The role of dolichol monophosphate in sugar transfer
The specificity of the transfer of monosaccharides from sugar nucleotides to dolichol monophosphate catalyzed by liver microsomes was studied. Besides uridine diphosphate glucose, uridine diphosphate-N-acetylglucosamine and guanosine diphosphate mannose were found to act as donors for the formation...
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1971
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Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00039861_v143_n2_p375_Behrens http://hdl.handle.net/20.500.12110/paper_00039861_v143_n2_p375_Behrens |
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paper:paper_00039861_v143_n2_p375_Behrens2023-06-08T14:24:56Z The role of dolichol monophosphate in sugar transfer Behrens, Nicolás H. Parodi, Armando José Krisman de Fischman, Clara Rebeca alkene amino acid bile acid cerebroside collagen fatty acid galactose glucosamine glucose glycol guanine nucleotide hexosamine hexose mannose nucleoside diphosphate sugar nucleotide organophosphorus compound phosphoric acid polymer pyrimidine nucleotide Surface Active Agents surfactant animal article brain catalysis drug stability enzymology liver microsome metabolism pH rat skin solubility temperature thin layer chromatography Alkenes Amino Acids Animal Animals, Newborn Bile Acids and Salts Brain Catalysis Cerebrosides Chromatography, Thin Layer Collagen Drug Stability Fatty Acids Galactose Glucosamine Glucose Glycols Guanine Nucleotides Hexosamines Hexoses Hydrogen-Ion Concentration Mannose Microsomes, Liver Nucleoside Diphosphate Sugars Nucleotides Organophosphorus Compounds Phosphoric Acids Polymers Rats Skin Solubility Surface-Active Agents Temperature Uracil Nucleotides The specificity of the transfer of monosaccharides from sugar nucleotides to dolichol monophosphate catalyzed by liver microsomes was studied. Besides uridine diphosphate glucose, uridine diphosphate-N-acetylglucosamine and guanosine diphosphate mannose were found to act as donors for the formation of the respective dolichol monophosphate sugars. Uridine diphosphate galactose and uridine diphosphate-N-acetylgalactosamine gave negative results. The optimal conditions for transfer from dolichol monophosphate glucose to endogenous acceptor was determined. Studies were carried out on the glucosylation of ceramide by brain extracts and of collagen by skin enzymes in order to find out if dolichol monophosphate glucose is an intermediate in these reactions. The results, while not definite, were not in favor of this assumption. © 1971. Fil:Behrens, N.H. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Parodi, A.J. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Krisman, C.R. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 1971 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00039861_v143_n2_p375_Behrens http://hdl.handle.net/20.500.12110/paper_00039861_v143_n2_p375_Behrens |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
alkene amino acid bile acid cerebroside collagen fatty acid galactose glucosamine glucose glycol guanine nucleotide hexosamine hexose mannose nucleoside diphosphate sugar nucleotide organophosphorus compound phosphoric acid polymer pyrimidine nucleotide Surface Active Agents surfactant animal article brain catalysis drug stability enzymology liver microsome metabolism pH rat skin solubility temperature thin layer chromatography Alkenes Amino Acids Animal Animals, Newborn Bile Acids and Salts Brain Catalysis Cerebrosides Chromatography, Thin Layer Collagen Drug Stability Fatty Acids Galactose Glucosamine Glucose Glycols Guanine Nucleotides Hexosamines Hexoses Hydrogen-Ion Concentration Mannose Microsomes, Liver Nucleoside Diphosphate Sugars Nucleotides Organophosphorus Compounds Phosphoric Acids Polymers Rats Skin Solubility Surface-Active Agents Temperature Uracil Nucleotides |
spellingShingle |
