Isolation, Structure Elucidation and Antifungal Activity of Angucycline Antibiotics from Streptomycete cellulosae

被引:2
|
作者
Xu, X. D. [1 ]
Zhao, Y. [1 ]
Bao, K. [1 ]
Miao, C. P. [1 ]
Tang, S. K. [1 ]
Wu, S. H. [1 ]
Li, Y. Q. [1 ]
机构
[1] Yunnan Univ, Coll Life Sci, Key Lab Microbial Divers Southwest China, Minist Educ, Kunming 650091, Peoples R China
基金
中国国家自然科学基金;
关键词
Streptomyces cellulosae; urdamycinone B; dehydroxyaquayamycin; isolation; PRODUCTS;
D O I
10.1134/S0003683823040178
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Streptomyces species are the major producers of antibiotics, and not many bioactive substances and antibiotics have been found in Streptomyces cellulosae. Two angucycline antibiotics were isolated from the ethyl acetate extract of the fermentation broth of the strain S. cellulosae YIM PH20352, they were identified as urdamycinone B (1) and dehydroxyaquayamycin (2) based on extensive spectroscopic analyses. Four root-rot pathogens of the Panax notoginseng including Alternaria panax, Plectosphaerella cucumerina, Fusarium oxysporum, and Fusarium solani were used for their antagonistic activity test. Compound 1 exhibited the most potent antifungal activity against A. panax and P. cucumerina with the MIC values at 16 and 64 & mu;g/mL, respectively; compound 2 exhibited antifungal activity against A. panax with the MIC value at 64 & mu;g/mL.
引用
收藏
页码:456 / 461
页数:6
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