血色素,酪氨酸酶的另一种底物。

IF 2.1 4区 医学 Q3 CHEMISTRY, MEDICINAL Planta medica Pub Date : 2024-10-01 Epub Date: 2024-08-19 DOI:10.1055/a-2381-5201
Chantalle Crous, Ivanke A Swart, Judey Pretorius, Frank van der Kooy, Jacobus P Petzer, Anél Petzer
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引用次数: 0

摘要

来自双孢蘑菇的蘑菇酪氨酸酶(abTYR)经常被用于开发药用和化妆品用途的酪氨酸酶抑制剂。在寻找新型酪氨酸酶抑制剂的过程中,本研究发现苏木精可作为 abTYR 的替代底物。研究人员通过分光光度法和色谱法分析了苏木精与 abTYR 的相互作用。结果表明,苏木精作为 abTYR 底物,在浓度低于 1.25 mM 时表现出 Michaelis-Menten 动力学行为。就 Km 而言,苏木精的底物特性与天然酪氨酸酶底物 L-3,4-二羟基苯丙氨酸(L-DOPA)相似,而 Vmax 则低八倍。经鉴定,abTYR 与苏木精反应过程中形成的主要氧化产物为血色素。这是首次报道苏木精与 abTYR 的相互作用。
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Hematoxylin, an Alternative Substrate of Tyrosinase.

Mushroom tyrosinase from Agaricus bisporus (abTYR) is often used during the development of tyrosinase inhibitors for medicinal and cosmetic purposes. In the search for novel tyrosinase inhibitors, this study identified hematoxylin as an alternative substrate for abTYR. The interaction of hematoxylin with abTYR was investigated through spectrophotometric and chromatographic analyses. The results showed that hematoxylin acted as an abTYR substrate and exhibited Michaelis-Menten kinetic behaviour at concentrations below 1.25 mM. The substrate properties of hematoxylin were similar to the natural tyrosinase substrate, L-3,4-dihydroxyphenylalanine (L-DOPA), with regards to Km, while Vmax was eightfold lower. The main oxidation product formed during the reaction of abTYR with hematoxylin was identified as hematein. This is the first report of the interaction of hematoxylin with abTYR.

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来源期刊
Planta medica
Planta medica 医学-药学
CiteScore
5.10
自引率
3.70%
发文量
101
审稿时长
1.8 months
期刊介绍: Planta Medica is one of the leading international journals in the field of natural products – including marine organisms, fungi as well as micro-organisms – and medicinal plants. Planta Medica accepts original research papers, reviews, minireviews and perspectives from researchers worldwide. The journal publishes 18 issues per year. The following areas of medicinal plants and natural product research are covered: -Biological and Pharmacological Activities -Natural Product Chemistry & Analytical Studies -Pharmacokinetic Investigations -Formulation and Delivery Systems of Natural Products. The journal explicitly encourages the submission of chemically characterized extracts.
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