Asymmetric enzymatic hydrophosphorylation through O 2 activation
Enzymatic carbon-phosphorus bond formation is extremely rare in nature, limiting biocatalytic access to phosphorus-containing compounds that are widely used in pharmaceuticals and agrochemicals. Here, we report an asymmetric enzymatic hydrophosphorylation through oxygen activation using a repurposed flavin-dependent enzyme. Mechanistic studies revealed that reactive oxygen species are converted into productive phosphorus-centered radicals, followed by radical addition and enzymatic hydrogen atom transfer, achieving high enantioselectivity. The enzyme accommodates diverse phosphorus-hydrogen donors that pose challenges to chemical catalysis, enabling the biosynthesis of valuable phosphorus-containing scaffolds. This work expands the scope of biocatalysis to programmable carbon-phosphorus bond formation and establishes a paradigm for channeling oxygen reactivity in enzymes.
Authors
- Huimin Zhao (ORCID: https://orcid.org/0000-0002-9069-6739)
- Y.-Y. Ge (ORCID: https://orcid.org/0009-0005-8336-126X)
- Wesley Harrison (ORCID: https://orcid.org/0000-0001-8256-5926)
- Yi Zhou (ORCID: https://orcid.org/0000-0002-0273-007X)
Institutions
- University of Illinois Urbana-Champaign (US)
- Center for Advanced Bioenergy and Bioproducts Innovation (US)
- Carl R. Woese Institute for Genomic Biology (US)
Publication Details
- Journal
- Science
- Published
- 2026-10-08
- DOI
- https://doi.org/10.1126/science.aef3001
- Primary Topic
- Enzyme Catalysis and Immobilization
- Type
- article
- Field-Weighted Citation Impact
- 0.00