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大肠杆菌K-12中β-葡萄糖醛酸酶合成的调控:uidA表达特异性去阻遏的组成型突变体。

Regulation of beta-glucuronidase synthesis in Escherichia coli K-12: constitutive mutants specifically derepressed for uidA expression.

作者信息

Novel M, Novel G

出版信息

J Bacteriol. 1976 Jul;127(1):406-17. doi: 10.1128/jb.127.1.406-417.1976.

Abstract

All methyl-beta-D-galacturonide-positive mutants isolated from Escherichia coli K-12 carry constitutive mutations for beta-glucuronidase (UID) synthesis. Most of these mutants are specific for UID synthesis and are distributed in three classes according to the derepression level of UID. Each specific mutant carries a mutation(s) near uidA, the structural gene for UID, at min 30.5 of the E. coli K-12 linkage map. The expression of UID synthesis in F-merodiploid strains carrying these mutations permits discrimination between dominant and recessive constitutivity over the wild-type allele. The first kind of mutation (dominant) should affect the operator site uidO of the structural gene uidA; the second type of mutation (recessive) should affect a regulatory gene, uidR, operating through a negative control. The isolation of mutants bearing at this locus superrepressed mutations, which can revert to produce a constitutive phenotype, confirms the occurrence of such a regulatory gene. The partially derepressed uidR mutants of the first class are normally inducible and remain constitutive at low temperature; their UID has the same thermal sensitivity as in the wild-type strains. The occurrence of similar regulatory gene mutants has been recently described in the lactose system (Shineberg, 1974).

摘要

从大肠杆菌K - 12中分离出的所有甲基 - β - D - 半乳糖醛酸阳性突变体都携带β - 葡萄糖醛酸酶(UID)合成的组成型突变。这些突变体中的大多数对UID合成具有特异性,并根据UID的去阻遏水平分为三类。每个特异性突变体在大肠杆菌K - 12连锁图谱的30.5分钟处,靠近UID的结构基因uidA处携带一个或多个突变。在携带这些突变的F - 部分二倍体菌株中UID合成的表达允许区分相对于野生型等位基因的显性和隐性组成型。第一种突变(显性)应影响结构基因uidA的操纵位点uidO;第二种突变类型(隐性)应影响通过负调控起作用的调控基因uidR。在该位点携带超阻遏突变的突变体的分离,这些突变体可以回复产生组成型表型,证实了这种调控基因的存在。第一类部分去阻遏的uidR突变体通常是可诱导的,并且在低温下保持组成型;它们的UID具有与野生型菌株相同的热敏感性。最近在乳糖系统中也描述了类似调控基因突变体的出现(Shineberg,1974)。

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本文引用的文献

8
[On the glucuronidase and galacturonidase activities of Escherichia coli ML 30].
C R Acad Hebd Seances Acad Sci D. 1968 Apr 29;266(18):1894-7.
9
[On the properties and the biosynthesis of beta-glucuronidase of Escherichia coli K 12].
C R Acad Hebd Seances Acad Sci D. 1968 May 6;266(19):2021-4.
10
Negative control of the galactose operon in E. coli.
Mol Gen Genet. 1968;102(1):79-88. doi: 10.1007/BF00341872.

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