Literature DB >> 18613236

The effect of the dilution rate on CHO cell physiology and recombinant interferon-gamma production in glucose-limited chemostat culture.

P M Hayter1, E M Curling, M L Gould, A J Baines, N Jenkins, I Salmon, P G Strange, A T Bull.   

Abstract

The physiology of a recombinant Chinese hamster ovary cell line in glucose-limited chemostat culture was studied over a range of dilution rates (D = 0.008 to 0.20 h(-1)). The specific growth rate (micro) deviated from D at low dilution rates due to an increased specific death rate. Extrapolation of these data suggested a minimum specific growth rate of 0.011 h(-1) (micro(max) = 0.025 h(-1)) The metabolism at each steady state was characterized by determining the metabolic quotients for glucose, lactate, ammonia, amino acids, and interferon-gamma (IFN-gamma). The specific rate of glucose uptake increased linearly with mu, and the saturation constant for glucose (K(s)) was calculated to be 59.6 microM. There was a linear increase in the rate of lactate production with a higher yield of lactate from glucose at high growth rates. The decline in the rate of production of lactate, alanine, and serine at low growth rate was consistent with the limitation of the glycolytic pathway by glucose. The specific rate of IFN-gamma production increased with mu in a manner indicative of a growth-related product. Despite changes in the IFN-gamma production rate and cell physiology, the pattern of IFN-gamma glycosylation was similar at all except the lowest growth rates where there was increased production of nonglycosylated IFN-gamma.

Entities:  

Year:  1993        PMID: 18613236     DOI: 10.1002/bit.260420909

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


  16 in total

1.  Optimization of the medium perfusion rate in a packed-bed bioreactor charged with CHO cells.

Authors:  F Meuwly; U von Stockar; A Kadouri
Journal:  Cytotechnology       Date:  2005-06-16       Impact factor: 2.058

2.  The role of the cell cycle in determining gene expression and productivity in CHO cells.

Authors:  D R Lloyd; V Leelavatcharamas; A N Emery; M Al-Rubeai
Journal:  Cytotechnology       Date:  1999-07       Impact factor: 2.058

3.  Use of cell cycle analysis to characterise growth and interferon-gamma production in perfusion culture of CHO cells.

Authors:  V Leelavatcharamas; A N Emery; M Al-Rubeai
Journal:  Cytotechnology       Date:  1999-07       Impact factor: 2.058

4.  Glycosylation and post-translational modification gene expression analysis by DNA microarrays for cultured mammalian cells.

Authors:  Arthur Nathan Brodsky; Mary Caldwell; Sarah W Harcum
Journal:  Methods       Date:  2011-10-19       Impact factor: 3.608

5.  CHO cell growth and recombinant interferon-γ production: Effects of BSA, Pluronic and lipids.

Authors:  P M Castro; A P Ison; P M Hayter; A T Bull
Journal:  Cytotechnology       Date:  1995-01       Impact factor: 2.058

6.  Effect of lipid supplements on the production and glycosylation of recombinant interferon-gamma expressed in CHO cells.

Authors:  N Jenkins; P Castro; S Menon; A Ison; A Bull
Journal:  Cytotechnology       Date:  1994       Impact factor: 2.058

7.  Growth and interferon-gamma production in batch culture of CHO cells.

Authors:  V Leelavatcharamas; A N Emery; M al-Rubeai
Journal:  Cytotechnology       Date:  1994       Impact factor: 2.058

8.  Plant protein hydrolysates support CHO-320 cells proliferation and recombinant IFN-gamma production in suspension and inside microcarriers in protein-free media.

Authors:  J S Ballez; J Mols; C Burteau; S N Agathos; Y J Schneider
Journal:  Cytotechnology       Date:  2004-03       Impact factor: 2.058

9.  Cell cycle phase dependent productivity of a recombinant Chinese hamster ovary cell line.

Authors:  Roshni L Dutton; Jeno Scharer; Murray Moo-Young
Journal:  Cytotechnology       Date:  2007-01-25       Impact factor: 2.058

10.  Enhanced erythropoietin heterogeneity in a CHO culture is caused by proteolytic degradation and can be eliminated by a high glutamine level.

Authors:  M Yang; M Butler
Journal:  Cytotechnology       Date:  2000-10       Impact factor: 2.058

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