2021
DOI: 10.1007/s12602-021-09813-4
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Bacteriocin-Like Inhibitory Substance (BLIS) Activity of Enterococcus faecium DB1 Against Biofilm Formation by Clostridium perfringens

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Cited by 8 publications
(5 citation statements)
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References 28 publications
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“…The potential bioactive compounds can be further purified from these fractions for various applications. Similar studies show BLIS from Enterococcus faecium strains could inhibit Clostridium perfringens biofilm formation ( 66 ). Studies have suggested that bacteriocins influence and regulate the human microbiome by eliminating pathogen invasion and colonization with effective modulation of their dynamic gene clusters and narrow range of activity ( 67 ).…”
Section: Discussionsupporting
confidence: 54%
“…The potential bioactive compounds can be further purified from these fractions for various applications. Similar studies show BLIS from Enterococcus faecium strains could inhibit Clostridium perfringens biofilm formation ( 66 ). Studies have suggested that bacteriocins influence and regulate the human microbiome by eliminating pathogen invasion and colonization with effective modulation of their dynamic gene clusters and narrow range of activity ( 67 ).…”
Section: Discussionsupporting
confidence: 54%
“…Lee et al [116] reported that BLIS obtained from Enterococcus faecium DB1 inhibited the growth and formation of biofilms of C. perfringens in chicken meat. The 2.5 mg/mL of DB1 BLIS suppressed the growth of C. perfringens by approximately 30%.…”
Section: Bacteriocin-like Inhibitory Substance (Blis)mentioning
confidence: 99%
“…The concentration of JM01 bacteriocin attached to the polystyrene surface was determined by the bicinchoninic acid (BCA) method by Lee et al . (2021) and Smith et al . (1985).…”
Section: Methodsmentioning
confidence: 96%
“…Adhesive property of JM01 bacteriocin to a polystyrene surface The concentration of JM01 bacteriocin attached to the polystyrene surface was determined by the bicinchoninic acid (BCA) method by Lee et al (2021) and Smith et al (1985). One hundred microlitres of JM01 bacteriocin (3.0 and 6.0 mg/mL) was added to each well of a 96-well polystyrene microplate, and the plates were incubated at 37 °C for 12 h. The supernatant of each well was gently washed, and then the remaining proteins in each well were resuspended with 25 μL of distilled water.…”
Section: Prevention Of Mrsa Adhesionmentioning
confidence: 99%