Denitrification

Nitrogen cycle.

Denitrification is a microbially facilitated process of nitrate reduction (performed by a large group of heterotrophic facultative anaerobic bacteria) that may ultimately produce molecular nitrogen (N2) through a series of intermediate gaseous nitrogen oxide products. This respiratory process reduces oxidized forms of nitrogen in response to the oxidation of an electron donor such as organic matter. The preferred nitrogen electron acceptors in order of most to least thermodynamically favorable include nitrate (NO3), nitrite (NO2), nitric oxide (NO), nitrous oxide (N2O) finally resulting in the production of dinitrogen (N2) completing the nitrogen cycle. Denitrifying microbes require a very low oxygen concentration of less than 10%, as well as organic C for energy. Since denitrification can lower leaching of NO3 to groundwater, it can be strategically used to treat sewage or animal residues of high nitrogen content. Denitrification allows for the production of N2O, which is a greenhouse gas that can have a considerable influence on global warming.

The process is performed primarily by heterotrophic bacteria (such as Paracoccus denitrificans and various pseudomonads),[1] although autotrophic denitrifiers have also been identified (e.g., Thiobacillus denitrificans).[2] Denitrifiers are represented in all main phylogenetic groups.[3] Generally several species of bacteria are involved in the complete reduction of nitrate to molecular nitrogen, and more than one enzymatic pathway has been identified in the reduction process.[4]

Direct reduction from nitrate to ammonium, a process known as dissimilatory nitrate reduction to ammonium or DNRA,[5] is also possible for organisms that have the nrf-gene.[6] This is less common than denitrification in most ecosystems as a means of nitrate reduction. Other genes known in microorganisms which denitrify include nir (nitrite reductase) and nos (nitrous oxide reductase) among others;[7] organisms identified as having these genes include Alcaligenes faecalis, Alcaligenes xylosoxidans, many in the Pseudomonas genus, Bradyrhizobium japonicum, and Blastobacter denitrificans.[8]

Nutrient limitation

All organisms require certain nutrients in their surroundings (available to them) for survival.[9] Depending upon the ecosystem, nitrogen is most likely the limiting nutrient, although phosphorus is the other primary limiting nutrient and these two elements interact chemically.[10] Some organisms appear to be able to denitrify and remove phosphorus.[11] The triple bond of N2 makes this a very stable compound; most organisms (i.e. plants) depend upon others to break this down to make it available for biochemical reactions.[12] See Nitrification. Symbiotic relationships between Rhizobium species and legumes are well-documented.[13]

Conditions required

Denitrification takes place under special conditions in both terrestrial and marine ecosystems.[14] In general, it occurs where oxygen, a more energetically favourable electron acceptor, is depleted, and bacteria respire nitrate as a substitute terminal electron acceptor. Due to the high concentration of oxygen in our atmosphere denitrification only takes place in anoxic environments where oxygen consumption exceeds the oxygen supply and where sufficient quantities of nitrate are present. These environments may include certain soils[15] and groundwater,[16] wetlands, oil reservoirs,[17] poorly ventilated corners of the ocean, and in seafloor sediments.

Denitrification generally proceeds through some combination of the following intermediate forms:

NO
3
NO
2
→ NO + N
2
O
N
2
(g)

The complete denitrification process can be expressed as a redox reaction:

2 NO3 + 10 e + 12 H+ → N2 + 6 H2O

This reaction shows a fractionation in isotope composition. Lighter isotopes of nitrogen are preferred in the reaction, leaving the heavier nitrogen isotopes in the residual matter. The process can cause delta-values of up to −40, where delta is a representation of the difference in isotopic composition . This can be used to identify denitrification processes in nature.

