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枯草芽孢杆菌芽孢形成基因座spoIIIC的转录调控与结构

Transcriptional regulation and structure of the Bacillus subtilis sporulation locus spoIIIC.

作者信息

Errington J, Rong S, Rosenkrantz M S, Sonenshein A L

机构信息

Department of Biochemistry, University of Oxford, United Kingdom.

出版信息

J Bacteriol. 1988 Mar;170(3):1162-7. doi: 10.1128/jb.170.3.1162-1167.1988.

Abstract

The spoIIIC locus of Bacillus subtilis has been cloned from the lambda library of Ferrari et al. (E. Ferrari, D. J. HEnner, and J. A. Hoch, J. Bacteriol. 146:430-432, 1981) by using as an assay transformation of the mutant allele spoIIIC94 to the wild type. Regulation of the spoIIIC locus was studied by hybridization of cloned spoIIIC DNA to RNA pulse-labeled at various times during growth and sporulation. The relative rate of transcription of the spoIIIC locus was highest 3 h after the end of growth. The DNA sequence of the spoIIIC transcription unit indicated the coding capacity for a small protein (138 amino acids) having significant similarity with one domain of RNA polymerase sigma factors. Interruption of this coding sequence by an insertion mutation caused cells to become Spo-.

摘要

通过将突变等位基因spoIIIC94转化为野生型作为一种检测方法,从法拉利等人(E. Ferrari、D. J. HEnner和J. A. Hoch,《细菌学杂志》146:430 - 432,1981年)的λ文库中克隆出了枯草芽孢杆菌的spoIIIC基因座。通过将克隆的spoIIIC DNA与在生长和芽孢形成过程中不同时间进行脉冲标记的RNA杂交,研究了spoIIIC基因座的调控。spoIIIC基因座的相对转录速率在生长结束后3小时最高。spoIIIC转录单元的DNA序列表明其编码一种小蛋白(138个氨基酸)的能力,该蛋白与RNA聚合酶σ因子的一个结构域具有显著相似性。插入突变打断该编码序列会导致细胞变为Spo- 。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae50/210887/cfc4a3feee57/jbacter00181-0147-a.jpg

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