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PMID: 2298487 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Regulation of expression of Streptococcus mutans genes important to virulence.

Infection and immunity ·Vol. 58 ·No. 2 ·1990-02-00 ·Pages 464-70

Hudson MC, Curtiss R

Abstract

Studies were initiated to investigate the regulation of Streptococcus mutans genes which are believed to be important to virulence. Operon fusions were constructed between S. mutans gene regulatory regions and a promoterless chloramphenicol acetyltransferase gene (cat) found on the plasmid pMH109. Specifically, fusions were generated between cat and the S. mutans genes encoding fructosyltransferase (ftf) and the glucosyltransferase B/C (gtfB/C) operon. Constructs were confirmed by restriction enzyme analysis, and the fusions were subcloned into the integration vehicle pVA891. Following generation of multimeric DNA, recombinant plasmids were introduced into the s. mutans genome by Campbell-type insertion, resulting in single-copy operon fusions. Chloramphenicol acetyltransferase specific activities were used to monitor the expression of the S. mutans gtfB/C operon and ftf determinants. The expression of these genes is increased by the presence of sucrose and is followed by a rapid decline in expression over time. Additionally, expression of the gtfB/C operon is increased in S. mutans cells bound to artificial tooth pellicles.

MeSH Terms
Chloramphenicol O-Acetyltransferase/analysis,genetics DNA, Bacterial/analysis Gene Expression Regulation, Bacterial Genes, Bacterial Nucleic Acid Hybridization Operon Plasmids Streptococcus mutans/genetics,pathogenicity Virulence
Chemicals
DNA, Bacterial Chloramphenicol O-Acetyltransferase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Hudson M C
Department of Biology, Washington University, St. Louis, Missouri 63130.
Curtiss R
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Article Info
Journal
Infection and immunity
Abbr.
Infect Immun
ISSN
0019-9567
Published
1990-02-00
Pages
464-70
Language
English
Region
United States
NLM ID
0246127
PMCID
PMC258480
Subset
IM
Grants
NIDCR NIH HHS · DE06801 · United States
NIDCR NIH HHS · F32-DE05493 · United States
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