Discovery and development of penicillin-binding protein-type thioesterases as biocatalysts
Cyclic peptides are promising drug candidates, but their synthesis, especially the synthesis of small, strained rings, remains challenging. Penicillin-binding protein-type thioesterases (PBP-TEs) have emerged as versatile biocatalysts that catalyze head-to-tail macrocyclization of nonribosomal peptides. Unlike canonical thioesterase domains, which catalyze diverse offloading outcomes, PBP-TEs exclusively promote head-to-tail cyclization, offering predictable reactivity. Their ability to act on diverse substrates in vitro further underscores their potential as tools for peptide drug discovery. This review highlights PBP-TE discovery and substrate scope investigation, along with recent advances in structural characterization and engineering, establishing these enzymes as a promising platform for the biocatalytic synthesis of cyclic peptides.
Authors
- Zachary L. Budimir
- Elizabeth I. Parkinson (ORCID: https://orcid.org/0000-0002-3665-5522)
Institutions
- Purdue University West Lafayette (US)
Publication Details
- Journal
- Current Opinion in Biotechnology
- Published
- 2025-12-22
- DOI
- https://doi.org/10.1016/j.copbio.2025.103417
- Primary Topic
- Microbial Natural Products and Biosynthesis
- Type
- article
- Field-Weighted Citation Impact
- 0.00