Gibberellin Biosynthesis in Maize. Metabolic Studies with GA15, GA24, GA25, GA7, and 2,3-Dehydro-GA9
ISSN: | 1532-2548 0032-0889 |
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DOI: | 10.1104/pp.121.3.1037 |
Přístupová URL adresa: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d5569d304a0fbd28825bc2d5dbb37ca https://doi.org/10.1104/pp.121.3.1037 |
Rights: | OPEN |
Přírůstkové číslo: | edsair.doi.dedup.....7d5569d304a0fbd28825bc2d5dbb37ca |
Autor: | Gordon Davis, Theo Lange, Jake MacMillan, Paul Gaskin, S. J. Croker, Bernard O. Phinney, Masatomo Kobayashi |
Rok vydání: | 1999 |
Předmět: | |
Zdroj: | Plant Physiology. 121:1037-1045 |
ISSN: | 1532-2548 0032-0889 |
DOI: | 10.1104/pp.121.3.1037 |
Popis: | [17-(14)C]-Labeled GA(15), GA(24), GA(25), GA(7), and 2,3-dehydro-GA(9) were separately injected into normal, dwarf-1 (d1), and dwarf-5 (d5) seedlings of maize (Zea mays L.). Purified radioactive metabolites from the plant tissues were identified by full-scan gas chromatography-mass spectrometry and Kovats retention index data. The metabolites from GA(15) were GA(44), GA(19), GA(20), GA(113), and GA(15)-15,16-ene (artifact?). GA(24) was metabolized to GA(19), GA(20), and GA(17). The metabolites from GA(25) were GA(17), GA(25) 16alpha,17-H(2)-17-OH, and HO-GA(25) (hydroxyl position not determined). GA(7) was metabolized to GA(30), GA(3), isoGA(3) (artifact?), and trace amounts of GA(7)-diene-diacid (artifact?). 2,3-Dehydro-GA(9) was metabolized to GA(5), GA(7) (trace amounts), 2,3-dehydro-GA(10) (artifact?), GA(31), and GA(62). Our results provide additional in vivo evidence of a metabolic grid in maize (i.e. pathway convergence). The grid connects members of a putative, non-early 3,13-hydroxylation branch pathway to the corresponding members of the previously documented early 13-hydroxylation branch pathway. The inability to detect the sequence GA(12) --> GA(15) --> GA(24) --> GA(9) indicates that the non-early 3,13-hydroxylation pathway probably plays a minor role in the origin of bioactive gibberellins in maize. |
Databáze: | OpenAIRE |
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