Issue 3, 2025, Issue in Progress

Genome mining of albocandins A–E from Streptomyces sp. YINM00030

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.

Graphical abstract: Genome mining of albocandins A–E from Streptomyces sp. YINM00030

Supplementary files

Article information

Article type
Paper
Submitted
29 Nov 2024
Accepted
13 Jan 2025
First published
21 Jan 2025
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2025,15, 1805-1812

Genome mining of albocandins A–E from Streptomyces sp. YINM00030

Z. Zhang, Z. Ren, X. Su, T. Xie, M. Yi, H. Zhou, M. Yin and Z. Ding, RSC Adv., 2025, 15, 1805 DOI: 10.1039/D4RA08447K

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements