Team:NTNU Trondheim

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<h3>Project</h3>
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<p align="left">The primary goal of this project is to aid CO2-capturing efforts by developing a chemically inducible gene expression system for the photosynthesizing cyanobacterium <i>Synechocystis sp. </i> PCC6803, and using it to increase the rate of carbon fixation in the bacterium. </p>
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<h3> Detailed project description</h3>
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<p align="left"> During the course of this project, our team will construct a new BioBrick that allows chemically inducible expression of transgenes in <a href="http://www.genome.jp/kegg-bin/show_organism?org=syn"><i>Synechocystis sp.</i> PCC6803.</a></p>
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<p align="left"> The new BioBrick will incorporate DNA sequences from four existing BioBricks, in addition to sequences from the <i>Synechocystis sp.</i> PC6803 genome.</p>
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<p align="left">We will use metabolic modelling methods such as <a href="http://www.nature.com/nbt/journal/v28/n3/abs/nbt.1614.html">Flux Balance Analysis</a> to identify bottlenecks in pathways involved with carbon fixation. Once bottlenecks are identified, we will look for high throughput orthologs of the genes corresponding to the identified bottlenecks, and include these in our BioBrick. Finally, the BioBrick carrying high throughput orthologs will be transformed into <i>Synechocystis sp.</i> PC6803 cells to increase their carbon fixation rate. </p>
 +
 
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<p align="left">Head over to our <a href="https://2014.igem.org/Team:NTNU_Trondheim/Project">project page</a> to read more about the project! </p>
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The primary goal of this project is to aid CO<sub>2</sub>-capturing efforts by developing a chemically inducible gene expression system for the photosynthesizing cyanobacterium Synechocystis sp. PCC6803, and using it to increase the rate of carbon fixation in the bacterium. This basic platform could then be used to offset CO<sub>2</sub> emissions at a higher rate than the naturally occurring organism.
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Revision as of 09:37, 25 June 2014

Team:NTNU_Trondheim - 2014.igem.org

 

Team:NTNU_Trondheim

From 2014.igem.org

Welcome to NTNU's iGEM Wiki 2014!

Scroll down to find more about our project!

Project

The primary goal of this project is to aid CO2-capturing efforts by developing a chemically inducible gene expression system for the photosynthesizing cyanobacterium Synechocystis sp. PCC6803, and using it to increase the rate of carbon fixation in the bacterium.

This basic platform could then be used to offset CO2 emissions at a higher rate than the naturally occurring organism.
Top

Detailed project description

During the course of this project, our team will construct a new BioBrick that allows chemically inducible expression of transgenes in Synechocystis sp. PCC6803.

The new BioBrick will incorporate DNA sequences from four existing BioBricks, in addition to sequences from the Synechocystis sp. PC6803 genome.

We will use metabolic modelling methods such as Flux Balance Analysis to identify bottlenecks in pathways involved with carbon fixation. Once bottlenecks are identified, we will look for high throughput orthologs of the genes corresponding to the identified bottlenecks, and include these in our BioBrick. Finally, the BioBrick carrying high throughput orthologs will be transformed into Synechocystis sp. PC6803 cells to increase their carbon fixation rate.

Head over to our project page to read more about the project!

Top

Who will your project help?

Tell your audience how your project will help the environment, science, medicine or everything else.
Top

Why did you choose this project?

What motivated you to work on this project? Tell us what inspires you.
Top

Here you can place the logos of your sponsors or other links!

Retrieved from "https://2014.igem.org/Team:UCL_Academy"

Retrieved from "http://2014.igem.org/Team:NTNU_Trondheim"