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Literature summary extracted from

  • Tu, Y.; Liu, F.; Guo, D.; Fan, L.; Zhu, Z.; Xue, Y.; Gao, Y.; Guo, M.
    Molecular characterization of flavanone 3-hydroxylase gene and flavonoid accumulation in two chemotyped safflower lines in response to methyl jasmonate stimulation (2016), BMC Plant Biol., 16, 132 .
    View publication on PubMedView publication on EuropePMC

Cloned(Commentary)

EC Number Cloned (Comment) Organism
1.14.11.9 gene CtF3H, DNA and amino acid sequence determination and analysis, phylogenic analysis, quantitative real-time PCR enzyme expression analysis, functional recombinant expression of MBP-tagged enzyme in Escherichia coli BL21(DE3)pLysS from vector pMAL-C5x leading to production of dihydrokaempferol when naringenin is available the substrate. Recombinant expression of GFP-tagged enzyme in onion cells via transfromation of Agrobacterium tumefaciens strain GV3101, where it is localized both in the nucleus and in the cytosol Carthamus tinctorius

Localization

EC Number Localization Comment Organism GeneOntology No. Textmining
1.14.11.9 cytosol
-
Carthamus tinctorius 5829
-
1.14.11.9 additional information subcellular localization study Carthamus tinctorius
-
-
1.14.11.9 nucleus
-
Carthamus tinctorius 5634
-

Metals/Ions

EC Number Metals/Ions Comment Organism Structure
1.14.11.9 Fe2+ dependent on, required for catalysis, the ferrous iron binding site HxDxnH is formed by His78, His121, His211, Asp213, His221, Asp 223, His265, His267, and His279 Carthamus tinctorius

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
1.14.11.9 a (2S)-flavan-4-one + 2-oxoglutarate + O2 Carthamus tinctorius
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a (2R,3R)-dihydroflavonol + succinate + CO2
-
?

Organism

EC Number Organism UniProt Comment Textmining
1.14.11.9 Carthamus tinctorius M9MTF3 a quinochalcone-type safflower line with orange-yellow flowers and a flavonol-type safflower line with white flowers, i.e. ZHH0119 line and XHH007 line, respectively
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Purification (Commentary)

EC Number Purification (Comment) Organism
1.14.11.9 recombinant MBP-tagged enzyme from Escherichia coli BL21(DE3)pLysS by amylose affinity chromatography Carthamus tinctorius

Source Tissue

EC Number Source Tissue Comment Organism Textmining
1.14.11.9 flower the transcriptome expression of CtF3H shows a diametrically opposed expression pattern in a quinochalcone-type safflower line (with orange-yellow flowers) and a flavonol-type safflower line (with white flowers) under external stimulation by methyl jasmonate (MeJA), which has been identified as an elicitor of flavonoid metabolites. High expression of CtF3H in quinochalcone-type safflower line Carthamus tinctorius
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Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1.14.11.9 a (2S)-flavan-4-one + 2-oxoglutarate + O2
-
Carthamus tinctorius a (2R,3R)-dihydroflavonol + succinate + CO2
-
?
1.14.11.9 a (2S)-flavan-4-one + 2-oxoglutarate + O2 the 2-oxoglutarate binding site RxS is formed by Arg289 and Ser291 Carthamus tinctorius a (2R,3R)-dihydroflavonol + succinate + CO2
-
?
1.14.11.9 additional information no activity with kaempferol, dihydrokaempferol, quercetin, and dihydroquercetin Carthamus tinctorius ?
-
?
1.14.11.9 naringenin + 2-oxoglutarate + O2
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Carthamus tinctorius dihydrokaempferol + succinate + CO2
-
?

Subunits

EC Number Subunits Comment Organism
1.14.11.9 ? x * 40720, sequence calculation, x * 40000, recombinant detagged enzyme, SDS-PAGE Carthamus tinctorius

Synonyms

EC Number Synonyms Comment Organism
1.14.11.9 CtF3H
-
Carthamus tinctorius
1.14.11.9 F3H
-
Carthamus tinctorius
1.14.11.9 flavanone 3-hydroxylase
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Carthamus tinctorius

pI Value

EC Number Organism Comment pI Value Maximum pI Value
1.14.11.9 Carthamus tinctorius sequence calculation
-
5.57

Expression

EC Number Organism Comment Expression
1.14.11.9 Carthamus tinctorius the enzyme flavanone 3-hydroxylase is induced by methyl jasmonate. Further metabolite analysis shows the increasing tendency of quinochalcones and flavonols, such as hydroxysafflor yellow A, kaempferol-3-O-beta-D-glucoside, kaempferol-3-O-beta-rutinoside, rutin, carthamin, and luteolin, in the quinochalcone-type safflower line. Also, the accumulation of kaempferol-3-O-beta-rutinoside and kaempferol-3-O-beta-D-glucoside in flavonols-typed safflower line shows enhanced accumulation pattern after methyl jasmonate treatment. Other flavonols, such as kaempferol, dihydrokaempferol and quercetin-3-O-beta-D-glucoside, in flavonols-typed safflower line present downregulation in respons to the methyl jasmonate stimulus up

General Information

EC Number General Information Comment Organism
1.14.11.9 evolution the enzyme belongs to the Fe2+/2–oxoglutarate-dependent dioxygenase superfamily Carthamus tinctorius
1.14.11.9 physiological function flavanone 3-hydroxylase (F3H) is one of the nuclear enzymes acting at the bifurcation of the flavonoid biosynthetic pathway, initiating catalysis of the 3-hydroxylation of (2S)-flavanones, such as naringenin to dihydroflavonols Carthamus tinctorius