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Mutans streptococci are major etiological agents of dental caries, and several of their secreted products contribute to bacterial accumulation on teeth. Of these, Streptococcus mutans glucan binding protein B (GbpB) is a novel, immunologically dominant protein. Its biological function is unclear, although GbpB shares homology with a putative peptidoglycan hydrolase from S. agalactiae and S. pneumoniae, indicative of a role in murein biosynthesis. To determine the cellular function of GbpB, we used several approaches to inactivate the gene, analyze its expression, and identify interacting proteins. None of the transformants analyzed were true gbpB mutants, since they all contained both disrupted and wild-type gene copies, and expression of functional GbpB was always conserved. Thus, the inability to obtain viable gbpB null mutants supports the notion that gbpB is an essential gene. Northern blot and real-time PCR analyses suggested that induction of gbpB expression in response to stress was a strain-dependent phenomenon. Proteins that interacted with GbpB were identified in pull-down and coimmunoprecipitation assays, and these data suggest that GbpB interacts with ribosomal protein L7/L12, possibly as part of a protein complex involved in peptidoglycan synthesis and cell division.
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http://dx.doi.org/10.1128/JB.01845-05 | DOI Listing |
Front Cell Infect Microbiol
December 2024
Department of Biotechnology, Alagappa University, Karaikudi, India.
is a well-recognized bacterium that plays a predominant role in the progression of dental caries. Its pathogenicity is linked to several key characteristics, including the ability to produce organic acids (acidogenicity), thrive in low pH environments (aciduricity), synthesize exopolysaccharides (EPS) glucosyltransferases, and form retentive biofilms. The treatment of dental caries with conventional antibiotics is often ineffective due to the bacterium's capacity to form recalcitrant biofilms.
View Article and Find Full Text PDFBMC Complement Med Ther
November 2024
Department of Operative Dentistry, School of Dentistry, Shahed University, Tehran, Iran.
Background: Biofilm formation has a crucial role in the cariogenic virulence of Streptococcus mutans, which leads to resistance to common antibacterials. The antimicrobial resistance crisis has led to increased research about traditional natural products.
Purpose: Quercus infectoria extract (QI extract) and nano hydrogels containing QI extract (QI-NH) and tannic acid (TA-NH) were evaluated against this pathogen.
Molecules
October 2024
Department of Oral Biochemistry, School of Dentistry, Wonkwang University, Iksan 54538, Republic of Korea.
This study aimed to identify the inhibitory effect of essential oil (AREO) on the cariogenic properties of , which causes dental caries and dental plaque formation. After extracting the AREO, their effects on the growth and acid production of were examined. Furthermore, biofilm formation was observed on the resin teeth surface.
View Article and Find Full Text PDFJ Am Chem Soc
August 2024
Department of Chemistry, Emory University, Atlanta, Georgia 30322, United States.
Natural products are important precursors for antibiotic drug design. These chemical scaffolds serve as synthetic inspiration for chemists who leverage their structures to develop novel antibacterials and chemical probes. We have previously studied carolacton, a natural product macrolactone from, and discovered a simplified derivative, , that maintained apparent biofilm inhibitory activity, although the biological target was unknown.
View Article and Find Full Text PDFInt Dent J
December 2024
Department of Biological Engineering, Sichuan University of Science & Engineering, Zigong, China. Electronic address:
Objective: The purpose of this work was to develop an anti-CAT-SYI immunoglobulin Y (IgY) antibody that targeted both GtfB (glucosyltransferase B) and GbpB (glucan-binding protein B) and test its anticaries properties in rats.
Methods: A new CAT-SYI fusion gene was created utilising functional DNA fragments from the GtfB and GbpB genes. The recombinant antigens, comprising the fused CAT-SYI antigen, GtfB, and GbpB, were expressed and purified using a prokaryotic expression and purification system.
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