Flavonoid biosynthesis

Flavonoids are synthesized by the phenylpropanoid metabolic pathway in which the amino acid phenylalanine is used to produce 4-coumaroyl-CoA.^[1] This can be combined with malonyl-CoA to yield the true backbone of flavonoids, a group of compounds called chalcones, which contain two phenyl rings. Conjugate ring-closure of chalcones results in the familiar form of flavonoids, the three-ringed structure of a flavone. The metabolic pathway continues through a series of enzymatic modifications to yield flavanones → dihydroflavonols → anthocyanins. Along this pathway, many products can be formed, including the flavonols, flavan-3-ols, proanthocyanidins (tannins) and a host of other various polyphenolics.

Flavanoids can possess chiral carbons. Methods of analysis should take this element into account^[2] especially regarding bioactivity or enzyme stereospecificity.^[3]

The biosynthesis of flavonoids involves several enzymes.

• Dihydrokaempferol 4-reductase
• Flavanone 4-reductase
• Anthocyanidin reductase
• Flavanone 3-dioxygenase
• Flavone synthase
• Flavonoid 3'-monooxygenase
• Flavonol synthase
• Leucocyanidin oxygenase
• Leucoanthocyanidin reductase
• Chalcone isomerase
• Naringenin-chalcone synthase

Methylation

• Apigenin 4'-O-methyltransferase
• Luteolin O-methyltransferase
• Quercetin 3-O-methyltransferase

Glycosylation

• Anthocyanidin 3-O-glucosyltransferase
• Flavone 7-O-beta-glucosyltransferase
• Flavone apiosyltransferase
• Flavonol-3-O-glucoside L-rhamnosyltransferase
• Flavonol 3-O-glucosyltransferase

Further acetylations

• Isoflavone-7-O-beta-glucoside 6"-O-malonyltransferase

References