Team:HKU-Hong Kong

From 2010.igem.org

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We are from the University of Hong Kong. Our team was formed in early April with 12 student members from different areas of studies.
We are from the University of Hong Kong. Our team was formed in early April with 12 student members from different areas of studies.
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[mailto:hkuigem2010@yahoo.com.hk contact us]
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'''[mailto:hkuigem2010@yahoo.com.hk Contact us]'''
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[http://www.youtube.com/user/hkuigem2010 Our official youtube channel]
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[http://www.flickr.com/photos/hkuigem2010 Our Gallery]
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<h1>Abstract of our project</h1>
<h1>Abstract of our project</h1>
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[[Image:Hkulogo1.png|250px|left|The "Bio-Safety Net"]]
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[[Image:Hkulogo1.png|280px|right|The "Bio-Safety Net"]]
{|style="background-color:transparent;" align="justify"
{|style="background-color:transparent;" align="justify"
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| Our team picked out the idea of engineering a mechanism that can act as a safety net to prevent genetically modified bacteria from performing undesired tasks in "inappropriate" environments.  
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| Our team’s project is a “bio-safety net” that limits the survival of bacteria according to tailored conditions.
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|Bacteria are genetically engineered to perform various functions.Prospective functions include biodegradation of crude oil and killing of cancer cells. Yet, undesired tasks might be performed by the baterium itself as well. The idea of the introduction of a "suicide" mechanism under specific conditions would serve the purpose of a "bio-safety net".
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Bacteria can be designed to perform promising tasks, such as the biodegradation of oil to clean up oil spills. Yet, there are risks associated with the possibility that living bacteria may perform undesired activities. Our goal is to introduce a “bio-safety net” that will apply to virtually all genetically engineered bacteria as a vital termination step after they have finished fulfilling their function.  
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|Mechanism and conditions for cell destruction were investigated. We found the biopart Bba_k112808 from the UC Berkeley team, (i.e. an enterobacteria phage T4 Lysis Device with no promotor)useful in attaining cell destruction. The idea of a bio-safety net is to limit the survival of the bacteria to (some) customized and specific condition(s).
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We will make this possible by introducing a "suicide" mechanism that is triggered under specific conditions. By using different promoters, the system can respond to changes in environmental factors and control expression specific to a chosen factor. Such mechanism can be easily assembled and incorporated into bacteria through the use of biobricks.
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|Matching of different promotors, corresponding to different environmental factors with the expression control of the lysis device, gives possibilities in designing biobricks that provide a "bio-safety net" to virtually all genetically engineered bacteria.
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In our project we aimed to and have created a “bio-safety net” that can limit the survival of bacteria according to tailored conditions. Although there are limitations to our findings we have highlighted problems and identified key areas for focus in future research.
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Latest revision as of 16:20, 26 October 2010

The Bio-Safety Net

Welcome to the wiki of the HKU igem team 2010

The title of our project this year is "The Bio-Safety Net"

We are from the University of Hong Kong. Our team was formed in early April with 12 student members from different areas of studies.

Contact us

Abstract of our project

The "Bio-Safety Net"
Bacteria can be designed to perform promising tasks, such as the biodegradation of oil to clean up oil spills. Yet, there are risks associated with the possibility that living bacteria may perform undesired activities. Our goal is to introduce a “bio-safety net” that will apply to virtually all genetically engineered bacteria as a vital termination step after they have finished fulfilling their function. We will make this possible by introducing a "suicide" mechanism that is triggered under specific conditions. By using different promoters, the system can respond to changes in environmental factors and control expression specific to a chosen factor. Such mechanism can be easily assembled and incorporated into bacteria through the use of biobricks.
Our team’s project is a “bio-safety net” that limits the survival of bacteria according to tailored conditions.

In our project we aimed to and have created a “bio-safety net” that can limit the survival of bacteria according to tailored conditions. Although there are limitations to our findings we have highlighted problems and identified key areas for focus in future research.


 

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