Biosynthesis of α- and β-ionone, prominent scent compounds, in flowers of Osmanthus fragrans.
Author(s) -
Susanne Baldermann,
Masaya Kato,
Peter Fleischmann,
Naoharu Watanabe
Publication year - 2012
Publication title -
acta biochimica polonica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.452
H-Index - 78
eISSN - 1734-154X
pISSN - 0001-527X
DOI - 10.18388/abp.2012_2176
Subject(s) - ionone , osmanthus fragrans , carotenoid , chemistry , lilac , terpene , botany , lycopene , flor , biology , stereochemistry , food science , biochemistry
Carotenoid derived volatiles are important fragrance compounds, which contribute to the scents of flowers from diverse taxa. A famous example is represented by the flowers of Osmanthus fragrans where apocarotenoids account for more than 20% of all volatiles. In the recent years, bio-degradation of carotenoids has been shown to be an important route for apocarotenoids formation. Here, we report on the contribution the O. fragrans carotenoid cleavage dioxygenase 1 to the synthesis of the two predominant C(13)-apocarotenoids, α- and β-ionone, derived from α-and β-carotene, respectively.
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