Team:EPF-Lausanne/Notebook/September2011

From 2011.igem.org

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(Wednesday, 14 September 2011)
(Thursday, September 1 2011)
 
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After taking a closer look at the plate from the platereader, it seems that none of the T7 variants did any lysing. This realization made it urgent that we discover whether or not the full T4-lysis cassette was really in these Gibson-assembled plasmids. The samples that had been sent in for sequencing had primers that seemed to amplify the backbone, instead of the lysis cassette. While this does not necessarily mean that the lysis is not there, it does suggest that all the PCRS and gels used to verify the presence of lysis were only showing the existence of the backbone.  
After taking a closer look at the plate from the platereader, it seems that none of the T7 variants did any lysing. This realization made it urgent that we discover whether or not the full T4-lysis cassette was really in these Gibson-assembled plasmids. The samples that had been sent in for sequencing had primers that seemed to amplify the backbone, instead of the lysis cassette. While this does not necessarily mean that the lysis is not there, it does suggest that all the PCRS and gels used to verify the presence of lysis were only showing the existence of the backbone.  
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Alina ran a PCR with different primers from Douglas' first attempts at putting together the 2700 bp cassette that amplify select regions of the cassette.  
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Alina ran a PCR with different primers from Douglas' first attempts at putting together the 2700 bp cassette that amplify select regions of the cassette.
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Lilia tested the expression of the TetR mutants with the T7 promoter. The expression mix contained the Green Lysine and the gel fluorescence was imaged and is shown on the next picture.
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[[File:EPFL2011_SDS-PAGE_ITT_expression_check_muTetRs_T7.png|400px]]
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The BP2col2 does not express, what explains the failure of the protein pool down at the MITOMI made on Wednesday.
== Friday, September 2 2011 ==
== Friday, September 2 2011 ==
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The results of the experiment indicate that not only do we have successful lysing of the relevant cells, but we also are able to recover the relevant DNA, not only as is found in the supernatant by qPCR but also by looking at the number of colonies produced by each hourly sample when transformed.  
The results of the experiment indicate that not only do we have successful lysing of the relevant cells, but we also are able to recover the relevant DNA, not only as is found in the supernatant by qPCR but also by looking at the number of colonies produced by each hourly sample when transformed.  
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[[File:colony_count_c2lys.png|700px]]
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[[File:colony_count_c2lys.png|350px]]
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[[File:mrfpgene_in_supernat_c2lys.png|350px]]
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[[File:od_lysis_invivo.png|350px]]
== Thursday, 15 September 2011 ==
== Thursday, 15 September 2011 ==
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Nadine ligated the Plac biobrick into pSB1C3 and transformed. She also purified the TetR genes with Gibson extensions, sending them for sequencing after having done a new Gibson reaction. The Gibson reactions were also transformed, hoping that this time it will work.
Nadine ligated the Plac biobrick into pSB1C3 and transformed. She also purified the TetR genes with Gibson extensions, sending them for sequencing after having done a new Gibson reaction. The Gibson reactions were also transformed, hoping that this time it will work.
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Second attempt to PCR tetR mutants with BioBrick primers yield in PCR product for all the mutants we have:
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[[File:EPF-Lausanne2011_Gel_mutagenesis.tif|600px]]
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We will now digest and ligate it to the pSB1C3 backbone!
== Saturday, 17 September 2011 ==
== Saturday, 17 September 2011 ==

Latest revision as of 08:43, 21 September 2011