TY - JOUR
T1 - Structural studies on the carbohydrate units of armadillo submandibular glycoprotein
AU - Wu, Albert M.
AU - Slomiany, Amalia
AU - Herp, Anthony
AU - Slomiany, Bronislaw L.
PY - 1979/6/19
Y1 - 1979/6/19
N2 - The structure of carbohydrate units of the major glycoprotein fraction of armadillo submandibular gland was investigated. Alkaline borohydride reductive cleavage of the glycoprotein resulted in the release of O-glycosidically linked mono- and disaccharide units. The monosaccharide was identified as N-acetylgalactosaminitol, whereas disaccharide contained of N-acetylneuraminic acid and N-acetylgalactosaminitol. Treatment of the native and desialyzed glycoprotein with α-N-acetylgalactosaminidase resulted in the removal of 60% and 96% of N-acetylgalactosamine, respectively. No cleavage of this sugar was affected by the action of β-N-acetylhexosaminidase. Both, N-acetylgalactosamine and N-acetylneuraminic acid were susceptible to oxidation with periodate. Analyses of the partially methylated N-acetylgalactosamine derivatives, obtained from the permethylated native glycoprotein, showed the presence of 3,4,6-tri-O-methyl-N-methylacetamidogalactose and 3,4-di-O-methyl-N-methylacetamidogalactose in a ratio of 1 : 0.4. Only 3,4,6-tri-O-methyl-N-methylacetamidogalactose was found in the hydrolysates of permethylated desialyzed glycoprotein. These results together with our previous data on chemical composition of the glycoprotein suggest that about 30% of the oligosaccharide chains consist of NeuAcα2 → 6GalNAcα1 → O-Thr(Ser) and 70% of GalNAcα → O-Thr(Ser).
AB - The structure of carbohydrate units of the major glycoprotein fraction of armadillo submandibular gland was investigated. Alkaline borohydride reductive cleavage of the glycoprotein resulted in the release of O-glycosidically linked mono- and disaccharide units. The monosaccharide was identified as N-acetylgalactosaminitol, whereas disaccharide contained of N-acetylneuraminic acid and N-acetylgalactosaminitol. Treatment of the native and desialyzed glycoprotein with α-N-acetylgalactosaminidase resulted in the removal of 60% and 96% of N-acetylgalactosamine, respectively. No cleavage of this sugar was affected by the action of β-N-acetylhexosaminidase. Both, N-acetylgalactosamine and N-acetylneuraminic acid were susceptible to oxidation with periodate. Analyses of the partially methylated N-acetylgalactosamine derivatives, obtained from the permethylated native glycoprotein, showed the presence of 3,4,6-tri-O-methyl-N-methylacetamidogalactose and 3,4-di-O-methyl-N-methylacetamidogalactose in a ratio of 1 : 0.4. Only 3,4,6-tri-O-methyl-N-methylacetamidogalactose was found in the hydrolysates of permethylated desialyzed glycoprotein. These results together with our previous data on chemical composition of the glycoprotein suggest that about 30% of the oligosaccharide chains consist of NeuAcα2 → 6GalNAcα1 → O-Thr(Ser) and 70% of GalNAcα → O-Thr(Ser).
KW - (Armadillo submandibular)
KW - Carbohydrate unit
KW - Exoglycosidase
KW - Glycoprotein
KW - Salivary mucin
UR - http://www.scopus.com/inward/record.url?scp=0018772222&partnerID=8YFLogxK
U2 - 10.1016/0005-2795(79)90160-0
DO - 10.1016/0005-2795(79)90160-0
M3 - 文章
C2 - 486529
AN - SCOPUS:0018772222
SN - 0005-2795
VL - 578
SP - 297
EP - 304
JO - BBA - Protein Structure
JF - BBA - Protein Structure
IS - 2
ER -