Nonheme iron enzymes are among nature's most versatile catalysts for molecular functionalization. Engineering nonheme enzymes for abiological reactions unlocks new catalytic possibilities beyond the limits of natural evolution. In this work, we engineered a nonheme enzyme, leucoanthocyanidin dioxygenase from Arabidopsis thaliana (AtLDOX), to catalyze an asymmetric 1,3-migratory nitrene C(sp3)─H insertion reaction. Through directed evolution, the final optimized AtLDOX_LS variant efficiently delivers a range of chiral α-amino acids derivatives with exceptional activity and enantioselectivity (up to 81% yield, 850 total turnover number, and 98:2 enantiomeric ratio). Preliminary mechanistic studies suggest the involvement of radical intermediates for this transformation. This work advances the biocatalytic toolbox for radical involved transformations and broadens the scope of enzymatic migration chemistry.
Directed Evolution of a Nonheme Iron Enzyme to Access Chiral α-Amino Acid Derivatives by 1,3-Migratory Nitrene C(sp3)─H Insertion.
Minghui Cheng,Tao Li,Yamei Gan,Wentao Zhang,Xu Chen,Qun Zhao
Published 2025 in Angewandte Chemie
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- Publication year
2025
- Venue
Angewandte Chemie
- Publication date
2025-11-10
- Fields of study
Biology, Medicine, Chemistry
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- Source metadata
Semantic Scholar, PubMed
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