Department of Microbiology, The Ohio State University, Columbus, Ohio, USA.
Division of Medicinal Chemistry and Pharmacognosy, The Ohio State University, Columbus, Ohio, USA.
Appl Environ Microbiol. 2023 Jun 28;89(6):e0033823. doi: 10.1128/aem.00338-23. Epub 2023 May 31.
Phosphonate natural products are renowned for inhibitory activities which underly their development as antibiotics and pesticides. Although most phosphonate natural products have been isolated from , bioinformatic surveys suggest that many other bacterial genera are replete with similar biosynthetic potential. While mining actinobacterial genomes, we encountered a contaminated data set which included a biosynthetic gene cluster predicted to produce novel phosphonate compounds. Sequence deconvolution revealed that the contig containing this cluster, as well as many others, belonged to a contaminating and is broadly conserved among multiple species, including the epiphyte Bacillus velezensis. Isolation and structure elucidation revealed a new di- and tripeptide composed of l-alanine and a C-terminal l-phosphonoalanine which we name phosphonoalamides E and F. These compounds exhibit broad-spectrum antibacterial activity, including strong inhibition against the agricultural pests responsible for vegetable soft rot (Erwinia rhapontici), onion rot (Pantoea ananatis), and American foulbrood (Paenibacillus larvae). This work expands our knowledge of phosphonate metabolism and underscores the importance of including underexplored microbial taxa in natural product discovery. Phosphonate natural products produced by bacteria have been a rich source of clinical antibiotics and commercial pesticides. Here, we describe the discovery of two new phosphonopeptides produced by with antibacterial activity against human and plant pathogens, including those responsible for widespread soft rot in crops and American foulbrood. Our results provide new insight on the natural chemical diversity of phosphonates and suggest that these compounds could be developed as effective antibiotics for use in medicine or agriculture.
膦酸天然产物以其作为抗生素和杀虫剂的抑制活性而闻名。尽管大多数膦酸天然产物已从 中分离出来,但生物信息调查表明,许多其他细菌属也具有类似的生物合成潜力。在挖掘放线菌基因组时,我们遇到了一个受污染的数据集,其中包括一个预测能产生新型膦酸化合物的生物合成基因簇。序列去卷积表明,包含该簇的 以及许多其他序列都属于一种污染,并且在包括附生细菌 Bacillus velezensis 在内的多种物种中广泛保守。分离和结构阐明揭示了一种由 l-丙氨酸和 C 末端 l-膦酰基丙氨酸组成的新型二肽和三肽,我们将其命名为膦酰基丙氨酸酰胺 E 和 F。这些化合物表现出广谱的抗菌活性,包括对导致蔬菜软腐病(Erwinia rhapontici)、洋葱腐烂(Pantoea ananatis)和美洲幼虫腐臭(Paenibacillus larvae)的农业害虫有很强的抑制作用。这项工作扩展了我们对膦酸代谢的认识,并强调了在天然产物发现中包括未充分探索的微生物类群的重要性。由细菌产生的膦酸天然产物一直是临床抗生素和商业杀虫剂的丰富来源。在这里,我们描述了由 产生的两种新型膦肽的发现,它们对人类和植物病原体具有抗菌活性,包括那些导致作物广泛软腐病和美洲幼虫腐臭的病原体。我们的结果提供了关于膦酸天然化学多样性的新见解,并表明这些化合物可以作为有效的抗生素开发,用于医学或农业。