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混合纤维弧菌中两个紧密连锁的纤维素酶基因的克隆与特性分析

Cloning and Characterization of Two Closely Linked Cellulase Genes from Cellvibrio mixtus.

作者信息

Kahler CM, Pemberton JM

机构信息

Department of Microbiology, University of Queensland, St. Lucia, 4072, Brisbane, Australia

出版信息

Curr Microbiol. 1996 Jul;33(1):60-6. doi: 10.1007/s002849900075.

Abstract

A 16.5-kb BamHI fragment of the Cellvibrio mixtus chromosome was found to direct carboxymethylcellulase, xylanase, and avicel hydrolysis. Two closely linked genes were subcloned from this insert. The gene, cmcI, was cloned as a 2.7-kb fragment and expressed in Escherichia coli. It encoded an enzyme of approximately 74 kDa which degraded carboxymethylcellulose and xylan but did not attack the microcrystalline cellulose substrate avicel. A second cellulase capable of degrading avicel, encoded by exoI, was found 5.5 kb downstream of cmcI. Two translation products of 53.7 kDa and 51.5 kDa were produced in E. coli strains expressing exoI. Northern analysis of total mRNA of C. mixtus grown on avicel, with a probe generated from cmcI, showed that cmcI and exoI were not cotranscribed in an operon.

摘要

发现混合纤维弧菌染色体的一个16.5kb的BamHI片段可指导羧甲基纤维素酶、木聚糖酶和微晶纤维素水解。从该插入片段中亚克隆出两个紧密连锁的基因。基因cmcI作为一个2.7kb的片段被克隆并在大肠杆菌中表达。它编码一种约74kDa的酶,该酶可降解羧甲基纤维素和木聚糖,但不作用于微晶纤维素底物微晶纤维素。在cmcI下游5.5kb处发现了由exoI编码的第二种能够降解微晶纤维素的纤维素酶。在表达exoI的大肠杆菌菌株中产生了53.7kDa和51.5kDa的两种翻译产物。用由cmcI产生的探针,对在微晶纤维素上生长的混合纤维弧菌的总mRNA进行Northern分析,结果表明cmcI和exoI不在一个操纵子中共转录。

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