Keeping Quality of Sea-Frozen Thawed Cod Fillets on Ice

The objective was to evaluate the suitability of sea‐frozen, thawed cod fillets for the “chilled” seafood market. Fillets were kept frozen for 17 mo. After thawing, fillets were kept iced and at 4°C. Microbiological research on fillets showed higher initial numbers in post‐rigor than pre‐rigor fillets. Pre‐rigor fillets were judged fresher after 2 mo of storage compared to post‐rigor. With longer freezer storage, lower initial freshness scores were obtained, and formation of trimethylamine in thawed fillets was slowed. Thawed fillets frozen prior to rigor merited higher scores for freshness than fillets frozen post‐rigor. This difference decreased with prolonged freezer storage. The results strongly indicate that fillets should be frozen pre‐rigor.     

Texture Changes of Frozen Stored Cod and Ocean Perch Minces

During frozen storage, minced cod and ocean perch were examined by expressible moisture (EM), water binding potential (WBP) and computerized texture profile analysis (TPA). The results suggested that a microcomputer interfaced with the Instron efficiently performed TPA. The texture and water loss of all fish minces changed more rapidly at -7°C storage than at -20°C and -40°C. Furthermore, cod, a gadoid with the ability to degrade trimethylamine oxide to dimethylamine and formaldehyde, deteriorated faster than ocean perch, which did not have this ability. EM was useful for examining the water loss of frozen fish at - 7°C only during the first two weeks of storage. The WBP at -7°C storage showed a good correlation with storage time for cod and ocean perch. This suggests that WBP might be a good indicator for examining water holding ability of fish proteins.     

Comparative rates of spoilage of fillets and whole fish during storage of haddock (Melanogrammus aeglefinus) and herring (Clupea harengus) as determined by the formation of non-volatile and volatile amines

The concentrations of the non-volatile and volatile amines that formed in herring ( Clupea harengus ) and haddock ( Melanogrammus aeglefinus ) during storage as fillets and as whole fish in ice and at 5°C were determined. Comparison of the rates of formation of the major non-volatile amines (histamine, cadaverine and putrescine) and trimethylamine showed that haddock fillets deteriorated more rapidly than the whole gutted fish and that ungutted herring spoiled more rapidly than fillets. The value of amines as indices of spoilage in fish is discussed.     

High-Resolution NMR and Magnetic Resonance Imaging (MRI) Studies on Fresh and Frozen Cod ( Gadus morhua) and Haddock (Melanogrammus aeglefinus)

Changes in the fish muscle from cod ( Gadus morhua ) and haddock ( Melanogrammus aeglefinus ) were investigated by high-resolution NMR and magnetic resonance imaging (MRI). Water- and salt-soluble extracts from fish stored at −20°C and −30°C were analysed by high-resolution proton NMR and enabled the identification of metabolites including trimethylamine oxide, trimethylamine (TMA) and dimethylamine. It was not possible to detect formaldehyde by NMR either in the stored fish samples or in spiked water or salt extracts even at high levels of formaldehyde addition, probably due to polymerisation. Systematic and controlled storage trials indicated the presence of dimethylamine at around 9 months for samples stored at −20°C, whereas no changes were detected at the control storage temperature of −30°C. A comparison of cod and haddock fillets stored for 1 year at −20 and −30°C confirmed the production of dimethylamine only in cod stored at −20°C. It was interesting to note that ‘fresh’ cod and haddock samples purchased from a local supermarket showed high levels of TMA indicating a breakdown of trimethylamine oxide to TMA by bacteria. TMA was not detected in the fish fillets especially obtained for the storage trials. MRI of fresh cod and fish stored at −8 and −30°C indicated that the fish half stored at −8°C exhibited dense lines or arches which are indicative of gaps in the tissue due to possible breakdown of the connective tissue. The images of fish stored at −30°C did not indicate any differences compared with the fresh fish. MRI also showed the presence of frozen and unfrozen areas in the fish non-destructively.     

