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pubmed-article:1417819pubmed:abstractTextA gene encoding cell-associated glucosyltransferase (CA-GTase) was cloned from Streptococcus mutans MT8148 into Escherichia coli DH5 alpha by using a low-copy-number plasmid, pMW119. After screening of a gene library with the oligonucleotide probe designed on the basis of a partial amino acid sequence of CA-GTase, a recombinant plasmid, pSK6, that had a 5.6 kb insert carrying the CA-GTase gene was selected. The gene product (recombinant CA-GTase) of pSK6 was expressed by using a lac promoter in pMW119. Western blotting revealed that rCA-GTase reacted with antibody to CA-GTase. rCA-GTase was found to synthesize water-insoluble glucans. Southern blotting indicated that the MT8148 chromosome contained another gene which was homologous to pSK6. A plasmid harboring this gene (pSK16) was also isolated from the gene library, the gene product of pSK16 exhibited GTase activity but ten times lower than that of pSK6.lld:pubmed
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pubmed-article:1417819pubmed:pagination1432-8lld:pubmed
pubmed-article:1417819pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:1417819pubmed:articleTitleMolecular characterization and expression of the cell-associated glucosyltransferase gene from Streptococcus mutans.lld:pubmed
pubmed-article:1417819pubmed:affiliationDepartment of Oral Microbiology, Osaka University Faculty of Dentistry, Japan.lld:pubmed
pubmed-article:1417819pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1417819pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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