Substituting a conserved histidine alleviates difluoroacetate-dependent isoaspartate formation in a fluoroacetate dehalogenase
- 1University of Groningen
Abstract
Organofluorides are ubiquitous in modern society, but their persistence poses significant environmental and health risks. Fluoroacetate dehalogenases (FAcDs) are promising candidates for the bioremediation of polyfluorinated substances, as they can hydrolyze C-F bonds efficiently under mild conditions. However, their activity toward gem-difluorinated carboxylic acids, such as 2,2-difluoroacetate (F2A), is typically poor, with rates orders of magnitude lower than for monofluorinated substrates (e.g. fluoroacetate). Here, we combine kinetic studies, mass spectrometric and biochemical analyses, and computational modeling to pinpoint the F2A-induced isomerization of the catalytic aspartate (Asp105) as a major inactivation pathway that severely limits sustained F2A turnover. To overcome this inhibition mechanism, we discovered that a highly conserved histidine (His104) acts as a gatekeeper for sustained F2A activity. Substituting His104 with the noncanonical N3-methylhistidine increased activity 14-fold, while replacement with asparagine boosted activity almost 50-fold, yielding a potent F2A defluorinase with an initial degradation rate of 0.3 s-1. Computational studies elucidated that these substitutions reshape the conformational landscape of Asp105, suppressing isoAsp-promoting conformations while preserving catalytically productive poses for F2A conversion. Notably, transplanting the His-to-Asn substitution into two homologous FAcDs drastically reduced their activity, highlighting H1 as a uniquely suitable scaffold for engineering promiscuous F2A conversion. Overall, this study demonstrates that targeting mechanistic intricacies can significantly enhance FAcD performance on F2A, providing a foundation for further engineering of H1 to degrade polyfluorinated pollutants.
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BibTeX
@misc{jansen2026substituting,
title = {{Substituting a conserved histidine alleviates difluoroacetate-dependent isoaspartate formation in a fluoroacetate dehalogenase}},
author = {S. C. Jansen and L. F. Guerra and C. Duran and M. M. Muelller and S. Osuna and C. Mayer},
howpublished = {bioRxiv},
year = {2026},
month = sep,
doi = {10.64898/2026.09.12.751135},
url = {https://www.biorxiv.org/content/10.64898/2026.09.12.751135v1},
note = {CC BY},
}
RIS
TY - UNPB
TI - Substituting a conserved histidine alleviates difluoroacetate-dependent isoaspartate formation in a fluoroacetate dehalogenase
AU - S. C. Jansen
AU - L. F. Guerra
AU - C. Duran
AU - M. M. Muelller
AU - S. Osuna
AU - C. Mayer
PY - 2026
DA - 2026/09/12
PB - bioRxiv
DO - 10.64898/2026.09.12.751135
UR - https://www.biorxiv.org/content/10.64898/2026.09.12.751135v1
AB - Organofluorides are ubiquitous in modern society, but their persistence poses significant environmental and health risks. Fluoroacetate dehalogenases (FAcDs) are promising candidates for the bioremediation of polyfluorinated substances, as they can hydrolyze C-F bonds efficiently under mild conditions. However, their activity toward gem-difluorinated carboxylic acids, such as 2,2-difluoroacetate (F2A), is typically poor, with rates orders of magnitude lower than for monofluorinated substrates (e.g. fluoroacetate). Here, we combine kinetic studies, mass spectrometric and biochemical analyses, and computational modeling to pinpoint the F2A-induced isomerization of the catalytic aspartate (Asp105) as a major inactivation pathway that severely limits sustained F2A turnover. To overcome this inhibition mechanism, we discovered that a highly conserved histidine (His104) acts as a gatekeeper for sustained F2A activity. Substituting His104 with the noncanonical N3-methylhistidine increased activity 14-fold, while replacement with asparagine boosted activity almost 50-fold, yielding a potent F2A defluorinase with an initial degradation rate of 0.3 s-1. Computational studies elucidated that these substitutions reshape the conformational landscape of Asp105, suppressing isoAsp-promoting conformations while preserving catalytically productive poses for F2A conversion. Notably, transplanting the His-to-Asn substitution into two homologous FAcDs drastically reduced their activity, highlighting H1 as a uniquely suitable scaffold for engineering promiscuous F2A conversion. Overall, this study demonstrates that targeting mechanistic intricacies can significantly enhance FAcD performance on F2A, providing a foundation for further engineering of H1 to degrade polyfluorinated pollutants.
ER -