Cell Density Effect in the Baculovirus-insect Cells System: A Quantitative Analysis of Energetic Metabolism

被引:100
作者
Bernal, Vicente [1 ]
Carinhas, Nuno [1 ]
Yokomizo, Adriana Y. [1 ]
Carrondo, Manuel J. T. [1 ,2 ]
Alves, Paula M. [1 ]
机构
[1] Univ Nova Lisboa, Inst Biol Expt & Tecnol, Inst Tecnol Quim & Biol, P-2780157 Oeiras, Portugal
[2] FCT UNL, Engn Bioquim Lab, Monte De Caparica, Portugal
关键词
Spodoptera frugiperda; cell density effect; metabolic burden; baculovirus production; protein production; metabolic flux analysis; SPODOPTERA-FRUGIPERDA SF9; FLUX ANALYSIS; GLUTAMINE-METABOLISM; PROTEIN-PRODUCTION; EXPRESSION SYSTEM; INTRACELLULAR ATP; HYBRIDOMA CELLS; INFECTION; CULTURES; GROWTH;
D O I
10.1002/bit.22364
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 cell density effect (i.e., the drop in the specific productivity in the baculovirus-insect cells expression system when cells are infected at high cell densities) has been extensively described in the literature. In this article, a model for the central metabolism of serum-free suspension cultures of Spodoptera frugiperda Sf9 cells is proposed and used to investigate the metabolic basis for this phenomenon. The main metabolic pathways (glycolysis, pentose phosphate pathway, tricarboxylic acids cycle, glutaminolysis, and amino acids metabolism), cellular growth and energetics were considered. The analysis of the stoichiometric model allowed further understanding of the interplay of the consumption of carbon and nitrogen sources in insect cells. Moreover, metabolic flux analysis revealed that Sf9 cells undergo a progressive inhibition of central metabolism when grown to high cell densities, for which the incorporation of amino acids carbon backbones into the TCA cycle (mainly glutamine) and the down-regulation of glycolysis are partially responsible. Following infection by baculovirus and cellular division arrest, central energy metabolism depended on the infection strategy chosen (cell concentration at the moment of infection and multiplicity of infection), inhibition being observed at high cell densities. Interestingly, the energetic status of the culture correlated with the decrease in cellular production of baculovirus, meaning that there is room for process optimization through the application of metabolic engineering techniques.
引用
收藏
页码:162 / 180
页数:19
相关论文
共 55 条
[31]   Structural and functional analysis of cellular networks with CellNetAnalyzer [J].
Klamt, Steffen ;
Saez-Rodriguez, Julio ;
Gilles, Ernst D. .
BMC SYSTEMS BIOLOGY, 2007, 1
[32]   Application of on-line OUR measurements to detect actions points to improve baculovirus-insect cell cultures in bioreactors [J].
Lecina, M. ;
Soley, A. ;
Gracia, J. ;
Espunya, E. ;
Lazaro, B. ;
Cairo, J. J. ;
Godia, F. .
JOURNAL OF BIOTECHNOLOGY, 2006, 125 (03) :385-394
[33]   Identification of metabolic fluxes in hepatic cells from transient 13C-labeling experiments:: Part II.: Flux estimation [J].
Maier, Klaus ;
Hofmann, Ute ;
Reuss, Matthias ;
Mauch, Klaus .
BIOTECHNOLOGY AND BIOENGINEERING, 2008, 100 (02) :355-370
[34]   Virus-like particle production at low multiplicities of infection with the baculovirus insect cell system [J].
Maranga, L ;
Brazao, TF ;
Carrondo, MJT .
BIOTECHNOLOGY AND BIOENGINEERING, 2003, 84 (02) :245-253
[35]   Lipid composition of Spodoptera frugiperda (Sf9) and Trichoplusia ni (Tn) insect cells used for baculovirus infection [J].
Marheineke, K ;
Grünewald, S ;
Christie, W ;
Reiländer, H .
FEBS LETTERS, 1998, 441 (01) :49-52
[36]   Low-protein medium affects the 293SF central metabolism during growth and infection with adenovirus [J].
Nadeau, I ;
Gilbert, PA ;
Jacob, D ;
Perrier, M ;
Kamen, A .
BIOTECHNOLOGY AND BIOENGINEERING, 2002, 77 (01) :91-104
[37]   293SF metabolic flux analysis during cell growth and infection with an adenoviral vector [J].
Nadeau, I ;
Jacob, D ;
Perrier, M ;
Kamen, A .
BIOTECHNOLOGY PROGRESS, 2000, 16 (05) :872-884
[38]  
Neermann J, 1996, J CELL PHYSIOL, V166, P152
[39]  
OHMAN L, 1995, APPL MICROBIOL BIOT, V43, P1006
[40]   Monitoring the progress of infection and recombinant protein production in insect cell cultures using intracellular ATP measurement [J].
Olejnik, AM ;
Czaczyk, K ;
Marecik, R ;
Grajek, W ;
Jankowski, T .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2004, 65 (01) :18-24