Team:British Columbia/Notebook QS

Electroporation protocol for S. aureus RN4220

1. Remove competent cells (70uL aliquots) from -80C and thaw on ice for 30 minutes
2. Add ligation mix (1ug of DNA)
3. Incubate on ice for 30 minutes
4. Transfer 60uL of cell suspension-DNA mixture to 0.1cm gap electroporation cuvette. Make sure the cuvettes are on ice prior to this.
5. Cells and DNA electroporated at 20C, 100ohm resistance, 25uF capacitance (optimum time constant = 2.5ms), and 2.3kV in a Gene Pulser apparatus with pulse controller.
6. Place cells on ice and immediately resuspend in 940uL of B2 broth.
7. Transfer cells, DNA, and broth to eppendorf microcentrifuge tube. Make sure microcentrifuge tubes were previously on ice.
8. Incubate for at least 2 hours at 37C.
9. Plate on Tryptic Soy Agar (TSA) or NYE agar with appropriate antibiotic. In this case, erthrymycin.
10. Incubate plates at 37C for 48 hours.

Lessons Learned

1. The 3-A method usually works. However, some parts seem harder to join to other parts. In the case of P2 (BBa_I764104), it took 4-5 times as long as expected to join it to 2 different GFP constructs. We haven't found a fix to this problem, even after varying several variables: insert:vector ratio, ligation volume, and changing ligase buffer.

2. PCR is a very good technique for verifying inserts. It is not so good for verifying small inserts (e.g. RBS) since the band would barely change. Sometimes, even when the PCR does not show correct bands, further restriction digests and sequencing yields the correct insert.

3. It is possible to clone genes directly from non-purified bacterial DNA. Simply pick a colony of cells containing the desired gene in the genome. This is of course harder to do than plasmid DNA. We've found that addition of DMSO (5-10%) helps the PCR (by presumably allowing primers and reagents to better reach the desired gene). This is true in the case of agrAC, where PCR was unsuccessful without the addition of DMSO.

4. Don't try to measure PCR product concentration using spectrophotometry right after a PCR. The concentration before and after reaction is basically the same because dNTP's also absorb similarly to strands of DNA. After purification, do measure DNA concentration.

5. Don't be afraid of going to the lab and start working. The best way to learn is through practice and troubleshooting. It also helps build up a good work flow.

6. Use polymerases with error checking ability (e.g. Phusion) when cloning genes.

7. Check antibiotics before using them.

8. DNA is incredibly stable. DNA stocks will last a long time when stored properly, even in water.

9. Don't be afraid of asking for help or asking to use other lab groups' equipment.

10. DNA purification kits don't always work very well. Do check with a nanodrop or other method. Pay close attention to contaminants absorbing at other wavelengths (large peak), as this can fool the machine into thinking there is DNA.

11. Always sequence constructs if possible, even if simply joining 2 registry parts together. It is the only way to be sure the right parts have joined and reduces panic when parts do not work as expected.

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