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Anaerobic ammonia oxidizing bacteria: ecological distribution, metabolism, and microbial interactions

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Abstract

Anammox (ANaerobic AMMonia OXidation) is a newly discovered pathway in the nitrogen cycle. This discovery has increased our knowledge of the global nitrogen cycle and triggered intense interest for anammox-based applications. Anammox bacteria are almost ubiquitous in the suboxic zones of almost all types of natural ecosystems and contribute significant to the global total nitrogen loss. In this paper, their ecological distributions and contributions to the nitrogen loss in marine, wetland, terrestrial ecosystems, and even extreme environments were reviewed. The unique metabolic mechanism of anammox bacteria was well described, including the particular cellular structures and genome compositions, which indicate the special evolutionary status of anammox bacteria. Finally, the ecological interactions among anammox bacteria and other organisms were discussed based on substrate availability and spatial organizations. This review attempts to summarize the fundamental understanding of anammox, provide an up-to-date summary of the knowledge of the overall anammox status, and propose future prospects for anammox. Based on novel findings, the metagenome has become a powerful tool for the genomic analysis of communities containing anammox bacteria; the metabolic diversity and biogeochemistry in the global nitrogen budget require more comprehensive studies.

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References

  1. Dalsgaard T, Thamdrup B, Canfield D E. Anaerobic ammonium oxidation (anammox) in the marine environment. Research in Microbiology, 2005, 156(4): 457–464

    Article  CAS  Google Scholar 

  2. Broda E. Two kinds of lithotrophs missing in nature. Zeitschrift fur allgemeine Mikrobiologie, 1977, 17(6): 491–493

    Article  CAS  Google Scholar 

  3. Mulder A, Graaf A, Robertson L, Kuenen J. Anaerobic ammonium oxidation discovered in a denitrifying fluidized bed reactor. FEMS Microbiology Ecology, 1995, 16(3): 177–184

    Article  CAS  Google Scholar 

  4. van de Graaf A A, Mulder A, de Bruijn P, Jetten M S, Robertson L A, Kuenen J G. Anaerobic oxidation of ammonium is a biologically mediated process. Applied and Environmental Microbiology, 1995, 61(4): 1246–1251

    Google Scholar 

  5. Liu S, Yang F, Gong Z, Meng F, Chen H, Xue Y, Furukawa K. Application of anaerobic ammonium-oxidizing consortium to achieve completely autotrophic ammonium and sulfate removal. Bioresource Technology, 2008, 99(15): 6817–6825

    Article  CAS  Google Scholar 

  6. Kuypers M M, Sliekers A O, Lavik G, Schmid M, Jørgensen B B, Kuenen J G, Sinninghe Damsté J S, Strous M, Jetten M S. Anaerobic ammonium oxidation by anammox bacteria in the Black Sea. Nature, 2003, 422(6932): 608–611

    Article  CAS  Google Scholar 

  7. Woebken D, Lam P, Kuypers M M, Naqvi SW, Kartal B, Strous M, Jetten M S, Fuchs B M, Amann R. A microdiversity study of anammox bacteria reveals a novel Candidatus Scalindua phylotype in marine oxygen minimum zones. Environmental Microbiology, 2008, 10(11): 3106–3119

    Article  CAS  Google Scholar 

  8. Li H, Chen S, Mu B Z, Gu J D. Molecular detection of anaerobic ammonium-oxidizing (anammox) bacteria in high-temperature petroleum reservoirs. Microbial Ecology, 2010, 60(4): 771–783

    Article  CAS  Google Scholar 

  9. Hong Y G, Li M, Cao H, Gu J D. Residence of habitat-specific anammox bacteria in the deep-sea subsurface sediments of the South China Sea: Analyses of marker gene abundance with physical chemical parameters. Microbial Ecology, 2011, 62(1): 36–47

    Article  Google Scholar 

  10. van de Vossenberg J, Woebken D, Maalcke WJ, Wessels H J, Dutilh B E, Kartal B, Janssen-Megens E M, Roeselers G, Yan J, Speth D, Gloerich J, Geerts W, van der Biezen E, Pluk W, Francoijs K J, Russ L, Lam P, Malfatti S A, Tringe S G, Haaijer S C, Op den Camp H J, Stunnenberg H G, Amann R, Kuypers M M, Jetten M S. The metagenome of the marine anammox bacterium ‘Candidatus Scalindua profunda’ illustrates the versatility of this globally important nitrogen cycle bacterium. Environmental Microbiology, 2013, 15(5): 1275–1289