Thawed Chilled Barents Sea Cod Fillets in Modified Atmosphere Packaging-Application of Multivariate Data Analysis to Select Key Parameters in Good Manufacturing Practice

The purpose of the present study was to select key parameters in good manufacturing practice for production of thawed chilled modified atmosphere packed (MAP) cod (Gadus morhua) fillets. The effect of frozen storage temperature (−20 and −30 °C), frozen storage period (3, 6, 9 and 12 mo) and chill storage periods up to 21 d at 2 °C were evaluated for thawed MAP Barents Sea cod fillets. Sensory, chemical, microbiological and physical quality attributes were evaluated and multivariate data analysis (principal component analysis and partial least-squares regression) applied for identification of key parameters in good manufacturing practice for this product. Frozen storage of up to 12 mo had no significant effect on quality attributes and shelf-life at 2 °C was above 14 d irrespective of the time of frozen storage. As compared to a previous study with Baltic Sea, cod drip losses during chill storage was low for thawed MAP Barents Sea cod and this fish raw material seemed the more appropriate for production of thawed chilled MAP products. Frozen storage inactivation of the spoilage bacteria of Photobacterium phosphoreum was modest in Barents Sea cod, possibly due to high trimethylamine oxide (TMAO) and NaCl contents.     

Effect of Delayed Filleting on Quality of Cod Flesh

A study was undertaken to determine the effect of delayed filleting on overall shelf life of cod. One lot of gutted cod was divided into three groups for iced storage and filleted 1,4 or 7 days postmortem. Quality of fillets during subsequent storage at 1–2°C was assessed by physical characteristics, trimethylamine values, and total aerobic plate counts. After day 7, comparison of fillets of the same postmortem age showed that fish which had been most recently filleted was superior to that processed one day after landing, and stored subsequently in plastic trays. Results indicated that maximum overall shelf life could be attained by minimizing time stored as flllets, i.e. delaying filleting.     

Elucidation of protein aggregation in frozen cod and haddock by transmission electron microscopy/immunocytochemistry,light microscopy and atomic force microscopy

Polyclonal antibodies raised to both native cod myosin and actin as well as to aggregated proteins obtained from frozen cod stored for 11 months at ?10 °C were used to investigate disposition of muscle proteins in frozen cod and haddock fillets by transmission electron microscopy. Specimens from cod and haddock fillets, stored at ?10 °C, treated with anti‐aggregate antibody as the primary antibody, showed significantly more gold particles, especially around the protein aggregates and muscle fibres compared with fish stored at ?30 °C. Samples that were treated with anti‐myosin or anti‐actin antibody showed opposite results. Similar binding properties were observed in ELISA experiments involving the reaction of actin and myosin to both native and aggregate antibodies; thus immunological tests can be used for monitoring aggregate and texture changes in frozen stored fish. In addition, atomic force microscopy images obtained from cod muscle also indicated structural changes in frozen cod muscle proteins. The mica surface was covered with a continuous layer of muscle proteins comprising mainly small globular particles and a few large particles for the control cod sample stored at ?30 °C for 11 months. In contrast, cod fillets stored at ?10 °C showed a thin layer of proteins with small holes and an increased number of large particles denoting aggregates. Formation of ice crystals between the muscle fibres of frozen cod and haddock muscle was monitored without thawing by light microscopy at ?20 °C. The micrographs showed a greater proportion of large ice crystals and extensive protein fibre changes in fillets stored at ?10 °C compared with the control at ?30 °C. Copyright © 2004 Society of Chemical Industry     

Microbiological quality and shelf life prediction of chilled fish

A number of storage experiments have been carried out with whole cod and vacuum-packed cod fillets stored in ice. The microbiological quality of the fish was determined on the basis of detection time estimated rapidly by conductance assays in a TMAO-containing medium at 25 degrees C. Detection time and sensory data have been incorporated into a predictive linear model to estimate the remaining shelf life of the products. It is concluded that the shelf life of iced whole cod can be predicted using this model but not that of vacuum-packed fillets because of the greater variability of bacterial activity in packaged fish.     

