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原核生物和真核生物微生物中多种潜在的碳分解代谢物阻遏机制。

A multiplicity of potential carbon catabolite repression mechanisms in prokaryotic and eukaryotic microorganisms.

作者信息

Saier M H

机构信息

Department of Biology, University of California, La Jolla 92093-0116.

出版信息

New Biol. 1991 Dec;3(12):1137-47.

PMID:1667478
Abstract

The discovery of cyclic AMP (cAMP) and its receptor protein in Escherichia coli and the convincing demonstration that these molecules mediate catabolite repression of the synthesis of carbohydrate catabolic enzymes led to the widespread belief that the phenomenon of catabolite repression in bacteria was understood. It is now recognized that cAMP-independent catabolite repression mechanisms are operative in both prokaryotic and eukaryotic microorganisms. New evidence has led to the identification of a diversity of cAMP-independent regulatory mechanisms that may mediate catabolite repression in bacteria. These mechanisms utilize (i) novel transcription factors, (ii) starvation-induced RNA polymerase sigma factors, and (iii) three evolutionarily distinct protein phosphorylating enzyme systems. Although these mechanisms are not fully understood, it is suggested that they exert their effects at the transcriptional level and that phosphorylation and allosteric control by regulatory proteins are involved in these processes.

摘要

环腺苷酸(cAMP)及其在大肠杆菌中的受体蛋白的发现,以及这些分子介导碳水化合物分解代谢酶合成的分解代谢物阻遏这一令人信服的证明,使得人们普遍认为细菌中的分解代谢物阻遏现象已被理解。现在人们认识到,不依赖cAMP的分解代谢物阻遏机制在原核和真核微生物中均起作用。新证据已导致鉴定出多种可能介导细菌中分解代谢物阻遏的不依赖cAMP的调节机制。这些机制利用(i)新型转录因子,(ii)饥饿诱导的RNA聚合酶σ因子,以及(iii)三种进化上不同的蛋白质磷酸化酶系统。尽管这些机制尚未完全被理解,但有人提出它们在转录水平发挥作用,并且调节蛋白的磷酸化和变构控制参与了这些过程。

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