Multifrequency EPR investigation of dimanganese catalase and related Mn(III)Mn(IV) complexes

被引:55
|
作者
Schäfer, KO
Bittl, R
Lendzian, F
Barynin, V
Weyhermüller, T
Wieghardt, K
Lubitz, W
机构
[1] Free Univ Berlin, Fachbereich Phys, D-14195 Berlin, Germany
[2] Tech Univ Berlin, Max Volmer Lab Biophys Chem, D-10623 Berlin, Germany
[3] Univ Sheffield, Dept Mol Biol & Biotechnol, Sheffield S10 2TN, S Yorkshire, England
[4] Max Planck Inst Strahlenchem, D-45470 Mulheim, Germany
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2003年 / 107卷 / 05期
关键词
D O I
10.1021/jp0259768
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The superoxidized (MnMnIV)-Mn-III state of dimanganese catalase from Thermus thermophilus and a series of structurally similar (MnMnIV)-Mn-III complexes were investigated using continuous wave (CW) and pulsed EPR spectroscopy at X- (9 GHz), Q- (34 GHz), and W-band (94 GHz) frequencies. The bis(mu-oxo) or bis(mu-oxo)(mu-carboxylato) bridged complexes exhibit strong antiferromagnetic coupling (\J\ > 100 cm(-1)). Relevant EPR parameters (G- and Mn-55 hyperfine coupling tensors) are obtained by spectral simulations and yield a consistent data set for all frequency bands. Two mechanisms that lead to EPR line broadening are discussed. The advantage of our fitting strategy, i.e., precise determination of the G-tensor from high-field/frequency and hyperfine couplings from low-frequency EPR spectra, over conventional procedures is outlined. Comparison of the G- and Mn-55 hyperfine tensors of the model complexes with those of dimanganese catalase show that both values are sensitive probes for small structural changes.
引用
收藏
页码:1242 / 1250
页数:9
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