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枯草芽孢杆菌degS和degU基因产物的分离与磷酸化

Isolation and phosphorylation of the Bacillus subtilis degS and degU gene products.

作者信息

Mukai K, Kawata M, Tanaka T

机构信息

Mitsubishi Kasei Institute of Life Sciences, Tokyo, Japan.

出版信息

J Biol Chem. 1990 Nov 15;265(32):20000-6.

PMID:2123196
Abstract

The Bacillus subtilis sacU locus consists of two genes, degS and degU, which positively regulate the synthesis of several extracellular enzymes including the neutral and alkaline proteases. Both the DegS and DegU proteins have been purified from overproducing Escherichia coli strains harboring degS or degU gene-carrying plasmids, and the following results were obtained. DegS was autophosphorylated in the presence of [gamma-32P]ATP, and transferred the phosphoryl group to DegU. The transfer reaction was rapid in contrast to the autophosphorylation reaction. The phosphoryl groups incorporated into DegS and DegU were released at their own specific rates, the latter being twice faster than the former. The linkage between DegS and the phosphoryl moiety was unstable at acidic pH, whereas reverse was the case for the linkage between DegU and its phosphoryl group, suggesting that His and Asp are involved in the formation of DegS-phosphate and DegU-phosphate, respectively. Deletion of degS resulted in the reduced expression of the exocellular alkaline protease gene, aprE. These results suggest that phosphorylation of DegS by its own kinase activity and subsequent transfer of the phosphoryl group to DegU play a role in the activation of the aprE gene.

摘要

枯草芽孢杆菌的sacU位点由degS和degU两个基因组成,它们正向调控包括中性和碱性蛋白酶在内的几种胞外酶的合成。DegS和DegU蛋白均已从携带degS或degU基因质粒的过量表达大肠杆菌菌株中纯化出来,并得到了以下结果。DegS在[γ-32P]ATP存在下进行自身磷酸化,并将磷酸基团转移至DegU。与自身磷酸化反应相比,转移反应速度很快。掺入DegS和DegU的磷酸基团以各自特定的速率释放,后者比前者快两倍。DegS与磷酸部分之间的连接在酸性pH下不稳定,而DegU与其磷酸基团之间的连接情况则相反,这表明His和Asp分别参与了DegS-磷酸和DegU-磷酸的形成。degS的缺失导致胞外碱性蛋白酶基因aprE的表达降低。这些结果表明,DegS通过自身激酶活性进行磷酸化以及随后将磷酸基团转移至DegU在aprE基因的激活中起作用。

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