Team:BYU Provo/Notebook/CholeraDetection/Fallexp/Period2/Dailylog

9/16/13

On Saturday we checked our bacteriophage spot test for plaques, but we saw none. Our bacteriophage lambda purification procedure failed. Dr. Grose thinks that inducing lambda to lysis by 43 degree heat shock must not have been sufficient stress. Since we know H202 does induce our phage, we're going to attempt to isolate bacteriophage lambda by doing a top agar plaque assay with a drop of hydrogen peroxide, then bathing the top agar in LB, sucking it all up and then purifying the bacteriophage by chloroform lysis procedure.

Clarice has been working on submitting parts to the registry. She has cloned the Ydiv gene into the iGEM backbone to submit the part; we purified the plasmid for submission.

KK, KP, CH

9/18/13

9/20/13

The electroporation transformation of pIG96 (iGEM backbone with YdiV/GFP insert) into mutant E.Coli lacking SdiA (the membrane receptor that detects cholera's AHL) yielded many colonies, four of which we streaked onto a plate for to sequence verify the plasmid.

We found the frozen strain of E.Coli K12, which we streaked today. Tomorrow we'll electroporate pIG96 into it.

The Children's Book has been distributed to all team members. All team members are to find three or four families with little children to whom they can administer the pre and post test.

We purified bacteriophage lambda from top agar plaque assay plates by flooding them with LB, the plates sit for 1 hour, then sucking the liquid up and using a chloroform lysis procedure to kill all remaining cells, and separation by centrifugation for 10 minutes at 8000 rpm. Spot tests will confirm tomorrow whether or not we actually isolated the bacteriophage.

Clarice re-transformed pIG91+SdiA ligation into DH5alpha. Four the fourth time haha. From yesterday's transformation we saw two white colonies, which we think indicates a successful ligation of the insert into the vector, but as a safeguard, Clarice redid the transformation today.