http://2009.igem.org/wiki/index.php?title=Jamboree/Project_Abstract/Team_Abstracts&feed=atom&action=historyJamboree/Project Abstract/Team Abstracts - Revision history2024-03-29T08:12:51ZRevision history for this page on the wikiMediaWiki 1.16.5http://2009.igem.org/wiki/index.php?title=Jamboree/Project_Abstract/Team_Abstracts&diff=169332&oldid=prevMeagan at 15:13, 5 November 20092009-11-05T15:13:14Z<p></p>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:Aberdeen_Scotland | Team Aberdeen_Scotland:]] A Synthetic Biology Approach to Pipe Repair: The Pico-Plumber===</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:Aberdeen_Scotland | Team Aberdeen_Scotland:]] A Synthetic Biology Approach to Pipe Repair: The Pico-Plumber===</div></td></tr>
</table>Meaganhttp://2009.igem.org/wiki/index.php?title=Jamboree/Project_Abstract/Team_Abstracts&diff=169331&oldid=prevMeagan at 15:11, 5 November 20092009-11-05T15:11:32Z<p></p>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:Aberdeen_Scotland | Team Aberdeen_Scotland:]] A Synthetic Biology Approach to Pipe Repair: The Pico-Plumber===</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:Aberdeen_Scotland | Team Aberdeen_Scotland:]] A Synthetic Biology Approach to Pipe Repair: The Pico-Plumber===</div></td></tr>
</table>Meaganhttp://2009.igem.org/wiki/index.php?title=Jamboree/Project_Abstract/Team_Abstracts&diff=169239&oldid=prevMeagan at 16:43, 24 October 20092009-10-24T16:43:54Z<p></p>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:IBB_Pune | Team IBB_Pune:]] Constructing multi-strain computational modules using Nucleotide and Protein mediated cell-cell signaling.===</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:IBB_Pune | Team IBB_Pune:]] Constructing multi-strain computational modules using Nucleotide and Protein mediated cell-cell signaling.===</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>Building complex genetic circuits in a single cell becomes difficult due to the formidable task of co-transforming large nucleotide sequences in addition to the imposed metabolic burden on the cell. Can a complex system be divided into independent modules that reside in different cells and interact with each other using nucleotide and protein mediated cell-cell signalling to act as a single unit? We seek to address this problem using a three pronged approach. Firstly, we are trying to introduce natural competance genes into the biobrick framework which will act as nucleotide importers. We are also building a protein export system using the TAT dependent export pathway. Finally, we are attempting to construct a multi-state turing machine which is a compound, modular computational system that has independent, interacting states which applies the above principle. We hope that this approach overcomes the obstacles in building more complex and composite circuits.</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>Building complex genetic circuits in a single cell becomes difficult due to the formidable task of co-transforming large nucleotide sequences in addition to the imposed metabolic burden on the cell. Can a complex system be divided into independent modules that reside in different cells and interact with each other using nucleotide and protein mediated cell-cell signalling to act as a single unit? We seek to address this problem using a three pronged approach. Firstly, we are trying to introduce natural competance genes into the biobrick framework which will act as nucleotide importers. We are also building a protein export system using the TAT dependent export pathway. Finally, we are attempting to construct a multi-state turing machine which is a compound, modular computational system that has independent, interacting states which applies the above principle. We hope that this approach overcomes the obstacles in building more complex and composite circuits.</div></td></tr>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del style="color: red; font-weight: bold; text-decoration: none;">===[[Team:IGIB-Delhi | Team IGIB-Delhi:]] ===</del></div></td><td colspan="2"> </td></tr>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:IIT_Bombay_India | Team IIT_Bombay_India:]] Analysis of multiple feedback loops using Synthetic Biology===</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:IIT_Bombay_India | Team IIT_Bombay_India:]] Analysis of multiple feedback loops using Synthetic Biology===</div></td></tr>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:Imperial College London | Team Imperial College London:]] The E.ncapsulator===</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:Imperial College London | Team Imperial College London:]] The E.ncapsulator===</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>For iGEM 2009 the Imperial College London team present you with The E.ncapsulator; a versatile manufacture and delivery platform by which therapeutics can be reliably targeted to the intestine. Our E.coli chassis progresses through a series of defined stages culminating in the production of a safe, inanimate pill. This sequential process involves drug production, self-encapsulation in a protective coating and genome deletion. The temporal transition through each of these stages has been individually optimised by both media and temperature. The E.ncapsulator provides an innovative method to deliver any biologically synthesisable compound and bypasses the need for expensive storage, packaging and purification processes. The E.ncapsulator is an attractive candidate for commercial pill development and demonstrates the massive manufacturing potential in Synthetic Biology.