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Plant Physiology 68:70-73 (1981)
© 1981 American Society of Plant Biologists

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Articles

Subcellular Location of NADP+-Isocitrate Dehydrogenase in Pisum sativum Leaves 1

Douglas D. Randall

Curtis V. Givan

Department of Biochemistry, University of Missouri, Columbia, Missouri 65211, Department of Plant Biology, University of Newcastle-upon-Tyne, Newcastle-upon-Tyne, United Kingdom NE1 7RU

The subcellular location of NADP+-isocitrate dehydrogenase was investigated by preparing protoplasts from leaves of pea seedlings. Washed protoplasts were gently lysed and the whole lysate separated on sucrose gradients by a rate-zonal centrifugation. Organelles were located by marker enzymes and chlorophyll analysis. Most of the NADP+-isocitrate dehydrogenase was in the soluble fraction. About 10% of the NADP+-isocitrate dehydrogenase was present in the chloroplasts as a partially latent enzyme. Less than 1% of the activity was found associated with the peroxisome fraction. NADP+-isocitrate dehydrogenase was partially characterized from highly purified chloroplasts isolated from shoot homogenates. The enzyme exhibited apparent Km values of 11 micromolar (NADP+), 35 micromolar (isocitrate), 78 micromolar (Mn2+), 0.3 millimolar (Mg2+) and showed optimum activity at pH 8 to 8.5 with Mn2+ and 8.8 to 9.2 with Mg2+. The NADP+-isocitrate dehydrogenase activity previously claimed in the peroxisomes by other workers is probably due to isolation procedures and/or nonspecific association. The NADP+-isocitrate dehydrogenase activity in the chloroplasts might help supply {alpha}-ketoglutarate for glutamate synthase action.


1 This research was supported by the Plant Biology Department, University of Newcastle-upon-Tyne, National Science Foundation Grant PCM-77-11390, and a Travel Grant from the University of Missouri-Columbia, Research Council. Missouri Agriculture Experiment Station Journal No. 8684.




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Copyright © 1981 by the American Society of Plant Biologists