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vancomycin resistant enterococcus faecium  (ATCC)


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    ATCC vancomycin resistant enterococcus faecium
    Examination of cell membrane permeability in VanA VRE (E. <t>faecium</t> BAA-2317) induced by compounds 1 and 2 (no induced permeability) versus 9a (induced permeability) at 10 μM (added at 5 min). Cell envelop permeability is indicated by an increase in fluorescence resulting from propidium iodide (PI) influx following compound administration.
    Vancomycin Resistant Enterococcus Faecium, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 96 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/vancomycin resistant enterococcus faecium/product/ATCC
    Average 95 stars, based on 96 article reviews
    vancomycin resistant enterococcus faecium - by Bioz Stars, 2026-03
    95/100 stars

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    1) Product Images from "Guanidiniocarbonyl-Pyrrole (GCP) C- and N-Terminus Modifications of Vancomycin"

    Article Title: Guanidiniocarbonyl-Pyrrole (GCP) C- and N-Terminus Modifications of Vancomycin

    Journal: The Journal of organic chemistry

    doi: 10.1021/acs.joc.5c02760

    Examination of cell membrane permeability in VanA VRE (E. faecium BAA-2317) induced by compounds 1 and 2 (no induced permeability) versus 9a (induced permeability) at 10 μM (added at 5 min). Cell envelop permeability is indicated by an increase in fluorescence resulting from propidium iodide (PI) influx following compound administration.
    Figure Legend Snippet: Examination of cell membrane permeability in VanA VRE (E. faecium BAA-2317) induced by compounds 1 and 2 (no induced permeability) versus 9a (induced permeability) at 10 μM (added at 5 min). Cell envelop permeability is indicated by an increase in fluorescence resulting from propidium iodide (PI) influx following compound administration.

    Techniques Used: Membrane, Permeability, Fluorescence



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    Examination of cell membrane permeability in VanA VRE (E. <t>faecium</t> BAA-2317) induced by compounds 1 and 2 (no induced permeability) versus 9a (induced permeability) at 10 μM (added at 5 min). Cell envelop permeability is indicated by an increase in fluorescence resulting from propidium iodide (PI) influx following compound administration.
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    Examination of cell membrane permeability in VanA VRE (E. <t>faecium</t> BAA-2317) induced by compounds 1 and 2 (no induced permeability) versus 9a (induced permeability) at 10 μM (added at 5 min). Cell envelop permeability is indicated by an increase in fluorescence resulting from propidium iodide (PI) influx following compound administration.
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    Examination of cell membrane permeability in VanA VRE (E. <t>faecium</t> BAA-2317) induced by compounds 1 and 2 (no induced permeability) versus 9a (induced permeability) at 10 μM (added at 5 min). Cell envelop permeability is indicated by an increase in fluorescence resulting from propidium iodide (PI) influx following compound administration.
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    Examination of cell membrane permeability in VanA VRE (E. faecium BAA-2317) induced by compounds 1 and 2 (no induced permeability) versus 9a (induced permeability) at 10 μM (added at 5 min). Cell envelop permeability is indicated by an increase in fluorescence resulting from propidium iodide (PI) influx following compound administration.

    Journal: The Journal of organic chemistry

    Article Title: Guanidiniocarbonyl-Pyrrole (GCP) C- and N-Terminus Modifications of Vancomycin

    doi: 10.1021/acs.joc.5c02760

    Figure Lengend Snippet: Examination of cell membrane permeability in VanA VRE (E. faecium BAA-2317) induced by compounds 1 and 2 (no induced permeability) versus 9a (induced permeability) at 10 μM (added at 5 min). Cell envelop permeability is indicated by an increase in fluorescence resulting from propidium iodide (PI) influx following compound administration.

    Article Snippet: 39 One day before experiments were run, cultures of vancomycin-resistant Enterococcus faecium (VanA VRE, ATCC BAA-2317) were inoculated and grown in an orbital shaker at 37 °C in 100% brain-heart infusion broth for 12 h. The above bacterial solution was subjected to a subculture to obtain fresh mid log phase bacterial cells (incubation time = 6 h).

    Techniques: Membrane, Permeability, Fluorescence