Team:Paris Saclay/Notebook/August/26
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Revision as of 08:05, 9 September 2013
Notebook : August 26
summary
- started the Restriction digestion and ligation to get the BioBrick fnr into plasmid PSB1C3 by using restrictin ensyme EcoRI and PstI.
- Sent an E-mail to M. Nesbeth from UCL for requesting the Biobrick BBa_K239005 which was created by iGEM UCL team in 2009
- Designed oligonucleotides for the gene coding for BphR2 (regulator, sensitive for PCBs), Transcriptional regulator of Pseudomonas oleovorans /pseudoalcaligenes group
lab work
- A.aero/anaerobic regulation system
- 1.BioBrick promotor fnr(repressor and activator) in plasmid PSB1C3
- Digestion for promoter fnr(repressor) in PSB1C3
- 2 enzymes SPE I and PST I
- For promoter fnr(repressor) :
DNA | 14µl |
SPE I | 2µl |
PST I | 2µl |
H2O | 0µl |
buffer | 2µl |
total | 20µl |
- For promoter fnr(activator)nirB clone 6:
DNA | 14µl |
SPE I | 2µl |
PST I | 2µl |
H2O | 0µl |
buffer | 2µl |
total | 20µl |
- For promoter fnr(activator)nark clone 6 :
DNA | 4µl |
SPE I | 2µl |
PST I | 2µl |
H2O | 10µl |
buffer | 2µl |
total | 20µl |
- For promoter fnr(activator)nirB clone 7 :
DNA | 14µl |
SPE I | 2µl |
PST I | 2µl |
H2O | 0µl |
buffer | 2µl |
total | 20µl |
- Ligation
- After 3h of digestion, we mixed the digestion products:
PCR product | 30µl |
PSB1C3 | 4µl |
Ligation buffer | 2µl |
H2O | 14µl |
- Then we performed a precipitation by ethanol in order to inactivate the enzymes. And suspended the deposit by:
mixture | control |
2µl ligation buffer | 2µl ligation buffer |
1µl ligase T4 | 1µl ligase T4+2µl PSB1C3 |
17µl H2O | 15µl H2O |
- The incubation was during 1H30.
- B.PCBs sensor system
- 1.BioBrick BphR2(regulator) in plasmid PSB1C3
- 1.BioBrick BphR2(regulator) in plasmid PSB1C3
- Using software gene manager to find the oligopeptide for amplification of BphR2.
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