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enterococcus faecium atcc10541 schleifer kilpper balz  (ATCC)


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    Structured Review

    ATCC enterococcus faecium atcc10541 schleifer kilpper balz
    Antimicrobial activity of essential oils (EOs) of plants belonging to the Verbenacea family against human pathogens (bacteria, fungi, or yeasts).
    Enterococcus Faecium Atcc10541 Schleifer Kilpper Balz, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 275 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fda/Enterococcus+hirae%3B+Strain+FDA+M19/pmc06017629-32-23-30
    Average 96 stars, based on 275 article reviews
    enterococcus faecium atcc10541 schleifer kilpper balz - by Bioz Stars, 2026-10
    96/100 stars

    Images

    1) Product Images from "Antimicrobial Activity and Chemical Composition of Essential Oils from Verbenaceae Species Growing in South America"

    Article Title: Antimicrobial Activity and Chemical Composition of Essential Oils from Verbenaceae Species Growing in South America

    Journal: Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry

    doi: 10.3390/molecules23030544

    Antimicrobial activity of essential oils (EOs) of plants belonging to the Verbenacea family against human pathogens (bacteria, fungi, or yeasts).
    Figure Legend Snippet: Antimicrobial activity of essential oils (EOs) of plants belonging to the Verbenacea family against human pathogens (bacteria, fungi, or yeasts).

    Techniques Used: Activity Assay, Bacteria, Isolation

    Related Articles

    Positive Control:

    Article Title: Antimicrobial Resistance in Escherichia coli from Captive Wild Felids: Associations with Host and Management Factors
    Article Snippet: .. In this assay, Enterococcus hirae ATCC 10541 was used as the positive control, and E. coli ATCC 25922 as the negative control. ..

    Negative Control:

    Article Title: Antimicrobial Resistance in Escherichia coli from Captive Wild Felids: Associations with Host and Management Factors
    Article Snippet: .. In this assay, Enterococcus hirae ATCC 10541 was used as the positive control, and E. coli ATCC 25922 as the negative control. ..

    other:

    Article Title: Susceptibility of Enterococcus spp. to chlorhexidine and Virkon® S: Effect of environmental factors, adaptation and implications for antimicrobial resistance.
    Article Snippet: Enterococcus spp. are potential hospital pathogens known for their intrinsic resistance to many antibiotics and resilience to many environmental factors.. Biocides are frequently used to eliminate these bacteria from surfaces within the hospital environment, yet reports of decreased susceptibility to these compounds and possible antibiotic cross-resistance have become sources of concern.. In this study, the susceptibility of 64 enterococci isolates to two biocides frequently used in clinical settings, Virkon® S and chlorhexidine, was tested in the absence and presence of two levels of organic matter.

    Article Title: In Vitro Evaluation of Halotolerant Bacillus velezensis 24.5 as a Promising Probiotic with Broad-Spectrum Antimicrobial Activity
    Article Snippet: Ent. hirae ATCC 10541 , , 5.33 ± 0.47 e , Ps. aeruginosa ATCC 27853 , , 2.00 ± 0.00 f , C. tropicalis ATCC 44508 , , 0.00 ± 0.00 g.

    Article Title: Susceptibility of Enterococcus spp. to chlorhexidine and Virkon® S: Effect of environmental factors, adaptation and implications for antimicrobial resistance.
    Article Snippet: Enterococcus spp. are potential hospital pathogens known for their intrinsic resistance to many antibiotics and resilience to many environmental factors.. Biocides are frequently used to eliminate these bacteria from surfaces within the hospital environment, yet reports of decreased susceptibility to these compounds and possible antibiotic cross-resistance have become sources of concern.. In this study, the susceptibility of 64 enterococci isolates to two biocides frequently used in clinical settings, Virkon S and chlorhexidine, was tested in the absence and presence of two levels of organic matter.

