Analysis of growth of Lactobacillus plantarum WCFS1 on a complex medium using a genome-scale metabolic model

被引:215
作者
Teusink, Bas
Wiersma, Anne
Molenaar, Douwe
Francke, Christof
de Vos, Willem M.
Siezen, Roland J.
Smid, Eddy J.
机构
[1] Wageningen Ctr Food Sci, NL-6700 AN Wageningen, Netherlands
[2] NIZO Food Res, NL-6710 BA Ede, Netherlands
[3] Radboud Univ Nijmegen, Ctr Mol & Biomol Informat, NL-6710 BA Nijmegen, Netherlands
关键词
D O I
10.1074/jbc.M606263200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A genome-scale metabolic model of the lactic acid bacterium Lactobacillus plantarum WCFS1 was constructed based on genomic content and experimental data. The complete model includes 721 genes, 643 reactions, and 531 metabolites. Different stoichiometric modeling techniques were used for interpretation of complex fermentation data, as L. plantarum is adapted to nutrient-rich environments and only grows in media supplemented with vitamins and amino acids. (i) Based on experimental input and output fluxes, maximal ATP production was estimated and related to growth rate. (ii) Optimization of ATP production further identified amino acid catabolic pathways that were not previously associated with free-energy metabolism. (iii) Genome-scale elementary flux mode analysis identified 28 potential futile cycles. (iv) Flux variability analysis supplemented the elementary mode analysis in identifying parallel pathways, e. g. pathways with identical end products but different co-factor usage. Strongly increased flexibility in the metabolic network was observed when strict coupling between catabolic ATP production and anabolic consumption was relaxed. These results illustrate how a genome-scale metabolic model and associated constraint-based modeling techniques can be used to analyze the physiology of growth on a complex medium rather than a minimal salts medium. However, optimization of biomass formation using the Flux Balance Analysis approach, reported to successfully predict growth rate and by product formation in Escherichia coli and Saccharomyces cerevisiae, predicted too high biomass yields that were incompatible with the observed lactate production. The reason is that this approach assumes optimal efficiency of substrate to biomass conversion, and can therefore not predict the metabolically inefficient lactate formation.
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页码:40041 / 40048
页数:8
相关论文
共 51 条
[1]   Energy balance for analysis of complex metabolic networks [J].
Beard, DA ;
Liang, SC ;
Qian, H .
BIOPHYSICAL JOURNAL, 2002, 83 (01) :79-86
[2]  
Bertsekas D.P., 1998, NETWORK OPTIMIZATION
[3]   Flux coupling analysis of genome-scale metabolic network reconstructions [J].
Burgard, AP ;
Nikolaev, EV ;
Schilling, CH ;
Maranas, CD .
GENOME RESEARCH, 2004, 14 (02) :301-312
[4]   Metabolic network analysis of Bacillus clausii on minimal and semirich medium using 13C-Labeled glucose [J].
Christiansen, T ;
Christensen, B ;
Nielsen, J .
METABOLIC ENGINEERING, 2002, 4 (02) :159-169
[5]   ENERGY-SPILLING REACTIONS OF STREPTOCOCCUS-BOVIS AND RESISTANCE OF ITS MEMBRANE TO PROTON CONDUCTANCE [J].
COOK, GM ;
RUSSELL, JB .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1994, 60 (06) :1942-1948
[6]   A method for classifying metabolites in topological pathway analyses based on minimization of pathway number [J].
Dandekar, T ;
Moldenhauer, F ;
Bulik, S ;
Bertram, H ;
Schuster, S .
BIOSYSTEMS, 2003, 70 (03) :255-270
[7]   Bacillus subtilis metabolism and energetics in carbon-limited and excess-carbon chemostat culture [J].
Dauner, M ;
Storni, T ;
Sauer, U .
JOURNAL OF BACTERIOLOGY, 2001, 183 (24) :7308-7317
[8]   Optimality and evolutionary tuning of the expression level of a protein [J].
Dekel, E ;
Alon, U .
NATURE, 2005, 436 (7050) :588-592
[9]   In silico predictions of Escherichia coli metabolic capabilities are consistent with experimental data [J].
Edwards, JS ;
Ibarra, RU ;
Palsson, BO .
NATURE BIOTECHNOLOGY, 2001, 19 (02) :125-130
[10]   Metabolic flux responses to pyruvate kinase knockout in Escherichia coli [J].
Emmerling, M ;
Dauner, M ;
Ponti, A ;
Fiaux, J ;
Hochuli, M ;
Szyperski, T ;
Wüthrich, K ;
Bailey, JE ;
Sauer, U .
JOURNAL OF BACTERIOLOGY, 2002, 184 (01) :152-164