Cacaoidin, First Member of the New Lanthidin RiPP Family

Javier Ortiz-Lopez, Francisco; Carretero-Molina, Daniel; Sanchez-Hidalgo, Marina; Martin, Jesus; Gonzalez, Ignacio; Roman-Hurtado, Fernando; de la Cruz, Mercedes; Garcia-Fernandez, Sergio; Reyes, Fernando; Patricia Deisinger, Julia; Mueller, Anna; Schneide

Publicación: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
2020
VL / 59 - BP / 12654 - EP / 12658
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.

Access level