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枯草芽孢杆菌的枯草杆菌蛋白酶E基因在体内由一个σ37启动子转录。

The subtilisin E gene of Bacillus subtilis is transcribed from a sigma 37 promoter in vivo.

作者信息

Wong S L, Price C W, Goldfarb D S, Doi R H

出版信息

Proc Natl Acad Sci U S A. 1984 Feb;81(4):1184-8. doi: 10.1073/pnas.81.4.1184.

Abstract

A cloned Bacillus subtilis gene (sprE) expressed only during the stationary growth phase is shown to encode the subtilisin E protease, an enzyme associated with sporulation. We have determined the DNA sequence of the sprE promoter region and the promoter-proximal half of the structural gene. The sprE gene codes for a putative 29-residue signal peptide and a 77-residue leader peptide preceding the mature subtilisin sequence. By plasmid integration and phage PBS1 transduction, we have mapped the sprE locus between glyB and metD on the B. subtilis chromosome, a region also containing the hyperprotease-producing hpr gene. In vitro the sprE gene is transcribed by the minor form of RNA polymerase containing a 37,000-dalton sigma factor (sigma 37). We show by S1 nuclease mapping that sprE transcription initiates at dual start sites both in vitro and in vivo and that the promoter for the downstream site has a characteristic sigma 37 recognition sequence. We propose that the physiological role of the sigma 37 RNA polymerase is to transcribe a class of genes that are catabolite repressed, that encode extracellular enzymes, or that are expressed only during the stationary phase of growth.

摘要

一个仅在稳定生长期表达的克隆枯草芽孢杆菌基因(sprE)被证明编码枯草杆菌蛋白酶E,一种与芽孢形成相关的酶。我们已经确定了sprE启动子区域和结构基因近端一半的DNA序列。sprE基因编码一个推测的29个氨基酸残基的信号肽和成熟枯草杆菌蛋白酶序列之前的一个77个氨基酸残基的前导肽。通过质粒整合和噬菌体PBS1转导,我们已将sprE基因座定位在枯草芽孢杆菌染色体上的glyB和metD之间,该区域还包含产生高蛋白酶的hpr基因。在体外,sprE基因由含有37000道尔顿σ因子(σ37)的RNA聚合酶的次要形式转录。我们通过S1核酸酶图谱分析表明,sprE转录在体外和体内均起始于双重起始位点,并且下游位点的启动子具有特征性的σ37识别序列。我们提出,σ37 RNA聚合酶的生理作用是转录一类受分解代谢物阻遏、编码细胞外酶或仅在生长稳定期表达的基因。

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