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.