Difference between revisions of "Team:Waterloo/Description"
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<div class="row"><div class="col"><div class="content-main"><h2 id="e-co-light-dynamic-optogenetic-control-of-co-cultures"><em>E. co-light</em> : Dynamic Optogenetic Control of Co-cultures</h2> | <div class="row"><div class="col"><div class="content-main"><h2 id="e-co-light-dynamic-optogenetic-control-of-co-cultures"><em>E. co-light</em> : Dynamic Optogenetic Control of Co-cultures</h2> | ||
| − | < | + | <video width="100%" height="480" controls> |
| + | <source src="https://static.igem.org/mediawiki/2018/e/e4/T--Waterloo--IntroVideo.mp4" type="video/mp4"> | ||
| + | </video> | ||
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| + | <p><a href="https://static.igem.org/mediawiki/2018/b/b5/T--Waterloo--IntroTranscript.pdf">Video Transcript</a></p> | ||
<p>Microorganisms exist in complex and diverse communities. This enables a variety of important interactions including co-metabolism and nutrient cycling. Yet, it can be difficult to culture species together in a laboratory setting. Mixed populations are difficult to maintain primarily due to competition: a difference in growth rates often results in one population outcompeting another. Our team aims to dynamically control E. coli growth by using optogenetics (light-induced gene expression) to regulate the production of MetE, an enzyme essential for bacterial growth. This kind of control could help us overcome a major barrier to maintaining co-cultures: competition between microorganisms. </p> | <p>Microorganisms exist in complex and diverse communities. This enables a variety of important interactions including co-metabolism and nutrient cycling. Yet, it can be difficult to culture species together in a laboratory setting. Mixed populations are difficult to maintain primarily due to competition: a difference in growth rates often results in one population outcompeting another. Our team aims to dynamically control E. coli growth by using optogenetics (light-induced gene expression) to regulate the production of MetE, an enzyme essential for bacterial growth. This kind of control could help us overcome a major barrier to maintaining co-cultures: competition between microorganisms. </p> | ||
<p>This would open several doors in biotech and research. For instance, metabolic engineering of microbial communities may improve the production of pharmaceuticals, biofuels, and other important materials. Moreover, controllable co-cultures would allow researchers to explore complex interactions between microbes and investigate questions that could not previously be answered due to co-culturing limitations.</p> | <p>This would open several doors in biotech and research. For instance, metabolic engineering of microbial communities may improve the production of pharmaceuticals, biofuels, and other important materials. Moreover, controllable co-cultures would allow researchers to explore complex interactions between microbes and investigate questions that could not previously be answered due to co-culturing limitations.</p> | ||
<h1 id="what-is-mete-">What is MetE?</h1> | <h1 id="what-is-mete-">What is MetE?</h1> | ||
| + | <p>We’re going to control the production of MetE, an enzyme that catalyses the rate-limiting step in methionine biosynthesis [1]. Methionine is an important amino acid bacteria need to make proteins and grow. Bacteria can get it from their environment or produce it themselves using the MetE enzyme. If placed in a medium that doesn’t contain methionine, bacteria can only grow if they produce this enzyme </p> | ||
<h1 id="what-is-ccas-r-">What is CcaS/R?</h1> | <h1 id="what-is-ccas-r-">What is CcaS/R?</h1> | ||
| + | <p>CcaS/R is a light-switchable system derived from cyanobacteria which can be introduced into E. coli [1]. This system can be used to create a long term optical feedback system for gene expression in the bacterial culture. CcaS/R is a three part system consisting of CcaS, CcaR and the associated promoter region. The gene of interest, MetE in our case, is placed under the promoter region so that its expression can be controlled. CcaS is the “sensor” protein which detects the wavelength of light. CcaR is the regulator protein which binds to the promoter, which modulates gene expression when green light is detected and stops expression when red light is detected [1].</p> | ||
| + | <h1 id="references">References</h1> | ||
| + | <p>[1] A. Milias-Argeitis, M. Rullan, S. K. Aoki, P. Buchmann, and M. Khammash, “Automated optogenetic feedback control for precise and robust regulation of gene expression and cell growth,” Nature Communications, vol. 7, p. 12546, 2016.</p> | ||
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Revision as of 23:02, 17 October 2018
Project Description
E. co-light : Dynamic Optogenetic Control of Co-cultures
Microorganisms exist in complex and diverse communities. This enables a variety of important interactions including co-metabolism and nutrient cycling. Yet, it can be difficult to culture species together in a laboratory setting. Mixed populations are difficult to maintain primarily due to competition: a difference in growth rates often results in one population outcompeting another. Our team aims to dynamically control E. coli growth by using optogenetics (light-induced gene expression) to regulate the production of MetE, an enzyme essential for bacterial growth. This kind of control could help us overcome a major barrier to maintaining co-cultures: competition between microorganisms.
This would open several doors in biotech and research. For instance, metabolic engineering of microbial communities may improve the production of pharmaceuticals, biofuels, and other important materials. Moreover, controllable co-cultures would allow researchers to explore complex interactions between microbes and investigate questions that could not previously be answered due to co-culturing limitations.
What is MetE?
We’re going to control the production of MetE, an enzyme that catalyses the rate-limiting step in methionine biosynthesis [1]. Methionine is an important amino acid bacteria need to make proteins and grow. Bacteria can get it from their environment or produce it themselves using the MetE enzyme. If placed in a medium that doesn’t contain methionine, bacteria can only grow if they produce this enzyme
What is CcaS/R?
CcaS/R is a light-switchable system derived from cyanobacteria which can be introduced into E. coli [1]. This system can be used to create a long term optical feedback system for gene expression in the bacterial culture. CcaS/R is a three part system consisting of CcaS, CcaR and the associated promoter region. The gene of interest, MetE in our case, is placed under the promoter region so that its expression can be controlled. CcaS is the “sensor” protein which detects the wavelength of light. CcaR is the regulator protein which binds to the promoter, which modulates gene expression when green light is detected and stops expression when red light is detected [1].
References
[1] A. Milias-Argeitis, M. Rullan, S. K. Aoki, P. Buchmann, and M. Khammash, “Automated optogenetic feedback control for precise and robust regulation of gene expression and cell growth,” Nature Communications, vol. 7, p. 12546, 2016.