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bacterial strains mrsa atcc 43300  (ATCC)


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    ATCC bacterial strains mrsa atcc 43300
    Bacterial Strains Mrsa Atcc 43300, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 3606 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/bacterial+strain+mrsa/Staphylococcus+aureus%3B+subsp%2E+aureus/pmc12736273-100-1-4
    Average 99 stars, based on 3606 article reviews
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    Article Title: Antibacterial and anti-inflammatory effects of genistein in Staphylococcus aureus induced osteomyelitis in rats.
    Article Snippet: Correspondence Xinyi Guo, Department of Orthopaedic Surgery, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Third Hosptial of Shanxi Medical University, Taiyuan 030032, China; Department of Orthopaedic Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China Email: xinyi.guo1@hotmail.com Abstract Methicillin‐resistant Staphylococcus aureus (MRSA) is a highly infectious Gram‐ positive pathogen known to cause severe diseases such as endocarditis, food poisoning, pneumonia, osteomyelitis, and septicemia.. MRSA is a major public health issue.. Among these, osteomyelitis is inflammation of the bone caused by the invasion of the bacterial pathogen in the bones.

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    Article Title: Modifying Antimicrobial Peptides with Albumin-Binding Molecules Enhances Membrane-Disrupting Efficacy by Modulating the Secondary Structure.
    Article Snippet: Antimicrobial peptides (AMPs) are powerful tools in combating drug-resistant bacteria.. However, their clinical application is hindered by poor pharmacokinetics and suboptimal antimicrobial activity.. This study proposes a strategy to enhance the antimicrobial activity and biosafety of AMPs by modification with albumin-binding molecules (ABMs).



