A comparative EPR investigation of the multicopper proteins nitrous-oxide reductase and cytochrome c oxidase.

The multicopper proteins, nitrous-oxide reductase (N2OR) and cytochrome c oxidase (COX), were investigated by EPR spectroscopy at microwave frequencies 2.4-35 GHz. Our results support a Cu-Cu interaction in COX and N2OR. At least 10 lines in the 2.7-GHz, 12 lines in the 4.6-GHz and 14 lines in the 9.2 GHz spectra were resolved for N2OR. Eight copper lines at 2.7 GHz, about nine lines at 4.6 GHz and about six lines at 9.2 GHz were resolved for COX. Simulations of the EPR spectra were consistent with most of the resonances of the multiline spectra, including regions in the center of the spectra where overlap of the three seven-line patterns is proposed. These simulations indicated that Cu-Cu interaction, in a mixed-valence [Cu(1.5) ... Cu(1.5)], S = 1/2 site is consistent with, if not proof of, the unusual spectral features observed for N2OR and COX.

[1]  H. Cuypers,et al.  Derived amino acid sequences of the nosZ gene (respiratory N2O reductase) from Alcaligenes eutrophus, Pseudomonas aeruginosa and Pseudomonas stutzeri reveal potential copper-binding residues. Implications for the CuA site of N2O reductase and cytochrome-c oxidase. , 1992, European journal of biochemistry.

[2]  G. Babcock,et al.  Oxygen activation and the conservation of energy in cell respiration , 1992, Nature.

[3]  D. Dooley,et al.  A model of the copper centres of nitrous oxide reductase (Pseudomonas stutzeri) , 1991, FEBS letters.

[4]  P. Stephens,et al.  Spectroscopic studies of the copper sites in wild-type Pseudomonas stutzeri N2O reductase and in an inactive protein isolated from a mutant deficient in copper-site biosynthesis , 1991 .

[5]  A. Azzi,et al.  Cytochromec oxidase metal centers: Location and function , 1991, Journal of bioenergetics and biomembranes.

[6]  G. Buse,et al.  Cytochromec oxidase inParacoccus denitrificans. Protein, chemical, structural, and evolutionary aspects , 1991, Journal of bioenergetics and biomembranes.

[7]  S. Chan,et al.  The nature of Cux in cytochrome c oxidase. , 1991, Journal of Biological Chemistry.

[8]  W. Zumft,et al.  Nitrous oxide reductase from denitrifying Pseudomonas stutzeri. Genes for copper-processing and properties of the deduced products, including a new member of the family of ATP/GTP-binding proteins. , 1990, European journal of biochemistry.

[9]  D. Kastrau,et al.  Multifrequency EPR evidence for a bimetallic center at the CuA site in cytochrome c oxidase , 1990, FEBS letters.

[10]  S. Chan,et al.  Cytochrome c oxidase: understanding nature's design of a proton pump. , 1990, Biochemistry.

[11]  B. Malmström,et al.  Analytical characterization of cytochrome oxidase preparations with regard to metal and phospholipid contents, peptide composition and catalytic activity. , 1989, Biochimica et biophysica acta.

[12]  B. Malmström The mechanism of proton translocation in respiration and photosynthesis , 1989, FEBS letters.

[13]  W. Zumft,et al.  Copper coordination in nitrous oxide reductase from Pseudomonas stutzeri , 1989 .

[14]  D. Dooley,et al.  Pseudomonas stutzeri N2O reductase contains CuA-type sites. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[15]  P. Kroneck,et al.  The nature of the cupric site in nitrous oxide reductase and of CuA in cytochrome c oxidase , 1989, FEBS letters.

[16]  P. Kroneck,et al.  Nitrous oxide reductase from Pseudomonas stutzeri. Redox properties and spectroscopic characterization of different forms of the multicopper enzyme. , 1989, European journal of biochemistry.

[17]  P. Kroneck,et al.  The cupric site in nitrous oxide reductase contains a mixed‐valence [Cu(II),Cu(I)] binuclear center: A multifrequency electron paramagnetic resonance investigation , 1988, FEBS letters.

[18]  W. Caughey,et al.  Metals of Bovine Heart Cytochrome c Oxidase a , 1988, Annals of the New York Academy of Sciences.

[19]  W. Zumft,et al.  Molecular cloning, heterologous expression, and primary structure of the structural gene for the copper enzyme nitrous oxide reductase from denitrifying Pseudomonas stutzeri , 1988, Journal of bacteriology.

[20]  F. Rusnak,et al.  Properties of a copper-containing cytochrome ba3: a second terminal oxidase from the extreme thermophile Thermus thermophilus. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[21]  S. Chan,et al.  On the nature of cysteine coordination to CuA in cytochrome c oxidase. , 1988, The Journal of biological chemistry.

