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枯草芽孢杆菌中鞭毛蛋白基因转录与鞭毛组装的偶联

Coupling of flagellin gene transcription to flagellar assembly in Bacillus subtilis.

作者信息

Barilla D, Caramori T, Galizzi A

机构信息

Dipartimento di Genetica e Microbiologia A. Buzzati-Traverso, Università degli Studi di Pavia, Italy.

出版信息

J Bacteriol. 1994 Aug;176(15):4558-64. doi: 10.1128/jb.176.15.4558-4564.1994.

Abstract

The regulation of flagellin gene expression in Bacillus subtilis was examined in vivo by means of a lacZ translational fusion to the flagellin structural gene (hag). We have tested the effects of two known mutations (flaA4 and flaA15) in the major flagellar operon and of three deletions. One deletion was in frame in the fliI cistron, one was out of frame in the fliK cistron, and the last spanned about 21 kb of the flaA operon. In all instances, the expression of the flagellin gene was defective. Flagellin gene expression was restored in the strain with the 21-kb deletion by overexpression of the sigD gene under control of the isopropyl-beta-D-thiogalactopyranoside (IPTG)-inducible spac promoter. These results indicate that transcription of the flagellin gene is dependent on the formation of the flagellar basal body but that such a requirement can be bypassed by overexpression of sigD. Lack of expression of hag was observed in the presence of flaD1, flaD2, and delta sin mutations as well.

摘要

通过将lacZ翻译融合到鞭毛蛋白结构基因(hag),在体内研究了枯草芽孢杆菌中鞭毛蛋白基因表达的调控。我们测试了主要鞭毛操纵子中两个已知突变(flaA4和flaA15)以及三个缺失的影响。一个缺失在fliI顺反子内符合读码框,一个在fliK顺反子内不符合读码框,最后一个跨越flaA操纵子约21 kb。在所有情况下,鞭毛蛋白基因的表达均有缺陷。在异丙基-β-D-硫代半乳糖苷(IPTG)诱导的spac启动子控制下,通过sigD基因的过表达,在具有21 kb缺失的菌株中恢复了鞭毛蛋白基因的表达。这些结果表明,鞭毛蛋白基因的转录依赖于鞭毛基体的形成,但这种需求可以通过sigD的过表达来绕过。在存在flaD1、flaD2和δsin突变的情况下,也观察到hag表达缺失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad36/196275/900cb194234a/jbacter00033-0106-a.jpg

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