Practical and theoretical considerations in the gas chromatography/combustion/isotope ratio mass spectrometry δ13C analysis of small polyfunctional compounds

被引:148
作者
Docherty, G [1 ]
Jones, V [1 ]
Evershed, RP [1 ]
机构
[1] Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
关键词
D O I
10.1002/rcm.270
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Carbohydrates and proteins are among the most abundant naturally occurring biomolecules and so suitable methods for their reliable stable isotope analysis by gas chromatography/combustion/ isotope ratio mass spectrometry (GC/C/IRMS) are required. Due to the non-volatile nature of these compounds they require hydrolytic cleavage to their lower molecular weight subunits and derivatisation prior to GC/C/IRMS analysis. The addition of carbon to the molecules and any kinetic isotopic fractionation associated with derivatisation must be accounted for in order to provide meaningful stable isotope values and estimates of propagated errors. To illustrate these points amino acid trifluoroacetate/isopropyl esters and alditol acetates were prepared from authentic amino acids and monosaccharides, respectively. As predicted from the derivatisation reaction mechanisms, a kinetic isotope effect was observed which precludes direct calculation of delta C-13 values of the amino acids and monosaccharides by simple mass balance equations. This study shows that the kinetic isotope effect associated with derivatisation is both reproducible and robust, thereby allowing the use of correction factors. We show how correction factors can be determined and accurately account for the addition of derivative carbon. As a consequence of the addition of a molar excess of carbon and the existence of a kinetic isotope effect during derivatisation, errors associated with determined delta C-13 values must be assessed. We illustrate how such errors can be quantified (for monosaccharides +/-1.3% and for amino acids between +/-0.8% and +/-1.4%). With the magnitude of the errors for a given delta C-13 value of a monosaccharide or amino acid quantified, it is possible to make reliable interpretations of delta C-13 values, thereby validating the determination of delta C-13 values of amino acids as TFA/IP esters and monosaccharides as alditol acetates. Copyright (C) 2001 John Wiley & Sons, Ltd.
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页码:730 / 738
页数:9
相关论文
共 12 条
[1]   A SIMPLE AND RAPID PREPARATION OF ALDITOL ACETATES FOR MONOSACCHARIDE ANALYSIS [J].
BLAKENEY, AB ;
HARRIS, PJ ;
HENRY, RJ ;
STONE, BA .
CARBOHYDRATE RESEARCH, 1983, 113 (02) :291-299
[2]   N-METHYLIMIDAZOLE AS A CATALYST FOR ANALYTICAL ACETYLATIONS OF HYDROXY COMPOUNDS [J].
CONNORS, KA ;
PANDIT, NK .
ANALYTICAL CHEMISTRY, 1978, 50 (11) :1542-1545
[3]   Allocation of nitrogen and carbon in leaves of Metrosideros polymorpha regulates carboxylation capacity and δ13C along an altitudinal gradient [J].
Cordell, S ;
Goldstein, G ;
Meinzer, FC ;
Handley, LL .
FUNCTIONAL ECOLOGY, 1999, 13 (06) :811-818
[4]   δ13C of CO2 respired in the dark in relation to δ13C of leaf carbohydrates in Phaseolus vulgaris L-under progressive drought [J].
Duranceau, M ;
Ghashghaie, J ;
Badeck, F ;
Deleens, E ;
Cornic, G .
PLANT CELL AND ENVIRONMENT, 1999, 22 (05) :515-523
[5]   Stable nitrogen isotope analysis of amino acid enantiomers by gas chromatography combustion/isotope ratio mass spectrometry [J].
Macko, SA ;
Uhle, ME ;
Engel, MH ;
Andrusevich, V .
ANALYTICAL CHEMISTRY, 1997, 69 (05) :926-929
[6]   Stable isotopic analysis of individual carbohydrates by gas chromatographic combustion/isotope ratio mass spectrometry [J].
Macko, SA ;
Ryan, M ;
Engel, MH .
CHEMICAL GEOLOGY, 1998, 152 (1-2) :205-210
[7]   Applied gas chromatography coupled to isotope ratio mass spectrometry [J].
Meier-Augenstein, W .
JOURNAL OF CHROMATOGRAPHY A, 1999, 842 (1-2) :351-371
[8]  
MEIERAUGENSTEIN W, 1997, LC GC EUR, V10, P17
[9]  
Melander L., 1980, Reaction Rates of Isotopic Molecules