Consensus DNA site for theEscherichia colicatabolite gene activator protein (CAP): CAP exhibits a 450-fold higher affinity for the consensus DNA site than for theE.coli lacDNA site

Abstract

We have synthesized two 40 base pair DNA fragments; one fragments contains the consensus DNA site for CAP (fragment ''ICP''); 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.