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灰色链霉菌的A因子结合蛋白负调控链霉素的产生和孢子形成。

The A-factor-binding protein of Streptomyces griseus negatively controls streptomycin production and sporulation.

作者信息

Miyake K, Kuzuyama T, Horinouchi S, Beppu T

机构信息

Department of Agricultural Chemistry, Faculty of Agriculture, University of Tokyo, Japan.

出版信息

J Bacteriol. 1990 Jun;172(6):3003-8. doi: 10.1128/jb.172.6.3003-3008.1990.

Abstract

A-factor, 2-(6'-methylheptanoyl)-3R-hydroxymethyl-4-butanolide, is an autoregulator essential for streptomycin production and sporulation in Streptomyces griseus. S. griseus 2247 that requires no A-factor for streptomycin production or sporulation was found to have a defect in the A-factor-binding protein. This observation implied that the A-factor-binding protein in the absence of A-factor repressed the expression of both phenotypes in the wild-type strain. Screening among mutagenized S. griseus colonies for strains producing streptomycin and sporulating in the absence of A-factor yielded three mutants that were also deficient in the A-factor-binding protein. Reversal of the defect in the A-factor-binding protein of these mutants led to the simultaneous loss of streptomycin production and sporulation. These data suggested that the A-factor-binding protein played a role in repressing both streptomycin production and sporulation and that the binding of A-factor to the protein released its repression. Mutants deficient in the A-factor-binding protein began to produce streptomycin and sporulate at an earlier stage of growth than did the wild-type strain. These mutants produced approximately 10 times more streptomycin than did the parental strain. These findings are consistent with the idea that the intracellular concentration of A-factor determines the timing of derepression of the gene(s) whose expression is repressed by the A-factor-binding protein.

摘要

A因子,即2-(6'-甲基庚酰基)-3R-羟甲基-4-丁醇内酯,是灰色链霉菌中链霉素产生和孢子形成所必需的一种自动调节因子。发现不依赖A因子进行链霉素产生或孢子形成的灰色链霉菌2247在A因子结合蛋白方面存在缺陷。这一观察结果表明,在野生型菌株中,缺乏A因子时,A因子结合蛋白会抑制这两种表型的表达。在诱变的灰色链霉菌菌落中筛选在无A因子情况下产生链霉素并形成孢子的菌株,得到了三个在A因子结合蛋白方面也存在缺陷的突变体。这些突变体A因子结合蛋白缺陷的逆转导致链霉素产生和孢子形成同时丧失。这些数据表明,A因子结合蛋白在抑制链霉素产生和孢子形成方面发挥作用,而A因子与该蛋白的结合会解除其抑制作用。缺乏A因子结合蛋白的突变体在生长早期就开始产生链霉素并形成孢子,比野生型菌株早。这些突变体产生的链霉素比亲本菌株多约10倍。这些发现与以下观点一致,即A因子的细胞内浓度决定了被A因子结合蛋白抑制表达的基因去阻遏的时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07c7/209100/e203618e50db/jbacter00160-0200-a.jpg

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