Erman J E, Yonetani T
Biochim Biophys Acta. 1975 Jun 26;393(2):343-9. doi: 10.1016/0005-2795(75)90060-4.
H2O2 reacts with cytochrome c peroxidase in a variety of ways. The initial reaction produces cytochrome c peroxidase Compound I. If more than a 10-fold excess of H2O2 is added to the enzyme, a portion of the H2O2 will react with Compound I to produce molecular oxygen. The remainder oxidizes the heme group and various amino acid residues in the protein. If less than a 10-fold excess of H2O2 is added to the enzyme, essentially all the H2O2 is utilized by oxidation of amino acid residues in the protein. The oxidation of the amino acid residues by H2O2 substantially modifies the reactivity of cytochrome c peroxidase. The modification of reactivity could be the direct result of amino acid oxidation or an indirect result caused by a perturbation of the protein structure at the active site. The products oxidized at pH 8 lose their ability to react with H2O2. The products oxidized at pH4 react with H2O2 but their reactivity toward Fe(CN)4-6 is substantially reduced.
过氧化氢以多种方式与细胞色素c过氧化物酶发生反应。初始反应生成细胞色素c过氧化物酶化合物I。如果向该酶中加入超过10倍过量的过氧化氢,一部分过氧化氢会与化合物I反应生成分子氧。其余的则氧化蛋白质中的血红素基团和各种氨基酸残基。如果向该酶中加入少于10倍过量的过氧化氢,基本上所有的过氧化氢都会通过氧化蛋白质中的氨基酸残基而被利用。过氧化氢对氨基酸残基的氧化会显著改变细胞色素c过氧化物酶的反应活性。反应活性的改变可能是氨基酸氧化的直接结果,也可能是活性位点处蛋白质结构扰动引起的间接结果。在pH 8条件下被氧化的产物失去了与过氧化氢反应的能力。在pH 4条件下被氧化的产物能与过氧化氢反应,但它们对Fe(CN)₄⁻⁶的反应活性大幅降低。