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微菌素C7产生及免疫的遗传决定因素的克隆与定位

Cloning and mapping of the genetic determinants for microcin C7 production and immunity.

作者信息

Novoa M A, Díaz-Guerra L, San Millán J L, Moreno F

出版信息

J Bacteriol. 1986 Dec;168(3):1384-91. doi: 10.1128/jb.168.3.1384-1391.1986.

Abstract

Microcin C7, a peptide antibiotic inhibitor of protein synthesis, is produced by Escherichia coli K-12 strains that carry the 43-kilobase low-copy-number plasmid pMccC7. Microcin C7 production and immunity determinants of this plasmid have been cloned into the vectors pBR322 and pACYC184. The resulting plasmids overproduce microcin C7 and express immunity against the microcin. Mcc- and Mcc- Imm- mutants have been isolated on recombinant plasmids by inserting transposable elements. Physical and phenotypic characterization of these mutants shows that a DNA region of 5 kilobases is required to produce microcin C7, and that two small regions located inside the producing region are also required to express immunity. Analysis of plasmids carrying mcc-lacZ gene fusions indicates that all microcin DNA is transcribed in the same direction. The results suggest that a structure like a polycistronic operon is responsible for microcin C7 production and immunity.

摘要

微菌素C7是一种蛋白质合成的肽类抗生素抑制剂,由携带43千碱基低拷贝数质粒pMccC7的大肠杆菌K - 12菌株产生。该质粒的微菌素C7产生和免疫决定簇已被克隆到载体pBR322和pACYC184中。所得质粒过量产生微菌素C7并表达对微菌素的免疫性。通过插入转座元件在重组质粒上分离出了Mcc - 和Mcc - Imm - 突变体。这些突变体的物理和表型特征表明,产生微菌素C7需要一个5千碱基的DNA区域,并且在产生区域内的两个小区域对于表达免疫性也是必需的。对携带mcc - lacZ基因融合体的质粒分析表明,所有微菌素DNA都以相同方向转录。结果表明,类似多顺反子操纵子的结构负责微菌素C7的产生和免疫性。

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