
doi: 10.1271/bbb.70692
pmid: 18391443
Arabidopsis thaliana lacks the flavone biosynthetic pathway, probably because of a lack or low activity of a flavone synthase. To establish this biosynthetic pathway in Arabidopsis, we subjected this model plant to transformation with the parsley gene for flavone synthase type I (FNS-I). Transgenic seedlings expressing FNS-I were cultured in liquid medium with or without naringenin, and plant extracts were then analyzed by high-performance liquid chromatography. In contrast to wild-type seedlings, the transgenic seedlings accumulated substantial amounts of apigenin, which is produced from naringenin by FNS-I, and the apigenin level correlated with the abundance of FNS-I mRNA in three different transgenic lines. These results indicate that the FNS-I transgene produces a functional enzyme that catalyzes the conversion of naringenin to apigenin in Arabidopsis. These FNS-I transgenic lines should prove useful in investigating the in vivo functions of enzymes that mediate the synthesis of the wide variety of flavones found in other plants.
apigenin, Flavonoids, naringenin, flavone synthase type I, Arabidopsis, <I>Arabidopsis thaliana</I>, Flavones, Plants, Genetically Modified, Mixed Function Oxygenases, Gene Expression Regulation, Plant, Flavanones, Petroselinum, Apigenin, Cloning, Molecular
apigenin, Flavonoids, naringenin, flavone synthase type I, Arabidopsis, <I>Arabidopsis thaliana</I>, Flavones, Plants, Genetically Modified, Mixed Function Oxygenases, Gene Expression Regulation, Plant, Flavanones, Petroselinum, Apigenin, Cloning, Molecular
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