"
Team:Wisconsin/Project
From 2008.igem.org
(Difference between revisions)
| Line 20: | Line 20: | ||
|Fuel consumption has come to the forefront as an important political and biological issue that has lead to innovative pursuits of renewable fuel as well as controversial exploitation of natural resources. Currently ethanol is the commercial biofuel of choice; however, current production and distillation of ethanol is inefficient. With this problem in mind, iGEM Wisconsin has looked for alternative ways to make not only ethanol, but other biofuels through synthetic biology. We've designed the following two projects using ''E. coli'' to produce biofuels in innovative ways: | |Fuel consumption has come to the forefront as an important political and biological issue that has lead to innovative pursuits of renewable fuel as well as controversial exploitation of natural resources. Currently ethanol is the commercial biofuel of choice; however, current production and distillation of ethanol is inefficient. With this problem in mind, iGEM Wisconsin has looked for alternative ways to make not only ethanol, but other biofuels through synthetic biology. We've designed the following two projects using ''E. coli'' to produce biofuels in innovative ways: | ||
| - | One project focuses on using ''E. coli'' to produce sorbitol, a sugar alcohol, in large quantities for eventual catalytic conversion to hydrocarbons. Along with producing sorbitol, we've modeled a way to alter ''E. coli'' as to make sorbitol production from a glycerol carbon source effective. Our aim is to modify a cell that can use glycerol byproduct from | + | One project focuses on using ''E. coli'' to produce sorbitol, a sugar alcohol, in large quantities for eventual catalytic conversion to hydrocarbons. Along with producing sorbitol, we've modeled a way to alter ''E. coli'' as to make sorbitol production from a glycerol carbon source effective. Our aim is to modify a cell that can use glycerol byproduct from biodiesel production and effectively create sorbitol. |
In the second project we will be attempting to use ''E. coli'' to break down lignin from plant matter into usable biofuels. We are currently aiming to insert fungal genes coding for lignin peroxidase into ''E. coli''. Lignin breakdown will be made possible through the transport of lignin peroxidase out of the cell. To achieve this, protein transporters will be added to the cell. | In the second project we will be attempting to use ''E. coli'' to break down lignin from plant matter into usable biofuels. We are currently aiming to insert fungal genes coding for lignin peroxidase into ''E. coli''. Lignin breakdown will be made possible through the transport of lignin peroxidase out of the cell. To achieve this, protein transporters will be added to the cell. | ||
Revision as of 01:37, 1 August 2008
| Home | The Team | The Project | Parts Submitted to the Registry | Modeling | Notebook |
|---|
| Overall Project |
| Fuel consumption has come to the forefront as an important political and biological issue that has lead to innovative pursuits of renewable fuel as well as controversial exploitation of natural resources. Currently ethanol is the commercial biofuel of choice; however, current production and distillation of ethanol is inefficient. With this problem in mind, iGEM Wisconsin has looked for alternative ways to make not only ethanol, but other biofuels through synthetic biology. We've designed the following two projects using E. coli to produce biofuels in innovative ways:
One project focuses on using E. coli to produce sorbitol, a sugar alcohol, in large quantities for eventual catalytic conversion to hydrocarbons. Along with producing sorbitol, we've modeled a way to alter E. coli as to make sorbitol production from a glycerol carbon source effective. Our aim is to modify a cell that can use glycerol byproduct from biodiesel production and effectively create sorbitol. In the second project we will be attempting to use E. coli to break down lignin from plant matter into usable biofuels. We are currently aiming to insert fungal genes coding for lignin peroxidase into E. coli. Lignin breakdown will be made possible through the transport of lignin peroxidase out of the cell. To achieve this, protein transporters will be added to the cell.
|
