MODEL-EQUATIONS FOR CONDENSATION BIOSYNTHESIS USING STABLE ISOTOPES AND RADIOISOTOPES

被引:101
作者
KELLEHER, JK
MASTERSON, TM
机构
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1992年 / 262卷 / 01期
关键词
MODELS; EXPERIMENTAL; THEORETICAL; MASS SPECTROMETRY; C-13; TRACER KINETICS; PALMITATE;
D O I
10.1152/ajpendo.1992.262.1.E118
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Important syntheses in living systems occur by condensation reactions of the type nA --> 1B (where n is the number of A molecules needed to synthesize 1 molecule of B). Quantitative relationships for estimating the rate of synthesis of B from radioactive and stable isotope tracers are compared. With radioisotope tracers, only a single quantity is detected, the amount of radioactivity in B. In contrast, isotopes of varying mass produce multiple mass isotopomers B that are detected using mass spectrometry. The analysis demonstrates that the rate of synthesis of B is identifiable from stable isotope data but not from radioisotope data. This results because the isotopomer distribution of B at any time after tracer addition is a function of only the multinomial distribution representing the synthesis of B from n molecules of A and two parameters representing the fractional fluxes of isotopically enriched molecules to the sampled compartment of B. The model considers the possibility that the sampled compartment of B may not reach isotopic steady state during the experiment. A graphical method for obtaining initial estimates of the two parameters is presented.
引用
收藏
页码:E118 / E125
页数:8
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