Integrated omics approach to unveil antifungal bacterial polyynes as acetyl-CoA acetyltransferase inhibitors

作者：Ching-Chih Lin, Sin Yong Hoo, Li‐Ting Ma, Chih Lin, Kai-Fa Huang, Ying-Ning Ho, Chi-Hui Sun, Han‐Jung Lee, Pi-Yu Chen, Lin‐Jie Shu, Bowei Wang, Wei-Chen Hsu, Tzu‐Ping Ko, Yuliang Yang · 发表于：Communications Biology · 年份：2022 · DOI：10.1038/s42003-022-03409-6 · 被引用次数：15 · 研究领域：Microbial Natural Products and Biosynthesis、Plant biochemistry and biosynthesis、Genomics and Phylogenetic Studies

Bacterial polyynes are highly active natural products with a broad spectrum of antimicrobial activities. However, their detailed mechanism of action remains unclear. By integrating comparative genomics, transcriptomics, functional genetics, and metabolomics analysis, we identified a unique polyyne resistance gene, masL (encoding acetyl-CoA acetyltransferase), in the biosynthesis gene cluster of antifungal polyynes (massilin A 1, massilin B 2, collimonin C 3, and collimonin D 4) of Massilia sp. YMA4. Crystallographic analysis indicated that bacterial polyynes serve as covalent inhibitors of acetyl-CoA acetyltransferase. Moreover, we confirmed that the bacterial polyynes disrupted cell membrane integrity and inhibited the cell viability of Candida albicans by targeting ERG10, the homolog of MasL. Thus, this study demonstrated that acetyl-CoA acetyltransferase is a potential target for developing antifungal agents.