Lipid-bound sugars in Rhizobium meliloti

Incubation of an enzyme preparation of Rhizobium meliloti with labeled uridine diphosphate glucose led to the formation of radioactive substances soluble in organic solvents. These substances are probably polyprenyl diphosphate saccharides. They behaved like these on treatment with ammonia or with h...

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Autores principales: Tolmasky, M.E., Staneloni, R.J., Ugalde, R.A., Leloir, L.F.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00039861_v203_n1_p358_Tolmasky
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spelling todo:paper_00039861_v203_n1_p358_Tolmasky2023-10-03T13:56:54Z Lipid-bound sugars in Rhizobium meliloti Tolmasky, M.E. Staneloni, R.J. Ugalde, R.A. Leloir, L.F. disaccharide galactose glucosyltransferase isoprenoid phosphate sugar solabiose uridine diphosphate glucose article biosynthesis enzyme specificity enzymology kinetics metabolism paper chromatography Rhizobium temperature thin layer chromatography Chromatography, Paper Chromatography, Thin Layer Disaccharides Galactose Glucosyltransferases Kinetics Polyisoprenyl Phosphate Sugars Rhizobium Substrate Specificity Temperature Uridine Diphosphate Glucose Incubation of an enzyme preparation of Rhizobium meliloti with labeled uridine diphosphate glucose led to the formation of radioactive substances soluble in organic solvents. These substances are probably polyprenyl diphosphate saccharides. They behaved like these on treatment with ammonia or with hot phenol and were decomposed by heating for 10 min at pH 2 yielding a mono- and a disaccharide. The monosaccharide was identified as galactose by paper chromatography. The disaccharide gave glucose and galactose by acid hydrolysis. Following reduction with borohydride it yielded glucose and galactitol. After treatment with periodate followed by paper chromatography only galactose was detectable. The disaccharide was hydrolyzed by β- but not by α-glucosidase. Therefore the disaccharide is glucosyl β1-3-galactose. © 1980, All rights reserved. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00039861_v203_n1_p358_Tolmasky
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic disaccharide
galactose
glucosyltransferase
isoprenoid phosphate sugar
solabiose
uridine diphosphate glucose
article
biosynthesis
enzyme specificity
enzymology
kinetics
metabolism
paper chromatography
Rhizobium
temperature
thin layer chromatography
Chromatography, Paper
Chromatography, Thin Layer
Disaccharides
Galactose
Glucosyltransferases
Kinetics
Polyisoprenyl Phosphate Sugars
Rhizobium
Substrate Specificity
Temperature
Uridine Diphosphate Glucose
spellingShingle disaccharide
galactose
glucosyltransferase
isoprenoid phosphate sugar
solabiose
uridine diphosphate glucose
article
biosynthesis
enzyme specificity
enzymology
kinetics
metabolism
paper chromatography
Rhizobium
temperature
thin layer chromatography
Chromatography, Paper
Chromatography, Thin Layer
Disaccharides
Galactose
Glucosyltransferases
Kinetics
Polyisoprenyl Phosphate Sugars
Rhizobium
Substrate Specificity
Temperature
Uridine Diphosphate Glucose
Tolmasky, M.E.
Staneloni, R.J.
Ugalde, R.A.
Leloir, L.F.
Lipid-bound sugars in Rhizobium meliloti
topic_facet disaccharide
galactose
glucosyltransferase
isoprenoid phosphate sugar
solabiose
uridine diphosphate glucose
article
biosynthesis
enzyme specificity
enzymology
kinetics
metabolism
paper chromatography
Rhizobium
temperature
thin layer chromatography
Chromatography, Paper
Chromatography, Thin Layer
Disaccharides
Galactose
Glucosyltransferases
Kinetics
Polyisoprenyl Phosphate Sugars
Rhizobium
Substrate Specificity
Temperature
Uridine Diphosphate Glucose
description Incubation of an enzyme preparation of Rhizobium meliloti with labeled uridine diphosphate glucose led to the formation of radioactive substances soluble in organic solvents. These substances are probably polyprenyl diphosphate saccharides. They behaved like these on treatment with ammonia or with hot phenol and were decomposed by heating for 10 min at pH 2 yielding a mono- and a disaccharide. The monosaccharide was identified as galactose by paper chromatography. The disaccharide gave glucose and galactose by acid hydrolysis. Following reduction with borohydride it yielded glucose and galactitol. After treatment with periodate followed by paper chromatography only galactose was detectable. The disaccharide was hydrolyzed by β- but not by α-glucosidase. Therefore the disaccharide is glucosyl β1-3-galactose. © 1980, All rights reserved.
format JOUR
author Tolmasky, M.E.
Staneloni, R.J.
Ugalde, R.A.
Leloir, L.F.
author_facet Tolmasky, M.E.
Staneloni, R.J.
Ugalde, R.A.
Leloir, L.F.
author_sort Tolmasky, M.E.
title Lipid-bound sugars in Rhizobium meliloti
title_short Lipid-bound sugars in Rhizobium meliloti
title_full Lipid-bound sugars in Rhizobium meliloti
title_fullStr Lipid-bound sugars in Rhizobium meliloti
title_full_unstemmed Lipid-bound sugars in Rhizobium meliloti
title_sort lipid-bound sugars in rhizobium meliloti
url http://hdl.handle.net/20.500.12110/paper_00039861_v203_n1_p358_Tolmasky
work_keys_str_mv AT tolmaskyme lipidboundsugarsinrhizobiummeliloti
AT stanelonirj lipidboundsugarsinrhizobiummeliloti
AT ugaldera lipidboundsugarsinrhizobiummeliloti
AT leloirlf lipidboundsugarsinrhizobiummeliloti
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