DRUM: A New Framework for Metabolic Modeling under Non-Balanced Growth. Application to the Carbon Metabolism of Unicellular Microalgae

被引:59
作者
Baroukh, Caroline [1 ,2 ]
Munoz-Tamayo, Rafael [2 ]
Steyer, Jean-Philippe [1 ]
Bernard, Olivier [2 ,3 ]
机构
[1] INRA, UR050, Lab Biotechnol Environm, Narbonne, France
[2] INRIA BIOCORE, Sophia Antipolis, France
[3] LOV UPMC CNRS, UMR 7093, Villefranche Sur Mer, France
关键词
ELEMENTARY FLUX MODES; PATHWAY ANALYSIS; BALANCE ANALYSIS; NETWORK; ACCUMULATION; BIODIESEL; IDENTIFICATION; MOBILIZATION; PREDICTION; ENERGETICS;
D O I
10.1371/journal.pone.0104499
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Metabolic modeling is a powerful tool to understand, predict and optimize bioprocesses, particularly when they imply intracellular molecules of interest. Unfortunately, the use of metabolic models for time varying metabolic fluxes is hampered by the lack of experimental data required to define and calibrate the kinetic reaction rates of the metabolic pathways. For this reason, metabolic models are often used under the balanced growth hypothesis. However, for some processes such as the photoautotrophic metabolism of microalgae, the balanced-growth assumption appears to be unreasonable because of the synchronization of their circadian cycle on the daily light. Yet, understanding microalgae metabolism is necessary to optimize the production yield of bioprocesses based on this microorganism, as for example production of third-generation biofuels. In this paper, we propose DRUM, a new dynamic metabolic modeling framework that handles the non-balanced growth condition and hence accumulation of intracellular metabolites. The first stage of the approach consists in splitting the metabolic network into sub-networks describing reactions which are spatially close, and which are assumed to satisfy balanced growth condition. The left metabolites interconnecting the sub-networks behave dynamically. Then, thanks to Elementary Flux Mode analysis, each sub-network is reduced to macroscopic reactions, for which simple kinetics are assumed. Finally, an Ordinary Differential Equation system is obtained to describe substrate consumption, biomass production, products excretion and accumulation of some internal metabolites. DRUM was applied to the accumulation of lipids and carbohydrates of the microalgae Tisochrysis lutea under day/night cycles. The resulting model describes accurately experimental data obtained in day/night conditions. It efficiently predicts the accumulation and consumption of lipids and carbohydrates.
引用
收藏
页数:15
相关论文
共 69 条
[1]   NEW LOOK AT STATISTICAL-MODEL IDENTIFICATION [J].
AKAIKE, H .
IEEE TRANSACTIONS ON AUTOMATIC CONTROL, 1974, AC19 (06) :716-723
[2]   Network biology:: Understanding the cell's functional organization [J].
Barabási, AL ;
Oltvai, ZN .
NATURE REVIEWS GENETICS, 2004, 5 (02) :101-U15
[3]  
Bastin G., 1990, On-line estimation and adaptive control of bioreactors
[4]   On the description of Tisochrysis lutea gen. nov sp nov and Isochrysis nuda sp nov in the Isochrysidales, and the transfer of Dicrateria to the Prymnesiales (Haptophyta) [J].
Bendif, El Mahdi ;
Probert, Ian ;
Schroeder, Declan C. ;
de Vargas, Colomban .
JOURNAL OF APPLIED PHYCOLOGY, 2013, 25 (06) :1763-1776
[5]   Identification of reaction networks for bioprocesses: determination of a partially unknown pseudo-stoichiometric matrix [J].
Bernard, O ;
Bastin, G .
BIOPROCESS AND BIOSYSTEMS ENGINEERING, 2005, 27 (05) :293-301
[6]   On the estimation of the pseudo-stoichiometric matrix for macroscopic mass balance modelling of biotechnological processes [J].
Bernard, O ;
Bastin, G .
MATHEMATICAL BIOSCIENCES, 2005, 193 (01) :51-77
[7]   Hurdles and challenges for modelling and control of microalgae for CO2 mitigation and biofuel production [J].
Bernard, Olivier .
JOURNAL OF PROCESS CONTROL, 2011, 21 (10) :1378-1389
[8]   Flux balance analysis of primary metabolism in Chlamydomonas reinhardtii [J].
Boyle, Nanette R. ;
Morgan, John A. .
BMC SYSTEMS BIOLOGY, 2009, 3
[9]   OptKnock: A bilevel programming framework for identifying gene knockout strategies for microbial strain optimization [J].
Burgard, AP ;
Pharkya, P ;
Maranas, CD .
BIOTECHNOLOGY AND BIOENGINEERING, 2003, 84 (06) :647-657
[10]   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