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Production of cellulosic ethanol in Saccharomyces cerevisiae heterologous expressing Clostridium thermocellum endoglucanase and Saccharomycopsis fibuligera beta-glucosidase genes

Authors
Jeon, EugeneHyeon, Jeong-eunSuh, Dong JinSuh, Young-WoongKim, Seoung WookSong, Kwang HoHan, Sung Ok
Issue Date
10월-2009
Publisher
KOREAN SOC MOLECULAR & CELLULAR BIOLOGY
Keywords
beta-glucosidase; cellulose degradation; Clostridium thermocellum; endoglucanase; ethanol production; extracellular expression; Saccharomyces cerevisiae
Citation
MOLECULES AND CELLS, v.28, no.4, pp.369 - 373
Indexed
SCIE
SCOPUS
KCI
Journal Title
MOLECULES AND CELLS
Volume
28
Number
4
Start Page
369
End Page
373
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/119196
DOI
10.1007/s10059-009-0131-y
ISSN
1016-8478
Abstract
Heterologous secretory expression of endoglucanase E (Clostridium thermocellum) and beta-glucosidase 1 (Saccharomycopsis fibuligera) was achieved in Saccharomyces cerevisiae fermentation cultures as an alpha-mating factor signal peptide fusion, based on the native enzyme coding sequence. Ethanol production depends on simultaneous saccharification of cellulose to glucose and fermentation of glucose to ethanol by a recombinant yeast strain as a microbial biocatalyst. Recombinant yeast strain expressing endoglucanase and beta-glucosidase was able to produce ethanol from beta-glucan, CMC and acid swollen cellulose. This indicates that the resultant yeast strain of this study acts efficiently as a whole cell biocatalyst.
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