Team:Evry/Sensor

From 2013.igem.org

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<h1>Sensor</h1>
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<h1>Iron Sensor</h1>
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We constructed iron sensors by combining 3 genetic parts: an E. coli promoter with a Fur binding site, the sfGFP fluorescent reporter, and a transcriptional terminator. These iron sensing elements were cloned in Biobrick compatible format as shown below.  
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We constructed iron sensors by combining 3 genetic parts: an E. coli promoter with a Fur binding site, a fluorescent reporter (sfGFP), and a transcriptional terminator. These iron-sensing elements repress expression of the reporter in response to iron and were cloned in Biobrick compatible format as shown below.  
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<div align='center'><img src="https://static.igem.org/mediawiki/2013/1/12/ColiSensor.png" width="75%"/></div>
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<b>Fig</b> Diagram of a genetic iron sensor. Iron bind the Ferric Uptake Regulator (Fur) to form a complex that binds the Fur box in the promoter, here shown as the aceB promoter. Once the iron-Fur complex is bound, it represses transcription of the target gene GFP.
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<b>Fig</b> Diagram of a genetic iron sensor. Iron binds the Ferric Uptake Regulator (Fur) to form a complex with high affinity for the Fur box in the promoter, here shown as the aceB promoter. Once the iron-Fur complex is bound to the promoter, it represses transcription of the target gene GFP.
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Revision as of 09:59, 4 October 2013

Iron coli project

Iron Sensor

We constructed iron sensors by combining 3 genetic parts: an E. coli promoter with a Fur binding site, a fluorescent reporter (sfGFP), and a transcriptional terminator. These iron-sensing elements repress expression of the reporter in response to iron and were cloned in Biobrick compatible format as shown below.



Fig Diagram of a genetic iron sensor. Iron binds the Ferric Uptake Regulator (Fur) to form a complex with high affinity for the Fur box in the promoter, here shown as the aceB promoter. Once the iron-Fur complex is bound to the promoter, it represses transcription of the target gene GFP.



Fig Construction of an iron-responsive genetic element by fusing a Fur-regulated promoter with a reporter gene. Promoter-reporter fusions were made with flanking restriction sites that are compatible with Biobrick-based cloning.

NAME FIGURE DESCRIPTION

E. coli promoter with Fur binding site

iron-Fur complex binds promoter to repress expression

sfGFP

Fluorescent reporter gene

Terminator

terminator to stop transcription

Plasmid

Biobrick-compatible plasmid backbone