1.14.11.9: flavanone 3-dioxygenase
This is an abbreviated version!
For detailed information about flavanone 3-dioxygenase, go to the full flat file.
Word Map on EC 1.14.11.9
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1.14.11.9
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chalcone
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anthocyanins
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dihydroflavonols
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flavonols
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anthocyanidin
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4-reductase
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ammonia-lyase
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3\'-hydroxylase
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petunia
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proanthocyanidins
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dihydrokaempferol
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leucoanthocyanidin
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3-o-glucosyltransferase
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2-oxoglutarate-dependent
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3',5'-hydroxylase
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r2r3-myb
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eriodictyol
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analysis
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testa
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udp-glucose:flavonoid
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2s-flavanones
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4-coumarate-coa
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dihydroflavonol-4-reductase
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dihydroquercetin
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2s-naringenin
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pelargonidin
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synthesis
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agriculture
- 1.14.11.9
- chalcone
- anthocyanins
- dihydroflavonols
- flavonols
- anthocyanidin
-
4-reductase
-
ammonia-lyase
-
3\'-hydroxylase
- petunia
- proanthocyanidins
- dihydrokaempferol
-
leucoanthocyanidin
- 3-o-glucosyltransferase
-
2-oxoglutarate-dependent
-
3',5'-hydroxylase
-
r2r3-myb
- eriodictyol
- analysis
-
testa
-
udp-glucose:flavonoid
-
2s-flavanones
-
4-coumarate-coa
- dihydroflavonol-4-reductase
- dihydroquercetin
- 2s-naringenin
- pelargonidin
- synthesis
- agriculture
Reaction
Synonyms
(2S)-flavanone 3-hydroxylase, AaF3H, AcF3H, BnF3H, CsF3H, CtF3H, F3H, F3H protein, F3H1, F3H2, FHT, FHTPH, flavanone 3-dioxygenase, flavanone 3-hydroxylase, flavanone 3beta-hydroxylase, flavanone synthase I, flavanone-3-hydroxylase, FLS1, FLS2, FS I, LcF3H, naringenin 3-dioxygenase, naringenin,2-oxoglutarate:oxygen oxidoreductase (3-hydroxylating), oxygenase, flavanone 3-di-, PeF3H, PgF3H, PnF3H, RtF3H1, RtF3H2, VcF3H
ECTree
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Application
Application on EC 1.14.11.9 - flavanone 3-dioxygenase
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agriculture
analysis
synthesis
additional information
F3H gene may be used as biomarker in tea breeding programs and genetic engineering to improve tea quality
basis for further research on the control of berry skin color and wine quality
agriculture
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the aim is to identify the soybean mosaic virus resistance associated single nucleotide polymorphism in the IFS1, IFS2 and F3H gene by association mapping in order to develop valuable genetic markers for future soybean mosaic virus resistance breeding efforts in soybean
agriculture
the aim is to identify the soybean mosaic virus resistance associated single nucleotide polymorphism in the IFS1, IFS2 and F3H gene by association mapping in order to develop valuable genetic markers for future soybean mosaic virus resistance breeding efforts in soybean
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an HPLC method for the determination of phenylalanine ammonia-lyase, flavanone 3-hydroxylase and flavonol synthase enzyme activity is proposed. This method is based on the determination of the compounds produced and consumed on the enzymatic reaction in just one chromatographic analysis. Optimisation of the method consideres kinetic studies to establish the incubation time to perform the assay. The method is an approach to measure the activities of the three enzymes simultaneously increasing the rapidity, selectivity and sensitivity over other exiting methods
analysis
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an HPLC method for the determination of phenylalanine ammonia-lyase, flavanone 3-hydroxylase and flavonol synthase enzyme activity is proposed. This method is based on the determination of the compounds produced and consumed on the enzymatic reaction in just one chromatographic analysis. Optimisation of the method consideres kinetic studies to establish the incubation time to perform the assay. The method is an approach to measure the activities of the three enzymes simultaneously increasing the rapidity, selectivity and sensitivity over other exiting methods
analysis
an HPLC method for the determination of phenylalanine ammonia-lyase, flavanone 3-hydroxylase and flavonol synthase enzyme activity is proposed. This method is based on the determination of the compounds produced and consumed on the enzymatic reaction in just one chromatographic analysis. Optimisation of the method consideres kinetic studies to establish the incubation time to perform the assay. The method is an approach to measure the activities of the three enzymes simultaneously increasing the rapidity, selectivity and sensitivity over other exiting methods
analysis
an HPLC method for the determination of phenylalanine ammonia-lyase, flavanone 3-hydroxylase and flavonol synthase enzyme activity is proposed. This method is based on the determination of the compounds produced and consumed on the enzymatic reaction in just one chromatographic analysis. Optimisation of the method consideres kinetic studies to establish the incubation time to perform the assay. The method is an approach to measure the activities of the three enzymes simultaneously increasing the rapidity, selectivity and sensitivity over other exiting methods
analysis
an HPLC method for the determination of phenylalanine ammonia-lyase, flavanone 3-hydroxylase and flavonol synthase enzyme activity is proposed. This method is based on the determination of the compounds produced and consumed on the enzymatic reaction in just one chromatographic analysis. Optimisation of the method consideres kinetic studies to establish the incubation time to perform the assay. The method is an approach to measure the activities of the three enzymes simultaneously increasing the rapidity, selectivity and sensitivity over other exiting methods
functional expression of plant-derived O-methyltransferase, flavanone 3-hydroxylase, and flavonol synthase in Corynebacterium glutamicum for production of pterostilbene, kaempferol, and quercetin
synthesis
expression of heterologous dioxygenase genes in (2S)-flavanone-producing Corynebacterium glutamicum strains enables the production of flavanonols and flavonols, e.g kaempferol and quercetin, starting from thephenylpropanoids p-coumaric acid and caffeic acid