Effects of Vacuum Packaging and Wrapping with Chitosan-Based Edible Film on the Extension of the Shelf Life of Sea Bass (Dicentrarchus labrax) Fillets in Cold Storage (4 °C)

In the present study, we assessed the possibility of improving the shelf life of fresh sea bass (Dicentrarchus labrax) fillets by using vacuum packaging and wrapping with chitosan-based edible films during cold storage at 4 °C. Sea bass fillet samples were periodically evaluated to assess chemical (pH, trimethylamine and total volatile basic nitrogen) and microbiological (presence of mesophilic aerobic bacteria and psychrotrophic bacteria) quality. Chemical spoilage (trimethylamine and total volatile basic nitrogen) and growth of microorganisms (total mesophilic and total psychrophilic aerobic bacterial counts) were significantly reduced (P?≤?0.05) in vacuum-packaged chitosan film wrapping during cold storage at 4 °C. The results showed that the shelf life of the control and vacuum-packaged groups ended within 5 days, whereas that of vacuum-packaged chitosan film-wrapped samples ended at 25 to 30 days. Therefore, the shelf life of sea bass fillets wrapped in chitosan was prolonged by about 20 days.     

Bulk Storage of Cod Fillets and Gutted Cod (Gadus morhua) Under Carbon Dioxide Atmosphere

The storage-life of bulk-stored cod under CO₂ atmosphere and air were compared. Gutted fish or fillets were distributed in bulk, among coolers containing 100% air or 25% CO₂-75% N₂, which were then stored at 0 ± 1°C for 20 days. Sensory assessments and chemical tests (pH, total volatile nitrogen) were carried out to estimate the raw-state quality and the bacterial spoilage. An important difference was observed between the storage life of cod under carbon dioxide atmosphere and air; microbiological and sensory assessments suggested a storage life exceeding 20 days and total volatile nitrogen results about 6–7 days under gas atmosphere, which was nearly twice as long as in air. Storage in CO₂ atmosphere was effective in inhibiting the growth of some bacteria on the fish, thereby contributing to the significant extension of the shelf life of the product.     

Structure of northern snakehead (Channa argus) meat: Effects of freezing method and frozen storage

This study was conducted to investigate the potential of cryogenic freezing with liquid nitrogen in the shelf-life extension of northern snakehead (Channa argus) and clarify the effects of temperature fluctuations after freezing on the quality attributes and tissue microstructure during frozen storage. The fish fillets were frozen by three methods including freezing using an ultra-low-temperature freezer (?80°C) to the core temperature of ?60°C (T1) or ?18°C (T2), or liquid nitrogen (T3) followed by storage at ?20°C for five months. Cryogenic freezing with liquid nitrogen postponed the decrease in pH and protein extractability. Temperature fluctuations after freezing might promote the accretion of ice crystals and resulted in the loss of tissue integrity and disorganization of myofibrils. The microstructural changes contributed greatly to the increased thawing loss and decreased resilience, as indicated by the enlarged extracellular spacing and the flakiness of myofibrils. Cryogenic freezing with liquid nitrogen showed no superiority in maintaining the microstructure of northern snakehead fillets, which was supposedly attributed to the cracking in tissue during freezing and the accretion of ice crystals during frozen storage.     

Shelf life of thawed cod fillets kept in ice

Summary Fillets of cod (Gadus morhua) were vacuum packed, frozen in an air-blast freezer and stored at –28°C. After 1 week, 3, 6 and 12 months, samples were thawed and stored in ice. Fresh fillets from the same batch were taken for reference and iced immediately. Organoleptic tests showed an extension of shelf life for the thawed fish of 2 days (1 week frozen storage) to 3–4 days (3 to 12 months storage) compared to the fresh fillets. The increase of pH, total volatile bases, trimethylamine and volatile acids was significantly retarded in the thawed fish. Relationships of these last three determinations with sensory assessment, however, were poor.

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Haltbarkeit aufgetauter und in Eis gelagerter Kabeljaufilets

Zusammenfassung Kabeljaufilets (Gadus morhua) wurden vakuumverpackt, in einem Luftfroster tiefgefroren und bei –28°C gelagert. Nach 1 Woche bzw. 3, 6 und 12 Monate wurden die Proben aufgetaut und in Eis gelagert.Sensorische Analysen zeigten, daß der aufgetaute Fisch ca. 2 Tage (1 Woche Gefrierlagerung) bis 3–4 Tage (3 bis 12 Monate Lagerung) länger haltbar war als die frischen Filets.Die Erhöhung der pH-Werte, des flüchtigen Basenstickstoffs, des Trimethylamins und der flüchtigen Säuren war in den aufgetauten Filets wesentlich verzögert. Jedoch korrelierten die drei letzten Befunde wenig mit den sensorischen.

