2.4.1.360: 2-hydroxyflavanone C-glucosyltransferase
This is an abbreviated version!
For detailed information about 2-hydroxyflavanone C-glucosyltransferase, go to the full flat file.
Word Map on EC 2.4.1.360
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2.4.1.360
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c-glucosylation
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flavonoid
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c-glycosyltransferases
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sativa
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o-glucosyltransferase
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dehydratase
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o-glycosylated
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planta
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c-glycosylflavones
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flavone
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cereals
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phloretin
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synthesis
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dibenzoylmethane
- 2.4.1.360
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c-glucosylation
- flavonoid
-
c-glycosyltransferases
- sativa
-
o-glucosyltransferase
- dehydratase
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o-glycosylated
-
planta
-
c-glycosylflavones
- flavone
-
cereals
- phloretin
- synthesis
- dibenzoylmethane
Reaction
Synonyms
CuCGT, FcCGT, OsCGT, UDP-glucose:2-hydroxyflavanone-6(or8)-C-glucosyltransferase, UGT708C1, UGT708C2
ECTree
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Application
Application on EC 2.4.1.360 - 2-hydroxyflavanone C-glucosyltransferase
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synthesis
biosynthesis of natural and novel C-glycosylflavones utilising recombinant Oryza sativa C-glycosyltransferase and Desmodium incanum root proteins
synthesis
production of C-glucosides of flavonoids and related compounds (i.e., 2-hydroxyflavanone, dihydrochalcone, and trihydroxyacetophenone) by Escherichia coli expressing C-glucosyltransferase from Fagopyrum esculentum. The substrates in their respective cultures were taken up by the cells and C-glucosylated, and the products were released into the culture media. The bioconversion process was completed in 1-2 h, but products were already observed immediately after addition of the substrates (0.2 mM). The conversion rates of these substrates reaches 80-95%