Angermüller S, Löffler M
Department of Anatomy and Cell Biology II, University of Heidelberg, Germany.
Histochem Cell Biol. 1995 Apr;103(4):287-92. doi: 10.1007/BF01457413.
Biochemical studies have demonstrated that dihydroorotate dehydrogenase (DHOdehase; EC 1.3.3.1 or 1.3.99.11) is the sole enzyme of de novo pyrimidine synthesis in mitochondria, whereas the rest of the pathway takes place in the cytosol. The dehydrogenation of dihydroorotate to orotate is linked to the respiratory chain via ubiquinone. In this study, we show for the first time the ultrastructural localization of DHOdehase. Since the purified enzyme was found to act both as dehydrogenase and as oxidase, the cerium capture technique for detecting enzymatically generated hydrogen peroxide could be applied to pin-point the in situ activity of DHOdehase oxidase in mitochondria of rat heart and kidney cortex. Cerium perhydroxide as the final reaction product was detected predominantly in the matrix with some focal condensation along the inner membrane, but not in the intermembrane space. From this pattern of localization, it is concluded that the active site of the membrane-bound enzyme could face the mitochondrial matrix similar to succinate dehydrogenase. The reliability of the applied method for the demonstration of DHOdehase oxidase was demonstrated by the addition of Brequinar sodium to the incubation medium. This quinoline-carboxylic acid derivative is a potent inhibitor of DHOdehase and has proven anti-proliferative activity. The present observations do not ascertain whether the oxidase is permanently active as a constant portion of the enzyme in vivo, similar to xanthine oxidase/dehydrogenase. However, DHOdehase should be considered as a source of radical oxygen species under pathophysiological conditions.
生化研究表明,二氢乳清酸脱氢酶(DHOdehase;EC 1.3.3.1或1.3.99.11)是线粒体中从头合成嘧啶的唯一酶,而该途径的其余部分发生在细胞质中。二氢乳清酸脱氢生成乳清酸的过程通过泛醌与呼吸链相连。在本研究中,我们首次展示了DHOdehase的超微结构定位。由于发现纯化后的该酶兼具脱氢酶和氧化酶的功能,因此可应用检测酶促产生过氧化氢的铈捕获技术来精确确定大鼠心脏和肾皮质线粒体中DHOdehase氧化酶的原位活性。作为最终反应产物的过氢氧化铈主要在基质中检测到,沿内膜有一些局灶性聚集,但在膜间隙中未检测到。根据这种定位模式,可以得出结论,膜结合酶的活性位点可能与琥珀酸脱氢酶类似,面向线粒体基质。通过在孵育培养基中添加布喹那钠,证明了用于展示DHOdehase氧化酶的方法的可靠性。这种喹啉羧酸衍生物是DHOdehase的有效抑制剂,并已证明具有抗增殖活性。目前的观察结果并未确定该氧化酶在体内是否像黄嘌呤氧化酶/脱氢酶一样作为酶的恒定部分永久具有活性。然而,在病理生理条件下,DHOdehase应被视为活性氧的来源。