Southern Marine Science and Engineering Guangdong Laboratory, Guangzhou, Guangdong, 511458 People's Republic of China.
Department of Ocean Science, The Hong Kong University of Science and Technology, Hong Kong, People's Republic of China.
J Nat Prod. 2022 Jul 22;85(7):1751-1762. doi: 10.1021/acs.jnatprod.2c00290. Epub 2022 Jun 15.
Bacteria in marine biofilms are a rich reservoir of natural products. To facilitate novel secondary metabolite discovery, we investigated the metabolic profile of a marine biofilm-derived sp. B19-2 by combining bioinformatics and LC-UV-MS analyses. After dereplication and purification of putatively unknown compounds, a new family of compounds - was uncovered and named bathiapeptides. Structural elucidation using NMR, HRESIMS, ozonolysis, advanced Marfey's analysis, and X-ray diffraction revealed that bathiapeptides are polypeptides that contain a rare polythiazole moiety. These compounds exhibited strong cytotoxicity against Hep G2, HeLa, MCF-7, and MGC-803 cell lines, and the lowest IC value was 0.5 μM. An iterative biosynthesis logic in bathiapeptides' biosynthesis was proposed based on the identified chemical structures and putative gene cluster analysis.
海洋生物膜中的细菌是天然产物的丰富资源库。为了促进新型次生代谢产物的发现,我们通过生物信息学和 LC-UV-MS 分析相结合,研究了海洋生物膜衍生的 sp. B19-2 的代谢谱。在对推定的未知化合物进行去重复和纯化后,发现并命名了一个新的化合物家族 - bathiapeptides。通过 NMR、HRESIMS、臭氧化、高级 Marfey 分析和 X 射线衍射进行结构阐明表明,bathiapeptides 是含有罕见的多噻唑部分的多肽。这些化合物对 Hep G2、HeLa、MCF-7 和 MGC-803 细胞系表现出强烈的细胞毒性,最低 IC 值为 0.5 μM。根据鉴定的化学结构和推定的基因簇分析,提出了 bathiapeptides 生物合成中的迭代生物合成逻辑。