Team:Utah State/usu home

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Mad yeasts on Mars?
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    <td bgcolor="#000000" cellpadding="0" cellspacing="0"> <img src="https://static.igem.org/mediawiki/2010/b/b0/USU_Main_Top.png" width="864" height="54" hspace="25" border="0" /></td>
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            <td bgcolor="#000000" cellpadding="0" cellspacing="0"><a href="https://2010.igem.org/Project_usu.html"><img src="https://static.igem.org/mediawiki/2010/2/23/Project_usu.png" width="57" height="60" border="0" /></a></td>
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            <td bgcolor="#000000" cellpadding="0" cellspacing="0"><a href="https://2010.igem.org/Design_usu.html"><img src="https://static.igem.org/mediawiki/2010/0/0a/Design.png" width="57" height="60" border="0" /></a></td>
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            <td width="224" bgcolor="#000000" cellpadding="0" cellspacing="0"><a href="https://2010.igem.org/Construction_usu.html"><img src="https://static.igem.org/mediawiki/2010/3/37/Construction.png" width="57" height="60" border="0" /></a></td>
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            <b><i>Welcome!</b></i></font>
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            <td bgcolor="#000000"><font face="Century Gothic, Arial, San Serif" color =#ffffff><p>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. </p></font></td>
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            <td bgcolor="#000000" cellpadding="0" cellspacing="0"><a href="https://2010.igem.org/Testing_usu.html"><img src="https://static.igem.org/mediawiki/2010/7/7f/Testing.png" width="57" height="60" border="0" /></a></td>
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            <td bgcolor="#000000" cellpadding="0" cellspacing="0"><a href="https://2010.igem.org/USU_protocol"><img src="https://static.igem.org/mediawiki/2010/1/1d/Protocols.png" width="57" height="60" border="0" /></a></td>
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            <td bgcolor="#000000" cellpadding="0" cellspacing="0"><a href="https://2010.igem.org/Results_usu.html"><img src="https://static.igem.org/mediawiki/2010/1/17/Results.png" width="57" height="60" border="0" /></a></td>
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Latest revision as of 08:35, 26 October 2010

USU_IGEM

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.