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Team:ITESM Mexico/Abstract
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::::::::::::::::::::::'''Dual light controlled arabinose biosensor''' | ::::::::::::::::::::::'''Dual light controlled arabinose biosensor''' | ||
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'''Integrating the work of many other previous iGEM teams (Tokyo NoKoGen 2010, Chiba 2009, 2010, British Columbia 2009, Cambridge 2010, UNAM-Genomics México 2010, ITESM Monterrey 2010), the aim of this project is to develop a way of giving a cell the command to perform a function at user’s will, improving current lock-and-key designs. A novel mechanism based on an ''E.coli'' chassis, was designed with two main objectives: to sense arabinose reporting its concentration and to use light receptors to trigger the expression of the required pathways. The first receptor enables ''E.coli'' to activate (express), the arabinose sensing mechanism; whereas the second receptor activates a quick deactivation(degradation), of the sensing mechanism depriving the cell of that capability.''' | '''Integrating the work of many other previous iGEM teams (Tokyo NoKoGen 2010, Chiba 2009, 2010, British Columbia 2009, Cambridge 2010, UNAM-Genomics México 2010, ITESM Monterrey 2010), the aim of this project is to develop a way of giving a cell the command to perform a function at user’s will, improving current lock-and-key designs. A novel mechanism based on an ''E.coli'' chassis, was designed with two main objectives: to sense arabinose reporting its concentration and to use light receptors to trigger the expression of the required pathways. The first receptor enables ''E.coli'' to activate (express), the arabinose sensing mechanism; whereas the second receptor activates a quick deactivation(degradation), of the sensing mechanism depriving the cell of that capability.''' | ||
Revision as of 20:52, 28 September 2011
ITESM MÉXICO
SensE.coli
-
- Dual light controlled arabinose biosensor
Integrating the work of many other previous iGEM teams (Tokyo NoKoGen 2010, Chiba 2009, 2010, British Columbia 2009, Cambridge 2010, UNAM-Genomics México 2010, ITESM Monterrey 2010), the aim of this project is to develop a way of giving a cell the command to perform a function at user’s will, improving current lock-and-key designs. A novel mechanism based on an E.coli chassis, was designed with two main objectives: to sense arabinose reporting its concentration and to use light receptors to trigger the expression of the required pathways. The first receptor enables E.coli to activate (express), the arabinose sensing mechanism; whereas the second receptor activates a quick deactivation(degradation), of the sensing mechanism depriving the cell of that capability.