    Article  Google Scholar 

  11. Fuchsman C A, Staley J T, Oakley B B, Kirkpatrick J B, Murray J W. Free-living and aggregate-associated Planctomycetes in the Black Sea. FEMS Microbiology Ecology, 2012, 80(2): 402–416

    Article  CAS  Google Scholar 

  12. Dalsgaard T, Canfield D E, Petersen J, Thamdrup B, Acuña-González J. N2 production by the anammox reaction in the anoxic water column of Golfo Dulce, Costa Rica. Nature, 2003, 422(6932): 606–608

    Article  CAS  Google Scholar 

  13. Lam P, Lavik G, Jensen M M, van de Vossenberg J, Schmid M, Woebken D, Gutiérrez D, Amann R, Jetten M S M, Kuypers M M M. Revising the nitrogen cycle in the Peruvian oxygen minimum zone. Proceedings of the National Academy of Sciences of the United States of America, 2009, 106(12): 4752–4757

    Article  CAS  Google Scholar 

  14. Rush D, Wakeham S G, Hopmans E C, Schouten S, Sinninghe Damsté J S. Biomarker evidence for anammox in the oxygen minimum zone of the Eastern Tropical North Pacific. Organic Geochemistry, 2012, 53: 80–87

    Article  CAS  Google Scholar 

  15. Nicholls J C, Davies C A, Trimmer M. High-resolution profiles and nitrogen isotope tracing reveal a dominant source of nitrous oxide and multiple pathways of nitrogen gas formation in the central Arabian Sea. Limnology and Oceanography, 2007, 52(1): 156–168

    Article  CAS  Google Scholar 

  16. Jensen M M, Lam P, Revsbech N P, Nagel B, Gaye B, Jetten M S, Kuypers M M. Intensive nitrogen loss over the Omani Shelf due to anammox coupled with dissimilatory nitrite reduction to ammonium. The ISME Journal, 2011, 5(10): 1660–1670

    CAS  Google Scholar 

  17. Kuypers M M, Lavik G, Woebken D, Schmid M, Fuchs B M, Amann R, Jørgensen B B, Jetten M S. Massive nitrogen loss from the Benguela upwelling system through anaerobic ammonium oxidation. Proceedings of the National Academy of Sciences of the United States of America, 2005, 102(18): 6478–6483

    Article  CAS  Google Scholar 

  18. Schneider B, Nausch G, Pohl C. Mineralization of organic matter and nitrogen transformations in the Gotland Sea deep water. Marine Chemistry, 2010, 119(1–4): 153–161

    Article  CAS  Google Scholar 

  19. Schmid MC, Risgaard-Petersen N, van de Vossenberg J, Kuypers M M, Lavik G, Petersen J, Hulth S, Thamdrup B, Canfield D, Dalsgaard T, Rysgaard S, Sejr M K, Strous M, den Camp H J, Jetten M S. Anaerobic ammonium-oxidizing bacteria in marine environments: Widespread occurrence but low diversity. Environmental Microbiology, 2007, 9(6): 1476–1484

    Article  CAS  Google Scholar 

  20. Thamdrup B, Dalsgaard T. Production of N2 through anaerobic ammonium oxidation coupled to nitrate reduction in marine sediments. Applied and Environmental Microbiology, 2002, 68(3): 1312–1318

    Article  CAS  Google Scholar 

  21. Shu Q, Jiao N. Profiling Planctomycetales diversity with reference to anammox-related bacteria in a South China Sea, deep-sea sediment. Marine Ecology (Berlin), 2008, 29(4): 413–420

    Article  CAS  Google Scholar 

  22. Trimmer M, Nicholls J C. Production of nitrogen gas via anammox and denitrification in intact sediment cores along a continental shelf to slope transect in the North Atlantic. Limnology and Oceanography, 2009, 54(2): 577–589

