Source:http://linkedlifedata.com/resource/pubmed/id/12948393
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2003-9-1
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pubmed:abstractText |
The products of the strong alkaline degradation of the lipopolysaccharide (LPS) of Pseudomonas aeruginosa immunotype 5 were separated by anion-exchange HPLC and studied by electrospray ionization mass spectrometry and NMR spectroscopy. It was found that two major products have the same inner core region and lipid A carbohydrate backbone (A) but different outer core regions (B and C). The difference is in the position of a rhamnose residue, which is substituted with either an additional glucose residue (B) or a disaccharide remainder of the degraded O-polysaccharide (C). The site and the configuration of the linkage between the O-polysaccharide and the core were determined and, together with published data, the structure of the so-called biological repeating unit of the O-antigen was defined (D). The glycosidic linkage of the quinovosamine residue is beta when it links the O-polysaccharide to the core (C) and alpha when it connects the interior repeating units of the O-polysaccharide to each other (D) [Formula: see text]. In the structures shown Rha stands for rhamnose, Kdo for 3-deoxy-D-manno-oct-2-ulosonic acid, Hep for L-glycero-D-manno-heptose, GalNAcA for 2-acetamido-2-deoxygalacturonic acid, QuiN for 2-amino-2,6-dideoxyglucose (quinovosamine), DeltaHexNA for 2-amino-2-deoxy-D-threo-hex-4-enuronic acid; all monosaccharides are in the pyranose form and have the D configuration, except for Rha and GalNAcA that have the L configuration. In C, the remainder of the degraded O-polysaccharide is shown in bold type.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/2-acetamido-2,6-dideoxy-glucose...,
http://linkedlifedata.com/resource/pubmed/chemical/Acetylglucosamine,
http://linkedlifedata.com/resource/pubmed/chemical/Lipid A,
http://linkedlifedata.com/resource/pubmed/chemical/Lipopolysaccharides,
http://linkedlifedata.com/resource/pubmed/chemical/O Antigens,
http://linkedlifedata.com/resource/pubmed/chemical/Rhamnose
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0006-2979
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
68
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
918-25
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:12948393-Acetylglucosamine,
pubmed-meshheading:12948393-Lipid A,
pubmed-meshheading:12948393-Lipopolysaccharides,
pubmed-meshheading:12948393-Magnetic Resonance Spectroscopy,
pubmed-meshheading:12948393-O Antigens,
pubmed-meshheading:12948393-Pseudomonas aeruginosa,
pubmed-meshheading:12948393-Rhamnose,
pubmed-meshheading:12948393-Spectrometry, Mass, Electrospray Ionization
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pubmed:year |
2003
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pubmed:articleTitle |
Elucidation of the structure of the lipopolysaccharide core and the linkage between the core and the O-antigen in Pseudomonas aeruginosa immunotype 5 using strong alkaline degradation of the lipopolysaccharide.
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pubmed:affiliation |
Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, 119991 Russia.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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