Influence of storage time and temperature on lipid deterioration during cod (Gadus morhua) and haddock (Melanogrammus aeglefinus) frozen storage

Lean fish deterioration during frozen storage (−30 and −10 °C) for up to 1 year was studied by the assessment of lipid changes. Comparison between a formaldehyde (FA)-forming species (cod) and a non-FA-forming one (haddock) was carried out. Lipid damages were measured on the basis of free fatty acids (FFA), peroxide value (PV), thiobarbituric acid index (TBA-i) and fluorescent compounds. In both species at −30 °C, most lipid damage indices showed significant correlations with the storage time. However, at −10 °C, only the FFA and fluorescence detections provided significant correlations with the storage time. Comparison between the fish species showed higher lipid oxidation (PV and TBA-i) and hydrolysis (FFA content) in haddock than in cod at −10 °C; however, a higher fluorescence development was observed in cod at the same temperature. At −30 °C, little differences in lipid damage indices were detected between the two species. © 1999 Society of Chemical Industry     

Lipolysis and Oxidation in Ultra‐High Temperature Milk Depend on Sampling Month,Storage Duration,and Temperature

During storage, some factors (for example, storage duration and temperature) can affect milk stability and consumer acceptability. Thiobarbituric acid reactive substances (TBARSs), lipid classes, and fatty acid profiles in stored ultra‐high temperature (UHT) milk were analyzed to assess the effects of storage time and temperature on lipid oxidation and lipolysis. With storage duration up to 12 months, the milk fat phase was separated and showed high levels of oxidation and lipolysis, manifested as increased levels of TBARS and free fatty acids. High oxidation levels decreased the percentage of unsaturated fatty acids (UFAs) in triacylglycerol and phospholipids. Higher storage temperatures (20, 30, and 37 °C) resulted in a higher degree of fat aggregation, oxidation, and lipolysis compared with refrigerated storage (4 °C). Additionally, sampling month of raw milk (May, July, and November) affected the lipid profiles of UHT milk during storage, with more UFA oxidized in July than in the other 2 months.     

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     

Antioxidants from barley husks impregnated in films of low-density polyethylene and their effect over lipid deterioration of frozen cod (Gadus morhua)

BACKGROUND: The changes in quality of cod fillets packaged in films with and without antioxidants during 12 months of frozen storage at ? 20 °C were investigated in the present study. The following parameters were determined in order to study lipid hydrolysis and primary and secondary lipid oxidation in the samples during frozen storage: peroxide value, conjugated dienes, conjugated triene hydroperoxides, free fatty acids, totox value, thiobarbituric acid‐reactive substances and p‐anisidine value. RESULTS: Films containing antioxidants isolated from barley husks were effective in slowing down lipid hydrolysis and primary and secondary lipid oxidation processes. Secondary lipid oxidation reached maximum values in the 12th month of storage in control samples and samples packaged with antioxidant‐containing film. Maximum lipid hydrolysis and lipid oxidation values for control cod samples were significantly higher than the maximum values found in samples packaged with antioxidant‐containing film. CONCLUSION: The results confirm the efficacy of natural antioxidants derived from barley husks in slowing down lipid hydrolysis and increasing the oxidative stability of cod flesh. They also demonstrate the potential usefulness of natural antioxidants extracted from barley husks in the development of active packaging films for food preservation. Copyright © 2011 Society of Chemical Industry     

Rheological and differential scanning calorimetry studies on structural and textural changes in frozen Atlantic mackerel (Scomber scombrus)

The viscoelastic behaviour and thermal stability of Atlantic mackerel fillets stored at ?20 and ?30 °C for up to 2 years were investigated. An increase in elastic (G′) and viscous (G″) modulus values, reflecting protein aggregation, was observed in samples stored at ?20 °C compared with those stored at ?30 °C, as well as with storage time. The results indicate that toughening on frozen storage is not just limited to lean gadoid fish but also occurs in fatty fish, leading to texture deterioration. Differential scanning calorimetry of fillets stored at ?20 °C showed a shift to a lower transition temperature (T_m) and a decrease in enthalpy (ΔH) compared with control fillets stored at ?30 °C; this change was enhanced when fillets were stored for a longer period of time, confirming protein denaturation and the formation of aggregates reported previously by the authors (J Sci Food Agric 82: 579–586 (2002)). The contribution of lipid oxidation to protein aggregation was shown by storing minced mackerel with or without the antioxidant vitamin E at ?10 °C. The G′ and G″ values were higher in samples stored without vitamin E than in samples stored with vitamin E; thus antioxidants may be used to minimise protein aggregation in fatty fish. The role of lipid oxidation in promoting protein aggregation and deterioration in the texture of fatty fish has not been reported hitherto. Antioxidants such as vitamin E may be used not only to prevent lipid oxidation but also to minimise protein damage in order to prolong the shelf‐life of fatty fish. Copyright © 2004 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.     

