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...
Publié dans: | Journal of experimental botany. - 1985. - 63(2012), 15 vom: 10. Sept., Seite 5607-12 |
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Auteur principal: | |
Autres auteurs: | , , , , |
Format: | Article en ligne |
Langue: | English |
Publié: |
2012
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Accès à la collection: | Journal of experimental botany |
Sujets: | Journal Article Research Support, Non-U.S. Gov't Xanthophylls zeta Carotene beta Carotene 01YAE03M7J fucoxanthin 06O0TC0VSM diadinoxanthin 18457-54-0 plus... |
Résumé: | 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 |
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Description: | Date Completed 31.12.2013 Date Revised 09.01.2024 published: Print-Electronic Citation Status MEDLINE |
ISSN: | 1460-2431 |
DOI: | 10.1093/jxb/ers211 |