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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Autores principales: Behrens, Nicolás H., Parodi, Armando José, Krisman de Fischman, Clara Rebeca
Publicado: 1971
Materias:
pH
rat
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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spelling 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
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