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atcc 271 medium  (ATCC)


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    Structured Review

    ATCC atcc 271 medium
    Atcc 271 Medium, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 18 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/atcc+271+medium/Rhodococcus+rhodochrous+formerly+rhodococcus/pm37299655-120-36-36
    Average 93 stars, based on 18 article reviews
    atcc 271 medium - by Bioz Stars, 2026-10
    93/100 stars

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    Related Articles

    Virus:

    Article Title: Enhancing Functionalization of Health Care Textiles with Gold Nanoparticle-Loaded Hydroxyapatite Composites.
    Article Snippet: To quantify MS2 plate forming units (PFU), its host E. coli (ATCC 15597) was used. .. Culture Media: Nutrient agar (NA) and nutrient broth (NB) were used as a medium for P. aeruginosa; Trypticase soy broth (TSB) and solid Trypticase soy agar (TSA) were used for E. coli and S. epidermidis; finally, ATCC 271 medium was used for virus and host manipulation. .. All reactants were purchased from Liofilchem (Téramo, Italy).

    Article Title: Enhancing Functionalization of Health Care Textiles with Gold Nanoparticle-Loaded Hydroxyapatite Composites
    Article Snippet: .. Briefly, 100 μL of AuNPs-HAp dispersions at different concentrations (0, 0.08, 0.1, and 0.2 mg/mL) were diluted with 100 μL of 1 × 10 7 colony-forming units (CFU)/mL of each microorganism (1 × 10 5 PFU/mL for MS2), and their optical density was determined by analysis in a spectrophotometer, before and after incubation at 37 °C, 120 rpm, for 24 h. Then, for the quantitative analysis, 200 μL of each AuNPs-HAp suspension with each microorganism was serially diluted with the medium NA for P. aeruginosa , TSA for S. epidermidis and E. coli , and ATCC 271 medium for MS2 virus (diluted 5 times, in a proportion of 1:10). (2) Optical density = O D T 24 − O D T 0 where: OD T24 —Optical density after 24 h. OD T0 —Optical density immediately after inoculation. (3) Log reduction = Log control − Log [ exposed ] where: Control—Inoculum microorganism concentration. ..

    Sterility:

    Article Title: Bioactive Compounds from Banana Leaf Extracts: Influence of Extraction Methodologies and Their Integration into Knitted Hemp Fabrics
    Article Snippet: .. Textile square samples of 6.25 cm 2 were inoculated with 50 μL of 1 × 10 7 Colony-Forming Units (CFUs)/mL of S. aureus and C. albicans , previously washed with sterile Phosphate-Buffered Saline (PBS), or 50 μL of 1 × 10 7 plate-forming units (PFUs)/mL of MS2 in ATCC 271 medium. ..

    Article Title: Bioactive Compounds from Banana Leaf Extracts: Influence of Extraction Methodologies and Their Integration into Knitted Hemp Fabrics.
    Article Snippet: .. Textile square samples of 6.25 cm2 were inoculated with 50 μL of 1 × 107 Colony-Forming Units (CFUs)/mL of S. aureus and C. albicans, previously washed with sterile Phosphate-Buffered Saline (PBS), or 50 μL of 1 × 107 plate-forming units (PFUs)/mL of MS2 in ATCC 271 medium. ..

    Saline:

    Article Title: Bioactive Compounds from Banana Leaf Extracts: Influence of Extraction Methodologies and Their Integration into Knitted Hemp Fabrics
    Article Snippet: .. Textile square samples of 6.25 cm 2 were inoculated with 50 μL of 1 × 10 7 Colony-Forming Units (CFUs)/mL of S. aureus and C. albicans , previously washed with sterile Phosphate-Buffered Saline (PBS), or 50 μL of 1 × 10 7 plate-forming units (PFUs)/mL of MS2 in ATCC 271 medium. ..

    Article Title: Bioactive Compounds from Banana Leaf Extracts: Influence of Extraction Methodologies and Their Integration into Knitted Hemp Fabrics.
    Article Snippet: .. Textile square samples of 6.25 cm2 were inoculated with 50 μL of 1 × 107 Colony-Forming Units (CFUs)/mL of S. aureus and C. albicans, previously washed with sterile Phosphate-Buffered Saline (PBS), or 50 μL of 1 × 107 plate-forming units (PFUs)/mL of MS2 in ATCC 271 medium. ..

    Bacteria:

    Article Title: Elastic bands antimicrobial functionalization
    Article Snippet: The samples, with 2.5 cm length, were inoculated with 50 μL containing 1 × 107 colony forming units (CFU) mL− 1 of S. aureus, and P. aeruginosa 1 × 107 PFU mL-1 in ATCC 271, for 1 h or 2 h for MS2, at room temperature. .. The samples were then immersed in 5 mL (PBS for bacteria or ATCC 271 medium for MS2) and thoroughly vortexed for at least 1 min. .. The washing liquid was serially diluted in PBS for bacteria or ATCC 271 for MS2, and subsequent dilutions were inoculated in solid medium.