    Article  CAS  Google Scholar 

  23. Shehzad A, Liu J, Yu M, Qismat S, Liu J, Zhang X H. Diversity, community composition and abundance of anammox bacteria in sediments of the North Marginal Seas of China. Microbes and Environments, 2016, 31(2): 111–120

    Article  Google Scholar 

  24. Kartal B, Kuypers MM, Lavik G, Schalk J, Op den Camp H J, Jetten M S, Strous M. Anammox bacteria disguised as denitrifiers: Nitrate reduction to dinitrogen gas via nitrite and ammonium. Environmental Microbiology, 2007, 9(3): 635–642

    Article  CAS  Google Scholar 

  25. Schubert C J, Durisch-Kaiser E, Wehrli B, Thamdrup B, Lam P, Kuypers M M. Anaerobic ammonium oxidation in a tropical freshwater system (Lake Tanganyika). Environmental Microbiology, 2006, 8(10): 1857–1863

    Article  CAS  Google Scholar 

  26. Penton C R, Devol A H, Tiedje J M. Molecular evidence for the broad distribution of anaerobic ammonium-oxidizing bacteria in freshwater and marine sediments. Applied and Environmental Microbiology, 2006, 72(10): 6829–6832

    Article  CAS  Google Scholar 

  27. Wang S, Zhu G, Peng Y, Jetten M S, Yin C. Anammox bacterial abundance, activity, and contribution in riparian sediments of the Pearl River estuary. Environmental Science & Technology, 2012, 46 (16): 8834–8842

    Article  CAS  Google Scholar 

  28. Han P, Gu J D. Further analysis of anammox bacterial community structures along an anthropogenic nitrogen-input gradient from the riparian sediments of the Pearl River Delta to the deep-ocean sediments of the South China Sea. Geomicrobiology Journal, 2015, 32(9): 789–798

    Article  CAS  Google Scholar 

  29. Hou L J, Zheng Y L, Liu M, Gong J, Zhang X L, Yin G Y, You L. Anaerobic ammonium oxidation (anammox) bacterial diversity, abundance, and activity in marsh sediments of the Yangtze Estuary. Journal of Geophysical Research. Biogeosciences, 2013, 118(3): 1237–1246

    Article  CAS  Google Scholar 

  30. Nicholls J C, Trimmer M. Widespread occurrence of the anammox reaction in estuarine sediments. Aquatic Microbial Ecology, 2009, 55(2): 105–113

    Article  Google Scholar 

  31. Fernandes S O, Michotey V D, Guasco S, Bonin P C, Bharathi P A. Denitrification prevails over anammox in tropical mangrove sediments (Goa, India). Marine Environmental Research, 2012, 74: 9–19

    Article  CAS  Google Scholar 

  32. Koop-Jakobsen K, Giblin A E. Anammox in tidal marsh sediments: The role of salinity, nitrogen loading, and marsh vegetation. Estuaries and Coasts, 2009, 32(2): 238–245

    Article  CAS  Google Scholar 

  33. Sato Y, Ohta H, Yamagishi T, Guo Y, Nishizawa T, Rahman M H, Kuroda H, Kato T, Saito M, Yoshinaga I, Inubushi K, Suwa Y. Detection of anammox activity and 16S rRNA genes in ravine paddy field soil. Microbes and Environments, 2012, 27(3): 316–319

    Article  Google Scholar 

  34. Hamersley M R, Woebken D, Boehrer B, Schultze M, Lavik G, Kuypers M M. Water column anammox and denitrification in a temperate permanently stratified lake (Lake Rassnitzer, Germany). Systematic and Applied Microbiology, 2009, 32(8): 571–582

    Article  CAS  Google Scholar 

  35. Dale O R, Tobias C R, Song B. Biogeographical distribution of diverse anaerobic ammonium oxidizing (anammox) bacteria in Cape Fear River Estuary. Environmental Microbiology, 2009, 11(5): 1194–1207

    Article  CAS  Google Scholar 

  36. Fu B, Liu J, Yang H, Hsu T C, He B, Dai M, Kao S J, Zhao M, Zhang X H. Shift of anammox bacterial community structure along the Pearl Estuary and the impact of environmental factors. Journal of Geophysical Research. Oceans, 2015, 120(4): 2869–2883

