The production of nitric oxide by marine ammonia-oxidizing archaea and inhibition of archaeal ammonia oxidation by a nitric oxide scavenger

Environ Microbiol. 2015 Jul;17(7):2261-74. doi: 10.1111/1462-2920.12677. Epub 2015 Jan 27.

Abstract

Nitrification is a critical process for the balance of reduced and oxidized nitrogen pools in nature, linking mineralization to the nitrogen loss processes of denitrification and anammox. Recent studies indicate a significant contribution of ammonia-oxidizing archaea (AOA) to nitrification. However, quantification of the relative contributions of AOA and ammonia-oxidizing bacteria (AOB) to in situ ammonia oxidation remains challenging. We show here the production of nitric oxide (NO) by Nitrosopumilus maritimus SCM1. Activity of SCM1 was always associated with the release of NO with quasi-steady state concentrations between 0.05 and 0.08 μM. NO production and metabolic activity were inhibited by the nitrogen free radical scavenger 2-phenyl-4,4,5,5,-tetramethylimidazoline-1-oxyl-3-oxide (PTIO). Comparison of marine and terrestrial AOB strains with SCM1 and the recently isolated marine AOA strain HCA1 demonstrated a differential sensitivity of AOB and AOA to PTIO and allylthiourea (ATU). Similar to the investigated AOA strains, bulk water column nitrification at coastal and open ocean sites with sub-micromolar ammonia/ammonium concentrations was inhibited by PTIO and insensitive to ATU. These experiments support predictions from kinetic, molecular and biogeochemical studies, indicating that marine nitrification at low ammonia/ammonium concentrations is largely driven by archaea and suggest an important role of NO in the archaeal metabolism.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Ammonia / metabolism*
  • Ammonium Compounds / metabolism
  • Aquatic Organisms / metabolism
  • Archaea / metabolism*
  • Betaproteobacteria / metabolism
  • Cyclic N-Oxides / pharmacology*
  • Denitrification
  • Imidazoles / pharmacology*
  • Nitric Oxide / biosynthesis
  • Nitric Oxide / metabolism*
  • Nitrification*
  • Nitrogen / metabolism
  • Oxidation-Reduction
  • Thiourea / analogs & derivatives*
  • Thiourea / pharmacology

Substances

  • Ammonium Compounds
  • Cyclic N-Oxides
  • Imidazoles
  • 2-phenyl-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide
  • Nitric Oxide
  • allylthiourea
  • Ammonia
  • Thiourea
  • Nitrogen