Team:BYU Provo/Notebook/Cholera - Enzymes/July-August

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: <u> '''Cholera Detection''' </u> </font>
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We continued to have issues with washing our biofilm during the biofilm assay without losing significant portions of the biofilm. We tried several different methods and found that the most consistent way to treat the biofilm during the assay is to pellet and resuspend the biofilm with each wash, allowing us to wash our sample without losing the biofilm itself.
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[[Team:BYU_Provo/Notebook/Cholera - Enzyme/July-August/Period1/Dailylog|Daily log]]
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[[Team:BYU_Provo/Notebook/Cholera - Enzyme/July-August/Period1/Progress Report|Progress Report]] </font>
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<font size="3" font face="Calibri"> We focused these two weeks on preparing our DspB and Savinase enzymes for protein purification so we could test them in our Biofilm Assay. We ran PCRs, restriction digests, ligations, and transformations on them.</font>
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<font size="3" font face="Calibri"> We checked the transformation products from our earlier work with colony PCR, but the transformations were unsuccessful. We worked this period on trying to get our ligations and transformations to work.</font>
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[[Team:BYU_Provo/Notebook/Cholera - Enzyme/July-August/Period3/Progress Report|Progress Report]]</font>
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<font size="3" font face="Calibri"> We continued working on getting DspB and Savinase ready for protein purification. We were having so many problems with Savinase that we went back and prepared new template DNA from ''Bacillus subtilis'' to use for our Savinase enzyme. </font>
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[[Team:BYU_Provo/Notebook/Cholera - Enzyme/July-August/Period4/Progress Report|Progress Report]]</font>
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Latest revision as of 21:07, 27 September 2013


Cholera - Enzyme Notebook July - August



Cholera Enzyme
March-April
May-June
July-August
September-October
Protocols

July 1 - July 14


We continued to have issues with washing our biofilm during the biofilm assay without losing significant portions of the biofilm. We tried several different methods and found that the most consistent way to treat the biofilm during the assay is to pellet and resuspend the biofilm with each wash, allowing us to wash our sample without losing the biofilm itself.


Daily log


Winter2.JPG
July 15 - July 31


We focused these two weeks on preparing our DspB and Savinase enzymes for protein purification so we could test them in our Biofilm Assay. We ran PCRs, restriction digests, ligations, and transformations on them.


Daily log



BYUCESummer3.JPG
August 1 - August 14


We checked the transformation products from our earlier work with colony PCR, but the transformations were unsuccessful. We worked this period on trying to get our ligations and transformations to work.


Daily log



BYU2013-CholeraGroup1.jpg
August 15 - August 31


We continued working on getting DspB and Savinase ready for protein purification. We were having so many problems with Savinase that we went back and prepared new template DNA from Bacillus subtilis to use for our Savinase enzyme.


Daily log



Gelnotebook2013.jpg