Team:Utah State

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    <td><a name="top"><img width="950" src="https://static.igem.org/mediawiki/2010/5/5e/Utah_State_logo.png" /></a></td>
 
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    <td align="center" ><a class="mainLinks" href="" >Project Summary</a> </td>
 
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    <td align="center" ><a class="mainLinks" href="" >Meet the Team</a> </td>
 
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    <td align="center"><a class="mainLinks" href=""  >Sponsors</a> </td>
 
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    <td align="center"><a class="mainLinks" href=""  >Something else</a> </td>
 
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    <td valign="top"><span style="font-size:23px">Welcome to the Utah State University's 2010 Wiki</span>
 
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      <p>The future of synthetic biology lies in expanding our ability to engineer genes in new organisms.
 
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        Our project develops a system to engineer the genome of the photosynthetic cyanobacterium Synechocystis sp. PCC6803, 
 
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        establishes expression standards for this species, and adds a set of characterized Synechocystis promoters and ribosome
 
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        binding sites to the BioBrick toolbox. We developed a BioBrick vector that can be used to assemble parts and devices in E.
 
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        coli. Upon transformation into Synechocystis, it integrates the device directly into the genome through homologous
 
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        recombination. We utilized genes that were activated under a variety of conditions, from those responding to heat stress to
 
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        ones oscillating under a circadian rhythm. The promoters and ribosome binding sites were converted into BioBrick-compatible
 
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        parts, and subsequently characterized. Our success will enable the use of existing parts in new species, and will expand the
 
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        range of devices that can be built. </p>
 
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            <p> <em>CyanoBricks</em> Description. </p></td>
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          <td style="padding-top:30px; padding-right:30px" valign="top" width="45%"><span style="font-size:18px">Another thing!</span>
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The future of synthetic biology lies in expanding our ability to engineer genes in new organisms. Our project develops a system to engineer the genome of the photosynthetic cyanobacterium Synechocystis sp. PCC6803, establishes expression standards for this species, and adds a set of characterized Synechocystis promoters and ribosome binding sites to the BioBrick toolbox. We developed a BioBrick vector that can be used to assemble parts and devices in E. coli. Upon transformation into Synechocystis, it integrates the device directly into the genome through homologous recombination. We utilized genes that were activated under a variety of conditions, from those responding to heat stress to ones oscillating under a circadian rhythm. The promoters and ribosome binding sites were converted into BioBrick-compatible parts, and subsequently characterized. Our success will enable the use of existing parts in new species, and will expand the range of devices that can be built.  
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            <p>Something else here.</p></td>
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<th align="center"><a href="/Team:Utah_State" title="Team:Utah State">Home</a>
 
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</th><th align="center"><a href="/Team:Utah_State/Team" title="Team:Utah State/Team">Team</a>
 
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Revision as of 00:50, 28 September 2010

Team:Utah State - 2009.igem.org

 

Team:Utah State

From 2009.igem.org

USU iGem Untitled Document

CyanoBricks
Project
Design
Construction
Modeling
Testing
Protocols
Results
Welcome!

The future of synthetic biology lies in expanding our ability to engineer genes in new organisms. Our project develops a system to engineer the genome of the photosynthetic cyanobacterium Synechocystis sp. PCC6803, establishes expression standards for this species, and adds a set of characterized Synechocystis promoters and ribosome binding sites to the BioBrick toolbox. We developed a BioBrick vector that can be used to assemble parts and devices in E. coli. Upon transformation into Synechocystis, it integrates the device directly into the genome through homologous recombination. We utilized genes that were activated under a variety of conditions, from those responding to heat stress to ones oscillating under a circadian rhythm. The promoters and ribosome binding sites were converted into BioBrick-compatible parts, and subsequently characterized. Our success will enable the use of existing parts in new species, and will expand the range of devices that can be built.



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