期刊
PHYTOCHEMISTRY
卷 207, 期 -, 页码 -出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.phytochem.2022.113568
关键词
Streptomyces aculeolatus Streptomycetaceae; Naphthoquinone; Siderophores; Antimalarial; Antimicrobial; Cytotoxicity
Seven undescribed compounds were isolated from the cultures of endophytic Streptomyces aculeolatus MS1-6, including four naphthoquinone terpenoids, one rare 2-nitropyrrole terpenoid, two hydroxamate siderophores, and one further undescribed compound. These compounds exhibited a broad spectrum of biological activities, including antimalarial, antitubercular, anti-plant pathogenic fungal, and antibacterial activities.
Seven undescribed compounds, including four naphthoquinone terpenoids (aculeolatins A - D), one rare 2-nitropyrrole terpenoid (nitropyrrolin F), and two hydroxamate siderophores (aculeolamides A and B) and one further undescribed compound (2,5,7-trihydroxy-3,6-dimethylnaphthalene-1,4-dione), together with eleven known compounds (arromycin, phenaziterpene A, nitropyrrolin A, heronapyrroles A and B, salaceyin A, 5,7-dihydroxy2-isopropylchromone, 1-hydroxyphenazine, 1-methoxyphenazine, 1-acetyl-beta-carboline, and N-(2-phenylethyl) acetamide), were isolated from the cultures of the endophytic Streptomyces aculeolatus MS1-6. The structures of the isolated compounds were determined using NMR spectroscopy and corroborated using chemical modification. These compounds exhibited a broad spectrum of biological activities, including antimalarial (IC50 6.03-9.84 mu g/mL), antitubercular (MIC 3.13-6.25 mu g/mL), anti-plant pathogenic fungal (MIC 25.0-50.0 mu g/mL), and antibacterial (MIC 3.03-50 mu g/mL) activities; however, they displayed unremarkable cytotoxicity against cancerous (MCF-7 and NCI-H187) and non-cancerous (Vero) cell lines.
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