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在邻苯二甲酸双加氧酶还原形式与氧气反应过程中邻苯二甲酸催化转化为其顺式二氢二醇的化学过程。

Chemistry of the catalytic conversion of phthalate into its cis-dihydrodiol during the reaction of oxygen with the reduced form of phthalate dioxygenase.

作者信息

Tarasev Michael, Ballou David P

机构信息

Department of Biological Chemistry, University of Michigan, 1301 Catherine Street, Ann Arbor, Michigan 48109-0606, USA.

出版信息

Biochemistry. 2005 Apr 26;44(16):6197-207. doi: 10.1021/bi047724y.

Abstract

The phthalate dioxygenase system, a Rieske non-heme iron dioxygenase, catalyzes the dihydroxylation of phthalate to form the 4,5-dihydro-cis-dihydrodiol of phthalate (DHD). It has two components: phthalate dioxygenase (PDO), a multimer with one Rieske-type [2Fe-2S] and one mononuclear Fe(II) center per monomer, and a reductase (PDR) that contains flavin mononucleotide (FMN) and a plant-type ferredoxin [2Fe-2S] center. This work shows that product formation in steady-state reactions is tightly coupled to electron delivery, with 1 dihydrodiol (DHD) of phthalate formed for every 2 electrons delivered from NADH. However, in reactions of reduced PDO with O(2), only about 0.5 DHD is formed per Rieske center that becomes oxidized. Although the product forms rapidly, its release from PDO is slow in these reactions with oxygen that do not include reductase and NADH. EPR data show that, at the completion of the oxidation, iron in the mononuclear center remains in the ferrous state. In contrast, naphthalene dioxygenase (NDO) [Wolfe, M. D., Parales, J. V., Gibson, D. T., and Lipscomb, J. D. (2001) J. Biol. Chem. 276, 1945-1953] and benzoate dioxygenase (BZDO) [Wolfe, M. D., Altier, D. J., Stubna, A., Popescu, C. V., Munck, E., and Lipscomb, J. D. (2002) Biochemistry, 41, 9611-9626], related Rieske non-heme iron dioxygenases, form 1 DHD per Rieske center oxidized, and the mononuclear center iron ends up ferric. Thus, both electrons from reduced NDO and BZDO monomers are used to form the product, whereas only the reduced Rieske centers in PDO become oxidized during production of DHD. This emphasizes the importance of PDO subunit interaction in catalysis. Electron redistribution was practically unaffected by the presence of oxidized PDR. A scheme is presented that emphasizes some of the differences in the mechanisms involved in substrate hydroxylation employed by PDO and either NDO or BZDO.

摘要

邻苯二甲酸双加氧酶系统是一种 Rieske 非血红素铁双加氧酶,催化邻苯二甲酸的二羟基化反应,形成邻苯二甲酸的 4,5 - 二氢 - 顺式 - 二氢二醇(DHD)。它有两个组分:邻苯二甲酸双加氧酶(PDO),每个单体含有一个 Rieske 型[2Fe - 2S]和一个单核 Fe(II)中心的多聚体,以及一种还原酶(PDR),其含有黄素单核苷酸(FMN)和一个植物型铁氧化还原蛋白[2Fe - 2S]中心。这项工作表明,稳态反应中的产物形成与电子传递紧密偶联,从 NADH 传递的每 2 个电子形成 1 个邻苯二甲酸二氢二醇(DHD)。然而,在还原态的 PDO 与 O₂ 的反应中,每个被氧化的 Rieske 中心仅形成约 0.5 个 DHD。尽管产物形成迅速,但在这些不包括还原酶和 NADH 的与氧气的反应中,其从 PDO 的释放缓慢。电子顺磁共振(EPR)数据表明,氧化完成时,单核中心的铁仍处于亚铁状态。相比之下,萘双加氧酶(NDO)[Wolfe, M. D., Parales, J. V., Gibson, D. T., and Lipscomb, J. D. (2001) J. Biol. Chem. 276, 1945 - 1953]和苯甲酸双加氧酶(BZDO)[Wolfe, M. D., Altier, D. J., Stubna, A., Popescu, C. V., Munck, E., and Lipscomb, J. D. (2002) Biochemistry, 41, 9611 - 9626],相关的 Rieske 非血红素铁双加氧酶,每个被氧化的 Rieske 中心形成 1 个 DHD,且单核中心的铁最终为三价铁。因此,来自还原态 NDO 和 BZDO 单体的两个电子都用于形成产物,而在 DHD 产生过程中只有 PDO 中被还原的 Rieske 中心被氧化。这强调了 PDO 亚基相互作用在催化中的重要性。电子重新分布实际上不受氧化态 PDR 存在的影响。本文提出了一个方案,强调了 PDO 与 NDO 或 BZDO 在底物羟基化机制上的一些差异。

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