Wednesday 29^th June

Lab work

Visualization

Culture of clones with gBlocks

By Lea and Marion

6 clones of each construction were selected and grown overnight in 3.5mL of LB (50µg/ml Amp) at 37°C, 180rpm.

BioBrick characterization

BL21 electro-competent cells preparation

By Charlene

200µL of BL21 pre-culture was added to 15mL of LB and incubated for 4h at 37°C. When abs_600nm=0.68, cells were centrifuged for 10 minutes at 4000rpm and washed twice with addition of 10mL glycerol (10%) followed by 10 minutes of centrifugation at 4000rpm. Cells were mixed with 200µL glycerol and kept -80°C.

BL21 electro-competent cells transformation

By Charlene

We realized four transformations with the following plasmids:

• K1372001
• K1372001+pcl_TAA
• K1372001+pcl_TAG
• K1372001+pcl_Tq

50µL of cells were added in the cuvettes with 1µL DNA (diluted 1/10). Everything was done at 4°C.

Transformation did not work for K1372001 and K1372001+pcl_TAA because the cuvettes were broken. Template:Font color. Cells died during transformation. Transformation worked for K1372001+pcl_TAG and K1372001+pcl_Tq. Template:Font color. We added 1mL of LB to the cells and incubated them for 1h at 37°C.

The following cells were plated on Petri dishes (30µg/mL Cm + 50µg/mL streptomycin):

• BL21|K1372001+pcl_TAG : 50µL of transformed cells
• BL21|K1372001+pcl_TAG : 500µL of transformed cells concentrated 5x.
• BL21|K1372001+pcl_Tq : 50µL cells
• BL21|K1372001+pcl Tq : 500µL of transformed cells concentrated 5x.

K1372001 plasmid digestion

By Naiane

K1372001 plasmid was digested with BglI using the following quantities: 3 µL DNA, 2µL buffer (O), 1 µL enzyme (BglI), 14µL water. The mix was incubated for 1h at 37°C and 10 min at 55°C and kept at -20°C until the gel electrophoresis was done. Fragments are expected to size 1.2kb and 2.4kb.

Bringing DNA closer

Plasmids digestion

By Naiane