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首页> 外文期刊>Inorganica Chimica Acta >Two proton-one electron coupled transfer in iron and manganese superoxide dismutases: A density functional study
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Two proton-one electron coupled transfer in iron and manganese superoxide dismutases: A density functional study

机译:铁和锰超氧化物歧化酶中两个质子一电子偶联转移:密度泛函研究

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A theoretical study on a simple model has been carried out to contribute to the elucidation of the reaction mechanism of iron and manganese superoxide dismutases (FeSOD and MnSOD). The presence of the water molecule in the reaction is very important since it is involved in a transfer process. In fact, this step is a complex coupled transfer process that involves two protons and one electron at the same time. This step is possible in a specific arrangement of superoxide anion in its coordination to the transition metal ion. The other possible conformations are the inactive species that evolves to the active complex in a slow way or that accepts an additional proton to produce a new species ("dead-end" complex) that is unable to evolve to hydrogen peroxide. Time-dependent formalism applied to the density functional calculations and compared to the experimental electronic spectra has allowed us to choose some possible candidates for the "dead-end" complex. Our results indicate that a hydroperoxo form (4-Mn) is the more probable candidate to it. However, other possibilities cannot be rejected. (c) 2006 Elsevier B.V. All rights reserved.
机译:已经进行了关于简单模型的理论研究,以有助于阐明铁和锰超氧化物歧化酶(FeSOD和MnSOD)的反应机理。反应中水分子的存在非常重要,因为它涉及转移过程。实际上,该步骤是一个复杂的耦合转移过程,涉及两个质子和一个电子。在与过渡金属离子配位的超氧化物阴离子的特定布置中,该步骤是可能的。其他可能的构象是非活性物质,其以缓慢的方式演变为活性复合物,或者接受额外的质子以产生不能进化为过氧化氢的新物质(“末端”复合物)。时间相关的形式主义应用于密度泛函计算,并与实验电子光谱进行比较,使我们能够为“死角”络合物选择一些可能的候选物。我们的结果表明氢过氧形式(4-Mn)是最可能的候选形式。但是,其他可能性不能被拒绝。 (c)2006 Elsevier B.V.保留所有权利。

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