Literature DB >> 16658714

An apparent oligomer of malate dehydrogenase from bean leaves.

W Habig1, D Racusen.   

Abstract

Two forms of malate dehydrogenase of widely differing molecular weight have been examined from primary leaves of Phaseolus vulgaris. In addition to the normal 69,000 molecular weight enzyme, an unusual form of 280,000 molecular weight may be detected by sucrose density gradient centrifugation or gel filtration with Sephadex G-200. Isopycnic density gradient centrifugation showed that both forms of malate dehydrogenase differed markedly from the bulk of the leaf protein by their low bouyant density of 1.261 g/cm(3).High molecular weight (280,000) malate dehydrogenase could be converted to active low molecular weight (69,000) malate dehydrogenase by treatment with 2.5 m CsCl, 1.0 m NaCl, 6 m urea, pH 6.5 or below, or one freeze-thaw cycle. Simple removal of salt or raising the pH were not effective in reforming the high molecular weight malate dehydrogenase after dissociation. The high molecular weight enzyme was not dissociated during prolonged dialysis against 0.1 m NaCl or 0.05 m phosphate, pH 7.0. Calcium at concentrations up to 0.1 m produced no activation or differential response in the two MDH forms.High and low molecular weight malate dehydrogenase were nearly identical in susceptibility to inhibition by various unreactive substrate analogs. However, there was a marked difference in the ability of the two forms of malate dehydrogenase to reduce 3-acetylpyridine-deamino-NAD. This difference in activity was the basis of a convenient assay for determining the ratio of high to low molecular weight malate dehydrogenase in crude extracts. The pH activity profiles and Michaelis constant for malate were nearly identical for the two molecular weight forms.Analysis by polyacrylamide gel electrophoresis revealed one high molecular weight and two low molecular weight malate dehydrogenase zones. Dissociation of high molecular weight malate dehydrogenase resulted in formation of low molecular weight enzyme whose electrophoretic properties differed from the normal low molecular weight forms.

Entities:  

Year:  1974        PMID: 16658714      PMCID: PMC543231          DOI: 10.1104/pp.53.3.402

Source DB:  PubMed          Journal:  Plant Physiol        ISSN: 0032-0889            Impact factor:   8.340


  34 in total

1.  Effect of sodium chloride on the activity of a soluble malate dehydrogenase from pea seeds.

Authors:  R Weimberg
Journal:  J Biol Chem       Date:  1967-06-25       Impact factor: 5.157

2.  The effects of adenine nucleotides on pig heart malate dehydrogenase.

Authors:  H K Kuramitsu
Journal:  Biochem Biophys Res Commun       Date:  1966-05-03       Impact factor: 3.575

3.  Reversible inactivation of dehydrogenases.

Authors:  O P Chilson; G B Kitto; J Pudles; N O Kaplan
Journal:  J Biol Chem       Date:  1966-05-25       Impact factor: 5.157

4.  Malate dehydrogenases. II. Purification and properties of Bacillus subtilis, Bacillus stearothermophilus, and Escherichia coli malate dehydrogenases.

Authors:  W H Murphey; C Barnaby; F J Lin; N O Kaplan
Journal:  J Biol Chem       Date:  1967-04-10       Impact factor: 5.157

5.  Malate dehydrogenases of leaf tissue from Spinacia oleracea: properties of three isoenzymes.

Authors:  V Rocha; I P Ting
Journal:  Arch Biochem Biophys       Date:  1971-11       Impact factor: 4.013

6.  Malic dehydrogenases in corn root tips.

Authors:  I P Ting
Journal:  Arch Biochem Biophys       Date:  1968-07       Impact factor: 4.013

7.  Ligand-induced association-dissociation as a means for enzyme purification.

Authors:  A Levitzki; D E Koshland
Journal:  Biochim Biophys Acta       Date:  1970-06-10

8.  [Molecular weight of Soya cotyledon malate dehydrogenase].

Authors:  Z S Bronovitskaia; V L Kretovich
Journal:  Dokl Akad Nauk SSSR       Date:  1970-01

9.  Characterization of some glyoxysomal proteins.

Authors:  R W Breidenbach
Journal:  Ann N Y Acad Sci       Date:  1969-12-19       Impact factor: 5.691

10.  Double-disc electrophoresis of proteins.

Authors:  D Racusen
Journal:  Nature       Date:  1967-03-04       Impact factor: 49.962

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  7 in total

1.  Glyoxysomal malate dehydrogenase of watermelon cotyledons: De novo synthesis on cytoplasmic ribosomes.

Authors:  R A Walk; B Hock
Journal:  Planta       Date:  1977-01       Impact factor: 4.116

2.  Chorion peroxidase-mediated NADH/O(2) oxidoreduction cooperated by chorion malate dehydrogenase-catalyzed NADH production: a feasible pathway leading to H(2)O(2) formation during chorion hardening in Aedes aegypti mosquitoes.

Authors:  Q Han; G Li; J Li
Journal:  Biochim Biophys Acta       Date:  2000-10-18

3.  Subcellular distribution and chemical form of cadmium in bean plants.

Authors:  H J Weigel; H J Jäger
Journal:  Plant Physiol       Date:  1980-03       Impact factor: 8.340

4.  Mitochondrial malate dehydrogenase of watermelon cotyledons: Time course and mode of enzyme activity changes during germination.

Authors:  R A Walk; B Hock
Journal:  Planta       Date:  1976-01       Impact factor: 4.116

5.  Glyoxysomal and mitochondrial malate dehydrogenase of watermelon (Citrullus vulgaris) cotyledons : I. Molecular properties of the purified isoenzymes.

Authors:  R A Walk; S Michaeli; B Hock
Journal:  Planta       Date:  1977-01       Impact factor: 4.116

6.  Glyoxysomal malate dehydrogenase and malate synthase from soybean cotyledons (Glycine max L.): enzyme association, antibody production and cDNA cloning.

Authors:  N Guex; H Henry; J Flach; H Richter; F Widmer
Journal:  Planta       Date:  1995       Impact factor: 4.116

7.  Purification and molecular properties of malate dehydrogenase from the marine diatom Nitzschia alba.

Authors:  A Y Yueh; C S Chung; Y K Lai
Journal:  Biochem J       Date:  1989-02-15       Impact factor: 3.857

  7 in total

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