Mass spectrometric determination of dioxygen bond splitting in the "peroxy" intermediate of cytochrome c oxidase

被引:105
作者
Fabian, M
Wong, WW
Gennis, RB
Palmer, G [1 ]
机构
[1] Rice Univ, Dept Biochem & Cell Biol, Houston, TX 77251 USA
[2] Baylor Univ, USDA ARS, Childrens Nutr Res Ctr, Coll Med,Dept Pediat, Houston, TX 77030 USA
[3] Univ Illinois, Dept Biochem, Urbana, IL 61801 USA
关键词
D O I
10.1073/pnas.96.23.13114
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The "peroxy" intermediate (P form) of bovine cytochrome c oxidase was prepared by reaction of the two-electron reduced mixed-valence CO complex with O-18(2) after photolytic removal of CO. The water present in the reaction mixture was recovered and analyzed for O-18 enrichment by mass spectrometry, It was found that approximately one oxygen atom (O-18) per one equivalent of the P form was present in the bulk water. The data show that the oxygen-oxygen dioxygen bond is already broken in the P intermediate and that one oxygen atom can be readily released or exchanged with the oxygen of the solvent water.
引用
收藏
页码:13114 / 13117
页数:4
相关论文
共 38 条