Aj. Barlow et al., Biosynthesis of the hemi- and monoterpene moieties of isoprenyl phenyl ethers from the liverwort Trichocolea tomentella, PHYTOCHEM, 57(1), 2001, pp. 7-14
The incorporation of C-13 labelled glucose into trichocolein, deoxytomentel
lin, trans-phytol and stigmasterol has been studied in axenic cultures of t
he liverwort Trichocolea tomentella. Quantitative C-13 NMR spectroscopic an
alysis of the resulting labelling patterns showed that the isoprene units o
f the hemi- and monoterpenoid moieties and the diterpene phytol are derived
from the methylerythritol phosphate pathway, whereas the isoprene units of
stigmasterol are built up via the mevalonic acid pathway. These results in
dicate the involvement of both IPP biosynthetic pathways in different cellu
lar compartments. A new, hydroperoxy geranyl phenyl ether derivative is als
o described. (C) 2001 Elsevier Science Ltd. All rights reserved.