escherichia coli rshm 4024  (ATCC)


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    ATCC escherichia coli rshm 4024
    Escherichia Coli Rshm 4024, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    escherichia coli  (ATCC)


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    ATCC escherichia coli
    Escherichia Coli, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    escherichia coli  (ATCC)


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    ATCC escherichia coli
    Escherichia Coli, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    escherichia coli mg 1655  (ATCC)


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    ATCC escherichia coli mg 1655
    Antimicrobial activity of MEs and the maximal MEs concentrations used (different MEs from M. purpureus (R) and Monascus sp. (C); for their complete description see Table ). Antimicrobial activity against Bacillus subtilis ATCC 6633 ( a ) and <t>Escherichia</t> <t>coli</t> MG1655 ( b ), under dark conditions and after irradiation is demonstrated as MBC values. All data are stated as the mean of at least three independent experiments and the bars represent standard deviations. The statistical analysis was performed using one-way ANOVA (* p < 0.05). Concentrations of MEs corresponding to the presented data are shown in Supplementary material—Table . The symbols represent: (•) the MBC values achieved under dark conditions; (•) the MBC values achieved under light conditions; (∆) the highest used concentration of MEs (6%) with no inhibition observed under dark conditions (values on the secondary y-axis), concentrations corresponding to 6% of MEs was used for one-way ANOVA statistical analysis; (∆) the highest used concentration of MEs (6%) with no inhibition observed under light conditions (values on the secondary y-axis), concentration corresponding to 6% of MEs was used for one-way ANOVA statistical analysis
    Escherichia Coli Mg 1655, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Screening Antibacterial Photodynamic Effect of Monascus Red Yeast Rice (Hong-Qu) and Mycelium Extracts"

    Article Title: Screening Antibacterial Photodynamic Effect of Monascus Red Yeast Rice (Hong-Qu) and Mycelium Extracts

    Journal: Current Microbiology

    doi: 10.1007/s00284-024-03725-6

    Antimicrobial activity of MEs and the maximal MEs concentrations used (different MEs from M. purpureus (R) and Monascus sp. (C); for their complete description see Table ). Antimicrobial activity against Bacillus subtilis ATCC 6633 ( a ) and Escherichia coli MG1655 ( b ), under dark conditions and after irradiation is demonstrated as MBC values. All data are stated as the mean of at least three independent experiments and the bars represent standard deviations. The statistical analysis was performed using one-way ANOVA (* p < 0.05). Concentrations of MEs corresponding to the presented data are shown in Supplementary material—Table . The symbols represent: (•) the MBC values achieved under dark conditions; (•) the MBC values achieved under light conditions; (∆) the highest used concentration of MEs (6%) with no inhibition observed under dark conditions (values on the secondary y-axis), concentrations corresponding to 6% of MEs was used for one-way ANOVA statistical analysis; (∆) the highest used concentration of MEs (6%) with no inhibition observed under light conditions (values on the secondary y-axis), concentration corresponding to 6% of MEs was used for one-way ANOVA statistical analysis
    Figure Legend Snippet: Antimicrobial activity of MEs and the maximal MEs concentrations used (different MEs from M. purpureus (R) and Monascus sp. (C); for their complete description see Table ). Antimicrobial activity against Bacillus subtilis ATCC 6633 ( a ) and Escherichia coli MG1655 ( b ), under dark conditions and after irradiation is demonstrated as MBC values. All data are stated as the mean of at least three independent experiments and the bars represent standard deviations. The statistical analysis was performed using one-way ANOVA (* p < 0.05). Concentrations of MEs corresponding to the presented data are shown in Supplementary material—Table . The symbols represent: (•) the MBC values achieved under dark conditions; (•) the MBC values achieved under light conditions; (∆) the highest used concentration of MEs (6%) with no inhibition observed under dark conditions (values on the secondary y-axis), concentrations corresponding to 6% of MEs was used for one-way ANOVA statistical analysis; (∆) the highest used concentration of MEs (6%) with no inhibition observed under light conditions (values on the secondary y-axis), concentration corresponding to 6% of MEs was used for one-way ANOVA statistical analysis

    Techniques Used: Activity Assay, Irradiation, Concentration Assay, Inhibition

    resistance against escherichia coli o157 h7  (ATCC)


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    ATCC resistance against escherichia coli o157 h7
    Resistance Against Escherichia Coli O157 H7, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    escherichia coli mg1655  (ATCC)


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    ATCC escherichia coli mg1655
    Antimicrobial activity of MEs and the maximal MEs concentrations used (different MEs from M. purpureus (R) and Monascus sp. (C); for their complete description see Table ). Antimicrobial activity against Bacillus subtilis ATCC 6633 ( a ) and <t>Escherichia</t> <t>coli</t> <t>MG1655</t> ( b ), under dark conditions and after irradiation is demonstrated as MBC values. All data are stated as the mean of at least three independent experiments and the bars represent standard deviations. The statistical analysis was performed using one-way ANOVA (* p < 0.05). Concentrations of MEs corresponding to the presented data are shown in Supplementary material—Table . The symbols represent: (•) the MBC values achieved under dark conditions; (•) the MBC values achieved under light conditions; (∆) the highest used concentration of MEs (6%) with no inhibition observed under dark conditions (values on the secondary y-axis), concentrations corresponding to 6% of MEs was used for one-way ANOVA statistical analysis; (∆) the highest used concentration of MEs (6%) with no inhibition observed under light conditions (values on the secondary y-axis), concentration corresponding to 6% of MEs was used for one-way ANOVA statistical analysis
    Escherichia Coli Mg1655, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Screening Antibacterial Photodynamic Effect of Monascus Red Yeast Rice (Hong-Qu) and Mycelium Extracts"

    Article Title: Screening Antibacterial Photodynamic Effect of Monascus Red Yeast Rice (Hong-Qu) and Mycelium Extracts

    Journal: Current Microbiology

    doi: 10.1007/s00284-024-03725-6

    Antimicrobial activity of MEs and the maximal MEs concentrations used (different MEs from M. purpureus (R) and Monascus sp. (C); for their complete description see Table ). Antimicrobial activity against Bacillus subtilis ATCC 6633 ( a ) and Escherichia coli MG1655 ( b ), under dark conditions and after irradiation is demonstrated as MBC values. All data are stated as the mean of at least three independent experiments and the bars represent standard deviations. The statistical analysis was performed using one-way ANOVA (* p < 0.05). Concentrations of MEs corresponding to the presented data are shown in Supplementary material—Table . The symbols represent: (•) the MBC values achieved under dark conditions; (•) the MBC values achieved under light conditions; (∆) the highest used concentration of MEs (6%) with no inhibition observed under dark conditions (values on the secondary y-axis), concentrations corresponding to 6% of MEs was used for one-way ANOVA statistical analysis; (∆) the highest used concentration of MEs (6%) with no inhibition observed under light conditions (values on the secondary y-axis), concentration corresponding to 6% of MEs was used for one-way ANOVA statistical analysis
    Figure Legend Snippet: Antimicrobial activity of MEs and the maximal MEs concentrations used (different MEs from M. purpureus (R) and Monascus sp. (C); for their complete description see Table ). Antimicrobial activity against Bacillus subtilis ATCC 6633 ( a ) and Escherichia coli MG1655 ( b ), under dark conditions and after irradiation is demonstrated as MBC values. All data are stated as the mean of at least three independent experiments and the bars represent standard deviations. The statistical analysis was performed using one-way ANOVA (* p < 0.05). Concentrations of MEs corresponding to the presented data are shown in Supplementary material—Table . The symbols represent: (•) the MBC values achieved under dark conditions; (•) the MBC values achieved under light conditions; (∆) the highest used concentration of MEs (6%) with no inhibition observed under dark conditions (values on the secondary y-axis), concentrations corresponding to 6% of MEs was used for one-way ANOVA statistical analysis; (∆) the highest used concentration of MEs (6%) with no inhibition observed under light conditions (values on the secondary y-axis), concentration corresponding to 6% of MEs was used for one-way ANOVA statistical analysis

    Techniques Used: Activity Assay, Irradiation, Concentration Assay, Inhibition

    escherichia coli  (ATCC)


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    ATCC escherichia coli
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    escherichia coli  (ATCC)


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    ATCC escherichia coli
    The resistance pattern of the isolates.
    Escherichia Coli, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Multidrug-resistance and extended-spectrum beta-lactamase-producing lactose-fermenting enterobacteriaceae in the human-dairy interface in northwest Ethiopia"

    Article Title: Multidrug-resistance and extended-spectrum beta-lactamase-producing lactose-fermenting enterobacteriaceae in the human-dairy interface in northwest Ethiopia

    Journal: PLOS ONE

    doi: 10.1371/journal.pone.0303872


    Figure Legend Snippet: The resistance pattern of the isolates.

    Techniques Used:


    Figure Legend Snippet: Multidrug resistance index and number isolates with greater than or equal to 0.2 index.

    Techniques Used: Bacteria, Sampling

    escherichia coli  (ATCC)


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    ATCC escherichia coli
    OMVs confer inter‐family protection and exhibit ex vivo as well as in vivo protection against PB. (a, b) The protection against PB mediated by OMVs from control or PB‐stressed bacteria was determined by performing bacterial growth kinetics. Growth kinetics were determined under continuous shaking at 37°C, and the OD 600 was measured every 30 min using a plate reader. All biological replicates were performed in technical triplicates. The highest concentration of PB that did not significantly alter bacterial growth compared to untreated control bacteria was used to calculate the fold change of Polymyxin B protection, indicating how much more PB the bacteria can tolerate in the presence of the respective OMVs. (a) Heatmap of the protection of different Enterobacteriaceae acceptor bacteria against PB in the presence of different Enterobacteriaceae OMVs isolated from control (ctr) or PB‐stressed donor bacteria. (b) Protection of Pseudomonas aeruginosa or Legionella pneumophila against PB mediated by Kp ‐PB OMVs or Kp ‐ctr OMVs. (c) Precision‐cut lung slices (PCLS) were infected with K. pneumoniae for 4 or 8 h, respectively, and additionally treated with 6 μg/mL PB with or without Kp ‐PB OMVs, each in technical duplicates. As a control, PCLS were infected with K. pneumoniae without any treatment. Bacterial load at the respective time points is displayed in CFU/mL. (d) Galleria mellonella were infected with K. pneumoniae by intra‐hemocoel injection through the last leg pair and additionally treated with either PB or PB in combination with OMVs. As controls, G. mellonella was infected with K. pneumoniae or OMVs together with PB. Survival was monitored for 7 days. Per group and replicate, 10–15 larvae were used. Graphs show mean values of 3–5 independent replicates ± SEM (c, d). Statistics: (c) two‐way ANOVA (Sidak`s multiple comparisons test); compared to respective control or (d) unpaired t ‐test; compared as indicated by brackets; * p < 0.05, ** p < 0.01; ns: not significant, PB: Polymyxin B, ctr: control; Kp : commercially available Klebsiella pneumoniae strain (MGH 78578); Kp ‐i: multi‐drug resistant Klebsiella pneumoniae clinical isolate; Ec: <t>Escherichia</t> coli ; Sal : Salmonella enterica serovar Typhimurium; n ≥ 3.
    Escherichia Coli, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Lipid A in outer membrane vesicles shields bacteria from polymyxins"

    Article Title: Lipid A in outer membrane vesicles shields bacteria from polymyxins

