The biosynthesis of a N,N′-diacetylchitobiose containing lipid by liver microsomes. A probable dolichol pyrophosphate derivative

Incubation of liver microsomes with dolichol monophosphate, Mg++ and UDP-[14C] -N-acetylglucosamine leads to the appearance of radioactivity in the lipid fraction. Mild acid treatment results in the formation of N-acetylglucosamine and N,N′-diacetylchitobiose (2-acetamido-2-deoxy-0-β-D-glucopyranosy...

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Detalles Bibliográficos
Autores principales:	Leloir, L.F., Staneloni, R.J., Carminatti, H., Behrens, N.H.
Formato:	JOUR
Materias:	acetic acid derivative borane derivative carbon disaccharide fatty alcohol glucosamine lipid magnesium terpene uridine diphosphate sugar animal article biosynthesis drug effect hydrolysis ion exchange chromatography liver microsome metabolism oxidation reduction reaction paper chromatography paper electrophoresis rat Acetic Acids Animal Borohydrides Carbon Isotopes Chromatography, DEAE-Cellulose Chromatography, Paper Disaccharides Electrophoresis, Paper Fatty Alcohols Glucosamine Hydrolysis Lipids Magnesium Microsomes, Liver Oxidation-Reduction Rats Terpenes Uridine Diphosphate Sugars
Acceso en línea:	http://hdl.handle.net/20.500.12110/paper_0006291X_v52_n4_p1285_Leloir
Aporte de:	Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires

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