Aono_2025_J.Antibiot.(Tokyo)__

The macrocyclic scaffolds of non-ribosomal peptides (NRPs) are typically constructed by thioesterase (TE) domains, alpha/beta-hydrolase fold enzymes located at the C-termini of non-ribosomal peptide synthetases (NRPSs). By employing various nucleophiles, TEs serve as sources of diversity in cyclization modes and ring-closing linkages of NRPs. The NRPS assembly line of momomycin, an unusual undecapeptidyl cyclic peptide with multiple backbone N-methylations, suggests that it is macrocyclized via the coupling of homochiral termini through a secondary amine nucleophile, which is rarely employed in TE-mediated cyclization. Here, we investigated the function of the momomycin cyclase, MmmB-TE. In vitro enzymatic assays revealed MmmB-TE's strict specificity for an L-configured cyclic amine nucleophile, as well as the incremental enhancements of cyclization efficiency conferred by backbone N-methylations. Mutagenesis studies, together with computational modeling of the peptide-O-enzyme complex, provided insights into the binding of the ring-closing residues in MmmB-TE.