Bioprocess and Biosystems Engineering

, Volume 40, Issue 5, pp 731–739 | Cite as

Rapid start-up of nitrifying MBBRs at low temperatures: nitrification, biofilm response and microbiome analysis

  • Bradley Young
  • Robert Delatolla
  • Turki Abujamel
  • Kevin Kennedy
  • Edith Laflamme
  • Alain Stintzi
Research Paper

Abstract

The moving bed biofilm reactor (MBBR), operated as a post carbon removal system, requires long start-up times in comparison to carbon removal systems due to slow growing autotrophic organisms. This study investigates the use of carriers seeded in a carbon rich treatment system prior to inoculation in a nitrifying MBBR system to promote the rapid development of nitrifying biofilm in an MBBR system at temperatures between 6 and 8 °C. Results show that nitrification was initiated by the carbon removal carriers after 22 h of operation. High throughput 16S-rDNA sequencing indicates that the sloughing period was a result of heterotrophic organism detachment and the recovery and stabilization period included a growth of Nitrosomonas and Nitrospira as the dominant ammonia oxidizing bacteria (AOB) and nitrite oxidizing bacteria (NOB) in the biofilm. Peripheral microorganisms such as Myxococcales, a rapid EPS producer, appear to have contributed to the recovery and stabilization of the biofilm.

Keywords

MBBR Ammonia removal System start-up Biofilm morphology Next generation sequencing 

Notes

Acknowledgements

The authors are grateful for the financial support from the Natural Science and Engineering Research Council of Canada and Veolia Water Technologies. The authors thank Daina Forrest, Walid Mottawea and James Butcher of the University of Ottawa for their technical support. The authors acknowledge the Saudi Arabian Cultural Bureau in Canada for scholarship contribution from King Abdulaziz University.

Supplementary material

449_2017_1739_MOESM1_ESM.docx (711 kb)
Supplementary material 1 (DOCX 710 KB)

