Difference between revisions of "Team:British Columbia/Basic Part"

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<h3>★  ALERT! </h3>
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<p>This page is used by the judges to evaluate your team for the <a href="https://2016.igem.org/Judging/Awards#Special_Prizes">basic part special prize</a>. </p>
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<p> Delete this box in order to be evaluated for this medal. See more information at <a href="https://2016.igem.org/Judging/Pages_for_Awards/Instructions"> Instructions for Pages for awards</a>.</p>
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        <strong><p style="font-size: 3em">Basic Part</p></strong>
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<strong>
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<a href="https://2016.igem.org/Team:British_Columbia">Home</a> /
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<a href="https://2016.igem.org/Team:British_Columbia/Basic_Part">Achievements - Parts - Basic Parts</a></strong>
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<h1>Favorite Basic Part: BBa_k2139003</h1>
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<p align="justify"> <a href= "http://parts.igem.org/wiki/index.php?title=Part:BBa_K2139003"> BBa_K2139003</a> is comprised of the coding region of E1. E1 was used as a fusion protein within the middle of <i>Caulobacter cresentus’s</i> RSA-A surface layer protein. We were able to show expression on the surface of <i>C. crescentus</i> and functionally characterize that it maintained functionality. You can see our data here. The part originated from <i>AcidoThermus cellulolyticus</i> and was codon optimized for expression in <i> C. crescentus</i>. Our biobrick contains only the catalytic domain of the full protein.</p>
  
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<p align="justify">   References: Linger, Jeffrey G., William S. Adney, and Al Darzins. "Heterologous Expression and Extracellular Secretion of Cellulolytic Enzymes by Zymomonas Mobilis." Applied and Environmental Microbiology, vol. 76, no. 19, 2010., pp. 6360-6369doi:10.1128/AEM.00230-10.
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A <b>basic part</b> is a functional unit of DNA that cannot be subdivided into smaller component parts. <a href="http://parts.igem.org/wiki/index.php/Part:BBa_R0051">BBa_R0051</a> is an example of a basic part, a promoter regulated by lambda cl.
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<p>Most genetically-encoded functions have not yet been converted to BioBrick parts. Thus, there are <b>many</b> opportunities to find new, cool, and important genetically encoded functions, and refine and convert the DNA encoding these functions into BioBrick standard biological parts. </p>
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<h4>Note</h4>
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<p>This page should list all the basic parts your team has made during your project. You must add all characterization information for your parts on the Registry. You should not put characterization information on this page.</p>
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<p id="read-more"><strong>Check out other parts of our project below!</strong></p>
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<a href="https://2016.igem.org/Team:British_Columbia/Achievements/Parts">
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<img src="https://static.igem.org/mediawiki/2016/6/60/T--British_Columbia--header-mountains.jpg"></a>
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<a href="https://2016.igem.org/Team:British_Columbia/Project/S-Layer/Cellulases">
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<strong><figcaption>Part List</figcaption></strong></a>
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<a href="https://2016.igem.org/Team:British_Columbia/Project/S-Layer/Cellulases">
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<strong><figcaption>Cellulases</figcaption></strong></a></div>
 
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Revision as of 14:48, 18 October 2016

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Basic Part

Basic Part

Favorite Basic Part: BBa_k2139003

BBa_K2139003 is comprised of the coding region of E1. E1 was used as a fusion protein within the middle of Caulobacter cresentus’s RSA-A surface layer protein. We were able to show expression on the surface of C. crescentus and functionally characterize that it maintained functionality. You can see our data here. The part originated from AcidoThermus cellulolyticus and was codon optimized for expression in C. crescentus. Our biobrick contains only the catalytic domain of the full protein.

References: Linger, Jeffrey G., William S. Adney, and Al Darzins. "Heterologous Expression and Extracellular Secretion of Cellulolytic Enzymes by Zymomonas Mobilis." Applied and Environmental Microbiology, vol. 76, no. 19, 2010., pp. 6360-6369doi:10.1128/AEM.00230-10.

Check out other parts of our project below!