Literature DB >> 4352836

D-3-hydroxybutyrate dehydrogenase from Rhodopseudomonas spheroides. Kinetics of radioisotope redistribution at chemical equilibrium catalysed by the enzyme in solutions.

M J Preuveneers, D Peacock, E M Crook, J B Clark, K Brocklehurst.   

Abstract

1. The reversible NAD(+)-linked oxidation of d-3-hydroxybutyrate to acetoacetate in 0.1m-sodium pyrophosphate buffer, pH8.5, at 25.0 degrees C, catalysed by d-3-hydroxybutyrate dehydrogenase (d-3-hydroxybutyrate-NAD(+) oxidoreductase, EC 1.1.1.30), was studied kinetically at chemical equilibrium by monitoring radioisotope redistribution with sodium dl-hydroxy[3-(14)C]butyrate and [4-(3)H]NAD(+)(labelled in the nicotinamide ring). 2. When all substrates are maintained at concentrations approaching saturation (approx. 3-50 times the K(m) values) the first-order rate constant for the enzyme-catalysed interconversion of NAD(+) and NADH is much smaller than that for the enzyme-catalysed interconversion of d-3-hydroxybutyrate and acetoacetate. 3. The rate of interconversion of NAD(+) and NADH increases initially with increasing concentrations of d-3-hydroxybutyrate and acetoacetate (ratio of concentrations maintained constant), passes through a maximum and approaches closely to zero at saturating concentrations of the latter substrates. 4. The rates of interconversion of NAD(+) and NADH and of d-3-hydroxybutyrate and acetoacetate increase with increasing concentration of NAD(+) (up to 66 times its K(m) value) and NADH (up to 180 times its K(m) value) (ratio of the concentrations of the nicotinamide nucleotides maintained constant). 5. These findings support the description of this catalysis as an ordered Bi Bi mechanism with no detectable alternative pathway, in which the interconversion of the central ternary complexes is not rate-limiting, and provide no evidence for the formation of dead-end complexes. 6. The solubility of 2,4-dinitrophenylhydrazine in HCl exhibits an acidity optimum, the maximum solubility at 25.0 degrees C (3.8mg/ml, 19mm) occurring at 2.29m-HCl; in solutions of this acidity acetone 2,4-dinitrophenylhydrazone is relatively insoluble (0.098mg/ml, 0.413mm).

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Year:  1973        PMID: 4352836      PMCID: PMC1177679          DOI: 10.1042/bj1330159

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  7 in total

1.  EQUILIBRIUM REACTION RATES AND THE MECHANISMS OF BOVINE HEART AND RABBIT MUSCLE LACTATE DEHYDROGENASES.

Authors:  E SILVERSTEIN; P D BOYER
Journal:  J Biol Chem       Date:  1964-11       Impact factor: 5.157

2.  Uses and limitations of measurements of rates of isotopic exchange and incorporation in catalyzed reactions.

Authors:  P D BOYER
Journal:  Arch Biochem Biophys       Date:  1959-06       Impact factor: 4.013

3.  Kinetic and isotope-exchange studies on shikimate dehydrogenase from Pisum sativum.

Authors:  D Balinsky; A W Dennis; W W Cleland
Journal:  Biochemistry       Date:  1971-05-11       Impact factor: 3.162

4.  Catalytic mechanism of pig heart mitochondrial malate dehydrogenase studied by kinetics at equilibrium.

Authors:  E Silverstein; G Sulebele
Journal:  Biochemistry       Date:  1969-06       Impact factor: 3.162

5.  The chemical estimation of ketone bodies.

Authors:  H G Britton
Journal:  Anal Biochem       Date:  1966-05       Impact factor: 3.365

6.  Separation of NAD+ and NADH and NADP+ aned NADPH by anion exchange on DEAE-cellulose paper.

Authors:  E Silverstein
Journal:  Biochim Biophys Acta       Date:  1970-07-21

7.  D-3-hydroxybutyrate dehydrogenase from Rhodopseudomonas spheroides. Kinetic mechanism from steady-state kinetics of the reaction catalysed by the enzyme in solution and covalently attached to diethylaminoethylcellulose.

Authors:  M J Preuveneers; D Peacock; E M Crook; J B Clark; K Brocklehurst
Journal:  Biochem J       Date:  1973-05       Impact factor: 3.857

  7 in total
  2 in total

1.  Impact of peripheral ketolytic deficiency on hepatic ketogenesis and gluconeogenesis during the transition to birth.

Authors:  David G Cotter; Baris Ercal; D André d'Avignon; Dennis J Dietzen; Peter A Crawford
Journal:  J Biol Chem       Date:  2013-05-20       Impact factor: 5.157

2.  D-3-hydroxybutyrate dehydrogenase from Rhodopseudomonas spheroides. Kinetic mechanism from steady-state kinetics of the reaction catalysed by the enzyme in solution and covalently attached to diethylaminoethylcellulose.

Authors:  M J Preuveneers; D Peacock; E M Crook; J B Clark; K Brocklehurst
Journal:  Biochem J       Date:  1973-05       Impact factor: 3.857

  2 in total

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