[22]  R. Moog,et al.  Characterization of the copper sites in Pseudomonas perfectomarina nitrous oxide reductase by resonance Raman spectroscopy , 1987 .

[23]  J. Gelles,et al.  Extended X-ray absorption fine structure of copper in CuA-depleted, p-(hydroxymercuri)benzoate-modified, and native cytochrome c oxidase. , 1987, Biochemistry.

[24]  G. Buse,et al.  Cytochrome c oxidase is a three-copper, two-heme-A protein. , 1987, European journal of biochemistry.

[25]  W. Jakob,et al.  Nitrous oxide reductase from denitrifying Pseudomonas perfectomarina. Purification and properties of a novel multicopper enzyme. , 1985, European journal of biochemistry.

[26]  J. S. Hyde,et al.  Direct evidence of nitrogen coupling in the copper(II) complex of bovine serum albumin by S-band electron spin resonance technique. , 1985, Journal of inorganic biochemistry.

[27]  J. Leigh,et al.  Distance between the visible copper and cytochrome a in bovine heart cytochrome oxidase. , 1985, Biochemistry.

[28]  D. Blair,et al.  Electron spin relaxation of CuA and cytochrome a in cytochrome c oxidase. Comparison to heme, copper, and sulfur radical complexes. , 1984, The Journal of biological chemistry.

[29]  H. Beinert,et al.  Multiple frequency EPR studies on three forms of oxidized cytochrome c oxidase. , 1983, Biochimica et biophysica acta.

[30]  Sunney I. Chan,et al.  The nature of CuA in cytochrome c oxidase , 1982, FEBS letters.

[31]  J. Hyde,et al.  The loop-gap resonator: a new microwave lumped circuit ESR sample structure , 1982 .

[32]  H. Gray,et al.  Extended x-ray absorption fine structure of copper in cytochrome c oxidase: Direct evidence for copper-sulfur ligation. , 1981, Proceedings of the National Academy of Sciences of the United States of America.

[33]  H. Beinert,et al.  Electron spin echo studies of cytochrome c oxidase. , 1980, The Journal of biological chemistry.

[34]  E. Margoliash,et al.  Copper electron-nuclear double resonance of cytochrome c oxidase. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[35]  J. S. Hyde,et al.  Hyperfine structure resolved by 2 to 4 GHz EPR of cytochrome c oxidase. , 1979, The Journal of biological chemistry.

[36]  S. Chan,et al.  An EPR study of the lineshape of copper in cytochrome c oxidase. , 1977, Biochimica et biophysica acta.

[37]  H. Beinert,et al.  Oxido-reductive titrations of cytochrome c oxidase followed by EPR spectroscopy. , 1976, Biochimica et biophysica acta.

[38]  T. Vänngård,et al.  EPR signals from cytochrome c oxidase. , 1976, Biochimica et biophysica acta.

[39]  J. Peisach,et al.  Structural implications derived from the analysis of electron paramagnetic resonance spectra of natural and artificial copper proteins. , 1974, Archives of biochemistry and biophysics.

[40]  H. Beinert,et al.  Studies of the heme components of cytochrome c oxidase by EPR spectroscopy. , 1969, Biochimica et biophysica acta.

[41]  P. Hemmerich,et al.  Binuclear mixed-valence copper acetate complex as a model for copper-copper interaction in enzymes , 1968 .

[42]  H. Beinert,et al.  OXIDATION-REDUCTION OF THE COPPER COMPONENT OF CYTOCHROME OXIDASE. KINETIC STUDIES WITH A RAPID FREEZING TECHNIQUE. , 1964, The Journal of biological chemistry.

[43]  H. Beinert,et al.  Properties of the copper associated with cytochrome oxidase as studied by paramagnetic resonance spectroscopy. , 1962, The Journal of biological chemistry.

[44]  W. Kaim,et al.  Detection of electron paramagnetic resonance signals from three different isotope combinations 63Cu/63Cu, 63Cu/65Cu and 65Cu/65Cu in stable dicopper(I) radical complexes , 1991 .

[45]  J. Pilbrow,et al.  Transition Ion Electron Paramagnetic Resonance , 1990 .

[46]  Harry Julius Emeléus,et al.  Advances in Inorganic Chemistry and Radiochemistry , 1982 .

[47]  K. Krab,et al.  Cytochrome oxidase : a synthesis , 1981 .

[48]  R. Lorence,et al.  Properties of a copper-containing cytochrome c1aa3 complex: a terminal oxidase of the extreme thermophile Thermus thermophilus HB8. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[49]  H. Beinert,et al.  Special techniques for the preparation of samples for low-temperature EPR spectroscopy. , 1978, Methods in enzymology.

[50]  J. Bolton,et al.  Biological applications of electron spin resonance , 1972 .