Zeitschrift für Naturforschung C · 1981 · 64 citations · 0 references
Life SciencesGeneticsPlant SciencesEnzymologyPlant BiochemistryPlant GeneticsChemical Defense In PlantsFlavonoid BiosynthesisPhenylpropanoid BiosynthesisPhenylpropanoid MetabolismPlant EnzymesPlant Natural Product BiosynthesisAnthocyanin Biosynthesis InhibitionAnthocyanin OxidationCofactor DependenceFlavanone 3-HydroxylaseFlavonoid MetabolismFlavonoid Pathway RegulationKnockout AllelesRecessive Lethal Alleles
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 C 15 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.