    Journal: Journal of Extracellular Vesicles

    doi: 10.1002/jev2.12447

    OMVs confer inter‐family protection and exhibit ex vivo as well as in vivo protection against PB. (a, b) The protection against PB mediated by OMVs from control or PB‐stressed bacteria was determined by performing bacterial growth kinetics. Growth kinetics were determined under continuous shaking at 37°C, and the OD 600 was measured every 30 min using a plate reader. All biological replicates were performed in technical triplicates. The highest concentration of PB that did not significantly alter bacterial growth compared to untreated control bacteria was used to calculate the fold change of Polymyxin B protection, indicating how much more PB the bacteria can tolerate in the presence of the respective OMVs. (a) Heatmap of the protection of different Enterobacteriaceae acceptor bacteria against PB in the presence of different Enterobacteriaceae OMVs isolated from control (ctr) or PB‐stressed donor bacteria. (b) Protection of Pseudomonas aeruginosa or Legionella pneumophila against PB mediated by Kp ‐PB OMVs or Kp ‐ctr OMVs. (c) Precision‐cut lung slices (PCLS) were infected with K. pneumoniae for 4 or 8 h, respectively, and additionally treated with 6 μg/mL PB with or without Kp ‐PB OMVs, each in technical duplicates. As a control, PCLS were infected with K. pneumoniae without any treatment. Bacterial load at the respective time points is displayed in CFU/mL. (d) Galleria mellonella were infected with K. pneumoniae by intra‐hemocoel injection through the last leg pair and additionally treated with either PB or PB in combination with OMVs. As controls, G. mellonella was infected with K. pneumoniae or OMVs together with PB. Survival was monitored for 7 days. Per group and replicate, 10–15 larvae were used. Graphs show mean values of 3–5 independent replicates ± SEM (c, d). Statistics: (c) two‐way ANOVA (Sidak`s multiple comparisons test); compared to respective control or (d) unpaired t ‐test; compared as indicated by brackets; * p < 0.05, ** p < 0.01; ns: not significant, PB: Polymyxin B, ctr: control; Kp : commercially available Klebsiella pneumoniae strain (MGH 78578); Kp ‐i: multi‐drug resistant Klebsiella pneumoniae clinical isolate; Ec: Escherichia coli ; Sal : Salmonella enterica serovar Typhimurium; n ≥ 3.
    Figure Legend Snippet: OMVs confer inter‐family protection and exhibit ex vivo as well as in vivo protection against PB. (a, b) The protection against PB mediated by OMVs from control or PB‐stressed bacteria was determined by performing bacterial growth kinetics. Growth kinetics were determined under continuous shaking at 37°C, and the OD 600 was measured every 30 min using a plate reader. All biological replicates were performed in technical triplicates. The highest concentration of PB that did not significantly alter bacterial growth compared to untreated control bacteria was used to calculate the fold change of Polymyxin B protection, indicating how much more PB the bacteria can tolerate in the presence of the respective OMVs. (a) Heatmap of the protection of different Enterobacteriaceae acceptor bacteria against PB in the presence of different Enterobacteriaceae OMVs isolated from control (ctr) or PB‐stressed donor bacteria. (b) Protection of Pseudomonas aeruginosa or Legionella pneumophila against PB mediated by Kp ‐PB OMVs or Kp ‐ctr OMVs. (c) Precision‐cut lung slices (PCLS) were infected with K. pneumoniae for 4 or 8 h, respectively, and additionally treated with 6 μg/mL PB with or without Kp ‐PB OMVs, each in technical duplicates. As a control, PCLS were infected with K. pneumoniae without any treatment. Bacterial load at the respective time points is displayed in CFU/mL. (d) Galleria mellonella were infected with K. pneumoniae by intra‐hemocoel injection through the last leg pair and additionally treated with either PB or PB in combination with OMVs. As controls, G. mellonella was infected with K. pneumoniae or OMVs together with PB. Survival was monitored for 7 days. Per group and replicate, 10–15 larvae were used. Graphs show mean values of 3–5 independent replicates ± SEM (c, d). Statistics: (c) two‐way ANOVA (Sidak`s multiple comparisons test); compared to respective control or (d) unpaired t ‐test; compared as indicated by brackets; * p < 0.05, ** p < 0.01; ns: not significant, PB: Polymyxin B, ctr: control; Kp : commercially available Klebsiella pneumoniae strain (MGH 78578); Kp ‐i: multi‐drug resistant Klebsiella pneumoniae clinical isolate; Ec: Escherichia coli ; Sal : Salmonella enterica serovar Typhimurium; n ≥ 3.

