Simultaneous secretion of seven lignocellulolytic enzymes by an industrial second-generation yeast strain enables efficient ethanol production from multiple polymeric substrates

被引:41
|
作者
Claes, Arne [1 ,2 ]
Deparis, Quinten [1 ,2 ]
Foulquie-Moreno, Maria R. [1 ,2 ]
Thevelein, Johan M. [1 ,2 ]
机构
[1] Katholieke Univ Leuven, Inst Bot & Microbiol, Lab Mol Cell Biol, Leuven, Belgium
[2] VIB, Ctr Microbiol, Kasteelpk Arenberg 31, B-3001 Leuven, Flanders, Belgium
关键词
Bioethanol; Yeast cell factory; Enzyme secretion; Consolidated bioprocessing; Lignocellulose; Xylan; CODISPLAYING; 3; TYPES; BIO-BASED CHEMICALS; SACCHAROMYCES-CEREVISIAE; ASPERGILLUS-NIGER; BETA-GLUCOSIDASE; CELLULOSE HYDROLYSIS; ENZYMATIC-HYDROLYSIS; TRICHODERMA-REESEI; XYLOSE-ISOMERASE; CLOSTRIDIUM-CELLULOVORANS;
D O I
10.1016/j.ymben.2020.02.004
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
A major hurdle in the production of bioethanol with second-generation feedstocks is the high cost of the enzymes for saccharification of the lignocellulosic biomass into fermentable sugars. Simultaneous saccharification and fermentation with Saccharomyces cerevisiae yeast that secretes a range of lignocellulolytic enzymes might address this problem, ideally leading to consolidated bioprocessing. However, it has been unclear how many enzymes can be secreted simultaneously and what the consequences would be on the C6 and C5 sugar fermentation performance and robustness of the second-generation yeast strain. We have successfully expressed seven secreted lignocellulolytic enzymes, namely endoglucanase, beta-glucosidase, cellobiohydrolase I and II, xylanase, beta-xylosidase and acetylxylan esterase, in a single second-generation industrial S. cerevisiae strain, reaching 94.5 FPU/g CDW and enabling direct conversion of lignocellulosic substrates into ethanol without preceding enzyme treatment. Neither glucose nor the engineered xylose fermentation were significantly affected by the heterologous enzyme secretion. This strain can therefore serve as a promising industrial platform strain for development of yeast cell factories that can significantly reduce the enzyme cost for saccharification of lignocellulosic feedstocks.
引用
收藏
页码:131 / 141
页数:11
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