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antimicrobial activity against s aureus atcc 9144  (ATCC)


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    Structured Review

    ATCC antimicrobial activity against s aureus atcc 9144
    (a) Results from screening Library 1 in the “catch all” KCl assay using POPC, POPG and POPE/POPG (2 : 1) vesicles, at 10 mol% with respect to lipid. The dotted line represents our cut-off criterion for further analysis (>70% efflux), used to identify the most active SSAs detailed in ; (b) S anion values for the most active SSAs in Library 1 against POPC and POPE/POPG (2 : 1) tested at 10 mol% w.r.t. lipid; (c) heatmaps detailing the percentage of antimicrobial growth inhibition obtained for Library 1 and AT at 100 µM against S. aureus <t>ATCC</t> <t>9144</t> and S. aureus NCTC 13616 at 20 hours. Heatmaps display the percent inhibition of either optical density (turbidity or growth), and inhibition of fluorescence (metabolic activity) at 20 hours. All values were blank adjusted and normalised to the positive control for complete inhibition (DMSO + broth, to calibrate 100% inhibition of growth/metabolic activity).
    Antimicrobial Activity Against S Aureus Atcc 9144, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 308 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/antimicrobial+activity+against+s+aureus/Staphylococcus+aureus%3B+subsp%2E+aureus/pmc12970626-213-22-27
    Average 96 stars, based on 308 article reviews
    antimicrobial activity against s aureus atcc 9144 - by Bioz Stars, 2026-09
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    Images

    1) Product Images from "An increased throughput workflow to identify ion transport and membrane lysis agents for antimicrobial discovery"

    Article Title: An increased throughput workflow to identify ion transport and membrane lysis agents for antimicrobial discovery

    Journal: Chemical Science

    doi: 10.1039/d5sc09781a

    (a) Results from screening Library 1 in the “catch all” KCl assay using POPC, POPG and POPE/POPG (2 : 1) vesicles, at 10 mol% with respect to lipid. The dotted line represents our cut-off criterion for further analysis (>70% efflux), used to identify the most active SSAs detailed in ; (b) S anion values for the most active SSAs in Library 1 against POPC and POPE/POPG (2 : 1) tested at 10 mol% w.r.t. lipid; (c) heatmaps detailing the percentage of antimicrobial growth inhibition obtained for Library 1 and AT at 100 µM against S. aureus ATCC 9144 and S. aureus NCTC 13616 at 20 hours. Heatmaps display the percent inhibition of either optical density (turbidity or growth), and inhibition of fluorescence (metabolic activity) at 20 hours. All values were blank adjusted and normalised to the positive control for complete inhibition (DMSO + broth, to calibrate 100% inhibition of growth/metabolic activity).
    Figure Legend Snippet: (a) Results from screening Library 1 in the “catch all” KCl assay using POPC, POPG and POPE/POPG (2 : 1) vesicles, at 10 mol% with respect to lipid. The dotted line represents our cut-off criterion for further analysis (>70% efflux), used to identify the most active SSAs detailed in ; (b) S anion values for the most active SSAs in Library 1 against POPC and POPE/POPG (2 : 1) tested at 10 mol% w.r.t. lipid; (c) heatmaps detailing the percentage of antimicrobial growth inhibition obtained for Library 1 and AT at 100 µM against S. aureus ATCC 9144 and S. aureus NCTC 13616 at 20 hours. Heatmaps display the percent inhibition of either optical density (turbidity or growth), and inhibition of fluorescence (metabolic activity) at 20 hours. All values were blank adjusted and normalised to the positive control for complete inhibition (DMSO + broth, to calibrate 100% inhibition of growth/metabolic activity).

    Techniques Used: Inhibition, Fluorescence, Activity Assay, Positive Control

    (a) Overlay of 31 P HSQC spectra of phospholipids extracted from S. aureus ATCC 9144 (red) and S. aureus NCTC 13616 (black); (b) differences in total phospholipid composition between S. aureus ATCC 9144 (blue) and S. aureus NCTC 13616 (orange).
    Figure Legend Snippet: (a) Overlay of 31 P HSQC spectra of phospholipids extracted from S. aureus ATCC 9144 (red) and S. aureus NCTC 13616 (black); (b) differences in total phospholipid composition between S. aureus ATCC 9144 (blue) and S. aureus NCTC 13616 (orange).

