Modular multi-enzyme cascades enable green and sustainable synthesis of non-canonical amino acids from glycerol.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 40883312.
- Also identified by DOI 10.1038/s41467-025-63341-1 and PMC identifier 12397247.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Non-canonical amino acids (ncAAs) bearing diverse functional groups hold transformative potential in drug discovery, protein engineering, and biomaterial science. However, their industrial-scale production remains constrained by the inefficiency, high cost, and environmental burden of conventional chemical and enzymatic methods. Here, we present a modular multi-enzyme cascade platform that leverages glycerol-an abundant and sustainable byproduct of biodiesel production-as a low-cost substrate for ncAAs synthesis. Directed evolution of O-phospho-L-serine sulfhydrylase (OPSS) enhances the catalytic efficiency of C-N bond formation by 5.6-fold, enabling the efficient synthesis of triazole-functionalized ncAAs. By integrating a plug-and-play enzymatic strategy, our system enables gram- to decagram-scale production of 22 ncAAs with C-S, C-Se, and C-N side chains and can be readily scaled up to a 2 liter reaction system. Notably, water is the sole byproduct, and all products exhibit an atomic economy of >75%, highlighting the environmental compatibility of this platform. This work establishes a green, cost-effective, and industrially viable approach to expanding amino acid diversity, providing a versatile toolkit for applications in pharmaceuticals, synthetic biology, and next-generation biomaterials.
Medical subject headings
- Amino Acids
- Glycerol
- Green Chemistry Technology