Team:Calgary/Project/Acomplishments

From 2011.igem.org

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<b>The University of Calgary iGEM Team has had many accomplishments this Summer</b><br><br>
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<h2>Results from the 2011 iGEM Americas Regionals</h2>
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<b>In our promoter project...</b><br>
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<a href="https://2011.igem.org/File:UCalgary2011_RegionalAwards.jpg"><img style="width: 300px; float: right; padding-left: 10px;" src="https://static.igem.org/mediawiki/2011/9/9c/UCalgary2011_RegionalAwards.jpg"></img></a>
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<ul><li>We designed a novel protocol to identify small hydrophobic molecule interacters within a cell.</li>
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<p>
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<li>We were able to successfully biotinylate a naphthenic acid, suggesting that we may be able to biotinylate other small hydrophobic molecuels to screen for interactors in the search for responsive elements.</li>
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We are pleased to report that iGEM Calgary came home with a gold medal and two of the eight special awards: Best Wiki and Best Experimental Measurement for our <a href="https://2011.igem.org/Team:Calgary/Project/Reporter">electrochemical reporter</a>. We will be proceeding on to the World Jamboree at MIT in November, after further refining of our project. Stay tuned for more on this!
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<li>We identified a gene that is upregulated in the presence of naphthenic acids, suggesting a possible responsive elements or degradative protein.</li><br><br>
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</p>
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<b>In our Reporter Project...</b><br>
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<p>See the rest of the Regionals results <a href="https://2011.igem.org/Jamborees">here</a>!</p>
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<li>We characterized a novel reporter function for the lacZ gene using an electrochemical output.</li>
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<br/><br/><br/><br/>
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<li>We laid the groundwork for future use of electrochemical reporting in iGEM</li><br><br>
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<br><p><b>The University of Calgary iGEM Team has had many accomplishments this summer:</b></p><br>
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<b>In our Chassis project...</b><br>
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<img style="float:right;" src="https://static.igem.org/mediawiki/2011/b/ba/UCalgary2011_BacterialPromoterSmall.png"></img>
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<li>We characterized a<i> Pseudomonas-E. coli</i> conjugation construct</li>
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<p><b>In our promoter project...</b></p>
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<li>We submitted parts and protocols for future work in both microalgae and <i>Pseudomonas</i></li>
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<ul><li><p>We designed a novel protocol to identify small hydrophobic molecule interactors within a cell.</p></li>
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<li>We characterized the viability of <i>Pseudomonas</i> and <i>E. coli</i> to grow and survive in tailings ponds</li>
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<li><p>We were able to successfully biotinylate a naphthenic acid, suggesting that it is possible to biotinylate other small hydrophobic molecules as well. This may be used to screen for various small molecule interactors.</p></li>
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</ul>
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<li><p>We identified a gene that is up-regulated in the presence of naphthenic acids, and cloned its promoter (putative) and submitted it to the registry as a stand-alone part, as well as part of a reporter system (with lacZ, oriT, and ori1600).</p></li><br></ul>
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<img style="float:right;" src="https://static.igem.org/mediawiki/2011/6/6c/UCalgary2011_BacterialGeneSmall.png"></img>
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<p><b>In our Reporter Project...</b></p><ul>
 +
<li><p>We characterized a novel reporter function for the <i>lacZ</i> gene using an electrochemical output.</p></li>
 +
<li><p>We laid the groundwork for future use of electrochemical reporting in iGEM.</p></li><br></ul>
 +
 