Effect of plant extracts on lipid oxidation during frozen storage of minced fish muscle

The aim of the study is to determine the effect of pomegranate seed extract (PSE) and grape seed extract (GSE) addition to chub mackerel minced muscle on lipid oxidation during frozen storage. Each extract was added to minced fish muscle at 2% concentration and then stored at ?18 °C for 3 months. The effect of plant dietary fibres to control lipid oxidation was compared with untreated samples (control). Formation of lipid hydroperoxides and thiobarbituric acid‐reactive substances (TBARS) was significantly inhibited by PSE and GSE addition when compared with control. Both extracts significantly retarded lipid oxidation according to the results of TBARS. A significant reduction of L* (lightness), a* (redness) and b* (yellowness) values was detected during frozen storage. GSE added samples had the highest redness and the lowest lightness and yellowness. However, samples with PSE showed the lowest redness and highest yellowness and h° (hue angle) values. The results from this study suggest GSE is a very effective inhibitor of primary and secondary oxidation products in minced fish muscle and have a potential as a natural antioxidant to control lipid oxidation during frozen storage of fatty fish.     

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.     

FISH MUSCLE LIPOLYSIS—A REVIEW

Lipolysis occurs extensively in fish muscle post-mortem and is associated with quality deterioration in the frozen tissue. Fish muscle lipolysis is presented in the context of basic fish muscle physiology and lipid composition. Phospholipase A and lipases from fish muscle have been described and characterized. The reaction is usually followed by measurement of free fatty acid production, and several colorimetric assays are available. Processing and storage treatments have been shown to influence the extent and rate of lipolysis in fish muscle; most of the research in this area has been directed at the effects of frozen storage. The interaction of lipolysis and lipid oxidation is a particularly intriguing area of study as triglyceride hydrolysis leads to increased oxidation while phospholipid hydrolysis produces the opposite effect.     

Enrichment of Chicken Nuggets with Microencapsulated Omega-3 Fish Oil: Effect of Frozen Storage Time on Oxidative Stability and Sensory Quality

This work studies for the first time the elaboration of frozen chicken nuggets enriched with microcapsules of omega-3 fatty acids using fish oil. Three types of chicken nuggets were prepared: control (C), enriched in bulk fish oil (BFO), and with added microencapsulated fish oil (MFO). Effect of length of frozen storage after pre-frying and before domestic frying was studied. The pre-fried nuggets were stored during 24 h at refrigeration temperature (0–2 °C) (T0) or during 1 month (T1M) or 3 months (T3M) in a domestic freezer at ?18 °C before frying. Length of frozen storage after pre-frying and before domestic frying promoted lipid and protein oxidative reactions in omega-3-enriched nuggets. Microencapsulation showed a protective effect against lipid and protein oxidation, especially during the first month of storage. In MFO, sensory traits were not affected by enrichment. In BFO-T0, a higher juiciness and saltiness and a less intense meat flavor in comparison with C-T0 and MFO-T0 was found. Time of frozen storage did not influence the sensory quality of chicken nuggets enriched with omega-3. Microencapsulation seems to be a promising method for enrichment of pre-fried frozen meat products with fish oil, improving the oxidative shelf life and preserving the sensory quality characteristics of the enriched products.     

Effects of frozen storage temperature on the quality and oxidative stability of bigeye tuna flesh after light salting

Effects of frozen storage temperature on the quality and oxidative stability of lightly salted tuna were investigated. The bright and vivid colour became totally brown after 4 weeks at −20 °C and 8 weeks at −30 °C, where the a^*/b^* value decreased from 1.35 to 0.38 and 0.58, respectively. Discoloration and lipid oxidation occurred concurrently in lightly salted tuna flesh, and it was speculated that the oxidation of oxymyoglobin to metmyoglobin exacerbated lipid oxidation and vice versa. Storage at −40 °C or lower temperatures effectively suppressed the discoloration and maintained the high water-holding capacity and unique textural properties of lightly salted flesh. It was attributed to the reduction in the conformational changes and particularly hydrophobic interactions among proteins, protecting the myoglobin from oxidative damages during frozen storage. Considering the quality maintenance and energy savings, storage at −40 °C was appropriate for lightly salted tuna flesh.     

