The 1-deoxy-D-xylulose-5-phosphate pathway of isoprenoid biosynthesis in plants

Citation
Hk. Lichtenthaler, The 1-deoxy-D-xylulose-5-phosphate pathway of isoprenoid biosynthesis in plants, ANN R PLANT, 50, 1999, pp. 47-65
Citations number
84
Categorie Soggetti
Plant Sciences","Animal & Plant Sciences
Journal title
ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY
ISSN journal
10402519 → ACNP
Volume
50
Year of publication
1999
Pages
47 - 65
Database
ISI
SICI code
1040-2519(1999)50:<47:T1POIB>2.0.ZU;2-G
Abstract
In plants the biosynthesis of prenyllipids and isoprenoids proceeds via two independent pathways: (a) the cytosolic classical acetate/mevalonate pathw ay for the biosynthesis of sterols, sesquiterpenes, triterpenoids; and (b) the alternative, non-mevalonate l-deoxy-D-xylulose 5-phosphate (DOXP) pathw ay for the biosynthesis of plastidic isoprenoids, such as carotenoids, phyt ol (a side-chain of chlorophylls), plastoquinone-9, isoprene, mono-, and di terpenes. Both pathways form the active C-5-unit isopentenyl diphosphate (I PP) as the precursor from which. all other isoprenoids are formed via head- to-tail addition. This review summarizes current knowledge of the novel 1-d eoxy-D-xylulose-5-phosphate (DOXP) pathway for isopentenyl diphosphate bios ynthesis, apparently located in plastids. The DOXP pathway of IPP formation starts from D-glyceraldehyde-3-phosphate (GA-3-P) and pyruvate, with DOXP- synthase as the starting enzyme. This pathway provides new insight into the regulation of chloroplast metabolism.