Sequential application of epsilon-polylysine, lauric arginate and acidic calcium sulfate for inactivation of pathogens on raw chicken and beef

dc.contributorKeeton, Jimmy T.
dc.creatorBenli, Hakan
dc.date.accessioned2010-01-15T00:07:51Z
dc.date.accessioned2010-01-16T01:08:59Z
dc.date.accessioned2017-04-07T19:55:45Z
dc.date.available2010-01-15T00:07:51Z
dc.date.available2010-01-16T01:08:59Z
dc.date.available2017-04-07T19:55:45Z
dc.date.created2008-08
dc.date.issued2009-05-15
dc.description.abstractSalmonella and Escherichia coli O157:H7 (EC) contamination continues to be one of the major concerns for the microbiological safety of raw poultry and beef products. Application of more than one decontamination agent as a multi-hurdle intervention to carcasses in a processing line might produce greater reductions than one treatment alone due to different modes of action of individual antimicrobials. In this study, sequential spray applications of e-polylysine (EPL), lauric arginate and acidic calcium sulfate (ACS) solutions were evaluated against Salmonella Enteritidis (SE) and Salmonella Typhimurium (ST) on artificially inoculated broiler carcasses and against ST and EC on beef rounds and ground beef derived from the rounds. All possible 2-way combinations and individual applications of 20 % ACS (ACS20), 300 mg/liter EPL (EPL300) and 200 mg/liter LAE (LAE200) were evaluated using a sterile membrane filter model system. The combinations that provided higher Salmonella reductions were further evaluated on inoculated chicken carcasses using either response surface methodology (RSM) or in various concentrations applied in a sequential manner. Sequential spray applications of EPL300 - ACS 30 % (ACS30) or LAE200-ACS30 produced the highest Salmonella reductions on inoculated chicken carcasses. In a subsequent experiment, treatment of Salmonella inoculated carcasses with EPL300-ACS30 or LAE200-ACS30 combinations were found effective for reducing initial Salmonella counts by 1.5 and 1.8 log CFU/ml, respectively, immediately after treatment and by 1.2 and 1.8 log CFU/ml, respectively, following 6 days of storage at 4.4 ?C. Evaluation of the resident microflora including aerobic plate counts (APC), E. coli, coliforms and psychrotrophs on uninoculated chicken carcasses after treatment with EPL300-ACS30 or LAE200-ACS30 and during storage indicated that these treatments have the potential to increase the shelf-life of poultry carcasses. Furthermore, application of warm (55 ?C) EPL300-ACS30 or LAE200-ACS30 onto inoculated beef rounds reduced both ST and EC counts over 6 days of storage at 4.4 ?C by 4.5 and 4.3 log CFU/cm2, respectively. Ground beef manufactured with EPL300-ACS30 or LAE200- ACS30 treated rounds had lower ST and EC counts initially and stayed lower over 4 days of storage at 4.4 ?C when compared to control.
dc.identifier.urihttp://hdl.handle.net/1969.1/ETD-TAMU-2965
dc.language.isoen_US
dc.subjectpathogen
dc.subjectdecontamination
dc.subjecthurdle
dc.subjectchicken
dc.subjectbeef
dc.titleSequential application of epsilon-polylysine, lauric arginate and acidic calcium sulfate for inactivation of pathogens on raw chicken and beef
dc.typeBook
dc.typeThesis

Files