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Team:Calgary/Project/Achievements
From 2010.igem.org
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<p>The CpxR reporter was found to report on misfolding protein. We characterized this promoter with varying concentrations of folding and misfolding proteins produced which we assumed is correlated to arabinose concentrations due to the use of AraC promoter. We also tested this promoter with NlpE, an outer membrane lipoprotein that literature has found activates the Cpx pathway. Finally, we tested this promoter in varying temperature to produce a heat shock response.</p></li> | <p>The CpxR reporter was found to report on misfolding protein. We characterized this promoter with varying concentrations of folding and misfolding proteins produced which we assumed is correlated to arabinose concentrations due to the use of AraC promoter. We also tested this promoter with NlpE, an outer membrane lipoprotein that literature has found activates the Cpx pathway. Finally, we tested this promoter in varying temperature to produce a heat shock response.</p></li> | ||
| - | <h3>Characterize the operation of at least one new BioBrick Part or Device and enter this information on the Parts or Device page via the Registry of Parts</h3> | + | <table> |
| + | <tr> | ||
| + | <td>INSERT CHECK MARK HERE</td> | ||
| + | <td><h3>Characterize the operation of at least one new BioBrick Part or Device and enter this information on the Parts or Device page via the Registry of Parts</h3></td> | ||
| + | </tr> | ||
| + | </table> | ||
<li>Both MalE and MalE31 also worked as expected, malE folding in the periplasm and malE31 showing a misfolding response. This was indicated through testing with a reporter from another lab (Raivio) (for more info click here) as well as tetsing with our cpxR reporter click here.</li> | <li>Both MalE and MalE31 also worked as expected, malE folding in the periplasm and malE31 showing a misfolding response. This was indicated through testing with a reporter from another lab (Raivio) (for more info click here) as well as tetsing with our cpxR reporter click here.</li> | ||
Revision as of 23:48, 27 October 2010
Achievements
Bronze Medal Requirements
| INSERT CHECK MARK HERE | Register the team |
| INSERT CHECK MARK HERE | Successfully complete and submit a project summary form |
| INSERT CHECK MARK HERE | Create a Wiki which includes all the details of the project |
| INSERT CHECK MARK HERE | Present a presentation and a poster at the iGEM Jamboree |
| INSERT CHECK MARK HERE For more information, please see our Parts page here. |
Enter information detailing at least one new standard BioBrick Part or Device in the Registry of Parts |
| INSERT CHECK MARK HERE For more information, please see our Parts page here. |
Submit DNA for at least one new BioBrick Part or Device to the Registry of Parts |
Silver Medal Requirements
| INSERT CHECK MARK HERE | Demonstrate that one of your parts works as expected |
- Through our characterization data, we showed that several of our parts worked as expected. Click here for more information.
The CpxR reporter was found to report on misfolding protein. We characterized this promoter with varying concentrations of folding and misfolding proteins produced which we assumed is correlated to arabinose concentrations due to the use of AraC promoter. We also tested this promoter with NlpE, an outer membrane lipoprotein that literature has found activates the Cpx pathway. Finally, we tested this promoter in varying temperature to produce a heat shock response.
- Both MalE and MalE31 also worked as expected, malE folding in the periplasm and malE31 showing a misfolding response. This was indicated through testing with a reporter from another lab (Raivio) (for more info click here) as well as tetsing with our cpxR reporter click here.
- We characterized the cpxR reporter, malE31, MalE and IbpAB. See characterization data here.
| INSERT CHECK MARK HERE | Characterize the operation of at least one new BioBrick Part or Device and enter this information on the Parts or Device page via the Registry of Parts |
Gold Medal Requirements
- we entered new DNA as well as new sequences for malE and malE31.
- we entered characterization data for the CpxR promoter.
- We tested out a part for Lethbridge. We characterized it for possible misfolding in the cytoplasm. Results can be found here.
- We also attended a regional workshop as well as a mock iGEM event with the University of Alberta as well as the University of Lethbridge. Here we helped each their out with our projects by practicing our presentations for each other, giving suggestions, future directions as well as troubleshooting
- Finally our team filled out surveys for the following teams:
- This year we chose to approach ethics by making a podscasts covering a few different ethical issues pertaining to synthetic biology. We felt tat this would be a novel way to increase awareness about the field of synthetic biology while having a discussion of important issues. We felt that this would be a much more accessible way for the public to gain a better understanding of what the real fears in synthetic biology is as well as to dispel some of the misleading impressions given by media sources.
