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

被引:27
作者
Ballez, JS
Mols, J
Burteau, C
Agathos, SN
Schneider, YJ
机构
[1] Catholic Univ Louvain, Lab Biochim Cellulaire, B-1348 Louvain, Belgium
[2] Catholic Univ Louvain, Unite Genie Biol, B-1348 Louvain, Belgium
[3] Catholic Univ Louvain, Inst Sci Vie, B-1348 Louvain, Belgium
关键词
bioreactor; CHO-320; cells; fibra-cel (R); interferon-gamma (IFNI-gamma); microcarriers; perfusion; plant protein hydrolysates (peptones); protein-free;
D O I
10.1007/s10616-004-1099-2
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We have recently developed a protein-free medium (PFS) able to support the growth of Chinese hamster ovary (CHO) cells in suspension. Upon further supplementation with some plant protein hydrolysates. medium performances reached what could be observed in serum-containing media [Burteau et al. In Vitro Cell. Dei,. Biol.-Anhn. 39 (2003) 291]. Now, we describe the use of rice and wheat protein hydrolysates. as non-nutritional additives to the culture medium to support productivity and cell growth in suspension or in microcarriers. When CHO-320 cells secreting recombinant interferon-gamma were cultivated in suspension in a bioreactor with our PFS supplemented with wheat hydrolysates. the maximum cell density increased by 25% and the IFN-gamma secretion by 60% compared to the control PFS. A small-scale perfusion system consisting of CHO-320 cells growing on and inside fibrous microcarriers under discontinuous operation was first developed. Under these conditions: rice protein hydrolysates stimulated recombinant IFN-gamma secretion by 30% compared to the control PFS. At the bioreactorscale. similar results were obtained but when compared to shake-flasks studies, nutrients, oxygen or toxic by-products gradients inside the microcarriers seemed to be the main limitation of the system. An increase of the perfusion rate to maintain glucose concentration over 5.5 mM and dissolved oxygen (DO) at 60% was able to stimulate the production of IFN-gamma to a level of 6.6 mug h(-1) g(-1) of microcarriers after 160 h when a cellular density of about 4 x 10 cell g(-1) of carriers was reached.
引用
收藏
页码:103 / 114
页数:12
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