Metabolism of Methanol in Plant Cells. Carbon-13 Nuclear Magnetic Resonance Studies

Author:

Gout Elizabeth1,Aubert Serge2,Bligny Richard2,Rébeillé Fabrice2,Nonomura Arthur R.3,Benson Andrew A.4,Douce Roland2

Affiliation:

1. Laboratoire de Résonance Magnétique en Biologie Métabolique, Département de Biologie Moléculaire et Structurale, CEA–38054, Grenoble cedex 9, France (E.G.);

2. Laboratoire de Physiologie Cellulaire Végétale, Unité de Recherche Associée 576 Commissariat à l'Energie Atomique/Centre National de la Recherche Scientifique/UniversitéJoseph Fourier, CEA–38054, Grenoble cedex 9, France (S.A., R.B., F.R., R.D.);

3. Farlow Herbarium, Harvard University, Cambridge, Massachusetts 02138 (A.R.N.); and

4. Scripps Institution of Oceanography, University of California, San Diego, California 92093–0202 (A.A.B.)

Abstract

Abstract Using 13C-NMR, we demonstrate that [13C]methanol readily entered sycamore (Acer pseudoplatanus L.) cells to be slowly metabolized to [3-13C]serine, [13CH3]methionine, and [13CH3]phosphatidylcholine. We conclude that the assimilation of [13C]methanol occurs through the formation of 13CH3H4Pte-glutamate (Glu)n and S-adenosyl-methionine, because feeding plant cells with [3-13CH3]serine, the direct precursor of13CH2H4Pte-Glun, can perfectly mimic [13CH3]methanol for folate-mediated single-carbon metabolism. On the other hand, the metabolism of [13C]methanol in plant cells revealed assimilation of label into a new cellular product that was identified as [13CH3]methyl-β-d-glucopyranoside. The de novo synthesis of methyl-β-d-glucopyranoside induced by methanol did not require the formation of13CH3H4Pte-Glun and was very likely catalyzed by a “transglycosylation” process.

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

Reference40 articles.

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3. Evidence for three serine hydroxymethyltransferases in green leaf cells: purification and characterization of the mitochondrial and chloroplastic isoforms.;Besson;Plant Physiol Biochem,1995

4. Techniques of cell suspension cultures.;Bligny;Methods Enzymol,1987

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