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1955
DOI: 10.1271/bbb1924.19.267
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Biochemical Studies on “Bakanae” Fungus

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Cited by 55 publications
(9 citation statements)
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“…and a comparison of its chemical properties with those of the British gibberellic acid revealed both compounds to be the same substance [7]. Further investigations on the Japanese gibberellin A allowed to separate it into three different products named gibberellin A1 (1), A2 (2) and A3 (3) [8]. The latter compound was identified to be the same as the gibberellic acid isolated by the British and American researchers.…”
Section: Gibberellins: a Historical Perspectivementioning
confidence: 77%
See 1 more Smart Citation
“…and a comparison of its chemical properties with those of the British gibberellic acid revealed both compounds to be the same substance [7]. Further investigations on the Japanese gibberellin A allowed to separate it into three different products named gibberellin A1 (1), A2 (2) and A3 (3) [8]. The latter compound was identified to be the same as the gibberellic acid isolated by the British and American researchers.…”
Section: Gibberellins: a Historical Perspectivementioning
confidence: 77%
“…Restricting ourselves to the fungal gibberellins, between 1962 and 1968 the British isolated nine others, GA7 (5) and GA9 through GA16 (6)(7)(8)(9)(10)(11)(12)(13) [10][11][12][13][14][15][16][17]. Later on, MacMillan and cols.…”
Section: Gibberellins: a Historical Perspectivementioning
confidence: 99%
“…Similar modulation of host physiology by pathogens has been documented in plants. For example, the plant hormone gibberellic acid 7 was originally discovered in the pathogenic fungus Gibberella fujikuroi , the causative agent of Bakanae disease in rice . This fungus produces these endogenous plant elongation growth regulators causing overextension and structural failure of rice seedling stems, resulting in very high economic losses of rice crops …”
Section: Small Molecules In Terrestrial Plant Symbiosesmentioning
confidence: 99%
“…These discoveries spurred the Tokyo group to reexamine their material, and they found that it could be separated into three gibberellins--A, A2, and A3 (14). Recently, another, A4, has been isolated (15).…”
Section: Chemistry Of the Gibberellinsmentioning
confidence: 99%
“…Gibberellic acid's ready aromatization after lactone cleavage and its over-all structure seem unique; no previously known natural products or synthetic compounds are closely related. Mono-or diacetylation of the hydroxyl groups has little influence on the hormone's action, but it has been found, in the few tests so far reported (1,14,20), that esterification of the acid group greatly reduces or removes biological effectiveness.…”
Section: Chemistry Of the Gibberellinsmentioning
confidence: 99%