Manipulating cell flocculation-associated protein kinases in Saccharomyces cerevisiae enables improved stress tolerance and efficient cellulosic ethanol production

被引:38
作者
Ye, Pei-Liang [1 ]
Wang, Xue-Qing [1 ]
Yuan, Bing [1 ]
Liu, Chen-Guang [1 ]
Zhao, Xin-Qing [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Life Sci & Biotechnol, State Key Lab Microbial Metab, Joint Int Res Lab Metab & Dev Sci, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
Saccharomyces cerevisiae; Cell flocculation; Stress tolerance; Protein kinase; Cellulosic ethanol; ACETIC-ACID; GENE-EXPRESSION; YEAST; PHOSPHORYLATION; OVEREXPRESSION; INVOLVEMENT; ENDOCYTOSIS; RESISTANT; PATHWAY; GLUCOSE;
D O I
10.1016/j.biortech.2022.126758
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
Cell self-flocculation endows yeast strains with improved environmental stress tolerance that benefits bioproduction. Exploration of the metabolic and regulatory network differences between the flocculating and nonflocculating cells is conducive to developing strains with satisfactory fermentation efficiency. In this work, integrated analyses of transcriptome, proteome, and phosphoproteome were performed using flocculating yeast Saccharomyces cerevisiae SPSC01 and its non-flocculating mutant grown under acetic acid stress, and the results revealed prominent changes in protein kinases. Overexpressing the mitogen-activated protein kinase Hog1 upregulated by flocculation led to reduced ROS accumulation and increased glutathione peroxidase activity, leading to improved ethanol production under stress. Among the seven genes encoding protein kinases that were tested, AKL1 showed the best performance when overexpressed, achieving higher ethanol productivity in both corncob hydrolysate and simulated corn stover hydrolysate. These results provide alternative strategies for improving cellulosic ethanol production by engineering key protein kinases in S. cerevisiae.
引用
收藏
页数:11
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