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天蓝色链霉菌relC突变的多效性效应

Pleiotropic effects of a relC mutation in Streptomyces antibioticus.

作者信息

Kelly K S, Ochi K, Jones G H

机构信息

Department of Biology, Emory University, Atlanta, Georgia 30322.

出版信息

J Bacteriol. 1991 Apr;173(7):2297-300. doi: 10.1128/jb.173.7.2297-2300.1991.

Abstract

Ochi (Agric. Biol. Chem. 51:829-835, 1987) has isolated a relaxed mutant of Streptomyces antibioticus, designated relC49, relC49 accumulates significantly lower levels of ppGpp than the parent stain, IMRU3720. At its maximum, the ppGpp level in relC49 was only one-fourth that observed in strain IMRU3720. Interestingly, a burst of ppGpp synthesis between 18 and 22 h of growth in IMRU3720 coincided with the onset of actinomycin production in that strain. As shown previously, the activity in protein synthesis of ribosomes from strain IMRU3720 decreases with the age of the culture. The decrease in activity was less pronounced in cultures of relC49. relC49 mycelium contains reduced levels of phenoxazinone synthase, a key enzyme involved in actinomycin biosynthesis. The rel mutation prevents the normal increase in the activity of one of the other enzymes required for production of the antibiotic, 3-hydroxyanthanilate-4-methyltransferase, and a third enzyme, actinomycin synthetase I, appears to be completely absent from relC49 mycelium. Levels of phenoxazinone synthease mRNA were examined by RNA dot blotting with the cloned phenoxazinone synthase gene as a probe. mRNA levels for phenoxazinone synthase were dramatically reduced in relC49 compared with strain IMRU3720. These results are discussed in terms of the possible regulation of the onset of actinomycin production by ppGpp.

摘要

落合(《农业与生物化学》51:829 - 835,1987年)分离出了天蓝色链霉菌的一个松弛型突变体,命名为relC49,relC49积累的鸟苷四磷酸(ppGpp)水平明显低于亲本菌株IMRU3720。在其最高水平时,relC49中的ppGpp水平仅为IMRU3720菌株中观察到水平的四分之一。有趣的是,IMRU3720在生长18至22小时之间ppGpp合成的爆发与该菌株中放线菌素产生的开始相吻合。如先前所示,IMRU3720菌株核糖体的蛋白质合成活性随着培养时间的延长而降低。在relC49培养物中活性的降低不太明显。relC49菌丝体中吩恶嗪酮合酶的水平降低,吩恶嗪酮合酶是放线菌素生物合成中的一种关键酶。rel突变阻止了抗生素生产所需的另一种酶3 - 羟基邻氨基苯甲酸 - 4 - 甲基转移酶活性的正常增加,并且relC49菌丝体中似乎完全不存在第三种酶放线菌素合成酶I。用克隆的吩恶嗪酮合酶基因作为探针,通过RNA斑点印迹法检测了吩恶嗪酮合酶mRNA的水平。与IMRU3720菌株相比,relC49中吩恶嗪酮合酶的mRNA水平显著降低。根据ppGpp对放线菌素产生开始的可能调节来讨论这些结果。

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