Difference between revisions of "Team:Amoy/Notebook"

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</div>
 
</div>
 
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<span id="node51_close" style="background: #f0f0f0 url(https://static.igem.org/mediawiki/2015/7/73/GalleryClose.gif) no-repeat center center; position: fixed; height: 18px; width: 18px; cursor: pointer; margin-top: 60px; right: 12%; z-index: 1002; display: none;"></span>
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<div style="width: 80%; margin-left: 10%;">
 +
<p class="detail_h1">Purpose:</br></p>
 +
<p class="detail_p">Make connection of gene and terminator</br></p>
 +
<p class="detail_h1">Steps:</br></p>
 +
<p class="detail_p">
 +
1. Double enzyme digestion of gene and terminator_B0015</br>
 +
2. Electrophoresis analysis of double digested result of plasmid</br>
 +
3. Extract double digested gene</br>
 +
4. Cycle purity of digested terminator</br>
 +
5. Link gene with terminator under 16℃ for 8 hours</br>
 +
6. Transformation</br></p>
 +
<img style="width: 30%; margin-right: 70%; margin-top: 10px; margin-bottom: 0px;" src="https://static.igem.org/mediawiki/2015/8/87/Amoy-Notebook_Node41_figure1.jpg" />
 +
<p class="detail_p"></br>
 +
7. Pick 8 single colonies from the agar plate using sterile pipette tips. Put it into 10ml LB of chloramphenicol</br>
 +
8. Extract the plasmids</br>
 +
9. Electrophoresis analysis of plasmids</br></p>
 +
<p class="detail_h1">Product:</br></p>
 +
<p class="detail_p">plasmid of gene ldh and terminator</br></p>
 +
</div>
 +
</div>
 +
<span id="node35_close" style="background: #f0f0f0 url(https://static.igem.org/mediawiki/2015/7/73/GalleryClose.gif) no-repeat center center; position: fixed; height: 18px; width: 18px; cursor: pointer; margin-top: 60px; right: 12%; z-index: 1002; display: none;"></span>
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 +
<div style="width: 80%; margin-left: 10%;">
 +
<p class="detail_h1">Purpose:</br></p>
 +
<p class="detail_p">make connection of gene and terminator</br></p>
 +
<p class="detail_h1">Steps:</br></p>
 +
<p class="detail_p">
 +
1. Double enzyme digestion of gene and terminator_B0015</br>
 +
2. Electrophoresis analysis of double digested result of plasmid</br>
 +
3. Extract double digested gene</br>
 +
4. Cycle purity of digested terminator</br>
 +
5. Link gene with terminator under 16℃ for 8 hours</br>
 +
6. Transformation</br></p>
 +
<img style="width: 30%; margin-right: 70%; margin-top: 10px; margin-bottom: 0px;" src="https://static.igem.org/mediawiki/2015/8/87/Amoy-Notebook_Node41_figure1.jpg" />
 +
<p class="detail_p"></br>
 +
7. Pick 8 single colonies from the agar plate using sterile pipette tips. Put it into 10ml LB of chloramphenicol</br>
 +
8. Extract the plasmids</br>
 +
9. Electrophoresis analysis of plasmids</br></p>
 +
<p class="detail_h1">Product:</br></p>
 +
<p class="detail_p">plasmid of gene fdh and terminator</br></p>
 +
</div>
 +
</div>
 +
<span id="node36_close" style="background: #f0f0f0 url(https://static.igem.org/mediawiki/2015/7/73/GalleryClose.gif) no-repeat center center; position: fixed; height: 18px; width: 18px; cursor: pointer; margin-top: 60px; right: 12%; z-index: 1002; display: none;"></span>
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 +
<div style="width: 80%; margin-left: 10%;">
 +
<p class="detail_h1">Purpose:</br></p>
 +
<p class="detail_p">make connection of gene and terminator</br></p>
 +
<p class="detail_h1">Steps:</br></p>
 +
<p class="detail_p">
