INVOLVEMENT OF THE MEVALONIC ACID PATHWAY AND THE GLYCERALDEHYDE-PYRUVATE PATHWAY IN TERPENOID BIOSYNTHESIS OF THE LIVERWORTS RICCIOCARPOS NATANS AND CONOCEPHALUM-CONICUM
Kp. Adam et al., INVOLVEMENT OF THE MEVALONIC ACID PATHWAY AND THE GLYCERALDEHYDE-PYRUVATE PATHWAY IN TERPENOID BIOSYNTHESIS OF THE LIVERWORTS RICCIOCARPOS NATANS AND CONOCEPHALUM-CONICUM, Archives of biochemistry and biophysics, 354(1), 1998, pp. 181-187
The incorporation of C-13-labeled glucose into borneol, bornyl acetate
, the sesquiterpenes cubebanol and ricciocarpin A, phytol, and stigmas
terol has been studied in axenic cultures of the liverworts Ricciocarp
os natans and Conocephalum conicum. Quantitative C-13 NMR spectroscopi
c analysis of the resulting labeling patterns showed that the isoprene
building blocks of the sesquiterpenes and stigmasterol are built up v
ia the mevalonic acid pathway, whereas the isoprene units of the monot
erpenes and the diterpene phytol are exclusively derived from the glyc
eraldehyde-pyruvate pathway, These results indicate the involvement of
both isopentenyl diphosphate biosynthetic pathways in different cellu
lar compartments. (C) 1998 Academic Press.