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Functional Plant Biology Functional Plant Biology Society
Plant function and evolutionary biology
RESEARCH ARTICLE

Endogenous Biosynthetic Precursors of (+)-Abscisic Acid. III. Incorporation of 2H from 2H2O and 18O from 18O2 into Precursors

A. G. Netting, M. L. Windsor and B. V. Milborrow

Australian Journal of Plant Physiology 24(2) 175 - 184
Published: 1997

Abstract

Deuterium from 2H2O was incorporated into the methyl abscisate released from components of the ‘adduct’ (Netting, Willows and Milborrow, Plant Growth Regulation11: 327–334, 1992) fraction and into the free abscisic acid in stressed tomato seedlings. Incorporation of deuterium after 7 or 10 days of daily wilt/recover cycles suggested that components of the adduct fraction could be precursors of free abscisic acid. It was then found that when seedlings, that had been through seven wilt/recover cycles in 2H2O were put through four wilt and recover cycles in 1H2O, the methyl abscisate released from the adduct components had significant incorporation of protium, as did the free abscisic acid from the same plant organs. The pattern of protium incorporation raised the possibility that some of the adduct components were synthesised in the roots in response to stress and were then transported to the shoot, where they broke down to liberate free abscisic acid.

When tomato shoots were wilted in an 18O2 atmosphere they incorporated 18O into the methyl abscisate plus abscisic acid released from the ‘ketone’ fraction of the adduct group of compounds at a high level in mildly stressed plants. It was possible that 18O was similarly incorporated into the methyl abscisate plus abscisic acid from the ‘enolate’ fraction of adduct when plants were wilted to between 4% and 17% water loss. These experiments led to the conclusion that components of the adduct fraction were the endogenous precursors of stress-induced abscisic acid. It appeared that they were produced from a precursor pool in response to stress and then rapidly broke down to liberate abscisic acid (and methyl abscisate).

https://doi.org/10.1071/PP96057

© CSIRO 1997

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