Effect of previous gutting on rancidity development in horse mackerel (Trachurus trachurus) during frozen storage at −20 °C

Gutting was applied to fresh horse mackerel (Trachurus trachurus) to study its effect on rancidity development during a prolonged frozen storage (up to 12 months at −20°C). To do so, chemical (free fatty acids, FFA; peroxide value, PV; thiobarbituric acid index, TBA-i; fluorescence ratio, FR) and sensory (odour and taste) analyses were carried out. The results showed that the gutting of horse mackerel led to a higher degree of oxidation in the frozen product, according to the chemical (PV, TBA-i and FR) and sensory (odour and taste) analyses. However, a lower extent of lipid hydrolysis (FFA formation) was detected at the end of the storage (twelfth month) as a result of gutting. It is concluded that the gutting of a medium-fat fish species such as horse mackerel is not recommended as previous treatment to frozen storage.     

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.     

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     

Effect of brine pre-treatment on lipid stability of frozen horse mackerel (<Emphasis Type="Italic">Trachurus trachurus</Emphasis>)

The rancidity development during the frozen storage (-20 °C) of an under-utilised medium-fat fish species (horse mackerel; Trachurus trachurus) was investigated. Special attention was given to a pre-freezing treatment consisting of an immersion in NaCl solution (5%, 10%, and 20%) and its effect on lipid damage during the fish frozen storage. Lipid hydrolysis (free fatty acid content) and oxidation (conjugated dienes formation; peroxide value, PV; thiobarbituric acid index, TBA-i; fluorescence formation, FR) were studied up to 270 days of frozen storage. Oxidative rancidity measured by the PV, TBA-i, and FR showed an increase with the frozen storage time and also as a result of an increasing salt content in fish muscle. A high peroxide formation was observed at day 210 of frozen storage, especially in the case of 20% NaCl treated samples. Lipid hydrolysis also increased with the frozen storage time; at the end of the experiment (270 days), a decreasing effect of muscle salt content on lipid hydrolysis was observed. Employment of appropriate antioxidant additions is recommended if salting pre-treatment is to be needed to avoid a large lipid oxidation development and ensure a longer shelf-life time.     

Influence of storage temperature on the quality of salted mackerel (Rastrelliger kangurta) and pink perch (Nemipterus japonicus)

Dry-salted mackerel and pink perch were stored at two temperatures: ambient (26·8 ± 3·3°C) and 2·5 ± 1°C. Changes in moisture content, salt content, water activity (a_w), peroxide value (PV), free fatty acid content (FFA), total volatile base nitrogen (TVBN) content, halophilic bacterial count and sensory scores for overall acceptability were studied. Loss of moisture and absorption of salt were considerably higher in the products stored at ambient temperature. The decrease in a_w was more pronounced at ambient temperature than at the lower temperature. Although the chemical indices of freshness (PV, FFA and TVBN) and the halophilic counts showed increasing trends, they were considerably lower in the products stored at the lower temperature. Sensory evaluation for overall acceptability indicated that storage at the lower temperature could considerably extend the shelf-life of salted fish.     

Differential lipid damage in various muscle zones of frozen hake (Merluccius merluccius)

 A comparison of the lipid damage produced in different hake zones was carried out during frozen storage at –11 and –18  °C. Three light muscle zones and the dark muscle were considered. Lipid oxidation [conjugated dienes; thiobarbituric acid index (TBA-i); fluorescence formation] and hydrolysis (free fatty acids, FFA) were determined. The most predominant lipid damage in all zones was hydrolysis, at the end of storage reaching values of about 40% (for the light muscle zones) and 12% (for the dark muscle) of the total lipids at –11  °C. Significant (P<0.05) correlation value (r=0.67–0.85) relationships between the frozen storage time and the FFA content were obtained for the four muscle zones at both temperatures. A comparison of the regression lines slopes in the different zones showed that a lower (P<0.05) lipolitic activity was produced in the dark muscle compared to the three light zones at both temperatures. A low lipid oxidation development was produced in the three light muscle parts, so that no significant differences between them could be assessed. However, the dark muscle showed a higher oxidation development (TBA-i and fluorescence formation) as a result of a higher lipid content and the presence of prooxidant constituents. Received: 16 June 1998     

Differential lipid damage in various muscle zones of frozen hake (Merluccius merluccius)

 A comparison of the lipid damage produced in different hake zones was carried out during frozen storage at –11 and –18  °C. Three light muscle zones and the dark muscle were considered. Lipid oxidation [conjugated dienes; thiobarbituric acid index (TBA-i); fluorescence formation] and hydrolysis (free fatty acids, FFA) were determined. The most predominant lipid damage in all zones was hydrolysis, at the end of storage reaching values of about 40% (for the light muscle zones) and 12% (for the dark muscle) of the total lipids at –11  °C. Significant (P<0.05) correlation value (r=0.67–0.85) relationships between the frozen storage time and the FFA content were obtained for the four muscle zones at both temperatures. A comparison of the regression lines slopes in the different zones showed that a lower (P<0.05) lipolitic activity was produced in the dark muscle compared to the three light zones at both temperatures. A low lipid oxidation development was produced in the three light muscle parts, so that no significant differences between them could be assessed. However, the dark muscle showed a higher oxidation development (TBA-i and fluorescence formation) as a result of a higher lipid content and the presence of prooxidant constituents.     

