Effect of Operating Conditions in Production of Diagnostic Salmonella Enteritidis O-Antigen-Specific Monoclonal Antibody in Different Bioreactor Systems
- 247 Downloads
- 2 Citations
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 filtrationNomenclature
- 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.
References
- 1.Coradin, T., Nassif, N., & Livage, J. (2003). Applied Microbiology and Biotechnology, 61, 429–434.CrossRefGoogle Scholar
- 2.Voigt, A., & Zintl, F. (1999). Journal of Biotechnology, 68, 213–226.CrossRefGoogle Scholar
- 3.Jain, E., & Kumar, A. (2008). Biotechnology Advances, 26, 46–72.CrossRefGoogle Scholar
- 4.Pol, L. V. D., & Tramper, J. (1998). Trends in Biotechnology, 16, 323–328.CrossRefGoogle Scholar
- 5.Legazpi, L., Diaz, J., Laca, A., & Diaz, M. (2005). Biochemical Engineering Journal, 26, 122–131.CrossRefGoogle Scholar
- 6.Ozturk, S. S., & Palsson, B. O. (1991). Biotechnology Progress, 7, 481–494.CrossRefGoogle Scholar
- 7.Ozturk, S. S., & Palsson, B. O. (1991). Biotechnology and Bioengineering, 37, 35–46.CrossRefGoogle Scholar
- 8.Ozturk, S. S., Riley, M. R., & Palsson, B. O. (1992). Biotechnology and Bioengineering, 39, 418–431.CrossRefGoogle Scholar
- 9.Ducommun, P., Ruffieux, P. A., Stockar, U., & Marison, I. (2001). Cytotech., 37, 65–73.CrossRefGoogle Scholar
- 10.Jan, D. C. H., Petch, D. A., Huzel, N., & Butler, M. (1997). Biotechnology and Bioengineering, 54, 153–164.CrossRefGoogle Scholar
- 11.Kretzmer, G. (2002). Applied Microbiology and Biotechnology, 59, 135–142.CrossRefGoogle Scholar
- 12.Marks, D. M. (2003). Cytotech., 42, 21–33.CrossRefGoogle Scholar
- 13.Nalbantsoy, A., Karaboz, I., & Deliloglu-Gurhan, I. (2010). HYBRIDOMA, 29, 414–423.CrossRefGoogle Scholar
- 14.Zijderveld, F. G. V., Bemmel-Zijderveld, A. M., & Anakotta, J. (1992). Journal of Clinical Microbiology, 30, 2560–2566.Google Scholar
- 15.Nalbantsoy, A., Karaboz, I., & Deliloglu-Gurhan, I. (2010). Foodborne Pathogens and Disease, 7, 1521–1529.CrossRefGoogle Scholar
- 16.Nalbantsoy, A., Bora, K., & Deliloglu-Gurhan, I. (2011). HYBRIDOMA, 30, 189–193.CrossRefGoogle Scholar
- 17.Nalbantsoy, A., Karaboz, I., Ivanova, R., & Deliloglu-Gurhan, I. (2011). Annals of Microbiology, 60, 565–571.CrossRefGoogle Scholar
- 18.Mirro, R., & Voll, K. (2009). BioProcess International., 7, 52–58.Google Scholar
- 19.Aslankaraoğlu, E., Gümüşderelioğlu, M., & Gürhan, S. I. (2003). Journal of Biomaterials Applications, 18, 137–148.CrossRefGoogle Scholar
- 20.Laemmli, U. K. (1970). Nature, 227, 680–685.CrossRefGoogle Scholar
- 21.Chu, L., & Robinson, D. K. (2003). Current Opinion in Biotechnology, 12, 180–187.CrossRefGoogle Scholar
- 22.Even, M. S., Sandusky, C. B., & Barnard, N. D. (2006). Trends in Biotechnology, 24, 105–108.CrossRefGoogle Scholar
- 23.Kim, D. Y., Lee, J. C., Chang, H. N., & Oha, D. J. (2006). Enzyme and Microbial Technology, 39, 426–433.CrossRefGoogle Scholar
- 24.Selvarasu, S., Wong, V. V. T., Karimi, I. A., & Lee, D. Y. (2009). Biotechnology and Bioengineering, 102, 1494–1504.CrossRefGoogle Scholar
- 25.Ozturk, S. S., & Palsson, B. O. (1990). Journal of Biotechnology, 16, 259–278.CrossRefGoogle Scholar
- 26.Gambhir, A., Korke, R., Lee, J., Fu, P. J., Europa, A., & Hu, W. S. (2003). Journal of Bioscience and Bioengineering, 95, 317–327.CrossRefGoogle Scholar
- 27.Dorka, P., Fischer, C., Budman, H., & Scharer, J. M. (2009). Bioprocess and Biosystems Engineering, 32, 183–196.CrossRefGoogle Scholar
- 28.Matsunaga, N., Kano, K., Maki, Y., & Dobashi, T. (2009). Journal of Bioscience and Bioengineering, 107, 419–424.CrossRefGoogle Scholar
- 29.Chisti, Y. (2000). Trends in Biotechnology, 18, 420–432.CrossRefGoogle Scholar
- 30.Krahe, M. (2003). Biochemical Engineering. In Ulmann’s encyclopedia of industrial chemistry (p. 2301). Weinheim: VCH Publishers.Google Scholar
- 31.McQueen, A., & Bailey, J. E. (1990). Biotechnology and Bioengineering, 35, 1065–1077.Google Scholar
- 32.Cruza, H. J., Freitasa, C. M., Alvesa, P. M., Moreiraa, J. L., & Carrondoa, M. J. T. (2000). Enzyme and Microbial Technology, 27, 43–52.CrossRefGoogle Scholar
- 33.Yang, S. T., Luo, J., & Chen, C. (2004). Advances in Biochemical Engineering/Biotechnology, 87, 61–96.CrossRefGoogle Scholar
- 34.Boraston, R., Thompson, P. W., Garland, S., & Birch, J. R. (1984). Developments in Biological Standardization, 55, 103–111.Google Scholar
- 35.Miller, W. M., Blanch, H. W., & Wilke, C. R. (1988). Biotechnology and Bioengineering, 32, 947–965.CrossRefGoogle Scholar
- 36.Sarkar, A. (2009). Laboratory methods, animal stem cells. In A. Sarkar (Ed.), Encyclopedia of stem cells (pp. 33–34). New Delhi: Discovery Publishing House.Google Scholar