alkene amino acid bile acid cerebroside collagen fatty acid galactose glucosamine glucose glycol guanine nucleotide hexosamine hexose mannose nucleoside diphosphate sugar nucleotide organophosphorus compound phosphoric acid polymer pyrimidine nucleotide Surface Active Agents surfactant animal article brain catalysis drug stability enzymology liver microsome metabolism pH rat skin solubility temperature thin layer chromatography Alkenes Amino Acids Animal Animals, Newborn Bile Acids and Salts Brain Catalysis Cerebrosides Chromatography, Thin Layer Collagen Drug Stability Fatty Acids Galactose Glucosamine Glucose Glycols Guanine Nucleotides Hexosamines Hexoses Hydrogen-Ion Concentration Mannose Microsomes, Liver Nucleoside Diphosphate Sugars Nucleotides Organophosphorus Compounds Phosphoric Acids Polymers Rats Skin Solubility Surface-Active Agents Temperature Uracil Nucleotides Behrens, Nicolás H. Parodi, Armando José Krisman de Fischman, Clara Rebeca The role of dolichol monophosphate in sugar transfer |
topic_facet |
alkene amino acid bile acid cerebroside collagen fatty acid galactose glucosamine glucose glycol guanine nucleotide hexosamine hexose mannose nucleoside diphosphate sugar nucleotide organophosphorus compound phosphoric acid polymer pyrimidine nucleotide Surface Active Agents surfactant animal article brain catalysis drug stability enzymology liver microsome metabolism pH rat skin solubility temperature thin layer chromatography Alkenes Amino Acids Animal Animals, Newborn Bile Acids and Salts Brain Catalysis Cerebrosides Chromatography, Thin Layer Collagen Drug Stability Fatty Acids Galactose Glucosamine Glucose Glycols Guanine Nucleotides Hexosamines Hexoses Hydrogen-Ion Concentration Mannose Microsomes, Liver Nucleoside Diphosphate Sugars Nucleotides Organophosphorus Compounds Phosphoric Acids Polymers Rats Skin Solubility Surface-Active Agents Temperature Uracil Nucleotides |
description |
The specificity of the transfer of monosaccharides from sugar nucleotides to dolichol monophosphate catalyzed by liver microsomes was studied. Besides uridine diphosphate glucose, uridine diphosphate-N-acetylglucosamine and guanosine diphosphate mannose were found to act as donors for the formation of the respective dolichol monophosphate sugars. Uridine diphosphate galactose and uridine diphosphate-N-acetylgalactosamine gave negative results. The optimal conditions for transfer from dolichol monophosphate glucose to endogenous acceptor was determined. Studies were carried out on the glucosylation of ceramide by brain extracts and of collagen by skin enzymes in order to find out if dolichol monophosphate glucose is an intermediate in these reactions. The results, while not definite, were not in favor of this assumption. © 1971. |
author |
Behrens, Nicolás H. Parodi, Armando José Krisman de Fischman, Clara Rebeca |
author_facet |
Behrens, Nicolás H. Parodi, Armando José Krisman de Fischman, Clara Rebeca |
author_sort |
Behrens, Nicolás H. |
title |
The role of dolichol monophosphate in sugar transfer |
title_short |
The role of dolichol monophosphate in sugar transfer |
title_full |
The role of dolichol monophosphate in sugar transfer |
title_fullStr |
The role of dolichol monophosphate in sugar transfer |
title_full_unstemmed |
The role of dolichol monophosphate in sugar transfer |
title_sort |
role of dolichol monophosphate in sugar transfer |
publishDate |
1971 |
url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00039861_v143_n2_p375_Behrens http://hdl.handle.net/20.500.12110/paper_00039861_v143_n2_p375_Behrens |
work_keys_str_mv |
AT behrensnicolash theroleofdolicholmonophosphateinsugartransfer AT parodiarmandojose theroleofdolicholmonophosphateinsugartransfer AT krismandefischmanclararebeca theroleofdolicholmonophosphateinsugartransfer AT behrensnicolash roleofdolicholmonophosphateinsugartransfer AT parodiarmandojose roleofdolicholmonophosphateinsugartransfer AT krismandefischmanclararebeca roleofdolicholmonophosphateinsugartransfer |
_version_ |
1768542153128017920 |