Mass isotopomer study of the nonoxidative pathways of the pentose cycle with [1,2-13C2]glucose

We present a single-tracer method for the study of the pentose phosphate pathway (PPP) using [1,2-C-13(2)]glucose and mass isotopomer analysis. The metabolism of [1,2-C-13(2)]glucose by the glucose-6-phosphate dehydrogenase, transketolase (TK), and transaldolase (TA) reactions results in unique pentose and lactate isotopomers with either one or two C-13 substitutions. The distribution of these isotopomers was used to estimate parameters of the PPP using the model of Katz and Rognstad (J. Katz and R. Rognstad. Biochemistry 6: 2227-2247, 1967). Mass and position isotopomers of ribose, and lactate and palmitate (products from triose phosphate) from human hepatoma cells (Hep G2) incubated with 30% enriched [1,2-C-13(2)]glucose were determined using gas chromatography mass spectrometry. After 24-72 h incubation, 1.9% of lactate molecules in the medium contained one C-13 substitution (m(1)) and 10% contained two C-13 substitutions (m(2)). A similar m(1)-to-m(2) ratio was found in palmitate as expected. Pentose cycle (PC) activity determined from incubation with [1,2-C-13(2)]glucose was 5.73 +/- 0.52% of the glucose flux, which was identical to the value of PC (5.55 +/- 0.73%) determined by separate incubations with [1-C-13] and [6-C-13]glucose. C-13 was found to be distributed in four ribose isotopomers ([1-C-13]-, [5-C-13]-, [1,2-C-13(2)]-, and [4,5-C-13(2)]ribose). The observed ribose isotopomer distribution was best matched with that provided from simulation by substituting 0.032 for TK and 0.85 for TA activity relative to glucose uptake into the model of Katz and Rognstad. The use of [1,2-C-13(2)]glucose not only permits the determination of PC but also allows estimation of relative rates through the TK and TA reactions.