4.8 Article

Ammonia oxidation at pH 2.5 by a new gammaproteobacterial ammonia-oxidizing bacterium

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ISME JOURNAL
卷 15, 期 4, 页码 1150-1164

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SPRINGERNATURE
DOI: 10.1038/s41396-020-00840-7

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资金

  1. European Research Council (ERC Advanced Grant project VOLCANO) [669371]
  2. European Research Council (ERC Advanced Grant project EcoMoM) [339880]
  3. Netherlands Organisation for Scientific Research (NWO Gravitation grant) [SIAM 024.002.002]
  4. Netherlands Organisation for Scientific Research (VIDI grant) [016.Vidi.189.050]
  5. European Research Council (ERC) [669371] Funding Source: European Research Council (ERC)

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The study discovered a novel gammaproteobacterial ammonia-oxidizing bacterium that can grow and oxidize ammonia at extremely acidic conditions (pH 2.5), showing high ammonia affinity and tolerance to toxic nitric oxide. This bacterium has a chemolithoautotrophic lifestyle and was characterized through physiological, genomic, and transcriptomic analyses. Phylogenetic analysis revealed it belongs to a novel bacterial genus, proposed to be named Candidatus Nitrosacidococcus tergens sp. RJ19.
Ammonia oxidation was considered impossible under highly acidic conditions, as the protonation of ammonia leads to decreased substrate availability and formation of toxic nitrogenous compounds. Recently, some studies described archaeal and bacterial ammonia oxidizers growing at pH as low as 4, while environmental studies observed nitrification at even lower pH values. In this work, we report on the discovery, cultivation, and physiological, genomic, and transcriptomic characterization of a novel gammaproteobacterial ammonia-oxidizing bacterium enriched via continuous bioreactor cultivation from an acidic air biofilter that was able to grow and oxidize ammonia at pH 2.5. This microorganism has a chemolithoautotrophic lifestyle, using ammonia as energy source. The observed growth rate on ammonia was 0.196 day(-1), with a doubling time of 3.5 days. The strain also displayed ureolytic activity and cultivation with urea as ammonia source resulted in a growth rate of 0.104 day(-1) and a doubling time of 6.7 days. A high ammonia affinity (K-m(app) = 147 +/- 14 nM) and high tolerance to toxic nitric oxide could represent an adaptation to acidic environments. Electron microscopic analysis showed coccoid cell morphology with a large amount of intracytoplasmic membrane stacks, typical of gammaproteobacterial ammonia oxidizers. Furthermore, genome and transcriptome analysis showed the presence and expression of diagnostic genes for nitrifiers (amoCAB, hao, nor, ure, cbbLS), but no nirK was identified. Phylogenetic analysis revealed that this strain belonged to a novel bacterial genus, for which we propose the name Candidatus Nitrosacidococcus tergens sp. RJ19.

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