Measuring multiple fluxes through plant metabolic networks

被引:189
作者
Ratcliffe, RG
Shachar-Hill, Y
机构
[1] Michigan State Univ, Dept Plant Biol, E Lansing, MI 48824 USA
[2] Univ Oxford, Dept Plant Sci, Oxford OX1 3RB, England
关键词
flux map; isotopomers; mass spectrometry; metabolic flux analysis; nuclear magnetic resonance spectroscopy; stable isotopes;
D O I
10.1111/j.1365-313X.2005.02649.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Fluxes through metabolic networks are crucial for cell function, and a knowledge of these fluxes is essential for understanding and manipulating metabolic phenotypes. Labeling provides the key to flux measurement, and in network flux analysis the measurement of multiple fluxes allows a flux map to be superimposed on the metabolic network. The principles and practice of two complementary methods, dynamic and steady-state labeling, are described, emphasizing best practice and illustrating their contribution to network flux analysis with examples taken from the plant and microbial literature. The principal analytical methods for the detection of stable isotopes are also described, as well as the procedures for obtaining flux maps from labeling data. A series of boxes summarizing the key concepts of network flux analysis is provided for convenience.
引用
收藏
页码:490 / 511
页数:22
相关论文
共 86 条
[1]   A new substrate cycle in plants. evidence for a high glucose-phosphate-to-glucose turnover from in vivo steady-state and pulse-labeling experiments with [13C] glucose and [14C] glucose [J].
Alonso, AP ;
Vigeolas, H ;
Raymond, P ;
Rolin, D ;
Dieuaide-Noubhani, M .
PLANT PHYSIOLOGY, 2005, 138 (04) :2220-2232
[2]  
Ap Rees T., 1994, Plant Cell and Environment, V17, P587, DOI 10.1111/j.1365-3040.1994.tb00151.x
[3]  
Bacher A, 1998, FEMS MICROBIOL REV, V22, P567
[4]   Response to Neuhaus et al.:: No need to shift the paradigm on the metabolic pathway to transitory starch in leaves [J].
Baroja-Fernández, E ;
Muñoz, FJ ;
Pozueta-Romero, J .
TRENDS IN PLANT SCIENCE, 2005, 10 (04) :156-158
[5]   Most of ADP-glucose linked to starch biosynthesis occurs outside the chloroplast in source leaves [J].
Baroja-Fernández, E ;
Muñoz, FJ ;
Zandueta-Criado, A ;
Morán-Zorzano, MT ;
Viale, AM ;
Alonso-Casajús, N ;
Pozueta-Romero, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (35) :13080-13085
[6]   Potential of metabolomics as a functional genomics tool [J].
Bino, RJ ;
Hall, RD ;
Fiehn, O ;
Kopka, J ;
Saito, K ;
Draper, J ;
Nikolau, BJ ;
Mendes, P ;
Roessner-Tunali, U ;
Beale, MH ;
Trethewey, RN ;
Lange, BM ;
Wurtele, ES ;
Sumner, LW .
TRENDS IN PLANT SCIENCE, 2004, 9 (09) :418-425
[7]   Understanding in vivo benzenoid metabolism in petunia petal tissue [J].
Boatright, J ;
Negre, F ;
Chen, XL ;
Kish, CM ;
Wood, B ;
Peel, G ;
Orlova, I ;
Gang, D ;
Rhodes, D ;
Dudareva, N .
PLANT PHYSIOLOGY, 2004, 135 (04) :1993-2011
[8]   Flux analysis of underdetermined metabolic networks: The quest for the missing constraints [J].
Bonarius, HPJ ;
Schmid, G ;
Tramper, J .
TRENDS IN BIOTECHNOLOGY, 1997, 15 (08) :308-314
[9]  
BOROWITZ MJ, 1977, J BIOL CHEM, V252, P1589
[10]   Isotopomer Analysis Using GC-MS [J].
Christensen, Bjarke ;
Nielsen, Jens .
METABOLIC ENGINEERING, 1999, 1 (04) :282-290