Biosynthesis of isoprenoids in higher plant chloroplasts proceeds via a mevalonate-independent pathway

被引:563
|
作者
Lichtenthaler, HK [1 ]
Schwender, J [1 ]
Disch, A [1 ]
Rohmer, M [1 ]
机构
[1] UNIV STRASBOURG 1,CNRS,INST LE BEL,F-67070 STRASBOURG,FRANCE
关键词
carotenoid; C-13-NMR-spectroscopy; glyceraldehyde phosphate; pyruvate; isopentenyl diphosphate; phytol; plastoquinone-9; sterol;
D O I
10.1016/S0014-5793(96)01404-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Isopentenyl diphosphate (IPP) is the biological C-5 precursor of isoprenoids. By labeling experiments using [1-C-13]glucose, higher plants were shown to possess two distinct biosynthetic routes for IPP biosynthesis: while the cytoplasmic sterols were formed via the acetate/mevalonate pathway, the chloroplast-bound isoprenoids (beta-carotene, lutein, prenyl chains of chlorophylls and plastoquinone-9) were synthesized via a novel IPP biosynthesis pathway (glyceraldehyde phosphate/pyruvate pathway) which was first found in eubacteria and a green alga. The dichotomy in isoprenoid biosynthesis in higher plants allows a reasonable interpretation of previous odd and inconclusive results concerning the biosynthesis of chloroplast isoprenoids, which so far had mainly been interpreted in the frame of models using compartmentation of the mevalonate pathway.
引用
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页码:271 / 274
页数:4
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