Journal of Biological Chemistry · 1976 · 336 citations · 24 references
Life SciencesBiochemistryEnzyme MechanismEnzymologyMicrobial MetabolismCatalytic MechanismsEnzyme KineticsOxygen EvolutionOxygen TransferRedox EnzymesAbsorbance SpectroscopyAbsorption SpectraAromatic Compound BindingOxygen Transfer ReactionsPseudomonas FluorescensPseudomonas SpeciesStopped-flow SpectroscopyTransient Intermediates
Para-hydroxybenzoate hydroxylase (EC 1.14.13.2) from Pseudomonas fluorescens is one of a group of flavoproteins which insert molecular oxygen into aromatic rings to form phenols. To determine the mechanism of oxygen insertion by this enzyme, an extensive study was made of the reaction with O2 of reduced enzyme in complex with various aromatic molecules. Reactions were studied by following absorbance changes with time with a stopped-flow spectrophotometer. Analysis of multiphasic reactions led to the detection of a minimum of three transient intermediates with characteristic absorption spectra involved in the process of hydroxylation. The initial interaction of oxygen with the reduced enzyme characteristically produces a derivative of FAD (maximum absorbance 380 to 390 nm) which is probably C(4a) peroxyflavin. Depending on the aromatic compound bound to the enzyme, this intermediate decays either to oxidized, enzyme-bound flavin and H2O2 or transfers an atom of oxygen to the aromatic compound. The process of oxygen transfer forms a derivative of FAD of unknown structure (maximum absorbance 390 to 420 nm), which subsequently decays to the third intermediate observed (maximum absorbance 380 to 385 nm), which is probably C(4a) hydroxyflavin. The decay of this last intermediate results in the formation of oxidized enzyme, and the liberation of hydroxylated product and H2O. In an extension of substrate specificity studies it was found that p-aminobenzoate is a substrate and 5-hydroxypicolinate is an effector for p-hydroxybenzoate hydroxylase. The binding of aromatic compounds to the reduced enzyme was observed by following shifts in the absorption spectrum of enzyme bound FADH2, permitting the determination of dissociation constants and kinetics of binding.
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Oxidases and Related Redox Systems
G. Milazzo · Bioelectrochemistry and Bioenergetics · 1975 · 677 citations
Molecular Mechanisms of Oxygen Activation
Philip J. Geary · Biochemical Society Transactions · 1975 · 570 citations
Vincent Massey, Sidney Strickland, Stephen G. Mayhew et al. · Biochemical and Biophysical Research Communications · 1969 · 426 citations · Full text
Fluorescence and optical characteristics of reduced flavines and flavoproteins
Sandro Ghisla, Vincent Massey, Jean‐Marc Lhoste et al. · Biochemistry · 1974 · 384 citations · Full text