    Techniques Used:

    Related Articles

    Activity Assay:

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    Article Snippet: .. The aqueous extract of E. amoenum , collected from Ardabil Province in Iran, has demonstrated antimicrobial activity against S. aureus (ATCC 8327) [ ]. ..

    Article Title: Composition and Activities of Carpesium macrocephalum Franch. & Sav. Essential Oils.
    Article Snippet: .. EOs from roots and aerial parts of T. speciosa collected in Bosnia and Herzegovina demonstrated antimicrobial activity against S. aureus (MIC: 1.1–15.0 mg/mL), P. aeruginosa (MIC: 4.0–11.0 mg/mL), E. coli ATCC 35210 (MIC: 1.0–7.0 mg/mL) and C. albicans (MIC: 1.0–15.0 mg/mL). ..

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    Article Snippet: The inhibition zone for MRSA ATCC 33592 and C. albicans ATCC 10231 was more than 20 mm; therefore, it was included in the very strong inhibitory category based on the classification by Abu-Zaid et al. (2022).Randu honey from Malang (RMH) forms an inhibitory zone diameter of 15.90 ± 0.57 to 21.58 ± 0.56 mm, which is included in the strong inhibitory category. .. The RMH sample exhibited the highest antimicrobial activity against S. aureus (ATCC 6538). ..

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    Article Snippet: .. The samples containing tetracycline or chloramphenicol exhibited antimicrobial activity against S. aureus (ATCC 6538) and P. aeruginosa (ATCC 10,154) strains. ..

    Article Title: A New Species and Eight New Records of Ascomycetes from Freshwater Niches in Korea
    Article Snippet: .. Moreover, six novel compounds and three known compounds obtained from the freshwater fungus Chaetomium sp. YMF 1.02105 exhibited antimicrobial activity against S. aureus (ATCC 6538) in standard disk assays [ ]. ..

    Article Title: Recent advances in piperazine derivatives as antibacterial agents: a comprehensive review (2020-2024).
    Article Snippet: Antimicrobial resistance (AMR) is a major global health challenge that requires the development of new therapeutic drugs.. Piperazine, a privileged nitrogen-containing heterocyclic scaffold, has been identified as a viable framework for antibacterial drug development.. This review examines current breakthroughs (2020–2024) in piperazine-based compounds with antibacterial activity.

    Article Title: Composition and Activities of Carpesium macrocephalum Franch. & Sav. Essential Oils
    Article Snippet: .. EOs from roots and aerial parts of T. speciosa collected in Bosnia and Herzegovina demonstrated antimicrobial activity against S. aureus (MIC: 1.1–15.0 mg/mL), P. aeruginosa (MIC: 4.0–11.0 mg/mL), E. coli ATCC 35210 (MIC: 1.0–7.0 mg/mL) and C. albicans (MIC: 1.0–15.0 mg/mL). ..

    Article Title: Antimicrobial and wound healing potential of naphthoquinones encapsulated in nanochitosan
    Article Snippet: Complete inhibition (MIC) upon CNP-NQ1 treatment was achieved against S. aureus (ATCC 14458), S. epidermidis and S. aureus (ATCC 29213), but not against S. pyogenes and P. aeruginosa . .. The inhibition curves produced by CNP-NQ2 treatment did not achieve 50% of antimicrobial activity against S. aureus (ATCC 29213) S. pyogenes and P. aeruginosa and, hence, their IC 50 were recorded as >5 mg/mL, the highest tested concentration. .. Complete growth inhibition (MIC) using CNP-NQ2 was only achieved against S. aureus (ATCC 14458) ( ; ).

    Synthesized:

    Article Title: Recent advances in piperazine derivatives as antibacterial agents: a comprehensive review (2020-2024).
    Article Snippet: Antimicrobial resistance (AMR) is a major global health challenge that requires the development of new therapeutic drugs.. Piperazine, a privileged nitrogen-containing heterocyclic scaffold, has been identified as a viable framework for antibacterial drug development.. This review examines current breakthroughs (2020–2024) in piperazine-based compounds with antibacterial activity.

    Inhibition:

    Article Title: Antimicrobial and wound healing potential of naphthoquinones encapsulated in nanochitosan
    Article Snippet: Complete inhibition (MIC) upon CNP-NQ1 treatment was achieved against S. aureus (ATCC 14458), S. epidermidis and S. aureus (ATCC 29213), but not against S. pyogenes and P. aeruginosa . .. The inhibition curves produced by CNP-NQ2 treatment did not achieve 50% of antimicrobial activity against S. aureus (ATCC 29213) S. pyogenes and P. aeruginosa and, hence, their IC 50 were recorded as >5 mg/mL, the highest tested concentration. .. Complete growth inhibition (MIC) using CNP-NQ2 was only achieved against S. aureus (ATCC 14458) ( ; ).

