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

Hartmut K. Lichtenthaler(Karlsruhe Institute of Technology), Jörg Schwender(Karlsruhe Institute of Technology), Andrea Disch(Centre National de la Recherche Scientifique), Michel Rohmer(Centre National de la Recherche Scientifique)
FEBS Letters
January 6, 1997
Cited by 707Open Access
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Abstract

Isopentenyl diphosphate (IPP) is the biological C5 precursor of isoprenoids. By labeling experiments using [1-(13)C]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.


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