PRECISE DELTA-C-13-DETERMINATION IN THE RANGE OF NATURAL-ABUNDANCE ONAMINO-ACIDS FROM PROTEIN HYDROLYSATES BY GAS-CHROMATOGRAPHY - ISOTOPERATIO MASS-SPECTROMETRY

Citation
H. Demmelmair et Hl. Schmidt, PRECISE DELTA-C-13-DETERMINATION IN THE RANGE OF NATURAL-ABUNDANCE ONAMINO-ACIDS FROM PROTEIN HYDROLYSATES BY GAS-CHROMATOGRAPHY - ISOTOPERATIO MASS-SPECTROMETRY, Isotopenpraxis, 29(3), 1993, pp. 237-250
Citations number
23
Categorie Soggetti
Chemistry Inorganic & Nuclear","Nuclear Sciences & Tecnology
Journal title
ISSN journal
00211915
Volume
29
Issue
3
Year of publication
1993
Pages
237 - 250
Database
ISI
SICI code
0021-1915(1993)29:3<237:PDITRO>2.0.ZU;2-N
Abstract
Routine on-line C-13-analysis by coupled gas chromatography - combusti on - isotope ratio - mass spectrometry of individual amino acids out o f mixtures in the natural abundance range demands their strictly stand ardized derivatization. For the N-acetyl-propylesters of amino acids f rom protein hydrolysates and blood serum a mean precision of 0.5 parts per thousand (1 SD) for derivatization, separation and measurement co uld be attained. From deltaC-13-values of derivatives deltaC-13-values of amino acids could be calculated by a carbon balance equation, impl ying an isotope effect on the C-1 of acetate of about 1.04 for nine am ino acids. The global deltaC-13-value of casein calculated from the in dividual amino acids differed by less than 1.5 parts per thousand from the directly determined value. The deltaC-13-values of amino acids fr om plant protein hydrolysates analyzed by the on-line method were in a greement with results obtained by classical procedures. The method per mits the delta-value determination of up to nine amino acids from 200 mug of a mixture in less than one hour. By this means the detection of C-13-labeled amino acids in nmole amounts diluted by the 5000-fold am ount of carrier becomes possible.