    Article Title: Comprehensive evaluation of the bactericidal and anti-pathogenic efficacy of chemical disinfectants against antibiotic resistant ESKAPE clinical strains
    Article Snippet: E. hirae ATCC 10541 , 80 , > 80 , 40 , 80 , 0.078 , 2.5 , 0.078 , 0.625 , 0.004 , 8 , 0.004 , 8.


    Incubation:

    Article Title: Antimicrobial Efficacy of a Taurolidine‐Based Antimicrobial Compound on Contaminated Surfaces Simulated in a Standardized 4‐Field Test
    Article Snippet: .. Reference microbial strains from the American Type Culture Collection (ATCC), including Staphylococcus aureus (ATCC 6538), Pseudomonas aeruginosa (ATCC 15 442), Enterococcus hirae (ATCC 10 541), and Candida albicans (ATCC 10 231), were grown on tryptic soy agar (TSA, Oxoid, catalog: CM0131R) and incubated at 36 °C ± 1.0 °C for 48 h (Binder BDS115‐230 V). .. Initial subcultures were prepared using sterile 1 μL inoculating loops (Roth selection), diluted in 1 mL of NaCl peptone (NaP, Oxoid, catalog: CM0982B), plated on TSA, and incubated under the same conditions.

    Library Screening:

    Article Title: Repurposing antibacterial drugs identifies ridinilazole and CRS3123 as promising candidates against vancomycin-resistant enterococci.
    Article Snippet: .. <0.007 0.031 0.5 >128 Enterococcus faecium UAA945 NR32094 <0.007 0.25 0.5 >128 Enterococcus faecalis B3336 NR-31887 <0.007 >64 0.5 >128 Enterococcus faecalis R712 HM-335 0.031 >64 0.5 128 Enterococcus faecalis NR31971 <0.007 2 0.5 32 Enterococcus faecalis NR31970 <0.007 4 0.5 0.5 Enterococcus faecalis NR31972 <0.007 64 0.5 >128 Enterococcus faecalis ATCC 29212 <0.007 0.5 0.5 >128 Enterococcus hirae ATCC 10541 <0.007 0.125 2 0.5 Enterococcus durans ATCC 11576 <0.007 <0.007 0.5 1 AR TIC LE IN PR ES S 499 500 501 Figure Legends: 502 503 Figure 1: MCE antibacterial library screening of 1135 compounds at 4 μM 504 against E. faecium NR-31909. ..



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    Image Search Results


    High-content image analysis/dimensionality reduction of drug screening data (A–C) Representative data of high content analysis across six GSC lines and three compound libraries (LOPAC, (A) Prestwick FDA (B) and C3L, (C) by 3D principal component analysis (PCA) (median aggregation to well level, n = 6 fields of view). DMSO controls circled in Black ( n = 48 per plate). Magnitude of vector co-ordinates for PC1, 2, 3 (sized by PC4) are indicated by color, red-pink (strong –PC1, –PC2), blue (strong +PC3, –PC2), green (strong +PC1 +PC2), yellow/gray (weaker phenotypes). PC1-4 factor loadings are given (%). Factor loadings are provided in . (D–F) Phenotypic distance of screened compounds (LOPAC, D, Prestwick FDA, E and C3L, F). We employed 20 principal components (>60% explained variance) to compute a phenotypic distance (Euclidean) for each compound. The corresponding p values are plotted against cell survival (normalized z scores, y axis). Legend indicates strength of –log 10 [ p value] distribution (five bins, red = maximal effect, reducing to gray where at = arbitrary threshold). Several example hits are labeled.

