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Team:UNIST Korea/project/future work
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| + | <font size=6><font color=cc0099><center>Future work & Application</center></font></font><br/><br/> | ||
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| + | <p align="justify">In the future our first effort will be to optimize the lysis module such that the Dpn enzymes are efficiently exploited by the synthetic microbes to eradicate its genetic material in a non-native environment. | ||
| + | On top of this, UNIST team will also introduce more controlled system into <i>E.coli</i> so that it can be more safe to the environment and easy to be handled in the laboratory. We would like to introduce the following components into our <i>Chop. coli</i> in order to achieve our goal;<br/><br/> | ||
| + | <center><b><font color=cc0066><font size="5">Second light receptor & Quorum Sensing System</font></font></b></center><br/></p> | ||
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| + | <p align="justify">Two light signals before lysis would help in providing a more tight control and ensure that the device would still work even when one of them is mutated.Our team will also introduce a fourth sensing module to the <i>Chop. coli</i> using the quorum sensing system. In case of fermentor <i>E. coli</i> will experience its native original quorum sensing molecule, AI2 | ||
| + | UNIST team is going to make that engineer <i>E.coli</i> to recognize different quorum sensing molecules such as AHL to differentiate between the fermentor and the real world. | ||
| + | This system will also help achieve an effective and tight control of lysis device. </br> | ||
| + | <br/><br/></p> | ||
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| + | <center><b><font color=cc0066><font size="5">With this approach it is also possible to create artificial cell<br/><br/> membrane for the transplantation of synthetic genome. </font></font></b></center><br/></p> | ||
| + | <center> <img src="https://static.igem.org/mediawiki/2011/d/d5/SKL30.png" width="500" height="500"/> | ||
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| + | <center><b>Figure explaining the future appearance of <i>Chop. coli</i></b></center> | ||
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Latest revision as of 02:36, 6 October 2011
In the future our first effort will be to optimize the lysis module such that the Dpn enzymes are efficiently exploited by the synthetic microbes to eradicate its genetic material in a non-native environment.
On top of this, UNIST team will also introduce more controlled system into E.coli so that it can be more safe to the environment and easy to be handled in the laboratory. We would like to introduce the following components into our Chop. coli in order to achieve our goal;
Two light signals before lysis would help in providing a more tight control and ensure that the device would still work even when one of them is mutated.Our team will also introduce a fourth sensing module to the Chop. coli using the quorum sensing system. In case of fermentor E. coli will experience its native original quorum sensing molecule, AI2
UNIST team is going to make that engineer E.coli to recognize different quorum sensing molecules such as AHL to differentiate between the fermentor and the real world.
This system will also help achieve an effective and tight control of lysis device.
membrane for the transplantation of synthetic genome.
