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The catalytic copper clusters of the particulate methane monooxygenase from methanotrophic bacteria: Electron paramagnetic resonance spectral simulations

机译:甲烷营养细菌中甲烷甲烷单加氧酶的催化铜簇:电子顺磁共振光谱模拟

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The pariculate methane monooxygenase (pMMO) from Methylococcus capsulatus contains 14-15 reduced copper ions, and it has been proposed that these copper ions are arranged in the form of trinuclear clusters. Two of these clusters have been referred to as catalytic clusters (C-clusters) and have been implicated in dioxygen activation and alkane hydroxylation. The remaining copper ions appear to provide a "reservoir" of reducing equivalents to replenish the electrons at the C-clusters following dioxygen activation at the C-clusters during turnover. Accordingly, they are normally reduced and have been called electron-transfer clusters (E-clusters). For pMMO prepared in highly enriched membranes, or purified as the pMMO-detergent complex from these membranes, only the C-cluster copper ions are oxidized. Recently, the low temperature EPR spectrum of as-isolated pMMO was deconvoluted into a type 2 Cu(II) signal and a broad, but nearly isotropic EPR signal centered at g similar to 2.1. Earlier magnetization and magnetic susceptibility measurements have suggested that the latter EPR signal, which is not sensitive to microwave power saturation, might arise from a ferromagnetically exchange-coupled trinuclear Cu(II) cluster with J approximate to 20 cm(-1) and D less than or equal to 0.05 cm(-1). Toward confirming these results, several triangular model Cu(II) complexes, both anti ferromagnetically and ferromagnetically coupled and with well-defined structural and ligand information, were reviewed to gain insights into magneto-structural correlations. Spectral simulations of the pMMO cluster EPR signals were then performed based on the structural and spectroscopic information provided by the ferromagnetic model complexes. We show that only Cu(II) ions with proper g-tensors and appropriate relative orientations between them can give rise to the unique EPR signal observed for the C-cluster(s) in pMMO. The putative C-cluster EPR signal observed for the as-isolatedpMMO at 3 K was best fitted by a triad of ferromagnetically coupled Cu(II) ions with the following sets of g-values: (1.983, 2.030, 2.218), (1.983, 2.029, 2.218) and (2.000, 2.033, 2.207); and zero-field splitting parameters D = 0.017 +/- 0.002 cm(-1) (175 25 Gauss) and E/D = 0.15. The fit was not sensitive to the value of J so long as the exchange interaction was much larger than the Zeeman interaction (J much greater than gbetaH).
机译:来自荚膜甲基球菌的颗粒状甲烷单加氧酶(pMMO)包含14-15个还原的铜离子,并且已提出这些铜离子以三核簇的形式排列。这些簇中的两个被称为催化簇(C-簇),并与双氧活化和烷烃羟基化有关。剩余的铜离子似乎提供了还原当量的“储层”,以在周转期间在C团簇处的双氧活化后补充C团簇处的电子。因此,它们通常被还原,并被称为电子转移簇(电子簇)。对于在高度富集的膜中制备的pMMO,或从这些膜中纯化为pMMO清洁剂的复合物,只有C簇铜离子被氧化。最近,已分离的pMMO的低温EPR光谱被反卷积为2型Cu(II)信号和一个宽大但几乎各向同性的EPR信号,其中心点g类似于2.1。较早的磁化和磁化率测量表明,对微波功率饱和不敏感的后一种EPR信号可能是由铁磁交换耦合的三核Cu(II)簇产生的,J约20 cm(-1),D少大于或等于0.05 cm(-1)。为了证实这些结果,对几种三角模型的Cu(II)络合物进行了反铁磁和铁磁耦合,并定义了明确的结构和配体信息,以深入了解磁结构相关性。然后根据铁磁模型复合体提供的结构和光谱信息对pMMO簇EPR信号进行光谱模拟。我们显示,只有具有适当g张量和它们之间适当相对方向的Cu(II)离子才能引起在pMMO中C簇观察到的独特EPR信号。铁磁耦合的Cu(II)离子三元组具有以下g值组,最适合在3 K下观察到的as-isolatedpMMO C-簇EPR信号:(1.983,2.030,2.218),(1.983, 2.029,2.218)和(2.000,2.033,2.207);和零场分裂参数D = 0.017 +/- 0.002 cm(-1)(175 25高斯)和E / D = 0.15。只要交换交互作用比Zeeman交互作用大得多(J远大于gbetaH),拟合对J的值就不敏感。

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