Functional intermediates in reaction of cytochrome oxidase with oxygen.
- 1 April 1975
- journal article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 72 (4), 1635-1640
- https://doi.org/10.1073/pnas.72.4.1635
Abstract
The development of a low temperature kinetic method for the flash photolysis of the compounds of membrane-bound cytochrome a3 with carbon monoxide in the presence of oxygen affords evidence for three categories of functional intermediate compounds of cytochrome a3 and oxygen. The three classes are identified as follows: Compounds of Type A are considered to be "oxy" compounds of the ferrous heme. They have the composition a3-2+. O2. Compounds of Type B are considered to be peroxide compounds (CU-2+A3-3+ O-2= or CU-2+A3-3+ O2H2) or the equivalent heme Fe-Cu peroxide bridge structures. Compounds of Type C are formed from the ferricyanide pretreated oxidase and may involve higher oxidation states of the heme iron such as quadrivalent iron, and peroxide. Kinetic and equilibrium studies show these compounds to be functional in oxygen reduction in the sequence A yields B yield cytochromes a, c, c1, etc.Keywords
This publication has 18 references indexed in Scilit:
- REACTIONS OF OXYGEN WITH HEMOGLOBIN, CYTOCHROME C OXIDASE AND OTHER HEMEPROTEINS*Annals of the New York Academy of Sciences, 1975
- ON THE MECHANISM OF THE REACTION OF CYTOCHROME OXIDASE WITH OXYGEN*Annals of the New York Academy of Sciences, 1975
- Heme—Heme interaction in cytochrome c oxidase in situ as measured by EPR spectroscopyArchives of Biochemistry and Biophysics, 1972
- The Influence of Deuterium Oxide and Organic Solvents on the Interaction of Respiratory Chain ComponentsJournal of Biological Chemistry, 1966
- Cytochrome oxidase and its derivatives V. The reaction of ferrous cytochrome c oxidase with oxygen and hydrogen peroxide in the presence of sodium dithioniteBiochimica et Biophysica Acta (BBA) - Enzymology and Biological Oxidation, 1966
- Kinetic Observations on the Near Infrared Band of Cytochrome c OxidaseJournal of Biological Chemistry, 1965
- Studies on Cytochrome aThe Journal of Biochemistry, 1963
- ON THE MECHANISM OF CHLOROPHYLL-CYTOCHROME INTERACTION: THE TEMPERATURE INSENSITIVITY OF LIGHT-INDUCED CYTOCHROME OXIDATION IN CHROMATIUMProceedings of the National Academy of Sciences, 1960
- Photosensitivity of Hæm CompoundsNature, 1957
- Enzyme‐Substrate CompoundsAdvances in enzymology and related areas of molecular biology, 1951