    Techniques Used: Ex Vivo, In Vivo, Bacteria, Concentration Assay, Isolation, Infection, Injection

    escherichia coli atcc  (ATCC)


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    ATCC escherichia coli atcc
    Comparative results for E. coli in both materials, box-and-whisker plot
    Escherichia Coli Atcc, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Biofilm on total joint replacement materials can be reduced through electromagnetic induction heating using a portable device"

    Article Title: Biofilm on total joint replacement materials can be reduced through electromagnetic induction heating using a portable device

    Journal: Journal of Orthopaedic Surgery and Research

    doi: 10.1186/s13018-024-04785-x

    Comparative results for E. coli in both materials, box-and-whisker plot
    Figure Legend Snippet: Comparative results for E. coli in both materials, box-and-whisker plot

    Techniques Used: Whisker Assay


    Figure Legend Snippet: Bacterial quantifications for E. coli on both materials, treated vs. control discs

    Techniques Used:

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    ATCC escherichia coli rshm 4024
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    ATCC escherichia coli mg 1655
    Antimicrobial activity of MEs and the maximal MEs concentrations used (different MEs from M. purpureus (R) and Monascus sp. (C); for their complete description see Table ). Antimicrobial activity against Bacillus subtilis ATCC 6633 ( a ) and <t>Escherichia</t> <t>coli</t> MG1655 ( b ), under dark conditions and after irradiation is demonstrated as MBC values. All data are stated as the mean of at least three independent experiments and the bars represent standard deviations. The statistical analysis was performed using one-way ANOVA (* p < 0.05). Concentrations of MEs corresponding to the presented data are shown in Supplementary material—Table . The symbols represent: (•) the MBC values achieved under dark conditions; (•) the MBC values achieved under light conditions; (∆) the highest used concentration of MEs (6%) with no inhibition observed under dark conditions (values on the secondary y-axis), concentrations corresponding to 6% of MEs was used for one-way ANOVA statistical analysis; (∆) the highest used concentration of MEs (6%) with no inhibition observed under light conditions (values on the secondary y-axis), concentration corresponding to 6% of MEs was used for one-way ANOVA statistical analysis
    Escherichia Coli Mg 1655, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC resistance against escherichia coli o157 h7
    Antimicrobial activity of MEs and the maximal MEs concentrations used (different MEs from M. purpureus (R) and Monascus sp. (C); for their complete description see Table ). Antimicrobial activity against Bacillus subtilis ATCC 6633 ( a ) and <t>Escherichia</t> <t>coli</t> MG1655 ( b ), under dark conditions and after irradiation is demonstrated as MBC values. All data are stated as the mean of at least three independent experiments and the bars represent standard deviations. The statistical analysis was performed using one-way ANOVA (* p < 0.05). Concentrations of MEs corresponding to the presented data are shown in Supplementary material—Table . The symbols represent: (•) the MBC values achieved under dark conditions; (•) the MBC values achieved under light conditions; (∆) the highest used concentration of MEs (6%) with no inhibition observed under dark conditions (values on the secondary y-axis), concentrations corresponding to 6% of MEs was used for one-way ANOVA statistical analysis; (∆) the highest used concentration of MEs (6%) with no inhibition observed under light conditions (values on the secondary y-axis), concentration corresponding to 6% of MEs was used for one-way ANOVA statistical analysis
    Resistance Against Escherichia Coli O157 H7, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC escherichia coli mg1655
    Antimicrobial activity of MEs and the maximal MEs concentrations used (different MEs from M. purpureus (R) and Monascus sp. (C); for their complete description see Table ). Antimicrobial activity against Bacillus subtilis ATCC 6633 ( a ) and <t>Escherichia</t> <t>coli</t> <t>MG1655</t> ( b ), under dark conditions and after irradiation is demonstrated as MBC values. All data are stated as the mean of at least three independent experiments and the bars represent standard deviations. The statistical analysis was performed using one-way ANOVA (* p < 0.05). Concentrations of MEs corresponding to the presented data are shown in Supplementary material—Table . The symbols represent: (•) the MBC values achieved under dark conditions; (•) the MBC values achieved under light conditions; (∆) the highest used concentration of MEs (6%) with no inhibition observed under dark conditions (values on the secondary y-axis), concentrations corresponding to 6% of MEs was used for one-way ANOVA statistical analysis; (∆) the highest used concentration of MEs (6%) with no inhibition observed under light conditions (values on the secondary y-axis), concentration corresponding to 6% of MEs was used for one-way ANOVA statistical analysis
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    ATCC escherichia coli atcc
    Comparative results for E. coli in both materials, box-and-whisker plot
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    Antimicrobial activity of MEs and the maximal MEs concentrations used (different MEs from M. purpureus (R) and Monascus sp. (C); for their complete description see Table ). Antimicrobial activity against Bacillus subtilis ATCC 6633 ( a ) and Escherichia coli MG1655 ( b ), under dark conditions and after irradiation is demonstrated as MBC values. All data are stated as the mean of at least three independent experiments and the bars represent standard deviations. The statistical analysis was performed using one-way ANOVA (* p < 0.05). Concentrations of MEs corresponding to the presented data are shown in Supplementary material—Table . The symbols represent: (•) the MBC values achieved under dark conditions; (•) the MBC values achieved under light conditions; (∆) the highest used concentration of MEs (6%) with no inhibition observed under dark conditions (values on the secondary y-axis), concentrations corresponding to 6% of MEs was used for one-way ANOVA statistical analysis; (∆) the highest used concentration of MEs (6%) with no inhibition observed under light conditions (values on the secondary y-axis), concentration corresponding to 6% of MEs was used for one-way ANOVA statistical analysis