</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>For iGEM 2009 the Imperial College London team present you with The E.ncapsulator; a versatile manufacture and delivery platform by which therapeutics can be reliably targeted to the intestine. Our E.coli chassis progresses through a series of defined stages culminating in the production of a safe, inanimate pill. This sequential process involves drug production, self-encapsulation in a protective coating and genome deletion. The temporal transition through each of these stages has been individually optimised by both media and temperature. The E.ncapsulator provides an innovative method to deliver any biologically synthesisable compound and bypasses the need for expensive storage, packaging and purification processes. The E.ncapsulator is an attractive candidate for commercial pill development and demonstrates the massive manufacturing potential in Synthetic Biology.</div></td></tr>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del style="color: red; font-weight: bold; text-decoration: none;">===[[Team:Indiana | Team Indiana:]] Introduction of DNA and protein into plants===</del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del style="color: red; font-weight: bold; text-decoration: none;">We are interested introducing a plant chassis to the iGEM registry. Our project follows two routes. First, we are developing a plant transformation vector that meets iGEM standards. This vector will allow for the introduction of standard parts into plants. Second, we seek to develop and test a synthetic cell penetrating peptide (CPP) to act as a macromolecule delivery vehicle. The membrane of the cell is impenetrable to most large molecules. It is possible that the completed BioBrick will provide the registry with an agent for the delivery of diverse materials across the lipid bilayer in a variety of organisms. </del></div></td><td colspan="2"> </td></tr>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:IPN-UNAM-Mexico | Team IPN-UNAM-Mexico:]] Turing meets synthetic biology: self-emerging patterns in an activator-inhibitor network.===</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:IPN-UNAM-Mexico | Team IPN-UNAM-Mexico:]] Turing meets synthetic biology: self-emerging patterns in an activator-inhibitor network.===</div></td></tr>
</table>Meaganhttp://2009.igem.org/wiki/index.php?title=Jamboree/Project_Abstract/Team_Abstracts&diff=127143&oldid=prevMeagan at 11:24, 20 October 20092009-10-20T11:24:50Z<p></p>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:Aberdeen_Scotland | Team Aberdeen_Scotland:]] A Synthetic Biology Approach to Pipe Repair: The Pico-Plumber===</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:Aberdeen_Scotland | Team Aberdeen_Scotland:]] A Synthetic Biology Approach to Pipe Repair: The Pico-Plumber===</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>Damage to inaccessible pipe systems, such as computer cooling circuits, is difficult to rectify. An Escherichia coli synthetic biology circuit for pipe repair was designed. Pipe breach detection and the restoration of pipe integrity were implemented through exploitation of chemotaxis, and cell lysis that releases a two-component protein-based glue (lysyl oxidase and tropoelastin). Control was achieved using an AND gate with quorum sensing and the lac inducer IPTG (released from the breach) as inputs. Deterministic and stochastic models of the genetic circuit, integrated with an agent-based model of E.coli cells, were used to define the effective radii of cell migration and timing of lysis. Constructed AND gate, quorum sensing and lysis timing modules were experimentally tested. The two-component glue concept was successfully validated using in vitro alpha-omega complementation of beta-galatosidase activity. Finally, a proposal for an igem.org-based parameter database was developed to aid the rapid identifation of BioBricks parameter values.</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>Damage to inaccessible pipe systems, such as computer cooling circuits, is difficult to rectify. An Escherichia coli synthetic biology circuit for pipe repair was designed. Pipe breach detection and the restoration of pipe integrity were implemented through exploitation of chemotaxis, and cell lysis that releases a two-component protein-based glue (lysyl oxidase and tropoelastin). Control was achieved using an AND gate with quorum sensing and the lac inducer IPTG (released from the breach) as inputs. Deterministic and stochastic models of the genetic circuit, integrated with an agent-based model of E.coli cells, were used to define the effective radii of cell migration and timing of lysis. Constructed AND gate, quorum sensing and lysis timing modules were experimentally tested. The two-component glue concept was successfully validated using in vitro alpha-omega complementation of beta-galatosidase activity. Finally, a proposal for an igem.org-based parameter database was developed to aid the rapid identifation of BioBricks parameter values.</div></td></tr>
