Nitrification Mechanisms for the P460 Enzymes

The oxidation of hydroxylamine was studied by quantum chemical modeling. Hydroxylamine is the product of ammonia oxidation in ammonia monooxygenase. That mechanism has been studied recently by quantum chemical modeling as here. Only two enzymes can oxidize hydroxylamine, hydroxylamine oxidase and cytochrome-P460. Both employ the unusual P460-heme cofactor. In hydroxylamine oxidase, there is a covalently linked tyrosine, while in cytochrome-P460, there is a covalently linked lysine. The calculations give explanations for the experimental findings that NO is the final product in hydroxylamine oxidase, while N<sub>2</sub>O is the final product in cytochrome-P460. The effect of the covalent attachments has been investigated, and reasons for their presence have been given. The methodology used, which was proven to give very good agreement with experiments for several redox enzymes, again leads to excellent agreement with experimental findings.

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Publication Details

Journal
The Journal of Physical Chemistry B
Published
2024-12-18
DOI
https://doi.org/10.1021/acs.jpcb.4c06537
Citations
4
Primary Topic
Metal-Catalyzed Oxygenation Mechanisms
Type
article
Field-Weighted Citation Impact
0.63

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article

Nitrification Mechanisms for the P460 Enzymes

Per E. M. Siegbahn
4 citations
The Journal of Physical Chemistry B
Metal-Catalyzed Oxygenation Mechanisms
0.63
article

Nitrification Mechanisms for the P460 Enzymes

Per E. M. Siegbahn
article en
4 citations

Abstract

The oxidation of hydroxylamine was studied by quantum chemical modeling. Hydroxylamine is the product of ammonia oxidation in ammonia monooxygenase. That mechanism has been studied recently by quantum chemical modeling as here. Only two enzymes can oxidize hydroxylamine, hydroxylamine oxidase and cytochrome-P460. Both employ the unusual P460-heme cofactor. In hydroxylamine oxidase, there is a covalently linked tyrosine, while in cytochrome-P460, there is a covalently linked lysine. The calculations give explanations for the experimental findings that NO is the final product in hydroxylamine oxidase, while N<sub>2</sub>O is the final product in cytochrome-P460. The effect of the covalent attachments has been investigated, and reasons for their presence have been given. The methodology used, which was proven to give very good agreement with experiments for several redox enzymes, again leads to excellent agreement with experimental findings.

The Journal of Physical Chemistry BVol. 129(1)
Stockholm University (SE)
Stockholms Universitet
Openalex Percentile: Top 36%
Metal-Catalyzed Oxygenation Mechanisms
0.63
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Nitrification Mechanisms for the P460 Enzymes — Per E. M. Siegbahn · The Journal of Physical Chemistry B (2024) | TGRS Research Map | TGRS