Metabolic flux distributions: genetic information, computational predictions, and experimental validation

被引:22
作者
Blank, Lars M. [1 ]
Kuepfer, Lars [2 ]
机构
[1] TU Dortmund, Lab Chem Biotechnol, Fac Biochem & Chem Engn, D-44221 Dortmund, Germany
[2] Bayer Technol Serv GmbH, Competence Ctr Syst Biol & Computat Solut, D-51368 Leverkusen, Germany
关键词
Flux balance analysis; Metabolic network analysis; C-13-metabolic flux analysis; Synthetic biology; Metabolic engineering; Industrial biotechnology; SUCCINIC ACID PRODUCTION; HIGHLY EXPRESSED GENES; L-LYSINE PRODUCTION; ESCHERICHIA-COLI; CORYNEBACTERIUM-GLUTAMICUM; AMINO-ACID; TRANSCRIPTIONAL REGULATION; PYRUVATE-CARBOXYLASE; PATHWAY ANALYSIS; NETWORK ANALYSIS;
D O I
10.1007/s00253-010-2506-6
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
Flux distributions in intracellular metabolic networks are of immense interest to fundamental and applied research, since they are quantitative descriptors of the phenotype and the operational mode of metabolism in the face of external growth conditions. In particular, fluxes are of relevance because they do not belong to the cellular inventory (e.g., transcriptome, proteome, metabolome), but are rather quantitative moieties, which link the phenotype of a cell to the specific metabolic mode of operation. A frequent application of measuring and redirecting intracellular fluxes is strain engineering, which ultimately aims at shifting metabolic activity toward a desired product to achieve a high yield and/or rate. In this article, we first review the assessment of intracellular flux distributions by either qualitative or rather quantitative computational methods and also discuss methods for experimental measurements. The tools at hand will then be exemplified on strain engineering projects from the literature. Finally, the achievements are discussed in the context of future developments in Metabolic Engineering and Synthetic Biology.
引用
收藏
页码:1243 / 1255
页数:13
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