Further studies on a glycolipid formed from dolichyl-d-glucosyl monophosphate
Incubation of liver microsomes with dolichyl-d-glucosyl-14C monophosphate led to the labelling of an endogenous acceptor. This compound seems to be also a dolichol derivative. It contains a high-molecular weight oligosaccharide bound to dolichol through a phosphate or pyrophosphate bond. Various tre...
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1973
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| Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00086215_v26_n2_p393_Parodi http://hdl.handle.net/20.500.12110/paper_00086215_v26_n2_p393_Parodi |
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paper:paper_00086215_v26_n2_p393_Parodi2023-06-08T14:32:32Z Further studies on a glycolipid formed from dolichyl-d-glucosyl monophosphate Parodi, Armando José Behrens, Nicolás H. Carminatti, Héctor Levy Sabaj, José A. borane derivative carbon concanavalin A fatty alcohol glucose phosphate glycolipid oligosaccharide periodic acid terpene tritium animal article binding site liver liver microsome metabolism oxidation reduction reaction paper chromatography rat swine time Animal Binding Sites Borohydrides Carbon Isotopes Chromatography, Paper Concanavalin A Fatty Alcohols Glucosephosphates Glycolipids Liver Microsomes, Liver Oligosaccharides Oxidation-Reduction Periodic Acid Rats Swine Terpenes Time Factors Tritium Incubation of liver microsomes with dolichyl-d-glucosyl-14C monophosphate led to the labelling of an endogenous acceptor. This compound seems to be also a dolichol derivative. It contains a high-molecular weight oligosaccharide bound to dolichol through a phosphate or pyrophosphate bond. Various treatments of the labelled oligosaccharide afforded further information on its structure: Reduction with sodium borohydride, followed by acid hydrolysis gave only radioactive d-glucose indicating that the labelled d-glucose is not incorporated at the reducing end of the oligosaccharide. The percentage of radioactivity, liberated as formic acid after periodate oxidation, indicates that more than one molecule of d-glucose is incorporated and that at least one of them is inside the oligosaccharide chain. Alkaline treatment of the otherwise neutral oligosaccharide gave two positively charged derivatives which could be neutralized by N-acetylation, indicating the presence of two hexosamine residues. The oligosaccharides isolated from different tissues by the same method as that used for rat liver, were similar as judged by their migration in paper chromatography and by the pattern of products liberated by acetolysis. © 1973. Fil:Parodi, A.J. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Behrens, N.H. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Carminatti, H. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Levy, J.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 1973 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00086215_v26_n2_p393_Parodi http://hdl.handle.net/20.500.12110/paper_00086215_v26_n2_p393_Parodi |
| institution |
Universidad de Buenos Aires |
| institution_str |
I-28 |
| repository_str |
R-134 |
| collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
| topic |
borane derivative carbon concanavalin A fatty alcohol glucose phosphate glycolipid oligosaccharide periodic acid terpene tritium animal article binding site liver liver microsome metabolism oxidation reduction reaction paper chromatography rat swine time Animal Binding Sites Borohydrides Carbon Isotopes Chromatography, Paper Concanavalin A Fatty Alcohols Glucosephosphates Glycolipids Liver Microsomes, Liver Oligosaccharides Oxidation-Reduction Periodic Acid Rats Swine Terpenes Time Factors Tritium |
| spellingShingle |
borane derivative carbon concanavalin A fatty alcohol glucose phosphate glycolipid oligosaccharide periodic acid terpene tritium animal article binding site liver liver microsome metabolism oxidation reduction reaction paper chromatography rat swine time Animal Binding Sites Borohydrides Carbon Isotopes Chromatography, Paper Concanavalin A Fatty Alcohols Glucosephosphates Glycolipids Liver Microsomes, Liver Oligosaccharides Oxidation-Reduction Periodic Acid Rats Swine Terpenes Time Factors Tritium Parodi, Armando José Behrens, Nicolás H. Carminatti, Héctor Levy Sabaj, José A. Further studies on a glycolipid formed from dolichyl-d-glucosyl monophosphate |
| topic_facet |
borane derivative carbon concanavalin A fatty alcohol glucose phosphate glycolipid oligosaccharide periodic acid terpene tritium animal article binding site liver liver microsome metabolism oxidation reduction reaction paper chromatography rat swine time Animal Binding Sites Borohydrides Carbon Isotopes Chromatography, Paper Concanavalin A Fatty Alcohols Glucosephosphates Glycolipids Liver Microsomes, Liver Oligosaccharides Oxidation-Reduction Periodic Acid Rats Swine Terpenes Time Factors Tritium |
| description |
Incubation of liver microsomes with dolichyl-d-glucosyl-14C monophosphate led to the labelling of an endogenous acceptor. This compound seems to be also a dolichol derivative. It contains a high-molecular weight oligosaccharide bound to dolichol through a phosphate or pyrophosphate bond. Various treatments of the labelled oligosaccharide afforded further information on its structure: Reduction with sodium borohydride, followed by acid hydrolysis gave only radioactive d-glucose indicating that the labelled d-glucose is not incorporated at the reducing end of the oligosaccharide. The percentage of radioactivity, liberated as formic acid after periodate oxidation, indicates that more than one molecule of d-glucose is incorporated and that at least one of them is inside the oligosaccharide chain. Alkaline treatment of the otherwise neutral oligosaccharide gave two positively charged derivatives which could be neutralized by N-acetylation, indicating the presence of two hexosamine residues. The oligosaccharides isolated from different tissues by the same method as that used for rat liver, were similar as judged by their migration in paper chromatography and by the pattern of products liberated by acetolysis. © 1973. |
| author |
Parodi, Armando José Behrens, Nicolás H. Carminatti, Héctor Levy Sabaj, José A. |
| author_facet |
Parodi, Armando José Behrens, Nicolás H. Carminatti, Héctor Levy Sabaj, José A. |
| author_sort |
Parodi, Armando José |
| title |
Further studies on a glycolipid formed from dolichyl-d-glucosyl monophosphate |
| title_short |
Further studies on a glycolipid formed from dolichyl-d-glucosyl monophosphate |
| title_full |
Further studies on a glycolipid formed from dolichyl-d-glucosyl monophosphate |
| title_fullStr |
Further studies on a glycolipid formed from dolichyl-d-glucosyl monophosphate |
| title_full_unstemmed |
Further studies on a glycolipid formed from dolichyl-d-glucosyl monophosphate |
| title_sort |
further studies on a glycolipid formed from dolichyl-d-glucosyl monophosphate |
| publishDate |
1973 |
| url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00086215_v26_n2_p393_Parodi http://hdl.handle.net/20.500.12110/paper_00086215_v26_n2_p393_Parodi |
| work_keys_str_mv |
AT parodiarmandojose furtherstudiesonaglycolipidformedfromdolichyldglucosylmonophosphate AT behrensnicolash furtherstudiesonaglycolipidformedfromdolichyldglucosylmonophosphate AT carminattihector furtherstudiesonaglycolipidformedfromdolichyldglucosylmonophosphate AT levysabajjosea furtherstudiesonaglycolipidformedfromdolichyldglucosylmonophosphate |
| _version_ |
1768544300982861824 |