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Plant Physiology 61:477-480 (1978) © 1978 American Society of Plant Biologists Malate Synthesis by Dark Carbon Dioxide Fixation in Leaves 1Institute for Photobiology of Cells and Organelles, Brandeis University, Waltham, Massachusetts 02154
The rates of dark CO2 fixation and the label distribution in malate following dark 14CO2 fixation in a C-4 plant (maize), a C-3 plant (sunflower), and two Crassulacean acid metabolism plants (Bryophyllum calycinum and Kalanchoë diagremontianum leaves and plantlets) are compared. Within the first 30 minutes of dark 14CO2 fixation, leaves of maize, B. calycinum, and sunflower, and K. diagremontianum plantlets fix CO2 at rates of 1.4, 3.4, 0.23, and 1.0 µmoles of CO2/mg of chlorophyll· hour, respectively. Net CO2 fixation stops within 3 hours in maize and sunflower, but Crassulaceans continue fixing CO2 for the duration of the 23-hour experiment.
A bacterial procedure using Lactobacillus plantarum ATCC No. 8014 and one using malic enzyme to remove the The contribution of carbon atom 1 of malate is between 18 and 21% of the total carboxyl label after 1 minute of dark CO2 fixation. Isotopic labeling in the two carboxyls approached unity with time. The rate of increase is greatest in sunflower leaves and Kalanchoë plantlets. In addition, Kalanchoë leaves fix 14CO2 more rapidly than Kalanchoë plantlets and the equilibration of the malate carboxyls occurs more slowly. The rates of fixation and the randomization are tissue-specific. The rate of fixation does not correlate with the rate of randomization of isotope in the malate carboxyls.
2 Predoctoral trainee, National Institutes of Health, Grant GM-1586-07. 3 Present address: Plant Growth Laboratory, College of Agricultural and Environmental Sciences, University of California, Davis, California 95616. 1 This research was supported by National Science Foundation Grant GB29126X2 and by United States Energy Research and Development Administration Grant ET 11-1 3231.
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