| Summary: | Farming of fish has become an increasingly important part of the Norwegian fishing industry. Furthermore, the Norwegian fishing sector represents one of the largest national industries in terms of economic value. Fish is a perishable product and a suitable substrate for chemical degradation and bacterial growth. Determinations of shelf-life of fish and fish products have traditionally been based on microbial, chemical and sensory evaluation. It is, however, important to have methods for a rapid and reliable assessment of the microflora, and to aid in the determination of the shelf-life of the fish products. This thesis discusses and describes the use of PCR and denaturing gradient gel electrophoresis (DGGE) to detect and characterise the microflora of farmed Atlantic halibut and cod. The aims were to introduce and apply molecular biological methods for characterisation of the microflora, and to use these methods to detect the changes in the microflora as a function of shelf-life extending treatments. An additional aim was to compare the results obtained from molecularbased and culture-based methods. The DGGE and subsequent sequencing approach displayed the bacterial flora of the farmed fish, and identified the predominant microflora. When applying the sequencing approach, Photobacterium spp., Pseudomonas spp., Brochothrix thermosphacta, Serratia sp., Yersinia sp., Micrococcus luteus and Shewanella spp. were found to be the predominant bacteria in farmed Atlantic cod and halibut, stored under modified atmosphere (MA). The method detected a more diverse bacterial flora than previously obtained when culture-based methods were applied. Bacterial DNA extracted directly from the sample, without prior cultivation, gave a more diverse bacterial community. Furthermore, the molecular methods have been used to study the effects of MA packaging and ozone treatment on the microflora composition. There was no observable effect of ozone treatment of farmed cod.
|
|---|