Difference between revisions of "Team:XJTLU-CHINA/Team"
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<li><a class="jump1" href="https://2015.igem.org/Team:XJTLU-CHINA/Description#J1">Map description</a></li> | <li><a class="jump1" href="https://2015.igem.org/Team:XJTLU-CHINA/Description#J1">Map description</a></li> | ||
− | <li><a class="jump2" href="https://2015.igem.org/Team:XJTLU-CHINA/ | + | <li><a class="jump2" href="https://2015.igem.org/Team:XJTLU-CHINA/Description#J2">RNAT</a></li> |
<li><a class="jump2" href="https://2015.igem.org/Team:XJTLU-CHINA/Description#J4">Improve experiment of RNAT</a></li> | <li><a class="jump2" href="https://2015.igem.org/Team:XJTLU-CHINA/Description#J4">Improve experiment of RNAT</a></li> | ||
<li><a class="jump2" href="https://2015.igem.org/Team:XJTLU-CHINA/Description#J4">Chromo-protein testing</a></li> | <li><a class="jump2" href="https://2015.igem.org/Team:XJTLU-CHINA/Description#J4">Chromo-protein testing</a></li> | ||
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<a class="primaryNavi" href="https://2015.igem.org/Team:XJTLU-CHINA/Parts">Parts</a> | <a class="primaryNavi" href="https://2015.igem.org/Team:XJTLU-CHINA/Parts">Parts</a> | ||
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− | <li><a class="jump1" href=" | + | <li><a class="jump1" href="#J1">Modularity</a></li> |
− | <li><a class="jump2" href=" | + | <li><a class="jump2" href="#J2">Part Detail</a></li> |
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<a class="primaryNavi" href="https://2015.igem.org/Team:XJTLU-CHINA/Team">Team</a> | <a class="primaryNavi" href="https://2015.igem.org/Team:XJTLU-CHINA/Team">Team</a> | ||
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− | <li><a class="jump1" href="#J1">Team introduction</a></li> | + | <li><a class="jump1" href="https://2015.igem.org/Team:XJTLU-CHINA/Team#J1">Team introduction</a></li> |
− | <li><a class="jump2" href="#J2">Attribution</a></li> | + | <li><a class="jump2" href="https://2015.igem.org/Team:XJTLU-CHINA/Team#J2">Attribution</a></li> |
<li><a class="jump2" href="https://2015.igem.org/Team:XJTLU-CHINA/Team#J3">Achievements</a></li> | <li><a class="jump2" href="https://2015.igem.org/Team:XJTLU-CHINA/Team#J3">Achievements</a></li> | ||
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<li><a class="jump1" href="https://2015.igem.org/Team:XJTLU-CHINA/Description#J1">Map description</a></li> | <li><a class="jump1" href="https://2015.igem.org/Team:XJTLU-CHINA/Description#J1">Map description</a></li> | ||
− | <li><a class="jump2" href=" | + | <li><a class="jump2" href="#J2">RNAT</a></li> |
− | <li><a class="jump2" href=" | + | <li><a class="jump2" href="#J4">Improve experiment of RNAT</a></li> |
− | <li><a class="jump2" href=" | + | <li><a class="jump2" href="#J4">Chromo-protein testing</a></li> |
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<a class="ZprimaryNavi" href="https://2015.igem.org/Team:XJTLU-CHINA/Parts">Parts</a> | <a class="ZprimaryNavi" href="https://2015.igem.org/Team:XJTLU-CHINA/Parts">Parts</a> | ||
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<ul> | <ul> | ||
− | <li><a class="jump1" href=" | + | <li><a class="jump1" href="#J1">Modularity</a></li> |
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− | < | + | <p>After the team had finished the genetic design of Land, Coast, Marine, and Polar bacteria, time was almost running out and there were still some concerns on the performance promoters and ribothermometers. To make sure we could have a chance to test the uncertain parts without delaying the whole circuits’ synthesis, instructor suggested us to modularize genetic circuits and then manipulate the modules using Gibson Assembly.</p> |
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− | + | <p>The team divided modules into two groups. One is “promoter + operator/ RBS/Ribothermometer”. The other one is “Coding sequence + terminator”. Details are in the following form. </p> | |
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− | + | <p>Actually in Land, Coast, Marine, and Polar bacteria there are several overlaps in the composition of genetic circuits. For instance, marine and polar bacteria both contain blue chromoprotein gene; coast and land bacteria both contain yellow chromoprotein gene. Each repeating part is only shown as one module.</p> | |
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− | < | + | <P>How can modularity help?</P> |
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− | < | + | <P>Firstly, the modules would be directly inserted to the plasmid pSB1C3, so that the team could hand in new parts immediately after characterizing them. </P> |
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− | < | + | <P>Secondly, this method ensures us to get the perfect circuits as soon as possible. It makes constructing long designed genetic circuit a more flexible process compared to the original gene synthesis and it is just the same way as an engineer welds all electronic components together to make a circuit board with expected function. Moreover, in this case, we didn’t need to repeat constructing the same modules used in different circuits. </P> |
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− | < | + | <P>Thirdly, Gibson assembly is capable for successful assembly of multiple DNA fragments. Hence, verified modules can later be integrated with others quickly. </P> |
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Revision as of 07:24, 18 September 2015
XJTLU-CHINA
Part
Modularity
After the team had finished the genetic design of Land, Coast, Marine, and Polar bacteria, time was almost running out and there were still some concerns on the performance promoters and ribothermometers. To make sure we could have a chance to test the uncertain parts without delaying the whole circuits’ synthesis, instructor suggested us to modularize genetic circuits and then manipulate the modules using Gibson Assembly.
The team divided modules into two groups. One is “promoter + operator/ RBS/Ribothermometer”. The other one is “Coding sequence + terminator”. Details are in the following form.
Actually in Land, Coast, Marine, and Polar bacteria there are several overlaps in the composition of genetic circuits. For instance, marine and polar bacteria both contain blue chromoprotein gene; coast and land bacteria both contain yellow chromoprotein gene. Each repeating part is only shown as one module.
How can modularity help?
Firstly, the modules would be directly inserted to the plasmid pSB1C3, so that the team could hand in new parts immediately after characterizing them.
Secondly, this method ensures us to get the perfect circuits as soon as possible. It makes constructing long designed genetic circuit a more flexible process compared to the original gene synthesis and it is just the same way as an engineer welds all electronic components together to make a circuit board with expected function. Moreover, in this case, we didn’t need to repeat constructing the same modules used in different circuits.
Thirdly, Gibson assembly is capable for successful assembly of multiple DNA fragments. Hence, verified modules can later be integrated with others quickly.