    Produced:

    Article Title: Antimicrobial and wound healing potential of naphthoquinones encapsulated in nanochitosan
    Article Snippet: Complete inhibition (MIC) upon CNP-NQ1 treatment was achieved against S. aureus (ATCC 14458), S. epidermidis and S. aureus (ATCC 29213), but not against S. pyogenes and P. aeruginosa . .. The inhibition curves produced by CNP-NQ2 treatment did not achieve 50% of antimicrobial activity against S. aureus (ATCC 29213) S. pyogenes and P. aeruginosa and, hence, their IC 50 were recorded as >5 mg/mL, the highest tested concentration. .. Complete growth inhibition (MIC) using CNP-NQ2 was only achieved against S. aureus (ATCC 14458) ( ; ).

    Concentration Assay:

    Article Title: Antimicrobial and wound healing potential of naphthoquinones encapsulated in nanochitosan
    Article Snippet: Complete inhibition (MIC) upon CNP-NQ1 treatment was achieved against S. aureus (ATCC 14458), S. epidermidis and S. aureus (ATCC 29213), but not against S. pyogenes and P. aeruginosa . .. The inhibition curves produced by CNP-NQ2 treatment did not achieve 50% of antimicrobial activity against S. aureus (ATCC 29213) S. pyogenes and P. aeruginosa and, hence, their IC 50 were recorded as >5 mg/mL, the highest tested concentration. .. Complete growth inhibition (MIC) using CNP-NQ2 was only achieved against S. aureus (ATCC 14458) ( ; ).



