Overexpression of Saccharomyces cerevisiae transcription factor and multidrug resistance genes conveys enhanced resistance to lignocellulose-derived fermentation inhibitors

被引:59
作者
Alriksson, Bjorn [2 ]
Horvath, Ilona Sarvari [2 ]
Jonsson, Leif J. [1 ,2 ]
机构
[1] Umea Univ, Dept Chem, SE-90187 Umea, Sweden
[2] Karlstad Univ, Dept Chem & Biomed Sci, SE-65188 Karlstad, Sweden
关键词
Lignocellulose; Ethanol; S; cerevisiae; ATR1; FLR1; YAP1; OXIDATIVE STRESS; FLR1; GENE; DEGRADATION-PRODUCTS; ETHANOL-PRODUCTION; YEAST; EXPRESSION; ACID; YAP1; DETOXIFICATION; WOOD;
D O I
10.1016/j.procbio.2009.09.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The presence of fermentation inhibitors in lignocellulose hydrolysates is an obstacle for achieving efficient fermentation of lignocellulose hydrolysates to ethanol and other commodities. In this investigation, the possibility of generating more inhibitor-resistant Saccharomyces cerevisiae by genetic engineering was explored. Based on previous results from studies of deletion mutants, three S. cerevisiae genes (ATR1, FLR1, YAP1) involved in multidrug resistance and stress response of yeast were selected for overexpression in three S. cerevisiae strains. The resistance of the transformed strains to lignocellulose-derived fermentation inhibitors and a dilute-acid spruce hydrolysate was evaluated in fermentation experiments. Overexpression of FLR1 resulted in enhanced resistance to the phenolic inhibitor coniferyl aldehyde and the furan aldehyde HMF (5-hydroxymethyl-2-furaldehyde). Overexpression of ATR1 conferred increased resistance to coniferyl aldehyde. Strains overexpressing YAP1, which encodes a transcription factor. displayed increased resistance to coniferyl aldehyde, HMF, and the spruce hydrolysate. An ethanol productivity of 0.17 g ethanol x l(-1) x h(-1) was achieved for a YAP1-overexpressing transformant cultivated in spruce hydrolysate, whereas a control transformant, which did not overexpress YAP1, only reached a productivity of 0.05 g ethanol x l(-1) x h(-1). (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:264 / 271
页数:8
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