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bacterial strains s mutans  (ATCC)


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    ATCC bacterial strains s mutans
    Bacterial Strains S Mutans, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 714 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/bacterial+strains+s+mutans/Streptococcus+mutans+Clarke/pm41951384-60-0-4
    Average 95 stars, based on 714 article reviews
    bacterial strains s mutans - by Bioz Stars, 2026-11
    95/100 stars

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    Cell Culture:

    Article Title: Anti-cariogenic property of Carica papaya , Trachyspermum ammi , Caesalpinia crista linn extracts and their effect on human oral keratinocytes
    Article Snippet: .. The bacterial strains S. mutans (American Type Culture Collection [ATCC]-25175); Lactobacillus species (ATCC 4356) and A. viscosus (ATCC 15987) were cultured in the specific culture media-Mitis Salivarius Bacitracin, Man Rogosa Sharpe and Enrichment media, respectively. ..

    other:

    Article Title: In vitro antimicrobial evaluation of toothpastes with natural compounds
    Article Snippet: The bacterial strains S. mutans (ATCC 25175), P. aeruginosa (ATCC 27853), and E. faecalis (ATCC 29212) were used for the antimicrobial analysis.

    Bacteria:

    Article Title: Borneol-grafted poly(amidoamine) dendrimer with dual antimicrobial and enamel-remineralizing activities against early-stage dental caries.
    Article Snippet: .. Bacterial strains S. mutans (ATCC 700610) and S. sanguinis (ATCC 10556) were used as model oral bacteria. .. Both strains were grown statically in brain heart infusion (BHI) broth (Oxoid, Basingstoke, UK) at 37°C in 5% CO2 for 14 h. Suspensions were adjusted to 0.5 McFarland using turbidity standards.



