Ammonia oxidation capacity of bacillus bacteria in swine wastewater after biogas treatment
Vol. 131 No. 1D (2022), Original Article
Vol. 131 No. 1D (2022)

Ammonia oxidation capacity of bacillus bacteria in swine wastewater after biogas treatment

Original Article
https://doi.org/10.26459/hueunijns.v131i1D.7006
Published 2022-12-31
Nguyen Huu Dong*
Ha Tinh University, Cam Vinh, Cam Xuyen, Ha Tinh, Vietnam
Nguyen Thi Viet
Hard Bee Scientific Research and Technology Transfer Joint Stock Company, A124 Portion, Phu My Thuong Urban area, Phu Thuong, Hue, Vietnam
Dinh Thi Thu Hang
Graduate University of Science and Technology - Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet St., Nghia Do, Cau Giay, Ha Noi, Vietnam
Phan Do Hung
Institute of Environmental Technology - Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet St., Nghia Do, Cau Giay, Ha Noi, Vietnam
Tran Hoa Dung
Hard Bee Scientific Research and Technology Transfer Joint Stock Company, A124 Portion, Phu My Thuong Urban area, Phu Thuong, Hue, Vietnam
PDF

Keywords

Bacillus; vi khuẩn oxy hóa amoni; sự nitrit hóa Bacillus
ammonium-oxidising bacteria
nitrification
denitrification

How to Cite

1.
Nguyen HD, Nguyen TV, Dinh TTH, Phan Do DH, Tran HD. Ammonia oxidation capacity of bacillus bacteria in swine wastewater after biogas treatment. hueuni-jns [Internet]. 2022Dec.31 [cited 2024Dec.5];131(1D):77-8. Available from: https://jos.hueuni.edu.vn/index.php/hujos-ns/article/view/7006
ACM ACS APA ABNT Chicago Harvard IEEE MLA Turabian Vancouver

Download Citation

Endnote/Zotero/Mendeley (RIS) BibTeX
Crossref
Scopus
Google Scholar
Europe PMC

Abstract

Nitrogen removal with biological methods plays a crucial role in wastewater treatment technology. The treatment begins with the oxidation of ammonia to nitrite to facilitate the subsequent nitrification and denitrification. Various strains of ammonia-oxidising bacteria have been reported. In this study, we use three Bacillus bacteria isolated from swine wastewater to oxidise ammonia. Different initial densities (103, 104, 105, and 106 CFU·mL–1) of each strain were examined. The results show that the combination of all the bacteria at a ratio of 1:1:1 and a density of 105 CFU·mL–1 exhibits the most effect. The findings contribute to the diversity of ammonia-oxidising bacterial species and pose a great potential for applying these strains in wastewater treatment.

