Orii Y
J Inorg Biochem. 1985 Mar-Apr;23(3-4):263-71. doi: 10.1016/0162-0134(85)85034-0.
CO added to dithionite-reduced cytochrome oxidase pretreated with azide, cyanide, or fluoride yielded CO-ferrous heme a3 trapping the unliganded reduced heme. Ferrous heme a3 was either an equilibrium species initially present, or provided by dissociation of ligand-bound ferric heme a3 followed by the reduction with dithionite. In the latter case the ligand dissociation was rate-limiting for the CO compound formation. Pretreatment of the enzyme with the inhibitory ligands affected neither photodissociation and reassociation of the CO compound thus formed, nor reaction with dioxygen initiated by the flow-flash method to any significant degree. Only the cyanide treatment slightly decreased the rate of intramolecular electron transfer. These results indicate that no inhibitory ligand but CO remains in the vicinity of the heme a3-CuB center in the CO compound of cytochrome oxidase.
向用叠氮化物、氰化物或氟化物预处理过的连二亚硫酸盐还原型细胞色素氧化酶中添加一氧化碳,会产生捕获未配位还原血红素的一氧化碳 - 亚铁血红素 a3。亚铁血红素 a3 要么是最初存在的平衡物种,要么是由与配体结合的高铁血红素 a3 解离,随后用连二亚硫酸盐还原产生的。在后一种情况下,配体解离是形成一氧化碳化合物的限速步骤。用抑制性配体对酶进行预处理,对如此形成的一氧化碳化合物的光解离和重新结合,以及通过流动 - 闪光法引发的与双氧的反应,均无显著影响。只有氰化物处理略微降低了分子内电子转移速率。这些结果表明,在细胞色素氧化酶的一氧化碳化合物中,血红素 a3 - 铜 B 中心附近除了一氧化碳外没有其他抑制性配体。