2.4.1.126: hydroxycinnamate 4-beta-glucosyltransferase

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For detailed information about hydroxycinnamate 4-beta-glucosyltransferase, go to the full flat file.

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Synonyms

glucosyltransferase, uridine diphosphoglucose-hydroxycinnamate, hydroxycinnamoyl glucosyltransferase, UDP-glucose-hydroxycinnamate glucosyltransferase, UDPglucose:trans-4-hydroxycinnamate 4-O-beta-D-glucosyltransferase, uridine diphosphoglucose-hydroxycinnamate glucosyltransferase

ECTree

     2 Transferases

         2.4 Glycosyltransferases

             2.4.1 Hexosyltransferases

                2.4.1.126 hydroxycinnamate 4-beta-glucosyltransferase

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Results	in table
6	AA Sequence
1	CAS Registry Number
1	Cloned(Commentary)
5	Expression
2	General Information
1	General Stability
7	Inhibitors
5	KM Value [mM]
1	Metals/Ions
1	Natural Substrates/ Products (Substrates)
2	Organism
2	Pathway
3	pH Optimum
1	Purification (Commentary)
1	Reaction
1	Reaction Type
2	Reference
4	Source Tissue
1	Specific Activity [micromol/min/mg]
2	Storage Stability
11	Substrates and Products (Substrate)
5	Synonyms
1	Systematic Name
1	Temperature Optimum [°C]

Cloned

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Cloned on EC 2.4.1.126 - hydroxycinnamate 4-beta-glucosyltransferase

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CLONED (Commentary)

ORGANISM

UNIPROT

LITERATURE

binary plasmid constructs for transformation of Arabidopsis are introduced into Agrobacterium tumefaciens by electroporation, plants are transformed by the floral dip method, for selection of transgenic plants T1 seeds are surface-sterilized in 70% ethanol for 2 min followed by a mixture of Tween 20 and sodium hypochloride for 10 min, seeds are rinsed thoroughly with sterile water and after swelling over night at 4°C plated on modified MS medium supplemented with carbenicillin and kanamycin, after scoring the development of antibiotic damage symptoms for 14 days post treatment, kanamycin resistant plants are transferred; binary plasmid constructs for transformation of Arabidopsis are introduced into Agrobacterium tumefaciens by electroporation, plants are transformed by the floral dip method, for selection of transgenic plants T1 seeds are surface-sterilized in 70% ethanol for 2 min followed by a mixture of Tween 20 and sodium hypochloride for 10 min, seeds are rinsed thoroughly with sterile water and after swelling over night at 4°C plated on modified MS medium supplemented with carbenicillin and kanamycin, after scoring the development of antibiotic damage symptoms for 14 days post treatment, kanamycin resistant plants are transferred; binary plasmid constructs for transformation of Arabidopsis are introduced into Agrobacterium tumefaciens by electroporation, plants are transformed by the floral dip method, for selection of transgenic plants T1 seeds are surface-sterilized in 70% ethanol for 2 min followed by a mixture of Tween 20 and sodium hypochloride for 10 min, seeds are rinsed thoroughly with sterile water and after swelling over night at 4°C plated on modified MS medium supplemented with carbenicillin and kanamycin, after scoring the development of antibiotic damage symptoms for 14 days post treatment, kanamycin resistant plants are transferred; binary plasmid constructs for transformation of Arabidopsis are introduced into Agrobacterium tumefaciens by electroporation, plants are transformed by the floral dip method, for selection of transgenic plants T1 seeds are surface-sterilized in 70% ethanol for 2 min followed by a mixture of Tween 20 and sodium hypochloride for 10 min, seeds are rinsed thoroughly with sterile water and after swelling over night at 4°C plated on modified MS medium supplemented with carbenicillin and kanamycin, after scoring the development of antibiotic damage symptoms for 14 days post treatment, kanamycin resistant plants are transferred

Arabidopsis thaliana

O23402

706373