Use in wastewater treatment

Further information: Sewage treatment

Denitrification is commonly used to remove nitrogen from sewage and municipal wastewater. It is also an instrumental process in constructed wetlands[18] and riparian zones[19] for the prevention of groundwater pollution with nitrate resulting from excessive agricultural or residential fertilizer usage.[20] Wood chip bioreactors have been studied since the 2000s and are effective in removing nitrate from agricultural run off[21] and even manure.[22]

Reduction under anoxic conditions can also occur through process called anaerobic ammonium oxidation (anammox):[23]

NH4+ + NO2 → N2 + 2 H2O

In some wastewater treatment plants, small amounts of methanol, ethanol, acetate, glycerin, or proprietary products are added to the wastewater to provide a carbon source for the denitrification bacteria.[24] Denitrification processes are also used in the treatment of industrial wastewater.[25]

Influence on global climate change

Increasing carbon dioxide levels within the atmosphere will influence global nutrient cycling, yet it is difficult to predict what those interactions might be.[26] Chemical interactions between soils and the atmosphere will be influenced by changes in atmospheric composition.[27] There are indications that increased fertilization of soils with nitrogen causes a decrease in carbon sequestration.[28]

It has been shown that streams and rivers receiving nitrogen inputs from urban and agricultural land uses are a significant source of nitrous oxide to the atmosphere.[29]

