Team:Trieste/parts/3

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<h2>Looking forward</h2>
<h2>Looking forward</h2>
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As we test that a single copy of CYM R in the plasmid can repress strictly the T5 cumate operator the next step is two integrate in the genome of the bacteria first a single copy of CYM R then the double copy. If this integration is verified we can have together with the T5 operator and the toxin a simple and efficient system for the control of bacteria proliferation  and for the elimination of the horizontal transfer.
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<h3><a href="http://partsregistry.org/Part:BBa_K875003"target="_blank">Link to the Registry</a></h3>
<h3><a href="http://partsregistry.org/Part:BBa_K875003"target="_blank">Link to the Registry</a></h3>

Revision as of 14:58, 25 September 2012

BBa_K875003

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Description

This composite produces constitutively the CymR regulator protein, that binds the Cumate Operator repressing the transcription from the promoter.


Assembly

Obtained by synthesis.

Results

CymR expression was confirmed by Western Blot analysis. Our CymR has a SV5 tag at the C-terminus in order to be detected by an anti-SV5 Ab. Its functionality was confirmed through the repression of T5 Cumate Operator-GFP.

Modelling


Looking forward

As we test that a single copy of CYM R in the plasmid can repress strictly the T5 cumate operator the next step is two integrate in the genome of the bacteria first a single copy of CYM R then the double copy. If this integration is verified we can have together with the T5 operator and the toxin a simple and efficient system for the control of bacteria proliferation and for the elimination of the horizontal transfer.

Link to the Registry


Università degli studi di Trieste ICGEB Illy Fondazione Cassa di Risparmio
iGEM 2012 iGEM 2012 iGEM 2012 iGEM 2012 iGEM 2012 iGEM 2012
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