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Plant Physiology 100:1369-1376 (1992)
© 1992 American Society of Plant Biologists

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Microbe-Plant Interactions

Inhibition of Phytoalexin Biosynthesis in Elicitor-Treated Tobacco Cell-Suspension Cultures by Calcium/Calmodulin Antagonists 1

Urs Vögeli2, Regina Vögeli-Lange3 and Joseph Chappell

Plant Physiology/Biochemistry Program, Agronomy Department, University of Kentucky, Lexington, Kentucky 40546-0091

A role for calcium/calcium-binding proteins in a mechanism of signaling elicitor-inducible phytoalexin biosynthesis was investigated. Two classes of calcium/calmodulin antagonists, phenothiazines and naphthalenesulfonamides, inhibited sesquiterpene phytoalexin accumulation in tobacco (Nicotiana tabacum) cell-suspension cultures when added 1 h before elicitor. The antagonists also inhibited the induction of sesquiterpene cyclase enzyme activity, a key regulatory enzyme for sesquiterpene biosynthesis. The antagonists suppressed the induction of sesquiterpene cyclase only if added before or simultaneously with elicitor. Additionally, the antagonists inhibited (a) accumulation of the cyclase protein as measured in immunoblots; (b) the in vivo synthesis rate of the cyclase protein, measured as the incorporation of [35S]methionine into immunoprecipitable cyclase protein; and (c) the cyclase mRNA translational activity, measured as the incorporation of [35S]methionine into immunoprecipitable cyclase protein synthesized by in vitro translation of RNA isolated from antagonist-treated, elicitor-induced cells. In contrast, elicitor-inducible phenylalanine ammonia lyase enzyme activity, the level of the enzyme protein, the in vivo synthesis rate, and the mRNA translational activity were not affected by any of the antagonist treatments. Uptake and incorporation of [35S]methionine into total cellular proteins and total in vitro translation products were also not indiscriminately altered by the antagonist treatments. The current results suggest that calcium and/or calmodulin-like proteins may be elements of a signal transduction pathway mediating elicitor-induced accumulation of phytoalexins in tobacco.


2 Present address: Ciba-Geigy AG, BU Disease Control, CH-8157 Dielsdorf, Switzerland.

3 Present address: Friedrich-Miescher-Institut, Postfach 2543, CH-4002 Basel, Switzerland.

1 This work was supported by the Kentucky Agricultural Experiment Station, a Swiss National Science Foundation fellowship (to U.V.), and the National Science Foundation (DMB 8806273). This is journal paper No. 92-3-9 of the Kentucky Agricultural Experiment Station.




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