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Four New Isocoumarins and a New Natural Tryptamine with Antifungal Activities from a Mangrove Endophytic Fungus Botryosphaeria ramosa L29.


ABSTRACT: Four new isocoumarin derivatives, botryospyrones A (1), B (2), C (3), and D (4), and a new natural tryptamine, (3aS, 8aS)-1-acetyl-1, 2, 3, 3a, 8, 8a-hexahydropyrrolo [2,3b] indol-3a-ol (5), were isolated from a marine mangrove endophytic fungus Botryosphaeria ramosa L29, obtained from the leaf of Myoporum bontioides. Their structures were elucidated using spectroscopic analysis. The absolute configurations of compounds 3, 4, and 5 were determined by comparison of their circular dichroism (CD) spectra with the calculated data. The inhibitory activities of compound 1 on Fusarium oxysporum, of compounds 2 and 3 on F. oxysporum and Fusarium graminearum, and of compound 5 on F. oxysporum, Penicillium italicum, and F. graminearum were higher than those of triadimefon, widely used as an agricultural fungicide. Compound 5 was produced after using the strategy we called "using inhibitory stress from components of the host" (UISCH), wherein (2R, 3R)-3, 5, 7-trihydroxyflavanone 3-acetate, a component of M. bontioides with weak growth inhibitory activity towards B. ramosa L29, was introduced into the culture medium.

SUBMITTER: Wu Z 

PROVIDER: S-EPMC6410081 | biostudies-literature | 2019 Feb

REPOSITORIES: biostudies-literature

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Four New Isocoumarins and a New Natural Tryptamine with Antifungal Activities from a Mangrove Endophytic Fungus <i>Botryosphaeria ramosa</i> L29.

Wu Zhihui Z   Chen Jiaqing J   Zhang Xiaolin X   Chen Zelin Z   Li Tong T   She Zhigang Z   Ding Weijia W   Li Chunyuan C  

Marine drugs 20190201 2


Four new isocoumarin derivatives, botryospyrones A (<b>1</b>), B (<b>2</b>), C (<b>3</b>), and D (<b>4</b>), and a new natural tryptamine, (3a<i>S</i>, 8a<i>S</i>)-1-acetyl-1, 2, 3, 3a, 8, 8a-hexahydropyrrolo [2,3b] indol-3a-ol (<b>5</b>), were isolated from a marine mangrove endophytic fungus <i>Botryosphaeria ramosa</i> L29, obtained from the leaf of <i>Myoporum bontioides</i>. Their structures were elucidated using spectroscopic analysis. The absolute configurations of compounds <b>3</b>, <b>  ...[more]

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