Native gibberellins and the metabolism of [14C]gibberellin A53 and of [17-13C, 17-3H2]gibberellin A20 in tassels of Zea mays |
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Authors: | Rick C. Heupel Bernard O. Phinney Clive R. Spray Paul Gaskin Jake MacMillan Peter Hedden Jan E. Graebe |
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Affiliation: | 1. School of Chemistry, University of Bristol, Bristol BS8 1TS, U.K.;2. Pflanzenphysiologisches Institut der Universität, 3400 Göttingen, West Germany |
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Abstract: | The native hormones from tassels of maize (Zea mays) were re-investigated. The previous identification by GC/SIM of GA1, GA8 and GA29 in normal tassels was confirmed by full GC/MS scans at the correct Kovats retention indices. In tassels of dwarf-1 mutants, GA44,?GA19, GA17, GA20 and the 16,17-dihydro, 7β,16α,17-trihydroxy derivative of ent-kaurenoic acid were identified by GC/MS. Gibberellin A1 was not found in the mutant tassels. [14C]Gibberellin A53 was fed to tassels of the dwarf-5 mutant. In the ethyl acetate-soluble acidic fraction from the feeds, [14C]GA44 was identified by GC/MS; [14C]GA19 and [14C]GA29 were identified by GC/SIM. The GA29 is probably a metabolite of the feeds because the dwarf-5 mutant is known to control the step copalyl pyrophosphate to ent-kaurene in the maize GA-biosynthetic pathway and because GA29 was not identified in a control experiment. The n-butanol fractions obtained from the feeds were shown, by GC/MS, to contain [14C]GA53 after hydrolysis, suggesting that conjugated [14C]GA53 is a major metabolite from GA53 feeds. [17-13C, 17-3H2]Gibberellin A20 was fed to normal, dwarf-1 and dwarf-5 tassels. In each case, analysis of the purified ethyl acetate-soluble acidic extracts by GC/MS led to the identification of [13C]GA29 and unmetabolized [13C]GA20 in which no 13C-isotope dilution was observed. |
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Keywords: | Gramineae tassels normal metabolism gibberellins GC/RC GC/MS and GC/SIM identification Kovats retention index. |
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