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reference strain staphylococcus aureus atcc 6538p fda 209p  (ATCC)


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    ATCC reference strain staphylococcus aureus atcc 6538p fda 209p
    Reference Strain Staphylococcus Aureus Atcc 6538p Fda 209p, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 3498 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/strains+staphylococcus+aureus+209p/Staphylococcus+aureus+subsp%2E+aureus+Rosenbach/10__1134_slash_s0026261725604385-31-17-21
    Average 99 stars, based on 3498 article reviews
    reference strain staphylococcus aureus atcc 6538p fda 209p - by Bioz Stars, 2026-09
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    Related Articles

    Activity Assay:

    Article Title: Synthesis and Antitumor and Antibacterial Activity of Sulfanyl-Substituted 3-(m-tolyl)-3H-spiro[benzo[h]quinazoline-5,1′-Cycloheptane]-4(6H)-ones
    Article Snippet: The reaction of ethyl 4 -amino-1 H-spiro[cycloheptane-1,2 -naphthalene]-3 -carboxylate withm-tolyl isothiocyanate and subsequent cyclization of the intermediate thiourea derivative synthesized 2-thioxo-3-(m-tolyl)2,3-dihydro-1H-spiro[benzo[h]quinazoline-5,1 -cycloheptane]-4(6H)-one.. The last was alkylated by various halides in the presence of alkali to form 2-thiosubstituted 3-(m-tolyl)-3H-spiro[benzo[h]-quinazoline5,1 -cycloheptane]-4(6H)-ones.. The antibacterial activity of the synthesized compounds was studied by the agar diffusion method using Gram-positive strains Staphylococcus aureus 209p and Bacillus subtilis ATCC 6633 and Gram-negative strains Shigella flexneri 6858 and Escherichia coli 0-55.

    Synthesized:

    Article Title: Synthesis and Antitumor and Antibacterial Activity of Sulfanyl-Substituted 3-(m-tolyl)-3H-spiro[benzo[h]quinazoline-5,1′-Cycloheptane]-4(6H)-ones
    Article Snippet: The reaction of ethyl 4 -amino-1 H-spiro[cycloheptane-1,2 -naphthalene]-3 -carboxylate withm-tolyl isothiocyanate and subsequent cyclization of the intermediate thiourea derivative synthesized 2-thioxo-3-(m-tolyl)2,3-dihydro-1H-spiro[benzo[h]quinazoline-5,1 -cycloheptane]-4(6H)-one.. The last was alkylated by various halides in the presence of alkali to form 2-thiosubstituted 3-(m-tolyl)-3H-spiro[benzo[h]-quinazoline5,1 -cycloheptane]-4(6H)-ones.. The antibacterial activity of the synthesized compounds was studied by the agar diffusion method using Gram-positive strains Staphylococcus aureus 209p and Bacillus subtilis ATCC 6633 and Gram-negative strains Shigella flexneri 6858 and Escherichia coli 0-55.

    Diffusion-based Assay:

    Article Title: Synthesis and Antitumor and Antibacterial Activity of Sulfanyl-Substituted 3-(m-tolyl)-3H-spiro[benzo[h]quinazoline-5,1′-Cycloheptane]-4(6H)-ones
    Article Snippet: The reaction of ethyl 4 -amino-1 H-spiro[cycloheptane-1,2 -naphthalene]-3 -carboxylate withm-tolyl isothiocyanate and subsequent cyclization of the intermediate thiourea derivative synthesized 2-thioxo-3-(m-tolyl)2,3-dihydro-1H-spiro[benzo[h]quinazoline-5,1 -cycloheptane]-4(6H)-one.. The last was alkylated by various halides in the presence of alkali to form 2-thiosubstituted 3-(m-tolyl)-3H-spiro[benzo[h]-quinazoline5,1 -cycloheptane]-4(6H)-ones.. The antibacterial activity of the synthesized compounds was studied by the agar diffusion method using Gram-positive strains Staphylococcus aureus 209p and Bacillus subtilis ATCC 6633 and Gram-negative strains Shigella flexneri 6858 and Escherichia coli 0-55.



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    reference strain staphylococcus aureus atcc 6538p fda 209p  (ATCC)
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    V31K S , R44K S , V31K S *, and R44K S * against S. aureus <t>209P</t> ( A ) and 129B ( B ) strains after 15 h ( A ) and 24 h ( B ) of incubation. Bacterial cultures in a liquid medium served as negative controls. Gentamicin sulfate and meropenem antibiotics were used as positive controls. Error bars show standard errors. Number of independent experiments is two. #—for significant differences with negative control p < 0.05.
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    Image Search Results


    V31K S , R44K S , V31K S *, and R44K S * against S. aureus 209P ( A ) and 129B ( B ) strains after 15 h ( A ) and 24 h ( B ) of incubation. Bacterial cultures in a liquid medium served as negative controls. Gentamicin sulfate and meropenem antibiotics were used as positive controls. Error bars show standard errors. Number of independent experiments is two. #—for significant differences with negative control p < 0.05.

