Issue 2, 2022

Discovery of gargantulides B and C, new 52-membered macrolactones from Amycolatopsis sp. Complete absolute stereochemistry of the gargantulide family

Abstract

Gargantulides B and C, two new and highly complex 52-membered glycosylated macrolactones, were isolated from Amycolatopsis sp. strain CA-230715 during an antibacterial screening campaign. The structures of these giant macrolides were elucidated by 2D NMR spectroscopy and shown to be related to gargantulide A, although containing additional β-glucopyranose and/or α-arabinofuranose monosaccharides separately attached to their backbones. Genome sequencing allowed the identification of a strikingly large 216 kbp biosynthetic gene cluster, among the largest type I PKS clusters described so far, and the proposal of a previously unreported biosynthetic pathway for gargantulides A–C. The absolute configurations of gargantulides B and C were assigned based on a combination of NMR and bioinformatics analysis of ketoreductase and enoylreductase domains within the multimodular type I PKS. In addition, the absolute stereochemistry of gargantulide A has now been revised and completed. Gargantulides B and C display potent antibacterial activity against a set of drug-resistant Gram-positive bacteria and moderate activity against the clinically relevant Gram-negative pathogen Acinetobacter baumannii.

Graphical abstract: Discovery of gargantulides B and C, new 52-membered macrolactones from Amycolatopsis sp. Complete absolute stereochemistry of the gargantulide family

Supplementary files

Article information

Article type
Research Article
Submitted
01 Oct 2021
Accepted
06 Dec 2021
First published
09 Dec 2021

Org. Chem. Front., 2022,9, 462-470

Discovery of gargantulides B and C, new 52-membered macrolactones from Amycolatopsis sp. Complete absolute stereochemistry of the gargantulide family

D. Carretero-Molina, F. J. Ortiz-López, T. Gren, D. Oves-Costales, J. Martín, F. Román-Hurtado, T. Sparholt Jørgensen, M. de la Cruz, C. Díaz, F. Vicente, K. Blin, F. Reyes, T. Weber and O. Genilloud, Org. Chem. Front., 2022, 9, 462 DOI: 10.1039/D1QO01480C

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