Team:Caltech

From 2012.igem.org

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=='''From Biofilms to Biofuel'''==
=='''From Biofilms to Biofuel'''==
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The following is plagiarized from someone: [[Team:Caltech/Project/General_information#iGEM|iGEM]] (international Genetically Engineered Machines Competition) is a competition organized by MIT (Massachusetts Institute of Technology) in Boston, USA, since 2005 and has become one of the largest international competitions in the field of science. This year 84 teams of undergraduate students compete against each other, and for the first time three teams from Germany join the competition. The project of the Heidelberg team is directed by Prof. Dr. Roland Eils from University of Heidelberg and the German Cancer Research Center (DKFZ).
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The iGEM (International Genetically Engineered Machine) competition started with a handful of teams competing at MIT, and has expanded to involve over one hundred and thirty college groups developing and implementing new applications of synthetic biology.  Over the summer, teams from each school utilize BioBricks supplied by MIT.  BioBricks are genetic libraries of promoters and genes that can be easily incorporated into other organisms’ genomes. This allows for relatively quick manipulation of organisms to express a certain product or perform a new function.  For example, the 2008 Caltech iGEM team, which won third place, manipulated E. coli (a beneficial resident of the intestine) to produce anti-pathenogenic products in addition to its typical functions in the body. The genetically engineered E. coli supplemented its typical role in the gut to mimic white blood cells’ anti-pathenogenic properties elsewhere in the body (1).
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Caltech’s 2012 iGEM team aims to manipulate bacteria to degrade stable organic polymers such as lignin and alginate; to use these substrates to synthesize biofuels, specifically biodiesel; and to direct their ATP synthesis mechanism to rely on proteorhodopsin as the source of the proton gradient, freeing NADH to interact in the synthetic pathway instead.  We will develop the three facets of the project in different strains of E. coli.  Depending on our success in each area, we will then splice the manipulated sequences into one new organism.
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[[Team:Caltech/Project/General_information#Synthetic Biology|Synthetic Biology]] is a young field in science, which combines classic gene technology with an engineering approach. Similar to the construction of an airplane, Synthetic Biology uses simple gene building blocks for the construction of new complex systems with distinct functions. These gene building blocks are collected in a database by iGEM and can be used by all participants of the competition. So far, the collection contains more than 1000 gene building blocks, due to the continuous development of new parts over the last years. This summer all teams work on self-developed projects which will then be presented in the beginning of November at the “Jamboree” in Boston. Several prizes in different categories will be awarded.
 
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Revision as of 18:28, 25 June 2012

From Biofilms to Biofuel

Title....

The iGEM (International Genetically Engineered Machine) competition started with a handful of teams competing at MIT, and has expanded to involve over one hundred and thirty college groups developing and implementing new applications of synthetic biology. Over the summer, teams from each school utilize BioBricks supplied by MIT. BioBricks are genetic libraries of promoters and genes that can be easily incorporated into other organisms’ genomes. This allows for relatively quick manipulation of organisms to express a certain product or perform a new function. For example, the 2008 Caltech iGEM team, which won third place, manipulated E. coli (a beneficial resident of the intestine) to produce anti-pathenogenic products in addition to its typical functions in the body. The genetically engineered E. coli supplemented its typical role in the gut to mimic white blood cells’ anti-pathenogenic properties elsewhere in the body (1). Caltech’s 2012 iGEM team aims to manipulate bacteria to degrade stable organic polymers such as lignin and alginate; to use these substrates to synthesize biofuels, specifically biodiesel; and to direct their ATP synthesis mechanism to rely on proteorhodopsin as the source of the proton gradient, freeing NADH to interact in the synthetic pathway instead. We will develop the three facets of the project in different strains of E. coli. Depending on our success in each area, we will then splice the manipulated sequences into one new organism.


News

29 Oct. 2008, Wiki-Freeze culminates into iGEM Ecolicence Song

To see our spontaneous iGEM Ecolicence composition click here


Sponsors

Klaus Tschira Foundation

German Cancer Research Center