https://doi.org/10.26459/hueunijns.v131i1D.7006
PDF

References

  1. Tua TV. Researching and applying advanced technology suitable to Vietnamese conditions to treat environmental pollution in combination with making use of waste from pig farms, Report on scientific and technological results of state-level topics KC08.04. Hanoi: Vietnam Academy of Science and Technology; 2015.
  2. Hong NT, Lieu PK. Treatment efficiencies of household-scale biogas systems on piggery wastewater in Thua Thien Hue province. Hue University Journal of Science. 2012;73(4):83-91.
  3. Ha NT, Anh NV, Anh NN. Assessment of wastewater flow and treatment in some pig breeding facilities. Environment Magazine. 2020;1.
  4. Lin L, Yuan S, Chen J, Xu Z, Lu X. Removal of ammonia nitrogen in wastewater by microwave radiation. Journal of hazardous materials. 2009; 161(2-3):1063-8.
  5. Dachs J, Eisenreich SJ, RM H. Influence of Eutrophication on air–water exchange, vertical fluxes, and phytoplankton concentrations of persistent organic pollutants. Environ Sci Technol. 2000;34(6):1095-102.
  6. Camargo JA, Alonso Á. Ecological and toxicological effects of inorganic nitrogen pollution in aquatic ecosystems: a global assessment. Environment International. 2006;32(6):831-49.
  7. Colt JE, Armstrong DA. Nitrogen toxicity to crustaceans, fish, and molluscs. In: LJ Allen, editors. Proceedings of the Bio-Engineering Symposium for Fish Culture Fish Culture Section, American Fisheries Society, Northeast Society of Conservation Engineers, Bethesda, MD; California: University of California; 1981. p. 34-47.
  8. Chen JC, Liu PC, Lei SC. Toxicity of ammonia and nitrit to Penaeus monodon adolescents. Aquaculture. 1990;89(2):127-37.
  9. Welander U, Henrysson T, Welander T. Biological nitrogen removal from municipal landfill leachate in a pilot scale suspended carrier biofilm process. Water research. 1998;32(5):1564-70.
  10. Zangeneh A, Sabzalipour S, Takdatsan A, Yengejeh RJ, Khafaie MA. Ammonia removal form municipal wastewater by air stripping process: An experimental study. South African Journal of Chemical Engineering. 2021;36:134-41.
  11. Li XZ, Zhao QL, Hao XD. Ammonium removal from landfill leachate by chemical precipitation. Waste Manage. 1999;19(6):409-15.
  12. Kim KW, Kim YJ, IT K, Park GI, Lee EH. Electrochemical conversion characteristics of ammonia to nitrogen. Water research. 2006; 40(7):1431-41.
  13. Focht DD, Chang AC. Nitrification and denitrification processes related to waste water treatment. Advances in applied microbiology. 1975; 19:153-86.
  14. Lee CG, Fletcher TD, Sun G. Nitrogen removal in constructed wetland systems. Engineering in life sciences. 2009;9(1):11-22.
  15. Prakasam TBS, Loehr RC. Microbial nitrification and denitrification in concentrated wastes. Water Research. 1972;6(7):859-69.
  16. Bock E, Wagner M. Oxidation of Inorganic Nitrogen Compounds as an Energy Source. In: Dworkin M, Falkow S, Rosenberg E, Schleifer K-H, Stackebrandt E, editors. The Prokaryotes: Volume 2: Ecophysiology and Biochemistry. New York, NY: Springer New York; 2006. p. 457-95.
  17. Bergey DH, Holt JG. Bergey's manual of determinative bacteriology. Ninth edition ed. Baltimore: Williams & Wilkins; 1994.
  18. Winogradsky S. Recherches sur les organismes de la nitrification. Ann inst Pasteur. 1890;4:213-31.
  19. Fujitani H, Kumagai A, Ushiki N, Momiuchi K, Tsuneda S. Selective isolation ammonia-oxidizing bacteria from autotrophic nitrifying granules by applying cell-sorting and sub-culturing of microcolonies. Frontiers in Microbiology. 2015; 6(1159):1-10.
  20. Itoh Y, Sakagami K, Uchino Y, Boonmak C, Oriyama T, Tojo F, et al. Isolation and characterization of a thermotolerant ammonia-oxidizing bacterium Nitrosomonas sp. JPCCT2 from a thermal Power station. Microbes and Environments. 2013;28(4):432-5.
  21. Satoh K, Tanaka T, Yuuichi O, Takahashi R, Tokuyama T. Improvement of preservation method for ammonia-oxidizing bacteria by freeze-drying. Soil Science Plant Nutrition. 2004;5(50):777-81.
  22. Shimaya C, Hashimoto T. Improvement of media for thermophilic ammonia-oxidizing bacteria in compost. Soil Science and Plant Nutrition. 2008; 54(4):529-33.
  23. Tokuyama T, Mine A, Kamiyama K, Yabe R, Satoh K, Masumoto H, Takahashi R, et al. Nitrosomonas communis strain YNSRA, an ammonia-oxidizing bacterium, isolated from the Reed Rhizoplane in an aquaponics plant. Journal of Bioscience and Bioengineering. 2004;98(4):309-12.
  24. Norton JM. Diversity and environmental distribution of ammonia-oxidizing bacteria. ASM Press, Washington. 2011;3:39-55.
  25. Rostron WM, Stuckey DC, Young AA. Nitrification of high strength ammonia wastewaters: comparative study of immobilization media. Water Research. 2001;35:1169-78.
  26. Van Loosdrecht MCM, Jetten MSM. Microbiological conversion in nitrogen removal. Water Science and Technology. 1998;38:1-7.
