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Plant Physiology 82:241-246 (1986)
© 1986 American Society of Plant Biologists

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Articles

Metabolism of Gibberellin A12-7-Aldehyde by Soybean Cotyledons and Its Use in Identifying Gibberellin A7 as an Endogenous Gibberellin 1

Paul R. Birnberg, Mark L. Brenner, Marcia C. Mardaus, Hiroshi Abe2 and Richard P. Pharis

Department of Horticultural Sciences and Landscape Architecture, University of Minnesota, St. Paul, Minnesota 55108, Metabolism and Radiation Research Laboratory, United States Department of Agriculture, Fargo, North Dakota 58105, Plant Physiology Research Group, Department of Biology, University of Calgary, Calgary, Alberta T2N1N4, Canada

The level of gibberellin(GA)-like material in cotyledons of soybean (Glycine max L.) was highest at mid-pod fill—about 10 nanograms GA3 equivalents per gram fresh weight of tissue, assayed in the immersion dwarf rice bioassay. This amount is about 1000-fold less than levels in Pisum and Phaseolus seed, other legume species whose spectrum of endogenous gibberellins (GAs) is well known. The metabolism of [14C]-GA12-7-aldehyde (GA12ald)—the universal GA precursor—by intact, mid-pod-fill, soybean cotyledons and their cell-free extracts was investigated. In 4 hours, extracts converted GA12ald to two products—[14C]GA12 (42% yield) and [14C]GA15 (7%). Within 5 minutes, intact embryos converted GA12ald to [14C]GA12 and [14C]GA15 in 15% yield; 4 hour incubations afforded at least 22 products (96% total yield). The putative [14C]GA12 was identified as a product of [14C]GA12ald metabolism on the basis of co-chromatography with authentic GA12 on a series of reversed and normal phase high pressure liquid chromatography (HPLC) and thin-layer chromatography (TLC) systems, and by a dual feed of the putative [14C]GA12 and authentic [14C]GA12 to cotyledons of both peas and soybeans. The [14C]GA15 was identified as a metabolite of [14C]GA12ald by capillary gas chromatography (GC)-mass-spectrometry-selected ion monitoring, GC-radiocounting, HPLC, and TLC. By adding the [14C] metabolites of [14C]GA12ald to a different and larger extract (about 0.2 kg fresh weight of soybean reproductive tissue) and purifying endogenous substances co-chromatographing with these metabolites, at least two GA-like substances were obtained and one identified as GA7 by GC-mass spectrometry. Since [14C]GA9 was not found as a [14C]metabolite of [14C]GA12ald, soybean embryos might have a pathway for biosynthesis of active, C-19 gibberellins like that of the cucurbits; GA12ald -> GA12 -> GA15 -> GA24 -> GA36 -> GA4 -> GA7.


2 Present address: Laboratory of Pesticide Chemistry, Department of Plant Protection, Faculty of Agriculture, Tokyo University of Agriculture and Technology, Saiwa-cho, Fucha, Tokyo 183, Japan.

1 Supported in part by Monsanto Agricultural Products, and Natural Sciences and Engineering Research Council of Canada, Grant No. A-2585. Contribution from the University of Minnesota Agricultural Experiment Station, St. Paul, MN. Paper No. 14650, Scientific Journal Series.







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ASPB Publications PLANT PHYSIOLOGY® THE PLANT CELL
Copyright © 1986 by the American Society of Plant Biologists