Effects of xylitol dehydrogenase (XYL2) on xylose fermentation by engineered Candida glycerinogenes.

Autor: Zong H; The Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, Research Centre of Industrial Microbiology, Jiangnan University, Wuxi, People's Republic of China., Zhang C; The Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, Research Centre of Industrial Microbiology, Jiangnan University, Wuxi, People's Republic of China., Zhuge B; The Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, Research Centre of Industrial Microbiology, Jiangnan University, Wuxi, People's Republic of China., Lu X; The Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, Research Centre of Industrial Microbiology, Jiangnan University, Wuxi, People's Republic of China., Fang H; The Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, Research Centre of Industrial Microbiology, Jiangnan University, Wuxi, People's Republic of China., Sun J; Zhejiang Condiments Industry Research Center, Zhejiang Zhengwei Food Co., Ltd., Yiwu, People's Republic of China.
Jazyk: angličtina
Zdroj: Biotechnology and applied biochemistry [Biotechnol Appl Biochem] 2017 Jul; Vol. 64 (4), pp. 590-599. Date of Electronic Publication: 2017 Mar 23.
DOI: 10.1002/bab.1514
Abstrakt: Efficient bioconversion of d-xylose into various biochemicals is critical for lignocelluloses application. Candida glycerinogenes, expressing the xylitol dehydrogenase (XYL2) gene, has the ability to produce glycerol from xylose entered into pentose phosphate pathway. In this study, we demonstrate that low expression levels of the XYL2 gene derived from Scheffersomyces stipitis in C. glycerinogenes is a major bottleneck in efficient xylose fermentation. Through a metabolic engineering approach using an integrative expression, XYL2 was identified as an overexpression target for improving xylose metabolism. Two recombinant strains with XYL2 overexpression were constructed to ferment a mixture of glucose and xylose simultaneously in batch fermentation. Compared with C. glycerinogenes (wild type), glycerol production from xylose by C. glycerinogenes (PURGAPX2) and C. glycerinogenes (PURGPDX2) was increased by 94.5% and 103.3%, respectively. It was also found that additional overexpression of XYL2 under the control of strong promoters in a xylose-fermenting strain not only reduced xylitol accumulation but also increased glycerol yields. As the expression levels of XYL2 increased, the glycerol yields gradually improved from 30.6 to 63.3 g/L, whereas the xylitol yields significantly decreased from 38.7 to 19.9 g/L. These results suggest that strong expression of XYL2 is a necessary condition for developing efficient xylose-fermenting strains.
(© 2016 International Union of Biochemistry and Molecular Biology, Inc.)
Databáze: MEDLINE
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