Nikol'skaia I I, Lopatina N G, Rekunova V N, Iurkevich A M, Debov S S
Vopr Med Khim. 1978 Mar-Apr;24(2):252-5.
It was studied effect of S-adenosyl, -uridyl, -citidyl and -inosyl homocysteines on activity of bacterial adenine and cytosine methylases from E. coli CK as well as on guanine methylase specific for DDVI phage. S-adenosyl homocysteine was shown to be the strong inhibitor of methylation; 10 micrometer of the substance inhibited all the enzymes studied by 98--99%. Use of total enzymatic preparations did not enable to find a difference in affinity of S-uridyl, -citidyl, and -inosyl homocysteines to various DNA methylases studied. All these preparations inhibited DNA methylases by 55--65%. Increase in concentration of inhibitor up to 20 micrometer did not elevate the inhibitory effect. Action of S-nucleosyl homocysteines did not depend on the type of acceptory DNA.
研究了S-腺苷同型半胱氨酸、S-尿苷同型半胱氨酸、S-胞苷同型半胱氨酸和S-肌苷同型半胱氨酸对大肠杆菌CK细菌腺嘌呤和胞嘧啶甲基化酶活性以及对DDVI噬菌体特异性鸟嘌呤甲基化酶活性的影响。结果表明,S-腺苷同型半胱氨酸是甲基化的强抑制剂;10微摩尔该物质可使所研究的所有酶的活性受到98%-99%的抑制。使用全酶制剂未能发现S-尿苷同型半胱氨酸、S-胞苷同型半胱氨酸和S-肌苷同型半胱氨酸对所研究的各种DNA甲基化酶的亲和力存在差异。所有这些制剂均可使DNA甲基化酶的活性受到55%-65%的抑制。将抑制剂浓度增加至20微摩尔并不会增强抑制作用。S-核苷同型半胱氨酸的作用不依赖于受体DNA的类型。