Xylose isomerase overexpression along with engineering of the pentose phosphate pathway and evolutionary engineering enable rapid xylose utilization and ethanol production by Saccharomyces cerevisiae

被引:222
|
作者
Zhou, Hang [1 ]
Cheng, Jing-sheng [1 ]
Wang, Benjamin L. [1 ]
Fink, Gerald R. [2 ]
Stephanopoulos, Gregory [1 ]
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[2] Whitehead Inst Biomed Res, Cambridge Ctr 9, Cambridge, MA 02142 USA
关键词
Xylose isomerase; Saccharomyces cerevisiae; Evolutionary engineering; Inverse metabolic engineering; Xylose utilization; Ethanol production; L-ARABINOSE; ALCOHOLIC FERMENTATION; FUNCTIONAL EXPRESSION; D-XYLULOKINASE; YEAST; GENE; STRAINS; METABOLISM; GLUCOSE; GROWTH;
D O I
10.1016/j.ymben.2012.07.011
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Xylose is the main pentose and second most abundant sugar in lignocellulosic feedstocks. To improve xylose utilization, necessary for the cost-effective bioconversion of lignocellulose, several metabolic engineering approaches have been employed in the yeast Saccharomyces cerevisiae. In this study, we describe the rational metabolic engineering of a S. cerevisiae strain, including overexpression of the Piromyces xylose isomerase gene (XYLA), Pichia stipitis xylulose kinase (XYL3) and genes of the non-oxidative pentose phosphate pathway (PPP). This engineered strain (H131-A3) was used to initialize a three-stage process of evolutionary engineering, through first aerobic and anaerobic sequential batch cultivation followed by growth in a xylose-limited chemostat. The evolved strain H131-A3-AL(CS) displayed significantly increased anaerobic growth rate (0.203 +/- 0.006 h(-1)) and xylose consumption rate (1.866 g g(-1) h(-1)) along with high ethanol conversion yield (0.41 g/g). These figures exceed by a significant margin any other performance metrics on xylose utilization and ethanol production by S. cerevisiae reported to-date. Further inverse metabolic engineering based on functional complementation suggested that efficient xylose assimilation is attributed, in part, to the elevated expression level of xylose isomerase, which was accomplished through the multiple-copy integration of XYLA in the chromosome of the evolved strain. (c) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:611 / 622
页数:12
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