    Journal: Current Microbiology

    Article Title: Screening Antibacterial Photodynamic Effect of Monascus Red Yeast Rice (Hong-Qu) and Mycelium Extracts

    doi: 10.1007/s00284-024-03725-6

    Figure Lengend Snippet: Antimicrobial activity of MEs and the maximal MEs concentrations used (different MEs from M. purpureus (R) and Monascus sp. (C); for their complete description see Table ). Antimicrobial activity against Bacillus subtilis ATCC 6633 ( a ) and Escherichia coli MG1655 ( b ), under dark conditions and after irradiation is demonstrated as MBC values. All data are stated as the mean of at least three independent experiments and the bars represent standard deviations. The statistical analysis was performed using one-way ANOVA (* p < 0.05). Concentrations of MEs corresponding to the presented data are shown in Supplementary material—Table . The symbols represent: (•) the MBC values achieved under dark conditions; (•) the MBC values achieved under light conditions; (∆) the highest used concentration of MEs (6%) with no inhibition observed under dark conditions (values on the secondary y-axis), concentrations corresponding to 6% of MEs was used for one-way ANOVA statistical analysis; (∆) the highest used concentration of MEs (6%) with no inhibition observed under light conditions (values on the secondary y-axis), concentration corresponding to 6% of MEs was used for one-way ANOVA statistical analysis

    Article Snippet: For the antimicrobial study, Escherichia coli MG 1655 [ ], Pseudomonas aeruginosa PAO1 [ ], Bacillus subtilis ATCC 6633 and Staphylococcus aureus ATCC 25923 were used.

