Team:CU-Boulder

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{{CU-Boulder-Header}}
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This is a template page. READ THESE INSTRUCTIONS.
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<a href="https://2012.igem.org/Team:CU-Boulder/Team"><img src="https://static.igem.org/mediawiki/2012/b/b9/Biofront2.jpg" height="310" width="1150" alt="Boulder-landscape2012-team" title="Team" id="wows0"/></a>
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<a href="https://2012.igem.org/Team:CU-Boulder/Project"><img src="https://static.igem.org/mediawiki/2012/7/75/Small_flowers1.jpg" alt="Boulder2012-project" title="Project" id="wows1"/></a>
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<a href="https://2012.igem.org/Team:CU-Boulder/Project"><img src="https://static.igem.org/mediawiki/2012/d/d6/010101.jpeg" height="350" width="1000" alt="Boulder2012-results" title="Results" id="wows2"/></a>
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<a href="https://2012.igem.org/Team:CU-Boulder/Modeling"><img src="https://static.igem.org/mediawiki/2012/d/d8/Synthetic_clip_image002.jpeg" height="350" width="1000" alt="Boulder2012-model" title="Model" id="wows3"/></a>
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<a href="https://2012.igem.org/Team:CU-Boulder/Safety"><img src="https://static.igem.org/mediawiki/2012/5/54/2012-06-25_09-51-34_418.jpg" title="Safety" id="wows4"/></a>
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<a href="https://2012.igem.org/Team:CU-Boulder/Attributions"><img src="https://static.igem.org/mediawiki/2012/a/aa/Boulder_panoramic.jpg" height="300" width="1100" alt="Boulder-panoramic2012" title="Attributions" id="wows5"/></a>
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You are provided with this team page template with which to start the iGEM season.  You may choose to personalize it to fit your team but keep the same "look." Or you may choose to take your team wiki to a different level and design your own wiki.  You can find some examples <a href="https://2009.igem.org/Help:Template/Examples">HERE</a>.
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<a href="#wows0" title="Team"><img src="https://static.igem.org/mediawiki/2012/b/b9/Biofront2.jpg" height="98" width="455" alt="Boulder-landscape2012"/>1</a>
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<a href="#wows1" title="Project"><img src="https://static.igem.org/mediawiki/2012/7/75/Small_flowers1.jpg" height="90" width="288" alt="Boulder-2012-project"/>2</a>
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<a href="#wows2" title="Results"><img src="https://static.igem.org/mediawiki/2012/d/d6/010101.jpeg" height="90" width="288" alt="Boulder-2012-results"/>3</a>
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You <strong>MUST</strong> have all of the pages listed in the menu below with the names specified. PLEASE keep all of your pages within your teams namespace. 
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<a href="#wows3" title="Model"><img src="https://static.igem.org/mediawiki/2012/d/d8/Synthetic_clip_image002.jpeg" height="90" width="288" alt="Boulder-2012-model"/>4</a>
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<a href="#wows4" title="Safety"><img src="https://static.igem.org/mediawiki/2012/5/54/2012-06-25_09-51-34_418.jpg" height="90" width="288" alt="Boulder-2012-safety"/>5</a>
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<a href="#wows5" title="Attributions"><img src="https://static.igem.org/mediawiki/2012/a/aa/Boulder_panoramic.jpg" height="90" width="288" alt="Boulder-2012-Attributions"/>6</a>
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|You can write a background of your team here. Give us a background of your team, the members, etc.  Or tell us more about something of your choosing.
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|[[Image:CU-Boulder_logo.png|200px|right|frame]]
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''Tell us more about your project. Give us background. Use this as the abstract of your project. Be descriptive but concise (1-2 paragraphs)''
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|[[Image:CU-Boulder_team.png|right|frame|Your team picture]]
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|align="center"|[[Team:CU-Boulder | Team CU-Boulder]]
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<!--- The Mission, Experiments --->
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<p style="text-align: center;"><a href="http://s10.flagcounter.com/more/5Qyt"><img src="http://s10.flagcounter.com/count/5Qyt/bg_FFFFFF/txt_000000/border_CCCCCC/columns_2/maxflags_12/viewers_0/labels_0/pageviews_0/flags_0/" alt="free counters" border="0"></a>
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!align="center"|[[Team:CU-Boulder|Home]]
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!align="center"|[[Team:CU-Boulder/Team|Team]]
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<p style="text-align: center;"><div class="fb-like" data-href="http://www.facebook.com/pages/CU-iGEM-2012/334455203291790" data-send="false" data-width="450" data-show-faces="false"></div></p>
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!align="center"|[https://igem.org/Team.cgi?year=2012&team_name=CU-Boulder Official Team Profile]
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!align="center"|[[Team:CU-Boulder/Project|Project]]
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!align="center"|[[Team:CU-Boulder/Parts|Parts Submitted to the Registry]]
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!align="center"|[[Team:CU-Boulder/Modeling|Modeling]]
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!align="center"|[[Team:CU-Boulder/Notebook|Notebook]]
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<p style="text-align: center;">Welcome to the CU-iGEM 2012 wiki! This is the first time the University of Colorado has competed in the International Genetically Engineered Machines competition, and we are excited to show you the science coming out of Boulder, Colorado! We are a team of five undergraduates advised by our two graduate mentors, and a smattering of post-docs. This year is also the grand opening of the brand new Biofrontiers building for bioscience, and biotechnology research. We have been fortunate enough to have lab space in the new building.</p>
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!align="center"|[[Team:CU-Boulder/Safety|Safety]]
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!align="center"|[[Team:CU-Boulder/Attributions|Attributions]]
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<center><h2>Quorum STOPPING</h2></center>
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<img src="https://static.igem.org/mediawiki/2012/d/d1/Media_5a7257dc5595cb7be3df7954509f3e90.jpeg" width=290 height=193 />
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&nbsp;&nbsp;&nbsp;&nbsp;Quorum sensing is a system of bacterial communication that coordinates gene expression based on population density. Quorum sensing dictates many functions within bacteria such as when pathogenic gene products are released, biofilm formation, and food rot. Inhibiting quorum sensing became the goal of CU-Boulder’s 2012 iGEM team. This led us to find or create many interesting BioBrick parts such as Aiia, a protein that degrades specific quorums, Sdia, a transcription factor that is more sensitive to AHLs than the standard LuxR, and NucB, a nuclease that degrades preexisting biofilm. <br>
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&nbsp;&nbsp;&nbsp;&nbsp;Instead of using a pathogenic bacteria, our team utilized the Lux gene brick from Vibrio fischeri. This gram-negative bacteria uses quorum sensing to produce bioluminescence, while living in the gut of bobtail squid (shown above). By using V. fischeri, our team eliminated the risk of working with pathogenic bacteria and bioluminescence proved to be easily quantifiable using plate reader experiments. As none of the presubmitted Lux bricks worked for our team, we isolated each of the 5 essential genes (LuxA,B,C,D,and E) and well an extremely important bioluminescent gene, LuxG, from a V. fischeri strain to create our model system. For more detailed information on our project visit our <a href="https://2012.igem.org/Team:CU-Boulder/Project">Project</a> page.
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The video below is an animated overview of quorum sensing.
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Latest revision as of 01:37, 4 October 2012

