Team:CIDEB-UANL Mexico/Project-Circuit

From 2013hs.igem.org

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For more details you can see the circuit:<a href="https://2013hs.igem.org/Team:CIDEB-UANL_Mexico/Project-Idea"><font color="blue"> Main Idea Description of the project. </font></a>
For more details you can see the circuit:<a href="https://2013hs.igem.org/Team:CIDEB-UANL_Mexico/Project-Idea"><font color="blue"> Main Idea Description of the project. </font></a>
<center><img src="https://static.igem.org/mediawiki/2013hs/3/37/Circuito2L.jpg" width="700px" height="300px" /></center> </p>
<center><img src="https://static.igem.org/mediawiki/2013hs/3/37/Circuito2L.jpg" width="700px" height="300px" /></center> </p>
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<p align="justify">One system is going to be repressing the other one with the riboswitch when the specific range of temperature is from 20oC to 37oC, but when the temperature is lower to this interval the first system is going to be off and then the second system is going to be active with the production of the pesticide (Vip3Ca3) and the GFP.
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When the temperature is low, the promoter (J23100) is going to inhibited and then the first system it’s going to shut down. Then the second system is activate it and the production of the pesticide (Vip3Ca3) is going to be active and also the GFP, that it is a mode to notice if it is producing the pesticide. As we know, the part that has the GFP reporter will be repressed after the 37ºC so it needs a degradation tag to reduce the fluorescence. Our circuit will be inserted into E. Coli. We had the idea of placing the bacteria in a gellan bead, like the team of Bristol 2010(https://2010.igem.org/Team:BCCS-Bristol), this is a way to enclose our bacteria and to maintain it safe from the environment and another things that could represent a risk for them and it help in bio safety because, the bacteria would not be in direct contact with the crops. Also this helps to extend the life period of the bacteria. </p>
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Revision as of 03:43, 21 June 2013

Project
Circuit

Circuit

The circuit works as the following way.
1. A pR (repressible promoter) is active and produces the Vip3Ca3 protein and the Green Fluorescent Protein as a reporter of the Vip3Ca3 production.
2. In the other part, there is a Constitutive promoter (pConst) but it works with a riboswitch.
3. The riboswitch is activated after the 32ºC and it starts trasnlation producing the cI protein which inhibits the pR turning off the Vip3Ca3 production.
In summary: The Vip3Ca3 production is regulated by temperature: it is produced below the 32ºC and at higher temperatures it is turned off.
For more details you can see the circuit: Main Idea Description of the project.

One system is going to be repressing the other one with the riboswitch when the specific range of temperature is from 20oC to 37oC, but when the temperature is lower to this interval the first system is going to be off and then the second system is going to be active with the production of the pesticide (Vip3Ca3) and the GFP. When the temperature is low, the promoter (J23100) is going to inhibited and then the first system it’s going to shut down. Then the second system is activate it and the production of the pesticide (Vip3Ca3) is going to be active and also the GFP, that it is a mode to notice if it is producing the pesticide. As we know, the part that has the GFP reporter will be repressed after the 37ºC so it needs a degradation tag to reduce the fluorescence. Our circuit will be inserted into E. Coli. We had the idea of placing the bacteria in a gellan bead, like the team of Bristol 2010(https://2010.igem.org/Team:BCCS-Bristol), this is a way to enclose our bacteria and to maintain it safe from the environment and another things that could represent a risk for them and it help in bio safety because, the bacteria would not be in direct contact with the crops. Also this helps to extend the life period of the bacteria.

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