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atcc 29213 mssa strains  (ATCC)


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    ATCC atcc 29213 mssa strains
    Atcc 29213 Mssa Strains, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 9738 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 99 stars, based on 9738 article reviews
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    Article Title: Anti- Staphylococcus aureus Activity of Volatile Phytochemicals and Their Combinations with Conventional Antibiotics Against Methicillin-Susceptible S. aureus (MSSA) and Methicillin-Resistant S. aureus (MRSA) Strains
    Article Snippet: For instance, borderline synergism was observed for CAR or THY combined with TET on MSSA strain ATCC 29213 (FICI = 0.53) and MRSA strain ATCC 43300 (FICI = 0.38) [ ], contrasting with our results.

    Article Title: A novel methionyl-tRNA synthetase inhibitor targeting gram-positive bacterial pathogens.
    Article Snippet: New antibiotics are needed to treat gram-positive bacterial pathogens.. MRS-2541 is a novel inhibitor of methionyl-tRNA synthetase with selective activity against gram-positive bacteria.. The minimum inhibitory concentrations (MICs) against Staphylococcus aureus, Streptococcus pyogenes, and Enterococcus species range from 0.063 to 0.5 μg/mL.

    Article Title: Integrating genomics and metabolomics to accelerate the discovery of anti-MRSA natural products from the endophytic fungus Neocucurbitaria sp. VM-36
    Article Snippet: Our findings further show that compound 1 has significant bactericidal effect on S. aureus , as exemplified for the three MRSA strains USA300, D15 and D17, and the MSSA strain ATCC 29213.

    Article Title: The efficacy of the food-grade antimicrobial xanthorrhizol against Staphylococcus aureus is associated with McsL channel expression
    Article Snippet: Since the MRSA strain ATCC 33592 is resistant to many antibiotics used in genetic experiments, such as erythromycin (100 μg/mL), kanamycin (25 μg/mL), and tetracycline (30 μg/mL) (our unpublished data), we plotted a time–kill curve for the MSSA strain ATCC 29213 ( ) using 0.5 × MIC xanthorrhizol for a more detailed study of its action against S. aureus.

    Article Title: The efficacy of the food-grade antimicrobial xanthorrhizol against Staphylococcus aureus is associated with McsL channel expression
    Article Snippet: The MIC of xanthorrhizol was determined to be 64 μg/mL for both the MRSA strain ATCC 33592 and the MSSA strain ATCC 29213.

    Article Title: The efficacy of the food-grade antimicrobial xanthorrhizol against Staphylococcus aureus is associated with McsL channel expression.
    Article Snippet: Rapid killing effect of xanthorrhizol against MRSA and MSSA strains The MIC of xanthorrhizol was determined to be 64 μg/mL for both the MRSA strain ATCC 33592 and the MSSA strain ATCC 29213.

    Isolation:

    Article Title: Algal extract for use in the treatment or prevention of post-traumatic immunosuppression
    Article Snippet: .. 0 point 1 point 2 points 3 points Weight loss <5% 5-12% 13-20% >20% Physical Normal Slightly Moderately Highly impaired appearance impaired impaired (spiky hairs and hunched back) Behaviour Normal Slightly Moderately Highly altered (isolation) altered altered (permanent isolation from the rest of the group) Bacterial Inoculum: The MSSA strain ATCC 29213 (hemolysin positive, Panton Valentine negative leucocidin) was used for all the experiments. ..

    Concentration Assay:

    Article Title: Role of methicillin-resistant Staphylococcus aureus in cutaneous infections: Current treatments and therapeutic approaches for future advancement.
    Article Snippet: Antibiotics are often prescribed as a first-line treatment for bacterial skin infections, particularly in severe and persistent cases.. However, the ability of the pathogen to develop antibiotic resistance complicates the treatment of these diseases.. Methicillin-resistant Staphylococcus aureus (MRSA) is one of the primary microorganisms implicated in skin and soft tissue infections, such as cellulitis, impetigo, and infections secondary to atopic dermatitis (AD) and has exerted significant pressure on the healthcare industry due to its resistance to conventional antibiotics, including beta-lactams.



