Monday 12^th July

Lab work

Bringing 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 usual protocol adapted to get 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.

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. 100µL (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.

Visualization

Transformation of gBlock 4.2 pPS16_008

By Mathilde and Laetitia

The gBlock 4.2 in the plasmid pPS16_008 was transformed with DH5α chimio competent cells following the protocol from the 11/07/2016.

Petri dishes peparation (x3) :

• 10µL of Ampycillin (50µg/mL)
• 5µL of Xgal (0,25µL/mL)
• 2µL of IPTG (0,1µL/mL)
• 20 mL of LB+Agar

The two gBlocks constructions were plated in duplicata (50µL and 150µL), and a controle construction was plated alone. The plates were put in incubation at 37°c overnight.