2018
DOI: 10.1016/j.ijfoodmicro.2018.04.010
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Selection procedure of bioprotective cultures for their combined use with High Pressure Processing to control spore-forming bacteria in cooked ham

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Cited by 28 publications
(28 citation statements)
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“…The use of controlled microbiota or antimicrobial flora for preserving meat during storage (principle of the bio-preservation) was reported in 14 studies [ 26 , 33 , 89 , 90 , 97 , 132 , 133 , 134 , 135 , 136 , 137 , 138 , 139 , 140 ]. These studies aimed generally to prevent spoilage occurrence or inhibit pathogenic bacteria to ensure safety by inoculating, during food processes, one or several microorganisms considered as protective cultures especially from LAB groups, or bacteriocins thereof.…”
Section: Resultsmentioning
confidence: 99%
“…The use of controlled microbiota or antimicrobial flora for preserving meat during storage (principle of the bio-preservation) was reported in 14 studies [ 26 , 33 , 89 , 90 , 97 , 132 , 133 , 134 , 135 , 136 , 137 , 138 , 139 , 140 ]. These studies aimed generally to prevent spoilage occurrence or inhibit pathogenic bacteria to ensure safety by inoculating, during food processes, one or several microorganisms considered as protective cultures especially from LAB groups, or bacteriocins thereof.…”
Section: Resultsmentioning
confidence: 99%
“…This is pointing out that there is a clear gap in our knowledge on the HPP efficiency towards various microbial communities which may be present on cooked ham. Although the technology could be a very promising strategy to improve the safety of nitrite-reduced cooked ham, it is necessary to investigate whether it should be used as hurdle with the combination of other strategies such as biopreservation (Ramaroson et al, 2018).…”
Section: Discussionmentioning
confidence: 99%
“…Lactococcus lactis CH-HP15 (Ramaroson et al, 2018) was first cultivated on M17 agar plates (Biokar diagnostic, Beauvais, France) at 30°C for 72 h. One colony was inoculated for preculture in Medium Modelling Ham (MMH) (Ramaroson et al, 2018, Modugno et al, 2019 at 30°C for 24 h, and then cultured in MMH at 30°C under agitation at 65 rpm for 13h until early stationary phase. Bacterial enumerations were performed by plating serial dilutions of bacterial cultures, microbiota or ham stomached samples.…”
Section: Bacterial Strains Media and Growth Conditionsmentioning
confidence: 99%
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