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Photochemical determinations of the oxidases of bacteria.
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A kinetic study of the mode of growth of surface colonies of bacteria and fungi.
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The reaction of Pseudomonas aeruginosa cytochrome c-551 oxidase with oxygen.
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Fast reactions in carbon monoxide binding to heme proteins.
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Low-temperature kinetics of the reaction of oxygen and solubilized cytochrome oxidase.
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Sequence of b cytochromes relative to ubiquinone in the electron transport chain of Escherichia coli.
J Bacteriol. 1978 Feb;133(2):477-84
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Low-temperature flash photolysis studies of cytochrome oxidase and its environment.
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Characterization and phenotypic control of the cytochrome content of Escherichia coli.
Biochem J. 1979 Aug 15;182(2):465-72
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Intermediates in the reaction of reduced cytochrome o (Vitreoscilla) with oxygen.
J Biol Chem. 1979 Jan 10;254(1):176-9
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Electron-accepting properties of cytochrome o purified from Vitreoscilla.
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The binding of cyanide and carbon monoxide to cytochrome o purified from Vitreoscilla. Evidence for subunit interaction in the reduced protein.
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Oxygenated Cytochrome o. An active intermediate observed in whole cells of Vitreoscilla.
J Biol Chem. 1977 Mar 25;252(6):1834-6
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Oxidation-reduction behavior of the heme c and heme d moieties of Pseudomonas aeruginosa nitrite reductase and the formation of an oxygenated intermediate at heme d1.
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Inhibition by cyanide of the respiratory chain oxidases of Escherichia coli.
Arch Biochem Biophys. 1974 Oct;164(2):682-93
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Energy-linked reduction of nicotinamide--adenine dinucleotide in membranes derived from normal and various respiratory-deficient mutant strains of Escherichia coli K12.
Biochem J. 1974 Oct;144(1):77-85
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Spectral characteristics and interconversions of the reduced oxidized, and oxygenated forms of purified cytochrome o.
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Reduced nicotinamide adenine dinucleotide cytochrome o reductase associated with cytochrome o purified from Vitreoscilla. Evidence for an intermediate oxygenated form of cytochrome o.
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Effects of sulphate-limited growth in continuous culture on the electron-transport chain and energy conservation in Escherichia coli K12.
Biochem J. 1975 Dec;152(3):537-46
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Cytochrome oxidase from Pseudomonas aeruginosa. IV. Reaction with oxygen and carbon monoxide.
Biochim Biophys Acta. 1976 Jun 8;430(3):445-53
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Kinetic characterization of the membrane-bound cytochromes of Escherichia coli grown under a variety of conditions by using a stopped-flow dual-wavelength spectrophotometer.
Biochem J. 1976 Feb 15;154(2):285-94
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Trapping of an intermediate in the oxidation-reduction cycle of cytochrome d in Escherichia coli.
FEBS Lett. 1976 Mar 1;62(3):330-3
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A versatile time-sharing multichannel spectrophotometer, reflectometer, and fluorometer.
Anal Biochem. 1975 Jun;66(2):498-514
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Low temperature trapping method for cytochrome oxidase oxygen intermediates.
Anal Biochem. 1975 Aug;67(2):552-79
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Functional intermediates in the reaction of membrane-bound cytochrome oxidase with oxygen.
J Biol Chem. 1975 Dec 25;250(24):9226-37
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The reaction of Pseudomonas aeruginosa cytochrome c oxidase with carbon monoxide.
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Dynamics of ligand binding to myoglobin.
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A rapid scanning dual wavelength spectrophotometer.
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Photosensitivity of haem compounds.
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