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
2009-10
Publisher
KOREAN SOC MOLECULAR & CELLULAR BIOLOGY
Citation
MOLECULES AND CELLS, v.28, no.4, pp.369 - 373
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.
Keywords
RECOMBINANT KLEBSIELLA-OXYTOCA; AMORPHOUS CELLULOSE; MICROCRYSTALLINE CELLULOSE; CRYSTALLINE CELLULOSE; YEAST-STRAIN; FERMENTATION; DEGRADATION; HYDROLYSIS; CELLULASES; CELLOBIOSE; RECOMBINANT KLEBSIELLA-OXYTOCA; AMORPHOUS CELLULOSE; MICROCRYSTALLINE CELLULOSE; CRYSTALLINE CELLULOSE; YEAST-STRAIN; FERMENTATION; DEGRADATION; HYDROLYSIS; CELLULASES; CELLOBIOSE; beta-glucosidase; cellulose degradation; Clostridium thermocellum; endoglucanase; ethanol production; extracellular expression; Saccharomyces cerevisiae
ISSN
1016-8478
URI
https://pubs.kist.re.kr/handle/201004/132078
DOI
10.1007/s10059-009-0131-y
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KIST Article > 2009
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