    Article  Google Scholar 

  37. Wang J, Gu J D. Dominance of Candidatus Scalindua species in anammox community revealed in soils with different duration of rice paddy cultivation in Northeast China. Applied Microbiology and Biotechnology, 2013, 97(4): 1785–1798

    Article  CAS  Google Scholar 

  38. Rich J J, Dale O R, Song B, Ward B B. Anaerobic ammonium oxidation (anammox) in Chesapeake Bay sediments. Microbial Ecology, 2008, 55(2): 311–320

    Article  CAS  Google Scholar 

  39. Zhu G, Wang S, Wang Y, Wang C, Risgaard-Petersen N, Jetten MS, Yin C. Anaerobic ammonia oxidation in a fertilized paddy soil. The ISME Journal, 2011, 5(12): 1905–1912

    CAS  Google Scholar 

  40. Li M, Cao H, Hong Y G, Gu J D. Seasonal dynamics of anammox bacteria in estuarial sediment of the Mai Po Nature Reserve revealed by analyzing the 16S rRNA and hydrazine oxidoreductase (hzo) genes. Microbes and Environments, 2011, 26(1): 15–22

    Article  CAS  Google Scholar 

  41. Sun W, Xu M Y, Wu W M, Guo J, Xia C Y, Sun G P, Wang A J. Molecular diversity and distribution of anammox community in sediments of the Dongjiang River, a drinking water source of Hong Kong. Journal of Applied Microbiology, 2014, 116(2): 464–476

    Article  CAS  Google Scholar 

  42. Moore T A. Detection of Anammox Bacteria in Ammonium-Contaminated Groundwater. Waterloo, Canada: University of Waterloo, 2011

    Google Scholar 

  43. Zhao Y, Xia Y, Kana T M, Wu Y, Li X, Yan X. Seasonal variation and controlling factors of anaerobic ammonium oxidation in freshwater river sediments in the Taihu Lake region of China. Chemosphere, 2013, 93(9): 2124–2131

    Article  CAS  Google Scholar 

  44. Lee K H, Wang Y F, Zhang G X, Gu J D. Distribution patterns of ammonia-oxidizing bacteria and anammox bacteria in the freshwater marsh of Honghe wetland in Northeast China. Ecotoxicology (London, England), 2014, 23(10): 1930–1942

    Article  CAS  Google Scholar 

  45. Naeher S, Huguet A, Roose-Amsaleg C L, Laverman AM, Fosse C, Lehmann M F, Derenne S, Zopfi J. Molecular and geochemical constraints on anaerobic ammonium oxidation (anammox) in a riparian zone of the Seine Estuary (France). Biogeochemistry, 2015, 123(1–2): 237–250

    Article  CAS  Google Scholar 

  46. Bernard R J, Mortazavi B, Kleinhuizen A A. Dissimilatory nitrate reduction to ammonium (DNRA) seasonally dominates NO3–reduction pathways in an anthropogenically impacted sub-tropical coastal lagoon. Biogeochemistry, 2015, 125(1): 47–64

    Article  CAS  Google Scholar 

  47. Deng F, Hou L, Liu M, Zheng Y, Yin G, Li X, Lin X, Chen F, Gao J, Jiang X. Dissimilatory nitrate reduction processes and associated contribution to nitrogen removal in sediments of the Yangtze Estuary. Journal of Geophysical Research. Biogeosciences, 2015, 120(8): 1521–1531

    Article  CAS  Google Scholar 

  48. Long A, Heitman J, Tobias C, Philips R, Song B. Co-occurring anammox, denitrification, and codenitrification in agricultural soils. Applied and Environmental Microbiology, 2013, 79(1): 168–176

    Article  CAS  Google Scholar 

  49. Humbert S, Tarnawski S, Fromin N, Mallet MP, Aragno M, Zopfi J. Molecular detection of anammox bacteria in terrestrial ecosystems: Distribution and diversity. The ISME Journal, 2010, 4(3): 450–454

    Article  Google Scholar 

  50. Hu B L, Rush D, van der Biezen E, Zheng P, van Mullekom M, Schouten S, Sinninghe Damsté J S, Smolders A J, Jetten MS, Kartal B. New anaerobic, ammonium-oxidizing community enriched from peat soil. Applied and Environmental Microbiology, 2011, 77(3): 966–971

