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Notebook : August 9

Lab work

A - Aerobic/Anaerobic regulation system

((((((((((((((((((((====1 - Obtaining Δ fnr E. coli strain by transduction to test our biobricks====

Abdou, Anais, Damir, Nadia, XiaoJing

We do the exprience again because the lysis made on wensday didn't happen. It's probably because the phage strain was too old ( 2001)

Protocol : transduction

Picture: lysed cells comparison.

0µl phage(control): the petri dish is cloudy, bacteria are not lysed.
50µl phage: the petri dish is clear, bacteria are lysed by phages.
We used a wild type strain to keep a stock and a Δ fnr E. coli strain to obtain phages that might have encapsidated a Δfnr::Km fragment.

10µl,50µl and 100µl petri dishes are clear so phages are multiplied.

We let the antibiotic over night to select the right strain. ))))))))))))))))))))))

Objective : obtaining Bba_K1155007

1 - Extraction of Bba_K115007 from DH5α

Abdou

Protocol : Hight copy plamid extraction

We used colonies number 10, 14 and 15.

Nanodrop

Bba_K1155007 in clone 10 : 38ng/µl
Bba_K1155007 in clone 14 : 48.5ng/µl
Bba_K1155007 in clone 15 : 52 ng/µl

the extraction was good. We will sequence our plasmid.

A - Aerobic/Anaerobic regulation system / B - PCB sensing system

Objective : Obtaining FNR and BphR2 proteins

1 - Electrophoresis of the PCR of BphR2 Part I, BphR2 Part II, RBS_BphR2 Part I, FNR Part I, FNR Part II, RBS_FNR Part I to check the gel purification

IMAGE

Well 1 : 6µL DNA Ladder
Well 2 : 5µL of BphR2 Part I+1µl of 6X loading dye
Well 3 : 5µL of BphR2 Part II+1µl of 6X loading dye
Well 4 : 5µL of RBS-BphR2 Part I+1µl of 6X loading dye
Well 5 : 5µL of FNR Part I+1µl of 6X loading dye
Well 6 : 5µL of FRN Part II+1µl of 6X loading dye
Well 7: 5µL of RBS-FNR Part I+1µl of 6X loading dye
Gel : 0.8%

Expected size :

BphR2 Part I :
BphR2 Part II :
RBS-BphR2 Part I :
FNR Part I :
FNR Part II :
RBS-FNR PartI :

We lost all our PCR fragments. We will do the PCR again.

2 - PCR of BphR2 Part I, BphR2 Part II, RBS-BphR2 Part I, FNR Part I, FNR Part II, RBS-FNR Part I

Anaïs, Damir, Nadia, XiaoJing

Used quantities :

Bphr2 Part I :
- Oligo 54F : 1µL
- Oligo 55R : 1µL
- Buffer Phusion : 10µL
- DNA of Pseudomonas pseudoalcaligenes : 1µL
- dNTP : 1µL
- Phusion : 0.5µL
- H2O : 35.5µL

Bphr2 Part II :
- Oligo 56F : 1µL
- Oligo 57R : 1µL
- Buffer Phusion : 10µL
- DNA Pseudomonas pseudoalcaligenes : 1µL
- dNTP : 1µL
- Phusion : 0.5µL
- H2O : 35.5µL

RBS-Bphr2 Part I :
- Oligo 58F : 1µL
- Oligo 57R : 1µL
- Buffer Phusion : 10µL
- DNA Pseudomonas pseudoalcaligenes : 1µL
- dNTP : 1µL
- Phusion : 0.5µL
- H2O : 35.5µL

FNR Part I :
- Oligo 59F : 1µL
- Oligo 60R : 1µL
- Buffer Phusion : 10µL
- DNA Escherichia coli : 1µL
- dNTP : 1µL
- Phusion : 0.5µL
- H2O : 35.5µL

FNR Part II :
- Oligo 61F : 1µL
- Oligo 62R : 1µL
- Buffer Phusion : 10µL
- DNA Escherichia coli : 1µL
- dNTP : 1µL
- Phusion : 0.5µL
- H2O : 35.5µL

RBS-FNR Part I :
- Oligo 63F : 1µL
- Oligo 62R : 1µL
- Buffer Phusion : 10µL
- DNA Escherichia coli : 1µL
- dNTP : 1µL
- Phusion : 0.5µL
- H2O : 35.5µL

PCR Program :

BphR2 Part I, BphR2 Part II, RBS-BphR2 Part I :

FNR Part I, FNR Part II, RBS-FNR Part I :

@@ Line 35: / Line 35: @@
 Abdou
-Protocol : [[Team:Paris_Saclay/Protocols/Hight copy plamid extraction|Hight copy plamid extraction]]
+Protocol : [[Team:Paris_Saclay/extraction|Hight copy plamid extraction]]
 We used colonies number 10, 14 and 15.
@@ Line 48: / Line 48: @@
 the extraction was good. We will sequence our plasmid.
 |}
 ==='''A - Aerobic/Anaerobic regulation system / B - PCB sensing system'''===

Team:Paris Saclay/Notebook/August/9