Feed development for fed-batch CHO production process by semisteady state analysis
- PMID: 20014108
- DOI: 10.1002/btpr.362
Feed development for fed-batch CHO production process by semisteady state analysis
Abstract
Semisteady state cultures are useful for studying cell physiology and facilitating media development. Two semisteady states with a viable cell density of 5.5 million cells/mL were obtained in CHO cell cultures and compared with a fed-batch mode control. In the first semisteady state, the culture was maintained at 5 mM glucose and 0.5 mM glutamine. The second condition had threefold higher concentrations of both nutrients, which led to a 10% increase in lactate production, a 78% increase in ammonia production, and a 30% reduction in cell growth rate. The differences between the two semisteady states indicate that maintaining relatively low levels of glucose and glutamine can reduce the production of lactate and ammonia. Specific amino acid production and consumption indicated further metabolic differences between the two semisteady states and fed-batch mode. The results from this experiment shed light in the feeding strategy for a fed-batch process and feed medium enhancement. The fed-batch process utilizes a feeding strategy whereby the feed added was based on glucose levels in the bioreactor. To evaluate if a fixed feed strategy would improve robustness and process consistency, two alternative feeding strategies were implemented. A constant volume feed of 30% or 40% of the initial culture volume fed over the course of cell culture was evaluated. The results indicate that a constant volumetric-based feed can be more beneficial than a glucose-based feeding strategy. This study demonstrated the applicability of analyzing CHO cultures in semisteady state for feed enhancement and continuous process improvement.
Copyright 2009 American Institute of Chemical Engineers
Similar articles
-
A single nutrient feed supports both chemically defined NS0 and CHO fed-batch processes: Improved productivity and lactate metabolism.Biotechnol Prog. 2009 Sep-Oct;25(5):1353-63. doi: 10.1002/btpr.238. Biotechnol Prog. 2009. PMID: 19637321
-
Low-glutamine fed-batch cultures of 293-HEK serum-free suspension cells for adenovirus production.Biotechnol Prog. 2003 Mar-Apr;19(2):501-9. doi: 10.1021/bp025638o. Biotechnol Prog. 2003. PMID: 12675594
-
Impact of dynamic online fed-batch strategies on metabolism, productivity and N-glycosylation quality in CHO cell cultures.Biotechnol Bioeng. 2005 Jan 20;89(2):164-77. doi: 10.1002/bit.20317. Biotechnol Bioeng. 2005. PMID: 15593097
-
Towards dynamic metabolic flux analysis in CHO cell cultures.Biotechnol J. 2012 Jan;7(1):61-74. doi: 10.1002/biot.201100052. Epub 2011 Nov 21. Biotechnol J. 2012. PMID: 22102428 Review.
-
Metabolic flux analysis in mammalian cell culture.Metab Eng. 2010 Mar;12(2):161-71. doi: 10.1016/j.ymben.2009.09.002. Epub 2009 Oct 13. Metab Eng. 2010. PMID: 19833223 Review.
Cited by
-
Enhanced production of human recombinant proteins from CHO cells grown to high densities in macroporous microcarriers.Mol Biotechnol. 2011 Nov;49(3):263-76. doi: 10.1007/s12033-011-9401-y. Mol Biotechnol. 2011. PMID: 21472499
-
Early integration of Design of Experiment (DOE) and multivariate statistics identifies feeding regimens suitable for CHO cell line development and screening.Cytotechnology. 2019 Dec;71(6):1137-1153. doi: 10.1007/s10616-019-00350-1. Epub 2019 Nov 9. Cytotechnology. 2019. PMID: 31705334 Free PMC article.
-
Effect of N-Glycan Profiles on Binding Affinity of Diagnostic Antibody Produced by Hybridomas in Serum-Free Suspension.J Microbiol Biotechnol. 2025 May 15;35:e2501036. doi: 10.4014/jmb.2501.01036. J Microbiol Biotechnol. 2025. PMID: 40374547 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources