Skip to main content

Advertisement

Log in

Mass production of nitrifying bacterial consortia for the rapid establishment of nitrification in saline recirculating aquaculture systems

  • Original Paper
  • Published:
World Journal of Microbiology and Biotechnology Aims and scope Submit manuscript

Abstract

Two distinct nitrifying bacterial consortia, namely an ammonia oxidizing non-penaeid culture (AMONPCU-1) and an ammonia oxidizing penaeid culture (AMOPCU-1), have been mass produced in a nitrifying bacterial consortia production unit (NBCPU). The consortia, maintained at 4°C were activated and cultured in a 2 l fermentor initially. At this stage the net biomass (0.105 and 0.112 g/l), maximum specific growth rate (0.112 and 0.105/h) and yield coefficients (1.315 and 2.08) were calculated respectively, for AMONPCU-1 and AMOPCU-1 on attaining stationary growth phase. Subsequently on mass production in a 200 l NBCPU under optimized culture conditions, the total amounts of NH4 +–N removed by AMONPCU-1 and AMOPCU-1 were 1.948 and 1.242 g/l within 160 and 270 days, respectively. Total alkalinity reduction of 11.7–14.4 and 7.5–9.1 g/l were observed which led to the consumption of 78 and 62 g Na2CO3. The yield coefficient and biomass of AMONPCU-1 were 0.67 and 125.3 g/l and those of AMOPCU-1 were 1.23 and 165 g/l. The higher yield coefficient and growth rate of AMOPCU-1 suggest better energy conversion efficiency and higher CO2 fixation potential. Both of the consortia were dominated by Nitrosomonas-like organisms. The consortia may find application in the establishment of nitrification within marine and brackish water culture systems.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  • Achuthan C, Kumar VJR, Manju NJ, Philip R, Singh ISB (2006) Development of nitrifying bacterial consortia for immobilizing in nitrifying bioreactors designed for penaeid and non-penaeid larval rearing systems in the tropics. Indian J Mar Sci 35:240–248

    CAS  Google Scholar 

  • Bendschneider K, Robinson RJ (1952) A spectrophotometric method for the determination of nitrite in seawater. J Mar Res 11:87–96

    CAS  Google Scholar 

  • Bovendeur J (1989) Fixed biofilm reactors applied to waste water treatment and aquacultural water recirculating systems. Dissertation, Department of Environmental Technology, Wageningen University, P.O. Box 8192, 6700 EV Wageningen, The Netherlands, 133 pp

  • Chapman BD, Schleicher M, Beuger A, Gostomski P, Thiele JH (2006) Improved methods for the cultivation of chemolithoautotrophic bacterium Nitrosomonas europea. J Microbiol Methods 65:96–106. doi:10.1016/j.mimet.2005.06.013

    Article  CAS  Google Scholar 

  • Cheng W, Hsiao IS, Chen JC (2004) Effect of nitrite on immune response of Taiwan abalone Haliotis diversicolor supertexta and its susceptibility to Vibrio parahaemolyticus. Dis Aquat Organ 60:157–164. doi:10.3354/dao060157

    Article  CAS  Google Scholar 

  • Diab S, Shilo M (1988) Transformation of nitrogen in sediments of fish ponds in Israel. Bamidgeh 38:67–88

    Google Scholar 

  • EPA (1975) Process design manual for nitrogen control. Environment protection agency (Brochure). Office of technology Transfer, Washington, DC

    Google Scholar 

  • Gernaey K, Vanrolleghem PA, Verstrate W (1998) Online estimation of Nitrosomonas kinetic parameters in activated sludge samples using titration in-sensor experiments. Water Res 32:71–80. doi:10.1016/S0043-1354(97)00185-1

    Article  CAS  Google Scholar 

  • Gray NF (1990) Activated sludge: theory and practice. Oxford University Press, Oxford, pp 153–176

    Google Scholar 

  • Johnstone BH, Jones RD (1988) Effects of light and CO on the survival of a marine ammonium-oxidizing bacterium during energy source deprivation. Appl Environ Microbiol 54:2890–2893

    CAS  Google Scholar 

  • Lawrence AW, McCarty PL (1970) United basis for biological treatment design and operation. J San Eng Div ASCE 96:757–778

    Google Scholar 

  • Nejidat A, Abeliovich A (1994) Detection of Nitrosomonas spp. by polymerase chain reaction. FEMS Microbiol Lett 120:191–194. doi:10.1111/j.1574-6968.1994.tb07029.x

    Article  CAS  Google Scholar 

  • Piedrahita RH (2003) Reducing the potential environmental impact of tank aquaculture effluents through intensification and recirculation. Aquaculture 226:35–44. doi:10.1016/S0044-8486(03)00465-4

    Article  CAS  Google Scholar 

  • Ramachandran K (1998) Development of bioreactors for nitrifying sewage. Ph.D. Thesis. Cochin University of Science and Technology. Kochi, India

  • Rittmann BE, Snoeyink VL (1984) Achieving biologically stable drinking water. J Am Wastewater Assoc 76(10):106–114

    CAS  Google Scholar 

  • Sharma B, Ahlert RC (1977) Nitrification and nitrogen removal. Water Res 11:897–925. doi:10.1016/0043-1354(77)90078-1

