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Team:OUC-China
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| - | <body > | + | <body> |
<div class="navbar navbar-inverse navbar-fixed-top" role="navigation"> | <div class="navbar navbar-inverse navbar-fixed-top" role="navigation"> | ||
<div class="navbar-header"> | <div class="navbar-header"> | ||
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<h1>WE DID IT !</h1> | <h1>WE DID IT !</h1> | ||
| - | <p>Constructing an Artificial | + | <p>Constructing an Artificial Organelle（Intracellular Compartment） in <i>E.coli</i></p> |
<a class="btn" href="https://2013.igem.org/Team:OUC-China/Results">learn the story behind this picture</a> | <a class="btn" href="https://2013.igem.org/Team:OUC-China/Results">learn the story behind this picture</a> | ||
</div> | </div> | ||
</li> | </li> | ||
| - | <li style="background-image: url('https://static.igem.org/mediawiki/ | + | <li style="background-image: url('https://static.igem.org/mediawiki/2013/7/7d/Cluster.png');"> |
<div class="inner"> | <div class="inner"> | ||
<h1>Compression of Metabolic Pathways</h1> | <h1>Compression of Metabolic Pathways</h1> | ||
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</div> | </div> | ||
</li> | </li> | ||
| - | <li style="background- | + | <li style="background-image: url('https://static.igem.org/mediawiki/2013/7/75/Ouc-slide4.jpg');"> |
<div class="inner"> | <div class="inner"> | ||
| - | <h1> | + | <h1>Factors Considered in RNA guardian</h1> |
| - | <p> | + | <p><br /></p> |
| - | <a class="btn" href=" | + | <a class="btn" href="https://2013.igem.org/Team:OUC-China/RNA_guardian/Design">Learn more</a> |
</div> | </div> | ||
</li> | </li> | ||
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<h3><b>Features Of Our Project</b></h3><hr> | <h3><b>Features Of Our Project</b></h3><hr> | ||
<li> | <li> | ||
| - | <b><span class="glyphicon glyphicon-ok-sign"></span> Artificial Organelle</b> | + | <b><span class="glyphicon glyphicon-ok-sign"></span> Artificial Organelle(Intracellular Compartment)</b> |
<p>We designed an artificial prokaryotic membranous organelle which is capable of anchoring proteins, opening up new possibilities for intracellular biochemistry reactions.</p> | <p>We designed an artificial prokaryotic membranous organelle which is capable of anchoring proteins, opening up new possibilities for intracellular biochemistry reactions.</p> | ||
<a class="btn btn-info" href="https://2013.igem.org/Team:OUC-China/Results">Learn more</a> | <a class="btn btn-info" href="https://2013.igem.org/Team:OUC-China/Results">Learn more</a> | ||
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</ul> | </ul> | ||
</div> | </div> | ||
| - | + | <div class="container"> | |
<h3><b>Introduction</b></h3><hr> | <h3><b>Introduction</b></h3><hr> | ||
<p>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. | <p>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: <i>Magnetosprillum Magneticum</i>, 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 <i><i>E.coli</i></i>, creating better conditions for efficient biological production.</p> | How could a membrane be constructed in a Prokaryote? The answer may lie in this species: <i>Magnetosprillum Magneticum</i>, 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 <i><i>E.coli</i></i>, creating better conditions for efficient biological production.</p> | ||
<p style="text-align:center"><a class="btn btn-large btn-info" href="https://2013.igem.org/Team:OUC-China/Overview">Learn more</a></p> | <p style="text-align:center"><a class="btn btn-large btn-info" href="https://2013.igem.org/Team:OUC-China/Overview">Learn more</a></p> | ||
| + | </div> | ||
| + | <!--footer--> | ||
| + | <footer> | ||
| + | <div class="container"> | ||
| + | <div class="row"> | ||
| + | <div class="col-md-1"></div> | ||
| + | <div class="col-md-6 footerleft"> | ||
| + | <h3 class="footer-title" style="color:#bdc1c5;">About</h3> | ||
| + | <p>Thanks to:</p> | ||
| + | <p> Bootstrap Flat-ui Unslider</p> | ||
| + | <p>Designed and built by <a href="http://copypeng.com">@PengYong</a> and <a href="http://www.renren.com/345094399/profile?ref=opensearch_normal#notice">@ZhengYuchen.</a></p> | ||
| + | <p>Code licensed under Apache License v2.0</p> | ||
| + | </div> | ||
| + | <div class="col-md-4"> | ||
| + | <div class="footer-banner"> | ||
| + | <h3 class="footer-title">Contact US</h3> | ||
| + | <ul> | ||
| + | <li>E-mail:<a href="mailto:oucigem@163.com"> oucigem@163.com</a></li> | ||
| + | <li><a href="http://oucast.com"> Official website</a></li> | ||
| + | <li><a href="http://www.renren.com/oast"> Find us on Renren</a></li> | ||
| + | <li><a href="http://weibo.com/u/2805858363"> Find us on Weibo</a></li> | ||
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<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> | ||
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Latest revision as of 03:38, 28 September 2013
-
Artificial Organelle(Intracellular Compartment)
We designed an artificial prokaryotic membranous organelle which is capable of anchoring proteins, opening up new possibilities for intracellular biochemistry reactions.
Learn more -
RNA Guardian
We took advantage of the 3D structure of RNA, using ribosomes as a barrier to stabilize RNA.
Learn more -
Microfluidic
We used Microfluidic Technology to detect the magnetism of our magnetic bacteria, Magnetospirillum Magneticum.
Learn more -
Preserving mamAB genes
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.
Learn more
Features Of Our Project
Introduction
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.
