Competition for energy between phosphoenolpyruvate and citrulline synthesis in guinea-pig liver mitochondria

1. The interrelationship between citrulline synthesis and phosphoenolpyruvate formation has been studied in guinea-pig liver mitochondria incubated with glutamate in State 3 and in the presence of uncoupler and oligomycin.

2. In coupled mitochondria the rate of phosphoenolpyruvate production was limited by a higher capacity of aspartate aminotransferase than that of phosphopyruvate carboxylase for the intramitochondrial oxalacetate. Citrulline formation was low due to the small production of NH₃ since glutamate oxidation in State 3 proceeds via the transamination pathway.

3. Inhibition of aspartate aminotransferase by aminooxyacetate in State 3 resulted in increases in both phosphoenolpyruvate and citrulline synthesis. Under uncoupled conditions, however, an increase of phosphoenolpyruvate formation was accompanied by a decrease of both citrulline production and the ATP content of the incubation medium. Restoration of the citrulline production was observed on the addition of exogenous ATP.

4. The results indicate that when energy is generated via substrate-level phosphorylation, the inhibition of citrulline production is probably due to a higher availability of GTP to the phosphopyruvate carboxylase than to the nucleoside diphosphate kinase.