Difference between revisions of "Team:UC Davis"

Line 332: Line 332:
 
               <div class="container">
 
               <div class="container">
 
                 <div class="carousel-caption">
 
                 <div class="carousel-caption">
                   <h1><font color = "#000000">SBiDer</font></h1>  
+
                   <h1><font color = "#000000">Measure Your Footprint</font></h1>  
 
                   <p><a class="btn btn-lg btn-primary" href="#" role="button">Take me to the app!</a></p>           
 
                   <p><a class="btn btn-lg btn-primary" href="#" role="button">Take me to the app!</a></p>           
 
                 </div>
 
                 </div>

Revision as of 18:54, 9 September 2015


Producing a Novel Antimicrobial Surface-Binding Peptide Using an Improved T7 Expression System

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.

Main Campus:
Molecular, Cellular & Developmental Biology
219 Prospect Street
P.O. Box 208103
New Haven, CT 06520
Phone: 203.432.3783
igem@yale.edu
natalie.ma@yale.edu (Graduate Advisor)
Copyright (c) 2014 Yale IGEM