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[对编码第二种嘌呤核苷磷酸化酶的结构基因和调控基因存在缺陷的大肠杆菌K-12突变体的遗传分析]

[Genetic analysis of Escherichia coli K-12 mutants defective for the structural and regulatory genes for second purine nucleoside phosphorylase].

作者信息

Kocharian Sh M, Melkumian M A

出版信息

Genetika. 1986 Aug;22(8):2055-65.

PMID:3095187
Abstract

Two types of mutants lacking the second purine nucleoside phosphorylase (PNPase 2) activity were isolated using the Escherichia coli K-12 pndR strains with constitutive or inosine-inducible synthesis of the PNPase 2. The mutations of the first type are recessive to the pndR+ allele on the F' episome. They are closely linked to the original pndR+ mutations and therefore affect the pndR gene encoding the activator protein. The mutations of the second type affect the PNPase 2 structural gene (pndA) and are recessive to the pndA+ allele on the F' episome. The nupC-pndR-pndA-ptsH-cysA gene order was established by means of four- and five-factorial transductional crosses.

摘要

利用大肠杆菌K-12 pndR菌株,通过组成型或肌苷诱导型合成嘌呤核苷磷酸化酶2(PNPase 2),分离出两种缺乏第二种嘌呤核苷磷酸化酶(PNPase 2)活性的突变体。第一类突变对F'附加体上的pndR +等位基因呈隐性。它们与原始的pndR +突变紧密连锁,因此影响编码激活蛋白的pndR基因。第二类突变影响PNPase 2结构基因(pndA),对F'附加体上的pndA +等位基因呈隐性。通过四因子和五因子转导杂交确定了nupC-pndR-pndA-ptsH-cysA基因顺序。

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