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Plant Physiology 100:1457-1463 (1992)
© 1992 American Society of Plant Biologists

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Development and Growth Regulation

Metabolism of Indole-3-Acetic Acid by Pericarp Discs from Immature and Mature Tomato (Lycopersicon esculentum Mill) 1

Carmen Catalá, Anders Östin, Jesús Chamarro, Göran Sandberg and Alan Crozier

Instituto de Agroquímica y Tecnología de Alimentos, Consejo Superior de Investigaciones Científicas, Jaime Roig 11, 46010 Valencia, Spain, Department of Forest Genetics and Plant Physiology, The Swedish University of Agricultural Sciences, S-901 83 Umeå, Sweden, Department of Botany, School of Biological Sciences, The University, Glasgow G12 8QQ, United Kingdom

[1'-14C, 13C6]Indole-3-acetic acid was infiltrated into immature pericarp discs from fruits of tomato (Lycopersicon esculentum Mill., cv Moneymaker). After a 24-h incubation period the discs were extracted with methanol and the partially purified extract was analyzed by reversed-phase high-performance liquid chromatography-radiocounting. Five metabolite peaks (1-5) were detected and subsequently analyzed by combined high-performance liquid chromatography-frit-fast atom bombardment-mass spectrometry. The metabolite 4 fraction was found to contain [13C6]-indole-3-acetylaspartic acid, and analysis of metabolite 5 identified [13C6]indole-3-acetyl-{beta}-D-glucose. The other metabolites could not be identified, but alkaline hydrolysis studies and gel permeation chromatography indicated that metabolites 1 and 3 were both amide conjugates with a molecular weight of approximately 600. Studies with radiolabeled indole-3-acetic acid, indole-3-acetylaspartic acid, and indole-3-acetyl-{beta}-D-glucose demonstrated that in immature pericarp indole-3-acetic acid is deactivated primarily via metabolism to indole-3-acetylaspartic acid, which is further converted to metabolites 1, 2, and 3. In mature, pink pericarp discs, indole-3-acetic acid is converted more extensively to its glucosyl conjugate. Conjugation of indole-3-acetic acid to indole-3-acetylaspartic acid appears to be dependent upon protein synthesis because it is inhibited by cycloheximide. In contrast, cycloheximide has little effect on the further conversion of indole-3-acetylaspartic acid to metabolites 1, 2, and 3.


1 This work constitutes partial fulfillment of the requirements for the degree of Ph.D. by C.C., who received a fellowship (Formacion de Personal Investigador) from the Ministerio Español de Educación y Ciencia and was supported by the Comisión Asesora de Investigación Científica y Técnica (ALI-88-256-CO2). Support was also received from The Thunholm Foundation (A.Ö.), The British Council (J.C., A.C.), and The Swedish Council for Forestry and Agricultural Research (G.S.).




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A. Jakubowska and S. Kowalczyk
The auxin conjugate 1-O-indole-3-acetyl-{beta}-D-glucose is synthesized in immature legume seeds by IAGlc synthase and may be used for modification of some high molecular weight compounds
J. Exp. Bot., April 1, 2004; 55(398): 791 - 801.
[Abstract] [Full Text] [PDF]




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Copyright © 1992 by the American Society of Plant Biologists