Effect of Oxygen and Carbon Dioxide on Photorespiratory Flux Determined from Glycine Accumulation in a Mutant of<i>Arabidopsis thaliana</i> — Shauna Somerville (1983) | RDL Network
Exposure to atmospheric conditions which promote photorespiration strongly inhibits photosynthesis in a mutant of <it>Arabidopsis</it> lacking mitochondrial serine transhydroxymethylase activity, and glycine accumulates as a stable end-product of photorespiratory carbon and nitrogen flow. By providing exogenous serine and ammonia to leaves of the mutant, wild-type photosynthesis rates can be temporarily maintained in the absence of photorespiratory CO<inf>2</inf> evolution. In these circumstances, the rate of glycine accumulation provides a direct measure of photorespiratory flux which is not complicated by the efflux and refixation of photorespired CO<inf>2</inf>, the dilution of radioactive label by endogenous metabolic pools, or non-specific effects of metabolic inhibitors. At the standard atmospheric concentration of CO<inf>2</inf>, the rate of glycine accumulation in the mutant was proportional to the oxygen concentration, amounting to 53&percnt; of the rate of gross CO<inf>2</inf>-fixation at 21&percnt; O<inf>2</inf>. At normal levels of O<inf>2</inf>, glycine accumulation was maximal at about 475 μl CO<inf>2</inf>1−1 and was reduced at higher or lower CO<inf>2</inf> concentrations, being almost abolished at 3000μ1 CO<inf>2</inf>1−1. These observations are discussed in the context of a model of photorespiration based on the properties of ribulose 1, 5-bisphosphate carboxylase&sol;oxygenase, and in relation to the results of previous attempts to measure photorespiration. Preliminary evidence from 14CO<inf>2</inf>-labelling experiments which suggests a non-photorespiratory pathway of serine synthesis is also presented.
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