Hydrolysis and Reconjugation of Gibberellin A20Glucosyl Ester by Seedlings of Zea mays L

The [6-2H]glucosyl ester of [17-13C,3H]gibberellin A20(GA20) was injected into light-grown 14-day-old seedlings of normal, dwarf-1, and dwarf-5 maize (Zea mays L.). The plant material was extracted 24 h later, and the extracts were purified by solvent partitioning, column chromatography, and HPLC.13...

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Published inProceedings of the National Academy of Sciences - PNAS Vol. 89; no. 17; pp. 8045 - 8048
Main Authors Schneider, Gernot, Jensen, Einar, Spray, Clive R., Phinney, Bernard O.
Format Journal Article
LanguageEnglish
Published National Academy of Sciences of the United States of America 01.09.1992
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Summary:The [6-2H]glucosyl ester of [17-13C,3H]gibberellin A20(GA20) was injected into light-grown 14-day-old seedlings of normal, dwarf-1, and dwarf-5 maize (Zea mays L.). The plant material was extracted 24 h later, and the extracts were purified by solvent partitioning, column chromatography, and HPLC.13C-labeled metabolites were identified from the purified extracts by full-scan gas chromatography/mass spectrometry and selected ion current monitoring in conjunction with Kovats retention indices. The metabolites, [13C]GA20, [13C]GA29, [13C]GA20-13-O-glucoside, and [13C]GA29-2-O-glucoside, were identified from normal, dwarf-1, and dwarf-5 seedlings. [13C]GA8and [13C]GA8-2-O-glucoside were also identified from normal and dwarf-5 seedlings but not from dwarf-1 seedlings. The data provide definitive evidence for the endogenous hydrolysis by the seedlings of the introduced conjugate and its reconjugation to three glucosides.
ISSN:0027-8424
1091-6490