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Team:BYU Provo/Notebook/CholeraDetection/Summerexp/Period5/Dailylog
From 2013.igem.org
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8/19/2013
We verified the PCR of RecA and cleaned it up. We were out of pIG12, so we did a plasmid prep of that and a digestion of the two. After we electroporate a plasmid into TT9907, we do see a few plaques. Perhaps if we perform an electroporation and then assay many colonies, we could find one that has taken up the plasmid AND remains vulnerable to lambda. We performed an electroporation today; in the next few days we’ll grow up many colonies and run a plaque assay. KK, KP
8/20/13
BIG news, or at least potentially big news: we believe that plating 9907 adjacent to cholera causes bacteriophage lambda to enter the lytic cycle! I was researching more to do with the RecA SOS pathway in E.Coli when I stumbled across and abstract that communicated evidence that high concentration of AHLs, homoserine lactones, cause lambda to enter the lytic cycle. Since AHLs are the molecules used in quorum sensing, and V.cholerae also releases them, I thought it might be possible that plating 9907 next to cholerae would trigger lambda to go lytic. I streaked a line of TT9907 next to a patch of cholera that I had grown for several days (we’ve noticed that it takes several days to get solid biofilm growth), and then another line away from cholera. The line perpendicular to and running away from cholera grew, while the streak adjacent to cholera did not! See the photo. Now – we need to verify that the cells don’t grew because lambda is killing them, and not because cholera secretes some toxin that does that. This opens a new avenue of possibilities. We need to discuss things with Dr. Grose, but probably we will abandon the idea of transforming a plasmid into TT9907. It took about 4 hours, but today I set up the experiment to test whether any of the post electroporation colonies retains the ability to be lysed by lambda. We grew up overnights from 40 colonies! The overnights were ready today, so prepared 40 top agar lawns and added a drop of H202 in the middle to stress lambda to lyse, should lambda still be a dormant lysogen in our host cell. We should see the results of the test tomorrow. We ran the digested RecA and pIG12 backbone vector on a low-melt gel. Under UV light we cut out a distinct band for RecA. It is ready for ligation. The plasmid, however, was smeared. Clarice is going to re-digest and re-run pIG12. KK, KP
8/23/13
We transformed pIG90 (RecA with a pIG12 backbone) into chemically competent cells via heat shock transformation. Dr. Grose thinks it would be best if at this point, the two cholera sub-groups united into one project. We began working with Nathan and Michael to purify biofilm-degrading enzymes. Work has been met with plenty of obstacles for them. Specifically, they are trying to PCR amplify a gene called dispersinB (DspB). They received the template from an iGEM team in France, successfully PCR-ed the gene, and performed a restriction digest. However, something went wrong and running the digested PCR on a low melt, they didn’t see a band. Since then, they had to re-PCR … but the tube with template DNA was misplaced! They’ve had to use a cleaned-up PCR as their template, but they haven’t been able to copy the gene. Michael and I started a reaction for DspB. KK, KP
8/26/13
Visualized on a gel, the DspB PCR smeared miserably along the length of its well. Tomorrow we’ll set up the reaction again. KK, KP
8/27/13
We performed PCR of DspB again using a cleaned-up PCR that Whitney did a while back. Hopefully we don’t see the same result as the last PCR reaction. KK, KP
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