Team:StanfordBrownSpelman/Cellulose Acetate
From 2014.igem.org
(Difference between revisions)
Angelofspeed (Talk | contribs) |
|||
Line 39: | Line 39: | ||
<nav id="navigation"> | <nav id="navigation"> | ||
- | <div class="projects underline"><h6><a href="https://2014.igem.org/Team:StanfordBrownSpelman | + | <div class="projects underline"><h6 id="projects"><a href="#SBS iGEM">Projects</a></h6> |
- | < | + | <h6><a href="https://2014.igem.org/Team:StanfordBrownSpelman/Achievements">Achievements</a></h6> |
- | < | + | <h6><a href="https://2014.igem.org/Team:StanfordBrownSpelman/Human_Practices">Policy and Practices</a></h6> |
- | <div id=" | + | <h6><a href="https://2014.igem.org/Team:StanfordBrownSpelman/Modelling">Modelling</a></h6> |
+ | <h6><a href="https://2014.igem.org/Team:StanfordBrownSpelman/Lab">In the Lab</a></h6> | ||
+ | <h6><a href="https://2014.igem.org/Team:StanfordBrownSpelman/Safety">Safety</a></h6> | ||
+ | <h6 id="team"><a href="#SBS iGEM">Team</a></h6> | ||
+ | <h6 id="contact"><a href="#SBS iGEM">Contact</a></h6> | ||
+ | </div> | ||
+ | <div id="wiki" class="wiki"><h6><a href="#SBS iGEM">Top</a></h6></div> | ||
+ | <div class="team"><h6><a href="#SBS iGEM">iGEM 2014<br>Stanford-Brown-Spelman</a></h6></div> | ||
</nav> | </nav> | ||
Line 52: | Line 59: | ||
<div id="header" class="small-8 small-centered columns"> | <div id="header" class="small-8 small-centered columns"> | ||
<h3><center><a href="https://2014.igem.org/Team:StanfordBrownSpelman/Cellulose_Acetate">Cellulose Acetate</a></h3> | <h3><center><a href="https://2014.igem.org/Team:StanfordBrownSpelman/Cellulose_Acetate">Cellulose Acetate</a></h3> | ||
- | < | + | <h7><center><a href="#" id="pics">Images</a> ● <a href="#" id="data">Results</a> ● <a href="#" id="methods">Methods</a> ● <a href="#" id="links">References</a> ● <a href="https://2014.igem.org/Team:StanfordBrownSpelman/BioBricks">BioBricks</a></h7> |
<h6> | <h6> | ||
The goal of this subproject is to engineer <i>Gluconacetobacter hansenii,</i> which produces large quantities of bacterial cellulose (BC), to use the acetylation machinery found in the wrinkly spreader isolate SBW25 of <i>Pseudomonas fluorescens</i> to produce bacterial cellulose acetate (BCOAc) towards its ultimate application as the foundation of a fully biological UAV. Industrially-produced cellulose acetate has many uses as a synthetic fiber and has advantages over pure BC in terms of material properties. However, its production presents some issues in that it requires harsh chemical processes, making the biological manufacturing method highly valuable. Using directed evolution, we plan to select for those organisms which produce the polymer with highest acetate content. In addition, we seek to create a fusion protein which will have the capacity to both cross-link BCOAc polymers (improving material properties) and allow the modular addition of any cell (e.g. a biosensor). This will be accomplished through the expression of a biotinylated membrane protein, through the protein’s streptavidin domain, making the UAV highly programmable. | The goal of this subproject is to engineer <i>Gluconacetobacter hansenii,</i> which produces large quantities of bacterial cellulose (BC), to use the acetylation machinery found in the wrinkly spreader isolate SBW25 of <i>Pseudomonas fluorescens</i> to produce bacterial cellulose acetate (BCOAc) towards its ultimate application as the foundation of a fully biological UAV. Industrially-produced cellulose acetate has many uses as a synthetic fiber and has advantages over pure BC in terms of material properties. However, its production presents some issues in that it requires harsh chemical processes, making the biological manufacturing method highly valuable. Using directed evolution, we plan to select for those organisms which produce the polymer with highest acetate content. In addition, we seek to create a fusion protein which will have the capacity to both cross-link BCOAc polymers (improving material properties) and allow the modular addition of any cell (e.g. a biosensor). This will be accomplished through the expression of a biotinylated membrane protein, through the protein’s streptavidin domain, making the UAV highly programmable. | ||
Line 197: | Line 204: | ||
<div class="row"> | <div class="row"> | ||
<div id="footer" class="small-8 small-centered columns"> | <div id="footer" class="small-8 small-centered columns"> | ||
- | < | + | <h6> |
Built atop Foundation. Content & Development © Stanford–Brown–Spelman iGEM 2014. | Built atop Foundation. Content & Development © Stanford–Brown–Spelman iGEM 2014. | ||
- | </ | + | </h6> |
</div> | </div> | ||
</div> | </div> |
Revision as of 17:13, 26 September 2014