Biological activity of some conjugated gibberellins
β Scribed by G. Sembdner; E. Borgmann; G. Schneider; H. W. Liebisch; O. Miersch; G. Adam; M. Lischewski; K. Schrefber
- Book ID
- 104757647
- Publisher
- Springer-Verlag
- Year
- 1976
- Tongue
- English
- Weight
- 764 KB
- Volume
- 132
- Category
- Article
- ISSN
- 0032-0935
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β¦ Synopsis
The biological activity of several gibberellin (GA) conjugates was studied and compared with that of the corresponding free GAs. The following conjugates were included: O(3)-/~-D-glucopyranosides of GA~, GA 3 and GA4; O(13)-fl-D-glucopyranosides of GA1, GA3 and GAs; O(13)-fl-D-glucopyranosyl-GAs-fl-D-glucopyranosyl ester; GA3-fl-D-glucopyranosyl ester and GA3-7-D-glucopyranosyl ester; N-GA3-0yl-glycine, its methyl ester, N-GA3-0yl-glycylglycine, and N-GA3-0yl-proline. All compounds were synthesized chemically but some of them are known to occur as endogenous plant products, or to be formed in plants upon application of a free GA. Activity was determined in the dwarf pea, dwarf corn, dwarf rice, and lettuce hypocotyl bioassays. The GA conjugates were found to possess different relative activities depending on the chemical structure, the bioassay system, and the site of application (shoot or roots). It is concluded that the activity of GA conjugates as measured in different bioassays is based upon the ability of plant enzymes and possibly of certain microorganisms to hydrolyze glucosidic, glucosyl ester, and amide-like linkages.
π SIMILAR VOLUMES
The biological activities of GA40, GA43, GA46, GA47, GA51 and GA4 20,4-lactone were tested over a wide range of concentrations in six plant bioassays. GA4 20,4-lactone showed the highest activity. Of the two 2Ξ±-hydroxylated compounds GA47 showed moderately high activity, and GA40 was slightly active