Abstract
Several of the key flavor compounds in rose essential oil are C13-norisoprenoids, such as β-damascenone, β-damascone, and β-ionone which are derived from carotenoid degradation. To search for genes putatively responsible for the cleavage of carotenoids, cloning of carotenoid cleavage (di-)oxygenase (CCD) genes from Rosa damascena was carried out by a degenerate primer approach and yielded a full-length cDNA (RdCCD1). The RdCCD1 gene was expressed in Escherichia coli and recombinant protein was assayed for its cleavage activity with a multitude of carotenoid substrates. The RdCCD1 protein was able to cleave a variety of carotenoids at the 9-10 and 9′-10′ positions to produce a C14 dialdehyde and two C13 products, which vary depending on the carotenoid substrates. RdCCD1 could also cleave lycopene at the 5-6 and 5′-6′ positions to produce 6-methyl-5-hepten-2-one. Expression of RdCCD1 was studied by real-time PCR in different tissues of rose. The RdCCD1 transcript was present predominantly in rose flower, where high levels of volatile C13-norisoprenoids are produced. Thus, the accumulation of C13-norisoprenoids in rose flower is correlated to the expression of RdCCD1.
Original language | English |
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Pages (from-to) | 457-464 |
Number of pages | 8 |
Journal | Phytochemistry |
Volume | 70 |
Issue number | 4 |
DOIs | |
State | Published - Mar 2009 |
Keywords
- (9Z)-, (9′Z)- and (di-Z)-carotenoids
- C-norisoprenoids
- Carotenoid cleavage oxygenase
- RdCCD1
- Rosa damascena
- Rose essential oil