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    ATCC bacterial strains s mutans
    Bacterial Strains S Mutans, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC bacterial strain s mutans ua159
    Inhibitory effect of BBR on the growth of bacteria. ( A ) The MIC and MBC values of BBR against planktonic bacteria. 10 6 CFU/mL bacteria in BHI broth were incubated with final concentrations of BBR ranging from 25 to 400 μg/mL anaerobically at 37°C for 24 h. The MIC was defined as the lowest concentration of BBR that inhibited visible bacterial growth. At the termination of the MIC assay, a volume of the culture was struck on BHIA and incubated to observe growth. The MBC was defined as the lowest concentration that yielded no colony growth by subculturing on BHIA plates. ( B–F ) The 24 h growth curve of planktonic S. mutans <t>UA159,</t> S. mutans ATCC 25175, S. mutans GS-5, S. gordonii DL-1, and S. mitis ATCC 6249 incubated under anaerobic conditions with/without treatment of BBR in a 96-well plate. The absorbance of each well was recorded every hour. ( G and H ) The short-term antibacterial effect of BBR on S. mutans UA159 was assessed by measuring the average number of CFU. S. mutans UA159 was treated with BBR for 5 min ( G ) and 10 min ( H ). The suspensions were then diluted and plated onto BHIA plates and incubated under anaerobic conditions at 37°C for 24 h to determine CFU counts. Values represent the means ± SD from three independent experiments (** P <0.01, *** P <0.001).
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    Inhibitory effect of BBR on the growth of bacteria. ( A ) The MIC and MBC values of BBR against planktonic bacteria. 10 6 CFU/mL bacteria in BHI broth were incubated with final concentrations of BBR ranging from 25 to 400 μg/mL anaerobically at 37°C for 24 h. The MIC was defined as the lowest concentration of BBR that inhibited visible bacterial growth. At the termination of the MIC assay, a volume of the culture was struck on BHIA and incubated to observe growth. The MBC was defined as the lowest concentration that yielded no colony growth by subculturing on BHIA plates. ( B–F ) The 24 h growth curve of planktonic S. mutans <t>UA159,</t> S. mutans ATCC 25175, S. mutans GS-5, S. gordonii DL-1, and S. mitis ATCC 6249 incubated under anaerobic conditions with/without treatment of BBR in a 96-well plate. The absorbance of each well was recorded every hour. ( G and H ) The short-term antibacterial effect of BBR on S. mutans UA159 was assessed by measuring the average number of CFU. S. mutans UA159 was treated with BBR for 5 min ( G ) and 10 min ( H ). The suspensions were then diluted and plated onto BHIA plates and incubated under anaerobic conditions at 37°C for 24 h to determine CFU counts. Values represent the means ± SD from three independent experiments (** P <0.01, *** P <0.001).
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    Inhibitory effect of BBR on the growth of bacteria. ( A ) The MIC and MBC values of BBR against planktonic bacteria. 10 6 CFU/mL bacteria in BHI broth were incubated with final concentrations of BBR ranging from 25 to 400 μg/mL anaerobically at 37°C for 24 h. The MIC was defined as the lowest concentration of BBR that inhibited visible bacterial growth. At the termination of the MIC assay, a volume of the culture was struck on BHIA and incubated to observe growth. The MBC was defined as the lowest concentration that yielded no colony growth by subculturing on BHIA plates. ( B–F ) The 24 h growth curve of planktonic S. mutans <t>UA159,</t> S. mutans ATCC 25175, S. mutans GS-5, S. gordonii DL-1, and S. mitis ATCC 6249 incubated under anaerobic conditions with/without treatment of BBR in a 96-well plate. The absorbance of each well was recorded every hour. ( G and H ) The short-term antibacterial effect of BBR on S. mutans UA159 was assessed by measuring the average number of CFU. S. mutans UA159 was treated with BBR for 5 min ( G ) and 10 min ( H ). The suspensions were then diluted and plated onto BHIA plates and incubated under anaerobic conditions at 37°C for 24 h to determine CFU counts. Values represent the means ± SD from three independent experiments (** P <0.01, *** P <0.001).
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    Inhibitory effect of BBR on the growth of bacteria. ( A ) The MIC and MBC values of BBR against planktonic bacteria. 10 6 CFU/mL bacteria in BHI broth were incubated with final concentrations of BBR ranging from 25 to 400 μg/mL anaerobically at 37°C for 24 h. The MIC was defined as the lowest concentration of BBR that inhibited visible bacterial growth. At the termination of the MIC assay, a volume of the culture was struck on BHIA and incubated to observe growth. The MBC was defined as the lowest concentration that yielded no colony growth by subculturing on BHIA plates. ( B–F ) The 24 h growth curve of planktonic S. mutans <t>UA159,</t> S. mutans ATCC 25175, S. mutans GS-5, S. gordonii DL-1, and S. mitis ATCC 6249 incubated under anaerobic conditions with/without treatment of BBR in a 96-well plate. The absorbance of each well was recorded every hour. ( G and H ) The short-term antibacterial effect of BBR on S. mutans UA159 was assessed by measuring the average number of CFU. S. mutans UA159 was treated with BBR for 5 min ( G ) and 10 min ( H ). The suspensions were then diluted and plated onto BHIA plates and incubated under anaerobic conditions at 37°C for 24 h to determine CFU counts. Values represent the means ± SD from three independent experiments (** P <0.01, *** P <0.001).
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    ATCC bacterial strain s mutans
    Multiple comparison of antibacterial effects of CS-NPs on <t> S. mutans </t> disc agar diffusion. CHX: chlorhexidine; CS-NPs: chitosan nanoparticles. *Statistical significance <0.05. ***Statistical significance <0.001.
    Bacterial Strain S Mutans, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Inhibitory effect of BBR on the growth of bacteria. ( A ) The MIC and MBC values of BBR against planktonic bacteria. 10 6 CFU/mL bacteria in BHI broth were incubated with final concentrations of BBR ranging from 25 to 400 μg/mL anaerobically at 37°C for 24 h. The MIC was defined as the lowest concentration of BBR that inhibited visible bacterial growth. At the termination of the MIC assay, a volume of the culture was struck on BHIA and incubated to observe growth. The MBC was defined as the lowest concentration that yielded no colony growth by subculturing on BHIA plates. ( B–F ) The 24 h growth curve of planktonic S. mutans UA159, S. mutans ATCC 25175, S. mutans GS-5, S. gordonii DL-1, and S. mitis ATCC 6249 incubated under anaerobic conditions with/without treatment of BBR in a 96-well plate. The absorbance of each well was recorded every hour. ( G and H ) The short-term antibacterial effect of BBR on S. mutans UA159 was assessed by measuring the average number of CFU. S. mutans UA159 was treated with BBR for 5 min ( G ) and 10 min ( H ). The suspensions were then diluted and plated onto BHIA plates and incubated under anaerobic conditions at 37°C for 24 h to determine CFU counts. Values represent the means ± SD from three independent experiments (** P <0.01, *** P <0.001).

