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Glycobiology Advance Access originally published online on June 2, 2005
Glycobiology 2005 15(10):895-904,; doi:10.1093/glycob/cwi084
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© Published by Oxford University Press 2005.

Structures of the O-linked oligosaccharides of a complex glycoconjugate from Pseudallescheria boydii

Marcia R. Pinto2, Philip A.J. Gorin3, Robin Wait4, Barbara Mulloy5 and Eliana Barreto-Bergter1,2

2 Instituto de Microbiologia, Universidade Federal do Rio de Janeiro, CCS, Bloco I, Ilha do Fundão, Rio de Janeiro, RJ 21941-970, Brazil; 3 Departamento de Bioquímica e Biologia Molecular, Universidade Federal do Paraná (UFPR), Curitiba, PR 81531-990, Brazil; 4 Faculty of Medicine, Kennedy Institute of Rheumatology Division, Imperial College London, 1, Aspenlea Road, Hammersmith, London W6 8LH, UK; and 5 Laboratory for Molecular Structure, National Institute for Biological Standards and Control, Blanche Lane, South Mimms, Potters Bar, Hertfordshire EN6 3QG, UK


1 To whom correspondence should be addressed; e-mail: eliana.bergter{at}micro.ufrj.br

Received on November 8, 2004; revised on May 20, 2005; accepted on May 23, 2005

Nonreducing O-linked oligosaccharides were obtained from the peptidorhamnomannan of mycelia of Pseudallescheria boydii by alkaline ß-elimination under reducing conditions. They were separated by gel filtration chromatography to give three oligosaccharide fractions. The major oligosaccharide from fraction 1 was characterized by a combination of techniques including electrospray ionization quadrupole time-of-flight tandem mass spectrometry (ESI MS/MS), matrix-assisted laser desorption ionization mass spectrometry (MALDI MS), nuclear magnetic resonance (NMR), and methylation gas–liquid chromatography-mass spectrometry (GC-MS) analysis. It was branched, with a principal chain of {alpha}-Rhap-(1 -> 3)-{alpha}-Rhap-(1 -> 3)-{alpha}-Manp-(1 -> 2)-Man-ol substituted at O-6 of mannitol with an {alpha}-Glcp-(1 -> 4)-ß-Galp group. Species containing one and two additional {alpha}-Glcp-(1 -> 4) substituents in the rhamnose branch were also present. The major component of fraction 2 was a substructure of oligosaccharide-1, lacking a hexose from the Glc-Gal branch. Fraction 3 contained a mixture of smaller, unbranched, oligosaccharides. In hapten inhibition tests, fractions 1 and 2 blocked the reaction between peptidorhamnomannan (PRM) and rabbit anti-P. boydii mycelium hyperimmune serum by ~75%, whereas fraction 3 inhibited by ~55%.

Key words: ELISA / ESI MS / MS / MALDI MS / methylation-GC-MS / Pseudallescheria boydii mycelia


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C. R. Thornton
Tracking the Emerging Human Pathogen Pseudallescheria boydii by Using Highly Specific Monoclonal Antibodies
Clin. Vaccine Immunol., May 1, 2009; 16(5): 756 - 764.
[Abstract] [Full Text] [PDF]



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