Team:XMU-China

From 2014.igem.org

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<p>This year, chemotaxis interests us a lot. We intend to reprogram the strain (CL-1) which lacks the CheZ gene to form mathematical patterns. CheZ gene belongs to chemotaxis family of E.coli, and protein CheZ can dephosphorylate CheY-P which allows E.coli to make smooth swimming. The  ΔCheZ bacteria can’t dephosphorylate CheY-P, therefore the strain isn’t motile until CheZ is involved in. Based on this, the motility of E.coli can be precisely controlled by stimulus (such as IPTG). We try to construct logic gene circuits to make E.coli recognize environmental stimulation, thus by utilizing the controlled chemotaxis which named pseudotaxis we could command bacteria to form patterns such as ellipse, hyperbola and so on.</p>
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&nbsp;<p>The intrinsic motivation that drive us striving for the above project is that we want to simulate the process of stem cell differentiation. In the organs development, stem cells differentiate while aggregate together to form heart, liver and kidney what have precise shapes. We think there must be some mathematical principles that govern the differentiation process. By simulating differentiation, we want to get a closer understanding of the differentiation process. However, E.coli can’t sense as much stimulus as stem cell, we intend to utilize RNA aptamers what has the potential to response to almost all stimulus to cover that shortage. Thus, we can get a more precise stimulation.</p>
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&nbsp; <p>We also try to utilize pseudotaxis to accomplish some experimental meaning. As far as we know, the motile ability is proportional to the amount of protein CheZ in certain range. By measuring the average chemotaxis distance, we can get a precise evaluation on the RBS efficiency which is evaluated by fluorescence strength previously.</p>
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Revision as of 04:20, 14 August 2014


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Project Description

This year, chemotaxis interests us a lot. We intend to reprogram the strain (CL-1) which lacks the CheZ gene to form mathematical patterns. CheZ gene belongs to chemotaxis family of E.coli, and protein CheZ can dephosphorylate CheY-P which allows E.coli to make smooth swimming. The ΔCheZ bacteria can’t dephosphorylate CheY-P, therefore the strain isn’t motile until CheZ is involved in. Based on this, the motility of E.coli can be precisely controlled by stimulus (such as IPTG). We try to construct logic gene circuits to make E.coli recognize environmental stimulation, thus by utilizing the controlled chemotaxis which named pseudotaxis we could command bacteria to form patterns such as ellipse, hyperbola and so on.

 

The intrinsic motivation that drive us striving for the above project is that we want to simulate the process of stem cell differentiation. In the organs development, stem cells differentiate while aggregate together to form heart, liver and kidney what have precise shapes. We think there must be some mathematical principles that govern the differentiation process. By simulating differentiation, we want to get a closer understanding of the differentiation process. However, E.coli can’t sense as much stimulus as stem cell, we intend to utilize RNA aptamers what has the potential to response to almost all stimulus to cover that shortage. Thus, we can get a more precise stimulation.

 

We also try to utilize pseudotaxis to accomplish some experimental meaning. As far as we know, the motile ability is proportional to the amount of protein CheZ in certain range. By measuring the average chemotaxis distance, we can get a precise evaluation on the RBS efficiency which is evaluated by fluorescence strength previously.