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首页> 外文期刊>Journal of biological inorganic chemistry: JBIC: a publication of the Society of Biological Inorganic Chemistry >Mediated catalysis of Paracoccus pantotrophus cytochrome c peroxidase by P-pantotrophus pseudoazurin: kinetics of intermolecular electron transfer
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Mediated catalysis of Paracoccus pantotrophus cytochrome c peroxidase by P-pantotrophus pseudoazurin: kinetics of intermolecular electron transfer

机译:P-泛营养假拟天青素介导的泛营养副球菌细胞色素C过氧化物酶催化:分子间电子转移动力学

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摘要

This work reports the direct electrochemistry of Paracoccus pantotrophus pseudoazurin and the mediated catalysis of cytochrome c peroxidase from the same organism. The voltammetric behaviour was examined at a gold membrane electrode, and the studies were performed in the presence of calcium to enable the peroxidase activation. A formal reduction potential, E (0)', of 230 +/- 5 mV was determined for pseudoazurin at pH 7.0. Its voltammetric signal presented a pH dependence, defined by pK values of 6.5 and 10.5 in the oxidised state and 7.2 in the reduced state, and was constant up to 1 M NaCl. This small copper protein was shown to be competent as an electron donor to cytochrome c peroxidase and the kinetics of intermolecular electron transfer was analysed. A second-order rate constant of 1.4 +/- 0.2 x 10(5) M-1 s(-1) was determined at 0 M NaCl. This parameter has a maximum at 0.3 M NaCl and is pH-independent between pH 5 and 9.
机译:这项工作报告了副球菌伪天青素的直接电化学和来自同一生物的细胞色素C过氧化物酶的介导催化作用。在金膜电极上检查了伏安行为,并在钙的存在下进行了研究以使过氧化物酶活化。测定在pH 7.0下假天青素的形式还原电位E(0)'为230 +/- 5 mV。它的伏安信号呈现pH依赖性,在氧化态下pK值为6.5和10.5,在还原态下pK值为7.2,直至1 M NaCl都是恒定的。该小铜蛋白被证明可作为细胞色素c过氧化物酶的电子供体,并分析了分子间电子转移的动力学。在0 M NaCl下测得的二阶速率常数为1.4 +/- 0.2 x 10(5)M-1 s(-1)。该参数在0.3 M NaCl时最大,在pH 5和9之间与pH无关。

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