2021
DOI: 10.1016/j.bcab.2021.102133
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Antagonistic activity of lipopeptide-biosurfactant producing Bacillus subtilis AKP, against Colletotrichum capsici, the causal organism of anthracnose disease of chilli

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Cited by 21 publications
(11 citation statements)
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“…One of the mechanisms of this antagonistic activity is direct antagonism against pathogenic fungi by inducing disruption of the plasma membrane. Another mechanism was reported in the lipopeptide iturin and fengycin by affecting the surface tension of the fungal cell membrane, causing the formation of micropores and ion leakage, which then led to cell death (Kumar et al 2021). Antifungal activity is also influenced by the carbon source used in the biosurfactant production media.…”
Section: Discussionmentioning
confidence: 99%
“…One of the mechanisms of this antagonistic activity is direct antagonism against pathogenic fungi by inducing disruption of the plasma membrane. Another mechanism was reported in the lipopeptide iturin and fengycin by affecting the surface tension of the fungal cell membrane, causing the formation of micropores and ion leakage, which then led to cell death (Kumar et al 2021). Antifungal activity is also influenced by the carbon source used in the biosurfactant production media.…”
Section: Discussionmentioning
confidence: 99%
“…In other previous studied cases, similar findings were reported where only one bacterial strain, Bacillus subtilis APK, exhibited significant antifungal potential against the anthracnose pathogen. This Bacillus strain demonstrated decreased pathogen mycelial growth in vitro and enhanced chili seedling growth under greenhouse conditions ( Kumar et al, 2021 ). Furthermore, a previous research has indicated that several Bacillus species can notably improve the growth and development of chili ( Peña-Yam et al, 2016 ).…”
Section: Discussionmentioning
confidence: 99%
“…The fermentation for bio‐surfactants production was done in a static batch culture of TGE medium (comprising glucose‐1%, tryptone‐1%, yeast‐1%, magnesium sulfate‐0.005%, manganese sulfate‐0.005%, pH 6.8 ± 2) at 37°C for 48 h. After incubation, the culture aliquot was harvested by centrifugation at 3174 × g for 10 min at 4°C. After that 50% methanol was added to the supernatant followed by vigorous shaking for 10 min (Kumar et al, 2021; Kumari et al, 2012). The culture aliquot was then concentrated in a rotary vacuum evaporator (Superfit R‐150, Mumbai, India).…”
Section: Methodsmentioning
confidence: 99%