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控制枯草芽孢杆菌中一类降解酶合成的信号转导途径:调控基因的表达及degS和degU突变分析

Signal transduction pathway controlling synthesis of a class of degradative enzymes in Bacillus subtilis: expression of the regulatory genes and analysis of mutations in degS and degU.

作者信息

Msadek T, Kunst F, Henner D, Klier A, Rapoport G, Dedonder R

机构信息

Unité de Biochimie Microbienne, Centre National de la Recherche Scientifique URA 1300, Institut Pasteur, Paris, France.

出版信息

J Bacteriol. 1990 Feb;172(2):824-34. doi: 10.1128/jb.172.2.824-834.1990.

DOI:10.1128/jb.172.2.824-834.1990
PMID:1688843
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC208512/
Abstract

The rates of synthesis of a class of both secreted and intracellular degradative enzymes in Bacillus subtilis are controlled by a signal transduction pathway defined by at least four regulatory genes: degS, degU, degQ (formerly sacQ), and degR (formerly prtR). The DegS-DegU proteins show amino acid similarities with two-component procaryotic modulator-effector pairs such as NtrB-NtrC, CheA-CheY, and EnvZ-OmpR. By analogy with these systems, it is possible that DegS is a protein kinase which could catalyze the transfer of a phosphoryl moiety to DegU, which acts as a positive regulator. DegR and DegQ correspond to polypeptides of 60 and 46 amino acids, respectively, which also activate the synthesis of degradative enzymes. We show that the degS and degU genes are organized in an operon. The putative sigma A promoter of the operon was mapped upstream from degS. Mutations in degS and degU were characterized at the molecular level, and their effects on transformability and cell motility were studied. The expression of degQ was shown to be subject both to catabolite repression and DegS-DegU-mediated control, allowing an increase in the rate of synthesis of degQ under conditions of nitrogen starvation. These results are consistent with the hypothesis that this control system responds to an environmental signal such as limitations of nitrogen, carbon, or phosphate sources.

摘要

枯草芽孢杆菌中一类分泌型和细胞内降解酶的合成速率受至少四个调控基因定义的信号转导途径控制

degS、degU、degQ(以前称为sacQ)和degR(以前称为prtR)。DegS-DegU蛋白与双组分原核调节剂-效应器对如NtrB-NtrC、CheA-CheY和EnvZ-OmpR具有氨基酸相似性。与这些系统类似,DegS可能是一种蛋白激酶,它可以催化磷酰基部分转移到作为正调控因子的DegU上。DegR和DegQ分别对应于60和46个氨基酸的多肽,它们也激活降解酶的合成。我们表明degS和degU基因组成一个操纵子。该操纵子假定的sigma A启动子定位在degS上游。在分子水平上对degS和degU中的突变进行了表征,并研究了它们对转化能力和细胞运动性的影响。已表明degQ的表达既受分解代谢物阻遏又受DegS-DegU介导的控制,从而在氮饥饿条件下允许degQ合成速率增加。这些结果与该控制系统对诸如氮、碳或磷源限制等环境信号作出反应的假设一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b716/208512/47864fcd8427/jbacter01044-0327-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b716/208512/47864fcd8427/jbacter01044-0327-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b716/208512/47864fcd8427/jbacter01044-0327-a.jpg

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