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Mutations in PurBox1 of the Bacillus subtilis pur operon control site affect adenine-regulated expression in vivo

机译:枯草芽孢杆菌pur操纵子控制位点的PurBox1中的突变影响体内腺嘌呤调节的表达。

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摘要

Transcription of the Bacillus subtilis pur operon is regulated by a purine repressor (PurR)-DNA control site interaction. The pur operon control site has two PurBoxes that are required for high-affinity PurR binding. An upstream, strong-binding PurBox1 is at position -81 to -68 relative to the transcription start site and a downstream weak-binding PurBox2 is at position -49 to -36. We constructed three PurBox1 mutations and the effects on binding of PurR to the control region in vitro and on regulation of pur operon expression in vivo were investigated. The mutations significantly reduced the binding of PurR to control region DNA. In strains with G-75A, G-75T and a five bp deletion (Δ5) pur operon repression was defective in vivo. In addition in vivo PurR titration was used to confirm that sequences flanking PurBoxl and PurBox2 are required for PurR binding to the pur operon control site.
机译:枯草芽孢杆菌pur操纵子的转录受嘌呤阻遏物(PurR)-DNA控制位点相互作用的调节。 pur操纵子控制位点具有两个高亲和力的PurR结合所需的PurBox。相对于转录起始位点,上游强结合型PurBox1位于-81至-68位置,下游弱结合型PurBox2在-49至-36位置。我们构建了三个PurBox1突变,并研究了其对PurR与对照区域的结合以及体外对pur操纵子表达的调节的影响。突变显着降低了PurR与控制区DNA的结合。在具有G-75A的菌株中,G-75T和5 bp的缺失(Δ5)在体内嘌呤操纵子阻遏是有缺陷的。另外,体内PurR滴定用于证实PurBox1和PurBox2侧翼的序列是PurR与pur操纵子控制位点结合所必需的。

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