Talk:Team:Nanjing-China/test

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<groupparts>iGEM013 Nanjing-China</groupparts>
 
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    <div class="logo"><a href="https://2013.igem.org/Main_Page" target="_blank" class="bl"></a><a href="https://igem.org/Team.cgi?year=2013&team_name=Nanjing-China" target="_blank" class="bl2"></a></div>
 
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          <li><a href="https://2013.igem.org/Team:Nanjing-China">Home</a></li>
 
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          <li><a href="https://2013.igem.org/Team:Nanjing-China/team">Team</a></li>
 
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          <li class="parts"><a href="https://2013.igem.org/Team:Nanjing-China/parts">Parts</a></li>
 
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          <li class="bar">Parts</li>
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          <li class=trunk onmouseover=listTrigger(0);><a href="https://2013.igem.org/Team:Nanjing-China/parts#trm">TRM</a></li>
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          <li class=trunk onmouseover=listTrigger(0);><a href="https://2013.igem.org/Team:Nanjing-China/parts#trzn">TrzN</a></li>
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          <li class=trunk onmouseover=listTrigger(0);><a href="https://2013.igem.org/Team:Nanjing-China/parts#rbs">Atrazine-RBS </a></li>
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          <li class=trunk onmouseover=listTrigger(0);><a href="https://2013.igem.org/Team:Nanjing-China/parts#plsr">Plsr</a></li>
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          <li class=trunk onmouseover=listTrigger(0);><a href="https://2013.igem.org/Team:Nanjing-China/parts#ci">Regulatory Parts</a></li>
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        <dt><a name="trm" href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K1145001" target="_blank">TRM(BBa_K1145001)</a></dt>
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            <dd class="dd_1"><p>TRM is a transmembrane transporter which is involved in transporting atrazine from the outside to the inside of the bacteria. It comes from the genome of Arthrobacter aurescens. The length of its gene is 1341bp. By using this part, we hope to increase the amount of atrazine inside the bacteria so that our Atrazine-RBS and TrzN can function better.</p></dd>
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        <dt><a name="trzn" href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K1145002" target="_blank">TrzN (BBa_K1145002)</a></dt>
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            <dd class="dd_1"><p>rzN is a fantastic degrading enzyme which can degrade atrazine into a nontoxic chemical substance. It also comes from the genome of Arthrobacter aurescens. The length of its gene is 1371bp. With the help of TRM, this part can function much more efficiently.</p></dd>
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==SJTU-BioX-Shanghai 2012 iGEM Team Parts==
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        <dt><a name="rbs" href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K1145003" target="_blank">Atrazine-RBS (BBa_K1145003)</a></dt>
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            <dd class="dd_1"><p>This is a brilliant switch which can be opened by atrazine. It comes from artificial synthesis. We use this part to recognize and detect atrazine. The length of this switch is 87bp. Once atrazine is detected, corresponding functions, for example recruiting partners, will take effect immediately.</p></dd>
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        <dt><a name="plsr" href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K1145004" target="_blank">Plsr (BBa_K1145004)</a></dt>
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            <dd class="dd_1"><p>This promoter comes from the genome of Escherichia coli. It can take effect when the density of bacteria hits certain value. By using this part, our bacteria can secrete TrzN only when enough bacteria gather around atrazine pollution centre.</p></dd>
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        <dt><a name="pa" href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K1145005" target="_blank">Coding Parts (BBa_K1145005)</a></dt>
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            <dd class="dd_1"><p>Pλ is a promoter which can be inhibited by protein CI. We use this part combined with CI to realize the main function of regulating the whole system.</p></dd>
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        <dt><a name="plac" href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K1145006" target="_blank">RBS Parts (BBa_K1145006)</a></dt>
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            <dd class="dd_1"><p>Promoter Plac/ara-1 is used to drive the expression of LuxRI in pLuxRI2 and its derivatives. It comes from artificial synthesis.</p></dd>
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        <dt><a name="ci" href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K1145007" target="_blank">Regulatory Parts (BBa_K1145007)</a></dt>
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            <dd class="dd_1"><p>CI is a protein which can inhibit the expression of Pλ, we use this part to regulate our whole system. It first comes from λ phage, and the length of its gene is 750bp. In our project, we modified this protein to make it better at inhibiting the expression of Pλ.</p></dd>
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==Overview==
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We have characterized and submitted 42 BioBricks which could either be used directly or serve as a universal tool readily for potential scientific or engineering use.
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Those BioBricks could be divided into 4 groups.
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<div id="footer">
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1.BioBricks in [https://2012.igem.org/Team:SJTU-BioX-Shanghai/Parts3 Basic Parts] are all basic components of the whole project. They can be assembled to carry out different tasks.
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    <a href="/Special:RecentChanges" title='Recent changes'>Recent changes</a>
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    <a href="/Special:WhatLinksHere/Team:Nanjing-China" title="List of all wiki pages that link here [j]" accesskey="j">What links here</a>
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2.BioBricks in [https://2012.igem.org/Team:SJTU-BioX-Shanghai/Parts2 Membrane Anchors] are fusion membrane proteins which could either constitutively aggregate or aggregate under signal induction.
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    <a href="/Special:RecentChangesLinked/Team:Nanjing-China" title="Recent changes in pages linked from this page [k]" accesskey="k">Related changes</a>
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3.BioBricks in [https://2012.igem.org/Team:SJTU-BioX-Shanghai/Parts4 Fatty-Acid-Producing Membrane Accelerator ] are Membrane Anchors linked with enzymes involved in fatty acid synthesis.
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    <a href="/Special:Preferences">My preferences</a>
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4.BioBricks in [https://2012.igem.org/Team:SJTU-BioX-Shanghai/Parts5 Ligh-Sensing Membrane Rudder] are Membrane Anchors linked with enzymes involved in Violacein synthesis and VVD protein.
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<groupparts>iGEM012 SJTU-BioX-Shanghai</groupparts>
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Revision as of 13:36, 27 September 2013

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SJTU-BioX-Shanghai 2012 iGEM Team Parts

Overview

We have characterized and submitted 42 BioBricks which could either be used directly or serve as a universal tool readily for potential scientific or engineering use.

Those BioBricks could be divided into 4 groups.

1.BioBricks in Basic Parts are all basic components of the whole project. They can be assembled to carry out different tasks.

2.BioBricks in Membrane Anchors are fusion membrane proteins which could either constitutively aggregate or aggregate under signal induction.

3.BioBricks in Fatty-Acid-Producing Membrane Accelerator are Membrane Anchors linked with enzymes involved in fatty acid synthesis.

4.BioBricks in Ligh-Sensing Membrane Rudder are Membrane Anchors linked with enzymes involved in Violacein synthesis and VVD protein.

<groupparts>iGEM012 SJTU-BioX-Shanghai</groupparts>


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