Abstract
In flower extracts of defined genotypes of Antirrhinum majus, two different hydroxylases were found catalysing the hydroxylation of naringenin and eriodictyol in the 3-position and of naringenin in the 3′-position. The 3-hydroxylase is a soluble enzyme and belongs according to its cofactor requirement to the 2-oxoglutarate-dependent dioxygenases. Investigations on different genotypes revealed a clear correlation between block of the anthocyanin pathway by recessive alleles of the gene inc and a complete lack of 3-hydroxylase activity. Chemogenetic studies on different genotypes suggested that the 3′-hydroxyl group of the B-ring of flavonoids is introduced at the stage of C15 intermediates. The corresponding 3′-hydroxylase was found to be localized in the microsomal fraction and required NADPH as cofactor. In confirmation of the chemogenetic studies, a strict correlation was found between 3′-hydroxylase activity and the gene eos which is known to control the hydroxylation of flavones, flavonols and anthocyanins in the 3′-position. These results are similar to those previously obtained with Matthioia incana.
Original language | English |
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Pages (from-to) | 411-416 |
Number of pages | 6 |
Journal | Zeitschrift fur Naturforschung - Section C Journal of Biosciences |
Volume | 36 |
Issue number | 5-6 |
DOIs | |
State | Published - 1 Jun 1981 |
Externally published | Yes |
Keywords
- Anthocyanin Biosynthesis
- Antirrhinum majus
- Flavanone 3-Hydroxylase
- Flavonoid 3′-Hydroxylase
- Flavonoids
- Genetic Control