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