On the treatment with acetic anhydride-pyridine at room temparature the four glucosldes gave the ccrresponding acetates. Chemical shifts in the NMR spectra of the glucosides and their acetates are summarized in Table. Esterification of a crystalline F-II tetraacetate (II), Cj~H40015H20\*\*, m.p. 20
Gibberellin in immature seeds of pharbitis nil
โ Scribed by Nobutaka Takahashi; Noboru Murofushi; Takao Yokota; Saburo Tamura
- Publisher
- Elsevier Science
- Year
- 1967
- Tongue
- French
- Weight
- 205 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
โฆ Synopsis
The presence of glbberellln-like substances in immature seeds of morning-glory (Pharbltis a)
has been suggested by Ogawa !
(1,2), Murakami (3) and Zeevaat (4). Now we wish to report the Isolation and structure of a new gibberellln, tentatively named Pharbltis Gibberellln, as well as the presence of gibberellln A3 (GA3) in the seeds. The ethyl acetate-soluble acidic fraction obtained from 60 kg of Immature seeds was successively subjected to ten transfers counter-current distribution method and charcoal chromatography. Elution with acetone-water mixtures, 50:50 and 70:30, gave active fractions, F-I and F-II, respectively. Histogram obtained from thin layer chromatography* and bioassay revealed that different active principles are contained in F-I and F-II. Each fraction was purified through successive procedures: sillcic acid adsorption, partition and preparative thin layer chromatography. F-I thus purified showed a fluorescent spot** at RGA 1.00 on thin layer chromatogram without heating. 3 This spot also exhibited marked growth promoting activity to dwarf maize mutant d-5. When methyl ester of pure F-I was subjected to thin layer chromatography, It revealed a fluorescent spot, whose Rf value was Identical with that of GA 3 methyl ester. Thus, the presence of GA3 In the seeds was established. * Solvent system: for acidic fraction, benzene-n-btitanol-acetic acid (70:25:5, v/v). Adsorbent: Silica gel G. ** When plates are sprayed with 70 $ (v/v) sulfuric acid and heated at 100ยฐ, all known gibberellins give blue or green fluorescent spots under ultraviolet light. GA3 and GA7 give fluorescence without heating.
๐ SIMILAR VOLUMES
We have isolated seven gibberellin glucosides (1, 2) from immature seeds of morning-glory (Pharbitis nil) and elucidated the structures of six of them - (3). Now we wish to report the structure of a new gibberellin glucoside, tentatively termed F-VII.
Isolation and. biological activities of new gibberellins A26 and A27 in immature seeds of the Japanese morning-glory (Pharbitis nil) have been reported - (1). We wish to report here the elucidation of their structures. Gibberellin A26 (GA26), m.p. 254-257", formed a monomethyl ester (II), m.p. 207
The presence of tkree water-soluble gibberellins was confirmed in immature seeds of morning-glory (Pharbitis nil). The structure of the main component has been elucidated as 2-O-fl-glucosyl-gibbereUin A s. It shows marked growth-promoting activity on rice seedlings but is far less active on dwarf ma
Gibberellin-like substances have been shown to occur in iss&ure seeds of Lupinus Zuteus (1-4) and an attempt was made to purify two active principles, which were tentatively named as Lupinus gibberellin I and II (5) . The former structure, whose provisional name was \*\* renamed as gibberellin Al8