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    ATCC s aureus mssa strain atcc 29213
    A. MRSA expresses five PBPs, PBP1, PBP2, PBP2A (pink), PBP3, and PBP4. B. FICI values calculated based on MRSA USA300 grown in the presence of BAY 11-7082 and another antibiotic. FICI values <0.5 represent synergy, values between 0.5-4 represent no interaction, and values >4 represent antagonism. C. FICI values for MRSA USA300 (pink) and MSSA <t>ATCC</t> <t>29213</t> (blue) grown in the presence of BAY 11-7082 and a β-lactam that synergizes with BAY 11-7082 in MRSA. Data represent an average of three independent experiments performed in triplicate.
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    ATCC reference mssa strain
    Synthesis and in vitro evaluation of 18 F-glucopyranosyl- d -sorbitol analogs. (A) Schematic of the synthesis of 18 F-glucopyranosyl- d -sorbitol analogs from [ 18 F]­FDG via reverse phosphorolysis and subsequent reduction. (B) Chemical structures of 18 F-glucopyranosyl- d -sorbitol analogs used in this study, which differ by glycosidic linkages and stereochemistry. The highlighted portions of analogs correspond to the [ 18 F]­FDS scaffold. RCY: radiochemical yield (nondecay corrected), RCP: radiochemical purity. (C,D) In vitro uptake of [ 18 F]­FNT, [ 18 F]­FMT, [ 18 F]­FLT, [ 18 F]­FCT, and [ 18 F]­FDS (control) by the indicated Gram-positive (C) and Gram-negative (D) bacterial pathogens. (E) Specificity of [ 18 F]­FNT uptake in S. aureus (Ctrl, ATCC 29213) reflected by reduced uptake in the presence of [ 19 F]­FNT (1 mM, blocking) and in heat killed bacteria. (F) Differential uptake of [ 18 F]­FNT in methicillin-resistant S. <t>aureus</t> <t>(MRSA)</t> and methicillin-sensitive S. aureus <t>(MSSA)</t> clinical isolates compared to reference strain ( S. aureus ATCC 29213; MSSA). **** P < 0.0001 by unpaired Student’s t -test.
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    ATCC bacterial strains methicillinsensitive staphylococcus aureus atcc 29213 mssa
    Synthesis and in vitro evaluation of 18 F-glucopyranosyl- d -sorbitol analogs. (A) Schematic of the synthesis of 18 F-glucopyranosyl- d -sorbitol analogs from [ 18 F]­FDG via reverse phosphorolysis and subsequent reduction. (B) Chemical structures of 18 F-glucopyranosyl- d -sorbitol analogs used in this study, which differ by glycosidic linkages and stereochemistry. The highlighted portions of analogs correspond to the [ 18 F]­FDS scaffold. RCY: radiochemical yield (nondecay corrected), RCP: radiochemical purity. (C,D) In vitro uptake of [ 18 F]­FNT, [ 18 F]­FMT, [ 18 F]­FLT, [ 18 F]­FCT, and [ 18 F]­FDS (control) by the indicated Gram-positive (C) and Gram-negative (D) bacterial pathogens. (E) Specificity of [ 18 F]­FNT uptake in S. aureus (Ctrl, ATCC 29213) reflected by reduced uptake in the presence of [ 19 F]­FNT (1 mM, blocking) and in heat killed bacteria. (F) Differential uptake of [ 18 F]­FNT in methicillin-resistant S. <t>aureus</t> <t>(MRSA)</t> and methicillin-sensitive S. aureus <t>(MSSA)</t> clinical isolates compared to reference strain ( S. aureus ATCC 29213; MSSA). **** P < 0.0001 by unpaired Student’s t -test.
    Bacterial Strains Methicillinsensitive Staphylococcus Aureus Atcc 29213 Mssa, 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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    ATCC strain atcc 29213 mssa
    Synthesis and in vitro evaluation of 18 F-glucopyranosyl- d -sorbitol analogs. (A) Schematic of the synthesis of 18 F-glucopyranosyl- d -sorbitol analogs from [ 18 F]­FDG via reverse phosphorolysis and subsequent reduction. (B) Chemical structures of 18 F-glucopyranosyl- d -sorbitol analogs used in this study, which differ by glycosidic linkages and stereochemistry. The highlighted portions of analogs correspond to the [ 18 F]­FDS scaffold. RCY: radiochemical yield (nondecay corrected), RCP: radiochemical purity. (C,D) In vitro uptake of [ 18 F]­FNT, [ 18 F]­FMT, [ 18 F]­FLT, [ 18 F]­FCT, and [ 18 F]­FDS (control) by the indicated Gram-positive (C) and Gram-negative (D) bacterial pathogens. (E) Specificity of [ 18 F]­FNT uptake in S. aureus (Ctrl, ATCC 29213) reflected by reduced uptake in the presence of [ 19 F]­FNT (1 mM, blocking) and in heat killed bacteria. (F) Differential uptake of [ 18 F]­FNT in methicillin-resistant S. <t>aureus</t> <t>(MRSA)</t> and methicillin-sensitive S. aureus <t>(MSSA)</t> clinical isolates compared to reference strain ( S. aureus ATCC 29213; MSSA). **** P < 0.0001 by unpaired Student’s t -test.
    Strain Atcc 29213 Mssa, 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. MRSA expresses five PBPs, PBP1, PBP2, PBP2A (pink), PBP3, and PBP4. B. FICI values calculated based on MRSA USA300 grown in the presence of BAY 11-7082 and another antibiotic. FICI values <0.5 represent synergy, values between 0.5-4 represent no interaction, and values >4 represent antagonism. C. FICI values for MRSA USA300 (pink) and MSSA ATCC 29213 (blue) grown in the presence of BAY 11-7082 and a β-lactam that synergizes with BAY 11-7082 in MRSA. Data represent an average of three independent experiments performed in triplicate.

