Skip to main content
Log in

Continuous insect cell (Sf-9) culture with aeration through sparging

  • Original Papers
  • Published:
Applied Microbiology and Biotechnology Aims and scope Submit manuscript

Abstract

The continuous growth of Spodoptera frugiperda Sf-9 cells in a 250-ml blown-glass jacketed spinner flask under a direct air sparging environment was investigated. Even at 220 ml working volume (about 90% of total volume), this spinner flask provided good mixing and oxygenation as demonstrated by a higher cell density compared with fermentor cultures. This eliminates a common limitation of the traditional spinner flask, namely much lower cell density at high working volume. Furthermore, this spinner flask has been run with Sf-9 cell culture at five different dilution rates and two different air sparging rates at steady state, demonstrating its utility in research applications where cell size, metabolic activity and environmental conditions can be constantly maintained. In addition to demonstrating the utility of the reactor, three novel points are made in this report. First, cell density in continuous cultures is increased significantly due to a high agitation rate and, especially, air sparging rate, which is seldom used in animal cell or insect cell culture. Second, there is no apparent difference in the specific death rate at two different sparging rates (0.0093 vvm and 0.0125 vvm). Finally, we have maintained Sf-9 cells for more than 4 months in a continuous culture using a serum-free medium without loss of recombinant protein expression in infected cells.

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.

Similar content being viewed by others

References

  • Armstrong RN, Levin W, Jerine DM (1980) Hepatic microsomal hydrolase. J Biol Chem 255:4698

    Google Scholar 

  • Batt BC, Kompala DS (1989) A structured kinetic modeling framework for the dynamic hybridoma growth and monoclonal antibody production in continuous suspension culture. Biotechnol Bioeng 34:515

    Google Scholar 

  • Caron AW, Kamen J, Massie B (1990) High-level recombinant protein production in bioreactors using the baculovirus insect cell expression system. Biotechnol Bioeng 36:1133–1140

    Google Scholar 

  • Cavegn C, Bertrand M, Payton MA, Bernard AR (1992) Optimization of high density insect cell cultures for the production of recombinant proteins. In: Extended Abstracts, American Institute of Chemical Engineers 1992 Annual Meeting, November 1–6, 1992, Miami Beach, Florida. American Institute of Chemical Engineers, New York, New York, p 363 (Abstract 152 h)

    Google Scholar 

  • Gooijer CD de, Lier FLJ van, End EJ van den, Vlak JM, Tramper J (1989) A model for baculovirus production with continuous insect cell cultures. Appl Microbiol Biotechnol 30:497–501

    Google Scholar 

  • Goosen MFA (1991) Insect cell cultivation techniques for the production of high-valued products. Can J Chem Eng 69:450–456

    Google Scholar 

  • Kamen AA, Tom RL, Caron AW, Chavarie C, Kamen J (1991) Culture of insect cells in a helical ribbon impeller bioreactor. Biotechnol Bioeng 38:619–628

    Google Scholar 

  • King G, Kuzio J, Daugulis A, Faulkner P, Allen B, Wu J, Goosen M (1991) Assessment of virus production and chloramphenicol acetyl transferase expression by insect cells in serum-free and serum-supplemented media using a temperature-sensitive baculovirus. Biotechnol Bioeng 38:1091–1099

    Google Scholar 

  • Kompier R, Tramper J, Vlak JM (1988) A continuous process for production of baculovirus using insect-cell cultures. Biotechnol Lett 10:849–854

    Google Scholar 

  • Licari P, Bailey JE (1991) Factors influencing recombinant protein yields in an insect cell-baculovirus expression system: multiplicity of infection and intracellular protein degradation. Biotechnol Bioeng 37:238–246

    Google Scholar 

  • Lier FLJ van, End EJ van den, Hooijer CD de, Vlak JM, Tramper J (1990) Continuous production of baculovirus in a cascade of insect-cell reactors. Appl Microbiol Biotechnol 33:43–47

    Google Scholar 

  • Lier FLJ van, Meijs WCJ van der, Grobben NG, Olie RA, Vlak JM, Tramper J (1992) Continuous β-galactosidase production with a recombinant baculovirus insect-cell system in bioreactors. J Biotechnol 22:291–298

    Google Scholar 

  • Low KS Harbour C, Barord JP (1987) A study of hybridoma cell growth and antibody production kinetic in continuous culture. Biotechnol Tech 1:239–244

    Google Scholar 

  • Luckow VA, Summers MD (1988) Trends in the development of baculovirus expression vectors. Bio/Technology 6:47

    Google Scholar 

  • Maiorella B, Inlow D, Shauger A, Harano D (1988) Large-scale insect cell culture for recombinant protein production. Bio/Technology 6:1406

    Google Scholar 

  • Miller WM, Blanch HW, Wilke CR (1988) A kinetic analysis of hybridoma growth and metabolism in batch and continuous suspension culture: effect of nutrient concentration, dilution rate, and pH. Biotechnol Bioeng 32:947–965

    Google Scholar 

  • Murhammer DW, Goochee CF (1988) Scaleup of insect cell cultures protective effects of pluronic F-68. Bio/Technology 6:1411–1418

    Google Scholar 

  • Ogonah O, Shuler ML, Granados RR (1991) Protein production (β-galactosidase) from a baculovirus vector in Spodoptera frugipedra and Trichpolusia ni cells in suspension culture. Biotechnol Lett 13:265

    Google Scholar 

  • O'Reilly DR, Miller LK, Luckow VA (1992) Baculovirus expression vectors: a laboratory manual, 1st edn. Freeman, New York

    Google Scholar 

  • Scott RI, Blanchard JH, Ferguson CHR (1992) Effects of oxygen on recombinant protein production by suspension cultures of Spodoptera frugiperda (Sf-9) insect cells. Enzyme Microb Technol 14:798–804

    Google Scholar 

  • Sinclair R (1974) Response of mammalian cells to controlled growth rates in steady-state continuous culture. In Vitro 10:295–305

    Google Scholar 

  • Taticek RA, Shuler ML (1992) A continuous flow bioreactor system for the production of recombinant proteins using the insect cell-baculovirus expression system. In: Extended Abstracts, American Institute of Chemical Engineers 1992 Annual Meeting, November 1–6, 1992, Miami Beach, Florida. American Institute of Chemical Engineers, New York, New York, p 363 (Abstract 152 g)

    Google Scholar 

  • Tramper J, Williams JB, Jous TD, Vlak JM (1986) Shear sensitivity of insect cells in suspension. Enzyme Microb Technol 8:3–36

    Google Scholar 

  • Tovey M, Bronty-Boye D (1976) Characteristics of the chemostst culture of murine leukemia L1210 cells. Exp Cell Res 101:346–354

    Google Scholar 

  • Wang MY, Vakharia V, Bentley WE (1993a) Expression of epoxide hydrolase in insect cells: a focus on the infected cell. Biotechnol Bioeng 42:240–247

    Google Scholar 

  • Wang MY, Simon K, Bentley WE (1993b) Effects of oxygen/glucose/glutamine feeding on insect cell baculovirus protein expression: a study of epoxide hydrolase production. Biotechnol Prog 9:355–361

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Wang, M.Y., Bentley, W.E. Continuous insect cell (Sf-9) culture with aeration through sparging. Appl Microbiol Biotechnol 41, 317–323 (1994). https://doi.org/10.1007/BF00221226

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00221226

Keywords

Navigation