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V. Frydman, J. Macmillan (1973)
Identification of gibberellins A20 and A29 in seed of Pisum sativum cv. Progress No. 9 by combined gas chromatography-mass spectrometryPlanta, 115
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H. Yamane, N. Murofushi, Hideo Osada, N. Takahashi (1977)
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N. Takahashi, N. Murofushi, T. Yokota (1972)
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J. Macmillan, C. Wels (1974)
Detailed analysis of metabolites from mevalonic lactone in Gibberella fujikuroiPhytochemistry, 13
V. Frydman, P. Gaskin, J. Macmillan (1974)
Qualitative and quantitative analyses of gibberellins throughout seed maturation in Pisum sativum cv. Progress No. 9Planta, 118
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The biosynthesis of a C19-gibberellin from mevalonic acid in a cell-free system from a higher plantPlanta, 120
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The biological activities of some new gibberellins (GAs) in six plant bioassaysPlanta, 135
I.D. Railton (1976)
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V. Frydman, J. Macmillan (1975)
The metabolism of gibberellins A9, A20 and A29 in immature seeds of Pisum sativum cv. Progress No. 9Planta, 125
J. Bearder, V. Frydman, P. Gaskin, I. Hatton, W. Harvey, J. Mcmillan, B. Phinney (1976)
Fungal products. Part XVII. Microbiological hydroxylation of gibberellin A9 and its methyl ester.Journal of the Chemical Society. Perkin transactions 1, 2
D.R. Reeve, A. Crozier (1975)
Gibberellins and plant growth
I. Yamaguchi, M. Miyamoto, H. Yamane, N. Murofushi, N. Takahashi, K. Fujita (1975)
Elucidation of the structure of gibberellin A40 from Gibberella fujikuroiJournal of The Chemical Society-perkin Transactions 1, 6
J. Macmillan (1977)
Some Aspects of Gibberellin Metabolism in Higher Plants
J. Bearder, V. Frydman, P. Gaskin, J. Macmillan, C. Wels, B. Phinney (1976)
Fungal products. Part XVI. Conversion of isosteviol and steviol acetate into gibberellin analogues by mutant b1-41a of Gibberella fujikuroi and the preparation of (3H)gibberellin A20.Journal of the Chemical Society. Perkin transactions 1, 2
Seed maturation of Pisum sativum cv. Progress No. 9 proceeds more slowly in winter than in summer even when the parent plants are grown in greenhouse conditions with light-and heat-supplementation. For parent plants grown under “summer” and “winter” conditions the metabolism of [3H]GA9 in cultured seeds is qualitatively different in seeds of equivalent age and qualitatively the same in seeds of equivalent weight. 13-Hydroxylation of [3H]GA9→[3H]GA20 is restricted to early stages of seed development. 2β-Hydroxylation of [3H]GA9→2β-OH-[3H]GA9 has only been observed at a stage of development after endogenous GA9 has accumulated. 2β-OH-GA9 has been shown to be endogenous to pea and is named GA51. H2-GA31 and its conjugate have not been shown to be present in pea and may be induced metabolites of [3H]GA9. The metabolism of GA20→GA29 is used to illustrate a technique of feeding [2H][3H]GAs in order to distinguish a metabolite from the same endogenous compound. The in vitro conversion of [3H]GA20→[3H]GA29, and the virtual non-metabolism of [3H]GA29 have been confirmed for seeds in intact fruits. These results are discussed in relation to the apparent absence of conjugated GAs in mature pea seeds.
Planta – Springer Journals
Published: Sep 13, 2004
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