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转录阻遏物LtnR对双组分羊毛硫抗生素lacticin 3147免疫性的调控。

Regulation of immunity to the two-component lantibiotic, lacticin 3147, by the transcriptional repressor LtnR.

作者信息

McAuliffe O, O'Keeffe T, Hill C, Ross R P

机构信息

Department of Microbiology and National Food Biotechnology Centre, University College Cork, Cork, Republic of Ireland.

出版信息

Mol Microbiol. 2001 Feb;39(4):982-93. doi: 10.1046/j.1365-2958.2001.02290.x.

Abstract

Lacticin 3147 is a membrane-active, two-component lantibiotic produced by Lactococcus lactis ssp. lactis DPC3147. In this study, the promoters of the lacticin 3147 gene cluster were mapped to the intergenic region between ltnR and ltnA1 (the genes encoding the regulatory protein LtnR and the first structural gene, LtnA1), and Northern analyses revealed that the biosynthetic and immunity genes are divergently transcribed in two operons, ltnA1A2M1TM2D and ltnRIFE respectively. Although the promoter controlling biosynthesis (Pbac) appears to be constitutive, characterization of a downstream beta-galactosidase (beta-gal) fusion beyond an intragenic stem-loop structure in ltnM1 confirmed that this putative transcriptional attenuator allows limited readthrough to the downstream biosynthetic genes, thus maintaining the correct stoichiometry between structural peptides and biosynthetic machinery. The promoter of the ltnRIFE operon (Pimm) was shown to be regulated by the transcriptional repressor LtnR. A mutant with a truncated ltnR gene exhibited a hyperimmune phenotype, whereas overexpression of ltnR resulted in cells with increased sensitivity to lacticin 3147. Gel mobility shift analysis indicated that LtnR binds to the Pimm promoter region, and fusion of this promoter to the beta-gal gene of pAK80 revealed that expression from Pimm is significantly reduced in the presence of LtnR. Thus, we have demonstrated that lacticin 3147 uses a regulatory mechanism not previously identified in lantibiotic systems.

摘要

Lacticin 3147是由乳酸乳球菌乳酸亚种DPC3147产生的一种具有膜活性的双组分羊毛硫抗生素。在本研究中,lacticin 3147基因簇的启动子被定位到ltnR和ltnA1(分别编码调控蛋白LtnR和第一个结构基因LtnA1的基因)之间的基因间区域,Northern分析表明生物合成基因和免疫基因分别在两个操纵子ltnA1A2M1TM2D和ltnRIFE中反向转录。尽管控制生物合成的启动子(Pbac)似乎是组成型的,但对ltnM1中基因内茎环结构下游的β-半乳糖苷酶(β-gal)融合体的表征证实,这种假定的转录衰减子允许有限的通读至下游生物合成基因,从而维持结构肽与生物合成机制之间的正确化学计量。ltnRIFE操纵子的启动子(Pimm)被证明受转录阻遏物LtnR调控。一个ltnR基因截短的突变体表现出超免疫表型,而ltnR的过表达导致细胞对lacticin 3147的敏感性增加。凝胶迁移率变动分析表明LtnR与Pimm启动子区域结合,并且该启动子与pAK80的β-gal基因融合表明在LtnR存在的情况下Pimm的表达显著降低。因此,我们证明了lacticin 3147使用了一种以前在羊毛硫抗生素系统中未发现的调控机制。

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