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     

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.     

Prediction of Quality in Frozen Cod (Gadus morhua) Fillets

Physical and chemical indices were determined on frozen cod (Gadus morhua) fillets stored for ca. 90 days at either - 12°C, - 15°C, - 22°C, - 30°C or under a set of simulated industrial fluctuating temperature conditions (SIFTC). Univariate and multivariate statistics on the quality indices gave a relationship between frozen storage textural deterioration and the chemical parameters as influenced by storage temperature. Results on the SIFTC resembled the - 12°C and - 15°C storage treatments. Chemical indices had lower activation energy values than those for the physical parameters. Ammonia, determined enzymatically, can be used as an index of frozen fish quality. The quadratic equations developed using the dependent variable of Instron raw peak force, independent of time and temperature, can predict the textural quality of frozen cod fillets.     

Effect of previous chilled storage on rancidity development in frozen horse mackerel (Trachurus trachurus)

Rancidity development during frozen storage (?20 °C) of an underutilised medium‐fat‐content fish species, horse mackerel (Trachurus trachurus), was studied. Special attention was given to the effect of previous chilled storage (0, 1, 3 and 5 days) on the quality of the frozen fish. For this, chemical (free fatty acid and conjugated diene contents; peroxide value, PV; thiobarbituric acid index, TBA‐i; fluorescent compound formation) and sensory (rancid odour and taste) analyses were carried out. Hydrolytic rancidity showed an increase with frozen storage time; however, no effect of previous chilling time was observed on the frozen product. Oxidative rancidity measured by chemical (PV, TBA‐i and fluorescence) and sensory (odour and taste) indices increased with frozen storage time and also with previous chilling time. Satisfactory quality was maintained up to 7 months of frozen storage of horse mackerel provided that a short chilling time (not longer than 3 days) was employed. © 2002 Society of Chemical Industry     

Changes in lipids,proteins and kamaboko forming ability of silver carp (Hypophthalmichthys molitrix) mince during frozen storage

Frozen storage of mechanically deboned silver carp (Hypophthalmichthys molitrix) mince for 180 days resulted in a significant (P⩽0.05) decrease in myofibrillar proteins. In contrast, peroxide value (PV), free fatty acids (FFA) and total volatile base nitrogen (TVBN) contents increased significantly (P⩽ 0.05) throughout the storage period. The kamaboko forming ability and the sensory scores of the silver carp mince decreased significantly (P⩽0.05) during the storage period. Texture of the mince was significantly (P ⩽ 0.001) correlated with the decrease in the myofibrillar proteins (salt-soluble proteins), jelly strength and folding test grades; and increase in expressible water percentage, PV, FFA and TVBN content. Based on ‘texture’ of the mince, the product was acceptable for 180 days at −18°C.     

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.     

Studies on fish muscle protein. Nutritional consequences of the changes occurring during frozen storage

Samples of cod, whiting, herring, lemon sole and skate muscle were frozen and stored at ? 8°C for up to 20 months. Samples of cod muscle were also stored at ? 30°C. During storage at ?8°C the decrease in the solubility of the muscle proteins in 5% NaCl (denaturation) was most rapid in whiting followed in order by skate, cod, herring and lemon sole. Little change was detected in the NaCl solubility of cod muscle protein stored at ? 30°C. An increase in the pH was found to occur in all the species examined. The relationship between these changes and the toughening that occurs in fish muscle during frozen storage is considered. No nutritionally significant decrease in the lysine availability or the in vitro digestibility of the muscle proteins was found to occur in any of the species examined. In whiting, lemon sole and skate very small, statistically significant, increases in the available lysine content were detected after 7 months of storage at ?8°C and this may indicate that unfolding of the protein chains had occurred.     

