Team:Utah State/Project

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!align="center"|[[Team:Utah_State|Home]]
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!align="center"|[[Team:Utah_State/Team|The Team]]
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!align="center"|[[Team:Utah_State/Project|The Project]]
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!align="center"|[[Team:Utah_State/Parts|Parts Submitted to the Registry]]
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!align="center"|[[Team:Utah_State/Modeling|Modeling]]
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!align="center"|[[Team:Utah_State/Notebook|Notebook]]
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== '''Overall project''' ==
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Your abstract
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        <td id="nav"><a href="https://2009.igem.org/Team:Utah_State"><font size = 4>HOME</font></a></td>
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        <td id="nav"><a href="https://2009.igem.org/Team:Utah_State/Team"><font size = 4>ABOUT US</font></a></td>
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        <td width="172" id="ana"><span class="currentPage"><font size = 4>PROJECT</font></span>
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        <a href="https://2009.igem.org/Team:Utah_State/Abstract">Abstract</a><br />
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<a href="https://2009.igem.org/Team:Utah_State/Introduction">Introduction</a><br />
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        <a href="https://2009.igem.org/Team:Utah_State/Broad-HostVectors">Broad-Host Vectors</a><br />
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        <a href="https://2009.igem.org/Team:Utah_State/Secretion">Secretion</a><br />
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        <a href="https://2009.igem.org/Team:Utah_State/Experiments">Experiments</a><br />
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        <a href="https://2009.igem.org/Team:Utah_State/FutureWork">Future Work</a><br />
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        <a href="https://2009.igem.org/Team:Utah_State/References">References</a><br />
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        <td id="nav"><a href="https://2009.igem.org/Team:Utah_State/Parts"><font size = 4>BIOBRICKS</font></a></td>
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      <td id="nav"><a href="https://2009.igem.org/Team:Utah_State/Achievements"><font size = 4>JUDGING</font></a></td>
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      <td id="nav"><a href="https://2009.igem.org/Team:Utah_State/Contact"><font size = 4>CONTACT</font></a></td>
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              <b><i>BioBricks without Borders:
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  Investigating a multi-host BioBrick vector and secretion of cellular products</font>
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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 Pseudomonas putida, Rhodobacter sphaeroides, and Synechocystis 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.
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== Project Details==
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=== Protocols ===
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=== Part 2 ===
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=== The Experiments ===
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=== Part 3 ===
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== Results ==
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Latest revision as of 02:00, 22 October 2009

USU iGem

Untitled Document

PROJECT Abstract
Introduction
Broad-Host Vectors
Secretion
Experiments
Future Work
References
BioBricks without Borders:
Investigating a multi-host BioBrick vector and secretion of cellular products

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 Pseudomonas putida, Rhodobacter sphaeroides, and Synechocystis 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.



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