Total Synthesis of Mutanobactins A, B from the Human Microbiome: Macrocyclization and Thiazepanone Assembly in a Single Step

Angew Chem Int Ed Engl. 2022 Jul 11;61(28):e202203051. doi: 10.1002/anie.202203051. Epub 2022 Jun 10.

Abstract

We report the first total syntheses of tricyclic mutanobactins A and B, lipopeptides incorporating a thiazepanone, isolated from Streptococcus mutans, a member of the human oral microbiome. A rapid, solid-phase peptide synthesis (SPPS) based route delivers these natural products from a cascade of cyclization reactions. This versatile process was also employed in a streamlined synthesis of mutanobactin D. Additionally, we provide an independent synthesis of a truncated mutanobactin A analog, utilizing a novel thiazepanone amino acid building block.

Keywords: Cyclization; Macrocycles; Peptide Synthesis; Total Synthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cyclization
  • Humans
  • Lipopeptides / chemistry
  • Microbiota*
  • Peptides, Cyclic* / chemistry
  • Solid-Phase Synthesis Techniques

Substances

  • Lipopeptides
  • Peptides, Cyclic