    Article  CAS  Google Scholar 

  • Seo JK, Jung IH, Kim MR, Kim BJ, Nam SW, Kim SK (2001) Nitrification performance of nitrifiers immobilized in PVA (polyvinyl alcohol) for a marine recirculating aquarium system. Aquacult Eng 24:181–194. doi:10.1016/S0144-8609(01)00063-2

    Article  Google Scholar 

  • Shnel N, Barak Y, Ezer T, Dafni Z, van Rijn J (2002) Design and performance of a zero-discharge tilapia recirculating system. Aquacult Eng 26:191–203. doi:10.1016/S0144-8609(02)00013-4

    Article  Google Scholar 

  • Singh ISB, Kumar VJR, Achuthan C, Manju NJ, Philip R (2007) Recirculation zero water exchange system for hatchery rearing of economically important marine organisms. In: Vijayan KK, Jayasankar P, Vijayagopal P (eds) Indian fisheries—a progressive outlook. Central Marine Fisheries Institute, Kochi, pp 139–155

    Google Scholar 

  • Solorzano L (1969) Determination of ammonia in natural waters by the phenol hypochlorite method. Limnol Oceanogr 14:799–801

    Article  CAS  Google Scholar 

  • Stensel HD, Barnard JL (1992) Principles of biological nutrient removal. In: Randal CW, Barnard JL, Stensel HD (eds) Design and retrofit wastewater treatment plants for biological nutrient removal. Technomic Pub. Co. Inc., Lancaster, pp 25–45

    Google Scholar 

  • Strickland JD, Parsons TR (1972) A practical handbook of seawater analysis, Bulletin 167. Fisheries Research Board of Canada, Ottawa, Canada, p 310

    Google Scholar 

  • Svobodova Z, Machova J, Poleszczu G, Hoda J, Hamaakova J, Kroupova H (2005) Nitrite poisoning of fish in aquaculture facilities with water-recirculating systems. Acta Vet Burnesis 74:129–137

    CAS  Google Scholar 

  • Tappe W, Tomaschewski C, Rittershaus S, Groeneweg J (1996) Cultivation of nitrifying bacteria in the retentostat, a simple fermenter with internal biomass retention. FEMS Microbiol Ecol 19:47–52. doi:10.1111/j.1574-6941.1996.tb00197.x

    Article  CAS  Google Scholar 

  • USEPA (1993) Process design manual of nitrogen control. EPA 625/r-93/010, Cincinnati, Ohio

  • Vadivelu VM, Keller J, Yuan Z (2006) Stoichiometric and kinetic characterization of Nitrosomonas sp. in mixed culture by decoupling the growth and energy generation processes. J Biotechnol 126:342–356. doi:10.1016/j.jbiotec.2006.04.017

    Article  CAS  Google Scholar 

  • Valenti WC, Daniels W (2000) Recirculation hatchery systems and management. In: New MB, Valenti WC (eds) Freshwater prawn culture: the farming of Macrobrachium rosenbergii. Blackwell Science, Oxford, England, pp 69–90

    Chapter  Google Scholar 

  • Van Hulle SWH, Volcke EIP, Lopez Teruel J, Donckels BV, Loosdrecht MCM, Vanrolleghem PA (2004) Influence of temperature and pH on the kinetics of the SHARON nitritation process. In: 4th IWA World Water Conference, Marrakech, Morocco

  • Voytek MA, Ward BB (1995) Detection of ammonium-oxidizing bacteria of the beta-subclass of the class Proteobacteria in aquatic samples with PCR. Appl Environ Microbiol 61:1444–1450

    CAS  Google Scholar 

  • Wagner M, Rath G, Koops HP, Flood J, Amann R (1996) In situ analysis of nitrifying bacteria in sewage treatment plants. Water Sci Technol 34:237–244. doi:10.1016/0273-1223(96)00514-8

    Article  CAS  Google Scholar 

  • Watson SW (1965) Characteristics of a marine nitrifying bacterium, Nitrosocystis oceanus sp. n. Limnol Oceanogr 10:274–289

    Google Scholar 

  • Wiesmann V (1994) Biological nitrogen removal from wastewater. In: Fiechter A (ed) Advances in biochemical engineering, vol 51. Springer-Verlag, Berlin, pp 113–154

    Google Scholar 

  • Zart D, Bock E (1998) High rate of aerobic nitrification and denitrification by Nitrosomonas eutropha grown in a fermentor with complete biomass retention in the presence of gaseous NO2 or NO. Arch Microbiol 169:282–286. doi:10.1007/s002030050573

    Article  CAS  Google Scholar 

Download references

Acknowledgements

This work was carried out with the financial assistance from Department of Biotechnology, Government of India under project no. BT/DRI 794/AAQ/03/092/99. Acknowledge Dr. Valsamma Joseph, Lecturer, NCAAH, CUSAT for analysis of the data and Prof. Robert H. Reed, Central Queensland University, Australia for language editing.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to I. S. Bright Singh.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Rejish Kumar, V.J., Achuthan, C., Manju, N.J. et al. Mass production of nitrifying bacterial consortia for the rapid establishment of nitrification in saline recirculating aquaculture systems. World J Microbiol Biotechnol 25, 407–414 (2009). https://doi.org/10.1007/s11274-008-9905-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11274-008-9905-1

Keywords

Navigation