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枯草芽孢杆菌spo0B基因的核苷酸序列及其表达调控

Nucleotide sequence of the spo0B gene of Bacillus subtilis and regulation of its expression.

作者信息

Bouvier J, Stragier P, Bonamy C, Szulmajster J

出版信息

Proc Natl Acad Sci U S A. 1984 Nov;81(22):7012-6. doi: 10.1073/pnas.81.22.7012.

Abstract

The spo0B gene is one of the genes involved in initiation of sporulation of Bacillus subtilis. This gene, previously cloned into the pHV33 shuttle vector, is expressed in Escherichia coli and B. subtilis. We have determined the sequence of 1118 base pairs (bp) of the DNA insert carrying the spo0B gene. The promoter sequence of this gene shows the canonical T-A-T-A-A-T region at 10 bp from the transcriptional start (-10 region) but an unusual sequence, T-T-T-T-C-T-, in the -35 region. The nucleotide sequence shows an open reading frame encoding a 192-amino-acid polypeptide of Mr 22,542, which is close to the molecular weight of the spo0B product synthesized in E. coli minicells. To investigate the regulation of the spo0B gene under a variety of physiological conditions, we constructed an in-frame fusion between the spo0B promoter proximal region and the lacZ gene of E. coli. This hybrid gene was subsequently integrated into the B. subtilis chromosome, and the beta-galactosidase activity was measured. It was found that the spo0B gene is preferentially expressed during exponential growth; it is not induced by exhaustion of the growth medium nor repressed by glucose.

摘要

spo0B基因是参与枯草芽孢杆菌芽孢形成起始过程的基因之一。该基因先前已克隆到pHV33穿梭载体中,可在大肠杆菌和枯草芽孢杆菌中表达。我们测定了携带spo0B基因的DNA插入片段的1118个碱基对(bp)的序列。该基因的启动子序列在转录起始点(-10区)上游10 bp处显示出典型的T-A-T-A-A-T区域,但在-35区有一个不寻常的序列T-T-T-T-C-T-。核苷酸序列显示一个开放阅读框,编码一个192个氨基酸的多肽,分子量为22,542,这与在大肠杆菌小细胞中合成的spo0B产物的分子量相近。为了研究spo0B基因在各种生理条件下的调控,我们构建了spo0B启动子近端区域与大肠杆菌lacZ基因的读码框内融合体。随后将这个杂种基因整合到枯草芽孢杆菌染色体中,并测定了β-半乳糖苷酶活性。结果发现,spo0B基因在指数生长期优先表达;它不受生长培养基耗尽的诱导,也不受葡萄糖的抑制。

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