RT Journal Article SR Electronic(1) A1 Wu, Ming L. A1 de Vries, Simon A1 van Alen, Theo A. A1 Butler, Margaret K. A1 Op den Camp, Huub J. M. A1 Keltjens, Jan T. A1 Jetten, Mike S. M. A1 Strous, MarcYR 2011 T1 Physiological role of the respiratory quinol oxidase in the anaerobic nitrite-reducing methanotroph ‘Candidatus Methylomirabilis oxyfera’ JF Microbiology, VO 157 IS 3 SP 890 OP 898 DO https://doi.org/10.1099/mic.0.045187-0 PB Microbiology Society, SN 1465-2080, AB The anaerobic nitrite-reducing methanotroph ‘Candidatus Methylomirabilis oxyfera’ (‘Ca. M. oxyfera’) produces oxygen from nitrite by a novel pathway. The major part of the O2 is used for methane activation and oxidation, which proceeds by the route well known for aerobic methanotrophs. Residual oxygen may serve other purposes, such as respiration. We have found that the genome of ‘Ca. M. oxyfera’ harbours four sets of genes encoding terminal respiratory oxidases: two cytochrome c oxidases, a third putative bo-type ubiquinol oxidase, and a cyanide-insensitive alternative oxidase. Illumina sequencing of reverse-transcribed total community RNA and quantitative real-time RT-PCR showed that all four sets of genes were transcribed, albeit at low levels. Oxygen-uptake and inhibition experiments, UV–visible absorption spectral characteristics and EPR spectroscopy of solubilized membranes showed that only one of the four oxidases is functionally produced by ‘Ca. M. oxyfera’, notably the membrane-bound bo-type terminal oxidase. These findings open a new role for terminal respiratory oxidases in anaerobic systems, and are an additional indication of the flexibility of terminal oxidases, of which the distribution among anaerobic micro-organisms may be largely underestimated., UL https://www.microbiologyresearch.org/content/journal/micro/10.1099/mic.0.045187-0