Abstract
The specific radioactivity of urinary hippurate glycine was determined after injecting guinea pigs with benzoate and either DL [2 14C]glutamate or DL[5 14C]glutamate. The isotope dilution factor for the formation of [14C]glycine was significantly greater (30%) with C 2 labelled glutamate. With either form of labelled glutamate the hippurate glycine was largely carboxyl group labelled. The observations suggest a route for the incorporation of glutamate carbon into glycine that involves C 5 but not C 2. A hypothesis for glycine biosynthesis from L glutamate is advanced, consistent with these findings, that includes conversion of L glutamate to 4 hydroxy 2 oxoglutarate, the scission of the latter to glyoxylate and pyruvate, and the formation of glycine by transamination.
Original language | English |
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Pages (from-to) | 357-363 |
Number of pages | 6 |
Journal | Biochemical Journal |
Volume | 152 |
Issue number | 2 |
Publication status | Published - 1975 |