    Article  CAS  Google Scholar 

  51. Rysgaard S, Glud R N, Sejr M K, Blicher M E, Stahl H J. Denitrification activity and oxygen dynamics in Arctic sea ice. Polar Biology, 2008, 31(5): 527–537

    Article  Google Scholar 

  52. Byrne N, Strous M, Crépeau V, Kartal B, Birrien J L, Schmid M, Lesongeur F, Schouten S, Jaeschke A, Jetten M, Prieur D, Godfroy A. Presence and activity of anaerobic ammonium-oxidizing bacteria at deep-sea hydrothermal vents. The ISME Journal, 2009, 3(1): 117–123

    Article  CAS  Google Scholar 

  53. Jaeschke A, Op den Camp H J, Harhangi H, Klimiuk A, Hopmans E C, Jetten M S, Schouten S, Sinninghe Damsté J S. 16S rRNA gene and lipid biomarker evidence for anaerobic ammonium-oxidizing bacteria (anammox) in California and Nevada hot springs. FEMS Microbiology Ecology, 2009, 67(3): 343–350

    Article  CAS  Google Scholar 

  54. Hong Y G, Yin B, Zheng T L. Diversity and abundance of anammox bacterial community in the deep-ocean surface sediment from equatorial Pacific. Applied Microbiology and Biotechnology, 2011, 89(4): 1233–1241

    Article  CAS  Google Scholar 

  55. Thamdrup B, Dalsgaard T, Jensen M M, Ulloa O, Farias L, Escribano R. Anaerobic ammonium oxidation in the oxygendeficient waters off northern Chile. Limnology and Oceanography, 2006, 51(5): 2145–2156

    Article  CAS  Google Scholar 

  56. Bulow S E, Rich J J, Naik H S, Pratihary A K, Ward B B. Denitrification exceeds anammox as a nitrogen loss pathway in the Arabian Sea oxygen minimum zone. Deep-sea Research. Part I, Oceanographic Research Papers, 2010, 57(3): 384–393

    Article  CAS  Google Scholar 

  57. Pitcher A, Villanueva L, Hopmans E C, Schouten S, Reichart G J, Sinninghe Damsté J S. Niche segregation of ammonia-oxidizing archaea and anammox bacteria in the Arabian Sea oxygen minimum zone. The ISME Journal, 2011, 5(12): 1896–1904

    CAS  Google Scholar 

  58. Hamersley M R, Lavik G, Woebken D, Rattray J E, Lam P, Hopmans E C, Damste J S S, Kruger S, Graco M, Gutierrez D, Kuypers M M M. Anaerobic ammonium oxidation in the Peruvian oxygen minimum zone. Limnology and Oceanography, 2007, 52(3): 923–933

    Article  CAS  Google Scholar 

  59. Rysgaard S, Glud R N, Risgaard Petersen N, Dalsgaard T. Denitrification and anammox activity in Arctic marine sediments. Limnology and Oceanography, 2004, 49(5): 1493–1502

    Article  CAS  Google Scholar 

  60. Gihring T M, Lavik G, Kuypers M M M, Kostka J E. Direct determination of nitrogen cycling rates and pathways in Arctic fjord sediments (Svalbard, Norway). Limnology and Oceanography, 2010, 55(2): 740–752

    Article  CAS  Google Scholar 

  61. Bale N J, Villanueva L, Fan H, Stal L J, Hopmans E C, Schouten S, Sinninghe Damsté J S. Occurrence and activity of anammox bacteria in surface sediments of the southern North Sea. FEMS Microbiology Ecology, 2014, 89(1): 99–110

    Article  CAS  Google Scholar 

  62. Brandsma J, van de Vossenberg J, Risgaard-Petersen N, Schmid M C, Engström P, Eurenius K, Hulth S, Jaeschke A, Abbas B, Hopmans E C, Strous M, Schouten S, Jetten M S, Damsté J S. A multi-proxy study of anaerobic ammonium oxidation in marine sediments of the Gullmar Fjord, Sweden. Environmental Microbiology Reports, 2011, 3(3): 360–366

