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Peer-reviewedCC BYChembiochem : a European journal of chemical biology

Explorations of the Hydrogenation of D₂ by Nitrogenase.

  • Ian Dance1
  1. 1School of Chemistry, UNSW Sydney, Sydney, New South Wales, Australia.
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Abstract

A non-physiological substrate of the enzyme nitrogenase, D₂, is doubly hydrogenated by the enzyme to produce 2HD. This 'HD reaction' is in competition with the native function of the enzyme, hydrogenating N₂ to NH₃. At the active site of the enzyme, a gallery of H atom donors is identified, and the proposed complete cycle mechanism for the N₂ reaction uses these donors eight times to generate the 2NH₃ + H₂ products. Here, the functionality of these H atom donors in hydrogenating D₂ to 2HD is investigated, applying density functional simulations to a 480+ atom model of the active site including all important surrounds. Many possible reaction trajectories were explored, and a revised mechanism for the HD reaction is presented. The mechanisms for hydrogenation of D₂ and of N₂ have common components, accounting for their experimentally known competition. Consideration of ten items of relevant experimental data about the HD reaction shows how the proposed mechanism complies with and interprets these data, although two experimental observations are still to be checked.

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Cite

BibTeXRIS
BibTeX
@article{dance2026explorations,
  title = {{Explorations of the Hydrogenation of D₂ by Nitrogenase.}},
  author = {Ian Dance},
  journal = {Chembiochem : a European journal of chemical biology},
  year = {2026},
  month = oct,
  doi = {10.1002/cbic.70570},
  url = {https://europepmc.org/article/MED/42952092},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Explorations of the Hydrogenation of D₂ by Nitrogenase.
AU  - Ian Dance
PY  - 2026
DA  - 2026/10/28
JO  - Chembiochem : a European journal of chemical biology
DO  - 10.1002/cbic.70570
UR  - https://europepmc.org/article/MED/42952092
AB  - A non-physiological substrate of the enzyme nitrogenase, D₂, is doubly hydrogenated by the enzyme to produce 2HD. This 'HD reaction' is in competition with the native function of the enzyme, hydrogenating N₂ to NH₃. At the active site of the enzyme, a gallery of H atom donors is identified, and the proposed complete cycle mechanism for the N₂ reaction uses these donors eight times to generate the 2NH₃ + H₂ products. Here, the functionality of these H atom donors in hydrogenating D₂ to 2HD is investigated, applying density functional simulations to a 480+ atom model of the active site including all important surrounds. Many possible reaction trajectories were explored, and a revised mechanism for the HD reaction is presented. The mechanisms for hydrogenation of D₂ and of N₂ have common components, accounting for their experimentally known competition. Consideration of ten items of relevant experimental data about the HD reaction shows how the proposed mechanism complies with and interprets these data, although two experimental observations are still to be checked.
SN  - 1439-4227
SN  - 1439-7633
ER  -