http://www.cnr.it/ontology/cnr/individuo/prodotto/ID210701
Structural Study of the Lipopolysaccharide O-Antigen Produced by the Emerging Cystic Fibrosis Pathogen Pandoraea pulmonicola (Articolo in rivista)
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- Structural Study of the Lipopolysaccharide O-Antigen Produced by the Emerging Cystic Fibrosis Pathogen Pandoraea pulmonicola (Articolo in rivista) (literal)
- Anno
- 2012-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1002/ejoc.201200047 (literal)
- Alternative label
F.Di Lorenzo, A.Silipo, A.Costello, L.Sturiale, D.Garozzo, M.Callaghan, R.Lanzetta, M.Parrilli, S.McClean, A.Molinaro (2012)
Structural Study of the Lipopolysaccharide O-Antigen Produced by the Emerging Cystic Fibrosis Pathogen Pandoraea pulmonicola
in European journal of organic chemistry (Print); Wiley-VCH Verlag Gmbh, Weinheim (Germania)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- F.Di Lorenzo, A.Silipo, A.Costello, L.Sturiale, D.Garozzo, M.Callaghan, R.Lanzetta, M.Parrilli, S.McClean, A.Molinaro (literal)
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- http://onlinelibrary.wiley.com/doi/10.1002/ejoc.201200047/abstract (literal)
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- Dipartimento di Scienze Chimiche, Università di Napoli \"Federico II\", Complesso Universitario Monte S. Angelo, Via Cintia 4, 80126 Napoli, Italy
Centre of Microbial Host Interactions, ITT Dublin, Tallaght, Dublin 24, Ireland
CNR Istituto per la Chimica e la Tecnologia dei Polimeri, Via P. Gaifami 18, 95126 Catania, Italy (literal)
- Titolo
- Structural Study of the Lipopolysaccharide O-Antigen Produced by the Emerging Cystic Fibrosis Pathogen Pandoraea pulmonicola (literal)
- Abstract
- This is the first report on the molecular structure of the O-chain of the lipopolysaccharide produced by the emerging and highly virulent clinical isolate Pandoraea pulmonicola strain LMG 18108, an opportunistic human pathogen in cystic fibrosis patients. Monosaccharide analysis and 2D NMR spectroscopy revealed a novel polysaccharide, the structure of which consists of the trisaccharide repeating unit [->2-?-d-Quip3NAcyl-(1->4)-?-d-GalpNAc-(1->3)-?-d-GlcpNAc-1->]n. The quinovosamine residue was found to be linked by a very unusual acyl substituent, a five-membered-ring acyl residue, the 3-hydroxy-2,3-dimethyl-5-oxoprolyl group. (literal)
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