Cutting the Gordian Knot: Identifiability of anaplerotic reactions in Corynebacterium glutamicum by means of 13C-metabolic flux analysis

被引:16
|
作者
Kappelmann, Jannick [1 ]
Wiechert, Wolfgang [1 ]
Noack, Stephan [1 ]
机构
[1] Forschungszentrum Julich, Inst Bio & Geosci, IBG Biotechnol 1, D-52425 Julich, Germany
关键词
C-13-metabolic flux analysis; anaplerosis; flux observability; structural identifiability; C; glutamicum; metabolic fluxes; BIDIRECTIONAL REACTION STEPS; PARALLEL LABELING EXPERIMENTS; CENTRAL CARBON METABOLITES; UNITS EMU; NETWORKS; QUANTIFICATION; SPECTROSCOPY; PRECISION; PATHWAYS; COMPLEX;
D O I
10.1002/bit.25833
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
Corynebacterium glutamicum is the major workhorse for the microbial production of several amino and organic acids. As long as these derive from tricarboxylic acid cycle intermediates, the activity of anaplerotic reactions is pivotal for a high biosynthetic yield. To determine single anaplerotic activities C-13-Metabolic Flux Analysis (C-13-MFA) has been extensively used for C. glutamicum, however with different network topologies, inconsistent or poorly determined anaplerotic reaction rates. Therefore, in this study we set out to investigate whether a focused isotopomer model of the anaplerotic node can at all admit a unique solution for all fluxes. By analyzing different scenarios of active anaplerotic reactions, we show in full generality that for C. glutamicum only certain anaplerotic deletion mutants allow to uniquely determine the anaplerotic fluxes from C-13-isotopomer data. We stress that the result of this analysis for different assumptions on active enzymes is directly transferable to other compartment-free organisms. Our results demonstrate that there exist biologically relevant metabolic network topologies for which the flux distribution cannot be inferred by classical C-13-MFA. Biotechnol. Bioeng. 2016;113: 661-674. (c) 2015 Wiley Periodicals, Inc.
引用
收藏
页码:661 / 674
页数:14
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