EC Number |
Natural Substrates |
---|
1.14.14.81 | 2,3-(trans)-(+)-catechin + [reduced NADPH-hemoprotein reductase] + O2 |
- |
1.14.14.81 | apigenin + [reduced NADPH-hemoprotein reductase] + O2 |
- |
1.14.14.81 | dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 |
- |
1.14.14.81 | dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 |
overall reaction |
1.14.14.81 | dihydrokaempferol + 2 [reduced NADPH-hemoprotein reductase] + 2 O2 |
leads to synthesis of delphinidin |
1.14.14.81 | dihydrokaempferol + [reduced NADPH-hemoprotein reductase] + O2 |
- |
1.14.14.81 | dihydroquercetin + [reduced NADPH-hemoprotein reductase] + O2 |
- |
1.14.14.81 | leucocyanidin + [reduced NADPH-hemoprotein reductase] + O2 |
- |
1.14.14.81 | more |
key enzyme in the synthesis of 3',5'-hydroxylated anthocyanins, which are generally required for blue or purple flowers |
1.14.14.81 | more |
key enzyme in the synthesis of 3',5'-hydroxylated anthocyanins, which are generally required for the expression of blue or purple flower color. Pigment composition analysis of transgenic plants suggests that the F3'5'H transgene not only creates or inhibits the biosynthetic pathway to 3',5'-hydroxylated anthocyanins but switches the pathway to 3',5'-hydroxylated or 3'-hydroxylated anthocyanins |