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首页> 外文期刊>Molecular Microbiology >The A-factor regulatory cascade leading to streptomycin biosynthesis in Streptomyces griseus : identification of a target gene of the A-factor receptor.
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The A-factor regulatory cascade leading to streptomycin biosynthesis in Streptomyces griseus : identification of a target gene of the A-factor receptor.

机译:A因子调节级联导致灰链霉菌中链霉素的生物合成:鉴定A因子受体的靶基因。

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In Streptomyces griseus, A-factor (2-isocapryloyl-3R-hydroxymethyl-gamma-butyrolactone) at an extremely low concentration triggers streptomycin biosynthesis and cell differentiation by binding a repressor-type receptor protein (ArpA) and dissociating it from DNA. An A-factor-responsive transcriptional activator (AdpA) able to bind the promoter of strR, a pathway-specific regulatory gene responsible for transcription of other streptomycin biosynthetic genes, was purified to homogeneity and adpA was cloned by PCR on the basis of amino acid sequences of purified AdpA. adpA encoding a 405-amino-acid protein containing a helix-turn-helix DNA-binding motif at the central region showed sequence similarity to transcriptional regulators in the AraC/XylS family. The -35 and -10 regions of the adpA promoter were found to be a target of ArpA; ArpA bound the promoter region in the absence of A-factor and exogenous addition of A-factor to the DNA-ArpA complex immediately released ArpA from the DNA. Consistent with this, S1 nuclease mapping showed that adpA was transcribed only in the presence of A-factor and strR was transcribed only in the presence of intact adpA. Furthermore, adpA disruptants produced no streptomycin and overexpression of adpA caused the wild-type S. griseus strain to produce streptomycin at an earlier growth stage in a larger amount. On the basis of these findings, we propose here a model to demonstrate how A-factor triggers streptomycin biosynthesis at a late exponential growth stage.
机译:在灰色链霉菌中,浓度极低的A因子(2-异辛酰基-3R-羟甲基-γ-丁内酯)通过结合阻遏物受体蛋白(ArpA)并将其与DNA分离,触发链霉素的生物合成和细胞分化。能够结合strR启动子的A因子响应转录激活剂(AdpA),strR是负责其他链霉素生物合成基因转录的途径特异性调控基因,被纯化至同质,并通过PCR在氨基酸的基础上克隆出adpA纯化的AdpA的序列。 adpA编码一个405个氨基酸的蛋白质,在中央区域包含一个螺旋-转-螺旋-DNA结合基序,与AraC / XylS家族的转录调节因子具有相似的序列。发现adpA启动子的-35和-10区域是ArpA的靶标; ArpA在不存在A因子的情况下结合启动子区域,并且向DNA-ArpA复合物中外源添加A因子会立即从DNA释放ArpA。与此相一致,S1核酸酶作图显示仅在A因子存在下转录adpA,而仅在完整adpA存在下转录strR。此外,adpA破坏剂不产生链霉素,并且adpA的过表达引起野生型灰葡萄链球菌菌株在更早的生长阶段大量产生链霉素。根据这些发现,我们在这里提出一个模型来证明A因子如何在指数增长后期触发链霉素的生物合成。

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