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Plant Physiology 51:793-797 (1973)
© 1973 American Society of Plant Biologists

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Articles

Metabolic Regulation in the Senescing Tobacco Leaf

I. Changes in Pattern of 32P Incorporation into Leaf Disc Metabolites 1

P. K. Macnicol2, R. E. Young3 and J. B. Biale

a Department of Botanical Sciences, University of California, Los Angeles, California 90024

Changes in phosphate metabolism were explored in discs from tobacco (Nicotiana tabacum) leaves of three contrasting types: green leaves which were fully expanded and attached to the plant, leaves which had yellowed following excision and dark starvation, and leaves which had yellowed while attached to the plant. 2,4-Dinitrophenol at 10–5M stimulated the respiration rate of discs from green and yellow-detached leaves only slightly, but markedly stimulated that of discs from yellow-attached leaves. Following a 10-minute uptake period the incorporation of 32P-orthophosphate into phosphate esters and lipids of discs from yellow-detached leaves was resistant to 2,4-dinitrophenol, whereas in discs from green and yellow-attached leaves it was inhibited by 2,4-dinitrophenol. Incorporation into a salt-soluble fraction containing unidentified nucleotide material showed converse behavior in that it was stimulated by 2,4-dinitrophenol in discs from green and yellow-attached leaves; in discs from yellow-detached leaves it was resistant to 2,4-dinitrophenol. In discs from yellow-detached and yellow-attached leaves there was a shift in the labeling pattern of phosphate esters toward increased label in hexose phosphates at the expense of adenine nucleotides, 3-phosphoglycerate, and phosphoenolpyruvate. It is concluded that incorporation into phosphate esters in discs from yellow-detached leaves is by substrate level phosphorylation coupled to enhanced aerobic glycolysis. In discs from yellow-attached leaves, on the other hand, incorporation depends on oxidation phosphorylation, and it is suggested that the shift in labeling pattern is caused by senescence-induced changes in activity of glycolytic enzymes.


2 Present address: Division of Plant Industry, Commonwealth Scientific and Industrial Research Organization, Canberra, A.C.T. 2601, Australia.

3 Present address: Department of Plant Science, University of California, Riverside, Calif. 92502.

1 Supported in part by United States Public Health Service Research Grant GM08224.







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Copyright © 1973 by the American Society of Plant Biologists