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Validation of brownie baking step for controlling Salmonella and Listeria monocytogenes

Pathogens, such as Salmonella and Listeria monocytogenes, can survive under the dry environment of flour for extended periods of time and could multiply when flour is hydrated to prepare batter or dough. Therefore, inactivation of these pathogens during the cooking/baking step is vital to ensure the...

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Detalles Bibliográficos
Autores principales: Unger, Phoebe, Channaiah, Lakshmikantha H., Singh, Arshdeep, Singh Sekhon, Amninder, Babb, Monipel, Yang, Yaeseol, Michael, Minto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7958536/
https://www.ncbi.nlm.nih.gov/pubmed/33747470
http://dx.doi.org/10.1002/fsn3.2132
Descripción
Sumario:Pathogens, such as Salmonella and Listeria monocytogenes, can survive under the dry environment of flour for extended periods of time and could multiply when flour is hydrated to prepare batter or dough. Therefore, inactivation of these pathogens during the cooking/baking step is vital to ensure the microbiological safety of bakery products such as brownies. The aim of this research was to validate a simulated commercial baking process as a kill‐step for controlling Salmonella and L. monocytogenes in brownies and to determine thermal inactivation parameters of these pathogens in brownie batter. Independent studies were conducted in a completely randomized design for each pathogen. All‐purpose flour was inoculated with a 5‐serovar Salmonella and 3‐strain L. monocytogenes cocktails. For baking validation, brownie batters were prepared from inoculated flour, and cooked in the oven set at 350°F (176.7°C) for 40 min followed by 15 min of ambient air cooling. For calculating D‐values, brownie batter was transferred into thermal‐death‐time disks, sealed, and placed in hot‐water baths. The samples were held for pre‐determined time intervals in hot‐water baths and immediately transferred to cold‐water baths. Microbial populations were enumerated using injury‐recovery media. At the end of baking, Salmonella and L. monocytogenes populations decreased by 6.3 and 5.9 log CFU/g, respectively. D‐values of Salmonella and L. monocytogenes cocktails were 53.4 and 37.5 min at 64°C; 27.2 and 16.9 min at 68°C; 10.7 and 9.1 min at 72°C; and 4.6 and 7.3 min at 76°C; respectively. The z‐values of Salmonella and L. monocytogenes cocktails were 11.1 and 16.4°C, respectively. This study can be used as a supporting document for the validation of similar brownie baking processes to control Salmonella and L. monocytogenes. The data from this study can also be employed for developing basic prediction models for the survival and thermal resistance of these pathogens during brownie baking step.