| Literature DB >> 29781256 |
Moritz K F Wolf1, Aurélie Closet1, Monika Bzowska2, Jean-Marc Bielser3, Jonathan Souquet3, Hervé Broly3, Massimo Morbidelli1.
Abstract
Mammalian cell perfusion cultures represent a promising alternative to the current fed-batch technology for the production of various biopharmaceuticals. Long-term operation at a fixed viable cell density (VCD) requires a viable culture and a constant removal of excessive cells. Product loss in the cell removing bleed stream deteriorates the process yield. In this study, the authors investigate the use of chemical and environmental growth inhibition on culture performance by either adding valeric acid (VA) to the production media or by reducing the culture temperature (33.0 °C) with respect to control conditions (36.5 °C, no VA). Low temperature significantly reduces cellular growth, thus, resulting in lower bleed rates accompanied by a reduced product loss of 11% compared to 26% under control conditions. Additionally, the cell specific productivity of the target protein improves and maintained stable leading to media savings per mass of product. VA shows initially an inhibitory effect on cellular growth. However, cells seemed to adapt to the presence of the inhibitor resulting in a recovery of the cellular growth. Cell cycle and Western blot analyses support the observed results. This work underlines the role of temperature as a key operating variable for the optimization of perfusion cultures.Entities:
Keywords: CHO cells; bioprocess engineering; bioreactor; cell culture; fermentation
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Year: 2018 PMID: 29781256 DOI: 10.1002/biot.201700722
Source DB: PubMed Journal: Biotechnol J ISSN: 1860-6768 Impact factor: 4.677