    Techniques: Activity Assay, Irradiation, Concentration Assay, Inhibition

    Antimicrobial activity of MEs and the maximal MEs concentrations used (different MEs from M. purpureus (R) and Monascus sp. (C); for their complete description see Table ). Antimicrobial activity against Bacillus subtilis ATCC 6633 ( a ) and Escherichia coli MG1655 ( b ), under dark conditions and after irradiation is demonstrated as MBC values. All data are stated as the mean of at least three independent experiments and the bars represent standard deviations. The statistical analysis was performed using one-way ANOVA (* p < 0.05). Concentrations of MEs corresponding to the presented data are shown in Supplementary material—Table . The symbols represent: (•) the MBC values achieved under dark conditions; (•) the MBC values achieved under light conditions; (∆) the highest used concentration of MEs (6%) with no inhibition observed under dark conditions (values on the secondary y-axis), concentrations corresponding to 6% of MEs was used for one-way ANOVA statistical analysis; (∆) the highest used concentration of MEs (6%) with no inhibition observed under light conditions (values on the secondary y-axis), concentration corresponding to 6% of MEs was used for one-way ANOVA statistical analysis

    Journal: Current Microbiology

    Article Title: Screening Antibacterial Photodynamic Effect of Monascus Red Yeast Rice (Hong-Qu) and Mycelium Extracts

    doi: 10.1007/s00284-024-03725-6

    Figure Lengend Snippet: Antimicrobial activity of MEs and the maximal MEs concentrations used (different MEs from M. purpureus (R) and Monascus sp. (C); for their complete description see Table ). Antimicrobial activity against Bacillus subtilis ATCC 6633 ( a ) and Escherichia coli MG1655 ( b ), under dark conditions and after irradiation is demonstrated as MBC values. All data are stated as the mean of at least three independent experiments and the bars represent standard deviations. The statistical analysis was performed using one-way ANOVA (* p < 0.05). Concentrations of MEs corresponding to the presented data are shown in Supplementary material—Table . The symbols represent: (•) the MBC values achieved under dark conditions; (•) the MBC values achieved under light conditions; (∆) the highest used concentration of MEs (6%) with no inhibition observed under dark conditions (values on the secondary y-axis), concentrations corresponding to 6% of MEs was used for one-way ANOVA statistical analysis; (∆) the highest used concentration of MEs (6%) with no inhibition observed under light conditions (values on the secondary y-axis), concentration corresponding to 6% of MEs was used for one-way ANOVA statistical analysis

    Article Snippet: Antimicrobial activity against Bacillus subtilis ATCC 6633 ( a ) and Escherichia coli MG1655 ( b ), under dark conditions and after irradiation is demonstrated as MBC values.

    Techniques: Activity Assay, Irradiation, Concentration Assay, Inhibition

    Comparative results for E. coli in both materials, box-and-whisker plot

    Journal: Journal of Orthopaedic Surgery and Research

    Article Title: Biofilm on total joint replacement materials can be reduced through electromagnetic induction heating using a portable device

    doi: 10.1186/s13018-024-04785-x

    Figure Lengend Snippet: Comparative results for E. coli in both materials, box-and-whisker plot

    Article Snippet: Three strains of bacterial species frequently found as arthroplasty infectious agents were selected: S epidermidis ATCC 35,984, S aureus ATCC 25,923, and Escherichia coli ATCC 25,922.

    Techniques: Whisker Assay

    Journal: Journal of Orthopaedic Surgery and Research

    Article Title: Biofilm on total joint replacement materials can be reduced through electromagnetic induction heating using a portable device

    doi: 10.1186/s13018-024-04785-x

    Figure Lengend Snippet: Bacterial quantifications for E. coli on both materials, treated vs. control discs

    Article Snippet: Three strains of bacterial species frequently found as arthroplasty infectious agents were selected: S epidermidis ATCC 35,984, S aureus ATCC 25,923, and Escherichia coli ATCC 25,922.

    Techniques: