"
Team:OUC-China
From 2013.igem.org
| Line 272: | Line 272: | ||
<a tabindex="-1" href="#">RNA guardian</a> | <a tabindex="-1" href="#">RNA guardian</a> | ||
<ul class="dropdown-menu"> | <ul class="dropdown-menu"> | ||
| - | <li><a tabindex="-1" href="https://2013.igem.org/Team:OUC-China/ | + | <li><a tabindex="-1" href="https://2013.igem.org/Team:OUC-China/Introduction">Introduction</a></li> |
<li><a tabindex="-1" href="https://2013.igem.org/Team:OUC-China/RNA guardian/Design">Design</a></li> | <li><a tabindex="-1" href="https://2013.igem.org/Team:OUC-China/RNA guardian/Design">Design</a></li> | ||
<li><a tabindex="-1" href="https://2013.igem.org/Team:OUC-China/RNA guardian/Results">Result</a></li> | <li><a tabindex="-1" href="https://2013.igem.org/Team:OUC-China/RNA guardian/Results">Result</a></li> | ||
| Line 347: | Line 347: | ||
</div> | </div> | ||
<!--the slidershow end--> | <!--the slidershow end--> | ||
| - | <div class="jumbotron"> | + | <div class="container"> |
| - | <h1> | + | <div class="jumbotron"> |
| - | <p class="lead"> | + | <h1>Features Of Our Project</h1> |
| - | + | <p class="lead">1.We designed an artificial prokaryotic membranous organelle which is capable of anchoring proteins, opening up new possibilities for intracellular biochemistry reactions.<br/>2.We took advantage of the 3D structure of RNA, using ribosomes as a barrier to stabilize RNA.<br/>3.We used Microfluidic Technology to detect the magnetism of our magnetic bacteria, Magnetospirillum Magneticum.<br/>4.We preserved Magnetospirillum Magneticum AMB-1 mamAB genes in E.coli, prevented the genes lose when AMB-1 strain was cultured in High oxygen partial pressure environment. | |
| + | </p> | ||
<a class="btn btn-large btn-success" href="#">Learn more</a> | <a class="btn btn-large btn-success" href="#">Learn more</a> | ||
</div> | </div> | ||
<hr> | <hr> | ||
| - | + | </div> | |
<div class="jumbotron"> | <div class="jumbotron"> | ||
| - | <h1> | + | <h1>Abstract</h1> |
| - | <p class="lead"> | + | <p class="lead">Putting biological resources into production has now become a hot topic since the development of technology and the draining of natural resources. For example, research about biofuel and biochemistry is now flourishing. But biological products have drawbacks of being inefficient and not broad-spectrum. Inspired by eukaryotic membranous organelles, we aim to construct a prokaryotic membranous organelle to realize division of work inside the cell and improve the efficiency of production. |
| - | + | How could a membrane be constructed in a Prokaryote? The answer may lie in this species: Magnetosprillum Magneticum, which can form a natural intracellular membrane. But this bacteria is slow-growing and requires demanding culture conditions, so the purpose of our project is to reconstruct the magnetosome membrane in E.coli, creating better conditions for efficient biological production.</p> | |
<a class="btn btn-large btn-success" href="#">Learn more</a> | <a class="btn btn-large btn-success" href="#">Learn more</a> | ||
</div> | </div> | ||
<hr> | <hr> | ||
| - | |||
<div class="jumbotron"> | <div class="jumbotron"> | ||
<header id="banner" class="hero-unit no-radius"> | <header id="banner" class="hero-unit no-radius"> | ||
| Line 373: | Line 373: | ||
<a class="btn btn-large btn-success" href="#">Learn more</a> | <a class="btn btn-large btn-success" href="#">Learn more</a> | ||
</div> | </div> | ||
| - | |||
<script src="http://netdna.bootstrapcdn.com/bootstrap/3.0.0/js/bootstrap.min.js"></script> | <script src="http://netdna.bootstrapcdn.com/bootstrap/3.0.0/js/bootstrap.min.js"></script> | ||
<script src="http://unslider.com/unslider.js"></script> | <script src="http://unslider.com/unslider.js"></script> | ||
Revision as of 17:45, 27 September 2013
Features Of Our Project
1.We designed an artificial prokaryotic membranous organelle which is capable of anchoring proteins, opening up new possibilities for intracellular biochemistry reactions.
2.We took advantage of the 3D structure of RNA, using ribosomes as a barrier to stabilize RNA.
3.We used Microfluidic Technology to detect the magnetism of our magnetic bacteria, Magnetospirillum Magneticum.
4.We preserved Magnetospirillum Magneticum AMB-1 mamAB genes in E.coli, prevented the genes lose when AMB-1 strain was cultured in High oxygen partial pressure environment.
Abstract
Putting biological resources into production has now become a hot topic since the development of technology and the draining of natural resources. For example, research about biofuel and biochemistry is now flourishing. But biological products have drawbacks of being inefficient and not broad-spectrum. Inspired by eukaryotic membranous organelles, we aim to construct a prokaryotic membranous organelle to realize division of work inside the cell and improve the efficiency of production. How could a membrane be constructed in a Prokaryote? The answer may lie in this species: Magnetosprillum Magneticum, which can form a natural intracellular membrane. But this bacteria is slow-growing and requires demanding culture conditions, so the purpose of our project is to reconstruct the magnetosome membrane in E.coli, creating better conditions for efficient biological production.
Learn more
