Modeling hybridoma cell metabolism using a generic genome-scale metabolic model of Mus musculus

被引:134
作者
Sheikh, K
Förster, J
Nielsen, LK [1 ]
机构
[1] Univ Queensland, Dept Chem Engn, St Lucia, Qld 4072, Australia
[2] Fluxome Sci AS, Soltofts Plads, DK-2800 Lyngby, Denmark
关键词
D O I
10.1021/bp0498138
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
The reconstructed cellular metabolic network of Mus musculus, based on annotated genomic data, pathway databases, and currently available biochemical and physiological information, is presented. Although incomplete, it represents the first attempt to collect and characterize the metabolic network of a mammalian cell on the basis of genomic data. The reaction network is generic in nature and attempts to capture the carbon, energy, and nitrogen metabolism of the cell. The metabolic reactions were compartmentalized between the cytosol and the mitochondria, including transport reactions between the compartments and the extracellular medium. The reaction list consists of 872 internal metabolites involved in a total of 1220 reactions, whereof 473 relate to known open reading frames. Initial in silico analysis of the reconstructed model is presented.
引用
收藏
页码:112 / 121
页数:10
相关论文
共 43 条
[1]   Integration of gene expression data into genome-scale metabolic models [J].
Åkesson, M ;
Förster, J ;
Nielsen, J .
METABOLIC ENGINEERING, 2004, 6 (04) :285-293
[2]   Analysis of CHO cells metabolic redistribution in a glutamate-based defined medium in continuous culture [J].
Altamirano, C ;
Illanes, A ;
Casablancas, A ;
Gámez, X ;
Cairó, JJ ;
Gòdia, C .
BIOTECHNOLOGY PROGRESS, 2001, 17 (06) :1032-1041
[3]   SERUM-FREE CELL-CULTURE - A UNIFYING APPROACH [J].
BARNES, D ;
SATO, G .
CELL, 1980, 22 (03) :649-655
[4]  
Bonarius HPJ, 1996, BIOTECHNOL BIOENG, V50, P299, DOI 10.1002/(SICI)1097-0290(19960505)50:3<299::AID-BIT9>3.0.CO
[5]  
2-B
[6]  
Chen KQ, 2001, BIOTECHNOL BIOENG, V72, P55, DOI 10.1002/1097-0290(20010105)72:1<55::AID-BIT8>3.0.CO
[7]  
2-4
[8]   Finishing the euchromatic sequence of the human genome [J].
Collins, FS ;
Lander, ES ;
Rogers, J ;
Waterston, RH .
NATURE, 2004, 431 (7011) :931-945
[9]   CELL-DEATH (APOPTOSIS) IN CELL-CULTURE SYSTEMS [J].
COTTER, TG ;
ALRUBEAI, M .
TRENDS IN BIOTECHNOLOGY, 1995, 13 (04) :150-155
[10]   Integrating high-throughput and computational data elucidates bacterial networks [J].
Covert, MW ;
Knight, EM ;
Reed, JL ;
Herrgard, MJ ;
Palsson, BO .
NATURE, 2004, 429 (6987) :92-96