 +
<img style="float:right;" src="https://static.igem.org/mediawiki/2011/0/02/UCalgary2011_BacterialChassisSmall.png"></img>
 +
<p><b>In our Chassis project...</b></p><ul>
 +
<li><p>We characterized a<i> Pseudomonas-E. coli</i> conjugation construct</p></li>
 +
<li><p>We submitted parts and protocols for future work in both microalgae and <i>Pseudomonas</i></p></li>
 +
<li><p>We characterized the viability of <i>Pseudomonas</i> and <i>E. coli</i> to grow and survive in tailings ponds</p></li>
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</ul><br>
<h2>Judging Requirements</h2>
<h2>Judging Requirements</h2>
<b>Bronze:</b>
<b>Bronze:</b>
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<ul><li><b>Team registration</b> - Our team successfully registered for the iGEM Competition
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<ul><li><b>Team registration</b> - Our team successfully registered for the iGEM Competition.
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<li><b>Complete Judging Form</b> - To view our Judging Form please <a>href="https://igem.org/2011_Judging_Form?id=640" click here</a>
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<li><b>Complete Judging Form</b> - To view our Judging Form please <a href="https://igem.org/2011_Judging_Form?id=640"> click here.</a>
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<li><b>Team Wiki</b> - Our team has successfully designed a wiki page for our project
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<li><b>Team Wiki</b> - Our team has successfully designed a wiki page for our project.
<li><b>Submit at least one new well-characterized standard BioBrick Part</b> - Our team has submitted several new parts all of which we have fully characterized.
<li><b>Submit at least one new well-characterized standard BioBrick Part</b> - Our team has submitted several new parts all of which we have fully characterized.
</ul>
</ul>
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<br>
<b>Silver:</b>
<b>Silver:</b>
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<ul><li><b>Demonstrate at least one new BioBrick part designed works as expected</b> - All of our parts have been carefully tested.  Our oriT-ori1600 <i>Psuedomonas</i> conjugation part has been well characterized.
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<ul><li><b>Demonstrate at least one new BioBrick part designed works as expected</b> - All of our parts have been carefully tested.  Our oriT-ori1600 <i>Pseudomonas</i> conjugation part has been well characterized.</li>
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<li>
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<li><b>Enter this information and other documentation on the part's 'Main Page' section of the Registry</b> - The data relating to our new BioBrick parts have all been added to the Registry.</li>
</ul>
</ul>
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<br>
<b>Gold:</b>  
<b>Gold:</b>  
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<ul><li><b>Improve the function of an existing BioBrick Part</b> - Our team utilized the <i>lacZ</i> gene to develop and characterize it as an electrochemical detector. Please see the <a href="https://2011.igem.org/Team:Calgary/Project/Reporter"> reporter section</a> for more information.</li>
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<li><b>Help another iGEM Team</b> - The University of Calgary iGEM Team collaborated with the University of Lethridge iGEM Team since both of our projects were involving tailings ponds water.  We characterized <i>E. coli</i> viability in our unique tailing ponds samples and developed a well standardized data set by working together.  For more information, <a href="https://2011.igem.org/Team:Calgary/Outreach/Collaboration"> click here</a></li>
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    Improve the function of an existing BioBrick Part or Device (created by another team or your own institution in a previous year) and enter this information in the Registry (in the “Experience” section of that BioBrick’s Registry entry), and don't forget to create a new registry page for the improved part.
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<li><b>Outline a new approach to an issue of Human Practice in Synthetic Biology</b> - In Canada, the government has mandated that oilsands companies must test for the presence of naphthenic acids four times a year in their tailings ponds. Obviously public opinion and government policy will influence the actions oil companies will make in Alberta. Our human practices is a report on the role of government and industry on tailings ponds bioremediation and how synthetic biology and our device will fit into the present policies and procedures implemented in Alberta. Please <a href="https://2011.igem.org/Team:Calgary/Outreach/Report"> click here</a> for more information.</li>
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    The growth of the Registry depends on having a broad base of reliable parts. This is why the improvement of an existing part is just as important as the creation and documentation of a new part. An "improvement" is anything that improves the functionality and ease-of-use of a part, so that it is more likely to be used by the community. For instance: strengthening the expression of a part by mutating the DNA sequence; modifying one or a few parts in construct (Device) so that it performs its intended job better; improving a cloning or expression vector that can be easily used by the entire community; and of course, troubleshooting and fixing a part reported to be non-functional. Data from an experimental comparison between the original and improved part/ device is strongly recommended.
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</ul>
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    Help another iGEM team by, for example, characterizing a part, debugging a construct, or modeling or simulating their system.
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    Outline and detail a new approach to an issue of Human Practice in synthetic biology as it relates to your project, such as safety, security, ethics, or ownership, sharing, and innovation.
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Latest revision as of 03:58, 29 October 2011


Accomplishments

Results from the 2011 iGEM Americas Regionals

We are pleased to report that iGEM Calgary came home with a gold medal and two of the eight special awards: Best Wiki and Best Experimental Measurement for our electrochemical reporter. We will be proceeding on to the World Jamboree at MIT in November, after further refining of our project. Stay tuned for more on this!

See the rest of the Regionals results here!






The University of Calgary iGEM Team has had many accomplishments this summer:


In our promoter project...

  • We designed a novel protocol to identify small hydrophobic molecule interactors within a cell.

  • We were able to successfully biotinylate a naphthenic acid, suggesting that it is possible to biotinylate other small hydrophobic molecules as well. This may be used to screen for various small molecule interactors.

  • We identified a gene that is up-regulated in the presence of naphthenic acids, and cloned its promoter (putative) and submitted it to the registry as a stand-alone part, as well as part of a reporter system (with lacZ, oriT, and ori1600).


In our Reporter Project...

  • We characterized a novel reporter function for the lacZ gene using an electrochemical output.

  • We laid the groundwork for future use of electrochemical reporting in iGEM.


In our Chassis project...

  • We characterized a Pseudomonas-E. coli conjugation construct

  • We submitted parts and protocols for future work in both microalgae and Pseudomonas

  • We characterized the viability of Pseudomonas and E. coli to grow and survive in tailings ponds


Judging Requirements

Bronze:
  • Team registration - Our team successfully registered for the iGEM Competition.
  • Complete Judging Form - To view our Judging Form please click here.
  • Team Wiki - Our team has successfully designed a wiki page for our project.
  • Submit at least one new well-characterized standard BioBrick Part - Our team has submitted several new parts all of which we have fully characterized.

Silver:
  • Demonstrate at least one new BioBrick part designed works as expected - All of our parts have been carefully tested. Our oriT-ori1600 Pseudomonas conjugation part has been well characterized.
  • Enter this information and other documentation on the part's 'Main Page' section of the Registry - The data relating to our new BioBrick parts have all been added to the Registry.

Gold:
  • Improve the function of an existing BioBrick Part - Our team utilized the lacZ gene to develop and characterize it as an electrochemical detector. Please see the reporter section for more information.
  • Help another iGEM Team - The University of Calgary iGEM Team collaborated with the University of Lethridge iGEM Team since both of our projects were involving tailings ponds water. We characterized E. coli viability in our unique tailing ponds samples and developed a well standardized data set by working together. For more information, click here
  • Outline a new approach to an issue of Human Practice in Synthetic Biology - In Canada, the government has mandated that oilsands companies must test for the presence of naphthenic acids four times a year in their tailings ponds. Obviously public opinion and government policy will influence the actions oil companies will make in Alberta. Our human practices is a report on the role of government and industry on tailings ponds bioremediation and how synthetic biology and our device will fit into the present policies and procedures implemented in Alberta. Please click here for more information.