Team:HKUST-Hong Kong/content.html

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<b>Hello!</b><br>
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<b>Greeting from the <b>2011 HKUST iGEM Team</b>!</b><br><br>
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Welcome to <b>HKUST</b> Team Wiki Page!<br><br>
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Welcome to our Wiki page!<br></p>
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We are the 2011 iGEM team from the <b><i>Hong Kong University of <br>Science and Technology</i> (HKUST)</b>.
 
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This is the fourth year for HKUST to<br> participate in this international synthetic biology competition.<br><br>
 
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This is the 4<sup>th</sup> time HKUST has participated in this international synthetic biology competition.<br>
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Thanks to our instructors' helpful advice, considerate advisors, and great enthusiasm and effort from all member of the HKUST iGEM 2011 team, we enjoyed a fantastic summer working with something that we feel will make a difference. <br><br>
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You may visit our <a href=gallery.html target=_top><font color=white><u>Gallery</u></font></a> to see what we do in the lab!
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Thanks to our experienced instructors, considerate advisors and <br>every team member from HKUST iGEM 2011 family, we enjoyed<br> a fantastic summer working cooperatively and effectively towards <br>our goal. <br><br>
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You may visit our <a href=gallery.html target=_top><font color=white><u>Gallery</u></font></a> to see how's our team was doing the lab.
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<a href="data.html" target=_top>Data Page</a><br>
<a href="data.html" target=_top>Data Page</a><br>
<span style="line-height:1; font-weight:600">Experiments and Results</span><br>
<span style="line-height:1; font-weight:600">Experiments and Results</span><br>
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<a href="asm.html"  target=_top>Strain construction</a> |  
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<a href="asm.html"  target=_top>Strain Construction</a> |  
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<a href="mic.html"  target=_top>Culture tests</a> |  
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<a href="mic.html"  target=_top>Culture Tests</a> |  
<a href="modeling.html"  target=_top>Modeling</a><br>
<a href="modeling.html"  target=_top>Modeling</a><br>
<span style="line-height:1; font-weight:600">Miscellaneous</span><br>
<span style="line-height:1; font-weight:600">Miscellaneous</span><br>
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<a href="future.html" target=_top>Future Plans</a> |
 
<a href="notebook.html" target=_top>Notebook</a>
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<a href="medal.html" target=_top>Medal Requirements</a> |  
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<font color=#CDD2C2>It has often been assumed that when an antibiotic is introduced to a bacterial community, only cells that carry resistance genes will survive and proliferate. However, recent findings have suggested that communities with a mixture of highly resistant (HR) and less resistant (LR) individuals are able to survive through ‘charity’ by HR individuals, which support LR individuals through indole signalling.</p><br>
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<font color=#CDD2C2>It has often been assumed that when an antibiotic is introduced to a bacterial community, only cells that carry resistance genes will survive and proliferate. However, recent findings suggest that communities with a mixture of highly resistant (HR) and less resistant (LR) individuals are able to survive through ‘charity’ by HR individuals, which support LR individuals through indole signalling.</p><br>
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<p>Our team aims to interfere with this signalling through introducing a disruptor <i>E. coli</i> into the bacterial community. This new strain will be able to degrade indole using a mutated toluene-4-monooxygenase (T4MO).  We hypothesize that LR cells in the community deprived of indole will undergo eliminated at lower antibiotic concentrations. If this demonstration is successful, indole degradation might prove to be a possible strategy in boosting antibiotics effectiveness in medical practice against bacteria that rely on such signalling.</p><br>
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<p>Our team aims to interfere with this signalling through introducing a disruptor <i>E. coli</i> into the bacterial community. This new strain will be able to degrade indole using a mutated toluene-4-monooxygenase (T4MO).  We hypothesize that LR cells in the community deprived of indole will undergo elimination at lower antibiotic concentrations. If this demonstration is successful, indole degradation might prove to be a possible strategy in boosting antibiotics effectiveness in medical practice against bacteria that rely on such signalling.</p><br>
<p>Along the way, we will also create a new strain of <i>E. coli</i> that utilizes an essential gene (<i>nadE</i>) as the selection marker for transformation, allowing antibiotics-free transformation and plasmid maintenance for regular laboratory manipulation. This new transformation method can be adopted for future iGEM teams, reducing their use of antibiotics without increasing the complexity of the transformation protocol.</p><br>
<p>Along the way, we will also create a new strain of <i>E. coli</i> that utilizes an essential gene (<i>nadE</i>) as the selection marker for transformation, allowing antibiotics-free transformation and plasmid maintenance for regular laboratory manipulation. This new transformation method can be adopted for future iGEM teams, reducing their use of antibiotics without increasing the complexity of the transformation protocol.</p><br>
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<b><font color="#FFE1E1" size=3>Home</font></b>
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<b><font color="green">Our Project</font></b></p>
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<a href="overview.html" target=_top>Overview</a><font color="green"> | </font>
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<a href="data.html" target=_top>Data Page</a><br></p>
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<b><font color="green">Experiments and Results</font></b></p>
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<a href="asm.html"  target=_top>Strain Construction</a><font color="green"> | </font>
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Our Project</font></b></p>
 