    Journal: International Journal of Molecular Sciences

    Article Title: Optimizing Antimicrobial Peptide Design: Integration of Cell-Penetrating Peptides, Amyloidogenic Fragments, and Amino Acid Residue Modifications

    doi: 10.3390/ijms25116030

    Figure Lengend Snippet: V31K S , R44K S , V31K S *, and R44K S * against S. aureus 209P ( A ) and 129B ( B ) strains after 15 h ( A ) and 24 h ( B ) of incubation. Bacterial cultures in a liquid medium served as negative controls. Gentamicin sulfate and meropenem antibiotics were used as positive controls. Error bars show standard errors. Number of independent experiments is two. #—for significant differences with negative control p < 0.05.

    Article Snippet: Apart from the previously mentioned data concerning susceptible strains 209P ( S. aureus ), ATCC 43300 (MRSA), strain IP 5832 ( B. cereus ), ATCC 28753 ( P. aeruginosa ), and K12 ( E. coli ), we also evaluated their effects on clinical isolate strains 129B ( S. aureus ), SA 180-F (MRSA), and 2943 ( P. aeruginosa ), as well as susceptible MG1655 ( E. coli ). presents comparative results for two strains of each organism.

    Techniques: Incubation, Negative Control

    Results of R23F S * ( A ), V31K S * ( B ), and R44K S * ( C ) test for antimicrobial effect against S. aureus (strain 209P), MRSA (strain ATCC 43300), B. cereus (strain IP 5832), P. aeruginosa (strain ATCC 28753), and E. coli (strain K12) after incubation for 15 h. The antibiotic gentamicin sulfate was used as a positive control. The concentration of gentamicin was 100 µM. Cell cultures in a liquid medium (Mueller–Hinton Broth) served as a negative control. Error bars show standard errors. Number of independent experiments is two. #—for significant differences with negative control p < 0.05.

    Journal: International Journal of Molecular Sciences

    Article Title: Optimizing Antimicrobial Peptide Design: Integration of Cell-Penetrating Peptides, Amyloidogenic Fragments, and Amino Acid Residue Modifications

    doi: 10.3390/ijms25116030

    Figure Lengend Snippet: Results of R23F S * ( A ), V31K S * ( B ), and R44K S * ( C ) test for antimicrobial effect against S. aureus (strain 209P), MRSA (strain ATCC 43300), B. cereus (strain IP 5832), P. aeruginosa (strain ATCC 28753), and E. coli (strain K12) after incubation for 15 h. The antibiotic gentamicin sulfate was used as a positive control. The concentration of gentamicin was 100 µM. Cell cultures in a liquid medium (Mueller–Hinton Broth) served as a negative control. Error bars show standard errors. Number of independent experiments is two. #—for significant differences with negative control p < 0.05.

    Article Snippet: Apart from the previously mentioned data concerning susceptible strains 209P ( S. aureus ), ATCC 43300 (MRSA), strain IP 5832 ( B. cereus ), ATCC 28753 ( P. aeruginosa ), and K12 ( E. coli ), we also evaluated their effects on clinical isolate strains 129B ( S. aureus ), SA 180-F (MRSA), and 2943 ( P. aeruginosa ), as well as susceptible MG1655 ( E. coli ). presents comparative results for two strains of each organism.

    Techniques: Incubation, Positive Control, Concentration Assay, Negative Control

    Results of testing peptides against diverse strains of pathogenic microorganisms.

    Journal: International Journal of Molecular Sciences

    Article Title: Optimizing Antimicrobial Peptide Design: Integration of Cell-Penetrating Peptides, Amyloidogenic Fragments, and Amino Acid Residue Modifications

    doi: 10.3390/ijms25116030

    Figure Lengend Snippet: Results of testing peptides against diverse strains of pathogenic microorganisms.

    Article Snippet: Apart from the previously mentioned data concerning susceptible strains 209P ( S. aureus ), ATCC 43300 (MRSA), strain IP 5832 ( B. cereus ), ATCC 28753 ( P. aeruginosa ), and K12 ( E. coli ), we also evaluated their effects on clinical isolate strains 129B ( S. aureus ), SA 180-F (MRSA), and 2943 ( P. aeruginosa ), as well as susceptible MG1655 ( E. coli ). presents comparative results for two strains of each organism.

    Techniques: Incubation