Atlantic salmon (Salmo salar,L) as raw material for the smoking industry. II: Effect of different smoking methods on losses of nutrients and on the oxidation of lipids

The changes in total fat content, fatty acid composition, tocopherol, ascorbic acid, pH and oxidation were analysed in Atlantic salmon (Salmo salar, L.) in response to either cold smoking (20 or 30 °C) or electrostatic smoking. Both fresh and frozen fillets were dry-salted before smoking. The fish smoked were the lean ocean-ranched salmon caught off Iceland in June 1998 and farmed Norwegian salmon, slaughtered in either November 1998 or April 1999, differing in fresh fillet fat content from 84 to 169 g·kg⁻¹ wet weight. The fresh material used in smoking significantly affected the smoking loss of nutritive components in the fillets. The leaner the fish the higher percentile loss in fillet fat. Ascorbic acid decreased about 80 percent from the fresh value, independent of smoking temperature (20 or 30 °C). The fish that were dry-salted and electrostatically smoked only lost about 10 percent of the fresh ascorbic acid content, independent of the type of raw material used, indicating a conserving effect on ascorbic acid by the electrostatic process. Also, the electrostatically smoked fish showed a smaller drop in fillet pH than cold-smoked fillets, while tocopherol was little affected by the smoking methods tested.     

Lipid and Protein Changes Related to Quality Loss in Frozen Sardine (<Emphasis Type="Italic">Sardina pilchardus</Emphasis>) Previously Processed Under High-Pressure Conditions

This research focuses on biochemical changes related to quality loss in frozen (?18 °C for 9 months) sardine (Sardina pilchardus) previously subjected to high-pressure (HP) processing (125–200 MPa). The inhibition (p < 0.05) of lipid hydrolysis development (lower free fatty acid formation and lipase activity), observed in frozen sardine as a result of the previous HP treatment, increased with the pressure level applied. Several parameters including peroxide value, thiobarbituric acid index, fluorescent compounds, and polyenes showed that the applied HP conditions prior to sardine freezing did not increase lipid oxidation. Also, HP did not induce a substantial modification of acid phosphatase and cathepsins B and D activities, and the electrophoretic patterns of sarcoplasmic and myofibrillar protein fractions did not change. However, HP processing led to a decrease in myofibrillar protein content in frozen pressure-treated fish, an effect that was higher in 175- and 200-MPa treated samples. In conclusion, this research showed that pressure treatments in the 125–200-MPa range with holding time of 0 min cause only minor modifications in biochemical indicators of deterioration throughout the subsequent frozen storage of samples for up to 9 months. This study shows the need to optimize HP conditions, particularly in the case of applications combining HP treatments, frozen storage, and thawing to obtain products with high quality and commercial viability.     

Browning of salted sun-dried fish

The lipid of traditional salted, sun-dried fish is highly susceptible to oxidation during processing and storage at tropical ambient temperatures (25–30°C), leading to browning and potential loss of nutritional and economic value of the product. Determinations of extractable fluorescence and soluble brown colour have been found to be relevant indicators of the high degree of lipid oxidation in such fish. Studies on model systems consisting of aerated fish oil and a range of components natural to fish confirmed that, at 25°C, the products of lipid oxidation reacted with phospholipids and amino acids to produce significant fluorescence. Similarly, proteins and amino acids interacted with lipid oxidation products to produce browning, although at 25°C, this only occurred in the presence of water. Temperatures above 50°C are required for the development of browning of aerated fish oil alone. The level of free amino acids in salted, sun-dried fish was found to decrease during storage which correlates with amino acid involvement in fluorescence and colour production. The fluorescence/colour can be related mechanistically to the development of lipid oxidation products and hence provides a realistic basis for their acting as indicators of extensive lipid oxidation.     

