Biosynthesis of the Halogenated Auxin, 4-Chloroindole-3-Acetic Acid

Author:

Tivendale Nathan D.1,Davidson Sandra E.1,Davies Noel W.1,Smith Jason A.1,Dalmais Marion1,Bendahmane Abdelhafid I.1,Quittenden Laura J.1,Sutton Lily1,Bala Raj K.1,Le Signor Christine1,Thompson Richard1,Horne James1,Reid James B.1,Ross John J.1

Affiliation:

1. School of Plant Science (N.D.T., S.E.D., L.J.Q., L.S., R.K.B., J.B.R., J.J.R.), Central Science Laboratory (N.W.D., J.H.), and School of Chemistry (N.D.T., J.A.S.), University of Tasmania, Sandy Bay, Tasmania, Australia 7005; Unité de Recherche en Génomique Végétale, 2 Evry, France 91018 (M.D., A.I.B.); and Unité Mixte de Recherche 1347 Agroécologie, Institut National de la Recherche Agronomique,

Abstract

Abstract Seeds of several agriculturally important legumes are rich sources of the only halogenated plant hormone, 4-chloroindole-3-acetic acid. However, the biosynthesis of this auxin is poorly understood. Here, we show that in pea (Pisum sativum) seeds, 4-chloroindole-3-acetic acid is synthesized via the novel intermediate 4-chloroindole-3-pyruvic acid, which is produced from 4-chlorotryptophan by two aminotransferases, TRYPTOPHAN AMINOTRANSFERASE RELATED1 and TRYPTOPHAN AMINOTRANSFERASE RELATED2. We characterize a tar2 mutant, obtained by Targeting Induced Local Lesions in Genomes, the seeds of which contain dramatically reduced 4-chloroindole-3-acetic acid levels as they mature. We also show that the widespread auxin, indole-3-acetic acid, is synthesized by a parallel pathway in pea.

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

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