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Plant Physiology 71:756-762 (1983)
© 1983 American Society of Plant Biologists

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Manipulation by Tridemorph, a Systemic Fungicide, of the Sterol Composition of Maize Leaves and Roots 1

Michèle Bladocha and Pierre Benveniste

Laboratoire de Biochimie Vegetale, Institut de Botanique, 67083—Strasbourg Cedex, France

The roots of maize (Zea mays L. var LG11) seedlings were watered with a solution of Tridemorph (2,6-dimethyl-N-tridecyl-morpholine), a systemic fungicide, for 3 to 4 weeks from the onset of germination. Very few {bigtriangleup}5-sterols, the major sterols of the control, were detected in the treated plants, and 9{beta},19-cyclopropyl sterols accumulated dramatically in both roots and leaves. {bigtriangleup}8-sterols were also found when low concentrations of the drug were used. The time course of the accumulation of the new sterols has been studied in plants treated with various concentrations (1-20 milligrams per liter) of Tridemorph. We found that: (a) cycloeucalenol-obtusifoliol isomerase, an enzyme opening the cyclopropane ring of cyclopropyl sterols, was strongly inhibited by the drug; and (b) the drug diffused readily from the roots to the whole plant and reached its enzymic targets in most of the leaf cells. The data obtained offer an opportunity to evaluate the physiological and biochemical consequence of the almost complete replacement of {bigtriangleup}5-sterols by cyclopropyl sterols in higher plant cells.


1 Supported by the Centre National de la Recherche Scientifique, Equipe de Recherche Associée 487, and Grant ATP No. 3998.




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M. A. Lovato, E. A. Hart, M. J. R. Segura, J.-L. Giner, and S. P. T. Matsuda
Functional Cloning of an Arabidopsis thaliana cDNA Encoding Cycloeucalenol Cycloisomerase
J. Biol. Chem., April 28, 2000; 275(18): 13394 - 13397.
[Abstract] [Full Text] [PDF]




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Copyright © 1983 by the American Society of Plant Biologists