Influence of intracellular nucleotide and nucleotide sugar contents on recombinant interferon-γ glycosylation during batch and fed-batch cultures of CHO cells

2008 ◽  
Vol 100 (4) ◽  
pp. 721-733 ◽  
Author(s):  
N. Kochanowski ◽  
F. Blanchard ◽  
R. Cacan ◽  
F. Chirat ◽  
E. Guedon ◽  
...  
2006 ◽  
Vol 8 (6) ◽  
pp. 509-522 ◽  
Author(s):  
Sing Fee Lim ◽  
Kok Hwee Chuan ◽  
Sen Liu ◽  
Sophia O.H. Loh ◽  
Beatrice Y.F. Chung ◽  
...  
Keyword(s):  

Author(s):  
Quentin Bethune ◽  
Cameron Harrington ◽  
Bhanu Mulukutla

CHO cells have been recently shown to produce amino acid catabolism derived byproducts, which accumulate in fed-batch cultures to growth-inhibitory levels. Residual amino acid limitation or genetic engineering strategies have been successfully employed to suppress production of these novel growth inhibitory metabolic byproducts. However, the growth advantage attained due to suppression of these metabolic byproducts in fed-batch cultures is more pronounced when lactate accumulation is also controlled. BCAT1 knock-out (KO) CHO cells, which produce negligible levels of the metabolic byproducts isovalerate, isobutyrate and 2-methylbutyrate, grow to significantly higher peak cell densities in fed-batch cultures with lactate control (HiPDOG) as compared to cultures without lactate control. Henceforth, strategies involving novel metabolic byproduct control should preferably include lactate control to more easily assess the enhanced cell growth and productivities attainable.


2007 ◽  
Vol 9 (5-6) ◽  
pp. 406-418 ◽  
Author(s):  
Chee Yong Yun ◽  
Sen Liu ◽  
Sing Fee Lim ◽  
Tianhua Wang ◽  
Beatrice Y.F. Chung ◽  
...  

2021 ◽  
Author(s):  
Johanna Vappiani ◽  
Tom Eyster ◽  
Keegan Orzechowski ◽  
Diana Ritz ◽  
Pramthesh Patel ◽  
...  

2016 ◽  
Vol 217 ◽  
pp. 122-131 ◽  
Author(s):  
Cécile Toussaint ◽  
Olivier Henry ◽  
Yves Durocher

Author(s):  
Cameron Harrington ◽  
Taylor Kalomeris ◽  
Michaela Jacobs ◽  
Gregory Hiller ◽  
Bhanu Chandra Mulukutla

Chinese hamster ovary (CHO) cells in fed-batch cultures produce several metabolic byproducts derived from amino acid catabolism, some of which accumulate to growth inhibitory levels. Controlling the accumulation of these byproducts has been shown to significantly enhance cell proliferation. Interestingly, some of these byproducts have physiological roles that go beyond inhibition of cell proliferation. In this study, we show that, in CHO cell fed-batch cultures, branched chain amino acid (BCAA) catabolism contributes to the formation of butyrate, a novel byproduct that is also a well-established specific productivity enhancer. Further, the other byproducts of BCAA catabolism, isovalerate and isobutyrate, which accumulate in CHO cell fed-batch cultures also enhance specific productivity. Additionally, the rate of production of these BCAA catabolic byproducts was negatively correlated with glucose uptake and lactate production rates. Limiting glucose supply to suppress glucose uptake and lactate production, like in case of fed-batch cultures employing HiPDOG technology, significantly enhances BCAA catabolic byproduct accumulation resulting in higher specific productivities.


2006 ◽  
Vol 51 (2) ◽  
pp. 67-79 ◽  
Author(s):  
Kok Hwee Chuan ◽  
Sing Fee Lim ◽  
Laurent Martin ◽  
Chee Yong Yun ◽  
Sophia O. H. Loh ◽  
...  

2008 ◽  
Vol 18 (5) ◽  
pp. 458-464 ◽  
Author(s):  
Gang Wang ◽  
Enmin Feng ◽  
Zhilong Xiu

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