</table>Meaganhttp://2009.igem.org/wiki/index.php?title=Jamboree/Project_Abstract/Team_Abstracts&diff=114076&oldid=prevGSee: /* Team Washington-Software: LegoRoboBricks for Automated BioBrick Assembly */2009-10-18T22:10:45Z<p><span class="autocomment">Team Washington-Software: LegoRoboBricks for Automated BioBrick Assembly</span></p>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:Washington-Software | Team Washington-Software:]] LegoRoboBricks for Automated BioBrick Assembly===</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:Washington-Software | Team Washington-Software:]] LegoRoboBricks for Automated BioBrick Assembly===</div></td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div>Commercial Liquid Handling Systems are extremely expensive, and are typically beyond the reach of the average molecular biologist interested in performing high throughput methods. To address this problem, we design and implement a liquid handling system built from commonly accessible Legos. Our goal is the automation of BioBrick assembly on a <del class="diffchange diffchange-inline">Lego </del>platform that can itself be easily replicated and we demonstrate a proof-of-principle for this system by transferring colored dye solutions on a 96-well plate. We introduce a new concept called LegoRoboBrick. The liquid handling system is build from 3 new LegoRoboBrick modular components: ALPHA (Automated Lego Pipette Head Assembly), BETA (BioBrick Environmental Testing Apparatus), and PHI (Pneumatic Handling Interface). We will demonstrate that the same BioBrick assembly software can run on multiple plug-and-play LegoRoboBrick instances with different physical dimensions and geometric configurations. The modular design of LegoRoboBricks allows easy extension of new laboratory functionalities in the future.</div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div>Commercial Liquid Handling Systems are extremely expensive, and are typically beyond the reach of the average molecular biologist interested in performing high throughput methods. To address this problem, we design and implement a liquid handling system built from commonly accessible Legos. Our goal is the automation of BioBrick assembly on a platform that can itself be easily replicated and we demonstrate a proof-of-principle for this system by transferring colored dye solutions on a 96-well plate. We introduce a new concept called LegoRoboBrick. The liquid handling system is build from 3 new LegoRoboBrick modular components: ALPHA (Automated Lego Pipette Head Assembly), BETA (BioBrick Environmental Testing Apparatus), and PHI (Pneumatic Handling Interface). We will demonstrate that the same BioBrick assembly software can run on multiple plug-and-play LegoRoboBrick instances with different physical dimensions and geometric configurations. The modular design of LegoRoboBricks allows easy extension of new laboratory functionalities in the future.</div></td></tr>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:Waterloo | Team Waterloo:]] Chromobricks: A Platform for Chromosome Engineering with BioBricks===</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:Waterloo | Team Waterloo:]] Chromobricks: A Platform for Chromosome Engineering with BioBricks===</div></td></tr>
</table>GSeehttp://2009.igem.org/wiki/index.php?title=Jamboree/Project_Abstract/Team_Abstracts&diff=114070&oldid=prevGSee: /* Team Washington-Software: LegoRoboBricks for Automated BioBrick Assembly */2009-10-18T22:09:50Z<p><span class="autocomment">Team Washington-Software: LegoRoboBricks for Automated BioBrick Assembly</span></p>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:Washington-Software | Team Washington-Software:]] LegoRoboBricks for Automated BioBrick Assembly===</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:Washington-Software | Team Washington-Software:]] LegoRoboBricks for Automated BioBrick Assembly===</div></td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div>Commercial Liquid Handling Systems are extremely expensive, and are typically beyond the reach of the average molecular biologist interested in performing high throughput methods. To address this problem, we design and implement a liquid handling system built from commonly accessible Legos. Our goal is the automation of BioBrick assembly on a Lego platform that can itself be easily replicated and we demonstrate a proof-of-principle <del class="diffchange diffchange-inline">use </del>for this system by transferring colored dye solutions on a 96-well plate. We introduce a new concept called LegoRoboBrick. The liquid handling system is build from 3 new LegoRoboBrick modular components: ALPHA (Automated Lego Pipette Head Assembly), BETA (BioBrick Environmental Testing Apparatus), and PHI (Pneumatic Handling Interface). We will demonstrate that the same BioBrick assembly software can run on multiple plug-and-play LegoRoboBrick instances with different physical dimensions and geometric configurations. The modular design of LegoRoboBricks allows easy extension of new laboratory functionalities in the future.