Lab Notebook

19 August 2009

Tim Weenink

After yesterdays horrible discovery that the I-SceI Homing Endonuclease we got from MIT was actually T4 DNA ligase we had to adjust our cloning strategy. The more primitive part without promoter was found to be the correct one, except that is was assembled with part !A instead of p(LacI). So we did that assembly again today. With p(LacI) from the delay team upstream, *T1 (downstream) and backbone pSB1C3 (also from the delay team). Both RbCl chemically comp and EC electrocomp cells were transformed.

Saeed

!Fr1n downstream will be purified from the gel by gel extraction and used for the new stategy as Tim mentioned before.

Daniel

Digestion of biobricks:

Assemblies 1A, 2A, 3A, 4A, 5A and 6A

Transformation and culture in plates and tubes

Calin

Good results on the conjugation test. All plates were imaged on the safe imager with the 5 Megapixel camera. Colony counting was done with [http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1770926 Clono-Counter].

For the trbK conjugation test:

also 3 positive control plates with no TrbK expression.

This successfully shows a reduction in the conjugation efficiency by four orders of magnitude when the entry exclusion protein is expressed.

For the oriTR conjugation test:

This shows that Conjugation Plasmid 1 is successfully transmitted but with a lower efficiency in the presence of R751.

Attempted 2nd knockout

Made 4 0.5xKAN plates, 2 0.1xKAN plates, 2 1xTRI plates and 2 5mL tubes with 0.5xKAN.

Started centrifuging when R751 was at OD 0.507.

Used 7 μL oriTR_PCR_KO vector for oriTR electroporation and 12 μL trbK_KO_PCR vector for trbK electroporation. Both time constants 3.7. In incubator at 4:13 pm.

Modifications made to protocol:

• Arabinose added the night before
• used 4 mL from the 5 mL culture, higher density of cells in elctroporation
• used 10% glycerol in the last spin down step