Team:Utah State/Parts

From 2009.igem.org

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     <td width="172" id="ana"><span class="currentPage"><font size = 4>BIOBRICKS</font></span>
     <td width="172" id="ana"><span class="currentPage"><font size = 4>BIOBRICKS</font></span>
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         <a href="#LaLa">Designed</a><br />
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         <a href="#tested">Tested</a><br/>
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        <a href="www.google.com">Submitted </a><br />
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      <a href="#submitted">Submitted </a><br />
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         <a href="www.google.com">Tested</a>
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               <b><i>BioBricks without Borders:</b></i></font>
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               <b><i>BioBricks</b></i></font>
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              <p><font face="Helvetica, Arial, San Serif" color =green>Investigating a multi-host BioBrick vector and secretion of cellular products</font></p><HR>
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<p class="class">The USU iGEM team has successfully constructed 49 BioBrick parts and devices. Of these, we have had the time to shown the functionality of 6 BioBricks, and had had 42 of them sequenced and shown to be correct. Check out our <a href="http://partsregistry.org/cgi/partsdb/pgroup.cgi?pgroup=iGEM2009&group=Utah_State/"><font color=#009900>BioBrick Registry</font></b></a> page to see all of these parts and to find more detailed information about them.
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<p> <font size="2.5" face=" Tahoma, Helvetica, Arial" color =#000000>The aim of the Utah State University iGEM project is to develop improved upstream and downstream processing strategies for manufacturing cellular products using the standardized BioBrick system. First, we altered the broad-host range vector pRL1383a to comply with BioBrick standards and enable use of BioBrick constructs in organisms like <i>Pseudomonas putida</i>, <i>Rhodobacter sphaeroides</i>, and <i>Synechocystis</i> PCC6803. This vector will facilitate exploitation of advantageous characteristics of these organisms, such as photosynthetic carbon assimilation.  Following expression, product recovery poses a difficult and expensive challenge. Downstream processing of cellular compounds, like polyhydroxyalkanoates (PHAs), commonly represents more than half of the total production expense.  To counter this problem, secretion-promoting BioBrick devices were constructed through genetic fusion of signal peptides with protein-coding regions.  To demonstrate this, the secretion of PHA granule-associated proteins and their affinity to PHA was investigated. Project success will facilitate expression and recovery of BioBrick-coded products in multiple organisms.</p>
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            <p>  <font size="4" face="Helvetica, Arial, San Serif" color =green>OUR SITE IS STILL UNDER CONSTRUCTION AND OUR INFORMATION IS BEING ADDED.  PLEASE COME BACK IN A FEW WEEKS TO SEE OUR PROJECT!</font></p>
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Revision as of 09:22, 21 October 2009

USU iGem Untitled Document

BIOBRICKS Tested
Submitted
Designed
BioBricks

The USU iGEM team has successfully constructed 49 BioBrick parts and devices. Of these, we have had the time to shown the functionality of 6 BioBricks, and had had 42 of them sequenced and shown to be correct. Check out our BioBrick Registry page to see all of these parts and to find more detailed information about them.


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