Isolation and structural studies of the neutral oligosaccharide units from bovine glycophorin
The O-glycosidically linked carbohydrate units of glycophorin from bovine erythrocyte membranes were released as reduced oligosaccharides by alkaline borohydride treatment. These oligosaccharides were separated by ion-exchange chromatography followed by gel filtration. Three oligosaccharides, a pent...
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Published in | Biochimica et Biophysica Acta (BBA) - General Subjects Vol. 677; no. 3; pp. 462 - 470 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
05.11.1981
Elsevier BV |
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Abstract | The
O-glycosidically linked carbohydrate units of glycophorin from bovine erythrocyte membranes were released as reduced oligosaccharides by alkaline borohydride treatment. These oligosaccharides were separated by ion-exchange chromatography followed by gel filtration. Three oligosaccharides, a penta- a hepta- and a decassacharide were obtained as the major components from the neutral fraction, and seven fractions were separated from the acidic fractions. All of the fractions were found to contain galactose and
N-acetylglucosamine in variable amounts, as well as
N-acetylgalactosaminitol. Studies of the neutral oligosaccharides by methylation analyses, nitrous acid deamination and Amith degradation, indicated the structure of the pentasaccharide to be Gal(1→3)-Gal(1→4)GlcNAc(1→3) Gal(1→3)GalNAcol and that of the heptasaccharide to be Gal91→3)Gal(1→4)-GlcNAc(1→3)Gal(1→4)GlcNAc(1→3)Gal(1→3)GalNAcol. The highest molecular weight fraction, decasaccharide in the neutral fraction had a branching point at C-6 of a galactose residue. |
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AbstractList | The O-glycosidically linked carbohydrate units of glycophorin from bovine erythrocyte membranes were released as reduced oligosaccharides by alkaline borohydride treatment. These oligosaccharides were separated by ion-exchange chromatography followed by gel filtration. Three oligosaccharides, a penta- a hepta- and a decasaccharide were obtained as the major components from the neutral fraction, and seven fractions were separated from the acidic fractions. All of the fractions were found to contain galactose and N-acetylglucosamine in variable amounts, as well as N-acetylgalactosaminitol. Studies of the neutral oligosaccharides by methylation analyses, nitrous acid deamination and Smith degradation, indicated the structure of the pentasaccharide to be Gal(1 leads to 3)Gal(1 leads to 4)GlcNAc(1 leads to 3)GalNAcol and that of the heptasaccharide to be Gal(1 leads to 3)Gal(1 leads to 4)GlcNAc(1 leads to 3)Gal(1 leads to 4)GlcNAc(1 leads to 3)Gal(1 leads to 3)GalNAcol. The highest molecular weight fraction, decasaccharide in the neutral fraction had a branching point at C-6 of a galactose residue. The O-glycosidically linked carbohydrate units of glycophorin from bovine erythrocyte membranes were released as reduced oligosaccharides by alkaline borohydride treatment. These oligosaccharides were separated by ion-exchange chromatography followed by gel filtration. Three oligosaccharides, a penta- a hepta- and a decasaccharide were obtained as the major components from the neutral fraction, and seven fractions were separated from the acidic fractions. All of the fractions were found to contain galactose and N-acetylglucosamine in variable amounts, as well as N-acetylgalactosaminitol. Studies of the neutral oligosaccharides by methylation analyses, nitrous acid deamination and Smith degradation, indicated the structure of the pentasaccharide to be Gal(1 leads to 3)Gal(1 leads to 4)GlcNAc(1 leads to 3)GalNAcol and that of the heptasaccharide to be Gal(1 leads to 3)Gal(1 leads to 4)GlcNAc(1 leads to 3)Gal(1 leads to 4)GlcNAc(1 leads to 3)Gal(1 leads to 3)GalNAcol. The highest molecular weight fraction, decasaccharide in the