</div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div>Commercial Liquid Handling Systems are extremely expensive, and are typically beyond the reach of the average molecular biologist interested in performing high throughput methods. To address this problem, we design and implement a liquid handling system built from commonly accessible Legos. Our goal is the automation of BioBrick assembly on a Lego platform that can itself be easily replicated and we demonstrate a proof-of-principle for this system by transferring colored dye solutions on a 96-well plate. We introduce a new concept called LegoRoboBrick. The liquid handling system is build from 3 new LegoRoboBrick modular components: ALPHA (Automated Lego Pipette Head Assembly), BETA (BioBrick Environmental Testing Apparatus), and PHI (Pneumatic Handling Interface). We will demonstrate that the same BioBrick assembly software can run on multiple plug-and-play LegoRoboBrick instances with different physical dimensions and geometric configurations. The modular design of LegoRoboBricks allows easy extension of new laboratory functionalities in the future.</div></td></tr>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:Waterloo | Team Waterloo:]] Chromobricks: A Platform for Chromosome Engineering with BioBricks===</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:Waterloo | Team Waterloo:]] Chromobricks: A Platform for Chromosome Engineering with BioBricks===</div></td></tr>
</table>GSeehttp://2009.igem.org/wiki/index.php?title=Jamboree/Project_Abstract/Team_Abstracts&diff=114065&oldid=prevGSee: /* Team Washington-Software: LegoRoboBricks for Automated BioBrick Assembly */2009-10-18T22:08:18Z<p><span class="autocomment">Team Washington-Software: LegoRoboBricks for Automated BioBrick Assembly</span></p>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:Washington-Software | Team Washington-Software:]] LegoRoboBricks for Automated BioBrick Assembly===</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:Washington-Software | Team Washington-Software:]] LegoRoboBricks for Automated BioBrick Assembly===</div></td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div>Commercial Liquid Handling Systems are extremely expensive, and are typically beyond the reach of the average molecular biologist interested in performing high throughput methods. <del class="diffchange diffchange-inline"> To </del>address this problem, <del class="diffchange diffchange-inline">our project consists of the </del>design and <del class="diffchange diffchange-inline">implementation of </del>a liquid handling system built from commonly accessible Legos. <del class="diffchange diffchange-inline"> We </del>demonstrate a proof-of-principle use for this system <del class="diffchange diffchange-inline">to perform BioBrick assembly </del>by transferring colored dye solutions on a 96-well plate. <del class="diffchange diffchange-inline"> </del>We introduce a new concept called LegoRoboBrick. <del class="diffchange diffchange-inline"> The </del>liquid handling system is build <del class="diffchange diffchange-inline">by designing and implementing </del>3 LegoRoboBrick modular components: ALPHA (Automated Lego Pipette Head Assembly), BETA (BioBrick Environmental Testing Apparatus), and PHI (Pneumatic Handling Interface). <del class="diffchange diffchange-inline"> We </del>will demonstrate that the same BioBrick assembly software can run on multiple plug-and-play LegoRoboBrick instances with different physical dimensions and geometric configurations. The modular design of LegoRoboBricks allows easy extension of new laboratory functionalities in the future.</div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div>Commercial Liquid Handling Systems are extremely expensive, and are typically beyond the reach of the average molecular biologist interested in performing high throughput methods. <ins class="diffchange diffchange-inline">To </ins>address this problem, <ins class="diffchange diffchange-inline">we </ins>design and <ins class="diffchange diffchange-inline">implement </ins>a liquid handling system built from commonly accessible Legos. <ins class="diffchange diffchange-inline">Our goal is the automation of BioBrick assembly on a Lego platform that can itself be easily replicated and we </ins>demonstrate a proof-of-principle use for this system by transferring colored dye solutions on a 96-well plate. We introduce a new concept called LegoRoboBrick. <ins class="diffchange diffchange-inline">The </ins>liquid handling system is build <ins class="diffchange diffchange-inline">from </ins>3 <ins class="diffchange diffchange-inline">new </ins>LegoRoboBrick modular components: ALPHA (Automated Lego Pipette Head Assembly), BETA (BioBrick Environmental Testing Apparatus), and PHI (Pneumatic Handling Interface). <ins class="diffchange diffchange-inline">We </ins>will demonstrate that the same BioBrick assembly software can run on multiple plug-and-play LegoRoboBrick instances with different physical dimensions and geometric configurations. The modular design of LegoRoboBricks allows easy extension of new laboratory functionalities in the future.</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:Waterloo | Team Waterloo:]] Chromobricks: A Platform for Chromosome Engineering with BioBricks===</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:Waterloo | Team Waterloo:]] Chromobricks: A Platform for Chromosome Engineering with BioBricks===</div></td></tr>
