Abstract:
:The incorporation of [1-13C]-labeled glucose into the irregular monoterpene artemisia ketone, the regular monoterpenes camphor and beta-thujone, the sesquiterpene germacrene D, the diterpene trans-phytol and beta-sitosterol and isofucosterol has been studied in axenic cultures of Tanacetum vulgare L. (Asteraceae). Quantitative 13C NMR spectroscopic analysis of the resulting labeling patterns showed that the isoprene units of the monoterpenes and the diterpene are formed via the methylerythritol phosphate (MEP) pathway, whereas the isoprene building blocks of the sesquiterpene and the sterols originate from the mevalonic acid (MVA) pathway.
journal_name
Phytochemistryjournal_title
Phytochemistryauthors
Umlauf D,Zapp J,Becker H,Adam KPdoi
10.1016/j.phytochem.2004.08.019subject
Has Abstractpub_date
2004-09-01 00:00:00pages
2463-70issue
17eissn
0031-9422issn
1873-3700pii
S0031-9422(04)00396-6journal_volume
65pub_type
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