Protein Scaffolds Modulate the Electronic Structure of a Common Ketyl Radical Intermediate in Thiamine Pyrophos-phate-Dependent Radical Biocatalysis: Insights from EPR and ENDOR Spectroscopy
- 1University of California Santa Barbara
Abstract
New-to-nature radical biocatalysis has emerged as a powerful strategy for asymmetric C--C bond formation, yet the enzyme-bound radi-cal intermediates that underpin these transformations have remained largely uncharacterized. Here, we combine photo biocatalytic reaction development with multifrequency electron paramagnetic resonance (EPR), electron-nuclear double resonance (ENDOR) spectroscopy, and density functional theory (DFT) calculations to elucidate the ketyl radical intermediates formed during thiamine pyrophosphate (TPP)-dependent radical biocatalysis. We first develop an oxidative photobiocatalytic cross-coupling of aldehydes with alkyltri-fluoroborates catalyzed by engineered benzoylformate decarboxylase (BFD) variants, providing enantioenriched -chiral ketones through a new oxidative radical manifold inaccessible to benzaldehyde lyases (BALs). Freeze-quench multifrequency EPR and ENDOR spectroscopy directly identify the catalytically generated TPP-bound ketyl radical and reveal that this common radical intermediate adopts distinct electronic structures in BFD and BAL despite their identical chemical composition. Analysis of 1H, 19F, 31P, and 14N hyper-fine interactions, together with DFT calculations, demonstrates that enzyme-specific active-site conformations redistribute spin density between the TPP cofactor and substrate fragment. Greater substrate-centered spin delocalization in BFD provides a mechanistic basis for its superior radical C--C coupling activity relative to BAL. These results establish a direct relationship between protein-controlled electronic structure and catalytic function in TPP-dependent radical biocatalysis and demonstrate that engineering the electronic properties of a common radical intermediate represents a useful strategy for controlling enzyme reactivity in radical biocatalysis.
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BibTeX
@misc{rao2026protein,
title = {{Protein Scaffolds Modulate the Electronic Structure of a Common Ketyl Radical Intermediate in Thiamine Pyrophos-phate-Dependent Radical Biocatalysis: Insights from EPR and ENDOR Spectroscopy}},
author = {G. Rao and Z. Zhang and X. Liu and A. Shiau and R. D. Britt and Y. Yang},
howpublished = {bioRxiv},
year = {2026},
month = oct,
doi = {10.64898/2026.10.15.759499},
url = {https://www.biorxiv.org/content/10.64898/2026.10.15.759499v1},
note = {CC BY},
}
RIS
TY - UNPB
TI - Protein Scaffolds Modulate the Electronic Structure of a Common Ketyl Radical Intermediate in Thiamine Pyrophos-phate-Dependent Radical Biocatalysis: Insights from EPR and ENDOR Spectroscopy
AU - G. Rao
AU - Z. Zhang
AU - X. Liu
AU - A. Shiau
AU - R. D. Britt
AU - Y. Yang
PY - 2026
DA - 2026/10/15
PB - bioRxiv
DO - 10.64898/2026.10.15.759499
UR - https://www.biorxiv.org/content/10.64898/2026.10.15.759499v1
AB - New-to-nature radical biocatalysis has emerged as a powerful strategy for asymmetric C--C bond formation, yet the enzyme-bound radi-cal intermediates that underpin these transformations have remained largely uncharacterized. Here, we combine photo biocatalytic reaction development with multifrequency electron paramagnetic resonance (EPR), electron-nuclear double resonance (ENDOR) spectroscopy, and density functional theory (DFT) calculations to elucidate the ketyl radical intermediates formed during thiamine pyrophosphate (TPP)-dependent radical biocatalysis. We first develop an oxidative photobiocatalytic cross-coupling of aldehydes with alkyltri-fluoroborates catalyzed by engineered benzoylformate decarboxylase (BFD) variants, providing enantioenriched -chiral ketones through a new oxidative radical manifold inaccessible to benzaldehyde lyases (BALs). Freeze-quench multifrequency EPR and ENDOR spectroscopy directly identify the catalytically generated TPP-bound ketyl radical and reveal that this common radical intermediate adopts distinct electronic structures in BFD and BAL despite their identical chemical composition. Analysis of 1H, 19F, 31P, and 14N hyper-fine interactions, together with DFT calculations, demonstrates that enzyme-specific active-site conformations redistribute spin density between the TPP cofactor and substrate fragment. Greater substrate-centered spin delocalization in BFD provides a mechanistic basis for its superior radical C--C coupling activity relative to BAL. These results establish a direct relationship between protein-controlled electronic structure and catalytic function in TPP-dependent radical biocatalysis and demonstrate that engineering the electronic properties of a common radical intermediate represents a useful strategy for controlling enzyme reactivity in radical biocatalysis.
ER -