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Título

Combined effect of high-pressure treatments and bacteriocin-producing lactic acid bacteria on inactivation of Escherichia coli O157H7 in raw-milk cheese

AutorRodríguez Mínguez, Eva; Arques Orobón, Juan Luis; Núñez Gutiérrez, Manuel; Gaya Sicilia, María Pilar; Medina, Milagros CSIC ORCID
Fecha de publicación2005
EditorAmerican Society for Microbiology
CitaciónApplied and Environmental Microbiology 71(7): 3399-3404 (2005)
ResumenThe effect of high-pressure (HP) treatments combined with bacteriocins of lactic acid bacteria (LAB) produced in situ on the survival of Escherichia coli O157H7 in cheese was investigated. Cheeses were manufactured from raw milk inoculated with E. coli O157H7 at approximately 105 CFU/ml. Seven different bacteriocin-producing LAB were added at approximately 106 CFU/ml as adjuncts to the starter. Cheeses were pressurized on day 2 or 50 at 300 MPa for 10 min or 500 MPa for 5 min, at 10°C in both cases. After 60 days, E. coli O157H7 counts in cheeses manufactured without bacteriocin-producing LAB and not pressurized were 5.1 log CFU/g. A higher inactivation of E. coli O157H7 was achieved in cheeses without bacteriocin-producing LAB when 300 MPa was applied on day 50 (3.8-log-unit reduction) than if applied on day 2 (1.3-log-unit reduction). Application of 500 MPa eliminated E. coli O157H7 in 60-day-old cheeses. Cheeses made with bacteriocin-producing LAB and not pressurized showed a slight reduction of the pathogen. Pressurization at 300 MPa on day 2 and addition of lacticin 481-, nisin A-, bacteriocin TAB 57-, or enterocin AS-48-producing LAB were synergistic and reduced E. coli O157H7 counts to levels below 2 log units in 60-day-old cheeses. Pressurization at 300 MPa on day 50 and addition of nisin A-, bacteriocin TAB 57-, enterocin I-, or enterocin AS-48-producing LAB completely inactivated E. coli O157H7 in 60-day-old cheeses. The application of reduced pressures combined with bacteriocin-producing LAB is a feasible procedure to improve cheese safety. Copyright © 2005, American Society for Microbiology. All Rights Reserved.
URIhttp://hdl.handle.net/10261/291804
DOI10.1128/AEM.71.7.3399-3404.2005
ISSN0099-2240
E-ISSN1098-5336
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