Lipid Oxidation in Microsomal Fraction of Squid Muscle (Loligo peali)

Frozen squid is susceptible to both lipid oxidation and yellow/brown discoloration during frozen storage. The involvement of lipid oxidation in the microsomal fraction of squid muscle on oxidative rancidity and discoloration was investigated using iron and either enzymatic or non‐enzymatic redox cycling pathways. Lipid oxidation was measured by thiobarbituric acid‐reactive substances (TBARS), and color changes were measured spectrophotometrically using an integrating sphere. The lipid oxidation was not observed in the squid microsomes in the presence of Fe³⁺ and β‐nicotinamide adenine dinucleotide disodium salt (NADH) or β‐nicotinamide adenine dinucleotide phosphate, reduced (NADPH), suggesting that the enzymatic redox cycling pathway was not active. Iron‐promoted TBARS formation was observed in the non‐enzymatic pathway when ascorbic acid was used as a reducing compound. Non‐enzymatic lipid oxidation increased with increasing temperature (4 °C to 37 °C), iron (0 to 100 μM), and ascorbic acid (0 to 200 μM) concentrations. As lipid oxidation in the microsomes or isolated microsomal lipids increased, color changes were observed as could be seen by an increase in b* values (yellowness) and a decrease in a* (redness) values. The ability of iron and ascorbate to promote both lipid oxidation and pigment formation in the microsomal fraction suggests that this pathway could be responsible for quality deterioration of squid muscle during storage.     

Lipid Peroxidation and Chemical Changes in Catfish (lctalurus puncfatus) Muscle Microsomes during Frozen Storage

An NADH-dependent lipid peroxidation system previously identified in channel catfish muscle microsomes functioned at ?10° in isolated microsomes. Below that, activity was inhibited. The amount of peroxidase activity remaining after thawing previously frozen isolated microsomes or intact catfish fillets was inversely related to storage temperature. Microsome yield and lipid content were lower in the fillets stored at - 10° than -40°. Most microsomal fatty acids, especially PUFAs, gradually decreased in the fish fillets stored at -10°. Prolonged storage of catfish fillets would require storage below -20°. Any thawing would result in reactivation of the peroxidase system.     

Stabilization of Lipids in Minced Fish by Freeze Texturization

Minced meats of Baltic cod (Gadus morhua) with added krill (Euphausia superba D.), krill precipitate, or bream (Abramis brama) were freeze-textured or frozen conventionally. Lipid composition and oxidation were analyzed after 6–8 mo storage at –20°C. Analyses included peroxide value, fluorescence, lipid classes (thin-layer chromatography), and fatty acid composition (gas chromatography). Peroxide value was 4–9 times lower in freeze-textured meat minces than in conventionally frozen samples. Docosahexaenoic acid (DHA) was higher, by 22% in bream minces to 80% in cod minces without additives, in all freeze-textured minces than in conventionally frozen samples. Texturization could reduce lipid oxidation in minced fish during frozen storage.     

Antioxidant Efficacy of Oleoresin Rosemary and Sodium Tripolyphosphate in Restructured Pork Steaks

Thiobarbituric acid (TBA) analysis, sensory evaluation and hexanal content (frozen storage only) monitored lipid oxidation. STPP significantly (P<0.01) reduced lipid oxidation in cooked steaks during refrigerated storage (ε4°C) for 8 days, and in raw steaks stored at ? 30°C for 8 mo. Lipid stability was not enhanced by OR/STPP treatments compared to STPP treatments. Water-soluble OR/STPP did not result in significantly (P>0.05) greater lipid stability than oil-soluble OR/STPP treatments. Hexanal content significantly (P<0.01) increased after 8 mo frozen storage.     

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.     

Antioxidant Extracts from Acorns (Quercus ilex L.) Effectively Protect Ready‐to‐Eat (RTE) Chicken Patties Irrespective of Packaging Atmosphere

This study evaluated the impact of a phenolic‐rich acorn extract (200 ppm gallic acid equivalents) and the concentration of oxygen in the packaging system (low‐oxygen modified atmosphere; 5% vs. normal‐oxygen; 21%) on lipid and protein oxidation and consumers acceptance of the ready‐to‐eat chicken patties. Samples were subjected to cooking (electric oven, 170 °C/16 min), cold storage (14 d at 4 °C), and reheating (microwave, 600 mW/1 min). Samples treated with acorn extract kept thiobarbituric acid‐reactive substances numbers and lipid‐derived volatiles at basal levels throughout the whole processing irrespective of the oxygen concentration in the packaging atmosphere. Consistently, treated patties had lower protein carbonyls than control ones. The acorn extract also controlled color and texture deterioration during chilled storage and reheating and improved the color and odor acceptance of the products. Formulating with acorn extract is a feasible strategy to inhibit the oxidation‐driven changes and preserve the quality of reheated samples as if there were freshly cooked. Compared to the effect of the antioxidant extract, the concentration of oxygen in the packaging system was negligible in terms of quality preservation.