Paris/July 16
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== Growth kinetics of w121 strain == | == Growth kinetics of w121 strain == | ||
Results of the previous day : we lost everything because of a crash of the computer :(. | Results of the previous day : we lost everything because of a crash of the computer :(. | ||
| + | == Transduction of MG1655 with P1 stock made on w121 == | ||
| + | * Control (1mL LB MgSO4 30mM; CaCl2 15mM) | ||
| + | * 5µL Phage + 900µL LB (MgSO4 30mM; CaCl2 15mM) + 100µL MG1655 Culture ON | ||
| + | * 50µL Phage + 900µL LB (MgSO4 30mM; CaCl2 15mM) + 100µL MG1655 Culture ON | ||
| + | * 500µL Phage + 500µL LB (MgSO4 30mM; CaCl2 15mM) + 100µL MG1655 Culture ON | ||
| + | =>For the n<sup>th</sup> time, it is not working : we have only contaminants. | ||
Revision as of 14:59, 16 July 2007
Plasmid pKs::DGAT expression in E. Coli
We tried to see TG with NR died on E. Coli cells transfected with pKs::DGAT, an IPTG-inducible promoter.
We tried different growth media containing more or less oleate, that should in theory increase TG synthesis.
Results : we don't see the inductible effect of IPTG. We can think that :
- Either the fluorescence without IPTG is due to a leak of the promoter
- Either DGAT is not induce in presence of IPTG, and the fluorescence we see is only a background.
Growth kinetics of w121 strain
Results of the previous day : we lost everything because of a crash of the computer :(.
Transduction of MG1655 with P1 stock made on w121
- Control (1mL LB MgSO4 30mM; CaCl2 15mM)
- 5µL Phage + 900µL LB (MgSO4 30mM; CaCl2 15mM) + 100µL MG1655 Culture ON
- 50µL Phage + 900µL LB (MgSO4 30mM; CaCl2 15mM) + 100µL MG1655 Culture ON
- 500µL Phage + 500µL LB (MgSO4 30mM; CaCl2 15mM) + 100µL MG1655 Culture ON
=>For the nth time, it is not working : we have only contaminants.
