Murray Leslie J, García-Serres Ricardo, McCormick Michael S, Davydov Roman, Naik Sunil G, Kim Sun-Hee, Hoffman Brian M, Huynh Boi Hanh, Lippard Stephen J
Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Biochemistry. 2007 Dec 25;46(51):14795-809. doi: 10.1021/bi7017128. Epub 2007 Nov 29.
At its carboxylate-bridged diiron active site, the hydroxylase component of toluene/o-xylene monooxygenase activates dioxygen for subsequent arene hydroxylation. In an I100W variant of this enzyme, we characterized the formation and decay of two species formed by addition of dioxygen to the reduced, diiron(II) state by rapid-freeze quench (RFQ) EPR, Mössbauer, and ENDOR spectroscopy. The dependence of the formation and decay rates of this mixed-valent transient on pH and the presence of phenol, propylene, or acetylene was investigated by double-mixing stopped-flow optical spectroscopy. Modification of the alpha-subunit of the hydroxylase after reaction of the reduced protein with dioxygen-saturated buffer was investigated by tryptic digestion coupled mass spectrometry. From these investigations, we conclude that (i) a diiron(III,IV)-W* transient, kinetically linked to a preceding diiron(III) intermediate, arises from the one-electron oxidation of W100, (ii) the tryptophan radical is deprotonated, (iii) rapid exchange of either a terminal water or hydroxide ion with water occurs at the ferric ion in the diiron(III,IV) cluster, and (iv) the diiron(III,IV) core and W* decay to the diiron(III) product by a common mechanism. No transient radical was observed by stopped-flow optical spectroscopy for reactions of the reduced hydroxylase variants I100Y, L208F, and F205W with dioxygen. The absence of such species, and the deprotonated state of the tryptophanyl radical in the diiron(III,IV)-W* transient, allow for a conservative estimate of the reduction potential of the diiron(III) intermediate as lying between 1.1 and 1.3 V. We also describe the X-ray crystal structure of the I100W variant of ToMOH.
在甲苯/邻二甲苯单加氧酶的羟化酶组分的羧酸盐桥连二铁活性位点,它能激活双加氧用于后续芳烃的羟基化反应。在该酶的I100W变体中,我们通过快速冷冻淬灭(RFQ)电子顺磁共振(EPR)、穆斯堡尔谱和电子核双共振(ENDOR)光谱,对在还原态二价铁状态下添加双加氧形成的两种物种的形成和衰减进行了表征。通过双混合停流光谱研究了这种混合价态瞬态的形成和衰减速率对pH以及苯酚、丙烯或乙炔存在的依赖性。通过胰蛋白酶消化结合质谱法研究了还原态蛋白质与双加氧饱和缓冲液反应后羟化酶α亚基的修饰情况。从这些研究中,我们得出以下结论:(i)动力学上与先前的二价铁(III)中间体相关联的二铁(III,IV)-W瞬态,源于W100的单电子氧化;(ii)色氨酸自由基去质子化;(iii)在二铁(III,IV)簇中的铁离子处,末端水或氢氧根离子与水发生快速交换;(iv)二铁(III,IV)核心和W通过共同机制衰减为二价铁(III)产物。对于还原态羟化酶变体I100Y、L208F和F205W与双加氧的反应,停流光谱未观察到瞬态自由基。这种物种的不存在以及二铁(III,IV)-W*瞬态中色氨酸自由基的去质子化状态,使得可以保守估计二价铁(III)中间体的还原电位在1.1至1.3 V之间。我们还描述了甲苯单加氧酶羟化酶(ToMOH)的I100W变体的X射线晶体结构。