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酪氨酸酶酪氨酸羟化酶和多巴氧化酶活性的新检测方法。

New assays for the tyrosine hydroxylase and dopa oxidase activities of tyrosinase.

作者信息

Winder A J, Harris H

机构信息

Sir William Dunn School of Pathology, University of Oxford, England.

出版信息

Eur J Biochem. 1991 Jun 1;198(2):317-26. doi: 10.1111/j.1432-1033.1991.tb16018.x.

Abstract

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.

摘要

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。

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