Gromova E S, Vinogradova M N, Uporova T M, Griaznova O I, Isaguliants M G
Bioorg Khim. 1987 Feb;13(2):269-72.
We studied the interaction of EcoRII and SsoII restriction endonucleases with synthetic DNA duplexes, containing 3'N----5'P and 3'P----5'N phosphoamide internucleotide bonds in one of the cleavage points. Enzymatic hydrolysis of the modified strand of the duplexes is blocked in all cases. The presence of phosphoamide bonds was found to reduce the rate of cleavage of the natural strand by EcoRII and to have no influence in case of SsoII. Properties of the EcoRII endonuclease complex with its substrate, containing non-cleavable 3'N----5'P internucleotide bonds in each cleavage point, were examined. In the presence of Mg2+ ions the equilibrium association constant of the enzyme-substrate complex is 3-fold reduced, and the dissociation rate constant of the complex is increased by 1.5 times.
我们研究了EcoRII和SsoII限制性内切酶与合成DNA双链体的相互作用,这些双链体在其中一个切割位点含有3'N→5'P和3'P→5'N磷酰胺核苷酸间键。在所有情况下,双链体修饰链的酶促水解均被阻断。发现磷酰胺键的存在会降低EcoRII对天然链的切割速率,而对SsoII则无影响。研究了EcoRII内切酶与其底物的复合物的性质,该底物在每个切割位点都含有不可切割的3'N→5'P核苷酸间键。在Mg2+离子存在下,酶-底物复合物的平衡缔合常数降低了3倍,复合物的解离速率常数增加了1.5倍。