See also

References

  1. Carlson, C. A.; Ingraham, J. L. (1983). "Comparison of denitrification by Pseudomonas stutzeri, Pseudomonas aeruginosa, and Paracoccus denitrificans". Appl. Environ. Microbiol 45: 1247–1253.
  2. Baalsrud, K., and K. S. Baalsrud. 1954. Studies on Thiobacillus denitrificans. Archives of Microbiology 20:34-62.
  3. Zumft, W (1997). "Cell biology and molecular basis of denitrification". Microbiol. Mol. Biol. Rev 61: 533–616.
  4. Atlas, R.M., Barthas, R. Microbial Ecology: Fundamentals and Applications. 3rd Ed. Benjamin-Cummings Publishing. ISBN 0-8053-0653-6
  5. An, S., and W. S. Gardner. 2002. Dissimilatory nitrate reduction to ammonium (DNRA) as a nitrogen link, versus denitrification as a sink in a shallow estuary (Laguna Madre/Baffin Bay, Texas). Marine Ecology Progress Series 237:41-50.
  6. Spanning, R., M. Delgado, and D. Richardson. 2005. "It is possible to encounter DNRA when your source of carbon is a fermentable substrate, as glucose, so if you wanna avoid DNRA use a non fermentable substrate. The Nitrogen Cycle: Denitrification and its Relationship to N2 Fixation, p. 277-342."
  7. Zumft, W (1997). "Cell biology and molecular basis of denitrification". Microbiol. Mol. Biol. Rev 61: 533–616.
  8. Liu, X.; Tiquia, S. M.; Holguin, G.; Wu, L.; Nold, S. C.; Devol, A. H.; Luo, K.; Palumbo, A. V.; Tiedje, J. M.; Zhou, J. (2003). "Molecular Diversity of Denitrifying Genes in Continental Margin Sediments within the Oxygen-Deficient Zone off the Pacific Coast of Mexico". Appl. Environ. Microbiol 69: 3549–3560. doi:10.1128/aem.69.6.3549-3560.2003.
  9. Howarth, R. W. 1988. Nutrient Limitation of Net Primary Production in Marine Ecosystems. Annual Review of Ecology and Systematics 19:89-110.
  10. Vance, C. P. (2001). "Symbiotic Nitrogen Fixation and Phosphorus Acquisition. Plant Nutrition in a World of Declining Renewable Resources". Plant Physiol 127: 390–397. doi:10.1104/pp.010331.
  11. Kuba, T., M. C. M. Van Loosdrecht, F. A. Brandse, and J. J. Heijnen. 1997. Occurrence of denitrifying phosphorus removing bacteria in modified UCT-type wastewater treatment plants. Water Research 31:777-786.
  12. Seitzinger, S.; Harrison, J. A.; Bohlke, J. K.; Bouwman, A. F.; Lowrance, R.; Peterson, B.; Tobias, C.; Drecht, G. V. (2006). "Denitrification Across Landscapes and Waterscapes: A Synthesis". Ecological Applications 16: 2064–2090. doi:10.1890/1051-0761(2006)016[2064:dalawa]2.0.co;2.
  13. Daniel, R. M., I. M. Smith, J. A. D. Phillip, H. D. Ratcliffe, J. W. Drozd, and A. T. Bull. 1980. Anaerobic Growth and Denitrification by Rhizobium japonicum and Other Rhizobia. J Gen Microbiol 120:517-521.
  14. Seitzinger, S.; Harrison, J. A.; Bohlke, J. K.; Bouwman, A. F.; Lowrance, R.; Peterson, B.; Tobias, C.; Drecht, G. V. (2006). "Denitrification Across Landscapes and Waterscapes: A Synthesis". Ecological Applications 16: 2064–2090. doi:10.1890/1051-0761(2006)016[2064:dalawa]2.0.co;2.
  15. Scaglia, J.; Lensi, R.; Chalamet, A. (1985). "Relationship between photosynthesis and denitrification in planted soil". Plant and Soil 84 (1): 37–43. doi:10.1007/BF02197865.
  16. Korom, Scott F. (1992). "Natural Denitrification in the Saturated Zone: A Review". Water Resources Research 28 (6): 1657–1668. Bibcode:1992WRR....28.1657K. doi:10.1029/92WR00252.
  17. Cornish Shartau, S. L.; Yurkiw, M.; Lin, S.; Grigoryan, A. A.; Lambo, A.; Park, H. S.; Lomans, B. P.; Van Der Biezen, E.; Jetten, M. S. M.; Voordouw, G. (2010). "Ammonium Concentrations in Produced Waters from a Mesothermic Oil Field Subjected to Nitrate Injection Decrease through Formation of Denitrifying Biomass and Anammox Activity". Applied and Environmental Microbiology 76 (15): 4977–4987. doi:10.1128/AEM.00596-10. PMC 2916462. PMID 20562276.
  18. Bachand, P. A. M., and A. J. Horne. 1999. Denitrification in constructed free-water surface wetlands: II. Effects of vegetation and temperature. Ecological Engineering 14:17-32.
  19. Martin, T. L., N. K. Kaushik, J. T. Trevors, and H. R. Whiteley. 1999. Review: Denitrification in temperate climate riparian zones. Water, Air, and Soil Pollution 111:171-186.
  20. Mulvaney, R. L., S. A. Khan, and C. S. Mulvaney. 1997. Nitrogen fertilizers promote denitrification. Biology and Fertility of Soils 24:211-220.
  21. Ghane E, Fausey NR, Brown LC. "Modeling nitrate removal in a denitrification bed. Water Res. 2015 Jan 30;71C:294-305. doi: 10.1016/j.watres.2014.10.039. PMID 25638338 (subscription required)
  22. Carney KN1, Rodgers M, Lawlor PG, Zhan X. "Treatment of separated piggery anaerobic digestate liquid using woodchip biofilters." Environ Technology. 2013 Mar-Apr;34(5-8):663-70. doi:10.1080/09593330.2012.710408 PMID 23837316 (subscription required)
  23. Dalsgaard, T.; Thamdrup, B.; Canfield, D. E. (2005). "Anaerobic ammonium oxidation (anammox) in the marine environment". Research in Microbiology 156: 457–464. doi:10.1016/j.resmic.2005.01.011.
  24. Chen, K.-C.; Lin, Y.-F. (1993). "The relationship between denitrifying bacteria and methanogenic bacteria in a mixed culture system of acclimated sludges". Water Research 27: 1749–1759. doi:10.1016/0043-1354(93)90113-v.
  25. Constantin, H.; Fick, M. (1997). "Influence of C-sources on the denitrification rate of a high-nitrate concentrated industrial wastewater". Water Research 31: 583–589. doi:10.1016/s0043-1354(96)00268-0.
  26. Sinclair, T. R. (1992). "Mineral Nutrition and Plant Growth Response to Climate Change". J. Exp. Bot. 43: 1141–1146. doi:10.1093/jxb/43.8.1141.
  27. Rosenzweig, C.; Hillel, D. (2000). "Soils and Global Climate Change: Challenges and Opportunities". Soil Science 165: 47–56. doi:10.1097/00010694-200001000-00007.
  28. Oren, R.; Ellsworth, D. S.; Johnsen, K. H.; Phillips, N.; Ewers, B. E.; Maier, C.; Schafer, K. V. R.; McCarthy, H.; Hendrey, G.; McNulty, S. G.; Katul, G. G. (2001). "Soil fertility limits carbon sequestration by forest ecosystems in a CO2-enriched atmosphere". Nature 411: 469–472.
  29. "New study focuses on nitrogen in waterways as cause of nitrous oxide in the atmosphere".

Literature

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