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Fine-structure mapping and complementation analysis of the Escherichia coli cysB gene.

机译:大肠杆菌cysB基因的精细结构定位和互补分析。

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摘要

Sixty-two point mutations were isolated in Escherichia coli by means of transduction with mutagenized phage P1. Twenty-two deletions extending into cysB but able to recombine with at least some of the point mutations were isolated on a transmissible E. coli plasmid. Mapping of the point mutations against the deletions divided the former into 16 deletion groups. Nine merodiploids were constructed in which the chromosome carried one of the three point mutations most distal to the trp operon and in which a plasmid carried one of the three point mutations most proximal to the trp operon. All of these showed a Cys-phenotype. It follows that mutations at the two extreme ends of the region belong to the same complementation group.
机译:通过诱变的噬菌体P1的转导,在大肠杆菌中分离出62个点突变。在可传播的大肠杆菌质粒上分离出22个缺失,延伸到cysB中,但能够与至少一些点突变重组。点突变对缺失的映射将前者分为16个缺失组。构建了九种类金属倍体,其中染色体带有最靠近trp操纵子的三个点突变之一,而质粒带有最靠近trp操纵子的三个点突变之一。所有这些均显示出Cys表型。因此,该区域两个末端的突变属于同一互补组。

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