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Consensus DNA site for the Escherichia coli catabolite gene activator protein (CAP): CAP exhibits a 450-fold higher affinity for the consensus DNA site than for the E.coli lac DNA site

机译:大肠杆菌分解代谢物基因激活蛋白(CAP)的共有DNA位点:CAP对共有DNA位点的亲和力比对大肠杆菌lac DNA位点的亲和力高450倍

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We have synthesized two 40 base pair DNA fragments; one fragment contains the consensus DNA site for CAP (fragment ‘ICAP'); the other fragment contains the E. coli lac promoter DNA site for CAP (fragment ‘LCAP'). We have investigated the binding of CAP to the two DNA fragments using the nitrocellulose filter binding assay. Under standard conditions ([NaCl) = 200 mM, pH = 7.3), CAP exhibits a 450–fold higher affinity for ICAP than for LCAP. The salt dependence of the binding equilibrium indicates that CAP makes eight ion pairs with ICAP, but only six ion pairs with LCAP. Approximately half of the difference in binding free energy for interaction of CAP with ICAP vs. LCAP is attributable to this difference in ion-pair formation. The pH dependence of the binding equilibrium indicates that the eight CAP-ICAP ion pairs and the six CAP-LCAP ion pairs do not involve His residues of CAP.
机译:我们合成了两个40个碱基对的DNA片段。一个片段包含CAP的共有DNA位点(片段“ ICAP”);另一个片段包含CAP的大肠杆菌lac启动子DNA位点(片段“ LCAP”)。我们已经使用硝酸纤维素滤膜结合试验研究了CAP与两个DNA片段的结合。在标准条件下([NaCl] = 200 mM,pH = 7.3),CAP对ICAP的亲和力比对LCAP高450倍。结合平衡的盐依赖性表明,CAP与ICAP形成8个离子对,而LCAP仅形成6个离子对。用于CAP与ICAP和LCAP相互作用的结合自由能的差异的大约一半归因于离子对形成的差异。结合平衡的pH依赖性表明,八个CAP-ICAP离子对和六个CAP-LCAP离子对不涉及CAP的His残基。

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