Winder A J, Harris H
Sir William Dunn School of Pathology, University of Oxford, England.
Eur J Biochem. 1991 Jun 1;198(2):317-26. doi: 10.1111/j.1432-1033.1991.tb16018.x.
New assays for the tyrosine hydroxylase and dopa oxidase activities of tyrosinase (EC 1.14.18.1) have been developed. The tyrosine hydroxylase assay uses L-[carboxy-14C]tyrosine as the substrate, 14CO2 is released from the products of the hydroxylation and further metabolism of L-[carboxy-14C]tyrosine by incubation with ferricyanide, and measured radiometrically. D-Dopa is a preferable cofactor to L-dopa for the assay. Dopa oxidase activity is measured spectrophotometrically. Dopaquinone, produced on the oxidation of L-dopa, reacts with Besthorn's hydrazone (3-methyl-2-benzothiazolinone hydrazone) to form a pink pigment with an absorbance maximum at 505 nm. Details of the optimisation of conditions for the assays and their specificities for the two enzyme activities are described.
已开发出用于酪氨酸酶(EC 1.14.18.1)酪氨酸羟化酶和多巴氧化酶活性的新测定方法。酪氨酸羟化酶测定法以L-[羧基-¹⁴C]酪氨酸为底物,通过与铁氰化物孵育,¹⁴CO₂从L-[羧基-¹⁴C]酪氨酸羟基化及进一步代谢的产物中释放出来,并通过放射性测量法进行测定。对于该测定,D-多巴是比L-多巴更合适的辅助因子。多巴氧化酶活性通过分光光度法进行测定。L-多巴氧化产生的多巴醌与贝斯索恩腙(3-甲基-2-苯并噻唑啉酮腙)反应形成一种粉红色色素,其最大吸光度在505 nm处。描述了测定条件优化的细节及其对两种酶活性的特异性。