The EPR-Detectable Copper of Nitrous Oxide Reductase as a Model for CuA in Cytochrome c Oxidase: A Multifrequency Electron Paramagnetic Resonance Investigation
The EPR-Detectable Copper of Nitrous Oxide Reductase as a Model for CuA in Cytochrome c Oxidase: A Multifrequency Electron Paramagnetic Resonance Investigation
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EPR 可检测的一氧化二氮还原酶铜作为细胞色素 c 氧化酶中 CuA 的模型:多频电子顺磁共振研究
DOI:
10.1007/978-94-011-6875-5_33
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发表时间:
1993
影响因子:
2.2
通讯作者:
W. Zumft
中科院分区:
文献类型:
--
作者:
P. Kroneck;W. Antholine;H. Koteich;D. Kastrau;F. Neese;W. Zumft
Nitrous oxide reductase (N2OR) is the terminal reductase in a respiratory chain converting N2O to N2 in the denitrifying bacteria:
$${N_2}O + 2{H^ + } + 2{e^ - } \to {N_2} + {H_2}O$$
([1])
Principal aspects of the subject have been covered recently, and these reviews may be consulted for primary reference.1,2 The high activity form of the enzyme from Pseudomonas stutzeri (N2OR I) has two identical subunits, each carrying a mixed-valence [Cu(1.5)...Cu(1.5)], S = 1/2 complex.3 A catalytically inactive derivative of the enzyme (N2OR V) has also the mixed-valence EPR-detectable site.4,5