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    bacterial strains mrsa atcc 43300  (ATCC)
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    ATCC bacterial strains mrsa atcc 43300
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    reference bacterial strain mrsa  (ATCC)
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    A–D Results of macromolecular biosynthesis assay. Inhibition of biosynthetic pathway is indicated by lower incorporation of radioactively <t>labeled</t> <t>precursors.</t> A [ 3 H] N -acetylglucosamine (peptidoglycan synthesis), B [ 3 H] uridine (RNA synthesis), C [ 3 H] thymidine (DNA synthesis) and D [ 3 H] leucine (protein synthesis) in <t>methicillin-resistant</t> <t>Staphylococcus</t> <t>aureus</t> (ATCC 43300) strain, treated for 2 h with 4 × MIC of VAN, RIF, CIP, CHL, CHX, and AB15. Results are expressed as the percentage of biomolecule incorporation related to untreated controls. The values shown are means of two independent experiments prepared in duplicates ± SEM. Significant reduction in biosynthetic pathway compared to control is indicated by p -value, where p < 0.05 was accepted as statistically significant (* p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001), determined by nonparametric one-way (ANOVA) test (Kruskal–Wallis test)
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    A–D Results of macromolecular biosynthesis assay. Inhibition of biosynthetic pathway is indicated by lower incorporation of radioactively <t>labeled</t> <t>precursors.</t> A [ 3 H] N -acetylglucosamine (peptidoglycan synthesis), B [ 3 H] uridine (RNA synthesis), C [ 3 H] thymidine (DNA synthesis) and D [ 3 H] leucine (protein synthesis) in <t>methicillin-resistant</t> <t>Staphylococcus</t> <t>aureus</t> (ATCC 43300) strain, treated for 2 h with 4 × MIC of VAN, RIF, CIP, CHL, CHX, and AB15. Results are expressed as the percentage of biomolecule incorporation related to untreated controls. The values shown are means of two independent experiments prepared in duplicates ± SEM. Significant reduction in biosynthetic pathway compared to control is indicated by p -value, where p < 0.05 was accepted as statistically significant (* p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001), determined by nonparametric one-way (ANOVA) test (Kruskal–Wallis test)
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    ATCC bacterial strain mrsa atcc 43300
    A–D Results of macromolecular biosynthesis assay. Inhibition of biosynthetic pathway is indicated by lower incorporation of radioactively <t>labeled</t> <t>precursors.</t> A [ 3 H] N -acetylglucosamine (peptidoglycan synthesis), B [ 3 H] uridine (RNA synthesis), C [ 3 H] thymidine (DNA synthesis) and D [ 3 H] leucine (protein synthesis) in <t>methicillin-resistant</t> <t>Staphylococcus</t> <t>aureus</t> (ATCC 43300) strain, treated for 2 h with 4 × MIC of VAN, RIF, CIP, CHL, CHX, and AB15. Results are expressed as the percentage of biomolecule incorporation related to untreated controls. The values shown are means of two independent experiments prepared in duplicates ± SEM. Significant reduction in biosynthetic pathway compared to control is indicated by p -value, where p < 0.05 was accepted as statistically significant (* p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001), determined by nonparametric one-way (ANOVA) test (Kruskal–Wallis test)
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    A–D Results of macromolecular biosynthesis assay. Inhibition of biosynthetic pathway is indicated by lower incorporation of radioactively <t>labeled</t> <t>precursors.</t> A [ 3 H] N -acetylglucosamine (peptidoglycan synthesis), B [ 3 H] uridine (RNA synthesis), C [ 3 H] thymidine (DNA synthesis) and D [ 3 H] leucine (protein synthesis) in <t>methicillin-resistant</t> <t>Staphylococcus</t> <t>aureus</t> (ATCC 43300) strain, treated for 2 h with 4 × MIC of VAN, RIF, CIP, CHL, CHX, and AB15. Results are expressed as the percentage of biomolecule incorporation related to untreated controls. The values shown are means of two independent experiments prepared in duplicates ± SEM. Significant reduction in biosynthetic pathway compared to control is indicated by p -value, where p < 0.05 was accepted as statistically significant (* p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001), determined by nonparametric one-way (ANOVA) test (Kruskal–Wallis test)
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    A–D Results of macromolecular biosynthesis assay. Inhibition of biosynthetic pathway is indicated by lower incorporation of radioactively <t>labeled</t> <t>precursors.</t> A [ 3 H] N -acetylglucosamine (peptidoglycan synthesis), B [ 3 H] uridine (RNA synthesis), C [ 3 H] thymidine (DNA synthesis) and D [ 3 H] leucine (protein synthesis) in <t>methicillin-resistant</t> <t>Staphylococcus</t> <t>aureus</t> (ATCC 43300) strain, treated for 2 h with 4 × MIC of VAN, RIF, CIP, CHL, CHX, and AB15. Results are expressed as the percentage of biomolecule incorporation related to untreated controls. The values shown are means of two independent experiments prepared in duplicates ± SEM. Significant reduction in biosynthetic pathway compared to control is indicated by p -value, where p < 0.05 was accepted as statistically significant (* p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001), determined by nonparametric one-way (ANOVA) test (Kruskal–Wallis test)
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    bacterial strains methicillin resistant staphylococcus aureus mrsa  (ATCC)
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    ATCC bacterial strains methicillin resistant staphylococcus aureus mrsa
    A–D Results of macromolecular biosynthesis assay. Inhibition of biosynthetic pathway is indicated by lower incorporation of radioactively <t>labeled</t> <t>precursors.</t> A [ 3 H] N -acetylglucosamine (peptidoglycan synthesis), B [ 3 H] uridine (RNA synthesis), C [ 3 H] thymidine (DNA synthesis) and D [ 3 H] leucine (protein synthesis) in <t>methicillin-resistant</t> <t>Staphylococcus</t> <t>aureus</t> (ATCC 43300) strain, treated for 2 h with 4 × MIC of VAN, RIF, CIP, CHL, CHX, and AB15. Results are expressed as the percentage of biomolecule incorporation related to untreated controls. The values shown are means of two independent experiments prepared in duplicates ± SEM. Significant reduction in biosynthetic pathway compared to control is indicated by p -value, where p < 0.05 was accepted as statistically significant (* p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001), determined by nonparametric one-way (ANOVA) test (Kruskal–Wallis test)
    Bacterial Strains Methicillin Resistant Staphylococcus Aureus Mrsa, 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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    A–D Results of macromolecular biosynthesis assay. Inhibition of biosynthetic pathway is indicated by lower incorporation of radioactively labeled precursors. A [ 3 H] N -acetylglucosamine (peptidoglycan synthesis), B [ 3 H] uridine (RNA synthesis), C [ 3 H] thymidine (DNA synthesis) and D [ 3 H] leucine (protein synthesis) in methicillin-resistant Staphylococcus aureus (ATCC 43300) strain, treated for 2 h with 4 × MIC of VAN, RIF, CIP, CHL, CHX, and AB15. Results are expressed as the percentage of biomolecule incorporation related to untreated controls. The values shown are means of two independent experiments prepared in duplicates ± SEM. Significant reduction in biosynthetic pathway compared to control is indicated by p -value, where p < 0.05 was accepted as statistically significant (* p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001), determined by nonparametric one-way (ANOVA) test (Kruskal–Wallis test)

