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通过X射线吸收光谱法研究的细胞色素氧化酶的“过氧化物酶体”形式。

"Peroxidatic" form of cytochrome oxidase as studied by X-ray absorption spectroscopy.

作者信息

Chance B, Kumar C, Powers L, Ching Y C

出版信息

Biophys J. 1983 Dec;44(3):353-63. doi: 10.1016/S0006-3495(83)84309-4.

DOI:10.1016/S0006-3495(83)84309-4
PMID:6318841
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1434835/
Abstract

X-ray absorption spectroscopy shows pulsed oxidase to be similar to resting oxidase but to lack the sulfur bridge between iron and copper of active sites (Powers, L., Y. Ching, B. Chance, and B. Muhoberac, 1982, Biophys. J., 37[2, Pt. 2]: 403a. [Abstr.] ) The first shell ligands and bond lengths of the pulsed oxidase active site heme most clearly fit the ferric peroxidases from horseradish and yeast, and the pulsed oxidase cyanide compound resembles the low spin hemoprotein cyanide compounds. The structural results are consistent with an aquo or a peroxo form for pulsed oxidase as is also observed by optical studies. These structural and chemical data are consistent with a role for the pulsed forms in a cyclic peroxidatic side reaction in which the pulsed and pulsed peroxide compounds act as peroxide scavengers. The peroxidatic role of cytochrome oxidase in the nonsulfur bridged form suggests the renaming of the "oxygenated" or "pulsed" forms on a functional basis as "peroxidatic" forms of cytochrome oxidase.

摘要

X射线吸收光谱显示,脉冲氧化酶与静止氧化酶相似,但活性位点的铁和铜之间缺乏硫桥(Powers, L., Y. Ching, B. Chance, and B. Muhoberac, 1982, Biophys. J., 37[2, Pt. 2]: 403a. [摘要])。脉冲氧化酶活性位点血红素的第一配位层配体和键长与辣根和酵母中的铁过氧化物酶最为吻合,且脉冲氧化酶氰化物化合物类似于低自旋血红素蛋白氰化物化合物。结构结果与光学研究中观察到的脉冲氧化酶的水合或过氧形式一致。这些结构和化学数据与脉冲形式在循环过氧化物酶副反应中的作用一致,在该反应中,脉冲和脉冲过氧化物化合物充当过氧化物清除剂。细胞色素氧化酶在非硫桥形式中的过氧化物酶作用表明,基于功能将“氧化”或“脉冲”形式重新命名为细胞色素氧化酶的“过氧化物酶”形式。

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引用本文的文献

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Biochem J. 1984 Nov 1;223(3):809-13. doi: 10.1042/bj2230809.
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Cytochrome c oxidase from Paracoccus denitrificans: both hemes are located in subunit I.反硝化副球菌的细胞色素c氧化酶:两个血红素均位于亚基I中。
Proc Natl Acad Sci U S A. 1988 Sep;85(18):6647-51. doi: 10.1073/pnas.85.18.6647.
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Cytochrome c oxidase metal centers: location and function.
J Bioenerg Biomembr. 1991 Apr;23(2):291-302. doi: 10.1007/BF00762223.

本文引用的文献

1
Extended x-ray absorption fine structure of copper in cytochrome c oxidase: Direct evidence for copper-sulfur ligation.细胞色素 c 氧化酶中铜的扩展 X 射线吸收精细结构:铜-硫配位的直接证据。
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The properties of the enzyme-substrate compounds of horseradish peroxidase and peroxides; the effect of pH upon the rate of reaction of complex II with several acceptors and its relation to their oxidation-reduction potential.辣根过氧化物酶与过氧化物的酶-底物化合物的性质;pH对复合物II与几种受体反应速率的影响及其与它们氧化还原电位的关系。
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Electronic structure of the peroxidase-peroxide complexes.过氧化物酶 - 过氧化物复合物的电子结构。
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Spectra and reaction kinetics of respiratory pigments of homogenized and intact cells.匀浆细胞和完整细胞呼吸色素的光谱及反应动力学
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Reaction of methmyoglobin with hydrogen peroxide.高铁肌红蛋白与过氧化氢的反应。
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STUDIES ON CYTOCHROME A. X. EFFECT OF HYDROGEN PEROXIDE ON ABSORPTION SPECTRA OF CYTOCHROME A.细胞色素A的研究。X. 过氧化氢对细胞色素A吸收光谱的影响
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Studies on cytochrome oxidase. I. Absolute and difference absorption spectra.细胞色素氧化酶的研究。I. 绝对吸收光谱和差示吸收光谱。
J Biol Chem. 1960 Mar;235:845-52.
9
The kinetics and stoichiometry of the transition from the primary to the secondary peroxidase peroxide complexes.从初级过氧化物酶-过氧化物复合物到次级过氧化物酶-过氧化物复合物转变的动力学和化学计量学。
Arch Biochem Biophys. 1952 Dec;41(2):416-24. doi: 10.1016/0003-9861(52)90470-0.
10
The spectra of the enzyme-substrate complexes of catalase and peroxidase.过氧化氢酶和过氧化物酶的酶-底物复合物光谱。
Arch Biochem Biophys. 1952 Dec;41(2):404-15. doi: 10.1016/0003-9861(52)90469-4.