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Updated: Jun 1, 2025

Mass Spectrometry-Guided Genome Mining as a Tool to Uncover Novel Natural Products
Published on: March 12, 2020
Genome mining of albocandins A-E from Streptomyces sp. YINM00030
Zhou-Tian-Le Zhang1, Zhen Ren2, Xiaoyu Su1
1Key Laboratory of Functional Molecules Analysis and Biotransformation of Universities in Yunnan Province, Yunnan Characteristic Plant Extraction Laboratory, School of Chemical Science and Technology, School of Medicine, Yunnan University Kunming Yunnan 650500 PR China yinmin@ynu.edu.cn haozhou@ynu.edu.cn ztding@ynu.edu.cn.
Abstract:
The natural products of 2,5-diketopiperazines have attracted considerable attention due to their potent pharmacological activities. Guided by genome mining techniques, five albonoursin analogues, designated as albocandins A-E (1-5), were isolated from Streptomyces sp. YINM00030, an actinomycete sourced from the rhizosphere soil of medicinal plants. The structures and absolute configurations of these compounds were elucidated through comprehensive spectroscopic analyses, HRESIMS, electronic circular dichroism (ECD) calculations, and single-crystal X-ray diffraction analyses. The biosynthetic pathway of these compounds were proposed. The investigation of biological activity showed that albocandins C and D exhibited cytotoxic activity against five human cancer cell lines (HL-60, A549, SMMC-7721, MDA-MB-231, SW480) in vitro with IC50 values ranging from 3.50 to 32.66 μM.
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