alcohol O-cinnamoyltransferase | |||||||||
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Identifiers | |||||||||
EC no. | 2.3.1.152 | ||||||||
CAS no. | 74082-53-4 | ||||||||
Databases | |||||||||
IntEnz | IntEnz view | ||||||||
BRENDA | BRENDA entry | ||||||||
ExPASy | NiceZyme view | ||||||||
KEGG | KEGG entry | ||||||||
MetaCyc | metabolic pathway | ||||||||
PRIAM | profile | ||||||||
PDB structures | RCSB PDB PDBe PDBsum | ||||||||
Gene Ontology | AmiGO / QuickGO | ||||||||
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In enzymology, an alcohol O-cinnamoyltransferase (EC 2.3.1.152) is an enzyme that catalyzes the chemical reaction
Thus, the two substrates of this enzyme are 1-O-trans-cinnamoyl-beta-D-glucopyranose and an alkanol (ROH), whereas its two products are alkyl cinnamate and glucose.
This enzyme belongs to the family of transferases, specifically those acyltransferases transferring groups other than aminoacyl groups. The systematic name of this enzyme class is 1-O-trans-cinnamoyl-beta-D-glucopyranose:alcohol O-cinnamoyltransferase.
Umbelliferone, also known as 7-hydroxycoumarin, hydrangine, skimmetine, and beta-umbelliferone, is a natural product of the coumarin family.
p-Coumaric acid is an organic compound with the formula HOC6H4CH=CHCO2H. It is one of the three isomers of hydroxycinnamic acid. It is a white solid that is only slightly soluble in water but very soluble in ethanol and diethyl ether.
The phenylpropanoids are a diverse family of organic compounds that are synthesized by plants from the amino acids phenylalanine and tyrosine. Their name is derived from the six-carbon, aromatic phenyl group and the three-carbon propene tail of coumaric acid, which is the central intermediate in phenylpropanoid biosynthesis. From 4-coumaroyl-CoA emanates the biosynthesis of myriad natural products including lignols, flavonoids, isoflavonoids, coumarins, aurones, stilbenes, catechin, and phenylpropanoids. The coumaroyl component is produced from cinnamic acid.
Pinosylvin is an organic compound with the formula C6H5CH=CHC6H3(OH)2. A white solid, it is related to trans-stilbene, but with two hydroxy groups on one of the phenyl substituents. It is very soluble in many organic solvents, such as acetone.
In enzymology, a caffeate O-methyltransferase is an enzyme that catalyzes the chemical reaction
In enzymology, a trans-cinnamate 2-monooxygenase (EC 1.14.13.14) is an enzyme that catalyzes the chemical reaction
In enzymology, a trans-cinnamate 4-monooxygenase (EC 1.14.14.91) is an enzyme that catalyzes the chemical reaction
The enzyme phenylalanine ammonia lyase (EC 4.3.1.24) catalyzes the conversion of L-phenylalanine to ammonia and trans-cinnamic acid.:
In enzymology, a sinapoylglucose---sinapoylglucose O-sinapoyltransferase is an enzyme that catalyzes the chemical reaction
In enzymology, a 2-coumarate O-beta-glucosyltransferase is an enzyme that catalyzes the chemical reaction
In enzymology, a 4-hydroxybenzoate 4-O-beta-D-glucosyltransferase is an enzyme that catalyzes the chemical reaction
In enzymology, a cinnamate beta-D-glucosyltransferase is an enzyme that catalyzes the chemical reaction
In enzymology, a cis-p-Coumarate glucosyltransferase is an enzyme that catalyzes the chemical reaction
In enzymology, a gallate 1-beta-glucosyltransferase is an enzyme that catalyzes the chemical reaction
In enzymology, a hydroquinone glucosyltransferase is an enzyme that catalyzes the chemical reaction
In enzymology, a nuatigenin 3beta-glucosyltransferase is an enzyme that catalyzes the chemical reaction
In enzymology, a sterol 3beta-glucosyltransferase is an enzyme that catalyzes the chemical reaction
In enzymology, a vomilenine glucosyltransferase is an enzyme that catalyzes the chemical reaction
1,2,3,4,6-Pentagalloylglucose is the pentagallic acid ester of glucose. It is a gallotannin and the precursor of ellagitannins.
The biosynthesis of phenylpropanoids involves a number of enzymes.