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变形链球菌中羊毛硫抗生素变链菌素II生物合成基因座中启动子的功能分析。

Functional analyses of the promoters in the lantibiotic mutacin II biosynthetic locus in Streptococcus mutans.

作者信息

Qi F, Chen P, Caufield P W

机构信息

Department of Oral Biology, School of Dentistry, University of Alabama at Birmingham, Birmingham, Alabama 35294, USA.

出版信息

Appl Environ Microbiol. 1999 Feb;65(2):652-8. doi: 10.1128/AEM.65.2.652-658.1999.

Abstract

The lantibiotic bacteriocin mutacin II is produced by the group II Streptococcus mutans. The mutacin II biosynthetic locus consists of seven genes, mutR, -A, -M, -T, -F, -E, and -G, organized as two operons. The mutAMTFEG operon is transcribed from the mutA promoter 55 bp upstream of the translation start codon for MutA, while the mutR promoter is 76 bp upstream of the mutR structural gene. Expression of the mutA promoter is regulated by the components of the growth medium, while the mutR promoter activity does not seem to be affected by these conditions. Inactivation of mutR abolishes transcription of the mutA operon but does not affect its own promoter activity. The expressions of both mutA and mutR promoters are independent of the growth stage, while the production of mutacin II is only elevated at the early stationary phase. Taken together, these results suggest that expression of the mutacin operon is regulated by a complex system involving transcriptional and posttranscriptional or posttranslational controls.

摘要

羊毛硫抗生素细菌素变链菌素II由II组变形链球菌产生。变链菌素II生物合成基因座由七个基因mutR、-A、-M、-T、-F、-E和-G组成,它们被组织成两个操纵子。mutAMTFEG操纵子从MutA翻译起始密码子上游55 bp处的mutA启动子转录,而mutR启动子在mutR结构基因上游76 bp处。mutA启动子的表达受生长培养基成分的调节,而mutR启动子活性似乎不受这些条件的影响。mutR的失活消除了mutA操纵子的转录,但不影响其自身的启动子活性。mutA和mutR启动子的表达均与生长阶段无关,而变链菌素II的产生仅在稳定期早期升高。综上所述,这些结果表明变链菌素操纵子的表达受一个复杂系统的调节,该系统涉及转录、转录后或翻译后控制。

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