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From 2008.igem.org

Friday, 20 June

• Taylor Stevenson:
  • Lysis Assay of VCS257 SupA+
  1. Cells were grown O/N @ 37*C in Lambda media.
  2. 4.5mL culture was infected with 4.5uL of phage packaging product from November, 2007 and allowed to incubate for 20min @ 37*C shaking @ 250 rpm.
  3. Infected culture was heat shocked @ 42*C for 20min, inducing lysis by denaturing the CI857 repressor.
  4. Cells were then grown and their optical density was measured at different time points after heat shock.
  • Lysogeny Screen
  1. Result-An infected VCS257 culture was streaked onto LB-agar. Isolated colonies were used to innoculate a 96 deep-well plate which was grown O/N @ 30*C shaking @ 300rpm. Using the well replicator, each of the wells was spotted onto two large petri dishes. One dish was grown @ 30*C and the other was grown @ 42*C O/N. Spots that grew on 30*C plates and not on 42*C plates are lysogens as the phage infected cells would lyse due to the temperature sensitive cI. The plates show that there is only one colony that could be a possible lysogen.
  2. The possible lysogen colony was streaked onto LB plates to be grown O/N @ 30*C and 42*C to verify temperature screen.
  3. A colony PCR was performed on the possible lysogen using the CroF and CroR primers. If a copy of the lambda genome is incorporated into the lysogen's, the PCR should result in amplification of the phage gene cro and produce a 400bp product. Additionally, three other PCR reactions were performed in parallel.
     1. -negative control using water
     2. -positive control using lambda DNA
     3. -second sample using lambda particles from stocks

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