Cn microspheres as surrogate membranes in glycosidase-catalysed hydrolysis of glycolipids
Literature Information
José A. R. Martins, David H. G. Crout, Peter Critchley
Glycosidase catalysed hydrolysis of glycolipids non-covalently attached to Cn microspheres proceeds to completion for appropriate glycolipid-microsphere combinations in contrast with hydrolysis of covalently immobilised analogues which in all cases studied stops significantly short of complete hydrolysis.
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![Bis(1,2,2,6,6-pentamethyl-4-piperidinyl) butyl[4-hydroxy-3,5-bis(2-methyl-2-propanyl)benzyl]malonate structure Bis(1,2,2,6,6-pentamethyl-4-piperidinyl) butyl[4-hydroxy-3,5-bis(2-methyl-2-propanyl)benzyl]malonate structure](https://static.chemtradehub.com/structs/638/63843-89-0-665e.webp)
![Disodium (6R,7R)-7-{[(2R)-2-hydroxy-2-phenylacetyl]amino}-8-oxo-3-({[1-(sulfonatomethyl)-1H-tetrazol-5-yl]sulfanyl}methyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate structure Disodium (6R,7R)-7-{[(2R)-2-hydroxy-2-phenylacetyl]amino}-8-oxo-3-({[1-(sulfonatomethyl)-1H-tetrazol-5-yl]sulfanyl}methyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate structure](https://static.chemtradehub.com/structs/612/61270-78-8-6b58.webp)

