Enantioselective Olefin Cyclopropanation with G-Quadruplex DNA-Based Biocatalysts
ACS Catal. 2020, 10, 6561-6567, 10.1021/acscatal.0c01203
Developing high-performance DNA-based biocatalysts for desired stereoselective syntheses remains a formidable challenge. Here, we report promising DNA-based catalysts comprised of G-quadruplex (G4) and Fe porphyrin for asymmetric olefin cyclopropanation. After the G4-based catalysts are optimized by several rounds of site mutation, their catalytic enantioselectivities achieve +81% and −86% enantiomeric excess (eetrans) at a turnover number (TON) as high as 500. The Fe porphyrin, binding upon the 5′,3′-end G-quartet, constitutes the active center for olefin cyclopropanation via an iron porphyrin carbene intermediate. The findings provide an opportunity for generating high-value chiral cyclopropane blocks via G4 biocatalysts and shed light on the potential of DNA as protein enzymes for catalysis.
Metal: FeLigand type: PorphyrinHost protein: DNAAnchoring strategy: SupramolecularOptimization: Chemical & geneticReaction: CyclopropanationMax TON: 500ee: 86PDB: ---Notes: ---