Biosynthesis of fucoxanthin and diadinoxanthin and function of initial pathway genes in Phaeodactylum tricornutum

The biosynthesis pathway to diadinoxanthin and fucoxanthin was elucidated in Phaeodactylum tricornutum by a combined approach involving metabolite analysis identification of gene function. For the initial steps leading to β-carotene, putative genes were selected from the genomic database and the fun...

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Veröffentlicht in:Journal of experimental botany. - 1985. - 63(2012), 15 vom: 10. Sept., Seite 5607-12
1. Verfasser: Dambek, Michael (VerfasserIn)
Weitere Verfasser: Eilers, Ulrike, Breitenbach, Jürgen, Steiger, Sabine, Büchel, Claudia, Sandmann, Gerhard
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2012
Zugriff auf das übergeordnete Werk:Journal of experimental botany
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Xanthophylls zeta Carotene beta Carotene 01YAE03M7J fucoxanthin 06O0TC0VSM diadinoxanthin 18457-54-0 mehr... Carotenoids 36-88-4 violaxanthin 51C926029A (all-E) phytoene 87E4NJ6N51 Oxidoreductases EC 1.- phytoene dehydrogenase EC 1.14.99.- zeta-carotene desaturase EC 1.3.3.- Geranylgeranyl-Diphosphate Geranylgeranyltransferase EC 2.5.1.32 Intramolecular Lyases EC 5.5.- lycopene cyclase-isomerase neoxanthin KK8M5T48AI
Beschreibung
Zusammenfassung:The biosynthesis pathway to diadinoxanthin and fucoxanthin was elucidated in Phaeodactylum tricornutum by a combined approach involving metabolite analysis identification of gene function. For the initial steps leading to β-carotene, putative genes were selected from the genomic database and the function of several of them identified by genetic pathway complementation in Escherichia coli. They included genes encoding a phytoene synthase, a phytoene desaturase, a ζ-carotene desaturase, and a lycopene β-cyclase. Intermediates of the pathway beyond β-carotene, present in trace amounts, were separated by TLC and identified as violaxanthin and neoxanthin in the enriched fraction. Neoxanthin is a branching point for the synthesis of both diadinoxanthin and fucoxanthin and the mechanisms for their formation were proposed. A single isomerization of one of the allenic double bounds in neoxanthin yields diadinoxanhin. Two reactions, hydroxylation at C8 in combination with a keto-enol tautomerization and acetylation of the 3'-HO group results in the formation of fucoxanthin
Beschreibung:Date Completed 31.12.2013
Date Revised 21.10.2021
published: Print-Electronic
Citation Status MEDLINE
ISSN:1460-2431
DOI:10.1093/jxb/ers211