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    ATCC antimicrobial activity against s aureus atcc 9144
    (a) Results from screening Library 1 in the “catch all” KCl assay using POPC, POPG and POPE/POPG (2 : 1) vesicles, at 10 mol% with respect to lipid. The dotted line represents our cut-off criterion for further analysis (>70% efflux), used to identify the most active SSAs detailed in ; (b) S anion values for the most active SSAs in Library 1 against POPC and POPE/POPG (2 : 1) tested at 10 mol% w.r.t. lipid; (c) heatmaps detailing the percentage of antimicrobial growth inhibition obtained for Library 1 and AT at 100 µM against S. aureus <t>ATCC</t> <t>9144</t> and S. aureus NCTC 13616 at 20 hours. Heatmaps display the percent inhibition of either optical density (turbidity or growth), and inhibition of fluorescence (metabolic activity) at 20 hours. All values were blank adjusted and normalised to the positive control for complete inhibition (DMSO + broth, to calibrate 100% inhibition of growth/metabolic activity).
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    (a) Results from screening Library 1 in the “catch all” KCl assay using POPC, POPG and POPE/POPG (2 : 1) vesicles, at 10 mol% with respect to lipid. The dotted line represents our cut-off criterion for further analysis (>70% efflux), used to identify the most active SSAs detailed in ; (b) S anion values for the most active SSAs in Library 1 against POPC and POPE/POPG (2 : 1) tested at 10 mol% w.r.t. lipid; (c) heatmaps detailing the percentage of antimicrobial growth inhibition obtained for Library 1 and AT at 100 µM against S. aureus <t>ATCC</t> <t>9144</t> and S. aureus NCTC 13616 at 20 hours. Heatmaps display the percent inhibition of either optical density (turbidity or growth), and inhibition of fluorescence (metabolic activity) at 20 hours. All values were blank adjusted and normalised to the positive control for complete inhibition (DMSO + broth, to calibrate 100% inhibition of growth/metabolic activity).
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    ATCC antimicrobial activity against s aureus atcc 6538
    (a) Results from screening Library 1 in the “catch all” KCl assay using POPC, POPG and POPE/POPG (2 : 1) vesicles, at 10 mol% with respect to lipid. The dotted line represents our cut-off criterion for further analysis (>70% efflux), used to identify the most active SSAs detailed in ; (b) S anion values for the most active SSAs in Library 1 against POPC and POPE/POPG (2 : 1) tested at 10 mol% w.r.t. lipid; (c) heatmaps detailing the percentage of antimicrobial growth inhibition obtained for Library 1 and AT at 100 µM against S. aureus <t>ATCC</t> <t>9144</t> and S. aureus NCTC 13616 at 20 hours. Heatmaps display the percent inhibition of either optical density (turbidity or growth), and inhibition of fluorescence (metabolic activity) at 20 hours. All values were blank adjusted and normalised to the positive control for complete inhibition (DMSO + broth, to calibrate 100% inhibition of growth/metabolic activity).
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    (a) Results from screening Library 1 in the “catch all” KCl assay using POPC, POPG and POPE/POPG (2 : 1) vesicles, at 10 mol% with respect to lipid. The dotted line represents our cut-off criterion for further analysis (>70% efflux), used to identify the most active SSAs detailed in ; (b) S anion values for the most active SSAs in Library 1 against POPC and POPE/POPG (2 : 1) tested at 10 mol% w.r.t. lipid; (c) heatmaps detailing the percentage of antimicrobial growth inhibition obtained for Library 1 and AT at 100 µM against S. aureus <t>ATCC</t> <t>9144</t> and S. aureus NCTC 13616 at 20 hours. Heatmaps display the percent inhibition of either optical density (turbidity or growth), and inhibition of fluorescence (metabolic activity) at 20 hours. All values were blank adjusted and normalised to the positive control for complete inhibition (DMSO + broth, to calibrate 100% inhibition of growth/metabolic activity).
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    (a) Results from screening Library 1 in the “catch all” KCl assay using POPC, POPG and POPE/POPG (2 : 1) vesicles, at 10 mol% with respect to lipid. The dotted line represents our cut-off criterion for further analysis (>70% efflux), used to identify the most active SSAs detailed in ; (b) S anion values for the most active SSAs in Library 1 against POPC and POPE/POPG (2 : 1) tested at 10 mol% w.r.t. lipid; (c) heatmaps detailing the percentage of antimicrobial growth inhibition obtained for Library 1 and AT at 100 µM against S. aureus <t>ATCC</t> <t>9144</t> and S. aureus NCTC 13616 at 20 hours. Heatmaps display the percent inhibition of either optical density (turbidity or growth), and inhibition of fluorescence (metabolic activity) at 20 hours. All values were blank adjusted and normalised to the positive control for complete inhibition (DMSO + broth, to calibrate 100% inhibition of growth/metabolic activity).
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    ATCC significant antimicrobial activity against s aureus atcc 9144
    (a) Results from screening Library 1 in the “catch all” KCl assay using POPC, POPG and POPE/POPG (2 : 1) vesicles, at 10 mol% with respect to lipid. The dotted line represents our cut-off criterion for further analysis (>70% efflux), used to identify the most active SSAs detailed in ; (b) S anion values for the most active SSAs in Library 1 against POPC and POPE/POPG (2 : 1) tested at 10 mol% w.r.t. lipid; (c) heatmaps detailing the percentage of antimicrobial growth inhibition obtained for Library 1 and AT at 100 µM against S. aureus <t>ATCC</t> <t>9144</t> and S. aureus NCTC 13616 at 20 hours. Heatmaps display the percent inhibition of either optical density (turbidity or growth), and inhibition of fluorescence (metabolic activity) at 20 hours. All values were blank adjusted and normalised to the positive control for complete inhibition (DMSO + broth, to calibrate 100% inhibition of growth/metabolic activity).
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    (a) Results from screening Library 1 in the “catch all” KCl assay using POPC, POPG and POPE/POPG (2 : 1) vesicles, at 10 mol% with respect to lipid. The dotted line represents our cut-off criterion for further analysis (>70% efflux), used to identify the most active SSAs detailed in ; (b) S anion values for the most active SSAs in Library 1 against POPC and POPE/POPG (2 : 1) tested at 10 mol% w.r.t. lipid; (c) heatmaps detailing the percentage of antimicrobial growth inhibition obtained for Library 1 and AT at 100 µM against S. aureus <t>ATCC</t> <t>9144</t> and S. aureus NCTC 13616 at 20 hours. Heatmaps display the percent inhibition of either optical density (turbidity or growth), and inhibition of fluorescence (metabolic activity) at 20 hours. All values were blank adjusted and normalised to the positive control for complete inhibition (DMSO + broth, to calibrate 100% inhibition of growth/metabolic activity).
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    ATCC antimicrobial activity against s aureus atcc 6538 p
    (a) Results from screening Library 1 in the “catch all” KCl assay using POPC, POPG and POPE/POPG (2 : 1) vesicles, at 10 mol% with respect to lipid. The dotted line represents our cut-off criterion for further analysis (>70% efflux), used to identify the most active SSAs detailed in ; (b) S anion values for the most active SSAs in Library 1 against POPC and POPE/POPG (2 : 1) tested at 10 mol% w.r.t. lipid; (c) heatmaps detailing the percentage of antimicrobial growth inhibition obtained for Library 1 and AT at 100 µM against S. aureus <t>ATCC</t> <t>9144</t> and S. aureus NCTC 13616 at 20 hours. Heatmaps display the percent inhibition of either optical density (turbidity or growth), and inhibition of fluorescence (metabolic activity) at 20 hours. All values were blank adjusted and normalised to the positive control for complete inhibition (DMSO + broth, to calibrate 100% inhibition of growth/metabolic activity).
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    Image Search Results


