Abstract

Nitric oxide (NO) and nitrous oxide (N2O) are among nature’s most powerful electron acceptors. In recent years it became clear that microorganisms can take advantage of the oxidizing power of these compounds to degrade aliphatic and aromatic hydrocarbons. For two unrelated bacterial species, the “NC10” phylum bacterium “Candidatus Methylomirabilis oxyfera” and the γ-proteobacterial strain HdN1 it has been suggested that under anoxic conditions with nitrate and/or nitrite, monooxygenases are used for methane and hexadecane oxidation, respectively. No degradation was observed with nitrous oxide only. Similarly, “aerobic” pathways for hydrocarbon degradation are employed by (per)chlorate-reducing bacteria, which are known to produce oxygen from chlorite . In the anaerobic methanotroph M. oxyfera, which lacks identifiable enzymes for nitrogen formation, substrate activation in the presence of nitrite was directly associated with both oxygen and nitrogen formation. These findings strongly argue for the role of NO, or an oxygen species derived from it, in the activation reaction of methane. Although oxygen generation elegantly explains the utilization of “aerobic” pathways under anoxic conditions, the underlying mechanism is still elusive. In this perspective, we review the current knowledge about intra-aerobic pathways, their potential presence in other organisms, and identify candidate enzymes related to quinol-dependent NO reductases (qNORs) that might be involved in the formation of oxygen.

Highlights

  • In dim anoxic waters of stratified lakes where oxygen-respiring organisms normally cannot survive, a tiny aerobic eukaryote makes a living

  • In the anaerobic methanotroph M. oxyfera, which lacks identifiable enzymes for nitrogen formation, substrate activation in the presence of nitrite was directly associated with both oxygen and nitrogen formation. These findings strongly argue for the role of nitric oxide (NO), or an oxygen species derived from it, in the activation reaction of methane

  • We review the current knowledge about intra-aerobic pathways, their potential presence in other organisms, and identify candidate enzymes related to quinol-dependent NO reductases that might be involved in the formation of oxygen

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Summary

INTRODUCTION

In dim anoxic waters of stratified lakes where oxygen-respiring organisms normally cannot survive, a tiny aerobic eukaryote makes a living. Functional chlorite dismutases have been found in Bacteria and Archaea that cannot grow with chlorate as electron acceptor, e.g., in the nitrite-oxidizing genera Nitrospira (Maixner et al, 2008) and Nitrobacter (Mlynek et al, 2011). In the latter species, Cld is significantly smaller and present as a homodimer. P. chloritidismutans is capable of respiring carbon substrates like fatty acids or alcohols with oxygen, chlorate, and nitrate, but growth on alkanes is not observed with nitrate as electron acceptor This suggests that oxygen, provided externally or from chlorate reduction, is required for the initial activation of the alkane, a hydroxylation to the corresponding alcohol (Heider, 2007). One of the prime questions was how it could be enzymatically activated under anaerobic

B NO2– nir
99 Gammaproteobacterium HdN1 NorZ1
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