Abstract
Experiments were designed to obtain evidence about the possible role of xanthophylls as abscisic acid (ABA) precursors in water-stressed leaves of Phaseolus vularis L. Leaves were exposed to 14CO2 and the specific activities of several major leaf xanthophylls and stress-induced ABA were determined after a chase in 12CO2 for varying periods of time. The ABA specific radioactivities were about 30 to 70% of that of lutein and violaxanthin regardless of the chase period. The specific activity of neoxanthin, however, was only about 15% of that of ABA. The effects of fluridone on xanthophyll and ABA levels and the extent of labeling of both from 14CO2 were determined. Fluridone did not inhibit the accumulation of ABA when leaves were stressed once, although subsequent stresses in the presence of fluridone did lead to a reduced ABA accumulation. The incorporation of 14C from 14CO2 into ABA and the xanthophylls was inhibited by fluridone and to about the same extent. The incorporation of 18O into ABA from violaxanthin which had been labeled in situ by means of the violaxanthin cycle was measured. The results indicated that a portion of the ABA accumulated during stress was formed from violaxanthin which had been labeled with 18O. The results of these experiments are consistent with a preformed xanthophyll(s) as the major ABA precursor in water-stressed bean leaves.
Full text
PDF





Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Creelman R. A., Zeevaart J. A. Incorporation of oxygen into abscisic Acid and phaseic Acid from molecular oxygen. Plant Physiol. 1984 May;75(1):166–169. doi: 10.1104/pp.75.1.166. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gamble P. E., Mullet J. E. Inhibition of carotenoid accumulation and abscisic acid biosynthesis in fluridone-treated dark-grown barley. Eur J Biochem. 1986 Oct 1;160(1):117–121. doi: 10.1111/j.1432-1033.1986.tb09947.x. [DOI] [PubMed] [Google Scholar]
- Milborrow B. V., Noddle R. C. Conversion of 5-(1,2-epoxy-2,6,6-trimethylcyclohexyl)-3-methylpenta-cis-2-trans-4-dienoic acid into abscisic acid in plants. Biochem J. 1970 Oct;119(4):727–734. doi: 10.1042/bj1190727. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Moore R., Smith J. D. Graviresponsiveness and abscisic-acid content of roots of carotenoid-deficient mutants of Zea mays L. Planta. 1985;164:126–128. [PubMed] [Google Scholar]
- Moore R., Smith J. D. Growth, graviresponsiveness and abscisic-acid content of Zea mays seedlings treated with fluridone. Planta. 1984;162:342–344. [PubMed] [Google Scholar]
- Noddle R. C., Robinson D. R. Biosynthesis of abscisic acid: incorporation of radioactivity from [2-14C]mevalonic acid by intact fruit. Biochem J. 1969 May;112(4):547–548. doi: 10.1042/bj1120547. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Taylor H. F., Smith T. A. Production of plant growth inhibitors from xanthophylls: a possible source of dormin. Nature. 1967 Sep 30;215(5109):1513–1514. doi: 10.1038/2151513a0. [DOI] [PubMed] [Google Scholar]
- Yamamoto H. Y., Higashi R. M. Violaxanthin de-epoxidase. Lipid composition and substrate specificity. Arch Biochem Biophys. 1978 Oct;190(2):514–522. doi: 10.1016/0003-9861(78)90305-3. [DOI] [PubMed] [Google Scholar]