Literature DB >> 15619325

Orbital shaker technology for the cultivation of mammalian cells in suspension.

Natalie Muller1, Philippe Girard, David L Hacker, Martin Jordan, Florian M Wurm.   

Abstract

For large-scale applications in biotechnology, cultivation of mammalian cells in suspension is an essential prerequisite. Typically, suspension cultures are grown in glass spinner flasks filled to less than 50% of the nominal volume. We propose a superior system for suspension cultures of mammalian cells based on orbital shaker technology. We found that "square-shaped" bottles (square bottles) provide an inexpensive but efficient means to grow HEK-293 EBNA and CHO-DG44 cells to high density. Cultures in agitated 1-L square bottles exceeded the performance of cultures in spinner flasks, reaching densities up to 7 x 10(6) cells/mL for HEK-293 EBNA cells and 5 x 10(6) cells/mL for CHO-DG44 cells in comparison to (2.5-4) x 10(6) cells/mL for cultures of the same cells grown in spinner flasks. For 1-L square bottles, optimal cell growth and viability were observed with a filling volume of 30-40% of the nominal volume and an agitation speed of 130 rpm at a rotational diameter of 2.5 cm. Transient reporter gene expression following gene delivery by calcium phosphate-DNA co-precipitation was the same or slightly better for HEK-293 EBNA cells grown in square bottles as compared to spinner flasks. Reductions in cost, simplified handling, and better performance in cell growth and viability make the agitated square bottle a new and very promising tool for the cultivation of mammalian cells in suspension.

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Year:  2005        PMID: 15619325     DOI: 10.1002/bit.20358

Source DB:  PubMed          Journal:  Biotechnol Bioeng        ISSN: 0006-3592            Impact factor:   4.530


  30 in total

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2.  Numerical simulation of scaling-up an inverted frusto-conical shaking bioreactor with low shear stress for mammalian cell suspension culture.

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3.  Productivity and quality of recombinant proteins produced by stable CHO cell clones can be predicted by transient expression in HEK cells.

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4.  Structures of the Toxoplasma gliding motility adhesin.

Authors:  Gaojie Song; Timothy A Springer
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5.  X-ray structure of the mouse serotonin 5-HT3 receptor.

Authors:  Ghérici Hassaine; Cédric Deluz; Luigino Grasso; Romain Wyss; Menno B Tol; Ruud Hovius; Alexandra Graff; Henning Stahlberg; Takashi Tomizaki; Aline Desmyter; Christophe Moreau; Xiao-Dan Li; Frédéric Poitevin; Horst Vogel; Hugues Nury
Journal:  Nature       Date:  2014-08-03       Impact factor: 49.962

6.  Production of lentiviral vectors in suspension cells using low proportion of supercoiled circular plasmid DNA.

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7.  Human Kunitz-type protease inhibitor engineered for enhanced matrix retention extends longevity of fibrin biomaterials.

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Review 8.  Recent advances in mammalian protein production.

Authors:  Ashok D Bandaranayake; Steven C Almo
Journal:  FEBS Lett       Date:  2013-12-06       Impact factor: 4.124

9.  In vitro enzymatic characterization of near full length EGFR in activated and inhibited states.

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10.  Serum-free transfection of CHO cells with chemically defined transfection systems and investigation of their potential for transient and stable transfection.

Authors:  Hannes Reisinger; Willibald Steinfellner; Hermann Katinger; Renate Kunert
Journal:  Cytotechnology       Date:  2009-09-17       Impact factor: 2.058

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