Influences of potassium ferrocyanide on lipid oxidation of salted cod (Gadus morhua) during processing, storage and rehydration

The effects of added potassium ferrocyanide (CN) in different concentrations (2.5 ppm, 7.5 ppm and 100 ppm), in salt, on lipid oxidation in cod during salting, storage and rehydration were examined in this study. An increase in CN concentration accelerated lipid oxidation of the salted cod, as observed by increases in lipid hydroperoxides (PV) and thiobarbituric acid-reactive substances (TBARS), as well as in the development of fluorescence compounds (δF_or and δF_aq). A yellow discolouration (higher b^∗ value) of salted cod was associated with higher levels of oxidation derivatives. High correlation between PV, TBARS and free fatty acid (FFA), as well as between FFA and δF_or, was found. The results of principal component analysis showed that TBARS, b^∗ value and δF_or were the strongest indicators of lipid oxidation during salting and storage.     

Cold storage properties of cooked fish (cod)

Results are reported for the storage properties of frozen cooked cod compared to uncooked cod. Development of cold-storage flavour was found to be less marked in the cooked fish. This difference was found with both fresh and stale raw material and at storage temperatures of -5 and -13 °C.     

Effect of lipid oxidation and frozen storage on muscle proteins of Atlantic mackerel (Scomber scombrus)

The effect of storage on the lipids and proteins in Atlantic mackerel stored for up to 24 months at ?20 and ?30 °C was studied. Traditional methods including the peroxide value, thiobarbituric acid‐reactive substances (TBARS) and a reverse phase HPLC method were used to determine the primary and secondary lipid oxidation products. All tests showed an increase in lipid oxidation products with storage time and at a higher storage temperature of ?20 °C compared with samples stored at ?30 °C. Antioxidants had a significant effect (P < 0.01) on the inhibition of lipid oxidation, as shown by the reduction in peroxide value and hydroxides, and malondialdehyde formation. Similarly, deterioration of protein structure and functionality in mackerel stored for 3, 6, 12 and 24 months was greater at ?20 than ?30 °C. ATPase activity in the myosin extract of Atlantic mackerel showed a significant decrease (P < 0.01) with progressive frozen storage. Protein solubility in high salt concentration (0.6 M NaCl) decreased (P < 0.01) during storage at both ?20 and ?30 °C but was greater at ?20 °C. Interestingly, antioxidants BHT, vitamin C and vitamin E protected the proteins against complete loss of ATPase activity and protein solubility to a significant level (P < 0.01) for up to 1 year at ?20 °C compared with samples stored without antioxidants. This study confirms the deleterious effect of lipid oxidation products on protein structure and function in frozen fatty fish. © 2002 Society of Chemical Industry     

The effects of spoilage on the dielectric properties of frozen fish

Using a time-domain technique to obtain low frequency dielectric data the effects of spoilage on certain dielectric properties of frozen cod (Gadus morhua), haddock (Melanogrammus aeglefinus) and lemon sole (Microstomus kitt) have been measured at ? 78.5°C in the frequency range 0.025–10 kHz. The spoilage varied with the period of storage in ice prior to freezing. The measurements revealed a relaxation, the frequency of which in cod and haddock depended on pre-freezing quality of the fish. The relationship is discussed between this dependence and various other parameters and the relaxation is tentatively identified as that of a Maxwell-Wagner mechanism.     

Synthesis and degradation of adenosine triphosphate in cod (Gadus morhua) at subzero temperatures

This study has demonstrated that the extraction step is very important when analysing ATP and its degradation products. An important factor is whether the sample is fresh, frozen or thawed when homogenised since thawing of the sample will lead to rapid loss of ATP. During frozen storage it was found that ATP in cod (Gadus morhua) was stable at −40 °C in small samples for at least 12 weeks. At −20 °C it was found that ATP content increases initially and thereafter falls. It was demonstrated that degradation of ATP in small samples occurs faster at 0 °C than at −2 and −5 °C. Furthermore, it was found that in whole cod ATP could be synthesised at a significant rate at −7 °C. © 1999 Society of Chemical Industry     

Effect of frozen storage on the quality of whole fish and fillets of horse mackerel (Trachurus trachurus) and mediterranean hake (Merluccius mediterraneus)

 Whole fish and fillets of horse mackerel (Trachurus trachurus) and mediterranean hake (Merluccius mediterraneus) were assessed for quality (physical, chemical and sensory attributes) changes throughout 12 months of frozen storage at −18 °C. The pH, expressible water (EXW), quantities of trimethylamine (TMA), dimethylamine (DMA), formaldehyde (FA), the total volatile base nitrogen (TVB-N) the thiobarbituric acid number (TBA), peroxide value (PV) and amount of free fatty acids (FFA) increased, while sensory attributes (odour, taste, texture) decreased during the frozen storage period. A comparison of quality scores between whole fish and fillets of horse mackerel and mediterranean hake showed that there were no significant differences (P>0.05) in attribute scores. There were, however, significant differences (P<0.05) in pH, EXW, TMA, DMA, FA, TVB-N, TBA, FFA and PV. Received: 19 April 1996/Revised version: 7 September 1996