Please use this identifier to cite or link to this item: http://10.1.7.192:80/jspui/handle/123456789/5224
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dc.contributor.authorJena, Prasant Kumar-
dc.contributor.authorTrivedi, Disha-
dc.contributor.authorChaudhary, Harshita-
dc.contributor.authorSahoo, Tapasa Kumar-
dc.contributor.authorSeshadri, Sriram-
dc.date.accessioned2014-12-06T06:09:45Z-
dc.date.available2014-12-06T06:09:45Z-
dc.date.issued2013-
dc.identifier.issn0273-2289-
dc.identifier.urihttp://hdl.handle.net/123456789/5224-
dc.descriptionApplled Biochemistry & Biotechnology, 169, 2088–2100en_US
dc.description.abstractThe increase of multidrug-resistant pathogens and the restriction on the use antibiotics due to its side effects have drawn attention to the search for possible alternatives. Bacteriocins are small antimicrobial peptides produced by numerous bacteria. Much interest has been focused on bacteriocins because they exhibit inhibitory activity against pathogens. Lactic acid bacteria possess the ability to synthesize antimicrobial compounds (like bacteriocin) during their growth. In this study, an antibacterial substance (bacteriocin PJ4) produced by Lactobacillus helveticus PJ4, isolated from rat gut microflora, was identified as bacteriocin. It was effective against wide assay of both Gram-positive and Gram-negative bacteria involved in various diseases, including Escherichia coli, Bacillus subtilis, Pseudomonas aeruginosa, Enterococcus faecalis, and Staphylococcus aureus. The antimicrobial peptide was relatively heatresistant and also active over a wide pH range of 2–10. It has been partially purified to homogeneity using ammonium sulfate precipitation and size exclusion chromatography and checked on reverse-phase high-performance liquid chromatography. Sodium dodecyl sulfate–polyacrylamide gel electrophoresis of bacteriocin PJ4 purified through size exclusion chromatography resolved ~6.5 kDa protein with bacteriocin activity. The peptide is inactivated by proteolytic enzymes, trypsin, and lipase but not when treated with catalase, α-amylase, and pepsin. It showed a bactericidal mode of action against the indicator strains E. coli MTCC443, Lactobacillus casei MTCC1423, and E. faecalis DT48. Such characteristics indicate that this bacteriocin may be a potential candidate for alternative agents to control important pathogensen_US
dc.language.isoen_USen_US
dc.publisherSpringeren_US
dc.subjectFaculty Paperen_US
dc.subjectFaculty Paper, Scienceen_US
dc.subjectScience, Faculty Paperen_US
dc.subjectLactobacillus helveticusen_US
dc.subjectBacteriocinen_US
dc.subjectPurificationen_US
dc.subjectCharacterizationen_US
dc.subjectMode of actionen_US
dc.subjectPathogenen_US
dc.titleBacteriocin PJ4 Active Against Enteric Pathogen Produced by Lactobacillus helveticus PJ4 Isolated from Gut Microflora of Wistar Rat (Rattus norvegicus): Partial Purification and Characterization of Bacteriocinen_US
dc.typeArticleen_US
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