Use of network analysis of metabolic systems in bioengineering

被引:62
作者
Schuster, S [1 ]
Klamt, S
Weckwerth, W
Moldenhauer, F
Pfeiffer, T
机构
[1] Max Delbruck Ctr Mol Med, Dept Bioinformat, D-13092 Berlin, Germany
[2] Max Plant Inst Dynam Complex Tech Syst, D-39106 Magdeburg, Germany
[3] Max Planck Inst Mol Plant Physiol, D-14476 Golm, Germany
[4] ETH Ctr Zurich, CH-8092 Zurich, Switzerland
关键词
D O I
10.1007/s004490100253
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
Basic ideas and recent developments in network analysis of metabolic systems and various applications of this analysis in bioengineering are reviewed. Central concepts are the null-space to the stoichiometry matrix and the elementary flux modes. The applicability of elementary-modes analysis in biotechnology is illustrated by the synthesis of the cyclooctadepsipeptides PF1022 in the fungus Mycelia sterilia. Network analysis is also useful in metabolic flux analysis. In particular, a procedure for finding out which reaction rates can be uniquely calculated in underdetermined reaction networks is outlined. The concept of 'enzyme subsets' is explained and its use for analysing genetic regulation is demonstrated. In particular, the correlation between expression data concerning the diauxic shift in yeast and the enzyme subsets in yeast metabolism is discussed.
引用
收藏
页码:363 / 372
页数:10
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