In Plants, 3-<i>O</i>-Methylglucose Is Phosphorylated by Hexokinase But Not Perceived as a Sugar

  • Sandra Cortès
    Commissariat à l'Energie Atomique, Centre National de la Recherche Scientifique, and Université Joseph Fourier, Unité Mixte de Recherche 5019 Physiologie Cellulaire Végétale, 17 rue des Martyrs, 38054 Grenoble cedex 9, France (S.C., M.G., A.E., C.R.);
  • Marina Gromova
    Commissariat à l'Energie Atomique, Centre National de la Recherche Scientifique, and Université Joseph Fourier, Unité Mixte de Recherche 5019 Physiologie Cellulaire Végétale, 17 rue des Martyrs, 38054 Grenoble cedex 9, France (S.C., M.G., A.E., C.R.);
  • Adeline Evrard
    Commissariat à l'Energie Atomique, Centre National de la Recherche Scientifique, and Université Joseph Fourier, Unité Mixte de Recherche 5019 Physiologie Cellulaire Végétale, 17 rue des Martyrs, 38054 Grenoble cedex 9, France (S.C., M.G., A.E., C.R.);
  • Claude Roby
    Commissariat à l'Energie Atomique, Centre National de la Recherche Scientifique, and Université Joseph Fourier, Unité Mixte de Recherche 5019 Physiologie Cellulaire Végétale, 17 rue des Martyrs, 38054 Grenoble cedex 9, France (S.C., M.G., A.E., C.R.);
  • Alain Heyraud
    Centre National de la Recherche Scientifique, Unité Propre de Recherche 5301 Centre de Recherches sur les Macromolécules Végétales, Boı̂te Postale 53, 38041 Grenoble cedex 9, France (A.H.); and
  • Dominique B. Rolin
    Institut National de la Recherche Agronomique and UniversitéVictor Segalen Bordeaux 2, Unité Mixte de Recherche 619 Biotechnologie et Physiologie Végétales, Boı̂te Postale 81, 33883 Villenave d'Ornon cedex, France (D.B.R., P.R., R.M.B.)
  • Philippe Raymond
    Institut National de la Recherche Agronomique and UniversitéVictor Segalen Bordeaux 2, Unité Mixte de Recherche 619 Biotechnologie et Physiologie Végétales, Boı̂te Postale 81, 33883 Villenave d'Ornon cedex, France (D.B.R., P.R., R.M.B.)
  • Renaud M. Brouquisse
    Institut National de la Recherche Agronomique and UniversitéVictor Segalen Bordeaux 2, Unité Mixte de Recherche 619 Biotechnologie et Physiologie Végétales, Boı̂te Postale 81, 33883 Villenave d'Ornon cedex, France (D.B.R., P.R., R.M.B.)

抄録

<jats:title>Abstract</jats:title> <jats:p>In plants, sugars are the main respiratory substrates and important signaling molecules in the regulation of carbon metabolism. Sugar signaling studies suggested that sugar sensing involves several key components, among them hexokinase (HXK). Although the sensing mechanism of HXK is unknown, several experiments support the hypothesis that hexose phosphorylation is a determining factor. Glucose (Glc) analogs transported into cells but not phosphorylated are frequently used to test this hypothesis, among them 3-O-methyl-Glc (3-OMG). The aim of the present work was to investigate the effects and fate of 3-OMG in heterotrophic plant cells. Measurements of respiration rates, protein and metabolite contents, and protease activities and amounts showed that 3-OMG is not a respiratory substrate and does not contribute to biosynthesis. Proteolysis and lipolysis are induced in 3-OMG-fed maize (Zea mays L. cv DEA) roots in the same way as in sugar-starved organs. However, contrary to the generally accepted idea, phosphorous and carbon nuclear magnetic resonance experiments and enzymatic assays prove that 3-OMG is phosphorylated to 3-OMG-6-phosphate, which accumulates in the cells. Insofar as plant HXK is involved in sugar sensing, these findings are discussed on the basis of the kinetic properties because the catalytic efficiency of HXK isolated from maize root tips is five orders of magnitude lower for 3-OMG than for Glc and Man.</jats:p>

収録刊行物

  • Plant Physiology

    Plant Physiology 131 (2), 824-837, 2003-02-01

    Oxford University Press (OUP)

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