pubmed-article:4212286 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:4212286 | lifeskim:mentions | umls-concept:C1265298 | lld:lifeskim |
pubmed-article:4212286 | lifeskim:mentions | umls-concept:C0524984 | lld:lifeskim |
pubmed-article:4212286 | lifeskim:mentions | umls-concept:C0007623 | lld:lifeskim |
pubmed-article:4212286 | lifeskim:mentions | umls-concept:C0003320 | lld:lifeskim |
pubmed-article:4212286 | lifeskim:mentions | umls-concept:C0032594 | lld:lifeskim |
pubmed-article:4212286 | lifeskim:mentions | umls-concept:C1998793 | lld:lifeskim |
pubmed-article:4212286 | lifeskim:mentions | umls-concept:C1880022 | lld:lifeskim |
pubmed-article:4212286 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:4212286 | pubmed:dateCreated | 1974-10-24 | lld:pubmed |
pubmed-article:4212286 | pubmed:abstractText | The Streptococcus mutans group d antigen of strain B13 has been purified and characterized with respect to chemical composition and immunochemical properties. The antigen was extracted from lyophilized cells or cell walls by using 5% trichloroacetic acid at 5 C for 16 h. The antigen could also be extracted with water or 0.01 N HCl at 100 C for 20 min. The antigen was purified by ion-exchange and gel chromatography and was found to contain 96% carbohydrate, 1.6% protein, and 0.3% phosphorus. Characterization by gas chromatography indicated that the polysaccharide was composed of galactose and glucose in a 2:1 ratio. The antigen contained two serologically active sites: one site specific for group d and a second site common to both group d and group a strains. Agar diffusion and immunoelectrophoresis indicated that the two sites existed on a single molecule. The immunological specificity of the group d polysaccharide site depended on a terminal d-galactose. The purified B13 antigen did not react with antisera specific for the glycerol teichoic acid from streptococci. Anti-d serum rapidly agglutinated whole cells, indicating that the antibody receptor sites of the polysaccharide antigen were at the surface of the streptococcal cell. | lld:pubmed |
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pubmed-article:4212286 | pubmed:language | eng | lld:pubmed |
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pubmed-article:4212286 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:4212286 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:4212286 | pubmed:month | Aug | lld:pubmed |
pubmed-article:4212286 | pubmed:issn | 0019-9567 | lld:pubmed |
pubmed-article:4212286 | pubmed:author | pubmed-author:SladeH DHD | lld:pubmed |
pubmed-article:4212286 | pubmed:author | pubmed-author:LinzerRR | lld:pubmed |
pubmed-article:4212286 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:4212286 | pubmed:volume | 10 | lld:pubmed |
pubmed-article:4212286 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:4212286 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:4212286 | pubmed:pagination | 361-8 | lld:pubmed |
pubmed-article:4212286 | pubmed:dateRevised | 2010-9-13 | lld:pubmed |
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pubmed-article:4212286 | pubmed:year | 1974 | lld:pubmed |
pubmed-article:4212286 | pubmed:articleTitle | Purification and characterization of Streptococcus mutans group d cell wall polysaccharide antigen. | lld:pubmed |
pubmed-article:4212286 | pubmed:publicationType | Journal Article | lld:pubmed |
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