    Journal: iScience

    Article Title: A comprehensive pharmacological survey across heterogeneous patient-derived glioblastoma stem cell models

    doi: 10.1016/j.isci.2026.115839

    Figure Lengend Snippet: High-content image analysis/dimensionality reduction of drug screening data (A–C) Representative data of high content analysis across six GSC lines and three compound libraries (LOPAC, (A) Prestwick FDA (B) and C3L, (C) by 3D principal component analysis (PCA) (median aggregation to well level, n = 6 fields of view). DMSO controls circled in Black ( n = 48 per plate). Magnitude of vector co-ordinates for PC1, 2, 3 (sized by PC4) are indicated by color, red-pink (strong –PC1, –PC2), blue (strong +PC3, –PC2), green (strong +PC1 +PC2), yellow/gray (weaker phenotypes). PC1-4 factor loadings are given (%). Factor loadings are provided in . (D–F) Phenotypic distance of screened compounds (LOPAC, D, Prestwick FDA, E and C3L, F). We employed 20 principal components (>60% explained variance) to compute a phenotypic distance (Euclidean) for each compound. The corresponding p values are plotted against cell survival (normalized z scores, y axis). Legend indicates strength of –log 10 [ p value] distribution (five bins, red = maximal effect, reducing to gray where at = arbitrary threshold). Several example hits are labeled.

    Article Snippet: Prestwick FDA approved Drug Library , Prestwick Chemical , https://www.prestwickchemical.com/screening-libraries/prestwick-chemical-library/.

    Techniques: Drug discovery, High Content Screening, Plasmid Preparation, Labeling

    High-content image analysis/dimensionality reduction of drug screening data (A–C) Representative data of high content analysis across six GSC lines and three compound libraries (LOPAC, (A) Prestwick FDA (B) and C3L, (C) by 3D principal component analysis (PCA) (median aggregation to well level, n = 6 fields of view). DMSO controls circled in Black ( n = 48 per plate). Magnitude of vector co-ordinates for PC1, 2, 3 (sized by PC4) are indicated by color, red-pink (strong –PC1, –PC2), blue (strong +PC3, –PC2), green (strong +PC1 +PC2), yellow/gray (weaker phenotypes). PC1-4 factor loadings are given (%). Factor loadings are provided in . (D–F) Phenotypic distance of screened compounds (LOPAC, D, Prestwick FDA, E and C3L, F). We employed 20 principal components (>60% explained variance) to compute a phenotypic distance (Euclidean) for each compound. The corresponding p values are plotted against cell survival (normalized z scores, y axis). Legend indicates strength of –log 10 [ p value] distribution (five bins, red = maximal effect, reducing to gray where at = arbitrary threshold). Several example hits are labeled.

    Journal: iScience

    Article Title: A comprehensive pharmacological survey across heterogeneous patient-derived glioblastoma stem cell models

    doi: 10.1016/j.isci.2026.115839

    Figure Lengend Snippet: High-content image analysis/dimensionality reduction of drug screening data (A–C) Representative data of high content analysis across six GSC lines and three compound libraries (LOPAC, (A) Prestwick FDA (B) and C3L, (C) by 3D principal component analysis (PCA) (median aggregation to well level, n = 6 fields of view). DMSO controls circled in Black ( n = 48 per plate). Magnitude of vector co-ordinates for PC1, 2, 3 (sized by PC4) are indicated by color, red-pink (strong –PC1, –PC2), blue (strong +PC3, –PC2), green (strong +PC1 +PC2), yellow/gray (weaker phenotypes). PC1-4 factor loadings are given (%). Factor loadings are provided in . (D–F) Phenotypic distance of screened compounds (LOPAC, D, Prestwick FDA, E and C3L, F). We employed 20 principal components (>60% explained variance) to compute a phenotypic distance (Euclidean) for each compound. The corresponding p values are plotted against cell survival (normalized z scores, y axis). Legend indicates strength of –log 10 [ p value] distribution (five bins, red = maximal effect, reducing to gray where at = arbitrary threshold). Several example hits are labeled.

    Article Snippet: Prestwick FDA , 1,280 , Prestwick Chemical (∼2016) https://www.prestwickchemical.com/screening-libraries/prestwick-chemical-library/ , 10,000, 1,000 , Staurosporine (1,000 nM).

    Techniques: Drug discovery, High Content Screening, Plasmid Preparation, Labeling