    Article  CAS  Google Scholar 

  63. Yang X R, Li H, Nie S A, Su J Q, Weng B S, Zhu G B, Yao H Y, Gilbert J A, Zhu Y G. Potential contribution of anammox to nitrogen loss from paddy soils in Southern China. Applied and Environmental Microbiology, 2015, 81(3): 938–947

    Article  Google Scholar 

  64. Nie S, Li H, Yang X, Zhang Z, Weng B, Huang F, Zhu G B, Zhu Y G. Nitrogen loss by anaerobic oxidation of ammonium in rice rhizosphere. The ISME Journal, 2015, 9(9): 2059–2067

    Article  CAS  Google Scholar 

  65. Shen L d, Zheng P h, Ma S j. Nitrogen loss through anaerobic ammonium oxidation in agricultural drainage ditches. Biology and Fertility of Soils, 2015, 52(2): 1–10

    Google Scholar 

  66. Boog J, Nivala J, Aubron T, Wallace S, van Afferden M, Müller R A. Hydraulic characterization and optimization of total nitrogen removal in an aerated vertical subsurface flow treatment wetland. Bioresource Technology, 2014, 162(0): 166–174

    Article  CAS  Google Scholar 

  67. van Niftrik L, Geerts W J C, van Donselaar E G, Humbel B M, Webb R I, Fuerst J A, Verkleij A J, Jetten MS M, Strous M. Linking ultrastructure and function in four genera of anaerobic ammoniumoxidizing bacteria: cell plan, glycogen storage, and localization of cytochrome C proteins. Journal of Bacteriology, 2008, 190(2): 708–717

    Article  Google Scholar 

  68. Rattray J E, van de Vossenberg J, Hopmans E C, Kartal B, van Niftrik L, Rijpstra W I C, Strous M, Jetten M S, Schouten S, Sinninghe Damsté J S. Ladderane lipid distribution in four genera of anammox bacteria. Archives of Microbiology, 2008, 190(1): 51–66

    Article  CAS  Google Scholar 

  69. Sinninghe Damsté J S, Strous M, Rijpstra W I C, Hopmans E C, Geenevasen J A J, van Duin A C T, van Niftrik L A, Jetten M S M. Linearly concatenated cyclobutane lipids form a dense bacterial membrane. Nature, 2002, 419(6908): 708–712

    Article  Google Scholar 

  70. van Niftrik L, van Helden M, Kirchen S, van Donselaar E G, Harhangi H R, Webb R I, Fuerst J A, Op den Camp H J, Jetten M S, Strous M. Intracellular localization of membrane-bound ATPases in the compartmentalized anammox bacterium “Candidatus Kuenenia stuttgartiensis”. Molecular Microbiology, 2010, 77(3): 701–715

    Article  Google Scholar 

  71. van Teeseling M C F, Mesman R J, Kuru E, Espaillat A, Cava F, Brun Y V, VanNieuwenhze M S, Kartal B, van Niftrik L. Anammox Planctomycetes have a peptidoglycan cell wall. Nature Communications, 2015, 6(1): 1–6

    Google Scholar 

  72. Schalk J, Oustad H, Kuenen J G, Jetten M S. The anaerobic oxidation of hydrazine: A novel reaction in microbial nitrogen metabolism. FEMS Microbiology Letters, 1998, 158(1): 61–67

    Article  CAS  Google Scholar 

  73. Jetten M S, Wagner M, Fuerst J, van Loosdrecht M, Kuenen G, Strous M. Microbiology and application of the anaerobic ammonium oxidation (“anammox”) process. Current Opinion in Biotechnology, 2001, 12(3): 283–288

    Article  CAS  Google Scholar 

  74. Oshiki M, Ali M, Shinyako-Hata K, Satoh H, Okabe S. Hydroxylamine-dependent anaerobic ammonium oxidation (anammox) by “Candidatus Brocadia sinica”. Environmental Microbiology, 2016, 18(9): 3133–3143

    Article  CAS  Google Scholar 

  75. Dietl A, Ferousi C, Maalcke W J, Menzel A, de Vries S, Keltjens J T, Jetten M S, Kartal B, Barends T R. The inner workings of the hydrazine synthase multiprotein complex. Nature, 2015, 527(7578): 394–397

