Difference between revisions of "Team:SHSID China/Parts"

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<div style="background: url(https://static.igem.org/mediawiki/2018/d/d6/T--SHSID_China--main_bg2.jpg); background-size: cover; background-position: center" class="link" id="Abstract">
 
<div style="background: url(https://static.igem.org/mediawiki/2018/d/d6/T--SHSID_China--main_bg2.jpg); background-size: cover; background-position: center" class="link" id="Abstract">
 
     <article style="color: white; font-size: 16px; padding-top: 10px">
 
     <article style="color: white; font-size: 16px; padding-top: 10px">
             <h2 style="color: white; font-family: 'Trocchi', serif; text-align: center">Part Table</h2>
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             <h2 style="color: white; font-family: 'Trocchi', serif; text-align: center">Parts Summary</h2>
             <p style="color: white; font-size: 16px; padding-top: 10px">We have referenced research papers and existing registry of biological parts on iGEM website to edit and produce parts. The following parts are luxG, luxCDEBAG+G, and grpE. </p>
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             <p style="color: white; font-size: 16px; padding-top: 10px; text-align: center">We have created and documented a total of 5 parts onto the Parts Registry.</p>
 
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             <groupparts>iGEM18 SHSID_China</groupparts>
 
             <groupparts>iGEM18 SHSID_China</groupparts>
 
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            <p style="color: white; font-size: 16px; padding-top: 10px">Part BBa_K2836001 is the luxG gene from <em>Aliivibrio fischeri</em> strain ES114, and encodes flavin reductase that participates in reduced flavin mononucleotide turnover, which is a substrate for the luciferase-catalyzed light emitting reaction encoded by the lux operon in bioluminescent bacteria. </p>
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            <p style="color: white; font-size: 16px; padding-top: 10px">Part BBa_K2836002 is a composite part consisting of the <em>lux</em> operon (part BBa_K325909) fused with an additional luxG gene (part BBa_K2836001), as luxG and flavin reductase have been shown to increase the intensity of light produced, thus improving upon the previous characterization of the lux operon (part BBa_K325909) by iGEM 10_Cambridge team. </p>
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            <p style="color: white; font-size: 16px; padding-top: 10px">Part BBa_K2836003 is the grpE promoter, which is a heat shock protein capable of increasing transcription rates when put under chemical stress from compounds such as ethanol, sodium propionate, sodium acetate, hydrogen peroxide, changes in temperature and UV radiation.</p>
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            <p style="color: white; font-size: 16px; padding-top: 10px">Parts BBa_K2836004 and BBa_K2836005 are composite parts made with the grpE promoter from BBa_K2836003 ligated with part BBa_K2836002 and part BBa_K325909 respectively to put bacterial autoluminescence under the control of a regulatory promoter.</p>
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            <h2 style="color: white; font-family: 'Trocchi', serif; text-align: center">Criteria for Medals:</h2>
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            <p style="color: white; font-size: 16px; padding-top: 10px">1. <strong>Silver #1</strong> (Validated Part): We submitted part BBa_K2836001 (http://parts.igem.org/Part:BBa_K2836001) as the new BioBrick part of our own creation. </p>
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            <p style="color: white; font-size: 16px; padding-top: 10px">2. <strong>Gold #2</strong> (Improve a Previous Part): We submitted part BBa_K2836002 (http://parts.igem.org/Part:BBa_K2836002) as a new BioBrick part that has a functional improvement upon an existing part (BBa_K325909). </p>
 
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Revision as of 20:45, 17 October 2018

Parts


The whole is the sum of its parts.