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New Hydroxydecanoic Acid Derivatives Produced by an Dndophytic Yeast Aureobasidium pullulans AJF1 from Flowers of Aconitum carmichaeli

机译:来自乌头菌的花朵,由浅褐酵母花香蛋白酶蛋白胶蛋白胶蛋白蛋白胶蛋白蛋白胶蛋白蛋白胶。

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摘要

Endophytes have been recognized as a source for structurally novel and biologically active secondary metabolites. Among the host plants for endophytes, some medicinal plants that produce pharmaceuticals have been reported to carry endophytes, which could also produce bioactive secondary metabolites. In this study, the medicinal plant Aconitum carmichaeli was selected as a potential source for endophytes. An endophytic microorganism, Aureobasidium pullulans AJF1, harbored in the flower of Aconitum carmichaeli, was cultured on a large scale and extracted with an organic solvent. Extensive chemical investigation of the extracts resulted in isolation of three lipid type compounds (1−3), which were identified to be (3R,5R)-3,5-dihydroxydecanoic acid (1), (3R,5R)-3-(((3R,5R)-3,5-dihydroxydecanoyl)oxy)-5-hydroxydecanoic acid (2), and (3R,5R)-3-(((3R,5R)-5-(((3R,5R)-3,5-dihydroxydecanoyl)oxy)-3-hydroxydecanoyl)oxy)-5-hydroxydecanoic acid (3) by chemical methods in combination with spectral analysis. Compounds 2 and 3 had new structures. Absolute configurations of the isolated compounds (1−3) were established using modified Mosher’s method together with analysis of NMR data for their acetonide derivatives. All the isolates (1−3) were evaluated for antibiotic activities against Escherichia coli, Staphylococcus aureus, Bacillus subtilis, Pseudomonas aeruginosa, and their cytotoxicities against MCF-7 cancer cells. Unfortunately, they showed low antibiotic activities and cytotoxic activities.
机译:Endophytes已被认为是在结构新颖和生物活性次级代谢物的结构上的源。在Endophytes的宿主植物中,据报道,一些产生药物的药用植物携带Endophytes,其也可以产生生物活性次级代谢物。在这项研究中,选择了药用植物的乌头菌Carmichaeli作为Endophytes的潜在来源。在Aconitum carmichaeli的花朵中,在大规模培养并用有机溶剂培养,在乌头姆核心群岛上培养并培养了内生微生物。提取物的广泛化学研究导致分离三种脂质型化合物(1-3),其被鉴定为(3R,5R)-3,5-二羟基二烷酸(1),(3R,5R)-3-( ((3R,5R)-3,5-二羟基二烷酰基)氧基)-5-羟基二癸酸(2),和(3R,5R)-3 - (((3R,5R)-5 - (((3R,5R) -3,5-二羟基二烷酰基)氧基)-3-羟基二烷酰基)氧基)-5-羟基癸酸(3)通过化学方法与光谱分析组合。化合物2和3具有新的结构。使用改性的Mosher的方法与其丙酮酮衍生物的NMR数据分析建立了分离的化合物(1-3)的绝对配置。针对大肠杆菌,金黄色葡萄球菌,枯草芽孢杆菌,假单胞菌植物,铜绿假单胞菌及其对MCF-7癌细胞的细胞毒性的抗生素活性评估了所有分离株(1-3)。不幸的是,它们显示出低抗生素活性和细胞毒性活动。

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