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在异源表达梭菌内切葡聚糖酶和纤维二糖裂合酶基因的酿酒酵母中生产纤维素乙醇。

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

机构信息

School of Life Science and Biotechnology, Korea University, Seoul 136-701, Korea.

出版信息

Mol Cells. 2009 Oct 31;28(4):369-73. doi: 10.1007/s10059-009-0131-y. Epub 2009 Sep 30.

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.

摘要

基于内切葡聚糖酶(Clostridium thermocellum)和β-葡萄糖苷酶 1(Saccharomycopsis fibuligera)的天然酶编码序列,通过α-交配因子信号肽融合,实现了它们在酿酒酵母发酵培养物中的异源分泌表达。乙醇的生产依赖于纤维素的同步糖化将其转化为葡萄糖,以及利用重组酵母菌株作为微生物生物催化剂将葡萄糖发酵为乙醇。表达内切葡聚糖酶和β-葡萄糖苷酶的重组酵母菌株能够从β-葡聚糖、CMC 和酸膨胀纤维素中生产乙醇。这表明,本研究中获得的酵母菌株作为全细胞生物催化剂能够有效地发挥作用。

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