    Article  CAS  Google Scholar 

  76. Jetten M S, Niftrik L, Strous M, Kartal B, Keltjens J T, Op den Camp H J. Biochemistry and molecular biology of anammox bacteria. Critical Reviews in Biochemistry and Molecular Biology, 2009, 44(2–3): 65–84

    Article  CAS  Google Scholar 

  77. van der Star W R, Dijkema C, de Waard P, Picioreanu C, Strous M, van Loosdrecht M C. An intracellular pH gradient in the anammox bacterium Kuenenia stuttgartiensis as evaluated by 31P NMR. Applied Microbiology and Biotechnology, 2010, 86(1): 311–317

    Article  CAS  Google Scholar 

  78. Strous M, Pelletier E, Mangenot S, Rattei T, Lehner A, TaylorMW, Horn M, Daims H, Bartol-Mavel D, Wincker P, Barbe V, Fonknechten N, Vallenet D, Segurens B, Schenowitz-Truong C, Médigue C, Collingro A, Snel B, Dutilh B E, Op den Camp H J, van der Drift C, Cirpus I, van de Pas-Schoonen K T, Harhangi H R, van Niftrik L, Schmid M, Keltjens J, van de Vossenberg J, Kartal B, Meier H, Frishman D, Huynen M A, Mewes H W, Weissenbach J, Jetten M S, Wagner M, Le Paslier D. Deciphering the evolution and metabolism of an anammox bacterium from a community genome. Nature, 2006, 440(7085): 790–794

    Article  Google Scholar 

  79. Kartal B, Maalcke W J, de Almeida N M, Cirpus I, Gloerich J, Geerts W, Op den Camp H J, Harhangi H R, Janssen-Megens E M, Francoijs K J, Stunnenberg H G, Keltjens J T, Jetten M S, Strous M. Molecular mechanism of anaerobic ammonium oxidation. Nature, 2011, 479(7371): 127–130

    Article  CAS  Google Scholar 

  80. Gori F, Tringe S G, Kartal B, Marchiori E, Jetten M S M. The metagenomic basis of anammox metabolism in Candidatus “Brocadia fulgida”. Biochemical Society Transactions, 2011, 39 (6): 1799–1804

    Article  CAS  Google Scholar 

  81. Hu Z, Speth D R, Francoijs K J, Quan Z X, Jetten MS. Metagenome analysis of a complex community reveals the metabolic blueprint of anammox bacterium “Candidatus Jettenia asiatica”. Frontiers in Microbiology, 2012, 3: 366

    Article  Google Scholar 

  82. Fuchsman C A, Rocap G. Whole-genome reciprocal BLAST analysis reveals that planctomycetes do not share an unusually large number of genes with Eukarya and Archaea. Applied and Environmental Microbiology, 2006, 72(10): 6841–6844

    Article  CAS  Google Scholar 

  83. De Clippeleir H, Defoirdt T, Vanhaecke L, Vlaeminck S E, Carballa M, Verstraete W, Boon N. Long-chain acylhomoserine lactones increase the anoxic ammonium oxidation rate in an OLAND biofilm. Applied Microbiology and Biotechnology, 2011, 90(4): 1511–1519

    Article  CAS  Google Scholar 

  84. Kartal B, Koleva M, Arsov R, van der Star W, Jetten MS, Strous M. Adaptation of a freshwater anammox population to high salinity wastewater. Journal of Biotechnology, 2006, 126(4): 546–553

    Article  CAS  Google Scholar 

  85. Kartal B, Rattray J, van Niftrik L A, van de Vossenberg J, Schmid M C, Webb R I, Schouten S, Fuerst J A, Damsté J S, Jetten M S, Strous M. Candidatus “Anammoxoglobus propionicus” a new propionate oxidizing species of anaerobic ammonium oxidizing bacteria. Systematic and Applied Microbiology, 2007, 30(1): 39–49

    Article  CAS  Google Scholar 

  86. Strous M, Kuenen J G, Jetten M S. Key physiology of anaerobic ammonium oxidation. Applied and Environmental Microbiology, 1999, 65(7): 3248–3250

    CAS  Google Scholar 

  87. Sonthiphand P, Hall M W, Neufeld J D. Biogeography of anaerobic ammonia-oxidizing (anammox) bacteria. Frontiers in Microbiology, 2014, 5: 1–14

