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  Comparison of the productivity of a new human cell line in different steady states of continuous cultivations using MFA

Freund, S., Rath, A., Sandig, V., Rose, T., & Reichl, U. (2012). Comparison of the productivity of a new human cell line in different steady states of continuous cultivations using MFA. Poster presented at Metabolic Engineering IX, Biarritz, France.

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 Creators:
Freund, Susann1, 2, Author           
Rath, Alexander1, Author           
Sandig, Volker, Author
Rose, Thomas, Author
Reichl, Udo1, 3, Author           
Affiliations:
1Bioprocess Engineering, Max Planck Institute for Dynamics of Complex Technical Systems, Max Planck Society, ou_1738140              
2International Max Planck Research School (IMPRS), Max Planck Institute for Dynamics of Complex Technical Systems, Max Planck Society, ou_1738143              
3Otto-von-Guericke-Universität Magdeburg, ou_1738156              

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 Abstract: Complex pharmaceutical glycoproteins are produced in mammalian cell lines. Efficient industrial production typically requires optimization of productivities and process conditions for the individual producer cell line. In that context system biology approaches, such as stationary metabolic flux analysis may provide a powerful tool for optimizing the production process. In addition this may allow for identification of superior targets for cell engineering to further enhance the yields. Cell metabolism and alpha1-antitrypsin (AAT) productivity was analyzed for different steady states in continuous culture. We demonstrate that the glucose to glutamine ratio in the feed medium have a significant impact on productivity. Depending on particular glucose/glutamine ratios and dilution rates cell specific AAT productivity was found to be up to 50% enhanced comparing different steady states.

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Language(s): eng - English
 Dates: 2012
 Publication Status: Not specified
 Pages: -
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 Table of Contents: -
 Rev. Type: -
 Identifiers: eDoc: 635009
 Degree: -

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Title: Metabolic Engineering IX
Place of Event: Biarritz, France
Start-/End Date: 2012-06-03 - 2012-06-07

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