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DC Field | Value | Language |
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dc.contributor.author | Varsha, K K | - |
dc.contributor.author | Nampoothiri, K M | - |
dc.contributor.author | Shilpa, G | - |
dc.contributor.author | Priya, S | - |
dc.date.accessioned | 2023-01-26T06:27:04Z | - |
dc.date.available | 2023-01-26T06:27:04Z | - |
dc.date.issued | 2021-06 | - |
dc.identifier.citation | Letters in Applied Microbiology;72(6):706-713 | en_US |
dc.identifier.uri | https://doi.org/10.1111/lam.13464 | - |
dc.identifier.uri | http://localhost:8080/xmlui/handle/123456789/4204 | - |
dc.description.abstract | A bioactive peptide of 8595 Da was purified from the cell free supernatant of Lactococcus garvieae subsp. bovis BSN307T . MALDI MS/MS peptide mapping and the data base search displayed no significant similarity to any reported antimicrobial peptide of LAB. This peptide at a dose concentration of 200 µg ml−1 inhibited the growth of both Gram-positive and Gram-negative bacteria by 58–89% and a dose of 500 µg ml−1 scavenged 50% of DPPH-free radicals generated. Interestingly, cytotoxicity assay demonstrated that 17 µg ml−1 of peptide selectively inhibited 50% proliferation of mammalian cancer cell lines HeLa and MCF-7 whereas normal H9c2 cells remained unaffected. Fluorescent microscopic analysis after DAPI nuclear staining of HeLa cells showed characteristics of apoptosis and activation of caspase-3 was ascertained by caspase-3 fluorescence assay. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.subject | antimicrobials | en_US |
dc.subject | cytotoxicity | en_US |
dc.subject | lactic acid bacteria | en_US |
dc.subject | peptides | en_US |
dc.subject | probiotics | en_US |
dc.title | Antimicrobial Activity and Cytotoxicity Trait of a Bioactive Peptide Purified from Lactococcus Garvieae Subsp. Bovis BSN307 T | en_US |
dc.type | Article | en_US |
Appears in Collections: | 2021 |
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Antimicrobial activity and cytotoxicity trait of a bioactive_Varsha_letters in applied microbiology.pdf Restricted Access | 887.48 kB | Adobe PDF | View/Open Request a copy |
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