    Spectrophotometry:

    Article Title: Enhancing Functionalization of Health Care Textiles with Gold Nanoparticle-Loaded Hydroxyapatite Composites
    Article Snippet: .. Briefly, 100 μL of AuNPs-HAp dispersions at different concentrations (0, 0.08, 0.1, and 0.2 mg/mL) were diluted with 100 μL of 1 × 10 7 colony-forming units (CFU)/mL of each microorganism (1 × 10 5 PFU/mL for MS2), and their optical density was determined by analysis in a spectrophotometer, before and after incubation at 37 °C, 120 rpm, for 24 h. Then, for the quantitative analysis, 200 μL of each AuNPs-HAp suspension with each microorganism was serially diluted with the medium NA for P. aeruginosa , TSA for S. epidermidis and E. coli , and ATCC 271 medium for MS2 virus (diluted 5 times, in a proportion of 1:10). (2) Optical density = O D T 24 − O D T 0 where: OD T24 —Optical density after 24 h. OD T0 —Optical density immediately after inoculation. (3) Log reduction = Log control − Log [ exposed ] where: Control—Inoculum microorganism concentration. ..

    Incubation:

    Article Title: Enhancing Functionalization of Health Care Textiles with Gold Nanoparticle-Loaded Hydroxyapatite Composites
    Article Snippet: .. Briefly, 100 μL of AuNPs-HAp dispersions at different concentrations (0, 0.08, 0.1, and 0.2 mg/mL) were diluted with 100 μL of 1 × 10 7 colony-forming units (CFU)/mL of each microorganism (1 × 10 5 PFU/mL for MS2), and their optical density was determined by analysis in a spectrophotometer, before and after incubation at 37 °C, 120 rpm, for 24 h. Then, for the quantitative analysis, 200 μL of each AuNPs-HAp suspension with each microorganism was serially diluted with the medium NA for P. aeruginosa , TSA for S. epidermidis and E. coli , and ATCC 271 medium for MS2 virus (diluted 5 times, in a proportion of 1:10). (2) Optical density = O D T 24 − O D T 0 where: OD T24 —Optical density after 24 h. OD T0 —Optical density immediately after inoculation. (3) Log reduction = Log control − Log [ exposed ] where: Control—Inoculum microorganism concentration. ..

    Suspension:

    Article Title: Enhancing Functionalization of Health Care Textiles with Gold Nanoparticle-Loaded Hydroxyapatite Composites
    Article Snippet: .. Briefly, 100 μL of AuNPs-HAp dispersions at different concentrations (0, 0.08, 0.1, and 0.2 mg/mL) were diluted with 100 μL of 1 × 10 7 colony-forming units (CFU)/mL of each microorganism (1 × 10 5 PFU/mL for MS2), and their optical density was determined by analysis in a spectrophotometer, before and after incubation at 37 °C, 120 rpm, for 24 h. Then, for the quantitative analysis, 200 μL of each AuNPs-HAp suspension with each microorganism was serially diluted with the medium NA for P. aeruginosa , TSA for S. epidermidis and E. coli , and ATCC 271 medium for MS2 virus (diluted 5 times, in a proportion of 1:10). (2) Optical density = O D T 24 − O D T 0 where: OD T24 —Optical density after 24 h. OD T0 —Optical density immediately after inoculation. (3) Log reduction = Log control − Log [ exposed ] where: Control—Inoculum microorganism concentration. ..

    Control:

    Article Title: Enhancing Functionalization of Health Care Textiles with Gold Nanoparticle-Loaded Hydroxyapatite Composites
    Article Snippet: .. Briefly, 100 μL of AuNPs-HAp dispersions at different concentrations (0, 0.08, 0.1, and 0.2 mg/mL) were diluted with 100 μL of 1 × 10 7 colony-forming units (CFU)/mL of each microorganism (1 × 10 5 PFU/mL for MS2), and their optical density was determined by analysis in a spectrophotometer, before and after incubation at 37 °C, 120 rpm, for 24 h. Then, for the quantitative analysis, 200 μL of each AuNPs-HAp suspension with each microorganism was serially diluted with the medium NA for P. aeruginosa , TSA for S. epidermidis and E. coli , and ATCC 271 medium for MS2 virus (diluted 5 times, in a proportion of 1:10). (2) Optical density = O D T 24 − O D T 0 where: OD T24 —Optical density after 24 h. OD T0 —Optical density immediately after inoculation. (3) Log reduction = Log control − Log [ exposed ] where: Control—Inoculum microorganism concentration. ..

    Concentration Assay:

    Article Title: Enhancing Functionalization of Health Care Textiles with Gold Nanoparticle-Loaded Hydroxyapatite Composites
    Article Snippet: .. Briefly, 100 μL of AuNPs-HAp dispersions at different concentrations (0, 0.08, 0.1, and 0.2 mg/mL) were diluted with 100 μL of 1 × 10 7 colony-forming units (CFU)/mL of each microorganism (1 × 10 5 PFU/mL for MS2), and their optical density was determined by analysis in a spectrophotometer, before and after incubation at 37 °C, 120 rpm, for 24 h. Then, for the quantitative analysis, 200 μL of each AuNPs-HAp suspension with each microorganism was serially diluted with the medium NA for P. aeruginosa , TSA for S. epidermidis and E. coli , and ATCC 271 medium for MS2 virus (diluted 5 times, in a proportion of 1:10). (2) Optical density = O D T 24 − O D T 0 where: OD T24 —Optical density after 24 h. OD T0 —Optical density immediately after inoculation. (3) Log reduction = Log control − Log [ exposed ] where: Control—Inoculum microorganism concentration. ..



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