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3 Food Science and Human Nutrition Department, Institute of Food and Agricultural Sciences 4 General Clinical Research Center 5 Division of Biostatistics, Department of Epidemiology and Health Policy Research 6 Division of Endocrinology and Metabolism, Department of Medicine 7 Department of Biochemistry and Molecular Biology, College of Medicine, University of Florida, Gainesville, FL 32611-0370
Glycine undergoes decarboxylation in the glycine cleavage system (GCS) to yield CO2, NH3, and a 1-carbon unit. CO2 also can be generated from the 2-carbon of glycine by 10-formyltetrahydrofolate-dehydrogenase and, after glycine-to-serine conversion by serine hydroxymethyltransferase, from the tricarboxylic acid cycle. To evaluate the relative fates of glycine carbons in CO2 generation in healthy volunteers (3 male, 3 female, aged 21–26 y), primed, constant infusions were conducted using 9.26 µmol·h–1·kg–1 of [1,2-13C]glycine and 1.87 µmol·h–1·kg–1 of [5,5,5-2H3]leucine, followed by an infusion protocol using [1-13C]glycine as the glycine tracer. The time period between the infusion protocols was >6 mo. In vivo rates of whole-body glycine and leucine flux were nearly identical in protocols with [1,2-13C]glycine and [5,5,5-2H3]leucine and with [1-13C]glycine and [5,5,5-2H3]leucine tracers, which showed high reproducibility between the tracer protocols. Using the [1-13C]glycine tracer, breath CO2 data showed a total rate of glycine decarboxylation of 96 ± 8 µmol·h–1·kg–1, which was 22 ± 3% of whole-body glycine flux. In contrast, infusion of [1,2-13C]glycine yielded a glycine-to-CO2 flux of 146 ± 37 µmol·h–1·kg–1 (P = 0.026). By difference, this implies a rate of CO2 formation from the glycine 2-carbon of 51 ± 40 µmol·h–1·kg–1, which accounts for
35% of the total CO2 generated in glycine catabolism. These findings also indicate that
65% of the CO2 generation from glycine occurs by decarboxylation, primarily from the GCS. Further, these results suggest that the GCS is responsible for the entry of 5,10-methylenetetrahydrofolate into 1-carbon metabolism at a very high rate (
96 µmol·h–1·kg–1), which is
20 times the demand for methyl groups for homocysteine remethylation.
* To whom correspondence should be addressed. E-mail: jfgy{at}ufl.edu.
Manuscript received 12 December 2008. Initial review completed 14 January 2009. Revision accepted 31 January 2009.