    Journal: Medical Microbiology and Immunology

    Article Title: A new bactericidal chlorinated derivative containing 2-aminooxazole potentiates antibacterial action of colistin against multidrug-resistant acinetobacter baumannii

    doi: 10.1007/s00430-025-00854-y

    Figure Lengend Snippet: A–D Results of macromolecular biosynthesis assay. Inhibition of biosynthetic pathway is indicated by lower incorporation of radioactively labeled precursors. A [ 3 H] N -acetylglucosamine (peptidoglycan synthesis), B [ 3 H] uridine (RNA synthesis), C [ 3 H] thymidine (DNA synthesis) and D [ 3 H] leucine (protein synthesis) in methicillin-resistant Staphylococcus aureus (ATCC 43300) strain, treated for 2 h with 4 × MIC of VAN, RIF, CIP, CHL, CHX, and AB15. Results are expressed as the percentage of biomolecule incorporation related to untreated controls. The values shown are means of two independent experiments prepared in duplicates ± SEM. Significant reduction in biosynthetic pathway compared to control is indicated by p -value, where p < 0.05 was accepted as statistically significant (* p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001), determined by nonparametric one-way (ANOVA) test (Kruskal–Wallis test)

    Article Snippet: As shown in Fig. , the action of AB15 resulted in a statistically significant decrease in the incorporation of radiolabeled precursors participating in the protein synthesis pathway (Fig. D) of the reference bacterial strain MRSA (ATCC 43300) (used according to a protocol described in Nowakowska et al., 2013) [ ].

    Techniques: Inhibition, Labeling, DNA Synthesis, Control

    Membrane depolarization assay. Membrane potential was monitored using the fluorescence dye, DiSC3(5), (λ Ex = 620 nm, λ Em = 680 nm). Methicillin-resistant Staphylococcus aureus (ATCC 43300) was stained with 0.5 mM DiSC3(5). After 10 min of measurement (black arrow), AB15, positive control represented by chlorhexidine (CHX), in final concentrations corresponding to 4 × MIC were added. The graph depicts the mean of six replicates and the standard deviation

    Journal: Medical Microbiology and Immunology

    Article Title: A new bactericidal chlorinated derivative containing 2-aminooxazole potentiates antibacterial action of colistin against multidrug-resistant acinetobacter baumannii

    doi: 10.1007/s00430-025-00854-y

    Figure Lengend Snippet: Membrane depolarization assay. Membrane potential was monitored using the fluorescence dye, DiSC3(5), (λ Ex = 620 nm, λ Em = 680 nm). Methicillin-resistant Staphylococcus aureus (ATCC 43300) was stained with 0.5 mM DiSC3(5). After 10 min of measurement (black arrow), AB15, positive control represented by chlorhexidine (CHX), in final concentrations corresponding to 4 × MIC were added. The graph depicts the mean of six replicates and the standard deviation

    Article Snippet: As shown in Fig. , the action of AB15 resulted in a statistically significant decrease in the incorporation of radiolabeled precursors participating in the protein synthesis pathway (Fig. D) of the reference bacterial strain MRSA (ATCC 43300) (used according to a protocol described in Nowakowska et al., 2013) [ ].

    Techniques: Membrane, Fluorescence, Staining, Positive Control, Standard Deviation