Jouve H, Jouve H, Melgar E, Lizárraga B
J Biol Chem. 1975 Sep 10;250(17):6631-5.
EPR studies of Mn2+ binding to bovine pancreatic deoxyribonuclease I show that the enzyme can bind three Mn2+ ions at pH 7.5 and 2 degrees. Two sites bind Mn2+ strongly, with a Kd of 10(-4)M, and the third binds Mn2+ weakly, with a Kd of 10(-3)M. Ca2+ competes with the two strong sites, whereas Mg2+ competes only with one of them, indicating that both sites are not equivalent. Mn2+ binding to DNA has been confirmed by EPR measurements. Two types of sites, with different affinities for Mn2+ binding, were found on DNA molecules, one with a Kd of 1.2 times 10(-4)M and the other with a Kd of 10(-3)M. Mg2+ ions can displace Mn2+ from the high affinity sites, but not from the low affinity sites. These results suggest the Mn2+ binds not only to the phosphate groups, but also to the electron donor groups of the base rings.
对锰离子(Mn2+)与牛胰脱氧核糖核酸酶I结合的电子顺磁共振(EPR)研究表明,在pH值为7.5和2摄氏度的条件下,该酶可结合三个Mn2+离子。其中两个位点与Mn2+紧密结合,解离常数(Kd)为10^(-4)M,第三个位点与Mn2+结合较弱,Kd为10^(-3)M。钙离子(Ca2+)与两个紧密结合位点竞争,而镁离子(Mg2+)仅与其中一个竞争,这表明这两个位点并不等同。通过EPR测量已证实Mn2+与DNA结合。在DNA分子上发现了两种对Mn2+结合具有不同亲和力的位点,一种Kd为1.2×10^(-4)M,另一种Kd为10^(-3)M。镁离子可从高亲和力位点取代Mn2+,但不能从低亲和力位点取代。这些结果表明,Mn2+不仅与磷酸基团结合,还与碱基环的电子供体基团结合。