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Molecular characterization and expression of the cell-associated glucosyltransferase gene from Streptococcus mutans.

作者信息

Fujiwara T, Kawabata S, Hamada S

机构信息

Department of Oral Microbiology, Osaka University Faculty of Dentistry, Japan.

出版信息

Biochem Biophys Res Commun. 1992 Sep 30;187(3):1432-8. doi: 10.1016/0006-291x(92)90462-t.

Abstract

A 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.

摘要

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