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<a href="data.html" target=_top>Data Page</a><br>
 
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<span style="line-height:1; font-weight:600">Experiments and Results</span><br>
 
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<a href="asm.html"  target=_top>Strain construction</a> |
 
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<span style="line-height:1; font-weight:600">Miscellaneous</span><br>
 
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iGEM Resources</font></b></p>
 
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<a href="team.html" target=_top>iGEM Member List</a> |
 
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<b><font color="#FFF4D0">iGEM Resources</font></b></p>
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<a href="acknowledgement.html" target=_top>Acknowledgements</a></p>
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<b><font color="#FFF4D0">The Team</font></b></p>
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<a href="team.html" target=_top>iGEM Member List</a><font color="#FFF4D0"> | </font>
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<a href="contribution.html" target=_top>Contributions</a><br></p>
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<b><font color="#FFF4D0">Achievements</font></b></p>
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<a href="medal.html" target=_top>Medal Requirements<font color="#FFF4D0"> | </font>
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<a href="biosafety.html" target=_top>BioSafety</a><br></p>
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<b><font color="#FFF4D0">BioBricks</font></b></p>
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Human Practice</font></b></p>
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Latest revision as of 10:40, 26 October 2011


Greeting from the 2011 HKUST iGEM Team!

Welcome to our Wiki page!

This is the 4th time HKUST has participated in this international synthetic biology competition.
Thanks to our instructors' helpful advice, considerate advisors, and great enthusiasm and effort from all member of the HKUST iGEM 2011 team, we enjoyed a fantastic summer working with something that we feel will make a difference.

You may visit our Gallery to see what we do in the lab!


Our Project

Overview | Data Page
Experiments and Results
Strain Construction | Culture Tests | Modeling
Miscellaneous
Notebook


iGEM Resources

Acknowledgements
The Team
iGEM Member List | Contributions
Achievements
Medal Requirements | BioSafety
BioBricks
Master List & Characterization Data



Human Practice

Workshop | Survey

Project Abstract


It has often been assumed that when an antibiotic is introduced to a bacterial community, only cells that carry resistance genes will survive and proliferate. However, recent findings suggest that communities with a mixture of highly resistant (HR) and less resistant (LR) individuals are able to survive through ‘charity’ by HR individuals, which support LR individuals through indole signalling.


Our team aims to interfere with this signalling through introducing a disruptor E. coli into the bacterial community. This new strain will be able to degrade indole using a mutated toluene-4-monooxygenase (T4MO). We hypothesize that LR cells in the community deprived of indole will undergo elimination at lower antibiotic concentrations. If this demonstration is successful, indole degradation might prove to be a possible strategy in boosting antibiotics effectiveness in medical practice against bacteria that rely on such signalling.


Along the way, we will also create a new strain of E. coli that utilizes an essential gene (nadE) as the selection marker for transformation, allowing antibiotics-free transformation and plasmid maintenance for regular laboratory manipulation. This new transformation method can be adopted for future iGEM teams, reducing their use of antibiotics without increasing the complexity of the transformation protocol.


Home

Our Project

Overview | Data Page

Experiments and Results

Strain Construction | Culture Tests | Modeling

Miscellaneous

Notebook

iGEM Resources

Acknowledgements

The Team

iGEM Member List | Contributions

Achievements

Medal Requirements | BioSafety

BioBricks

Master List & Characterization Data

Human Practice

Workshop | Survey

Retrieved from "http://2011.igem.org/Team:HKUST-Hong_Kong/content.html"