    (a) Results from screening Library 1 in the “catch all” KCl assay using POPC, POPG and POPE/POPG (2 : 1) vesicles, at 10 mol% with respect to lipid. The dotted line represents our cut-off criterion for further analysis (>70% efflux), used to identify the most active SSAs detailed in ; (b) S anion values for the most active SSAs in Library 1 against POPC and POPE/POPG (2 : 1) tested at 10 mol% w.r.t. lipid; (c) heatmaps detailing the percentage of antimicrobial growth inhibition obtained for Library 1 and AT at 100 µM against S. aureus ATCC 9144 and S. aureus NCTC 13616 at 20 hours. Heatmaps display the percent inhibition of either optical density (turbidity or growth), and inhibition of fluorescence (metabolic activity) at 20 hours. All values were blank adjusted and normalised to the positive control for complete inhibition (DMSO + broth, to calibrate 100% inhibition of growth/metabolic activity).

    Journal: Chemical Science

    Article Title: An increased throughput workflow to identify ion transport and membrane lysis agents for antimicrobial discovery

    doi: 10.1039/d5sc09781a

    Figure Lengend Snippet: (a) Results from screening Library 1 in the “catch all” KCl assay using POPC, POPG and POPE/POPG (2 : 1) vesicles, at 10 mol% with respect to lipid. The dotted line represents our cut-off criterion for further analysis (>70% efflux), used to identify the most active SSAs detailed in ; (b) S anion values for the most active SSAs in Library 1 against POPC and POPE/POPG (2 : 1) tested at 10 mol% w.r.t. lipid; (c) heatmaps detailing the percentage of antimicrobial growth inhibition obtained for Library 1 and AT at 100 µM against S. aureus ATCC 9144 and S. aureus NCTC 13616 at 20 hours. Heatmaps display the percent inhibition of either optical density (turbidity or growth), and inhibition of fluorescence (metabolic activity) at 20 hours. All values were blank adjusted and normalised to the positive control for complete inhibition (DMSO + broth, to calibrate 100% inhibition of growth/metabolic activity).

    Article Snippet: We found no difference in modal MIC values from our inverted protocols, except for SSA 8, which exhibited a 16-fold decrease in antimicrobial activity against S. aureus ATCC 9144, and a 64-fold decrease in antimicrobial activity against S. aureus NCTC 13616 under these traditional assay conditions.

    Techniques: Inhibition, Fluorescence, Activity Assay, Positive Control

    (a) Overlay of 31 P HSQC spectra of phospholipids extracted from S. aureus ATCC 9144 (red) and S. aureus NCTC 13616 (black); (b) differences in total phospholipid composition between S. aureus ATCC 9144 (blue) and S. aureus NCTC 13616 (orange).

    Journal: Chemical Science

    Article Title: An increased throughput workflow to identify ion transport and membrane lysis agents for antimicrobial discovery

    doi: 10.1039/d5sc09781a

    Figure Lengend Snippet: (a) Overlay of 31 P HSQC spectra of phospholipids extracted from S. aureus ATCC 9144 (red) and S. aureus NCTC 13616 (black); (b) differences in total phospholipid composition between S. aureus ATCC 9144 (blue) and S. aureus NCTC 13616 (orange).

    Article Snippet: We found no difference in modal MIC values from our inverted protocols, except for SSA 8, which exhibited a 16-fold decrease in antimicrobial activity against S. aureus ATCC 9144, and a 64-fold decrease in antimicrobial activity against S. aureus NCTC 13616 under these traditional assay conditions.

    Techniques: