13C metabolic flux analysis: optimal design of isotopic labeling experiments

被引:87
作者
Antoniewicz, Maciek R. [1 ]
机构
[1] Univ Delaware, Metab Engn & Syst Biol Lab, Dept Chem & Biomol Engn, Newark, DE 19716 USA
基金
美国国家科学基金会;
关键词
AMINO-ACIDS; UNITS EMU; SYSTEMS; TRACERS; NETWORK; MICROORGANISMS; DISTRIBUTIONS; FRAMEWORK; STRAIN; FUTURE;
D O I
10.1016/j.copbio.2013.02.003
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Measuring fluxes by C-13 metabolic flux analysis (C-13-MFA) has become a key activity in chemical and pharmaceutical biotechnology. Optimal design of isotopic labeling experiments is of central importance to C-13-MFA as it determines the precision with which fluxes can be estimated. Traditional methods for selecting isotopic tracers and labeling measurements did not fully utilize the power of C-13-MFA. Recently, new approaches were developed for optimal design of isotopic labeling experiments based on parallel labeling experiments and algorithms for rational selection of tracers. In addition, advanced isotopic labeling measurements were developed based on tandem mass spectrometry. Combined, these approaches can dramatically improve the quality of C-13-MFA results with important applications in metabolic engineering and biotechnology.
引用
收藏
页码:1116 / 1121
页数:6
相关论文
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