Boulder-landscape2012-team Boulder2012-project Boulder2012-results Boulder2012-model Boulder-panoramic2012
Boulder-landscape20121 Boulder-2012-project2 Boulder-2012-results3 Boulder-2012-model4 Boulder-2012-safety5 Boulder-2012-Attributions6

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Welcome to the CU-iGEM 2012 wiki! This is the first time the University of Colorado has competed in the International Genetically Engineered Machines competition, and we are excited to show you the science coming out of Boulder, Colorado! We are a team of five undergraduates advised by our two graduate mentors, and a smattering of post-docs. This year is also the grand opening of the brand new Biofrontiers building for bioscience, and biotechnology research. We have been fortunate enough to have lab space in the new building.



Quorum STOPPING



    Quorum sensing is a system of bacterial communication that coordinates gene expression based on population density. Quorum sensing dictates many functions within bacteria such as when pathogenic gene products are released, biofilm formation, and food rot. Inhibiting quorum sensing became the goal of CU-Boulder’s 2012 iGEM team. This led us to find or create many interesting BioBrick parts such as Aiia, a protein that degrades specific quorums, Sdia, a transcription factor that is more sensitive to AHLs than the standard LuxR, and NucB, a nuclease that degrades preexisting biofilm.
    Instead of using a pathogenic bacteria, our team utilized the Lux gene brick from Vibrio fischeri. This gram-negative bacteria uses quorum sensing to produce bioluminescence, while living in the gut of bobtail squid (shown above). By using V. fischeri, our team eliminated the risk of working with pathogenic bacteria and bioluminescence proved to be easily quantifiable using plate reader experiments. As none of the presubmitted Lux bricks worked for our team, we isolated each of the 5 essential genes (LuxA,B,C,D,and E) and well an extremely important bioluminescent gene, LuxG, from a V. fischeri strain to create our model system. For more detailed information on our project visit our Project page.

The video below is an animated overview of quorum sensing.