The chemical synthesis of -acyl indoles is hindered by the poor nucleophilicity of indolic nitrogen, necessitating the use of strongly basic reaction conditions that encumber elaboration of highly functionalized scaffolds. Herein, we describe the total chemoenzymatic synthesis of the bulbiferamide natural products by the biochemical activity reconstitution of a nonribosomal peptide synthetase assembly line-derived (NRPS-derived) thioesterase that neatly installs the macrocyclizing indolylamide. The enzyme represents a starting point for biocatalytic access to macrocyclic indolylamide peptides and natural products.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11536411PMC
http://dx.doi.org/10.1021/acs.orglett.4c03648DOI Listing

Publication Analysis

Top Keywords

natural products
8
activity biocatalytic
4
biocatalytic potential
4
potential indolylamide
4
indolylamide generating
4
generating thioesterase
4
thioesterase chemical
4
chemical synthesis
4
synthesis -acyl
4
-acyl indoles
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!