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寡霉素 A 和 C,从新分离的链霉菌中分离得到的主要次级代谢产物。

Oligomycins A and C, major secondary metabolites isolated from the newly isolated strain Streptomyces diastaticus.

机构信息

Key Laboratory for Microbial Resources, Ministry of Education, and Laboratory for Conservation and Utilization of Bio-Resources, Yunnan Institute of Microbiology, Yunnan University, Kunming, Yunnan 650091, P.R. China.

出版信息

Folia Microbiol (Praha). 2010 Jan;55(1):10-6. doi: 10.1007/s12223-010-0002-0. Epub 2010 Mar 25.

Abstract

During the screening program for fungicides, one actinomycete strain ECO 00047 was isolated with the potential activity against fungus. According to the morphology and analysis of the nucleotide sequence of the 16S rRNA gene (1500 bp) this isolate was identified as Streptomyces diastaticus. The active compounds were separated by silica gel column chromatography, Sephadex LH-20 gel filtration and then purified by flash chromatography on C18 (20-45 microm). The chemical structure of the bioactive compounds I and II were elucidated, based on the spectroscopic data of MS, IR, UV, 1H-NMR, 13C-NMR and X-ray single crystal diffraction analysis. Compounds I and II were identical with oligomycins A and C, the macrolide antibiotics which have been known to be produced by Streptomyces diastatochromogenes, S. libani and S. avermitilis. The two compounds exhibited a strong activity against Aspergillus niger, Alternaria alternata, Botrytis cinerea and Phytophthora capsici but no activity toward bacteria. Although the two above antibiotics were known, their isolation has so far not been reported from S. diastaticus.

摘要

在杀菌剂的筛选计划中,分离到一株具有抗真菌活性的放线菌 ECO 00047。根据形态学和 16S rRNA 基因(1500bp)的核苷酸序列分析,该分离株被鉴定为解淀粉链霉菌。通过硅胶柱层析、葡聚糖 LH-20 凝胶过滤和 C18(20-45μm)快速色谱进一步分离活性化合物。根据 MS、IR、UV、1H-NMR、13C-NMR 和 X 射线单晶衍射分析的光谱数据,阐明了生物活性化合物 I 和 II 的化学结构。化合物 I 和 II 与寡霉素 A 和 C 一致,寡霉素 A 和 C 是已知由解淀粉链霉菌、利邦链霉菌和阿维链霉菌产生的大环内酯类抗生素。这两种化合物对黑曲霉、链格孢、灰葡萄孢和辣椒疫霉表现出很强的活性,但对细菌没有活性。尽管这两种抗生素是已知的,但迄今为止尚未从解淀粉链霉菌中分离得到。

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