Difference between revisions of "Team:Bordeaux/Results"
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+ | <h5 align="left">crdS, crdA and crdC genes ?</h5> | ||
<p align=justify>✵ <b>crdS gene</b> codes the Curdlan synthase. | <p align=justify>✵ <b>crdS gene</b> codes the Curdlan synthase. | ||
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<br>N.B : We tried to work on these three genes. However, amplification attempts by PCR were unsuccessful for crdA and crdC genes.So, in a first time, we focused on cloning crdS gene only.</p> | <br>N.B : We tried to work on these three genes. However, amplification attempts by PCR were unsuccessful for crdA and crdC genes.So, in a first time, we focused on cloning crdS gene only.</p> | ||
+ | </div> | ||
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<h5 align="left">OsmY promoter</h5> | <h5 align="left">OsmY promoter</h5> | ||
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<p align="justify">Curdlan production was carried out in two different media: LB medium and M63 medium. | <p align="justify">Curdlan production was carried out in two different media: LB medium and M63 medium. | ||
<br>✵ We worked on M63 medium because this one is cited in literature. M63 is a minimal, low osmolarity medium for E.coli, resulting in slower growth rate of these cells. | <br>✵ We worked on M63 medium because this one is cited in literature. M63 is a minimal, low osmolarity medium for E.coli, resulting in slower growth rate of these cells. | ||
− | XXX Mettre la reference de la publication XXX | + | <br>XXX Mettre la reference de la publication XXX |
− | →With this medium of known composition we were able to control parameters for the production of our molecule of interest. | + | <br>→With this medium of known composition we were able to control parameters for the production of our molecule of interest. |
<br>✵We worked also on LB medium because this is the most common medium used in the laboratory.</p> | <br>✵We worked also on LB medium because this is the most common medium used in the laboratory.</p> | ||
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</div> | </div> |
Revision as of 14:08, 9 September 2015