Metabolic isotopomer labeling systems. Part II: structural flux identifiability analysis

被引:35
作者
Isermann, N [1 ]
Wiechert, W [1 ]
机构
[1] Univ Gesamthsch Siegen, IMR, Dept simulat, D-57068 Siegen, Germany
关键词
metabolic engineering; metabolic flux analysis; carbon labeling experiments; isotopomer labeling systems; structural identifiability;
D O I
10.1016/S0025-5564(02)00222-5
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Metabolic flux analysis using carbon labeling experiments (CLEs) is an important tool in metabolic engineering where the intracellular fluxes have to be computed from the measured extracellular fluxes and the partially measured distribution of C-13 labeling within the intracellular metabolite pools. The relation between unknown fluxes and measurements is described by,an isotopomer labeling system (ILS) (see Part I [Math. Biosci. 169 (2001) 173]). Part II deals with the structural flux identifiability of measured ILSs in the steady state. The central question is whether the measured data contains sufficient information to determine the unknown intracellular fluxes. This question has to be decided a priori, i.e. before the CLE is carried out. In structural identifiability analysis the measurements are assumed to be noise-free. A general theory of structural flux identifiability for measured ILSs is presented and several algorithms are developed to solve the identifiability problem. In the particular case of maximal measurement information, a symbolical algorithm is presented that decides the identifiability question by means of linear methods. Several upper bounds of the number of identifiable fluxes are derived, and the influence of the chosen inputs is evaluated. By introducing integer arithmetic this algorithm can even be applied to large networks. For the general case of arbitrary measurement information, identifiability is decided by a local criterion. A new algorithm based on integer arithmetic enables an a priori local identifiability analysis to be performed for networks of arbitrary size. All algorithms have been implemented and flux identifiability is investigated for the network of the central metabolic pathways of a microorganism. Moreover, several small examples are worked out to illustrate the influence of input metabolite labeling and the paradox of information loss due to network simplification. (C) 2003 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:175 / 214
页数:40
相关论文
共 40 条
[1]  
[Anonymous], COMPUTATIONAL APPROA
[2]   TOWARD A SCIENCE OF METABOLIC ENGINEERING [J].
BAILEY, JE .
SCIENCE, 1991, 252 (5013) :1668-1675
[3]   Identifiability and distinguishability concepts in electrochemistry [J].
Berthier, F ;
Diard, JP ;
Pronzato, L ;
Walter, E .
AUTOMATICA, 1996, 32 (07) :973-984
[4]   Isotopomer Analysis Using GC-MS [J].
Christensen, Bjarke ;
Nielsen, Jens .
METABOLIC ENGINEERING, 1999, 1 (04) :282-290
[5]  
COX D, 1992, IDEALS VARIETIES ALG
[6]   Determination of full 13C isotopomer distributions for metabolic flux analysis using heteronuclear spin echo difference NMR spectroscopy [J].
de Graaf, AA ;
Mahle, M ;
Möllney, M ;
Wiechert, W ;
Stahmann, P ;
Sahm, H .
JOURNAL OF BIOTECHNOLOGY, 2000, 77 (01) :25-35
[7]  
DEGRAAF AA, 2000, NMR MICROBIOLOGY THE
[8]  
DELFORGE J, 1987, IDENTIFIABILITY PARA, P21
[9]  
Golub GH, 2013, Matrix Computations, V4