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Results 1 - 4 of 4

EC Number	Substrates	Commentary Substrates	Organism	Products	Commentary (Products)	Reversibility
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	delphinidin 3-rutinoside-7-(6-(p-hydroxybenzoyl)-glucoside) + p-hydroxybenzoyl-glucose	-	Delphinium grandiflorum	delphinidin 3-rutinoside-7-(6-(4-(glucosyl)-oxybenzoyl)-glucoside) + 4-hydroxybenzol	-	?
2.4.1.B70	more	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	?	-	?
2.4.1.B70	more	anthocyanin profiling in sepals	Delphinium grandiflorum	?	-	-

Results 1 - 4 of 4

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Release 2023.1 (January 2023)