    Journal: Microbiology Spectrum

    Article Title: Inhibitory effects of berberine against Streptococcus mutans : an in vitro insight on its anticaries potential

    doi: 10.1128/spectrum.00700-25

    Figure Lengend Snippet: Inhibitory effect of BBR on the growth of bacteria. ( A ) The MIC and MBC values of BBR against planktonic bacteria. 10 6 CFU/mL bacteria in BHI broth were incubated with final concentrations of BBR ranging from 25 to 400 μg/mL anaerobically at 37°C for 24 h. The MIC was defined as the lowest concentration of BBR that inhibited visible bacterial growth. At the termination of the MIC assay, a volume of the culture was struck on BHIA and incubated to observe growth. The MBC was defined as the lowest concentration that yielded no colony growth by subculturing on BHIA plates. ( B–F ) The 24 h growth curve of planktonic S. mutans UA159, S. mutans ATCC 25175, S. mutans GS-5, S. gordonii DL-1, and S. mitis ATCC 6249 incubated under anaerobic conditions with/without treatment of BBR in a 96-well plate. The absorbance of each well was recorded every hour. ( G and H ) The short-term antibacterial effect of BBR on S. mutans UA159 was assessed by measuring the average number of CFU. S. mutans UA159 was treated with BBR for 5 min ( G ) and 10 min ( H ). The suspensions were then diluted and plated onto BHIA plates and incubated under anaerobic conditions at 37°C for 24 h to determine CFU counts. Values represent the means ± SD from three independent experiments (** P <0.01, *** P <0.001).

    Article Snippet: The bacterial strain S. mutans UA159 was obtained from the American Type Culture Collection (ATCC).

    Techniques: Bacteria, Incubation, Concentration Assay, Subculturing Assay

    Effect of BBR on the biofilm formation of S. mutans . In these assays, BBR was incubated with S. mutans in BHIS for 24 h to evaluate its effect on the biofilm formation. ( A ) The crystal violet staining of S. mutans 24 h biofilms under the treatment of BBR. The images were taken from a 24-well cell culture plate. ( B ) The results of the crystal violet staining assay applied to S. mutans biofilms after treated with different concentrations of BBR for 24 h in BHIS. ( C ) SEM micro-images of S. mutans 24 h biofilms on glass coverslips. In the control group, S. mutans bacteria formed dense biofilms covered with large amounts of EPS (red arrows). Disrupted biofilm skeleton (yellow arrows) and enlarged biofilm pores (green arrows) were observed under the treatment of 50 µg/mL of BBR. Only a small number of morphologically irregular S. mutans and cell contents were observed under the treatment of 100 µg/mL and 200 µg/mL of BBR (purple arrows). Values represent the means ± SD from three independent experiments (*** P <0.001).

    Journal: Microbiology Spectrum

    Article Title: Inhibitory effects of berberine against Streptococcus mutans : an in vitro insight on its anticaries potential

    doi: 10.1128/spectrum.00700-25

    Figure Lengend Snippet: Effect of BBR on the biofilm formation of S. mutans . In these assays, BBR was incubated with S. mutans in BHIS for 24 h to evaluate its effect on the biofilm formation. ( A ) The crystal violet staining of S. mutans 24 h biofilms under the treatment of BBR. The images were taken from a 24-well cell culture plate. ( B ) The results of the crystal violet staining assay applied to S. mutans biofilms after treated with different concentrations of BBR for 24 h in BHIS. ( C ) SEM micro-images of S. mutans 24 h biofilms on glass coverslips. In the control group, S. mutans bacteria formed dense biofilms covered with large amounts of EPS (red arrows). Disrupted biofilm skeleton (yellow arrows) and enlarged biofilm pores (green arrows) were observed under the treatment of 50 µg/mL of BBR. Only a small number of morphologically irregular S. mutans and cell contents were observed under the treatment of 100 µg/mL and 200 µg/mL of BBR (purple arrows). Values represent the means ± SD from three independent experiments (*** P <0.001).

    Article Snippet: The bacterial strain S. mutans UA159 was obtained from the American Type Culture Collection (ATCC).

    Techniques: Incubation, Staining, Cell Culture, Control, Bacteria

    Quantification of S. mutans biofilm after treatment of BBR. ( A ) Double-labeling imaging of S. mutans 24 h biofilms formed on glass coverslips. Live bacteria were green-labeled, and dead bacteria were red-labeled. ( B ) BBR reduced the proportion of live bacteria in S. mutans biofilms. ( C ) The effect of BBR on S. mutans biofilm formation was assessed by measuring the average number of CFU in the biofilm in one well of the culture plate. The analysis was performed using Image J COMSTAT software. Values represent the means ± SD from three independent experiments (*** P <0.001).

