Cold glycerol-saline:: The promising quenching solution for accurate intracellular metabolite analysis of microbial cells

被引:123
作者
Villas-Boas, Silas G.
Bruheim, Per
机构
[1] AgResearch Ltd, Grassland Res Ctr, Palmerston North 4442, New Zealand
[2] Norwegian Univ Sci & Technol, Fac Nat Sci & Technol, Dept Biotechnol, N-7491 Trondheim, Norway
[3] SINTEF, Mat & Chem, Dept Biotechnol, N-7465 Trondheim, Norway
关键词
D O I
10.1016/j.ab.2007.06.028
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Microbial metabolomics has been seriously limited by our inability to perform a reliable separation of intra- and extracellular metabolites with efficient quenching of cell metabolism. Microbial cells are sensitive to most (if not all) quenching agents developed to date, resulting in leakage of intracellular metabolites to the extracellular medium during quenching. Therefore, as yet we are unable to obtain an accurate concentration of intracellular metabolites from microbial cell cultures. However, knowledge of the in vivo concentrations of intermediary metabolites is of fundamental importance for the characterization of microbial metabolism so as to integrate meaningful metabolomics data with other levels of functional genomics analysis. In this article, we report a novel and robust quenching method for microbial cell cultures based on cold glycerol-saline solution as the quenching agent that prevents significant leakage of intracellular metabolites and, therefore, permits more accurate measurement of intracellular metabolite concentrations in microbial cells. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:87 / 97
页数:11
相关论文
共 22 条
[1]   Sampling for metabolome analysis of microorganisms [J].
Bolten, Christoph J. ;
Kiefer, Patrick ;
Letisse, Fabien ;
Portais, Jean-Charles ;
Wittmann, Christoph .
ANALYTICAL CHEMISTRY, 2007, 79 (10) :3843-3849
[2]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[3]   Conservation of the metabolomic response to starvation across two divergent microbes [J].
Brauer, Matthew J. ;
Yuan, Jie ;
Bennett, Bryson D. ;
Lu, Wenyun ;
Kimball, Elizabeth ;
Botstein, David ;
Rabinowitz, Joshua D. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (51) :19302-19307
[4]   Industrial production of amino acids by coryneform bacteria [J].
Hermann, T .
JOURNAL OF BIOTECHNOLOGY, 2003, 104 (1-3) :155-172
[5]   Microbial metabolomics: past, present and future methodologies [J].
Mashego, Mlawule R. ;
Rumbold, Karl ;
De Mey, Marjan ;
Vandamme, Erick ;
Soetaert, Wim ;
Heijnen, Joseph J. .
BIOTECHNOLOGY LETTERS, 2007, 29 (01) :1-16
[6]   MIRACLE:: mass isotopomer ratio analysis of U-13C-labeled extracts.: A new method for accurate quantification of changes in concentrations of intracellular metabolites [J].
Mashego, MR ;
Wu, L ;
Van Dam, JC ;
Ras, C ;
Vinke, JL ;
Van Winden, WA ;
Van Gulik, WM ;
Heijnen, JJ .
BIOTECHNOLOGY AND BIOENGINEERING, 2004, 85 (06) :620-628
[7]   The next wave in metabolome analysis [J].
Nielsen, J ;
Oliver, S .
TRENDS IN BIOTECHNOLOGY, 2005, 23 (11) :544-546
[8]   It is all about metabolic fluxes [J].
Nielsen, J .
JOURNAL OF BACTERIOLOGY, 2003, 185 (24) :7031-7035
[9]   Systematic functional analysis of the yeast genome (vol 16, pg 373, 1998) [J].
Oliver, SG .
TRENDS IN BIOTECHNOLOGY, 1998, 16 (10) :447-447
[10]   A functional genomics strategy that uses metabolome data to reveal the phenotype of silent mutations [J].
Raamsdonk, LM ;
Teusink, B ;
Broadhurst, D ;
Zhang, NS ;
Hayes, A ;
Walsh, MC ;
Berden, JA ;
Brindle, KM ;
Kell, DB ;
Rowland, JJ ;
Westerhoff, HV ;
van Dam, K ;
Oliver, SG .
NATURE BIOTECHNOLOGY, 2001, 19 (01) :45-50