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Evaluation of quality parameters and shelf life of fresh cheese packed under modified atmosphere.

ABSTRACT: Fresh (acid coagulated) cheeses belong to a group of soft unripen cheeses which are very popular among consumers. However, owing to the specific composition and properties, these cheeses have a limited shelf life. The aim of this study was to investigate the effect of modified atmosphere packaging (MAP) onto fresh cheese and to compare it with the commonly used packaging under atmospheric air and vacuum. The produced fresh cheese was packed under normal atmosphere (air), vacuum and modified atmosphere of following composition: (1) 60%N₂:40%CO₂; (2) 70%N₂:30%CO₂. All cheese samples were cool stored for 18 days, whereby the sampling and analyses were conducted every 3 days. During the storage period, there was a continuous decrease in acidity (from 4.66 to 4.47), while the viable counts of the monitored microorganisms increased in the control sample. However, in samples packaged under vacuum and modified atmosphere a slighter decrease in acidity (no result under 4.50) and inhibited microbiological growth were detected. Scores of sensory evaluations were high for all samples (17.63-19.73), whereby the sample packed under MAP with ratio 70%CO₂:30%N₂ obtained the best average score of 17.72 at the end of the 18-day storage period. Other analyses confirmed that vacuum and MAP prolong the shelf life of fresh cheese while preserving its physico-chemical and sensory characteristics.

SUBMITTER: Barukcic I

PROVIDER: S-EPMC7270376 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Project description:Modified-atmosphere packaging (MAP) of foods in combination with low-temperature storage extends product shelf life by limiting microbial growth. We investigated the microbial biodiversity of MAP salmon and coalfish by using an explorative approach and analyzing both the total amounts of bacteria and the microbial group composition (both aerobic and anaerobic bacteria). Real-time PCR analyses revealed a surprisingly large difference in the microbial loads for the different fish samples. The microbial composition was determined by examining partial 16S rRNA gene sequences from 180 bacterial isolates, as well as by performing terminal restriction fragment length polymorphism analysis and cloning 92 sequences from PCR products of DNA directly retrieved from the fish matrix. Twenty different bacterial groups were identified. Partial least-squares (PLS) regression was used to relate the major groups of bacteria identified to the fish matrix and storage time. A strong association of coalfish with Photobacterium phosphoreum was observed. Brochothrix spp. and Carnobacterium spp., on the other hand, were associated with salmon. These bacteria dominated the fish matrixes after a storage period. Twelve Carnobacterium isolates were identified as either Carnobacterium piscicola (five isolates) or Carnobacterium divergens (seven isolates), while the eight Brochothrix isolates were identified as Brochothrix thermosphacta by full-length 16S rRNA gene sequencing. Principal-component analyses and PLS analysis of the growth characteristics (with 49 different substrates) showed that C. piscicola had distinct substrate requirements, while the requirements of B. thermosphacta and C. piscicola were quite divergent. In conclusion, our explorative multivariate approach gave a picture of the total microbial biodiversity in MAP fish that was more comprehensive than the picture that could be obtained previously. Such information is crucial in controlled food production when, for example, the hazard analysis of critical control points principle is used.

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Evaluation of quality parameters and shelf life of fresh cheese packed under modified atmosphere.

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