     

Toxin Development by Clostridium botulinum in Modified Atmosphere-Packaged Fresh Tilapia Fillets During Storage

Potential for toxin development by Clostridium botulinum type E was investigated in retail-type packages of fresh tilapia fillets packaged in high barrier film under selected atmospheres [100% air, a modified atmosphere (MA) containing 75%CO₂:25%N₂, and vacuum] and stored under refrigeration (4°C) and abuse temperatures (8 and 16°C). Toxin development coincided with sensory spoilage at 16°C storage for fillets packaged in either MA, or vacuum. At 8°C, toxin development in fillets packaged in either of the atmospheres occurred 7-23 days after sensory spoilage. At 4°C, none of MA-packaged fillets became toxic until 10 days after onset of sensory spoilage. Toxin development did not precede sensory spoilage in any treatments or temperatures studied.     

Deterioration of European hake (Merluccius merluccius) during frozen storage

European hake (Merluccius merluccius (L)) was frozen as whole fish and as fillets and stored at ?18°C, ?24°C and ?30°C for up to 39 weeks. Sensory properties, peroxide value and thiobarbituric acid value, lipid fatty acid composition, adenosine nucleotide degradation products, dimethylamine and formaldehyde were measured at intervals during storage. Changes at ?30°C were negligible, otherwise fillets deteriorated faster than whole fish. Hedonic rating gave a storage life of around 9 months for whole fish stored at ?18°C.     

Effect of Phosphate Blends on Stability of Cod Fillets in Frozen Storage

Atlantic cod fillets were dipped in commercial tripoly or metaphosphate solutions, frozen and stored at either –12 ° 0.5°C or –30°C (constant or with daily programmed fluctuations to ?26°C) for up to 26 wk. Phosphate treatments at both storage temperatures decreased thaw drip and cooked drip and yielded a product with higher raw and cooked moisture. Protein content of cooked drip from fillets stored at –12°C was reduced by phosphate treatment; no significant difference was found between treated and control samples at –30°C. Although salt extractable protein was lowered, phosphate treatment did not affect dimethylamine/formaldehyde formation. Sensory evaluation of treated fillets stored at –30°C (with daily fluctuation to –26°C) revealed phosphated fillets to be the most tender and, after 26 wk storage, the most highly acceptable. Tripolyphosphate treatment significantly retarded the increase of expressible fluid under abusive conditions of frozen storage.     

Freshness Assessment of Thawed and Chilled Cod Fillets Packed in Modified Atmosphere Using Near-infrared Spectroscopy

Near-infrared reflectance (NIR) spectra was recorded of 105 samples of cod mince prepared from chill stored thawed cod fillets of varying quality in modified atmosphere packaging (MAP). Traditional chemical, physical, microbiological and sensory quality methods developed for assessing fresh fish products were determined on the same cod fillets. The purpose was to evaluate the potential of NIR spectroscopy for estimating (i) frozen storage temperature, (ii) frozen storage period and (iii) chill storage period of thawed-chilled MAP Barents Sea cod fillets. Furthermore, the potential for measuring of selected quality attributes as drip loss, water holding capacity and content of dimethylamine by NIR was evaluated. The results of the investigation were presented using multivariate modelling methods such as partial least-squares regression (PLSR) and discriminant partial least-squares regression (DPLSR). Systematic differences in the NIR measurements on minced cod fillets were primarily due to the chill storage duration (days at 2°C) on thawed-chilled MAP fillets. PLSR models based on wavelengths selected by a new Jack-knife method resulted in a correlation coefficient of 0.90 between measured and predicted duration of chill storage period (days at 2°C). The root-mean-square error of cross-validation (RMSECV) was 3.4 d at 2°C. NIR measurements provided promising results for evaluation of freshness for thawed-chilled MAP cod fillets completing the traditionally quality methods. However, it is necessary to study the effect of e.g. sample preparation, season, fishing ground and cod size together with more sophisticated pre-treatments of NIR spectra before the NIR method can be integrated as a method for evaluation of thawed-chilled MAP cod fillets.     

