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黄酮类生物合成中三种依赖2-氧代戊二酸的加氧酶的机制研究:花青素合酶、黄酮醇合酶和黄烷酮3β-羟化酶。

Mechanistic studies on three 2-oxoglutarate-dependent oxygenases of flavonoid biosynthesis: anthocyanidin synthase, flavonol synthase, and flavanone 3beta-hydroxylase.

作者信息

Turnbull Jonathan J, Nakajima Jun-Ichiro, Welford Richard W D, Yamazaki Mami, Saito Kazuki, Schofield Christopher J

机构信息

The Dyson Perrins Laboratory and The Oxford Centre for Molecular Sciences, South Parks Road, Oxford OX1 3QY, United Kingdom.

出版信息

J Biol Chem. 2004 Jan 9;279(2):1206-16. doi: 10.1074/jbc.M309228200. Epub 2003 Oct 21.

Abstract

Anthocyanidin synthase (ANS), flavonol synthase (FLS), and flavanone 3beta-hydroxylase (FHT) are involved in the biosynthesis of flavonoids in plants and are all members of the family of 2-oxoglutarate- and ferrous iron-dependent oxygenases. ANS, FLS, and FHT are closely related by sequence and catalyze oxidation of the flavonoid "C ring"; they have been shown to have overlapping substrate and product selectivities. In the initial steps of catalysis, 2-oxoglutarate and dioxygen are thought to react at the ferrous iron center producing succinate, carbon dioxide, and a reactive ferryl intermediate, the latter of which can then affect oxidation of the flavonoid substrate. Here we describe work on ANS, FLS, and FHT utilizing several different substrates carried out in 18O2/16OH2, 16O2/18OH2, and 18O2/18OH2 atmospheres. In the 18O2/16OH2 atmosphere close to complete incorporation of a single 18O label was observed in the dihydroflavonol products (e.g. (2R,3R)-trans-dihydrokaempferol) from incubations of flavanones (e.g. (2S)naringenin) with FHT, ANS, and FLS. This and other evidence supports the intermediacy of a reactive oxidizing species, the oxygen of which does not exchange with that of water. In the case of products formed by oxidation of flavonoid substrates with a C-3 hydroxyl group (e.g. (2R,3R)-trans-dihydroquercetin), the results imply that oxygen exchange can occur at a stage subsequent to initial oxidation of the C-ring, probably via an enzyme-bound C-3 ketone/3,3-gem-diol intermediate.

摘要

花青素合酶(ANS)、黄酮醇合酶(FLS)和黄烷酮3β-羟化酶(FHT)参与植物类黄酮的生物合成,它们均属于2-氧代戊二酸和亚铁离子依赖性加氧酶家族。ANS、FLS和FHT在序列上密切相关,并催化类黄酮“C环”的氧化;已证明它们具有重叠的底物和产物选择性。在催化的初始步骤中,2-氧代戊二酸和双加氧被认为在亚铁离子中心发生反应,生成琥珀酸、二氧化碳和一种活性铁氧中间体,后者随后可影响类黄酮底物的氧化。在此,我们描述了在18O2/16OH2、16O2/18OH2和18O2/18OH2气氛中利用几种不同底物对ANS、FLS和FHT进行的研究。在18O2/16OH2气氛中,观察到黄烷酮(如(2S)柚皮素)与FHT、ANS和FLS孵育产生的二氢黄酮醇产物(如(2R,3R)-反式二氢山奈酚)中几乎完全掺入了单个18O标记。这一证据以及其他证据支持了一种活性氧化物种的中间体的存在,其氧不与水的氧交换。对于由具有C-3羟基的类黄酮底物氧化形成的产物(如(2R,3R)-反式二氢槲皮素),结果表明氧交换可能发生在C环初始氧化后的一个阶段,可能是通过酶结合的C-3酮/3,3-偕二醇中间体。

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