Reversible Interconversion of Nitrate and Nitrite Catalyzed by Periplasmic Nitrate Reductase from <i>Campylobacter jejuni</i>

The periplasmic nitrate reductase catalytic subunit (NapA) belongs to the DMSO reductase (DMSOR) family of the molybdenum cofactor (Moco) containing enzymes and catalyzes nitrate reduction to nitrite. Some members of the DMSOR family (e.g., DMSO reductase, formate dehydrogenase, nitrite oxidoreductase, and arsenate reductase) catalyze the reversible interconversion of the substrate and product with varying efficiency. Here, we demonstrate that NapA not only can reduce nitrate to nitrite but also can also oxidize nitrite to nitrate. At least three mechanisms involving the oxygen atom transfer (OAT) process have been proposed for NapA-catalyzed nitrate reduction. NapA can also oxidize nitrite via an OAT process. However, there is no experimental evidence for any of these OAT processes using isolated pure enzymes so far. Here, we provide the first experimental evidence for OAT reactions in both forward (i.e., nitrate reduction) and backward (i.e., nitrite oxidation) reactions catalyzed by NapA using isotope labeling, mass spectrometry, and NMR experiments. Finally, we propose a mechanistic scheme supported by experiment and computation consistent with atom transfer as the rate-limiting step.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-04-09
DOI
https://doi.org/10.1021/jacs.4c17874
Citations
6
Primary Topic
Metalloenzymes and iron-sulfur proteins
Type
article
Field-Weighted Citation Impact
2.18

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article

Reversible Interconversion of Nitrate and Nitrite Catalyzed by Periplasmic Nitrate Reductase from Campylobacter jejuni

Partha Basu, Maciej Szaleniec, Nicholas E. Manicke, Nitai Charan Giri et al.
6 citations
Journal of the American Chemical Society
Metalloenzymes and iron-sulfur proteins
2.18
article

Reversible Interconversion of Nitrate and Nitrite Catalyzed by Periplasmic Nitrate Reductase from Campylobacter jejuni

Partha Basu, Maciej Szaleniec, Nicholas E. Manicke, Nitai Charan Giri, Lahiru Wedasingha
article en
6 citations

Abstract

The periplasmic nitrate reductase catalytic subunit (NapA) belongs to the DMSO reductase (DMSOR) family of the molybdenum cofactor (Moco) containing enzymes and catalyzes nitrate reduction to nitrite. Some members of the DMSOR family (e.g., DMSO reductase, formate dehydrogenase, nitrite oxidoreductase, and arsenate reductase) catalyze the reversible interconversion of the substrate and product with varying efficiency. Here, we demonstrate that NapA not only can reduce nitrate to nitrite but also can also oxidize nitrite to nitrate. At least three mechanisms involving the oxygen atom transfer (OAT) process have been proposed for NapA-catalyzed nitrate reduction. NapA can also oxidize nitrite via an OAT process. However, there is no experimental evidence for any of these OAT processes using isolated pure enzymes so far. Here, we provide the first experimental evidence for OAT reactions in both forward (i.e., nitrate reduction) and backward (i.e., nitrite oxidation) reactions catalyzed by NapA using isotope labeling, mass spectrometry, and NMR experiments. Finally, we propose a mechanistic scheme supported by experiment and computation consistent with atom transfer as the rate-limiting step.

Journal of the American Chemical SocietyVol. 147(16)
Jerzy Haber Institute of Catalysis and Surface Chemistry, Polish Academy of Sciences (PL), Indiana University Indianapolis (US), Indiana University – Purdue University Indianapolis (US)
National Institute of General Medical Sciences, Division of Chemistry
Openalex Percentile: Top 13%
Metalloenzymes and iron-sulfur proteins
2.18
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Reversible Interconversion of Nitrate and Nitrite Catalyzed by Periplasmic Nitrate Reductase from <i>Campylobacter jejuni</i> — Partha Basu, Maciej Szaleniec, et al. · Journal of the American Chemical Society (2025) | TGRS Research Map | TGRS