Development of highly efficient bioethanol production yeast by genetic engineering
Project/Area Number |
23603003
|
Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Biomass energy
|
Research Institution | Kyoto University |
Principal Investigator |
KODAKI TSUTOMU 京都大学, エネルギー理工学研究所, 准教授 (70170264)
|
Project Period (FY) |
2011 – 2013
|
Project Status |
Completed (Fiscal Year 2013)
|
Budget Amount *help |
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2013: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2012: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2011: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
|
Keywords | バイオエタノール / 酵母 / キシロース / タンパク質工学 |
Research Abstract |
Since xylose is one of the major fermentable sugars present in lignocellulosic biomass, the efficient fermentation of xylose is required to develop economically viable processes for producing bioethanol. In this study, construction of the strictly NADPH dependent xylose reductase from Pichia stipitis was succeeded by site directed mutagenesis. The more efficient xylose fermentation and the decrease of xylitol excretion was observed by introducing the strictly NADPH dependent XR with the strictly NADP+ dependent XDH. Next, by introducing many putative genes of xylose transporters of P. stipitis, the XUT1 and SUT1 genes of Pichia stipitis were shown to be the most effective on xylose consumption. Furthermore, Overexpression of the enzymes involved in the pentose phosphate pathway was shown to have positive effects on xylose fermentation.
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Report
(4 results)
Research Products
(5 results)
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[Book] Green Energy and Technology "Zero-Carbon Energy Kyoto 2010"2011
Author(s)
Khattab, S. M. R., Watanabe, S., Saimura, M., Afifi, M. M., Zohri, A.-N. A., Abdul-Raouf, U. M., and Kodaki, T.
Publisher
Construction of a novel strictly NADPH-dependent Pichia stipitis xylose reductase by site-directed mutagenesis for effective bioethanol production
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