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Team:Lyon-INSA-ENS/Realisation/ExperimentalSchedule
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| - | <li style="margin-left:10%"> The first one is the construction of a part containing the OmpR234 curli regulator under the control of the cobalt inducible rcnA gene promotor.</li> | + | <li style="margin-left:10%"> The first one is the construction of a part containing the OmpR234 curli regulator under the control of the cobalt inducible ''rcnA'' gene promotor.</li> |
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| - | <li style="margin-left:10%"> The second one is the construction of a part containing the entire curli operon (csgBAEFG genes)under the control of the cobalt inducible rcnA gene promotor. </li> | + | <li style="margin-left:10%"> The second one is the construction of a part containing the entire curli operon (''csgBAEFG'' genes)under the control of the cobalt inducible rcnA gene promotor. </li> |
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<img src="https://static.igem.org/mediawiki/2011/b/b9/Partcsg.jpg" ; width ="250px" ; height = "95px"/> | <img src="https://static.igem.org/mediawiki/2011/b/b9/Partcsg.jpg" ; width ="250px" ; height = "95px"/> | ||
Revision as of 19:47, 22 August 2011
Experimental Schedule
The goal of the "Cobalt buster" project is to construct a bacterial strain which will be able to produce adherence structures (curlis) when cobalt is encountered in the liquid medium.
To make it possible we chose two strategies :