    Article  Google Scholar 

  88. Lam P, Jensen M M, Lavik G, McGinnis D F, Müller B, Schubert C J, Amann R, Thamdrup B, Kuypers M M. Linking crenarchaeal and bacterial nitrification to anammox in the Black Sea. Proceedings of the National Academy of Sciences of the United States of America, 2007, 104(17): 7104–7109

    Article  CAS  Google Scholar 

  89. Woebken D, Fuchs B M, Kuypers M M, Amann R. Potential interactions of particle-associated anammox bacteria with bacterial and archaeal partners in the Namibian upwelling system. Applied and Environmental Microbiology, 2007, 73(14): 4648–4657

    Article  CAS  Google Scholar 

  90. Sliekers A O, Haaijer S, Schmid M, Harhangi H, Verwegen K, Kuenen J G, Jetten M S. Nitrification and anammox with urea as the energy source. Systematic and Applied Microbiology, 2004, 27(3): 271–278

    Article  CAS  Google Scholar 

  91. Vázquez-Padín J, Mosquera-Corral A, Campos J L, Méndez R, Revsbech N P. Microbial community distribution and activity dynamics of granular biomass in a CANON reactor. Water Research, 2010, 44(15): 4359–4370

    Article  Google Scholar 

  92. van Kessel M A, Speth D R, Albertsen M, Nielsen P H, Op den Camp H J, Kartal B, Jetten M S, Lücker S. Complete nitrification by a single microorganism. Nature, 2015, 528(7583): 555–559

    Article  Google Scholar 

  93. Dalsgaard T, Thamdrup B, Farias L, Revsbech N P. Anammox and denitrification in the oxygen minimum zone of the eastern South Pacific. Limnology and Oceanography, 2012, 57(5): 1331–1346

    Article  CAS  Google Scholar 

  94. Du R, Cao S, Li B, Niu M, Wang S, Peng Y. Performance and microbial community analysis of a novel DEAMOX based on partial-denitrification and anammox treating ammonia and nitrate wastewaters. Water Research, 2017, 108: 46–56

    Article  CAS  Google Scholar 

  95. Zhang X, Zhang H, Ye C, Wei M, Du J. Effect of COD/N ratio on nitrogen removal and microbial communities of CANON process in membrane bioreactors. Bioresource Technology, 2015, 189: 302–308

    Article  CAS  Google Scholar 

  96. Okabe S, Oshiki M, Takahashi Y, Satoh H. N2O emission from a partial nitrification-anammox process and identification of a key biological process of N2O emission from anammox granules. Water Research, 2011, 45(19): 6461–6470

    Article  CAS  Google Scholar 

  97. Ding J, Fu L, Ding Z W, Lu Y Z, Cheng S H, Zeng R J. Environmental evaluation of coexistence of denitrifying anaerobic methane-oxidizing archaea and bacteria in a paddy field. Applied Microbiology and Biotechnology, 2015, 100(1): 1–8

    Google Scholar 

  98. Kindaichi T, Yuri S, Ozaki N, Ohashi A. Ecophysiological role and function of uncultured Chloroflexi in an anammox reactor. Water Science and Technology, 2012, 66(12): 2556–2561

    Article  CAS  Google Scholar 

  99. Prokopenko M G, Hirst M B, De Brabandere L, Lawrence D J, Berelson W M, Granger J, Chang B X, Dawson S, Crane E J, Chong L, Thamdrup B, Townsend-Small A, Sigman D M. Nitrogen losses in anoxic marine sediments driven by Thioploca-anammox bacterial consortia. Nature, 2013, 500(7461): 194–198

    Article  CAS  Google Scholar 

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Acknowledgements

This work was supported by National Natural Science Foundation of China (Grant No. 31470543), Natural Science Foundation of Heilongjiang Province (No. ZD201412) and Harbin Science and Technology Program (No. 2016RAXXJ010).

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Correspondence to Dawen Gao.

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Gao, D., Wang, X., Liang, H. et al. Anaerobic ammonia oxidizing bacteria: ecological distribution, metabolism, and microbial interactions. Front. Environ. Sci. Eng. 12, 10 (2018). https://doi.org/10.1007/s11783-018-1035-x

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  • DOI: https://doi.org/10.1007/s11783-018-1035-x

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