Discovery and Biosynthesis of Ureidopeptide Natural Products Macrocyclized via Indole N‐acylation in Marine Microbulbifer spp. Bacteria

The discovery, structure elucidation, biosynthesis, and possible molecular logic of bulbiferamides – macrocyclic ureidopeptides containing N-acyl tryptophan indoles.

Abstract

Commensal bacteria associated with marine invertebrates are underappreciated sources of chemically novel natural products. Using mass spectrometry, we had previously detected the presence of peptidic natural products in obligate marine bacteria of the genus Microbulbifer cultured from marine sponges. In this report, the isolation and structural characterization of a panel of ureidohexapeptide natural products, termed the bulbiferamides, from Microbulbifer strains is reported wherein the tryptophan side chain indole participates in a macrocyclizing peptide bond formation. Genome sequencing identifies biosynthetic gene clusters encoding production of the bulbiferamides and implicates the involvement of a thioesterase in the indolic macrocycle formation. The structural diversity and widespread presence of bulbiferamides in commensal microbiomes of marine invertebrates point toward a possible ecological role for these natural products.

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