Team:Evry/Sensor
From 2013.igem.org
Line 23: | Line 23: | ||
<li>yncE promoter</li> | <li>yncE promoter</li> | ||
</ul> | </ul> | ||
+ | |||
+ | <p> | ||
+ | Using PCR on <i>E. coli</i> genome, we extracted these four promoters. Then we construct our biosensors fusing these promoter with a reporter gene (see Figure 1 below). Promoter-reporter fusions were made with flanking restriction sites that are compatible with Biobrick-based cloning. | ||
+ | </p> | ||
+ | |||
+ | <div align='center'><img src="https://static.igem.org/mediawiki/2013/7/7b/P1-GFP.png" width="75%"/></div> | ||
+ | |||
+ | <div align='center'><img src="https://static.igem.org/mediawiki/2013/f/f3/P1-Nat_Prom.png" width="58%"/></div> | ||
+ | |||
+ | <p> | ||
+ | <b>Fig. 1</b> Construction of an iron-responsive genetic element by fusing a Fur-regulated promoter with a reporter gene. | ||
+ | </p> | ||
<p> | <p> |
Revision as of 17:51, 28 October 2013
Iron Sensor
Construction of the iron-responsive biosensors
E. coli's genome is composed of many Fur binding site. Based on a genome study, we identified 4 promoters which are controled by the FUR protein.
- AceB promoter
- Fes promoter
- FecA promoter
- yncE promoter
Using PCR on E. coli genome, we extracted these four promoters. Then we construct our biosensors fusing these promoter with a reporter gene (see Figure 1 below). Promoter-reporter fusions were made with flanking restriction sites that are compatible with Biobrick-based cloning.
Fig. 1 Construction of an iron-responsive genetic element by fusing a Fur-regulated promoter with a reporter gene.
We constructed iron-responsive biosensors by combining 3 genetic parts: an E. coli promoter with a Ferric Uptake Regulator (Fur) binding site, a fluorescent reporter (sfGFP), and a transcriptional terminator. These sensors respond to ambient iron by using the Fur system to repress a target gene.
We constructed 4 differents iron sensor using promoters regions from aceB (BBa_K1163102), fes (BBa_K1163108), fepA (BBa_K1163105) and yncE (BBa_K1163111). Finally, pAceB appears to be the best candidate to build our sensor system. See our results
Fig 1 Diagram of our 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. GFP expression is thus negatively correlated with iron availability.
Fig 2 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 |
Table I Genetic elements used to make iron-responsive sensors.