Retzlaff L, Distler J
Institut für Chemische Mikrobiologie, Bergische Universität GH Wuppertal, Germany.
Mol Microbiol. 1995 Oct;18(1):151-62. doi: 10.1111/j.1365-2958.1995.mmi_18010151.x.
In Streptomyces griseus the expression of at least one streptomycin biosynthetic gene, strB1, is dependent on the pathway-specific activator protein StrR. We show here that StrR is a DNA-binding protein which specifically interacts with the strB1 promoter fragment. Footprinting experiments demonstrate that the StrR protein binds to an inverted repeat located upstream of the strB1 promoter. Further StrR-binding sites having the consensus sequence GTTCGActG(N)11CagTcGAAc were identified in the str-sts gene clusters of S. griseus and Streptomyces glaucescens by sequence comparison, gel retardation, and footprinting studies. The genetic and biochemical evidence strongly supports the model of the StrR protein activating the expression of streptomycin biosynthetic genes by interacting with multiple binding sites within the str-sts gene clusters of S. griseus and S. glaucescens.
在灰色链霉菌中,至少一个链霉素生物合成基因strB1的表达依赖于途径特异性激活蛋白StrR。我们在此表明,StrR是一种DNA结合蛋白,它与strB1启动子片段特异性相互作用。足迹实验表明,StrR蛋白与位于strB1启动子上游的一个反向重复序列结合。通过序列比较、凝胶阻滞和足迹研究,在灰色链霉菌和浅蓝链霉菌的str-sts基因簇中鉴定出具有一致序列GTTCGActG(N)11CagTcGAAc的其他StrR结合位点。遗传和生化证据有力地支持了StrR蛋白通过与灰色链霉菌和浅蓝链霉菌的str-sts基因簇内的多个结合位点相互作用来激活链霉素生物合成基因表达的模型。