Low-protein medium affects the 293SF central metabolism during growth and infection with adenovirus

被引:38
作者
Nadeau, I
Gilbert, PA
Jacob, D
Perrier, M
Kamen, A
机构
[1] Biotechnol Res Inst, CNRC, Montreal, PQ H4P 2R2, Canada
[2] Ecole Polytech, Montreal, PQ H3C 3A7, Canada
关键词
metabolis flux analysis; human cell line HEK-293; adenovires vector; bioprocess; bioreactor; genetherapy; medium;
D O I
10.1002/bit.10128
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
In this study the metabolism of 293SF cells grown in serum-free and low-protein medium was analyzed. This cell line is known for its ability to replicate recombinant adenovirus, mainly used in gene tzherapy applications. A complete model composed of the main glycolytic, glutaminolytic, and amino acids pathways, as well as the internalization fluxes of certain compounds into the mitochondria, is used for metabolic flux calculations. The pentose-phosphate cycle is also added to the biochemical reactions set and was independently measured with labeled C-14-glucose. Different feeding strategies in two different media were analyzed with the model, and the theoretical ATP production was also calculated. The two media were similar in their glucose and amino acid composition, but one contained BSA at 1g/L whereas the other had a very low protein content. Use of low-protein medium resulted in up to fourfold higher adenoviral vector production. In this medium, glucose utilization was more efficient, as it entered the TCA cycle more efficiently. Also, lower glutamine and amino acids consumption were observed as well as lower lactate and ammonia production. This increased TCA activity led to a twofold higher ATP production in the low-protein medium. (C) 2002 John Wiley Sons, Inc.
引用
收藏
页码:91 / 104
页数:14
相关论文
共 49 条
[1]   DETERMINATION OF THE RESPIRATION QUOTIENT IN MAMMALIAN-CELL CULTURE IN BICARBONATE BUFFERED MEDIA [J].
BONARIUS, HPJ ;
DEGOOIJER, CD ;
TRAMPER, J ;
SCHMID, G .
BIOTECHNOLOGY AND BIOENGINEERING, 1995, 45 (06) :524-535
[2]   Error analysis of metabolic-rate measurements in mammalian-cell culture by carbon and nitrogen balances [J].
Bonarius, HPJ ;
Houtman, JHM ;
Schmid, G ;
de Gooijer, CD ;
Tramper, J .
CYTOTECHNOLOGY, 1999, 29 (03) :167-175
[3]  
Bonarius HPJ, 1998, BIOTECHNOL BIOENG, V58, P258, DOI 10.1002/(SICI)1097-0290(19980420)58:2/3<258::AID-BIT20>3.0.CO
[4]  
2-7
[5]   Flux analysis of underdetermined metabolic networks: The quest for the missing constraints [J].
Bonarius, HPJ ;
Schmid, G ;
Tramper, J .
TRENDS IN BIOTECHNOLOGY, 1997, 15 (08) :308-314
[6]  
Bonarius HPJ, 1996, BIOTECHNOL BIOENG, V50, P299, DOI 10.1002/(SICI)1097-0290(19960505)50:3<299::AID-BIT9>3.0.CO
[7]  
2-B
[8]   Study of adenovirus production in serum-free 293SF suspension culture by GFP-expression monitoring [J].
Cote, J ;
Bourget, L ;
Garnier, A ;
Kamen, A .
BIOTECHNOLOGY PROGRESS, 1997, 13 (06) :709-714
[9]  
Côté J, 1998, BIOTECHNOL BIOENG, V59, P567, DOI 10.1002/(SICI)1097-0290(19980905)59:5<567::AID-BIT6>3.0.CO
[10]  
2-8