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Construction of a red fluorescent shuttle vector controlled by recA operon promoter of Streptococcus mutans / 中华口腔医学杂志
Chinese Journal of Stomatology ; (12): 291-295, 2012.
Article in Chinese | WPRIM | ID: wpr-281610
ABSTRACT
<p><b>OBJECTIVE</b>To construct a red fluorescent shuttle vector controlled by recA operon promoter to transform Streptococcus mutans.</p><p><b>METHODS</b>The promoter of recA was amplified from Streptococcus mutans UA159, and connected to plasmid pDsRed2-N1 to construct pRred with a red fluorescent coding gene, which was then inserted into the shuttle vector pDL276 to construct pLRred.</p><p><b>RESULTS</b>pLRred was successfully constructed, and Escherichia coli transformed with the pLRred plasmid could express reporter gene DsRed.</p><p><b>CONCLUSIONS</b>The recombination plasmid pLRred can be used in the further research of the expression of cariogenic virulence factor gene by Streptococcus mutans in biofilm.</p>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Operon / Plasmids / Rec A Recombinases / Streptococcus mutans / Transformation, Bacterial / Recombinant Proteins / Promoter Regions, Genetic / Genes, Reporter / Genes, Essential / Escherichia coli Language: Chinese Journal: Chinese Journal of Stomatology Year: 2012 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Operon / Plasmids / Rec A Recombinases / Streptococcus mutans / Transformation, Bacterial / Recombinant Proteins / Promoter Regions, Genetic / Genes, Reporter / Genes, Essential / Escherichia coli Language: Chinese Journal: Chinese Journal of Stomatology Year: 2012 Type: Article