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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882685Generated: October 25, 2026

Udp-Glucose → UDP GalN biotin

https://huagongshe.com/reaction/882685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUdp-GlucoseHCID 8629—
ReactantUDP-galactosamineHCID 161225—
Reactant6-[5-[(3aS,4S,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanoylamino]-2-(2,5-dioxopyrrolidin-1-yl)-2-sulfohexanoateHCID 131729864—
ProductUDP GalN biotinHCID 131729863—

Reaction Steps

UDP-galactosamine (UDP-GalN) is formed from UDP-Glc and galactosamine-1-phosphate by the action of galactose-1-phosphate uridyltransferase (E.C. 2.7.7.12; Sigma, USA). A typical synthesis protocol is described below. The reaction mixture contains 10 mM galactosamine-1-phosphate, 20 mM UDP-Glc, 5 U/ml of galactose-1-phosphate uridyltransferase, 100 mM Na-HEPES pH 8.0, 5 mM MgCl2, and 5 mM β-mercaptoethanol. The reaction vessel is incubated at room temperature under nitrogen atmosphere for 3 days, after which nucleotide sugars are isolated from the reaction mixture with a graphitised carbon column essentially as in (Mäki et al., 2002). The nucleotide sugar mixture, containing UDP-Glc and UDP-GalN, is incubated with a molar excess of sulfosuccinimidyl-6-(biotinamido)hexanoate (sulfo-NHS-LC-biotin; Pierce, USA) in 50 mM NH4HCO3 at room temperature for 2.5 hours. The product, UDP-GalN-biotin, uridine 5′-diphospho-N-(6-biotinamidohexanoyl)galactosamine, is purified by gel filtration and reversed phase HPLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236487B2
Source datasetuspto-grants-2012_08
ORD IDord-3619111ce1b54746beae6e022093081f
Source noteuspto-grants-2012_08