Metabolic flux analysis in mammalian cell culture

被引:155
作者
Quek, Lake-Ee [1 ]
Dietmair, Stefanie [1 ]
Kroemer, Jens O. [1 ]
Nielsen, Lars K. [1 ]
机构
[1] Univ Queensland, AIBN, Brisbane, Qld 4072, Australia
关键词
Metabolic flux analysis (MFA); Mammalian cells; Review; Constrained-based analysis; Hybridoma; CHO; RECOMBINANT MONOCLONAL-ANTIBODY; MAGNETIC-RESONANCE SPECTROSCOPY; BIOCHEMICAL REACTION SYSTEMS; LINEAR CONSTRAINT RELATIONS; YEAST PYRUVATE-CARBOXYLASE; FED-BATCH CULTURE; HYBRIDOMA CELLS; MYELOMA CELLS; GLUTAMINE-METABOLISM; MASS BALANCES;
D O I
10.1016/j.ymben.2009.09.002
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
Mammalian cell culture metabolism is characterized by glucoglutaminolysis, that is, high glucose and glutamine uptake combined with a high rate of lactate and non-essential amino acid secretion. Stress associated with acid neutralization and ammonia accumulation necessitates complex feeding schemes and limits cell densities achieved in fed-batch culture. Conventional and constraint-based metabolic flux analysis has been successfully used to study the metabolic phenotype of mammalian cells in culture, while C-13 tracer analysis has been used to study small network models and validate assumptions of metabolism. Large-scale C-13 metabolic flux analysis, which is required to improve confidence in the network models and their predictions, remains a major challenge. Advances in both modeling and analytical techniques are bringing this challenge within sight. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:161 / 171
页数:11
相关论文
共 80 条
  • [1] Analysis of CHO cells metabolic redistribution in a glutamate-based defined medium in continuous culture
    Altamirano, C
    Illanes, A
    Casablancas, A
    Gámez, X
    Cairó, JJ
    Gòdia, C
    [J]. BIOTECHNOLOGY PROGRESS, 2001, 17 (06) : 1032 - 1041
  • [2] Elementary metabolite units (EMU): A novel framework for modeling isotopic distributions
    Antoniewicz, Maciek R.
    Kelleher, Joanne K.
    Stephanopoulos, Gregory
    [J]. METABOLIC ENGINEERING, 2007, 9 (01) : 68 - 86
  • [3] Inverse metabolic engineering: A strategy for directed genetic engineering of useful phenotypes
    Bailey, JE
    Sburlati, A
    Hatzimanikatis, V
    Lee, K
    Renner, WA
    Tsai, PS
    [J]. BIOTECHNOLOGY AND BIOENGINEERING, 2002, 79 (05) : 568 - 579
  • [4] HIGH-LEVEL EXPRESSION OF A RECOMBINANT ANTIBODY FROM MYELOMA CELLS USING A GLUTAMINE-SYNTHETASE GENE AS AN AMPLIFIABLE SELECTABLE MARKER
    BEBBINGTON, CR
    RENNER, G
    THOMSON, S
    KING, D
    ABRAMS, D
    YARRANTON, GT
    [J]. BIO-TECHNOLOGY, 1992, 10 (02): : 169 - 175
  • [5] GENETIC-ENGINEERING OF HYBRIDOMA GLUTAMINE-METABOLISM
    BELL, SL
    BEBBINGTON, C
    SCOTT, MF
    WARDELL, JN
    SPIER, RE
    BUSHELL, ME
    SANDERS, PG
    [J]. ENZYME AND MICROBIAL TECHNOLOGY, 1995, 17 (02) : 98 - 106
  • [6] SELECTING AND DESIGNING CELL-LINES FOR IMPROVED PHYSIOLOGICAL-CHARACTERISTICS
    BIRCH, JR
    BORASTON, RC
    METCALFE, H
    BROWN, ME
    BEBBINGTON, CR
    FIELD, RP
    [J]. CYTOTECHNOLOGY, 1994, 15 (1-3) : 11 - 16
  • [7] DETERMINATION OF THE RESPIRATION QUOTIENT IN MAMMALIAN-CELL CULTURE IN BICARBONATE BUFFERED MEDIA
    BONARIUS, HPJ
    DEGOOIJER, CD
    TRAMPER, J
    SCHMID, G
    [J]. BIOTECHNOLOGY AND BIOENGINEERING, 1995, 45 (06) : 524 - 535
  • [8] Bonarius HPJ, 1998, BIOTECHNOL BIOENG, V58, P258, DOI 10.1002/(SICI)1097-0290(19980420)58:2/3<258::AID-BIT20>3.0.CO
  • [9] 2-7
  • [10] Bonarius HPJ, 1996, BIOTECHNOL BIOENG, V50, P299, DOI 10.1002/(SICI)1097-0290(19960505)50:3<299::AID-BIT9>3.0.CO