Variability of Salt Absorption by Brine Dipped Fillets of Cod (Gadus morhua), Blackback Flounder (Pseudopleuronectes americanus), and Ocean Perch (Sebastes marinus)

Major changes in sodium content of fillets of cod, blackback flounder, and ocean perch resulted from varying concentration of brine solution (5, 10, or 15%), duration of dip (30, 60 or 90 sec), fillet thickness, season of catch, and rinsing or skinning fillets before cooking. Postmortem age (1-5 days) of fish, temperature of brine solution (6, 12, or 20°C), and cooking had minor effects on final sodium concentration.     

COMPARISON OF MARGIN OF SAFETY BETWEEN SENSORY SPOILAGE AND ONSET OF CLOSTRIDIUM BOTULINUM TOXIN DEVELOPMENT DURING STORAGE OF MODIFIED ATMOSPHERE (MA)-PACKAGED FRESH MARINE COD FILLETS WITH MA-PACKAGED AQUACULTURED FISH FILLETS

The margin of safety between shelf-life (onset of sensory spoilage) and potential time to toxin production by Clostridium botulinum type E in retail type packages of fresh marine cod fillets packaged in high barrier film under selected atmospheres [100% air, a modified atmosphere (MA) containing 75% CO₂:25% N₂, and vacuum] and stored under refrigeration (4C) and temperature-abuse conditions (8 and 16C) was investigated. Margin of safety data of MA-packaged marine cod fillets was also compared with MA-packaged aquacultured tilapia, catfish, and salmon fillets. Sensory spoilage preceded onset of toxin presence for the marine cod fillets packaged in any of the atmospheres and storage temperatures tested. At 4C, none of the marine cod fillets packaged in either atmosphere developed toxin, even 20 days after spoilage, as determined by sensory characteristics. During storage at refrigeration and mild (8C) temperature-abuse conditions, MA-packaged marine cod showed a greater margin of safety compared to aquacultured tilapia, catfish, and salmon packaged under the same atmospheres and conditions. Fat content appeared to potentially influence the margin of safety in MA-packaged aquacultured fresh fish fillets during storage.     

A comparison of biochemical changes in cod (Gadus morhua) and haddock (Melanogrammus aeglefinus) fillets during frozen storage

Changes in the muscle proteins of frozen cod fillets, which produce significant amounts of formaldehyde, and frozen haddock fillets, which produce negligible formaldehyde, were compared. Protein extractability and hydrophobicity and the amino acid contents of soluble and insoluble proteins, as well as formaldehyde formation, were investigated in matching pairs of cod and haddock fillets stored at ?10 and ?30 °C (control). Formaldehyde production in cod was much higher (845 and 1065 nmol g^?1 at 20 and 30 weeks respectively) than in haddock (93 and 101 nmol g^?1 after 20 and 30 weeks respectively) at ?10 °C. However, a rapid decrease in solubility of proteins, increase in hydrophobicity and decrease in the amino acid content of salt‐soluble proteins at ?10 compared with ?30 °C were observed in both species. The results showed that there were no significant differences in the nature of the protein changes between these two species, thus indicating that factors other than formaldehyde were involved in the denaturation of proteins and the formation of aggregates during frozen storage of cod and haddock fillets, especially at ?10 °C. © 2001 Society of Chemical Industry     

The effect of powdered thyme sprinkling on quality changes of wild and farmed gilthead sea bream fillets stored in ice

The effect of powdered thyme sprinkling on the quality characteristics of fresh and ice-stored wild and farmed gilthead sea bream fillets was assessed. Initially, significant differences in proximate composition and quality attributes were found between wild and farmed fresh sea bream flesh. Throughout ice storage, biochemical alteration appeared more pronounced in farmed fish fillets with significantly higher levels of TVB-N, TMA-N, and TBA; and a lower liquid-holding capacity (LHC). Thyme powder addition (1% w/w) exhibited a preservative effect in both fish lots since significant lower levels of TVB-N, TMA-N, free amino acids (NPS), TBA and LHC were observed in thyme-treated fillets during ice storage. However, thyme inhibitory effect was more marked in wild than farmed fish. As revealed by partial least square regression, LHC in both groups was positively influenced by storage time and trimethylamine accumulation factors, while it was negatively influenced by thyme treatment and fish origin. Hence, LHC was suggested to be related to spoilage bacterial growth. The use of dried thyme extended the shelf life of fish fillets by about 5 days and appeared to be highly valuable to the fish industry as a natural preservative.