非核糖体肽
化学
基因簇
抗真菌
基因
肽
计算生物学
小分子
抗菌剂
细菌
生物合成
生物化学
组合化学
微生物学
生物
遗传学
有机化学
作者
Xavier Vila‐Farrés,John Chu,Daigo Inoyama,Melinda A. Ternei,Christophe Lemetre,Louis Cohen,Wooyoung Cho,Boojala Vijay B. Reddy,Henry Zebroski,Joel S. Freundlich,David S. Perlin,Sean F. Brady
摘要
Bacterial culture broth extracts have been the starting point for the development of numerous therapeutics. However, only a small fraction of bacterial biosynthetic diversity is accessible using this strategy. Here, we apply a discovery approach that bypasses the culturing step entirely by bioinformatically predicting small molecule structures from the primary sequences of the biosynthetic gene clusters. These structures are then chemically synthesized to give synthetic-bioinformatic natural products (syn-BNPs). Using this approach, we screened syn-BNPs inspired by nonribosomal peptide synthetases against microbial pathogens, and discovered an antibiotic for which no resistance could be identified and an antifungal agent with activity against diverse fungal pathogens.
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