Influence of culture conditions on recombinant Drosophila melanogaster S2 cells producing rabies virus glycoprotein cultivated in serum-free medium

Batista FRX, Moraes AM, Büntemeyer H, Noll T (2009)
BIOLOGICALS 37(2): 108-118.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
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Autor*in
Batista, Fabiana R. X.; Moraes, Angela M.; Büntemeyer, HeinoUniBi; Noll, ThomasUniBi
Abstract / Bemerkung
The recombinant G glycoprotein from the surface of the rabies virus (RVGP) is a promising candidate as a rabies vaccine component and also for diagnostic purposes. In this study, RVGP production by transfected Drosophila melanogaster S2 cells cultivated in a serum-free medium (Supplemented IPL-41 medium) was carried out. The effects of pH and pO(2) were evaluated in batch culture in parallel spinner flasks. The use of a pH equal to 6.3 and a pO(2) of 40% air saturation resulted in the highest RVGP content. These conditions were also used in fed-batch mode, yielding a RVGP content level of 98 g/10(7) cells. The main nutrients consumed were glucose, glutamine, asparagine, serine and proline and the major metabolites produced were alanine and ammonia, according to the metabolism studies performed. Since RVGP is a transmembrane protein, two different methods for protein recovery were assessed and compared. Detergent-based cell disruption showed to be more effective than mechanical disruption with glass beads for glycoprotein recovery. (C) 2008 The International Association for Biologicals. Published by Elsevier Ltd. All rights reserved.
Stichworte
S2 cells; Growth kinetics; Aeration; Fed-batch culture; RVGP
Erscheinungsjahr
2009
Zeitschriftentitel
BIOLOGICALS
Band
37
Ausgabe
2
Seite(n)
108-118
ISSN
1045-1056
Page URI
https://pub.uni-bielefeld.de/record/1633988

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Batista FRX, Moraes AM, Büntemeyer H, Noll T. Influence of culture conditions on recombinant Drosophila melanogaster S2 cells producing rabies virus glycoprotein cultivated in serum-free medium. BIOLOGICALS. 2009;37(2):108-118.
Batista, F. R. X., Moraes, A. M., Büntemeyer, H., & Noll, T. (2009). Influence of culture conditions on recombinant Drosophila melanogaster S2 cells producing rabies virus glycoprotein cultivated in serum-free medium. BIOLOGICALS, 37(2), 108-118. https://doi.org/10.1016/j.biologicals.2008.11.001
Batista, Fabiana R. X., Moraes, Angela M., Büntemeyer, Heino, and Noll, Thomas. 2009. “Influence of culture conditions on recombinant Drosophila melanogaster S2 cells producing rabies virus glycoprotein cultivated in serum-free medium”. BIOLOGICALS 37 (2): 108-118.
Batista, F. R. X., Moraes, A. M., Büntemeyer, H., and Noll, T. (2009). Influence of culture conditions on recombinant Drosophila melanogaster S2 cells producing rabies virus glycoprotein cultivated in serum-free medium. BIOLOGICALS 37, 108-118.
Batista, F.R.X., et al., 2009. Influence of culture conditions on recombinant Drosophila melanogaster S2 cells producing rabies virus glycoprotein cultivated in serum-free medium. BIOLOGICALS, 37(2), p 108-118.
F.R.X. Batista, et al., “Influence of culture conditions on recombinant Drosophila melanogaster S2 cells producing rabies virus glycoprotein cultivated in serum-free medium”, BIOLOGICALS, vol. 37, 2009, pp. 108-118.
Batista, F.R.X., Moraes, A.M., Büntemeyer, H., Noll, T.: Influence of culture conditions on recombinant Drosophila melanogaster S2 cells producing rabies virus glycoprotein cultivated in serum-free medium. BIOLOGICALS. 37, 108-118 (2009).
Batista, Fabiana R. X., Moraes, Angela M., Büntemeyer, Heino, and Noll, Thomas. “Influence of culture conditions on recombinant Drosophila melanogaster S2 cells producing rabies virus glycoprotein cultivated in serum-free medium”. BIOLOGICALS 37.2 (2009): 108-118.