    Journal: bioRxiv

    Article Title: BAY 11-7082 potentiates select β-lactams to inhibit growth of methicillin-resistant Staphylococcus aureus

    doi: 10.64898/2026.01.13.699313

    Figure Lengend Snippet: A. MRSA expresses five PBPs, PBP1, PBP2, PBP2A (pink), PBP3, and PBP4. B. FICI values calculated based on MRSA USA300 grown in the presence of BAY 11-7082 and another antibiotic. FICI values <0.5 represent synergy, values between 0.5-4 represent no interaction, and values >4 represent antagonism. C. FICI values for MRSA USA300 (pink) and MSSA ATCC 29213 (blue) grown in the presence of BAY 11-7082 and a β-lactam that synergizes with BAY 11-7082 in MRSA. Data represent an average of three independent experiments performed in triplicate.

    Article Snippet: We conducted checkerboard assays with MRSA strain USA300, which has mecA ( , Figure S2 ), as well as methicillin-sensitive S. aureus (MSSA) strain ATCC 29213, which does not, to understand the potential role of PBP2a ( , Figure S3 ).

    Techniques:

    Synthesis and in vitro evaluation of 18 F-glucopyranosyl- d -sorbitol analogs. (A) Schematic of the synthesis of 18 F-glucopyranosyl- d -sorbitol analogs from [ 18 F]­FDG via reverse phosphorolysis and subsequent reduction. (B) Chemical structures of 18 F-glucopyranosyl- d -sorbitol analogs used in this study, which differ by glycosidic linkages and stereochemistry. The highlighted portions of analogs correspond to the [ 18 F]­FDS scaffold. RCY: radiochemical yield (nondecay corrected), RCP: radiochemical purity. (C,D) In vitro uptake of [ 18 F]­FNT, [ 18 F]­FMT, [ 18 F]­FLT, [ 18 F]­FCT, and [ 18 F]­FDS (control) by the indicated Gram-positive (C) and Gram-negative (D) bacterial pathogens. (E) Specificity of [ 18 F]­FNT uptake in S. aureus (Ctrl, ATCC 29213) reflected by reduced uptake in the presence of [ 19 F]­FNT (1 mM, blocking) and in heat killed bacteria. (F) Differential uptake of [ 18 F]­FNT in methicillin-resistant S. aureus (MRSA) and methicillin-sensitive S. aureus (MSSA) clinical isolates compared to reference strain ( S. aureus ATCC 29213; MSSA). **** P < 0.0001 by unpaired Student’s t -test.

    Journal: JACS Au

    Article Title: Regioselective Glycosylation of Fluorine-18-Labeled Sorbitol for Enhanced Bacterial Detection In Vivo Using PET

    doi: 10.1021/jacsau.5c01153

    Figure Lengend Snippet: Synthesis and in vitro evaluation of 18 F-glucopyranosyl- d -sorbitol analogs. (A) Schematic of the synthesis of 18 F-glucopyranosyl- d -sorbitol analogs from [ 18 F]­FDG via reverse phosphorolysis and subsequent reduction. (B) Chemical structures of 18 F-glucopyranosyl- d -sorbitol analogs used in this study, which differ by glycosidic linkages and stereochemistry. The highlighted portions of analogs correspond to the [ 18 F]­FDS scaffold. RCY: radiochemical yield (nondecay corrected), RCP: radiochemical purity. (C,D) In vitro uptake of [ 18 F]­FNT, [ 18 F]­FMT, [ 18 F]­FLT, [ 18 F]­FCT, and [ 18 F]­FDS (control) by the indicated Gram-positive (C) and Gram-negative (D) bacterial pathogens. (E) Specificity of [ 18 F]­FNT uptake in S. aureus (Ctrl, ATCC 29213) reflected by reduced uptake in the presence of [ 19 F]­FNT (1 mM, blocking) and in heat killed bacteria. (F) Differential uptake of [ 18 F]­FNT in methicillin-resistant S. aureus (MRSA) and methicillin-sensitive S. aureus (MSSA) clinical isolates compared to reference strain ( S. aureus ATCC 29213; MSSA). **** P < 0.0001 by unpaired Student’s t -test.

    Article Snippet: [ 18 F] FNT exhibited higher uptake in clinical MSSA and MRSA isolates compared to the reference MSSA strain ( F, S. aureus ATCC 29213, P < 0.0001).

    Techniques: In Vitro, Control, Blocking Assay, Bacteria