Team:UT Dallas/Project

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       <h1><a href="index.html"><span>UTDallas</span> iGem 2011<small></small></a></h1>
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       <h1><span>UTDallas</span> iGem<small></small></h1>
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         <li><a href="https://2011.igem.org/Team:UT_Dallas/Protocols"><font size="3" face="verdana">Protocols</a></font></li>
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         <h3>Creating Futures</h3>
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           <p> <font size="3" face="verdana">The human bowel hosts a rich diversity of symbiotic microflora that provides a powerful engineering platform for intelligent probiotics. These “immunobots” will ideally work in-sync and enhance natural self-repair mechanisms for a range of intestinal diseases associated with tissue damage. Towards this end, we engineered a bacterial chemotaxis pathway that utilizes a chimeric receptor to successfully interface with the immune system. In addition, we introduced an inducible secondary bacterial population that can trigger system-wide self-destruction, conferring an additional level of user control. Each module of our system was characterized using fluorescent reporters and the integrated parts were evaluated by controlled experiments involving wound signal gradients. We envision a probiotic solution that can facilitate localized tissue repair for damage resulting from inflammatory bowel diseases, including ulcerative colitis and Crohn’s disease.
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          <p><b><font size="4" face="Arial">&nbsp;&nbsp;&nbsp;Dr. Leonidas Bleris</b></font></p>
 
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          <p><b><font size="4" face="Arial">&nbsp;&nbsp;Dr. Hyun-Joo</b></font></p>
 
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          <p><b><font size="4" face="Arial">&nbsp;&nbsp;Dr. Lan Ma</b></p>
 
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          <p><b><font size="4" face="Arial">&nbsp;&nbsp;&nbsp;Sameer Sant</b></font></p>
 
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          <p><b><font size="4" face="Arial">&nbsp;&nbsp;Tyler Guinn</b></font></p>
 
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          <p><b><font size="4" face="Arial">&nbsp;&nbsp;&nbsp;Mitu Bhattatiry</b></font></p>
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          <p><b><font size="4" face="Arial">&nbsp;&nbsp;Jennifer Olbeter</b></p>
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          <p><b><font size="4" face="Arial">&nbsp;&nbsp;Saurav</b></font></p>
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" width="58" height="58" alt="" /></a> <a href="#"><img src="https://static.igem.org/mediawiki/2011/e/e8/Pic_3.jpg" width="58" height="58" alt="" /></a> <a href="#"><img src="https://static.igem.org/mediawiki/2011/2/2a/Pic_4.jpg" width="58" height="58" alt="" /></a> <a href="#"><img src="https://static.igem.org/mediawiki/2011/1/17/Pic_5.jpg" width="58" height="58" alt="" /></a> <a href="#"><img src="https://static.igem.org/mediawiki/2011/7/76/Pic_6.jpg" width="58" height="58" alt="" /></a> </div>
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       <h2><span><font size="5" face="verdana">UT Dallas</span></font></h2>
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      A little portal to learn more about UTD if anyone wants to. Learn more about where we work and some fun facts about UTD. *Add picture of Nserl.</p><p><a href="#"><font size="3" face="verdana">Click here to learn more about UTD</a></font></p>
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       <p>This will just give a brief description of what we've been doing and then link to the Notebook page when anyone clicks the "Learn More" link. See what we've been doing over the past few months.
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Latest revision as of 23:59, 5 September 2011

biz solution

Overview

The human bowel hosts a rich diversity of symbiotic microflora that provides a powerful engineering platform for intelligent probiotics. These “immunobots” will ideally work in-sync and enhance natural self-repair mechanisms for a range of intestinal diseases associated with tissue damage. Towards this end, we engineered a bacterial chemotaxis pathway that utilizes a chimeric receptor to successfully interface with the immune system. In addition, we introduced an inducible secondary bacterial population that can trigger system-wide self-destruction, conferring an additional level of user control. Each module of our system was characterized using fluorescent reporters and the integrated parts were evaluated by controlled experiments involving wound signal gradients. We envision a probiotic solution that can facilitate localized tissue repair for damage resulting from inflammatory bowel diseases, including ulcerative colitis and Crohn’s disease.