Team:Imperial College/Major Results

From 2008.igem.org

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We studied the motility of ''B. subtilis'' and developed an elegant mechanical model to describe cell trajectory. We fitted our model to our laboratory data and discovered that our model matches cell trajectory data extremely well.
We studied the motility of ''B. subtilis'' and developed an elegant mechanical model to describe cell trajectory. We fitted our model to our laboratory data and discovered that our model matches cell trajectory data extremely well.
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{{Imperial/Box1|Characterisation of Chloramphenicol Acetyltransferase|<br>
{{Imperial/Box1|Characterisation of Chloramphenicol Acetyltransferase|<br>

Revision as of 22:18, 29 October 2008


Experimental Results

Major results are shown in this section; this page will be updated shortly. For minor results, please refer to our Notebook.


Our Work With B. subtilis Chassis

Please click here for more information
B.subtilis has great potential as a chassis for synthetic biology. However it is not commonly used in iGEM competitions and very few B. subtilis BioBricks are available. In order to increase the accessibility of B.subtilis as a chassis, we have created 41 new BioBricks which are specific to B. subtilis. We have also successfully transformed it and characterised its growth.

B subtilis Clutch Mechanism.png


Control of Motility

Please click here for the Motility Control Results Page
We studied the motility of B. subtilis and developed an elegant mechanical model to describe cell trajectory. We fitted our model to our laboratory data and discovered that our model matches cell trajectory data extremely well.

GFP2.gif


Characterisation of Chloramphenicol Acetyltransferase


Please click here for the chloramphenicol acetyltransferase Characterisation Summary Page
We have characterised the ability of Chloramphenicol acetyltransferase ([http://partsregistry.org/wiki/index.php?title=Part:BBa_J31005 BBa_J31005]) to provide resistance to Chlroamphenicol. This has shown that a variety of our parts are functional including integration sites, promoters and ribosome binding sites and the range of chloramphenicol concentrations at which a cell will be protected by Chloramphenicol acetyltransferase.


Characterisation of BioBricks

Please click here for the BioBricks Characterisation Summary Page
We have characterised several of our testing constructs in B. subtilis.This has shown that a variety of our parts are functional including integration sites, antibiotic resistance, promoters and ribosome binding sites.




General lab work and smaller results are put up on the calendar on the dates they were done; they can therefore be found in the >>> Notebook >>>