References

  1. 1.
    Canada Gazette (2012) Wastewater systems effluent regulations. Part II. 146(15)Google Scholar
  2. 2.
    Metcalf and Eddy (2003) Wastewater engineering: treatment and reuse, 4th edn. McGraw-Hill, New YorkGoogle Scholar
  3. 3.
    Maas CL, Parker WJ, Legge RL (2008) Detachment of solids and nitrifiers in integrated, fixed-film activated sludge systems. Water Environ Res 80(12):2202–2208CrossRefGoogle Scholar
  4. 4.
    Flemming HC, Wingender J (2010) The biofilm matrix. Nat Rev Microbiol 8(9):623f–633Google Scholar
  5. 5.
    Delatolla R, Tufenkji N, Comeau Y, Gadbois A, Lamarre D, Berk D (2012) Effects of long exposure to low temperatures on nitrifying biofilm and biomass in wastewater treatment. Water Environ Res 84(4):328–338CrossRefGoogle Scholar
  6. 6.
    Di Trapani D, Christensson M, Torregrossa M, Viviani G, Ødegaard H (2013) Performance of a hybrid activated sludge/biofilm process for wastewater treatment in a cold climate region: influence of operating conditions. Biochem Eng J 77:214–219CrossRefGoogle Scholar
  7. 7.
    Hoang V, Delatolla R, Abujamel T, Mottawea W, Gadbois A, Laflamme E, Stintzi A (2014) Nitrifying moving bed biofilm reactor (MBBR) biofilm and biomass response to long term exposure to 1 °C. Water Res 49:215–224CrossRefGoogle Scholar
  8. 8.
    Hibiya K, Tsuneda S, Hirata A (2000) Formation and characteristics of nitrifying biofilm on a membrane modified with positively-charged polymer chains. Coll Surf B Biointerfaces 18(2):105–112CrossRefGoogle Scholar
  9. 9.
    Tsuneda S, Park S, Hayashi H, Jung J, Hirata A (2001) Enhancement of nitrifying biofilm formation using selected EPS produced by heterotrophic bacteria. Water Sci Technol 43(6):197–204Google Scholar
  10. 10.
    Wijffels RH, Englund G, Hunik JH, Leenen EJTM, Bakketun A, Gunther A, Obon de Castro JM, Tramper J (1994) Effects of diffusion limitation on immobilized nitrifying microorganisms at low temperatures. Biotechnol Bioeng 45:1–9CrossRefGoogle Scholar
  11. 11.
    Sumino T, Nakamura H, Mori N, Kawaguchi Y (1992) Immobilization of nitrifying bacteria by polyethylene glycol prepolymer. J Ferment Bioeng 73(1):37–42CrossRefGoogle Scholar
  12. 12.
    Sriwiriyarat T, Ungkurarate W, Fongsatitkul P, Chinwetkitvanich S (2008) Effects of dissolved oxygen on biological nitrogen removal in integrated fixed film activated sludge (IFAS) wastewater treatment process. J Environ Sci Health Part A Tox/Hazard Subst Environ Eng 43(5):518–527CrossRefGoogle Scholar
  13. 13.
    Kwon S, Kim T, Yu GH, Jung J, Park H (2010) Bacterial community composition and diversity of a full-scale integrated fixed-film activated sludge system as investigated by pyrosequencing. J Microbiol Biotechnol 20(12):1717–1723Google Scholar
  14. 14.
    Telgmann U, Horn H, Morgenroth E (2004) Influence of growth history on sloughing and erosion from biofilms. Water Res 38(17):3671–3684CrossRefGoogle Scholar
  15. 15.
    APHA A WEF (ed) (1995) Standard methods for the examination of water and wastewater. 19 edn. A.P.H.A.A.W.W.A.W.E. Federation, Washington DC, USAGoogle Scholar
  16. 16.
    Delatolla R, Berk D, Tufenkji N (2008) Rapid and reliable quantification of biofilm weight and nitrogen content of biofilm attached to polystyrene beads. Water Res 42:3082–3088CrossRefGoogle Scholar
  17. 17.
    Delatolla R, Berk D, Tufenkji N (2009) In-situ characterization of nitrifying biofilm: minimizing biomass loss and preserving perspective. Water Res 43:1775–1787CrossRefGoogle Scholar
  18. 18.
    Young B, Banihashemi B, Forrest D, Kennedy K, Stintzi A, Delatolla R (2016) Meso and micro-scale response of post carbon removal nitrifying MBBR biofilm across carrier type and loading. Water Res 91:235–243CrossRefGoogle Scholar
  19. 19.
    Magoč T, Salzberg SL (2011) FLASH: fast length adjustment of short reads to improve genome assemblies. Bioinform 27(21):2957–2963CrossRefGoogle Scholar
