Skip to main content
Applied and Environmental Microbiology logoLink to Applied and Environmental Microbiology
. 1995 Apr;61(4):1246–1251. doi: 10.1128/aem.61.4.1246-1251.1995

Anaerobic oxidation of ammonium is a biologically mediated process.

A A van de Graaf 1, A Mulder 1, P de Bruijn 1, M S Jetten 1, L A Robertson 1, J G Kuenen 1
PMCID: PMC167380  PMID: 7747947

Abstract

A newly discovered process by which ammonium is converted to dinitrogen gas under anaerobic conditions (the Anammox process) has now been examined in detail. In order to confirm the biological nature of this process, anaerobic batch culture experiments were used. All of the ammonium provided in the medium was oxidized within 9 days. In control experiments with autoclaved or raw wastewater, without added sludge or with added sterilized (either autoclaved or gamma irradiated) sludge, no changes in the ammonium and nitrate concentrations were observed. Chemical reactions could therefore not be responsible for the ammonium conversion. The addition of chloramphenicol, ampicillin, 2,4-dinitrophenol, carbonyl cyanide m-chlorophenyl-hydrazone (CCCP), and mercuric chloride (HgIICl2) completely inhibited the activity of the ammonium-oxidizing sludge. Furthermore, the rate of ammonium oxidation was proportional to the initial amount of sludge used. It was therefore concluded that anaerobic ammonium oxidation was a microbiological process. As the experiments were carried out in an oxygen-free atmosphere, the conversion of ammonium to dinitrogen gas did not even require a trace of O2. That the end product of the reaction was nitrogen gas has been confirmed by using 15NH4+ and 14NO3-. The dominant product was 14-15N2. Only 1.7% of the total labelled nitrogen gas produced was 15-15N2. It is therefore proposed that the N2 produced by the Anammox process is formed from equimolar amounts of NH4+ and NO3-.

Full Text

The Full Text of this article is available as a PDF (236.1 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Broda E. Two kinds of lithotrophs missing in nature. Z Allg Mikrobiol. 1977;17(6):491–493. doi: 10.1002/jobm.3630170611. [DOI] [PubMed] [Google Scholar]
  2. Brooks M. H., Smith R. L., Macalady D. L. Inhibition of existing denitrification enzyme activity by chloramphenicol. Appl Environ Microbiol. 1992 May;58(5):1746–1753. doi: 10.1128/aem.58.5.1746-1753.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. FAWCETT J. K., SCOTT J. E. A rapid and precise method for the determination of urea. J Clin Pathol. 1960 Mar;13:156–159. doi: 10.1136/jcp.13.2.156. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Poth M. Dinitrogen production from nitrite by a nitrosomonas isolate. Appl Environ Microbiol. 1986 Oct;52(4):957–959. doi: 10.1128/aem.52.4.957-959.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Poth M., Focht D. D. N Kinetic Analysis of N(2)O Production by Nitrosomonas europaea: an Examination of Nitrifier Denitrification. Appl Environ Microbiol. 1985 May;49(5):1134–1141. doi: 10.1128/aem.49.5.1134-1141.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Ritchie G. A., Nicholas D. J. Identification of the sources of nitrous oxide produced by oxidative and reductive processes in Nitrosomonas europaea. Biochem J. 1972 Mar;126(5):1181–1191. doi: 10.1042/bj1261181. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Thauer R. K., Jungermann K., Decker K. Energy conservation in chemotrophic anaerobic bacteria. Bacteriol Rev. 1977 Mar;41(1):100–180. doi: 10.1128/br.41.1.100-180.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Applied and Environmental Microbiology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES