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EC 1.14.13.88 Details
EC number
1.14.13.88
Accepted name
flavanoid 3′,5′-hydroxylase
Reaction
a flavanone + 2 NADPH + 2 H+ + 2 O2 = a 3′,5′-dihydroxyflavanone + 2 NADP+ + 2 H2O (overall reaction);;(1a) a flavanone + NADPH + H+ + O2 = a 3′-hydroxyflavanone + NADP+ + H2O;;(1b) a 3′-hydroxyflavanone + NADPH + H+ + O2 = a 3′,5′-dihydroxyflavanone + NADP+ + H2O
Other name(s)
flavonoid 3′,5′-hydroxylase
Systematic name
flavanone,NADPH:oxygen oxidoreductase
CAS registry number
94047-23-1
Comment
A heme-thiolate protein (P-450). The 3′,5′-dihydroxyflavanone is formed via the 3′-hydroxyflavanone. In Petunia hybrida the enzyme acts on naringenin, eriodictyol, dihydroquercetin (taxifolin) and dihydrokaempferol (aromadendrin). The enzyme catalyses the hydroxylation of 5,7,4′-trihydroxyflavanone (naringenin) at either the 3′ position to form eriodictyol or at both the 3′ and 5′ positions to form 5,7,3′,4′,5′-pentahydroxyflavanone (dihydrotricetin). The enzyme also catalyses the hydroxylation of 3,5,7,3′,4′-pentahydroxyflavanone (taxifolin) at the 5′ position, forming ampelopsin. NADH is not a good substitute for NADPH.
History
created 2004, deleted 2018
EC Tree
1.6.4.1 created 1961, deleted 2002
1.6.4.2 created 1961, modified 1989, deleted 2002
1.6.4.3 created 1961, modified 1976, deleted 1983
1.6.4.4 created 1965, deleted 2002
1.6.4.5 created 1972, deleted 2002
1.6.4.6 created 1972, deleted 2002
1.6.4.7 created 1978, deleted 2002
1.6.4.8 created 1989, deleted 2002
1.6.4.9 created 1992, deleted 2002
1.6.4.10 created 1992, deleted 2002
1.14.13.45 created 1992, deleted 2003