6 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

An effective and simplified DO-stat control strategy for production of rabies glycoprotein in Pichia pastoris.
Picotto LD, Sguazza GH, Tizzano MA, Galosi CM, Cavalitto SF, Pecoraro MR., Protein Expr Purif 132(), 2017
PMID: 28189633
Culturing Drosophila melanogaster (S2) in a chemostat.
Vieira PB, da Costa BL, de Fatima Pires Augusto E, Tonso A., Biotechnol Lett 37(3), 2015
PMID: 25367803
Behavior of wild-type and transfected S2 cells cultured in two different media.
Batista FR, Greco KN, Astray RM, Jorge SA, Augusto EF, Pereira CA, Mendonça RZ, Moraes AM., Appl Biochem Biotechnol 163(1), 2011
PMID: 21161610

28 References

Daten bereitgestellt von Europe PubMed Central.

Comparative production of human interleukin-2 fused with green fluorescent protein in several recombinant expression systems
Cha, Biochem Eng J 24(), 2005
Observation and modeling of induction effect on human transferring production from stably transfected Drosophila S2 cell culture
Lim, Enz Microb Technol 39(), 2006
Production and purification of human menin from Drosophila melanogaster S2 cells using stirred tank reactor.
Valle MA, Kester MB, Burns AL, Marx SJ, Spiegel AM, Shiloach J., Cytotechnology 35(2), 2001
PMID: 19003289
Expression of human plasminogen in Drosophila Schneider S2 cells.
Nilsen SL, Castellino FJ., Protein Expr. Purif. 16(1), 1999
PMID: 10336871
The ascension of wildlife rabies: a cause for public health concern or intervention?
Rupprecht CE, Smith JS, Fekadu M, Childs JE., Emerging Infect. Dis. 1(4), 1995
PMID: 8903179
Production methods for rabies vaccine.
Perez O, Paolazzi CC., J. Ind. Microbiol. Biotechnol. 18(5), 1997
PMID: 9218362
Animal sera derivatives and substitutes used in the manufacture of pharmaceuticals: viral safety and regulatory aspects
Castle, Dev Biol Standard 99(), 1999
Fedbatch culture and dynamic nutrient feeding
Wlaschin, 2006
Mendonça RZ, Pereira CA, Moraes AM. Evaluation of concentrated milk whey as a supplement for Sf9 Spodoptera frugiperda cells in culture
Batista, Electron J Biotechnol 9(), 2006
Formulation of a protein-free medium based on IPL-41 for the sustained growth of Drosophila melanogaster S2 cells.
Batista FR, Pereira CA, Mendonca RZ, Moraes AM., Cytotechnology 57(1), 2008
PMID: 19003168
Rabies virus glycoprotein expression in Drosophila S2 cells. I. Functional recombinant protein in stable co-transfected cell line.
Yokomizo AY, Jorge SA, Astray RM, Fernandes I, Ribeiro OG, Horton DS, Tonso A, Tordo N, Pereira CA., Biotechnol J 2(1), 2007
PMID: 17225257
Methods for off-line analysis of nutrients and products in mammalian cell culture
Büntemeyer, 2007
Characterization of growth and metabolism of Drosophila melanogaster cells transfected with the rabies-virus glycoprotein gene.
Swiech K, da Silva CS, Arantes MK, dos Santos AS, Astray RM, Pereira CA, Suazo CA., Biotechnol. Appl. Biochem. 49(Pt 1), 2008
PMID: 17570830

Echalier, 1997
Bioprocess development for the production of a recombinant MUC1 fusion protein expressed by CHO-K1 cells in protein-free medium.
Link T, Backstrom M, Graham R, Essers R, Zorner K, Gatgens J, Burchell J, Taylor-Papadimitriou J, Hansson GC, Noll T., J. Biotechnol. 110(1), 2004
PMID: 15099905
An insight into insect cell metabolism through selective nutrient manipulation
Mendonça, Biotechnol Progr 72(), 1999
Optimization of a feed medium for fed-batch culture of insect cells using a genetic algorithm.
Marteijn RC, Jurrius O, Dhont J, de Gooijer CD, Tramper J, Martens DE., Biotechnol. Bioeng. 81(3), 2003
PMID: 12474249
Effect of hyperosmolarity on recombinant protein productivity in baculovirus expression system.
Olejnik A, Grajek W, Marecik R., J. Biotechnol. 102(3), 2003
PMID: 12730004
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