    Journal: Microbiology Spectrum

    Article Title: Inhibitory effects of berberine against Streptococcus mutans : an in vitro insight on its anticaries potential

    doi: 10.1128/spectrum.00700-25

    Figure Lengend Snippet: Quantification of S. mutans biofilm after treatment of BBR. ( A ) Double-labeling imaging of S. mutans 24 h biofilms formed on glass coverslips. Live bacteria were green-labeled, and dead bacteria were red-labeled. ( B ) BBR reduced the proportion of live bacteria in S. mutans biofilms. ( C ) The effect of BBR on S. mutans biofilm formation was assessed by measuring the average number of CFU in the biofilm in one well of the culture plate. The analysis was performed using Image J COMSTAT software. Values represent the means ± SD from three independent experiments (*** P <0.001).

    Article Snippet: The bacterial strain S. mutans UA159 was obtained from the American Type Culture Collection (ATCC).

    Techniques: Labeling, Imaging, Bacteria, Software

    Effect of BBR on eradicating the S. mutans mature biofilms. ( A ) Double-labeling imaging of S. mutans mature biofilms treated with BBR. Live and dead bacteria were green-labeled and red-labeled, respectively. ( B ) BBR decreases the proportion of live bacteria in S. mutans mature biofilms. ( C ) The effect of BBR on eradicating the S. mutans mature biofilms was measured by the determination of the average number of CFUs in the biofilm. The S. mutans biofilms were cultured for 24 h without BBR. Then, BBR solution was added to each well for another 24 h. The data were collected at 48 h. The analysis was performed using Image J COMSTAT software. Values represent the means ± SD from three independent experiments (*** P <0.001).

    Journal: Microbiology Spectrum

    Article Title: Inhibitory effects of berberine against Streptococcus mutans : an in vitro insight on its anticaries potential

    doi: 10.1128/spectrum.00700-25

    Figure Lengend Snippet: Effect of BBR on eradicating the S. mutans mature biofilms. ( A ) Double-labeling imaging of S. mutans mature biofilms treated with BBR. Live and dead bacteria were green-labeled and red-labeled, respectively. ( B ) BBR decreases the proportion of live bacteria in S. mutans mature biofilms. ( C ) The effect of BBR on eradicating the S. mutans mature biofilms was measured by the determination of the average number of CFUs in the biofilm. The S. mutans biofilms were cultured for 24 h without BBR. Then, BBR solution was added to each well for another 24 h. The data were collected at 48 h. The analysis was performed using Image J COMSTAT software. Values represent the means ± SD from three independent experiments (*** P <0.001).

    Article Snippet: The bacterial strain S. mutans UA159 was obtained from the American Type Culture Collection (ATCC).

    Techniques: Labeling, Imaging, Bacteria, Cell Culture, Software

    BBR inhibited S. mutans virulence factors. ( A ) Effect of BBR on the biofilm structure of S. mutans observed by CLSM. Double-labeling imaging of S. mutans 24 h biofilm formed on glass coverslips. The fluorescence (SYTO 9) marks the live bacteria, while the red fluorescence (Concanavalin A-TRITC) marks the EPS synthesized by S. mutans . ( B ) Quantification of the amounts of EPS and bacteria in each scanned layer of S. mutans 24 h biofilm without the treatment of BBR. ( C ) Quantification of the amounts of EPS and bacteria in each scanned layer of S. mutans 24 h biofilm with the treatment of 50 µg/mL BBR. ( D ) Quantitative measurement of water-insoluble EPS by anthrone-sulfuric method. ( E ) Measurement of lactic acid production. ( F and G ) Effect of BBR on S. mutans glycolytic pH drop under 1% ( F ) and 0.1% ( G ) glucose. Values represent the means ± SD from three independent experiments (*** P <0.001).