</table>GSeehttp://2009.igem.org/wiki/index.php?title=Jamboree/Project_Abstract/Team_Abstracts&diff=82120&oldid=prevVinoo at 19:06, 2 October 20092009-10-02T19:06:55Z<p></p>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:Yeshiva_NYC | Team Yeshiva_NYC:]] Spatially encoding temporal information: using diffusional escape of periplasmic reporter proteins as a clock.===</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>===[[Team:Yeshiva_NYC | Team Yeshiva_NYC:]] Spatially encoding temporal information: using diffusional escape of periplasmic reporter proteins as a clock.===</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>We were inspired by iGEM projects that utilize colored or fluorescent reporter molecules. Specifically, we thought “wouldn’t it be nice to be able to leave a plate out in the field, collect it a day or two later, and be able to tell at what time the synthesis of the reporter molecules was triggered?” Ideally, protein reporters would leave the cell and diffuse through the agar, leaving a clear history of their expression. To this end, we are 1) creating a library of Sec and Tat leader sequence biobricks for directing expressed proteins to the periplasm, 2) making an E. coli expression strain with a weakened outer cell wall that leaks most of the periplasmic proteins to the environment, and 3) measuring and modeling the diffusion of small molecules and proteins in agar to ascertain the ability to derive the times and conditions under which they originated.</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>We were inspired by iGEM projects that utilize colored or fluorescent reporter molecules. Specifically, we thought “wouldn’t it be nice to be able to leave a plate out in the field, collect it a day or two later, and be able to tell at what time the synthesis of the reporter molecules was triggered?” Ideally, protein reporters would leave the cell and diffuse through the agar, leaving a clear history of their expression. To this end, we are 1) creating a library of Sec and Tat leader sequence biobricks for directing expressed proteins to the periplasm, 2) making an E. coli expression strain with a weakened outer cell wall that leaks most of the periplasmic proteins to the environment, and 3) measuring and modeling the diffusion of small molecules and proteins in agar to ascertain the ability to derive the times and conditions under which they originated.</div></td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del style="color: red; font-weight: bold; text-decoration: none;">------- </del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del style="color: red; font-weight: bold; text-decoration: none;"></del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del style="color: red; font-weight: bold; text-decoration: none;">===[https://2009.igem.org/Team:TUDelft Team TU Delft:] Bacterial Relay Race===</del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del style="color: red; font-weight: bold; text-decoration: none;">In our project, we aim at creating a cell-to-cell communication system that allows the propagation of a set of instructions coded on a plasmid, and not just binary information as in quorum sensing. To achieve this goal, we have designed a communication system based on three different modules: a conjugation system, a time-delay genetic circuit, and a self-destructive plasmid.<br></del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del style="color: red; font-weight: bold; text-decoration: none;">Cell-to-cell communication systems are important because, in most synthetic biology applications, the desired tasks are generally accomplished by a population of cells, rather than by a single cell. The proposed communication system could be used for creating a distributed sensors network, or it could help to better understand and possibly reduce antibiotic resistance in bacteria.<br></del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del style="color: red; font-weight: bold; text-decoration: none;">Furthermore, we have conducted a survey to study the perception on synthetic biology and related ethical issues, among iGEM participants, students and supervisors. We have focused on the top-down and bottom-up approaches as applied to biology.