Biosynthesis of Chloroplastidic and Extrachloroplastidic Terpenoids in Liverwort Cultured Cells: 13C Serine as a Probe of Terpene Biosynthesis via Mevalonate and Non-mevalonate Pathways
Daisuke Itoh, Kyouhei Kawano, Kensuke Nabeta
Abstract
Daisuke Itoh, Kyouhei Kawano, Kensuke Nabeta
Abstract
Two terpenoid biosynthetic pathways, the mevalonate and non-mevalonate (glyceraldehyde phosphate-pyruvate) routes, were examined by feeding (13)C-labeled serines ([1-(13)C]- and [3-(13)C]-) to the cultured cells of the liverwort, Heteroscyphus planus. The labeling patterns observed in the isoprenoid unit of the biosynthetically (13)C-labeled stigmasterol corresponded to those expected from the mevalonate pathway, while those of the phytyl side chain corresponded to those from the non-mevalonate pathway. Thus, serine is a potential probe to determine the origin of terpenoid biosynthesis, in either the mevalonate or non-mevalonate pathway.
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Two terpenoid biosynthetic pathways, the mevalonate and non-mevalonate (glyceraldehyde phosphate-pyruvate) routes, were examined by feeding (13)C-labeled serines ([1-(13)C]- and [3-(13)C]-) to the cultured cells of the liverwort, Heteroscyphus planus. The labeling patterns observed in the isoprenoid unit of the biosynthetically (13)C-labeled stigmasterol corresponded to those expected from the mevalonate pathway, while those of the phytyl side chain corresponded to those from the non-mevalonate pathway. Thus, serine is a potential probe to determine the origin of terpenoid biosynthesis, in either the mevalonate or non-mevalonate pathway.
Key concepts: Mevalonate pathway, Mevalonic acid, Terpenoid, Biosynthesis, Biochemistry, Serine, Biology, Terpene