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来自黄色瘤胃球菌的纤维素酶基因在大肠杆菌中的克隆与表达

Cloning and expression in Escherichia coli of a cellulase gene from Ruminococcus flavefaciens.

作者信息

Barros M E, Thomson J A

出版信息

J Bacteriol. 1987 Apr;169(4):1760-2. doi: 10.1128/jb.169.4.1760-1762.1987.

DOI:10.1128/jb.169.4.1760-1762.1987
PMID:3549703
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC212014/
Abstract

An endoglucanase gene of Ruminococcus flavefaciens FD1 was cloned on the vector pEcoR251 to form the recombinant plasmid pMEB200. The cloned endoglucanase gene showed carboxymethylcellulase enzyme activity but no degradation of Avicel (FMC Corp., Philadelphia, Pa.) or filter paper. Carboxymethylcellulase activity was found during the late-exponential-growth phase and accumulated in the periplasmic fraction. Enzyme production was not subject to catabolite repression by glucose.

摘要

将黄化瘤胃球菌FD1的一种内切葡聚糖酶基因克隆到载体pEcoR251上,构建重组质粒pMEB200。克隆的内切葡聚糖酶基因具有羧甲基纤维素酶活性,但对微晶纤维素(FMC公司,宾夕法尼亚州费城)或滤纸无降解作用。羧甲基纤维素酶活性在指数生长后期出现,并在周质部分积累。酶的产生不受葡萄糖的分解代谢物阻遏。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d981/212014/7def0b9ebcd8/jbacter00194-0407-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d981/212014/83ac4b470fbc/jbacter00194-0406-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d981/212014/7def0b9ebcd8/jbacter00194-0407-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d981/212014/83ac4b470fbc/jbacter00194-0406-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d981/212014/7def0b9ebcd8/jbacter00194-0407-a.jpg

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本文引用的文献

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