Further studies on high molecular weight liver glycogen

A simple method for the extraction of undegraded liver glycogen is described. The molecular weight distribution curve as measured by gradient centrifugation was quite variable and was found to be unrelated to glycogen content. The concentration of malto-oligosaccharides in liver was estimated by a n...

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Detalles Bibliográficos
Autor principal: Krisman de Fischman, Clara Rebeca
Publicado: 1966
Materias:
rat
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00039861_v113_n2_p265_Mordoh
http://hdl.handle.net/20.500.12110/paper_00039861_v113_n2_p265_Mordoh
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spelling paper:paper_00039861_v113_n2_p265_Mordoh2023-06-08T14:24:51Z Further studies on high molecular weight liver glycogen Krisman de Fischman, Clara Rebeca guanidine derivative oligosaccharide sodium hydroxide urea animal article cell fractionation chemistry glycogen liver level heat in vitro study molecular weight rat ultrasound Animal Chemistry Guanidines Heat In Vitro Liver Glycogen Molecular Weight Oligosaccharides Rats Sodium Hydroxide Subcellular Fractions Ultrasonics Urea A simple method for the extraction of undegraded liver glycogen is described. The molecular weight distribution curve as measured by gradient centrifugation was quite variable and was found to be unrelated to glycogen content. The concentration of malto-oligosaccharides in liver was estimated by a new method and was found to remain constant under conditions in which glycogen content varied considerably. Native glycogen was compared with that prepared in vitro with purified enzymes. Although both preparations were similar in molecular weight and in their appearance under the electron microscope, they differed in the type of breakdown produced by acid, alkali, heat, and ultrasonic vibrations. When glycogen prepared in vitro was submitted to these procedures, its sedimentation coefficient decreased progressively, while native glycogen was broken down preferentially to a lighter population of about S = 100. © 1966. Fil:Krisman, C.R. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 1966 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00039861_v113_n2_p265_Mordoh http://hdl.handle.net/20.500.12110/paper_00039861_v113_n2_p265_Mordoh
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic guanidine derivative
oligosaccharide
sodium hydroxide
urea
animal
article
cell fractionation
chemistry
glycogen liver level
heat
in vitro study
molecular weight
rat
ultrasound
Animal
Chemistry
Guanidines
Heat
In Vitro
Liver Glycogen
Molecular Weight
Oligosaccharides
Rats
Sodium Hydroxide
Subcellular Fractions
Ultrasonics
Urea
spellingShingle guanidine derivative
oligosaccharide
sodium hydroxide
urea
animal
article
cell fractionation
chemistry
glycogen liver level
heat
in vitro study
molecular weight
rat
ultrasound
Animal
Chemistry
Guanidines
Heat
In Vitro
Liver Glycogen
Molecular Weight
Oligosaccharides
Rats
Sodium Hydroxide
Subcellular Fractions
Ultrasonics
Urea
Krisman de Fischman, Clara Rebeca
Further studies on high molecular weight liver glycogen
topic_facet guanidine derivative
oligosaccharide
sodium hydroxide
urea
animal
article
cell fractionation
chemistry
glycogen liver level
heat
in vitro study
molecular weight
rat
ultrasound
Animal
Chemistry
Guanidines
Heat
In Vitro
Liver Glycogen
Molecular Weight
Oligosaccharides
Rats
Sodium Hydroxide
Subcellular Fractions
Ultrasonics
Urea
description A simple method for the extraction of undegraded liver glycogen is described. The molecular weight distribution curve as measured by gradient centrifugation was quite variable and was found to be unrelated to glycogen content. The concentration of malto-oligosaccharides in liver was estimated by a new method and was found to remain constant under conditions in which glycogen content varied considerably. Native glycogen was compared with that prepared in vitro with purified enzymes. Although both preparations were similar in molecular weight and in their appearance under the electron microscope, they differed in the type of breakdown produced by acid, alkali, heat, and ultrasonic vibrations. When glycogen prepared in vitro was submitted to these procedures, its sedimentation coefficient decreased progressively, while native glycogen was broken down preferentially to a lighter population of about S = 100. © 1966.
author Krisman de Fischman, Clara Rebeca
author_facet Krisman de Fischman, Clara Rebeca
author_sort Krisman de Fischman, Clara Rebeca
title Further studies on high molecular weight liver glycogen
title_short Further studies on high molecular weight liver glycogen
title_full Further studies on high molecular weight liver glycogen
title_fullStr Further studies on high molecular weight liver glycogen
title_full_unstemmed Further studies on high molecular weight liver glycogen
title_sort further studies on high molecular weight liver glycogen
publishDate 1966
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00039861_v113_n2_p265_Mordoh
http://hdl.handle.net/20.500.12110/paper_00039861_v113_n2_p265_Mordoh
work_keys_str_mv AT krismandefischmanclararebeca furtherstudiesonhighmolecularweightliverglycogen
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