Monday 12^th July

Lab work

Getting DNA closer

Amplification of DS-TDcasN-, DS-SPcasN- and pZA21 plasmids

By Caroline

Plasmids extracted the 4/07/16 were used to amplify the dCas9 needed for the get DNA closer tool and the pZA21 plasmid in which the tool will be inserted. A PCR was carry out following PCR with Q5^® High-Fidelity 2X Master Mix from the usual protocol adapted to have 50µL at the end.

Liquid culture of transformed NM, TD, ST1 and SP cas9

By Mathilde and Laetitia

Two colonies from each petri dishes were cultured in 1mL of LB and Spectinomycin (50µg/mL). Our 8 cultures were put in incubation at 37°c, 180 rpm OV.

Electrophoresis of the PCR amplification

By Caroline

5µL of the amplifications are mixed with 1µL of purple loading dye. The solutions are put into a 0.8% agarose gel and migrated for 25min.

Biobrick characterization

Electrocompetents and transformation by electroporation of BL21

By Charlene

Cells transformed on 11/07/16 grew overnight. However no colony was observed. To control if there is a bacteria transformed which was not put on Petri dish, we performed another experiment. 100 µL (500µL concentrated) of transformed bacteria for each condition, conserved at -4°C from yesterday, were split in 3 solutions :

• 30µL of bacteria + 3mL LB + Streptomycin (50µg/mL) + Chloramphenicol (30µg/mL)
• 30µL of bacteria + 3mL LB + Streptomycin (50µg/mL)
• 30µL of bacteria + 3mL LB + Chloramphenicol (30µg/mL)

Cells were incubated for 8h at 37°C, 200 RPM.

No bacteria grew so we concluded that there was a problem with the transformation.