  20. 20.
    Goecks J, Nekrutenko A, Taylor J, The Galaxy Team (2010) Galaxy: a comprehensive approach for supporting accessible, reproducible, and transparent computational research in the life sciences. Genome Biol 11:R86CrossRefGoogle Scholar
  21. 21.
    Caporaso JG, Kuczynski J, Stombaugh J, Bittinger K, Bushman FD, Costello EK, Fierer N, Gonzalez Peña A, Goodrich JK, Gordon JI, Huttley GA, Kelley ST, Knights D, Koenig JE, Ley RE, Lozupone CA, McDonald D, Muegge BD, Pirrung M, Reeder J, Sevinsky JR, Turnbaugh PJ, Walters WA, Widmann J, Yatzunenko T, Zaneveld J, Knight R (2010) QIIME allows analysis of high-throughput community sequencing data. Nat Methods 7(5):335–336CrossRefGoogle Scholar
  22. 22.
    Giardine B, Riemer C, Hardison RC, Burhans R, Shah P, Zhang Y, Blankenberg D, Albert I, Taylor J, Miller W, Kent J, Nekrutenko A (2005) Galaxy: a platform for interactive large-scale genome analysis. Genome Res 15:1451–1455CrossRefGoogle Scholar
  23. 23.
    Blankenberg D, Von Kuster G, Coraor N., Ananda G, Lazarus R, Mangan M, Nekrutenko A, Taylor J (2010) Galaxy: a web-based genome analysis tool for experimentalists. Curr Protoc Mol Biol 19.10.1–19.10.21Google Scholar
  24. 24.
    Segata N, Izard J, Waldron L, Gevers D, Miropolsky L, Garrett WS, Huttenhower C (2011) Metagenomic biomarker discovery and explanation. Genome Biol 12(6):R60CrossRefGoogle Scholar
  25. 25.
    WEF (2010) Design of municipal wastewater treatment plants: WEF manual of practice no. 8, 5th edn. McGraw-Hill, New YorkGoogle Scholar
  26. 26.
    Laspidou CS, Rittmann BE (2004) Evaluating trends in biofilm density using the UMCCA model. Water Res 38(14–15):3362–3372CrossRefGoogle Scholar
  27. 27.
    Dugan P, Stoner D, Pickrum H (2006) The Genus Zoogloea. Prokaryotes 7:960–970Google Scholar
  28. 28.
    Bryan C, Marchal M, Battaglia-Brunet F, Kugler V, Lemaitre-Guillier C, Liévremont D, Bertin P, Arséne-Ploetze F (2009) Carbon and arsenic metabolism in Thiomonas strains : differences revealed diverse adaptation processes. BMC Microbiol 9(127): doi: 10.1186/1471-2180-9-127
  29. 29.
    Kertesz M, Kawaski A (2010) In: Timmis KN (ed) Handbook of hydrocarbon and lipid microbiology. Springer, BerlinGoogle Scholar
  30. 30.
    Cottrell MT, Kirchman DL (2000) Natural assemblages of marine proteobacteria and members of the Cytophaga-Flavobacter cluster consuming low- and high-molecular-weight dissolved organic matter. Appl Environ Microbiol 66(4):1692–1697CrossRefGoogle Scholar
  31. 31.
    Lee SH, Ka JO, Cho JC (2008) Members of the phylum Acidobacteria are dominant and metabolically active in rhizosphere soil. FEMS Microbiol Lett 285:263–269CrossRefGoogle Scholar
  32. 32.
    Kulichevskaya IS, Suzina NE, Liesack W, Dedysh SN (2010) Bryobacter aggregatus gen. nov., sp. nov., a peat-inhabiting, aerobic chemo-organotroph from subdivision 3 of the Acidobacteria. Int J Syst Evol Microbiol 60(Pt 2):301–306CrossRefGoogle Scholar
  33. 33.
    Lee LY, Ong SL, Ng WJ (2004) Biofilm morphology and nitrification activities: recovery of nitrifying biofilm particles covered with heterotrophic outgrowth. Bioresour Technol 95(2):209–214CrossRefGoogle Scholar

Copyright information

© Springer-Verlag Berlin Heidelberg 2017

Authors and Affiliations

  • Bradley Young
    • 1
  • Robert Delatolla
    • 1
  • Turki Abujamel
    • 2
    • 3
  • Kevin Kennedy
    • 1
  • Edith Laflamme
    • 4
  • Alain Stintzi
    • 2
  1. 1.Department of Civil Engineering, Faculty of EngineeringUniversity of OttawaOttawaCanada
  2. 2.Department of Biochemistry, Microbiology and Immunology, Faculty of MedicineOttawa Institute of Systems Biology, University of OttawaOttawaCanada
  3. 3.Department of Medical Technology, Faculty of Applied Medical SciencesKing Abdulaziz UniversityJeddahSaudi Arabia
  4. 4.Veolia Water Technologies CanadaMontrealCanada

Personalised recommendations