we tested both products of the digestions in order to verify the success of the reaction (Process A), which remained for 25 minutes in 100V. Once the sizes of the digestion's products confirmed, we did the Process B (1 hour in 100V) in order to segregate a good amount of DNA to the next step.

Process A

  1. BBa_J61051
  2. BBa_K228001

Process B

  1. BBa_J61051 strains from the bottom band of process A

Results:

  • A #1: Success, we can clearly see the vector and the core of the BioBrick after the digestion.
  • A #2: Success, the digested BioBrick was cut one time and has the expected size.
  • B: Success, we have a very good concentration of the BBa_J61051's core.

BioBrick Assembly - Segregate Process Protocol

Lemon scent

Transformation of electrocompetent cells

by Arnaud & Terry

Strain used: DY330. Plasmid used: pJBEI-6409 (code for enzymes to produce limonene from glucose in E. coli)

Make 2 électroporations in cold electroporation cuvettes:

  • A control cuvette(without DNA): 50µl of DY330.
  • A second cuvette: 50µl of DY330 culture + 1µl of pJBEI-6409 plasmid.

Electroporation : 2500V, 132W, 40µF.

After that, add 1ml of cold LB in each cuvette and transfer in 2 tubes to incubate during 1 to 2h at 30°C.

Spread on 4 dishes LB + Cm:

  • 100µl of control (without plasmid)
  • 50µl of transformed DY330 with pJBEI-6409
  • 100µl of transformed DY330 with pJBEI-6409
  • The rest of transformed DY330 with pJBEI-6409 (concentrate in approximately 150µl)

Incubate for the weekend at 30°C.

PCR of BBa_K762100

by Sean

Oligonucleotides used: iPS66, iPS67

Oligonucleotides were diluted twice from 100µM to 50µM.

Protocol

Add into a PCR tube the following:

Component For a total volume of 50μl
H2O 35.5μl
Phusion buffer 5X 10μl
dNTPs 1μl
iPS66 1μl
iPS67 1μl
BBa_K762100 1μl
Phusion DNA polymerase 0.25μl

Tube was placed in PCR machine with the following parameters.

Cycle step Temperature Time Cycle

Initial denaturation

98°C

1 min

1

Denaturation 98°C 15 s 25 - 30
Annealing 55°C variable 25 - 30
Extension 72°C 45 s 25-30
Final extension 72°C 10 min 1
Final extension 8°C hold 1


Photo of the Day

Paris Saclay 29 july.jpg

Members there:

  • Instructors and advisors: Alice, Solenne and Sylvie.
  • Students: Arnaud, Fabio, Romain, Sean and Terry.

Back to the calendar

Retrieved from "http://2014.igem.org/Team:Paris_Saclay/Notebook/July/29"