Isoprenoid biosynthesis. Metabolite profiling of peppermint oil gland secretory cells and application to herbicide target analysis

Citation
Bm. Lange et al., Isoprenoid biosynthesis. Metabolite profiling of peppermint oil gland secretory cells and application to herbicide target analysis, PLANT PHYSL, 127(1), 2001, pp. 305-314
Citations number
53
Categorie Soggetti
Plant Sciences","Animal & Plant Sciences
Journal title
PLANT PHYSIOLOGY
ISSN journal
00320889 → ACNP
Volume
127
Issue
1
Year of publication
2001
Pages
305 - 314
Database
ISI
SICI code
0032-0889(200109)127:1<305:IBMPOP>2.0.ZU;2-7
Abstract
Two independent pathways operate in plants for the synthesis of isopentenyl diphosphate and dimethylallyl diphosphate, the central intermediates in th e 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 effe cts of the herbicides fosmido-mycin, phosphonothrixin, methyl viologen, ben zyl viologen, clomazone, 2-(dimethylamino)ethyl diphosphate, alendronate, a nd pamidronate on the pools of metabolites related to monoterpene biosynthe sis via the mevalonate-independent pathway. A newly developed isolation pro tocol for polar metabolites together with an improved separation and detect ion method based on liquid chromatography-mass spectrometry have allowed as sessment of the enzyme targets for a number of these herbicides.