Team:HKUST-Hong Kong/content.html

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<font color=gray><h3>Hong Kong University of Science and Technology</h3></font>
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[Greetings + General description to project/site]
 
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//We are the 2010 iGEM team from the Hong Kong University of Science and Technology (HKUST) .
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<b>Greeting from the <b>2011 HKUST iGEM Team</b>!</b><br><br>
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This is the third year for HKUST tynthetic biology
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competition. //We are the 2010 iGEM team from the Hong Kong University of Science and Technology (HKUST).
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Welcome to our Wiki page!<br></p>
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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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//We are the 2010 iGEM team from the Hong Kong University of Science and Technology (HKUST) .
 
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competition. //We are the 2010 iGEM team from the Hong Kong University of Science and Technology (HKUST).
 
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//We are the 2010 iGEM team from the Hong Kong University of Science and Technology (HKUST) .
 
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competition. //We are the 2010 iGEM team from the Hong Kong University of Science and Technology (HKUST).
 
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Our Project
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//We are the 2010 iGEM team from the Hong Kong University of Science and Technology (HKUST) .
 
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<a href="overview.html" target=_top>Overview</a> |
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<span style="line-height:1; font-weight:600">Experiments and Results</span><br>
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[Highlights]//........We are the 2010 iGEM team from the Hong Kong University of Science and Technology (HKUST) .
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//........We are the 2010 iGEM team from the Hong Kong University of Science and Technology (HKUST) .
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iGEM Resources</font></b></p>
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<a href="acknowledgement.html" target=_top>Acknowledgements</a><br>
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<span style="line-height:0.7; font-weight:600">The Team</span><br>
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<a href="team.html" target=_top>iGEM Member List</a> |
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//........We are the 2010 iGEM team from the Hong Kong University of Science and Technology (HKUST) .
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<BR><BR>Human Practice</font></b></p>
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<TD bgcolor=white><p>[Accomplishment]//We are the 2010 iGEM team from the Hong Kong University of Science and Technology (HKUST) .
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On this Wiki page, we are presenting how synthetic biology could contribute to health and medical studies. We are here introducing an idea – an interspecies quorum-quenching system in which non-pathogenic Lactobacillus could sense and reduce the virulence of Staphylococcus aureus. Such a model system should not yield a strong selective pressure for development of resistance, and would therefore be an attractive concept for preventive medicine.Click here to read more about our project
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<b><u>Project Abstract</u></b></font></p><br>
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Thanks to our experienced instructors, considerate advisors and every team member from HKUST iGEM 2010 family, we enjoyed a fantastic summer working cooperatively and effectively towards our goal. The logo below demonstrates our project idea: having non-pathogenic Lactobacillus (left) ‘working’ against virulent S. aureus (right):
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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 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>
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<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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Services[Quick links with brief introduction]</font></b></p>
 
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Professional and cost effective web development <a href=.html><font color=white>[Read more...]</font></a></font></p>
 
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The HKUST Team</font></b></p>
 
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This is our ? time joining the iGem project. We are enthusiastic about synthetic biology. Click to know more about our team.<a href=team.html><font color=green>[Read more...]
 
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<b><font color="#FFE1E1" size=3>Home</font></b>
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Contact  Us</font></b></p>
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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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<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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<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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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

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