</del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del style="color: red; font-weight: bold; text-decoration: none;"></del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del style="color: red; font-weight: bold; text-decoration: none;">===[https://2009.igem.org/Team:Groningen Team Groningen:] Heavy metal scavengers with a vertical gas drive===</del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del style="color: red; font-weight: bold; text-decoration: none;"></del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del style="color: red; font-weight: bold; text-decoration: none;">Heavy metal pollution of water and sediment endangers human health and the environment. To battle this problem, a purification strategy was developed in which arsenic, zinc or copper are removed from metal-polluted water and sediment. In this approach Escherichia coli bacteria accumulate metal ions from solutions, after which they produce gas vesicles and start floating. This biological device encompasses two integrated systems: one for metal accumulation, the other for metal-induced buoyancy. The uptake and storage system consists of a metal transporter and metallothioneins (metal binding proteins). The buoyancy system is made up of a metal-induced promoter upstream of a gas vesicle gene cluster. This device can be changed to scavenge for any compound by altering the accumulation and the induction modules. The combination of both systems enables the efficient decontamination of polluted water and sediment in a biological manner.</del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del style="color: red; font-weight: bold; text-decoration: none;"></del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del style="color: red; font-weight: bold; text-decoration: none;">===[https://2009.igem.org/Team:PKU_Beijing Team PKU_Beijing:] Conditioned Reflex Mimicking in ''E.coli''===</del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del style="color: red; font-weight: bold; text-decoration: none;"></del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del style="color: red; font-weight: bold; text-decoration: none;">We are engineering our E. coli cells to process the correlation information of two enviornmental signal, similar to the process of conditioning in higher orgamisms. We have constructed and tested a series of AND gates which can sense the two signals: the conditioned and unconditioned stimuli. With the presence of both signals, the AND gate outputs a repressor protein and then changes the state of the bistable switch, which acts as a memory module. In this way, our E. coli cells can convert the information about the concurrence of the two signals into its memory. After the memory module is switched and given the "conditioned stimulus", the E. coli cells will pass the information to the reporter module and thus exhibit the "conditioned response."</del></div></td><td colspan="2"> </td></tr>
</table>Vinoohttp://2009.igem.org/wiki/index.php?title=Jamboree/Project_Abstract/Team_Abstracts&diff=82119&oldid=prevVinoo at 19:06, 2 October 20092009-10-02T19:06:31Z<p></p>
<a href="http://2009.igem.org/wiki/index.php?title=Jamboree/Project_Abstract/Team_Abstracts&diff=82119&oldid=82111">Show changes</a>Vinoohttp://2009.igem.org/wiki/index.php?title=Jamboree/Project_Abstract/Team_Abstracts&diff=82111&oldid=prevVinoo at 18:04, 2 October 20092009-10-02T18:04:49Z<p></p>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>Tokyo-NokoGen has developed the Escherichia coli Auto Protein Synthesizer (ESCAPES), an E. coli machine that greatly simplifies the production of your favorite protein. We created a green light-activated actuator to respond to external light signals, as well as a riboregulator-based signal counter to count the number of flashes. In ESCAPES, the first green light flash induces the E. coli to self-aggregate, while the second flash causes them to auto-lyse, thus greatly simplifying the protein preparation process. The light-activated actuator was constructed by fusing the light responsive domain of the Synechocystis photoreceptor CcaS with the EnvZ histidine kinase domain. Self-aggregation is achieved by the induction of the Antigen43 gene, which we isolated from E. coli, while autolysis took advantage of the available BioBrick parts endolysin and holin. ESCAPES helps you “escape” from tedious protein preparation steps, such as centrifugation and cell disruption. </div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>Tokyo-NokoGen has developed the Escherichia coli Auto Protein Synthesizer (ESCAPES), an E. coli machine that greatly simplifies the production of your favorite protein. We created a green light-activated actuator to respond to external light signals, as well as a riboregulator-based signal counter to count the number of flashes. In ESCAPES, the first green light flash induces the E. coli to self-aggregate, while the second flash causes them to auto-lyse, thus greatly simplifying the protein preparation process. The light-activated actuator was constructed by fusing the light responsive domain of the Synechocystis photoreceptor CcaS with the EnvZ histidine kinase domain. Self-aggregation is achieved by the induction of the Antigen43 gene, which we isolated from E. coli, while autolysis took advantage of the available BioBrick parts endolysin and holin. ESCAPES helps you “escape” from tedious protein preparation steps, such as centrifugation and cell