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Steffimycin E,一种新型抗分枝杆菌药物,针对鸟分枝杆菌复合群,由链霉菌 OPMA02852 产生。

Steffimycin E, a new anti-mycobacterial agent against Mycobacterium avium complex, produced by Streptomyces sp. OPMA02852.

机构信息

Department of Microbial Chemistry, Graduate School of Pharmaceutical Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo, 108-8641, Japan.

Medicinal Research Laboratories, School of Pharmacy, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo, 108-8641, Japan.

出版信息

J Antibiot (Tokyo). 2020 Aug;73(8):581-584. doi: 10.1038/s41429-020-0290-9. Epub 2020 Mar 4.

DOI:10.1038/s41429-020-0290-9
PMID:32132675
Abstract

The marine actinomycete strain OPMA02852, identified as the genus Streptomyces, was found to produce anti-mycobacterial compounds against Mycobacterium avium complex (MAC). One new compound, designated as steffimycin E (1), was isolated together with three known steffimycins (steffimycin (2), 10-dihydrosteffimycin (3), and 8-demethoxysteffimycin (4)) from the culture broth of this producing microorganism by solvent extraction, ODS column chromatography, and preparative HPLC. Compound 1 has a tetracyclic quinone structure with a sugar moiety. Compound 1 exhibited anti-mycobacterial activity against M. intracellulare, M. bovis BCG, and M. smegmatis.

摘要

海洋放线菌 OPMA02852 菌株被鉴定为链霉菌属,能够产生抗分枝杆菌化合物来抑制鸟分枝杆菌复合群(MAC)。从该产生菌的发酵液中,通过溶剂萃取、ODS 柱层析和制备型 HPLC,分离得到一个新化合物,命名为 steffimycin E(1),以及三个已知化合物 steffimycin(2)、10-二氢 steffimycin(3)和 8-去甲氧基 steffimycin(4)。化合物 1 具有四环醌结构和糖部分。化合物 1 对胞内分枝杆菌、牛分枝杆菌 BCG 和耻垢分枝杆菌表现出抗分枝杆菌活性。

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