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  Dynamic pathway allocation in early terpenoid biosynthesis of stress-induced lima bean leaves

Bartram, S., Jux, A., Gleixner, G., & Boland, W. (2006). Dynamic pathway allocation in early terpenoid biosynthesis of stress-induced lima bean leaves. Phytochemistry, 67(15), 1661-1672.

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Bartram, S., Author
Jux, A., Author
Gleixner, G.1, Author           
Boland, W., Author
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1Molecular Biogeochemistry Group, Dr. G. Gleixner, Department Biogeochemical Processes, Prof. E.-D. Schulze, Max Planck Institute for Biogeochemistry, Max Planck Society, ou_1497773              

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Free keywords: Phaseolus lunatus Leguminosae Lima bean Isoprenoid biosynthesis Cross talk 1-deoxy-d-xylulose Mevalonate Terpenoids Volatiles Isotopically labeled Inhibitors Irms Isotopic discrimination Mevalonate-independent pathway Isoprenoid biosynthesis Arabidopsis-thaliana Nonmevalonate pathway Plastidial pathways Higher-plants Cross-talk Units 1-deoxy-d-xylulose Homoterpenes
 Abstract: Two independent pathways contribute in higher plants to the formation of isopentenyl diphosphate (IDP), the central building block of isoprenoids. In general, the cytosolic mevalonate pathway (MVA) provides the precursors for sesquiterpenes and sterols, whereas the plastidial methylerythritol pathway (MEP) furnishes the monoterpene-, diterpene- and carotenoids. Administration of deuterium labeled 1-deoxy-D-xylulose and mevalolactone to lima beans (Phaseolus lunatus), followed by gas chromatographic separation and mass spectro-metric analysis of de novo produced volatiles revealed that the strict separation of both pathways does not exist. This could be confirmed by blocking the pathways individually with cerivastatin (R) (MVA) and fosmidomycin (MEP), respectively. Isotopic ratio mass spectrometry (IRMS) at natural abundance levels demonstrated independently and without the need for labeled precursors a dynamic allocation of the MVA- or the MEP-pathway in the biosynthesis of the nerolidol-derived homoterpene 4,8-dimethyl-nona-1,3,7-triene (DMNT). Insect-feeding upregulated predominantly the MVA-pathway, while the fungal elicitor alamethicin stimulated the biosynthesis of DMNT via the MEP-pathway. (c) 2006 Elsevier Ltd. All rights reserved. [References: 40]

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 Dates: 2006
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 Identifiers: Other: BGC0928
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Title: Phytochemistry
Source Genre: Journal
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Publ. Info: Oxford : Pergamon
Pages: - Volume / Issue: 67 (15) Sequence Number: - Start / End Page: 1661 - 1672 Identifier: CoNE: https://pure.mpg.de/cone/journals/resource/954925433416
ISSN: 0031-9422