Team:Paris Saclay/Notebook/July/25
From 2014.igem.org
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- | 8 liquid cultures | + | To insure a resonate quantity of DNA, we made two liquid cultures from each box of the [https://2014.igem.org/Team:Paris_Saclay/Notebook/July/24#Transformation_of_competent_E.coli_cells last process], resulting in a total of 8 liquid cultures composed by 5ml of LB, 5µl of Amp, and respective colonies (4 with '''BBa_J61051''' and 4 with '''BBa_K228001''') (at 9am - 37°C - 150 rpm). |
+ | |||
+ | The cultures number 1 and 3 were collect from concentrated colonies' boxes and number 2 and 4, from undiluted colonies' boxes. At the end of the process, tubes 1 and 3 resulted in BioBricks' clones 1 and tubes 2 and 4, BioBricks' clones 2. | ||
==Reunion== | ==Reunion== |
Revision as of 15:30, 29 July 2014
Contents |
Friday 25th July
Lab work
? - ????
PCR on odor-free E. coli
by Sean
We want to be sure that the odor-free E. coli really is E. coli. We will use a postitive control.
Protocol
C - Lemon scent
Results PCR targeting
by Romain
After the night, the electrophoresis revealed the oligonucleotides iPS70 and iPS71 prepared with the GoTaq enzyme.
We made a PCR Clean-up. Protocol
After that, we made another electrophoresis which revealed successfully the purification.
Preparation of electrocompetent cells
by Romain
Strain used: DY330.
Protocol:
Dilution of 300µl of bacterial culture DY330 in 30ml of LB at 30°C.
When the culture OD650 = 0,6:
- put in ice during 10min.
- centriguge at 4°C, 5min, 4000rpm.
- Discard the supernatant, and resuspend the pellet in 30ml glycerol 10% COLD.
- centriguge at 4°C, 5min, 4000rpm.
- Discard the supernatant, and resuspend the pellet in 15ml glycerol 10% COLD.
- centriguge at 4°C, 5min, 4000rpm.
- Discard the supernatant, and resuspend the pellet in 200µl glycerol 10% COLD.
Transformation of electrocompetent cells
by Romain
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.
E - Salicylate Inducible Suppressing System
Bacterial culture:
by Fabio
To insure a resonate quantity of DNA, we made two liquid cultures from each box of the last process, resulting in a total of 8 liquid cultures composed by 5ml of LB, 5µl of Amp, and respective colonies (4 with BBa_J61051 and 4 with BBa_K228001) (at 9am - 37°C - 150 rpm).
The cultures number 1 and 3 were collect from concentrated colonies' boxes and number 2 and 4, from undiluted colonies' boxes. At the end of the process, tubes 1 and 3 resulted in BioBricks' clones 1 and tubes 2 and 4, BioBricks' clones 2.
Reunion
With Arnaud, Fabio, Sean, Terry, Alice, Solenne, Sylvie & Philippe
Members present:
- Instructors and advisors: Solenne.
- Students: Arnaud, Fabio, Juliette, Pierre, Romain, Sean and Terry.