Abstract
A K270R mutation of xylose reductase (XR) was constructed by site-direct mutagenesis. Fermentation results of the F106X and F106KR strains, which carried wild type XR and K270R respectively, were compared using different substrate concentrations (from 55 to 220. g/L). After 72. h, F106X produced less ethanol than xylitol, while F106KR produced ethanol at a constant yield of 0.36. g/g for all xylose concentrations. The xylose consumption rate and ethanol productivity increased with increasing xylose concentrations in F106KR strain. In particular, F106KR produced 77.6. g/L ethanol from 220. g/L xylose and converted 100. g/L glucose and 100. g/L xylose into 89.0. g/L ethanol in 72. h, but the corresponding values of F106X strain are 7.5 and 65.8. g/L. The ethanol yield of F106KR from glucose and xylose was 0.42. g/g, which was 82.3% of the theoretical yield. These results suggest that the F106KR strain is an excellent producer of ethanol from xylose.
Original language | English |
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Pages (from-to) | 9206-9215 |
Number of pages | 10 |
Journal | Bioresource Technology |
Volume | 102 |
Issue number | 19 |
DOIs | |
Publication status | Published - 1 Oct 2011 |
Externally published | Yes |
Keywords
- Ethanol
- Redox imbalance
- Saccharomyces cerevisiae
- Xylose
- Xylose reductase
ASJC Scopus subject areas
- Bioengineering
- Environmental Engineering
- Renewable Energy, Sustainability and the Environment
- Waste Management and Disposal