Team:Ionis Paris/10 06 16
To test the competency of the BL21 cells done on the 09/06/16 with the stock of pSB1C3-RFP plasmid. Plasmid DNA : pSB1C3-RFP at 200 pg/µL BL21 competent cells (See 09/06/16) Petri dish LB+Cm: Cm concentration = 25 µg/mL Thaw 1 tube of BL21 competent cells on ice for 10 min. Mix gently and carefully pipette 50 µL of cells into 2 transformation tubes on ice. Add 1 µL (200 pg) of plasmid DNA to the cell mixture. Carefully flick the tube 4-5 times to mix cells and DNA. Do not vortex. Place the mixture on ice for 30 min. Do not mix. Heat shock at exactly 42°C for 30 s. Do not mix. Place on ice for 5 min. Do not mix. Pipette 950 µL of room temperature SOC into the mixture. Place at 37°C for 60 min at 250 rpm. Warm selection plates to 25°C. Mix the cells thoroughly by flicking the tube and inverting. Spread 100 µL of each dilution (100%,10%,1%) onto a selection plate. Pellet the remaining cells (except for the control), discard mostly all the supernatant and resuspend the remaining cells in 100 µL of LB. Spread 100 µL onto a selection plate. Incubate all the plates O/N at 37°C. Some colonies on the petri dishes LB+Cm plated with 1% of transformed bacteria, more with 10%, a lot with 100% and a bacterial lawn with the pellet. Obtained results: The transformation worked, as we obtained satisfying results. Colonies contain a plasmid with the Chloramphenicol resistance gene, present in pSB1C3. The BL21 cells are therefore competent.
Transformation efficiency test : Competent BL21 cells with pSB1C3-RFP plasmid
Objectives
Materials
Protocol
Results
Expected results :
A bacterial lawn is expected on the LB petri dish plated with pSB1C3-RFP (+ control).
No colony is expected on the 2 petri dishes plated with no plasmid (- control).
All obtained colonies are expected to be red because of the RFP gene that codes for a red fluorescent protein.
We obtained expected results.Interpretation