neutral fraction had a branching point at C-6 of a galactose residue.The O-glycosidically linked carbohydrate units of glycophorin from bovine erythrocyte membranes were released as reduced oligosaccharides by alkaline borohydride treatment. These oligosaccharides were separated by ion-exchange chromatography followed by gel filtration. Three oligosaccharides, a penta- a hepta- and a decasaccharide were obtained as the major components from the neutral fraction, and seven fractions were separated from the acidic fractions. All of the fractions were found to contain galactose and N-acetylglucosamine in variable amounts, as well as N-acetylgalactosaminitol. Studies of the neutral oligosaccharides by methylation analyses, nitrous acid deamination and Smith degradation, indicated the structure of the pentasaccharide to be Gal(1 leads to 3)Gal(1 leads to 4)GlcNAc(1 leads to 3)GalNAcol and that of the heptasaccharide to be Gal(1 leads to 3)Gal(1 leads to 4)GlcNAc(1 leads to 3)Gal(1 leads to 4)GlcNAc(1 leads to 3)Gal(1 leads to 3)GalNAcol. The highest molecular weight fraction, decasaccharide in the neutral fraction had a branching point at C-6 of a galactose residue. The O-glycosidically linked carbohydrate units of glycophorin from bovine erythrocyte membranes were released as reduced oligosaccharides by alkaline borohydride treatment. These oligosaccharides were separated by ion-exchange chromatography followed by gel filtration. Three oligosaccharides, a penta- a hepta- and a decassacharide were obtained as the major components from the neutral fraction, and seven fractions were separated from the acidic fractions. All of the fractions were found to contain galactose and N-acetylglucosamine in variable amounts, as well as N-acetylgalactosaminitol. Studies of the neutral oligosaccharides by methylation analyses, nitrous acid deamination and Amith degradation, indicated the structure of the pentasaccharide to be Gal(1→3)-Gal(1→4)GlcNAc(1→3) Gal(1→3)GalNAcol and that of the heptasaccharide to be Gal91→3)Gal(1→4)-GlcNAc(1→3)Gal(1→4)GlcNAc(1→3)Gal(1→3)GalNAcol. The highest molecular weight fraction, decasaccharide in the neutral fraction had a branching point at C-6 of a galactose residue. |
Author | Akira Hamada Motowo Tomita Kayoko Fukuda |
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CitedBy_id | crossref_primary_10_1016_0304_4165_83_90269_6 crossref_primary_10_1016_0008_6215_87_80221_5 crossref_primary_10_1007_BF01048330 crossref_primary_10_1016_0304_4165_85_90177_1 crossref_primary_10_1016_0304_4165_84_90205_8 crossref_primary_10_1016_S0021_9258_19_57237_4 crossref_primary_10_1016_0304_4165_87_90229_7 crossref_primary_10_1016_0304_4165_82_90180_5 crossref_primary_10_1111_j_1432_1033_1986_tb09482_x crossref_primary_10_1016_0008_6215_88_80100_9 crossref_primary_10_1111_j_1432_1033_1982_tb06694_x |
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Keywords | Oligosaccharide structure Glycophorin Bovine erthrocyte |
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O-glycosidically linked carbohydrate units of glycophorin from bovine erythrocyte membranes were released as reduced oligosaccharides by alkaline... The O-glycosidically linked carbohydrate units of glycophorin from bovine erythrocyte membranes were released as reduced oligosaccharides by alkaline... |
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SubjectTerms | Animals Borohydrides Bovine erthrocyte Carbohydrate Conformation Carbohydrates Carbohydrates - analysis Cattle Chemical Phenomena Chemistry Chromatography, Gel Chromium Chromium Compounds Glycophorin Glycophorin - analysis Glycophorins Hydrolysis Methylation Oligosaccharide structure Oligosaccharides Oligosaccharides - isolation & purification Oxides Sialoglycoproteins Sialoglycoproteins - analysis |
Title | Isolation and structural studies of the neutral oligosaccharide units from bovine glycophorin |
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