Kaiser I I, Kladianos D M, Van Kirk E A, Haley B E
J Biol Chem. 1983 Feb 10;258(3):1747-51.
An in vitro system using an enzyme extract containing ATP:L-methionine S-adenosyltransferase from Escherichia coli MRE 600 cells was used to synthesize 8-azido-S-adenosyl-L-methionine from methionine and 8-azidoadenosine 5'-triphosphate. In the absence of ultraviolet light and analog can serve as a methyl donor for porcine catechol O-methyltransferase. Photolysis of 8-azido-S-adenosyl[35S]methionine in the presence of catechol O-methyltransferase results in covalent incorporation. Addition of either authentic S-adenosylmethionine or S-adenosylhomocysteine, but not adenosine 5'-monophosphate, to the photolysis reaction mixture eliminates the photoincorporation. These results indicate that the incorporation is occurring at the S-adenosylmethionine binding site in the catechol O-methyltransferase.
利用一种含有来自大肠杆菌MRE 600细胞的ATP:L-甲硫氨酸S-腺苷转移酶的酶提取物的体外系统,从甲硫氨酸和8-叠氮腺苷5'-三磷酸合成8-叠氮-S-腺苷-L-甲硫氨酸。在没有紫外线的情况下,该类似物可作为猪儿茶酚O-甲基转移酶的甲基供体。在儿茶酚O-甲基转移酶存在下对8-叠氮-S-腺苷[35S]甲硫氨酸进行光解会导致共价掺入。向光解反应混合物中添加 authentic S-腺苷甲硫氨酸或S-腺苷高半胱氨酸,但不添加5'-单磷酸腺苷,可消除光掺入。这些结果表明掺入发生在儿茶酚O-甲基转移酶的S-腺苷甲硫氨酸结合位点。