Threonine dehydrogenase is a minor degradative pathway of threonine catabolism in adult humans

The threonine dehydrogenase (TDG) pathway is a significant route of threoni ne degradation, yielding glycine in experimental animals, but has not been accurately quantitated in humans. Therefore, the effect of a large excess o f dietary threonine, given either as free amino acid (+Thr) or as a constit uent of protein (+P-Thr), on threonine catabolism to CO2 and to glycine was studied in six healthy adult males using a 4-h constant infusion of L-[1-C -13]threonine and [N-15]glycine. Gas chromatography-combustion isotope rati o mass spectrometry was used to determine [C-13]glycine produced from label ed threonine. Threonine intakes were higher on +Thr and +P-Thr diets compar ed with control (126, 126, and 50 mu mol.kg(-1).h(-1), SD 8, P < 0.0001). T hreonine oxidation to CO2 increased threefold in subjects on +Thr and +P-Th r vs. control (49, 45, and 15 mu mol.kg(-1).h(-1), SD 6, P < 0.0001). Threo nine conversion to glycine tended to be higher on +Thr and +P-Thr vs. contr ol (3.5, 3.4, and 1.6 mu mol.kg(-1).h(-1), Sn 1.3, P = 0.06). The TDG pathw ay accounted for only 7-11% of total threonine catabolism and therefore is a minor pathway in the human adult.