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顶头孢霉编码乙酰转移酶的基因cefG的克隆、特性分析及其在菌株改良中的应用

Cloning, characterization, and use in strain improvement of the Cephalosporium acremonium gene cefG encoding acetyl transferase.

作者信息

Mathison L, Soliday C, Stepan T, Aldrich T, Rambosek J

机构信息

Panlabs, Inc. Bothell, WA 98011.

出版信息

Curr Genet. 1993 Jan;23(1):33-41. doi: 10.1007/BF00336747.

DOI:10.1007/BF00336747
PMID:8428381
Abstract

A long open reading frame (ORF) closely linked to the Cephalosporium acremonium gene cefEF was identified by DNA sequencing. The cefEF gene encodes the enzyme involved in cephalosporin C (CPC) biosynthesis known as expandase/hydroxylase. Complementation of a C. acremonium cefG mutant, as well as expression of the gene in Aspergillus niger, showed this ORF to be the cefG gene, encoding cephalosporin C acetyltransferase, which catalyzes the last step in CPC biosynthesis. Analysis of transformants containing additional copies of this gene showed that a direct relationship exists between cefG copy number, cefG message levels, and CPC titers. This gene encodes an enzyme for what may be a rate-limiting step in CPC production.

摘要

通过DNA测序鉴定出一个与顶头孢霉基因cefEF紧密相连的长开放阅读框(ORF)。cefEF基因编码参与头孢菌素C(CPC)生物合成的酶,即扩张酶/羟化酶。顶头孢霉cefG突变体的互补以及该基因在黑曲霉中的表达表明,这个ORF就是cefG基因,它编码头孢菌素C乙酰转移酶,催化CPC生物合成的最后一步。对含有该基因额外拷贝的转化体的分析表明,cefG拷贝数、cefG信使水平和CPC滴度之间存在直接关系。该基因编码一种酶,可能参与CPC生产中的限速步骤。

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1
Cloning, characterization, and use in strain improvement of the Cephalosporium acremonium gene cefG encoding acetyl transferase.顶头孢霉编码乙酰转移酶的基因cefG的克隆、特性分析及其在菌株改良中的应用
Curr Genet. 1993 Jan;23(1):33-41. doi: 10.1007/BF00336747.
2
The cefG gene of Cephalosporium acremonium is linked to the cefEF gene and encodes a deacetylcephalosporin C acetyltransferase closely related to homoserine O-acetyltransferase.顶头孢霉的cefG基因与cefEF基因相连,编码一种与高丝氨酸O - 乙酰转移酶密切相关的去乙酰头孢菌素C乙酰转移酶。
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Cloning and sequencing of the beta-lactam hydroxylase gene (cefF) from Streptomyces clavuligerus: gene duplication may have led to separate hydroxylase and expandase activities in the actinomycetes.来自棒状链霉菌的β-内酰胺羟化酶基因(cefF)的克隆与测序:基因复制可能导致放线菌中羟化酶和扩环酶活性的分离。
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