| Literature DB >> 32407589 |
Francisco Javier Ortiz-López1, Daniel Carretero-Molina1, Marina Sánchez-Hidalgo1, Jesús Martín1, Ignacio González1, Fernando Román-Hurtado1, Mercedes de la Cruz1, Sergio García-Fernández2, Fernando Reyes1, Julia Patricia Deisinger3,4, Anna Müller3, Tanja Schneider3,4, Olga Genilloud1.
Abstract
Lantibiotics are ribosomally synthesized and post-translationally modified peptides (RiPPs) characterized by the presence of lanthionine or methyllanthionine rings and their antimicrobial activity. Cacaoidin, a novel glycosylated lantibiotic, was isolated from a Streptomyces cacaoi strain and fully characterized by NMR, mass spectrometry, chemical derivatization approaches and genome analysis. The new molecule combines outstanding structural features, such as a high number of d-amino acids, an uncommon glycosylated tyrosine residue and an unprecedented N,N-dimethyl lanthionine. This latter feature places cacaoidin within a new RiPP family located between lanthipeptides and linaridins, here termed lanthidins. Cacaoidin displayed potent antibacterial activity against Gram-positive pathogens including Clostridium difficile. The biosynthetic gene cluster showed low homology with those of other known lanthipeptides or linaridins, suggesting a new RiPP biosynthetic pathway.Entities:
Keywords: RiPP family; lanthidin; lantibiotic; natural products; tyrosine-O-glycosylation
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Year: 2020 PMID: 32407589 DOI: 10.1002/anie.202005187
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336