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Nitrous oxide production via enzymatic nitroxyl from the nitrifying archaeon Nitrosopumilus maritimus .

Authors :
Voland RW
Wang H
Abruña HD
Lancaster KM
Source :
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2025 Jan 21; Vol. 122 (3), pp. e2416971122. Date of Electronic Publication: 2025 Jan 17.
Publication Year :
2025

Abstract

Ammonia oxidizing archaea (AOA) are among the most abundant microorganisms on earth and are known to be a major source of nitrous oxide (N <subscript>2</subscript> O) emissions, although biochemical origins of this N <subscript>2</subscript> O remain unknown. Enzymological details of AOA nitrogen metabolism are broadly unavailable. We report the recombinant expression, purification, and characterization of a multicopper oxidase, Nmar_1354, from the AOA Nitrosopumilus maritimus . We show that Nmar_1354 selectively produces nitroxyl (HNO) by coupling the oxidation of the obligate nitrification intermediate hydroxylamine (NH <subscript>2</subscript> OH) to dioxygen (O <subscript>2</subscript> ) reduction. This HNO undergoes several downstream reactions, although the major fates are production of N <subscript>2</subscript> via reaction with NH <subscript>2</subscript> OH and dimerization with itself to yield N <subscript>2</subscript> O. These results afford one plausible enzymatic origin for N <subscript>2</subscript> O release by AOA. Moreover, these results reveal a physiologically relevant enzymatic reaction for producing HNO, an enigmatic nitrogen oxide speculated to be operative in cellular signaling and in energy transduction.<br />Competing Interests: Competing interests statement:The authors declare no competing interest.

Details

Language :
English
ISSN :
1091-6490
Volume :
122
Issue :
3
Database :
MEDLINE
Journal :
Proceedings of the National Academy of Sciences of the United States of America
Publication Type :
Academic Journal
Accession number :
39823305
Full Text :
https://doi.org/10.1073/pnas.2416971122