Abstract
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]GA8 and [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.
Full text
PDF



Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Fujioka S., Yamane H., Spray C. R., Phinney B. O., Gaskin P., Macmillan J., Takahashi N. Gibberellin A(3) Is Biosynthesized from Gibberellin A(20) via Gibberellin A(5) in Shoots of Zea mays L. Plant Physiol. 1990 Sep;94(1):127–131. doi: 10.1104/pp.94.1.127. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rood S. B., Koshioka M., Douglas T. J., Pharis R. P. Metabolism of tritiated gibberellin a(20) in maize. Plant Physiol. 1982 Dec;70(6):1614–1618. doi: 10.1104/pp.70.6.1614. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rood S. B., Pharis R. P., Koshioka M. Reversible conjugation of gibberellins in situ in maize. Plant Physiol. 1983 Oct;73(2):340–346. doi: 10.1104/pp.73.2.340. [DOI] [PMC free article] [PubMed] [Google Scholar]