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Détails bibliographiques
Auteurs principaux: Hong, Li-Li, Cheng, Yijia, Zhang, Wenyu, Luo, Jiaming, Yang, Fan, Zhang, Cui-Xian, Lin, Hou-Wen, Zhou, Yongjun
Format: Artículo científico
Langue:en
Publié: Journal of agricultural and food chemistry 2026
Sujets:
Accès en ligne:https://pubmed.ncbi.nlm.nih.gov/42037158/
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Table des matières:
  • Elucidating the Biosynthetic Pathway of Lactone-Type Spirotetronate Polyketide PA-46101s with Inhibitory Activities against Aquatic Pathogenic Bacteria. Hong, Li-Li Cheng, Yijia Zhang, Wenyu Luo, Jiaming Yang, Fan Zhang, Cui-Xian Lin, Hou-Wen Zhou, Yongjun Streptomyces Anti-Bacterial Agents Polyketides Lactones Biosynthetic Pathways Bacterial Proteins Multigene Family Molecular Structure The spirotetronate polyketides are a class of microbial antibiotics structurally featuring a macrocycle core embedded with a cyclohexene ring spiro-linked to tetronic acid and/or a decalin ring. Of them, PA-46101s are characterized with an extra lactone moiety in the macrocycle scaffold. Despite the remarkable antibacterial activities, the biosynthetic pathway of PA-46101s has not been investigated. Herein, the PA-46101s biosynthetic gene cluster was identified from a species. Overexpression of a LuxR transcriptional regulator led to around a 15-fold rise of PA-46101s production. Characterization of an intermediate accumulated upon deletion of the Baeyer-Villiger monooxygenase homologous gene E1 revealed the first lactone-formation gene from spirotetronate biosynthetic pathways. Characterization of the metabolites of glycosyltransferase gene mutants allowed us to dissect the tailoring glycosylation orders. The obtained PA-46101s analogs exhibited obvious inhibitory activities against the aquatic pathogenic bacteria and . This study paves the way for the structural diversification of PA-46101s through combinatorial biology.