  27. Barnes D, Bliss PJ. Biological Control of Nitrogen in Wastewater Treatment. Cambridge: Cambridge University Press; 1983.
  28. Joo HS, Hirai M, Shoda M. Nitrification and denitrification in high strength ammonium by Alcaligenes feacalis. Biotechnology Letters. 2005; 27(11):773-8.
  29. Kim DJ, Lee DI, Keller J. Effect of temperature and free ammonia on nitrification and nitrite accumulation in landfill leachate and analysis of its nitrifying bacterial community by FISH. Bioresource Technology. 2006;97:459-64.
  30. Zhao B, He YL, Hughes J, Zhang XF. Heterotrophic nitrogen removal by a newly isolated Acinetobacter calcoaceticus HNR. Bioresource Technology. 2010; 101(14):5194-200.
  31. Zhao B, An Q, He YL, Guo JS. N2O and N2 production during heterotrophic nitrification by Alcaligenes faecalis strain NR. Bioresource technology. 2012;116:379-85.
  32. Ren YX, Yang L, Liang X. The characteristics of a novel heterotrophic nitrifying and aerobic denitrifying bacterium, Acinetobacter junii YB. Bioresource Technology. 2014;171:1-9.
  33. Muller T, Walter B, Wirtz A, Barkovski A. Ammonium toxicity in bacteria. Current Microbiology. 2006;52:400-6.
  34. Sheela B, Khasim BS, Yellaji RO. Bioremediation of ammonia using ammonia oxidizing bacteria isolated from sewage. International Journal of Environmental Bioremediation & Biodegradation. 2014;2(4):146-50.
  35. Kim JK, Park JK, Cho KS, Nam SW, Park TJ, Bajpai R. Aerobic nitrification-denitrification by heterotrophic Bacillus species strains. Bioresource Technology. 2005;96:1897-906.
  36. Yang XP, Wang SM, Zhang DW, Zhou LX. Isolation and nitrogen removal characteristics of an aerobic heterotrophic nitrifying-denitrifying bacterium, Bacillus subtilis A1. Bioresource Technology. 2011; 102:854-62.
  37. Lin Y, Kong HN, He YL, Lui BB, Inamori Y, Yan L. Isolation and characterization of a new heterotrophic nitrifying Bacillus sp. strain. Biomedical and Environmental Sciences. 2007; 20:450-5.
  38. Leejeerajumnean A, Ames JM, Owens JD. Effect of ammonia on the growth of Bacillus species and some other bacteria. Letters in Applied microbiology. 2000;30:385-9.
  39. Atlas RM. Handbook of Media for Environmental Microbiology (2nd ed.). Boca Raton: CRC Press:. 2005. 672 p.
  40. Hong HA, Duc H, Cutting SM. The use of bacterial spore formers as probiotics. FEMS Microbiol Rev. 2005;29(4):813-35.
  41. Loncar N, Gligorijević N, Božić NA, Vujčić Z. Congo red degrading laccases from Bacillus amyloliquefaciens strains isolated from salt spring in Serbia. Int Biodeter Biodegr. 2014;91:18-23.
  42. Mahdhi A, Esteban M, Hmila Z, Bekir K, Kamoun F, Bakhrouf A, Krifi B. Survival and retention of the probiotic properties of Bacillus sp. strains under marine stress starvation conditions and their potential use as a probiotic in Artemia culture. Res Vet Sci. 2012;93:1151-9.
  43. Reda R, Selim K. Evaluation of Bacillus amyloliquefaciens on the growth performance, intestinal morphology, hematology and body compo-sition of Nile tilapia, Oreochromis niloticus. Aquacult Int. 2015;23:203-17.
  44. Cao H, He S, Wei R, Diong M, Lu L. Bacillus amyloliquefaciens G1: a potential antagonistic bacterium against eel-pathogenic Aeromonas hydrophila. Evi-dence-based complement Altern Med. 2011:1-7.
  45. Li K, Zheng T, Tian Y, Xi F, Yuan J, Zhang G, Hong H. Beneficial effects of Bacillus licheniformis on the intestinal microflora and immunity of the white shrimp, Litopenaeus vannamei. Biotechnology Letters. 2007;29:525-30.
  46. Aftabuddin S, Kashem MA, Kader MA, Sikder MNA, Hakim MA. Use of Streptomyces fradiae and Bacillus megaterium as probiotics in the experimental culture of tiger shrimp Penaeus monodon (Crustacea, Penaeidae). Aquaculture, Aquarium, Conservation & Legislation. 2013;6(3): 253-67.
  47. Meng R, He L, Xi B, Hu X, Li Y. Experimental study on purifying aquaculture wastewater between Bacillus and nitrifying bacteria. Environmental Science & Technology (China). 2009;3(11):28-31.
  48. Liu L, Gao J, Huang Z, Li Y, Shang N, Gao J, Cai M. Potential Application of a Pseudomonas geniculata ATCC 19374 and Bacillus cereus EC3 Mixture in Livestock Wastewater Treatment. Waste and Biomass Valorization. 2021;12(7):3927-38.
  49. Guo J, Chen C, Chen W, Jiang J, Chen B, Zheng F. Effective immobilization of Bacillus subtilis in chitosan-sodium alginate composite carrier for ammonia removal from anaerobically digested swine wastewater. Chemosphere. 2021;284:131266.
  50. Tien HV, Diep CN, Ngon TT. TOptimization of bioflocculant produced by Bacillus aryabhattai KG12S and its application in piggery wastewater treament after biogas system. Part B: Agriculture, Fisheries and Biotechnology, Can Tho University Journal of Science. 2015;37(1):32-41.
Creative Commons License

This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.

Copyright (c) 2022 Array