The aim of this study was to assess the microbial populations causing the spoilage of chilled beef during storage and to evaluate the effect of the use of an antimicrobial packaging for the meat storage. A nisin activated antimicrobial packaging was developed by using a nisin, HCL and EDTA solution and used for the storage of beef cuts at 1 °C. The common spoilage related microbial groups were monitored during the storage of beef in activated and non activated plastic bags by using selective media. The use of the antimicrobial packaging caused an overall significant reduction of viable counts of Gram positive bacteria such as carnobacteria, lactic acid bacteria and Brochotrix thermosphacta whose development was inhibited for at least 11 days of storage compared to the control. Moreover, a 1-3 log cycles reduction of enterobacteria was also registered between 22 and 32 days of storage. The microbiota was assessed at species level by using Polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE) analysis of 16S rRNA gene of DNA extracted directly from meat and from bulk cells from selective media plates and showed that the species occurring within the targeted microbial groups did not change according to storage conditions. In conclusion, the use of the nisin activated packaging reduced the number of spoilage populations but did not affect the species diversity. Improved antimicrobial packaging is needed, possibly coupled with vacuum storage, to possibly achieve a simultaneous inhibition of more spoilage microbial groups and to preserve the microbiological quality of beef during chilled storage. © 2009 Elsevier Ltd. All rights reserved.

Development of spoilage microbiota in beef stored in nisin activated packaging

FERROCINO, ILARIO;
2010-01-01

Abstract

The aim of this study was to assess the microbial populations causing the spoilage of chilled beef during storage and to evaluate the effect of the use of an antimicrobial packaging for the meat storage. A nisin activated antimicrobial packaging was developed by using a nisin, HCL and EDTA solution and used for the storage of beef cuts at 1 °C. The common spoilage related microbial groups were monitored during the storage of beef in activated and non activated plastic bags by using selective media. The use of the antimicrobial packaging caused an overall significant reduction of viable counts of Gram positive bacteria such as carnobacteria, lactic acid bacteria and Brochotrix thermosphacta whose development was inhibited for at least 11 days of storage compared to the control. Moreover, a 1-3 log cycles reduction of enterobacteria was also registered between 22 and 32 days of storage. The microbiota was assessed at species level by using Polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE) analysis of 16S rRNA gene of DNA extracted directly from meat and from bulk cells from selective media plates and showed that the species occurring within the targeted microbial groups did not change according to storage conditions. In conclusion, the use of the nisin activated packaging reduced the number of spoilage populations but did not affect the species diversity. Improved antimicrobial packaging is needed, possibly coupled with vacuum storage, to possibly achieve a simultaneous inhibition of more spoilage microbial groups and to preserve the microbiological quality of beef during chilled storage. © 2009 Elsevier Ltd. All rights reserved.
2010
27
137
143
http://www.scopus.com/inward/record.url?eid=2-s2.0-70449106034&partnerID=40&md5=8b6de4ed1539628a1529ebae06411983
antiinfective agent, nisin; animal, article, bacterium, cattle, classification, drug effect, evaluation, food handling, food packaging, genetics, isolation and purification, meat, methodology, microbial viability, microbiology, molecular genetics; Animals, Anti-Bacterial Agents, Bacteria, Cattle, Food Handling, Food Packaging, Meat, Microbial Viability, Molecular Sequence Data, Nisin; Bacteria (microorganisms), Brochothrix thermosphacta, Enterobacteriaceae, Posibacteria
D. Ercolini;I. Ferrocino;A. L. Storia;G. Mauriello;S. Gigli;P. Masi;F. Villani
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/156947
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