Difference between revisions of "Part:BBa K763002:Experience"

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<I>iGEM TU-Eindhoven 2013</I>
 
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For the 2013 TU-Eindhoven iGEM project we wished to express MRI contrast providing proteins upon bacteria entering anaerobic tumours. To induce the expression of these proteins we would be making use of an FNR promoter just like the NirB promoter. To design our promoter we made use of an article (Anne M.L. Barnard, Jeffrey Green, and Stephen J.W. Busby, Transcription regulation by tandem-bound FNR at Escherichia coli promoters. Journal of bacteriology 185.20, 5993-6004 (2003)). From this article we extracted the data for our promoter, by choosing the most optimal promoter given in the articles selection.  
 
For the 2013 TU-Eindhoven iGEM project we wished to express MRI contrast providing proteins upon bacteria entering anaerobic tumours. To induce the expression of these proteins we would be making use of an FNR promoter just like the NirB promoter. To design our promoter we made use of an article (Anne M.L. Barnard, Jeffrey Green, and Stephen J.W. Busby, Transcription regulation by tandem-bound FNR at Escherichia coli promoters. Journal of bacteriology 185.20, 5993-6004 (2003)). From this article we extracted the data for our promoter, by choosing the most optimal promoter given in the articles selection.  

Revision as of 21:43, 4 October 2013


This experience page is provided so that any user may enter their experience using this part.
Please enter how you used this part and how it worked out.

Applications of BBa_K763002

User Reviews

UNIQ3cef667241c02334-partinfo-00000000-QINU

Review number not understood iGEM TU-Eindhoven 2013

For the 2013 TU-Eindhoven iGEM project we wished to express MRI contrast providing proteins upon bacteria entering anaerobic tumours. To induce the expression of these proteins we would be making use of an FNR promoter just like the NirB promoter. To design our promoter we made use of an article (Anne M.L. Barnard, Jeffrey Green, and Stephen J.W. Busby, Transcription regulation by tandem-bound FNR at Escherichia coli promoters. Journal of bacteriology 185.20, 5993-6004 (2003)). From this article we extracted the data for our promoter, by choosing the most optimal promoter given in the articles selection. To test the efficiency of this promoter we, much like the Valencia 2012 team, expressed EGFP under anaerobic conditions in which, again like the Valencia 2012 team were successful. Based on the research by Barnard and al. and our measurements (see [Part:BBa_K1123005 | BBa_K1123005] and [Part:BBa_K1123000 | BBa_K1123000]) seems to have more potential as an FNR promoter with higher activity.

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UNIQ3cef667241c02334-partinfo-00000002-QINU