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Energy-dependent changes in the ATP/ADP ratio at the tight nucleotide binding site of chloroplast ATP synthase
Authors:Alexander N Malyan  Heinrich Strotmann
Institution:(1) Institute of Soil Science and Photosynthesis, Russian Academy of Science, 142292 Pushchino, Moscow Region, Russia;(2) Institut für Biochemie der Pflanzen, H. Heine Universität Dusseldorf, D-4000 Dusseldorf, Germany
Abstract:Using DTT-modulated thylakoid membranes we studied tight nucleotide binding and ATP content in bound nucleotides and in the reaction mixture during 14C] ADP photophosphorylation. The increasing light intensity caused an increase in the rate of 14C] ADP incorporation and a decrease in the steady-state level of tightly bound nucleotides. Within the light intensity range from 11 to 710 w m–2, ATP content in bound nucleotides was larger than that in nucleotides of the reaction mixture; the most prominent difference was observed at low degrees of ADP phosphorylation. The increasing light intensity was accompanied by a significant increase of the relative ATP content in tightly bound nucleotides. The ratio between substrates and products formed at the tight nucleotide binding site during photophosphorylation was suggested to depend on the light-induced proton gradient across the thylakoid membrane.Abbreviations AdN adenine nucleotide - Chl chlorophyll - DTT dithiothreitol - FCCP carbonylcianide p-trifluoromethoxyphenilhydrazone - Pi inorganic orthophosphate - PMS phenazine methosulfate - TLC thin-layer chromatography - Tricine N-tris(hydroxymethyl)methyl] glycine
Keywords:ATP synthase  chloroplast  nucleotide binding  photophosphorylation
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