disruption. </div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"></td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div>===[[Team:<del class="diffchange diffchange-inline">BLANK </del>| Team <del class="diffchange diffchange-inline">BLANK</del>:]] ===</div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div>===[[Team:<ins class="diffchange diffchange-inline">TorontoMaRSDiscovery </ins>| Team <ins class="diffchange diffchange-inline">TorontoMaRSDiscovery</ins>:]] <ins class="diffchange diffchange-inline">Engineering bacterial micro-compartments to investigate metabolic channeling and its potential uses in biotechnological applications===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:Tsinghua | Team Tsinghua:]] Syn-genome Based Gensniper===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:TUDelft | Team TUDelft:]] Bacterial Relay Race===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:TzuChiU_Formosa | Team TzuChiU_Formosa:]] Midnight Apollo===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:UAB-Barcelona | Team UAB-Barcelona:]] A toxics biosensor. Could bacteria detect instantaneous and simultaneously several types of pollutants?===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:UC_Davis | Team UC_Davis:]] A Bacterial Secretion System Motivated the Goal of Managing Celiac===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:UChicago | Team UChicago:]] An enhanced yeast-based system for detection and decontamination of organophosphate neurotoxins.===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:UCL_London | Team UCL_London:]] Stress Light===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:UCSF | Team UCSF:]] Engineering the Movement of Cellular Robots===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:ULB-Brussels | Team ULB-Brussels:]] GluColi, a new generation of glue===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:UNICAMP-Brazil | Team UNICAMP-Brazil:]] The Microguards===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:UNIPV-Pavia | Team UNIPV-Pavia:]] Ethanol? Whey not!===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:uOttawa | Team uOttawa:]] A probiotic Lactobacillus strain which produces cellulose===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:Uppsala-Sweden | Team Uppsala-Sweden:]] Booze Bugs : Sun To Alcohol===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:UQ-Australia | Team UQ-Australia:]] Mercury sequestration using a multicomponent operon, and increasing the temperature tolerance range of P. syringae.===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:USTC | Team USTC:]] E. coli Automatic Directed Evolution Machine: a Universal Framework for Evolutionary Approaches in Synthetic Biology===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:USTC_Software | Team USTC_Software:]] Automatic Biological Circuit Design===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:Utah_State | Team Utah_State:]] BioBricks without Borders: Investigating a multi-host BioBrick vector and secretion of cellular products===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:Valencia | Team Valencia:]] iLCD: iGEM Lighting Cell Display===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:Victoria_Australia | Team Victoria_Australia:]] An environmentally sustainable biological lighting system ===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:VictoriaBC | Team VictoriaBC:]] Signal Integration: Applications of RNA Riboregulator Capabilities===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:Virginia | Team Virginia:]] Arsenic Sequestration for Groundwater Decontamination===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:Virginia_Commonwealth | Team Virginia_Commonwealth:]] Promoter design, characterization and consequences===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:Warsaw | Team Warsaw:]] BacInVader – a new system for cancer genetic therapy===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:Wash_U | Team Wash_U:]] Improved Photosynthetic Productivity for Rhodobacter sphaeroides via Synthetic Regulation of the Light Harvesting Antenna LH2===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:Washington | Team Washington:]] The Ideal Protein Purification System===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:Washington-Software | Team Washington-Software:]] LegoRoboBricks for Automated BioBrick Assembly===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:Waterloo | Team Waterloo:]] Chromobricks: A Platform for Chromosome Engineering with BioBricks===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:Wisconsin-Madison | Team Wisconsin-Madison:]] Ocean Fuel: increased salt tolerance through glycine betaine production===</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> </div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">===[[Team:Yeshiva_NYC | Team Yeshiva_NYC:]] Spatially encoding temporal information: using diffusional escape of periplasmic reporter proteins as a clock.</ins>===</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>------- </div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>------- </div></td></tr>
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</table>Vinoo