 +
1. Double enzyme digestion of gene and terminator_B1006</br>
 +
2. Electrophoresis analysis of double digested result of plasmid</br>
 +
3. Extract double digested gene</br>
 +
4. Cycle purity of digested terminator</br>
 +
5. Link gene with terminator under 16℃ for 8 hours</br>
 +
6. Transformation</br></p>
 +
<img style="width: 30%; margin-right: 70%; margin-top: 10px; margin-bottom: 0px;" src="https://static.igem.org/mediawiki/2015/8/87/Amoy-Notebook_Node41_figure1.jpg" />
 +
<p class="detail_p"></br>
 +
7. Pick 8 single colonies from the agar plate using sterile pipette tips. Put it into 10ml LB of chloramphenicol</br>
 +
8. Extract the plasmids</br>
 +
9. Electrophoresis analysis of plasmids</br></p>
 +
<p class="detail_h1">Product:</br></p>
 +
<p class="detail_p">plasmid of gene ldh and terminator</br></p>
 +
</div>
 +
</div>
 +
<span id="node37_close" style="background: #f0f0f0 url(https://static.igem.org/mediawiki/2015/7/73/GalleryClose.gif) no-repeat center center; position: fixed; height: 18px; width: 18px; cursor: pointer; margin-top: 60px; right: 12%; z-index: 1002; display: none;"></span>
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 +
<div style="width: 80%; margin-left: 10%;">
 +
<p class="detail_h1">Purpose:</br></p>
 +
<p class="detail_p">make connection of gene and terminator</br></p>
 +
<p class="detail_h1">Steps:</br></p>
 +
<p class="detail_p">
 +
1. Double enzyme digestion of gene and terminator_B1006</br>
 +
2. Electrophoresis analysis of double digested result of plasmid</br>
 +
3. Extract double digested gene</br>
 +
4. Cycle purity of digested terminator</br>
 +
5. Link gene with terminator under 16℃ for 8 hours</br>
 +
6. Transformation</br></p>
 +
<img style="width: 30%; margin-right: 70%; margin-top: 10px; margin-bottom: 0px;" src="https://static.igem.org/mediawiki/2015/8/87/Amoy-Notebook_Node41_figure1.jpg" />
 +
<p class="detail_p"></br>
 +
7. Pick 8 single colonies from the agar plate using sterile pipette tips. Put it into 10ml LB of chloramphenicol</br>
 +
8. Extract the plasmids</br>
 +
9. Electrophoresis analysis of plasmids</br></p>
 +
<p class="detail_h1">Product:</br></p>
 +
<p class="detail_p">plasmid of gene and terminator</br></p>
 +
</div>
 +
</div>
 +
<span id="node38_close" style="background: #f0f0f0 url(https://static.igem.org/mediawiki/2015/7/73/GalleryClose.gif) no-repeat center center; position: fixed; height: 18px; width: 18px; cursor: pointer; margin-top: 60px; right: 12%; z-index: 1002; display: none;"></span>
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Revision as of 06:10, 12 September 2015

Aomy/Project

NOTEBOOK

Initially, they used isolated enzymes, which can be disadvantageous for the reason that enzymes are always destabilized in the isolation and purification process. What's more, the cofactor-NADH is rather an expensive raw material, which will enhance the cost of L-tert-leucine production. So scientists introduced whole-cell biocatalysts to L-tert-leucine production. Whole-cell biocatalysts could stabilize enzymes and reduce the addition level of cofactor NADH.

In the path of building our biobricks, we divided the circuits into two modules. One is promoter linked with rbs and the other is gene linked with terminator. The dendrogram below is our experiments detail. Click each bottom for more information.

CONTACT US

Email: igemxmu@gmail.com

Website: 2015.igem.org/Team:Amoy

Address: Xiamen University, No. 422, Siming South Road, Xiamen, Fujian, P.R.China 361005