Team:HKUST-Hong Kong/Project

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This is a template page. READ THESE INSTRUCTIONS.
You are provided with this team page template with which to start the iGEM season. You may choose to personalize it to fit your team but keep the same "look." Or you may choose to take your team wiki to a different level and design your own wiki. You can find some examples HERE.
You MUST have a team description page, a project abstract, a complete project description, a lab notebook, and a safety page. PLEASE keep all of your pages within your teams namespace.


You can write a background of your team here. Give us a background of your team, the members, etc. Or tell us more about something of your choosing.

Tell us more about your project. Give us background. Use this is the abstract of your project. Be descriptive but concise (1-2 paragraphs)

Team Example


Home Team Official Team Profile Project Parts Submitted to the Registry Modeling Notebook Safety Attributions



Contents

Project Abstract

   It has long been assumed that when antibiotic is introduced to a bacterial community, only those that carry resistance genes for that particular antibiotic 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.
   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, being deprived of indole, will undergo massive cell death 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 recycled for future iGEM teams, reducing their use of antibiotics without increasing the complexity of the transformation protocol.

Project Details

Part 2

The Experiments

Part 3

Results