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Plant Physiol, September 2001, Vol. 127, pp. 305-314

Isoprenoid Biosynthesis. Metabolite Profiling of Peppermint Oil Gland Secretory Cells and Application to Herbicide Target Analysis1

B. Markus Lange,2 Raymond E.B. Ketchum, and Rodney B. Croteau*

Institute of Biological Chemistry, Washington State University, Pullman, Washington 99164-6340

Two independent pathways operate in plants for the synthesis of isopentenyl diphosphate and dimethylallyl diphosphate, the central intermediates in the biosynthesis of all isoprenoids. The mevalonate pathway is present in the cytosol, whereas the recently discovered mevalonate-independent pathway is localized to plastids. We have used isolated peppermint (Mentha piperita) oil gland secretory cells as an experimental model system to study the effects of the herbicides fosmidomycin, phosphonothrixin, methyl viologen, benzyl viologen, clomazone, 2-(dimethylamino)ethyl diphosphate, alendronate, and pamidronate on the pools of metabolites related to monoterpene biosynthesis via the mevalonate-independent pathway. A newly developed isolation protocol for polar metabolites together with an improved separation and detection method based on liquid chromatography-mass spectrometry have allowed assessment of the enzyme targets for a number of these herbicides.


1 This work was supported by a grant from the U.S. Department of Energy.

2 Present address: Torrey Mesa Research Institute, Syngenta, Research and Technology, 3115 Merryfield Row, San Diego, CA 92121-1125.

* Corresponding author; e-mail croteau{at}mail.wsu.edu; fax 509-335-7643.

© 2001 American Society of Plant Physiologists



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