Applied Biochemistry and Biotechnology

, Volume 172, Issue 1, pp 224–236 | Cite as

Effect of Operating Conditions in Production of Diagnostic Salmonella Enteritidis O-Antigen-Specific Monoclonal Antibody in Different Bioreactor Systems

  • Duygu Ayyildiz-Tamis
  • Ayse Nalbantsoy
  • Murat Elibol
  • Saime Ismet Deliloglu-Gurhan
Article

Abstract

In this study, different cultivation systems such as roller bottles (RB), 5-L stirred-tank bioreactor (STR), and disposable bioreactors were used to cultivate hybridoma for lab-scale production of Salmonella Enteritidis O-antigen-specific monoclonal antibody (MAb). Hybridoma cell line was cultivated in either serum-containing or serum-free medium (SFM) culture conditions. In STR, MAb production scaled up to 4 L, and production capabilities of the cells were also evaluated in different featured production systems. Moreover, the growth parameters of the cells in all production systems such as glucose consumption, lactate and ammonia production, and also MAb productivities were determined. Collected supernatants from the reactors were concentrated by a cross-flow filtration system. In conclusion, cells were not adapted to SFM in RB and STR. Therefore, less MAb titer in both STR and RB systems with SFM was observed compared to the cultures containing fetal bovine serum-supplemented medium. A higher MAb titer was gained in the membrane-aerated system compared to those in STR and RB. Although the highest MAb titer was obtained in the static membrane bioreactor system, the highest productivity was obtained in STR operated in semicontinuous mode with overlay aeration.

Keywords

Hybridoma Monoclonal antibody Salmonella Enteritidis Bioreactors Cross-flow filtration 

Nomenclature

dCO2

Dissolved carbon dioxide concentration (%)

dO2

Dissolved oxygen concentration (%)

kLa

Oxygen mass transfer coefficient

pMAb

MAb productivity (mg L−1 day−1)

qGlu

Specific glucose consumption rate (mg L−1 day−1 cell−1)

pLac

Specific lactate production rate (mg L−1 day−1 cell−1)

pAmmonia

Specific ammonia production rate (mg L−1 day−1 cell−1)

Notes

Acknowledgments

This research was supported by The Scientific and Technological Research Council of Turkey (TUBITAK) with 108M578 project number.

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Copyright information

© Springer Science+Business Media New York 2013

Authors and Affiliations

  • Duygu Ayyildiz-Tamis
    • 1
  • Ayse Nalbantsoy
    • 1
  • Murat Elibol
    • 1
  • Saime Ismet Deliloglu-Gurhan
    • 1
  1. 1.Department of Bioengineering, Faculty of EngineeringEge UniversityIzmirTurkey

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