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大肠杆菌K-12中苏氨酸操纵子的精细结构分析。

Fine structure analysis of the threonine operon in Escherichia coli K-12.

作者信息

Saint-Girons I, Margarita D

出版信息

Mol Gen Genet. 1978 Jun 1;162(1):101-7. doi: 10.1007/BF00333856.

Abstract

A fine structure analysis of the threonine operon in Escherichia coli K-12 was performed by deletion mapping. Lambda transducing bacteriophages carrying various parts of the threonine operon were isolated from strains in which the lacZ gene was fused to a thr gene. We tested for recombination between deletions of the threonine promotor extending into the threonine operon, carried by the phage, and bacterial thr auxotrophs. The relative order of thrO (operator) mutations was established. We propose that an operator region is located between a promoter region and the structural genes. Mutations leading to the desensitization of the aspartokinase I-homoserine dehydrogenase I towards threonine were localized in two different regions of the thrA gene.

摘要

通过缺失作图对大肠杆菌K-12中的苏氨酸操纵子进行了精细结构分析。从lacZ基因与thr基因融合的菌株中分离出携带苏氨酸操纵子不同部分的λ转导噬菌体。我们检测了噬菌体携带的延伸至苏氨酸操纵子的苏氨酸启动子缺失与细菌苏氨酸营养缺陷型之间的重组情况。确定了thrO(操纵基因)突变的相对顺序。我们提出操纵基因区域位于启动子区域和结构基因之间。导致天冬氨酸激酶I-高丝氨酸脱氢酶I对苏氨酸脱敏的突变定位于thrA基因的两个不同区域。

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