Inhibition of Photorespiration and Increase of Net Photosynthesis in Isolated Maize Bundle Sheath Cells Treated with Glutamate or Aspartate
Author(s) -
David J. Oliver
Publication year - 1978
Publication title -
plant physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.554
H-Index - 312
eISSN - 1532-2548
pISSN - 0032-0889
DOI - 10.1104/pp.62.5.690
Subject(s) - photorespiration , photosynthesis , glutamate receptor , biology , vascular bundle , biochemistry , stimulation , biophysics , carbon fixation , glutamate dehydrogenase , botany , endocrinology , receptor
Net photosynthetic (14)CO(2) fixation by isolated maize (Zea mays) bundle sheath strands was stimulated 20 to 35% by the inclusion of l-glutamate or l-aspartate in the reaction mixture. Maximal stimulation occurred at a 7.5 mm concentration of either amino acid. Since the photosynthetic rate and the glutamate-dependent stimulation in the rate were equally sensitive to a photosynthetic electron transport inhibitor, 3-(p-chlorophenyl)-1,1-dimethylurea, it was concluded that glutamate did not stimulate CO(2) fixation by supplying needed NADPH (NADH) through glutamate dehydrogenase. Treatment of the bundle sheath strands with glutamate inhibited glycolate synthesis by 59%. Photorespiration in this tissue, measured as the O(2) inhibition of CO(2) fixation (the Warburg effect), was inhibited by treatment with glutamate. The stimulation in net photosynthetic CO(2) fixation probably results from the decrease in photorespiratory CO(2) loss. This metabolic regulation of the rate of glycolate synthesis and photorespiration observed with isolated bundle sheath strands could account for the inability to detect rapid photorespiration in the mature intact maize leaf.
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