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| + | #REDIRECT [[PennState]] |
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| - | |[[PennState|Home]]
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| - | |[[PennState/Project|Project Descriptions]]
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| - | |<html><a id="faces"><img src="http://www.fablevision.com/northstar/make/characters/face1.gif" width="30" /></a></html>[[PennState/People|People]]
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| - | |<html><a id="faces"><img src="http://www.websters-online-dictionary.org/coreimages/clipart/988/988925.jpg" width="60" /></a></html>[[PennState/Lab|Lab]]
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| - | |[[PennState/Parts|Parts]]
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| - | |[[PennState/Acknowledgements|Acknowledgements]]
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| - | |[[PennState/Links|Links]]
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| - | {| cellspacing="2px" cellpadding="0" border="0" style="padding: 10px; width: 435px; color: #501100; background-color: #000044;|
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| - | |width=435px style="padding: 10px; background-color: #000033; border: 2px solid #8FB08C;" |
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| - | <font color="#FFFFFF" size="6"><html></html>Diauxie Elimination</font>
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| - | <p><font color="#FFFFFF" size="3">Increasing energy demands have brought about the need for a renewable, efficient energy source. Using microorganisms to convert biomass to fuel offers a promising alternative to traditional energy sources, but still faces developmental challenges. Microbes such as Escherichia coli have evolved to preferentially metabolize sugars in a process knows as diauxie. Engineering bacteria to eliminate diauxie with the common lignocellulose sugar xylose would allow faster digestion of ordinary plant biomass while simultaneously reducing the costly sugar residues of wild type bacterial digests. Such modified strains of E. coli need to reduce or eliminate glucose’s repression of catabolization proteins necessary to utilize the energy stored in xylose. The effect of such augmentation would be readily assayed with fluorescent proteins placed downstream of xylose regulatory regions.
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| - | <font face="Tahoma" color="#FFFFFF"><font color="#646B86" size="6"><html></html>Bio Dosimeter</font>
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Latest revision as of 22:34, 26 October 2007
- REDIRECT PennState
