Department of Chemistry and the Oxford Centre for Integrative Systems Biology, University of Oxford, Oxford, UK.
FEBS J. 2012 May;279(9):1563-75. doi: 10.1111/j.1742-4658.2012.08496.x. Epub 2012 Feb 20.
Ferrous iron and 2-oxoglutarate-dependent oxygenases and related enzymes catalyse a range of oxidative reactions, possibly the widest of any enzyme family. Their catalytic flexibility is proposed to be related to their nonhaem iron-binding site, which utilizes two or three protein-based ligands. A possible penalty for this flexibility is that they may be more prone to oxidative damage than the P450 oxidases, where the iron is arguably located in a more controlled environment. We review the evidence for autocatalysed oxidative modifications to 2-oxoglutarate-dependent oxygenases, including the recently reported studies on human enzymes, as well as the oxidative fragmentations observed in the case of the plant ethylene-forming enzyme (1-aminocyclopropane-1-carboxylic acid oxidase).
亚铁离子和 2-氧代戊二酸依赖性加氧酶及相关酶催化一系列氧化反应,可能是任何酶家族中最广泛的。它们的催化灵活性与其非血红素铁结合位点有关,该位点利用两个或三个基于蛋白质的配体。这种灵活性的一个可能代价是,与 P450 氧化酶相比,它们可能更容易受到氧化损伤,因为铁据称位于更受控制的环境中。我们回顾了对 2-氧代戊二酸依赖性加氧酶的自动催化氧化修饰的证据,包括最近关于人类酶的研究,以及在植物乙烯形成酶(1-氨基环丙烷-1-羧酸氧化酶)情况下观察到的氧化片段化。