Team:NCTU Formosa/Project

From 2012.igem.org

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<p>This is our biobrick. The most important part of our biobrick is 37°C ribosome binding site gene. We separate our biobrick into two parts . The first part is which has 37℃ ribosome binding site gene and the second part is under the first one.</p>
<p>This is our biobrick. The most important part of our biobrick is 37°C ribosome binding site gene. We separate our biobrick into two parts . The first part is which has 37℃ ribosome binding site gene and the second part is under the first one.</p>
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<img src="https://static.igem.org/mediawiki/2012/4/42/Loading.gif" alt="" />
 
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<p>The report shows that we use fluorescene protein to mark the second part of our biobrick . We can see that fluorescene protein staying in 30°C environment will have higher expression than staying in 37°C environment . According to it , we can see that our system do truly work!</p>
 
<p>And now we're introducing how our system works.</p>
<p>And now we're introducing how our system works.</p>
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<p>After getting enough 2-Ketoisovalerate , E.coli will stay in 30°C environment. The ribosome will not bind the 37°C ribosome binding site and tetR genes will not be translated. Then the second part will be translated successfully. At the end , we can get the isobutanol.</p>
<p>After getting enough 2-Ketoisovalerate , E.coli will stay in 30°C environment. The ribosome will not bind the 37°C ribosome binding site and tetR genes will not be translated. Then the second part will be translated successfully. At the end , we can get the isobutanol.</p>
<h2 id="project-s2-s-title" class="project-s-title"> <span>Result</span></h2>
<h2 id="project-s2-s-title" class="project-s-title"> <span>Result</span></h2>
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<p>(developing)</p>
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<img src="https://static.igem.org/mediawiki/2012/4/42/Loading.gif" alt="" />
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<p>The report shows that we use fluorescene protein to mark the second part of our biobrick . We can see that fluorescene protein staying in 30°C environment will have higher expression than staying in 37°C environment . According to it , we can see that our system do truly work!</p>
<h2 id="project-s2-3-title" class="project-s-title"> <span>Zinc finger</span></h2>
<h2 id="project-s2-3-title" class="project-s-title"> <span>Zinc finger</span></h2>
<p>(developing)</p>
<p>(developing)</p>

Revision as of 09:45, 8 September 2012

Team:NCTU Formosa - 2012.igem.org

 Introduction to the project

(developing)

 Project details

 Enzyme for isobutanol

(developing)

 Temperature control system

The low temperature release system is a way to let e.coli produce isobutanol efficiently . Because isobutanol and isobutyaldehyde are toxic to the e.coli , the system avoid e.coli facing them at the beginning . The following picture is our system.

At the beginning , we will let E.coli stay in 37°C environment. After having enough 2-Ketoisovalerate , we will move E.coli into 30°C environment for producing the final product , isobutanol. It can make us get isobutanol successfully and efficiently.

This is our biobrick. The most important part of our biobrick is 37°C ribosome binding site gene. We separate our biobrick into two parts . The first part is which has 37℃ ribosome binding site gene and the second part is under the first one.

And now we're introducing how our system works.

When being in 37°C environment, the first part will be translated and produce tetR protein to inhibit Ptet promoter. The second part will not be translated. Then we can produce intermediate , 2-Ketoisovalerate.

After getting enough 2-Ketoisovalerate , E.coli will stay in 30°C environment. The ribosome will not bind the 37°C ribosome binding site and tetR genes will not be translated. Then the second part will be translated successfully. At the end , we can get the isobutanol.

 Result

The report shows that we use fluorescene protein to mark the second part of our biobrick . We can see that fluorescene protein staying in 30°C environment will have higher expression than staying in 37°C environment . According to it , we can see that our system do truly work!

 Zinc finger

(developing)

 Result

(developing)

 Instrument

(developing)

 Conclusion

(developing)