scholarly journals Species specificity of O-linked carbohydrate chains of the oviducal mucins in amphibians: structural analysis of neutral oligosaccharide alditols released by reductive β-elimination from the egg-jelly coats of Rana clamitans

2002 ◽  
Vol 363 (3) ◽  
pp. 457 ◽  
Author(s):  
Florence DELPLACE ◽  
Emmanuel MAES ◽  
Jérme LEMOINE ◽  
Gérard STRECKER
2002 ◽  
Vol 363 (3) ◽  
pp. 457-471 ◽  
Author(s):  
Florence DELPLACE ◽  
Emmanuel MAES ◽  
Jérôme LEMOINE ◽  
Gérard STRECKER

The extracellular matrix (the so-called jelly coat) surrounding amphibian eggs mainly comprises highly O-glycosylated proteins. These oviducal mucins have an important role in the fertilization process, and their carbohydrate chains are remarkably species-specific. Alkaline reductive treatment of the jelly-coat material of the frog Rana clamitans led to the release of oligosaccharide alditols. The neutral oligosaccharide alditols were fractionated and purified by successive chromatographic techniques. The structures of 27 of them, ranging from three to sixteen monosaccharides, were established by a combination of NMR spectroscopy, methylation analyses and matrix-assisted laser-desorption ionization—time of flight MS. Typically, some of the neutral compounds appeared to possess the core structure: Gal(β1–3)[GlcNAc(β1–6)]Gal(β1–3)[GlcNAc(β1–6)]GalNAc-ol (where GalNAc-ol represents N-acetylgalactosaminitol). Moreover, a novel type of chain termination, characterized by an unusual sequence {Fuc(α1–2)Gal(α1–3)Gal(α1–4)Gal(β1–3/4)} was observed. Indeed, the most complex representative structure of this series was found to be: Fuc(α1–2)Gal(α1–3)Gal(α1–4)Gal(β1–3)[Fuc(α1–2)Gal(α1–3)Gal(α1–4)Gal(β1–4)GlcNAc(β1–6)]Gal(β1–3)[Fuc(α1–2)Gal(α1–3)Gal(α1–4)Gal(β1–4)GlcNAc(β1–6)]GalNAc-ol.


Glycobiology ◽  
1994 ◽  
Vol 4 (5) ◽  
pp. 605-609 ◽  
Author(s):  
Gèrard Strecker ◽  
Jean Michel ◽  
Wleruszeski ◽  
Marie Dominique ◽  
Fontaine ◽  
...  

1985 ◽  
Vol 232 (3) ◽  
pp. 637-641 ◽  
Author(s):  
B Overdijk ◽  
E P Beem ◽  
G J van Steijn ◽  
L A Trippelvitz ◽  
J J Lisman ◽  
...  

The oligosaccharide structures of bovine brain beta-N-acetylhexosaminidases A and B (EC 3.2.1.30) were studied at the glycopeptide level by employing 500 MHz 1H-n.m.r. spectroscopy and methylation analysis involving g.l.c.-m.s. More than 90% of the chains were found to be of the oligomannoside type, containing, on average, five to six mannose residues. Biantennary N-acetyl-lactosamine-type chains terminated in N-acetylneuraminic acid were found to comprise the remaining 5-10% of the total carbohydrate. The isoenzyme forms A and B do not differ from each other in the structure of their carbohydrate moiety, but do deviate in carbohydrate content and, in consequence, in the number of carbohydrate chains per molecule.


1998 ◽  
Vol 62 (6) ◽  
pp. 1211-1215 ◽  
Author(s):  
Yasushi SHIKATA ◽  
Hiroshi OHE ◽  
Nariyasu MANO ◽  
Manabu KUWADA ◽  
Naoki ASAKAWA

1993 ◽  
Vol 10 (4) ◽  
pp. 284-284
Author(s):  
N. P. Arbatsky ◽  
H. A. Zenkevich ◽  
V. P. Slanke ◽  
Z. M. Latze ◽  
A. O. Zhefova ◽  
...  

2002 ◽  
Vol 337 (2) ◽  
pp. 121-132 ◽  
Author(s):  
Alexandra Coppin ◽  
Emmanuel Maes ◽  
Gérard Strecker

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