Biosynthesis of 2-C-methyl-D-erythritol in plants by rearrangement of the terpenoid precursor, 1-deoxy-D-xylulose 5-phosphate

Autor:	Wolfgang Eisenreich, Adelbert Bacher, Monika Fellermeier, Meinhart H. Zenk, Christoph Latzel, Silvia Sagner
Rok vydání:	1998
Předmět:	Terpenoid biosynthesis Liriodendron tulipifera Organic Chemistry Erythritol Biochemistry Terpenoid Terpene chemistry.chemical_compound 1-deoxy-D-xylulose 5-phosphate chemistry Biosynthesis Drug Discovery Side product
Zdroj:	Tetrahedron Letters. 39:2091-2094
ISSN:	0040-4039
DOI:	10.1016/s0040-4039(98)00296-2
Popis:	Leaves of Liriodendron tulipifera convert 1-deoxy-D-xylulose to 2-C-methyl-D-erythritol via a skeletal rearrangement reminiscent of the formation of terpene precursors from 1-deoxy-D-xylulose. The data suggest that 2-C-methyl-D-erythritol 4-phosphate is either an intermediate or a side product of the deoxyxylulose 4-phosphate pathway of terpenoid biosynthesis.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::3cc3c2d72d6bec66042ee27bf46df221 https://doi.org/10.1016/s0040-4039(98)00296-2 Zobrazit plný text záznamu Full Text from ScienceDirect