    Journal: Microbiology Spectrum

    Article Title: Inhibitory effects of berberine against Streptococcus mutans : an in vitro insight on its anticaries potential

    doi: 10.1128/spectrum.00700-25

    Figure Lengend Snippet: BBR inhibited S. mutans virulence factors. ( A ) Effect of BBR on the biofilm structure of S. mutans observed by CLSM. Double-labeling imaging of S. mutans 24 h biofilm formed on glass coverslips. The fluorescence (SYTO 9) marks the live bacteria, while the red fluorescence (Concanavalin A-TRITC) marks the EPS synthesized by S. mutans . ( B ) Quantification of the amounts of EPS and bacteria in each scanned layer of S. mutans 24 h biofilm without the treatment of BBR. ( C ) Quantification of the amounts of EPS and bacteria in each scanned layer of S. mutans 24 h biofilm with the treatment of 50 µg/mL BBR. ( D ) Quantitative measurement of water-insoluble EPS by anthrone-sulfuric method. ( E ) Measurement of lactic acid production. ( F and G ) Effect of BBR on S. mutans glycolytic pH drop under 1% ( F ) and 0.1% ( G ) glucose. Values represent the means ± SD from three independent experiments (*** P <0.001).

    Article Snippet: The bacterial strain S. mutans UA159 was obtained from the American Type Culture Collection (ATCC).

    Techniques: Labeling, Imaging, Fluorescence, Bacteria, Synthesized

    The bactericidal mechanism of BBR on S. mutans . ( A ) Effect of BBR on aggregation. ( B ) Membrane depolarization activity of BBR was tested using DiSC3(5). ( C ) TEM micrographs of S. mutans . Values represent the means ± SD from three independent experiments (* P <0.05, *** P <0.001).

    Journal: Microbiology Spectrum

    Article Title: Inhibitory effects of berberine against Streptococcus mutans : an in vitro insight on its anticaries potential

    doi: 10.1128/spectrum.00700-25

    Figure Lengend Snippet: The bactericidal mechanism of BBR on S. mutans . ( A ) Effect of BBR on aggregation. ( B ) Membrane depolarization activity of BBR was tested using DiSC3(5). ( C ) TEM micrographs of S. mutans . Values represent the means ± SD from three independent experiments (* P <0.05, *** P <0.001).

    Article Snippet: The bacterial strain S. mutans UA159 was obtained from the American Type Culture Collection (ATCC).

    Techniques: Membrane, Activity Assay

    Effects of BBR on S. mutans gene expression. The relative mRNA expressions of gtfB , gtfC , gtfD , ldh , vicR , liaR , and comD were measured by qRT-PCR. S. mutans UA159 16S rRNA was used as an internal control. Values represent the means ± SD from three independent experiments (*** P <0.001, ns, not statistically significant compared to the untreated control group).

    Journal: Microbiology Spectrum

    Article Title: Inhibitory effects of berberine against Streptococcus mutans : an in vitro insight on its anticaries potential

    doi: 10.1128/spectrum.00700-25

    Figure Lengend Snippet: Effects of BBR on S. mutans gene expression. The relative mRNA expressions of gtfB , gtfC , gtfD , ldh , vicR , liaR , and comD were measured by qRT-PCR. S. mutans UA159 16S rRNA was used as an internal control. Values represent the means ± SD from three independent experiments (*** P <0.001, ns, not statistically significant compared to the untreated control group).

    Article Snippet: The bacterial strain S. mutans UA159 was obtained from the American Type Culture Collection (ATCC).

    Techniques: Gene Expression, Quantitative RT-PCR, Control

    Journal: Microbiology Spectrum

    Article Title: Inhibitory effects of berberine against Streptococcus mutans : an in vitro insight on its anticaries potential

    doi: 10.1128/spectrum.00700-25

    Figure Lengend Snippet: Sequences of primers used in this study

    Article Snippet: The bacterial strain S. mutans UA159 was obtained from the American Type Culture Collection (ATCC).

    Techniques:

    Multiple comparison of antibacterial effects of CS-NPs on  S. mutans  disc agar diffusion. CHX: chlorhexidine; CS-NPs: chitosan nanoparticles. *Statistical significance <0.05. ***Statistical significance <0.001.

    Journal: Cureus

    Article Title: Antibacterial Activity and Shear Bond Strength of Orthodontic Adhesive Containing Various Sizes of Chitosan Nanoparticles: An In Vitro Study

    doi: 10.7759/cureus.54098

    Figure Lengend Snippet: Multiple comparison of antibacterial effects of CS-NPs on S. mutans disc agar diffusion. CHX: chlorhexidine; CS-NPs: chitosan nanoparticles. *Statistical significance <0.05. ***Statistical significance <0.001.

    Article Snippet: Bacterial strain growth conditions and collection The bacterial strain S. mutans (ATCC© 25175TM) was purchased from the American Type Culture Collection (ATCC, Manassas, VA, USA).

    Techniques: Comparison, Diffusion-based Assay, Control