Nonradioactive assay for cellular dimethylallyl diphosphate

被引:44
作者
Fisher, AJ
Rosenstiel, TN
Shirk, MC
Fall, R
机构
[1] Univ Colorado, Dept Chem & Biochem, Boulder, CO 80309 USA
[2] Univ Colorado, Cooperat Inst Res Environm Sci, Boulder, CO 80309 USA
[3] Univ Colorado, Dept Environm Populat & Organism Biol, Boulder, CO 80309 USA
基金
美国国家科学基金会;
关键词
dimethylallyl diphosphate; isoprenoid; isoprenoid diphosphate; acid-catalyzed hydrolysis; isoprene; methylbutenol; gas chromatography;
D O I
10.1006/abio.2001.5079
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A sensitive, nonradioactive method was developed to measure cellular levels of dimethylallyl diphosphate (DMAPP), a central intermediate of isoprenoid metabolism in nature. The assay is based on the hydrolysis of DMAPP in acid to the volatile hydrocarbon isoprene (2-methyl-1,3-butadiene), with subsequent analysis of isoprene by headspace gas chromatography with reduction gas detection. In the assay, cell samples are directly acidified with 4 M H2SO4 in sealed reaction vials. Therefore, there is no need to extract metabolites, purify them, and keep them stable prior to analysis, and degradative enzymatic activities are destroyed. DMAPP levels of 23 +/- 4 nmol (g fresh weight)(-1) [ca. 85 nmol (g dry weight)(-1)] and 80 +/- 14 nmol (g fresh weight)(-1) [ca. 296 nmol (g dry weight)(-1)] were measured in dark- and light-adapted leaves of Populus deltoides (Eastern cottonwood), respectively. Evidence is presented to show that DMAPP is the major leaf metabolite giving rise to isoprene following acid hydrolysis. DMAPP levels in Bacillus subtilis and Saccharomyces cerevisiae were determined to be 40.8 +/- 16.7 pmol (OD600)(-1) [ca. 638 pmol (mg dry weight)(-1)] and 6.3 +/- 3.7 pmol (OD600)(-1) [ca. 139 pmol (mg dry weight)(-1)], respectively. The method should be suitable for any cell or tissue type and isolated cellular organelles. (C) 2001 Academic Press.
引用
收藏
页码:272 / 279
页数:8
相关论文
共 38 条
[1]   Yeast intracellular water determination by thermogravimetry [J].
Alcázar, EB ;
Rocha-Leao, MHM ;
Dweck, J .
JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY, 2000, 59 (03) :643-648
[2]   Mevalonate biosynthesis in plants [J].
Bach, TJ ;
Boronat, A ;
Campos, N ;
Ferrer, A ;
Vollack, KU .
CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1999, 34 (02) :107-122
[3]  
BAKER BM, 2000, THESIS U COLORADO BO
[4]   Competition between a sterol biosynthetic enzyme and tRNA modification in addition to changes in the protein synthesis machinery causes altered nonsense suppression [J].
Benko, AL ;
Vaduva, G ;
Martin, NC ;
Hopper, AK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (01) :61-66
[5]   DETERMINATION OF PHYTYL DIPHOSPHATE AND GERANYLGERANYL DIPHOSPHATE IN ETIOLATED OAT SEEDLINGS [J].
BENZ, J ;
FISCHER, I ;
RUDIGER, W .
PHYTOCHEMISTRY, 1983, 22 (12) :2801-2804
[6]   STEROL PATHWAY IN YEAST - IDENTIFICATION AND PROPERTIES OF MUTANT STRAINS DEFECTIVE IN MEVALONATE DIPHOSPHATE DECARBOXYLASE AND FARNESYL DIPHOSPHATE SYNTHETASE [J].
CHAMBON, C ;
LADEVEZE, V ;
SERVOUSE, M ;
BLANCHARD, L ;
JAVELOT, C ;
VLADESCU, B ;
KARST, F .
LIPIDS, 1991, 26 (08) :633-636
[7]   BIOCHEMISTRY AND MOLECULAR-BIOLOGY OF THE ISOPRENOID BIOSYNTHETIC-PATHWAY IN PLANTS [J].
CHAPPELL, J .
ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY, 1995, 46 :521-547
[8]  
DAVISSON VJ, 1985, METHOD ENZYMOL, V110, P130
[9]  
DENERIS ES, 1985, J BIOL CHEM, V260, P1382
[10]  
EDMOND J, 1974, J BIOL CHEM, V249, P66