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Structural studies of capsular polysaccharide of type XII diplococcus pneumoniae

dc.contributor.authorDuke, Jodie L.en_US
dc.contributor.authorGoldstein, Irwin J.en_US
dc.contributor.authorCifonelli, Joseph A.en_US
dc.date.accessioned2006-04-07T16:43:44Z
dc.date.available2006-04-07T16:43:44Z
dc.date.issued1974-10en_US
dc.identifier.citationDuke, Jodie L., Goldstein, Irwin J., Cifonelli, Joseph A. (1974/10)."Structural studies of capsular polysaccharide of type XII diplococcus pneumoniae." Carbohydrate Research 37(1): 81-88. <http://hdl.handle.net/2027.42/22259>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6TFF-42HPJN7-78/2/d683e95536ecd3bd9c2ef06e6fe86c16en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/22259
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=4154145&dopt=citationen_US
dc.description.abstractThe capsular polysaccharide of Diplococcus pneumoniae Type XII contains residues of -glucose and -galactose in a molar ratio of 2:1. The methylated polysaccharide yielded upon hydrolysis 2,3,4,6-tetra- and 3,4,6-tri-O-methyl--glucose and 2,3,4,6-tetra-O-methyl--galactose as the only neutral methyl sugars. Periodate oxidation of the polysaccharide resulted in destruction of all neutral sugars and immunochemical activity against rabbit antisera. Periodate oxidation of the methyl O-methylglycosides obtained after hydrolysis of the methylated polysaccharide indicated that at least 30% of the -fucosamine residues are substituted at C-4 in the polysaccharide. It is concluded that the polysaccharide consists of a hexosamine backbone that is substituted by -galactosyl and kojibiosyl side-chains. The proposed terminal -galactosyl residues apparently are sterically hindered from interacting with several -galactose-binding proteins.en_US
dc.format.extent591839 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleStructural studies of capsular polysaccharide of type XII diplococcus pneumoniaeen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Biological Chemistry, The University of Michigan Medical School, Ann Arbor, Michigan 48104 U.S.A.en_US
dc.contributor.affiliationumDepartment of Biological Chemistry, The University of Michigan Medical School, Ann Arbor, Michigan 48104 U.S.A.en_US
dc.contributor.affiliationotherLa Rabida Institute, University of Chicago, and Department of Biochemistry, The University of Chicago, Chicago, Illinois 60637 U.S.A.en_US
dc.identifier.pmid4154145en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/22259/1/0000696.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/S0008-6215(00)87065-2en_US
dc.identifier.sourceCarbohydrate Researchen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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