Delocalization over the heme and the axial ligands of one of the two oxidizing equivalents stored above the ferric state in the peroxidase and catalase Compound-I intermediates: Indirect participation of the proximal axial ligand of iron in the oxidation reactions catalyzed by heme-based peroxidases and catalases?
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作者:
Weiss, R
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机构:UNIV LUBECK,INST PHYS,D-23538 LUBECK,GERMANY
Weiss, R
Mandon, D
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机构:UNIV LUBECK,INST PHYS,D-23538 LUBECK,GERMANY
Mandon, D
Wolter, T
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机构:UNIV LUBECK,INST PHYS,D-23538 LUBECK,GERMANY
Wolter, T
Trautwein, AX
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机构:UNIV LUBECK,INST PHYS,D-23538 LUBECK,GERMANY
Trautwein, AX
Muther, M
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机构:UNIV LUBECK,INST PHYS,D-23538 LUBECK,GERMANY
Muther, M
Bill, E
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机构:UNIV LUBECK,INST PHYS,D-23538 LUBECK,GERMANY
Bill, E
Gold, A
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机构:UNIV LUBECK,INST PHYS,D-23538 LUBECK,GERMANY
Gold, A
Jayaraj, K
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机构:UNIV LUBECK,INST PHYS,D-23538 LUBECK,GERMANY
Jayaraj, K
Terner, J
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机构:UNIV LUBECK,INST PHYS,D-23538 LUBECK,GERMANY
Terner, J
机构:
[1] UNIV LUBECK,INST PHYS,D-23538 LUBECK,GERMANY
[2] MAX PLANCK INST STRAHLENCHEM,D-45470 MULHEIM,GERMANY
[3] UNIV N CAROLINA,DEPT ENVIRONM SCI & ENGN,CHAPEL HILL,NC 27599
[4] VIRGINIA COMMONWEALTH UNIV,DEPT CHEM,RICHMOND,VA 23284
A comparison of the exchange interactions arising in the peroxidase and catalase Compound I intermediates and their iron(IV)-oxo porphyrin pi-cation radical models, both of which are two oxidizing equivalents above the ferric state, suggests that in the models the oxidizing equivalent is localized on the porphyrin ring, while in the proteins it is partly delocalized onto the proximal ligand. Thus, the proximal axial ligand of iron participates indirectly in the oxidation reactions catalyzed by the enzymes. Possible roles of the axial ligand in the catalytic mechanism of these heme-based enzymes are discussed.