Difference between revisions of "Team:UC Davis"
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+ | <div class="footbox"> | ||
+ | <a href="https://2014.igem.org/Team:Yale"> | ||
+ | <img src="https://static.igem.org/mediawiki/2014/thumb/5/5c/G3071.png/528px-G3071.png" height="130px"/> | ||
+ | </a> | ||
+ | </div> | ||
+ | <div class="footbox" style=""> | ||
+ | Main Campus: </br> | ||
+ | Molecular, Cellular & Developmental Biology</br> | ||
+ | 219 Prospect Street</br> | ||
+ | P.O. Box 208103</br> | ||
+ | New Haven, CT 06520</br> | ||
+ | <img src="https://static.igem.org/mediawiki/2013/a/a7/PB_footerphone.png" height="10px"/> Phone: 203.432.3783</br> | ||
+ | <img src="https://static.igem.org/mediawiki/2013/7/74/PB_footeremail.png" height="10px"/> <a href="mailto:igem@yale.edu">igem@yale.edu </a> <br> | ||
+ | <img src="https://static.igem.org/mediawiki/2013/7/74/PB_footeremail.png" height="10px"/> <a href="mailto:natalie.ma@yale.edu">natalie.ma@yale.edu (Graduate Advisor)</a><br /> | ||
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+ | </div> | ||
+ | <div class="footbox" style="margin-left:20px;margin-top:20px;"> | ||
+ | <a href="http://www.yale.edu/"> | ||
+ | <img src="http://placehold.it/400x90/293660/FFFFFFF/&text=Yale+iGem+Team" height="90px" style="display:none"/> | ||
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+ | <div class="footbox" style="float:right;margin-top:20px;margin-right:20px"> | ||
+ | <a href="https://2014.igem.org/Main_Page"> | ||
+ | <img src="https://static.igem.org/mediawiki/2014/b/b0/IGEMLogo2014v2white.png" height="60px"/> | ||
+ | </a> | ||
+ | </div> | ||
+ | <div style="clear: both;"></div> | ||
+ | <center> | ||
+ | Copyright (c) 2014 Yale IGEM | ||
+ | </center> | ||
+ | </div> | ||
+ | </body> | ||
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Revision as of 17:30, 6 September 2015
Biofilm formation on surfaces is an issue in the medical field, naval industry, and other areas. We developed an anti-fouling peptide with two modular components: a mussel adhesion protein (MAP) anchor and LL-37, an antimicrobial peptide. MAPs can selectively attach to metal and organic surfaces via L-3,5-dihydroxyphenylalanine (L-DOPA), a nonstandard amino acid that was incorporated using a genetically recoded organism (GRO). Because this peptide is toxic to the GRO in which it is produced, we designed a better controlled inducible system that limits basal expression. This was achieved through a novel T7 riboregulation system that controls expression at both the transcriptional and translational levels. This improved system is a precise synthetic switch for the expression of cytotoxic substances in the already robust T7 system. Lastly, the antimicrobial surface-binding peptide was assayed for functionality.