Team:Paris Bettencourt/Experiments/ComS diffusion

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<h2>Constructs done</h2>
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ComS diffusion
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<p>The ComS gene was synthetized by GeneArt but also insulated by PCR colony, changing the start and the stop codon, and then clones in pSB1C3. Then we cloned in front of a pVeg-SpoVG promoter and behind a RBA RFP double terminator.</p>
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<p>Then the construct was moved into an integration vector and also a multihost plasmid, called pHM3 from the Harald Putzer laboratory.</p>
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<p>Then the construct has been electropoprated and is waiting for caracterization.</p>
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<h2>Creation of the ∆CodY strain with the reporter</h2>
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<p>The genomic DNA from the CodY::spc strain from Linc Sonensheim laboratory was extracted and purified. The Elowitz's reporter strains where leaded to starvation, in order to make them competent, and then incubated for 30min with the genomic DNA. In this time laps, the strain is randomly making recombination of the outside DNA with its own genome, and make the KO in themself.</p>
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<p>Then, the B. Subtilis are selected on Spectinomycine plates, and only the KO clones where selected. At our great surprise, this protocol works very well and we got a huge number of recombinants.</p>
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 +
<h2>Caracterization of the ComS biobrick</h2>
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<p>The construct was cloned into our multihost vector and electroporated into Elowitz reporter strain. The YFP expressed in the cell indicates that the ComS gene created is active and the CFP reports that the ComK production has been triggered by overexpression of ComS.</p>
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Revision as of 15:08, 19 September 2011

Team IGEM Paris 2011

Constructs done

The ComS gene was synthetized by GeneArt but also insulated by PCR colony, changing the start and the stop codon, and then clones in pSB1C3. Then we cloned in front of a pVeg-SpoVG promoter and behind a RBA RFP double terminator.

Then the construct was moved into an integration vector and also a multihost plasmid, called pHM3 from the Harald Putzer laboratory.

Then the construct has been electropoprated and is waiting for caracterization.

Creation of the ∆CodY strain with the reporter

The genomic DNA from the CodY::spc strain from Linc Sonensheim laboratory was extracted and purified. The Elowitz's reporter strains where leaded to starvation, in order to make them competent, and then incubated for 30min with the genomic DNA. In this time laps, the strain is randomly making recombination of the outside DNA with its own genome, and make the KO in themself.

Then, the B. Subtilis are selected on Spectinomycine plates, and only the KO clones where selected. At our great surprise, this protocol works very well and we got a huge number of recombinants.

Caracterization of the ComS biobrick

The construct was cloned into our multihost vector and electroporated into Elowitz reporter strain. The YFP expressed in the cell indicates that the ComS gene created is active and the CFP reports that the ComK production has been triggered by overexpression of ComS.



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