Issue 27, 2024

Putative reaction mechanism of nitrogenase with a half-dissociated S2B ligand

Abstract

We have studied whether dissociation of the S2B sulfide ligand from one of its two coordinating Fe ions may affect the later parts of the reaction mechanism of nitrogenase. Such dissociation has been shown to be favourable for the E2–E4 states in the reaction mechanism, but previous studies have assumed that S2B either remains bridging or has fully dissociated from the active-site FeMo cluster. We employ combined quantum mechanical and molecular mechanical (QM/MM) calculations with two density-functional theory methods, r2SCAN and TPSSh. To make dissociation of S2B possible, we have added a proton to this group throughout the reaction. We study the reaction starting from the E4 state with N2H2 bound to the cluster. Our results indicate that half-dissociation of S2B is unfavourable in most steps of the reaction mechanism. We observe favourable half-dissociation of S2B only when NH or NH2 is bound to the cluster, bridging Fe2 and Fe6. However, the former state is most likely not involved in the reaction mechanism and the latter state is only an intermittent intermediate of the E7 state. Therefore, half-dissociation of S2B seems to play only a minor role in the later parts of the reaction mechanism of nitrogenase. Our suggested mechanism with a protonated S2B is alternating (the two N atoms of the substrate is protonated in an alternating manner) and the substrate prefers to bind to Fe2, in contrast to the preferred binding to Fe6 observed when S2B is unprotonated and bridging Fe2 and Fe6.

Graphical abstract: Putative reaction mechanism of nitrogenase with a half-dissociated S2B ligand

Supplementary files

Article information

Article type
Paper
Submitted
29 mar. 2024
Accepted
15 jun. 2024
First published
20 jun. 2024
This article is Open Access
Creative Commons BY-NC license

Dalton Trans., 2024,53, 11500-11513

Putative reaction mechanism of nitrogenase with a half-dissociated S2B ligand

H. Jiang and U. Ryde, Dalton Trans., 2024, 53, 11500 DOI: 10.1039/D4DT00937A

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