Literature DB >> 14968968

Control of bacterial pathogens during processing of cold-smoked and dried salmon strips.

M W Eklund1, M E Peterson, F T Poysky, R N Paranjpye, G A Pelroy.   

Abstract

Microbiological and chemical changes were determined during the smoking and drying of salmon strips processed at 29 to 31 degrees C for 4 days at a facility in Alaska in 1993. During the process, Staphylococcus aureus populations increased to more than 10(5) CFU/g after 2 to 3 days of processing. Subsequent laboratory studies showed that a pellicle (dried skinlike surface) formed rapidly on the strips when there was rapid air circulation in the smokehouse and that bacteria embedded in or under the pellicle were able to grow even when heavy smoke deposition occurred. Under these conditions, an inoculum of 26 CFU/g of S. aureus increased to 10(5) CFU/g after 3 days of processing. Elimination of preprocess drying and reduction in air flow during smoking resulted in smoke deposition before pellicle formation and enabled the product to reach levels of water-phase salt and water activity that inhibit the growth of S. aureus and Listeria monocytogenes. In 1994, these modifications were then applied during processing at an Alaskan facility, and S. aureus could not be detected in the finished product. L. monocytogenes was detected in the raw product area, on the processing tables, and on the raw salmon strips, but it was not detected in the finished product when the smoke was applied before pellicle formation.

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Year:  2004        PMID: 14968968     DOI: 10.4315/0362-028x-67.2.347

Source DB:  PubMed          Journal:  J Food Prot        ISSN: 0362-028X            Impact factor:   2.077


  2 in total

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Authors:  Helga Hernández; Adéla Fraňková; Pavel Klouček; Jan Banout
Journal:  J Vis Exp       Date:  2018-03-14       Impact factor: 1.355

2.  Epidemiological Survey of Listeria monocytogenes in a gravlax salmon processing line.

Authors:  C D Cruz; F A Silvestre; E M Kinoshita; M Landgraf; B D G M Franco; M T Destro
Journal:  Braz J Microbiol       Date:  2008-06-01       Impact factor: 2.476

  2 in total

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