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Team:Uppsala-Sweden/Ethanol
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The source of carbon for the ethanol is pyruvate which is also used in the krebs cycle. To get a higher yield the pyruvate pool must be large enough for the ethanol anabolism. By blocking the pyruvate dehydrogenase the usage of pyruvate in the Krebs cycle can be reduced and the pyruvate used for ethanol production instead. | The source of carbon for the ethanol is pyruvate which is also used in the krebs cycle. To get a higher yield the pyruvate pool must be large enough for the ethanol anabolism. By blocking the pyruvate dehydrogenase the usage of pyruvate in the Krebs cycle can be reduced and the pyruvate used for ethanol production instead. | ||
| - | ==The | + | ==The Constructs== |
| - | + | We designed multiple constructs as we ran into some unexpected restriciton site problem during the assembling process. The <i>Z. mobilis</i> strain which was source of the pdc and adh, actually had a most probably a mutation inside the adh2 gene, which lead to a novel EcoRI restriction site. Thus we switched to the adh2 from <i>S. cerevisiae</i>. | |
| - | [[Image: | + | We build as well versions for testing purposes in <i>E. Coli</i>. |
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| + | <h3><partinfo>BBa_K273056</partinfo> : The Construct for Testing Purposes in <i>E. Coli</i> with adh2 from <i>Z. mobilis</i></h3> | ||
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| + | <center>[[Image:ethanol1_ecoli.png]]</center> | ||
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| + | <h3><partinfo>BBa_K273057</partinfo> : The Final Construct for <i>Synechocystis sp PCC6803</i> with adh2 from <i>Z. mobilis</i></h3> | ||
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| + | <center>[[ethanol1.png]]</center> | ||
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| + | <h3><partinfo>BBa_K273015</partinfo> : The Construct for Testing Purposes in <i>E. Coli</i> with adh2 from <i>S. cerevisiae</i></h3> | ||
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| + | <center>[[Image:ethanol2_ecoli.png]]</center> | ||
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| + | <h3><partinfo>BBa_K273016</partinfo> : The Final Construct for <i>Synechocystis sp PCC6803</i> with adh2 from <i>S. cerevisiae</i></h3> | ||
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| + | <center>[[Image:ethanol2.png]]</center> | ||
==Progress== | ==Progress== | ||
Revision as of 22:29, 19 October 2009
The Ethanol Project
Our goal is to introduce ethanol producing capability into a cyanobacteria using the biobrick system.
How to
Cyanobacteria have the capability to harvest the energy from the sun and convert it into other forms of energy. The natural way for these organisms is to store it as sugars or other carbohydrates in a way similar to plants. By introducing a casette of genes for ethanol production, we could get a cyanobacteria to start producing ethanol. However the yield from this might be very low since the bacteria have already evolved good pathways in the metabolism to take care of the energy. The source of carbon for the ethanol is pyruvate which is also used in the krebs cycle. To get a higher yield the pyruvate pool must be large enough for the ethanol anabolism. By blocking the pyruvate dehydrogenase the usage of pyruvate in the Krebs cycle can be reduced and the pyruvate used for ethanol production instead.
The Constructs
We designed multiple constructs as we ran into some unexpected restriciton site problem during the assembling process. The Z. mobilis strain which was source of the pdc and adh, actually had a most probably a mutation inside the adh2 gene, which lead to a novel EcoRI restriction site. Thus we switched to the adh2 from S. cerevisiae.
We build as well versions for testing purposes in E. Coli.
: The Construct for Testing Purposes in E. Coli with adh2 from Z. mobilis
: The Final Construct for Synechocystis sp PCC6803 with adh2 from Z. mobilis
: The Construct for Testing Purposes in E. Coli with adh2 from S. cerevisiae
: The Final Construct for Synechocystis sp PCC6803 with adh2 from S. cerevisiae
Progress
as of 2009-1018
