Abstract
Considerable evidence exists that the carboxyl-carbon atom of glycolic acid is the primary source of the CO(2) produced during photorespiration by leaves of many species of plants, including tobacco. Experiments were conducted to determine whether glyoxylate or glycine, both products of glycolic acid metabolism, is the more immediate precursor of photorespiratory CO(2).Illuminated tobacco leaf disks were floated on 18 mm solutions of glycolate-1-(14)C or glycine-1-(14)C in CO(2)-free air. The (14)CO(2) released and the (14)C content of several postulated intermediates were determined when the substrate solutions were provided alone or with one of the following: 9 mm alpha-hydroxy-2-pyridine-methanesulfonic acid, an inhibitor of the oxidation of glycolate to glyoxylate; 9 mm isonicotinyl hydrazide, an inhibitor of the conversion of glycine to serine; or 18 mm nonradioactive glycine or glycolate with the other radioactive substrate.Both inhibitors decreased the rate of photorespiration in tobacco leaf disks by the (14)C-assay. The alpha-hydroxy-2-pyridine-methanesulfonic acid severely blocked (14)CO(2) production and labeling of the glycolate pathway from glycolate-1-(14)C. Isonicotinyl hydrazide had little effect on the (14)CO(2) released from glycine-1-(14)C although the glycine to serine conversion was severely inhibited.These results and other data in the literature indicate that the glycolate pathway of carbohydrate metabolism does not supply sufficient CO(2) during the synthesis of serine from glycine to account for the rates of photorespiration observed in many species. A direct decarboxylation of glyoxylate is more likely the main source of photorespiratory CO(2).