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Literature summary extracted from

  • Miyahara, T.; Sakiyama, R.; Ozeki, Y.; Sasaki, N.
    Acyl-glucose-dependent glucosyltransferase catalyzes the final step of anthocyanin formation in Arabidopsis (2013), J. Plant Physiol., 170, 619-624.
    View publication on PubMed

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
2.4.1.B70 1-O-(4-coumaroyl)-beta-D-glucose + cyanidin 3-O-[2-O-(2-O-(sinapoyl)-beta-D-xylosyl)-6-O-(6-(4-coumaroyl))-beta-D-glucoside] 5-O-[6-O-(malonyl)-beta-D-glucoside] Arabidopsis thaliana i.e. A9 anthocyanin molecule 4-coumarate + cyanidin 3-O-[2-O-(2-O-(sinapoyl)-beta-D-xylosyl)-6-O-(6-(4-O-beta-D-glucosyl)-4-coumaroyl)-beta-D-glucoside] 5-O-[6-O-(malonyl)-beta-D-glucoside] i.e. A11 anthocyanin molecule ?
2.4.1.B70 additional information Arabidopsis thaliana glucosylation occurs at the 4-coumarate moiety of the anthocyanin molecule cyanidin 3-O-[2-O-(2-O-(sinapoyl)xylosyl) 6-O-(p-coumaroyl) glucoside] 5-O-[6-O-(malonyl) glucoside] leading to completion of the main anthocyanin structure. Enzyme is more efficient with hydroxycinnamoyl-glucoses (C6-C3-glucoses) than benzoyl-glucose derivatives ?
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 ?

Organism

EC Number Organism UniProt Comment Textmining
2.4.1.B70 Arabidopsis thaliana Q93ZI4 cf. EC 3.2.1.21
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Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
2.4.1.B70 1-O-(4-coumaroyl)-beta-D-glucose + cyanidin 3-O-[2-O-(2-O-(sinapoyl)-beta-D-xylosyl)-6-O-(6-(4-coumaroyl))-beta-D-glucoside] 5-O-[6-O-(malonyl)-beta-D-glucoside] i.e. A9 anthocyanin molecule Arabidopsis thaliana 4-coumarate + cyanidin 3-O-[2-O-(2-O-(sinapoyl)-beta-D-xylosyl)-6-O-(6-(4-O-beta-D-glucosyl)-4-coumaroyl)-beta-D-glucoside] 5-O-[6-O-(malonyl)-beta-D-glucoside] i.e. A11 anthocyanin molecule ?
2.4.1.B70 additional information glucosylation occurs at the 4-coumarate moiety of the anthocyanin molecule cyanidin 3-O-[2-O-(2-O-(sinapoyl)xylosyl) 6-O-(p-coumaroyl) glucoside] 5-O-[6-O-(malonyl) glucoside] leading to completion of the main anthocyanin structure. Enzyme is more efficient with hydroxycinnamoyl-glucoses (C6-C3-glucoses) than benzoyl-glucose derivatives Arabidopsis thaliana ?
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 ?

Synonyms

EC Number Synonyms Comment Organism
2.4.1.B70 AAGT
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 Arabidopsis thaliana
2.4.1.B70 acyl-glucose-dependent anthocyanin glucosyltransferase
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 Arabidopsis thaliana
2.4.1.B70 BGLU10
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 Arabidopsis thaliana

Temperature Optimum [°C]

EC Number Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
2.4.1.B70 25 30
-
 Arabidopsis thaliana

pH Range

EC Number pH Minimum pH Maximum Comment Organism
2.4.1.B70 6 6.5
-
 Arabidopsis thaliana

Expression

EC Number Organism Comment Expression
2.4.1.B70 Arabidopsis thaliana highest levels of BGLU10 expression are observed on day 4 after anthocyanin induction additional information

General Information

EC Number General Information Comment Organism
2.4.1.B70 physiological function BGLU10 KO lines accumulate substrate cyanidin 3-O-[2-O-(2-O-(sinapoyl)xylosyl) 6-O-(p-coumaroyl) glucoside] 5-O-[6-O-(malonyl) glucoside]. The expression pattern of BGLU10 and the increase in acyl-glucose-dependent anthocyanin glucosyltransferase activity are consistent with the ratio of accumulating A11 to A9 anthocyanin Arabidopsis thaliana