Textural and physicochemical changes in salmon (Salmo salar) treated with commercial liquid smoke flavourings

The textural and physicochemical properties of fillets of farmed Atlantic salmon (Salmo salar) treated with two commercial liquid smoke flavourings (LS1 and LS2) were examined after 15, 30 and 45 days of storage at 2 °C in oxygen impermeable bags. Salmon flesh treated with LS1 was characterized by high water-soluble protein, fat and moisture contents, plus low hardness, fracturability, gumminess and chewiness, and a low alkali-insoluble protein content. These characteristics were similar to those of control salmon (not treated with liquid smoke flavouring). Storage time changed these properties similarly in both. Salmon flesh treated with LS2 was characterized by high hardness, fracturability, gumminess, chewiness and alkali-insoluble protein levels, plus low water-soluble protein, fat and moisture contents. Storage time appeared to have a far less important effect on salmon flesh treated with LS2.     

Evaluating instrumental colour and texture of thermally treated New Zealand King Salmon (Oncorhynchus tshawytscha) and their relation to sensory properties

Farmed New Zealand King Salmon (Oncorhynchus tshawytscha) was prepared according to common consumer techniques, namely poached, steamed, microwaved, pan fried (no oil), oven baked (no oil) and deep fried (in sunflower oil). Colour and texture were measured instrumentally and a sensory evaluation comprising of a generic QDA was conducted for the intensity and overall liking of the properties of colour, texture, flavour and aroma.During the thermal treatment (cooking), the outer colour of the King Salmon fillets became lighter, more red and yellow. Thermal treatment increased the texture firmness, chewiness and springiness of King Salmon as measured by texture analyser. Overall, the sensory panel preferred the oven baked King Salmon but least liked the poached and microwaved King Salmon. The instrumental texture measurements of the cooked King Salmon were closely linked with the texture ratings from the sensory panel. These experiments provide useful data for determining the optimal preparation techniques that in turn can facilitate the farming of NZ King Salmon to directly benefit the consumer.     

Classification of fresh Atlantic salmon (Salmo salar L.) fillets stored under different atmospheres by hyperspectral imaging

Hyperspectral imaging (HSI) was used to investigate spectroscopic changes in fresh salmon stored under different atmospheres (air, 60% CO₂/40% N₂ and 90% vacuum) and to determine whether HSI can classify fillets by the type of packaging. Hyperspectral images of samples kept at 4 °C were acquired and bacterial growth and lipid oxidation were measured. Principal component analysis was applied to study spectral development of samples during storage and K nearest-neighbour classifier was used for the classification of fillets by packaging type. Partial least squares regression was run to reduce the number of wavelengths included in the classification model. The results demonstrated that spectral variations could be observed in the different packaging atmospheres primarily at the wavelengths 606 and 636 nm. Using HSI, successful classification of fillets according to the packaging used (>88%) was achieved and this was largely dependent on spectral characteristics at the wavelengths 606 and 636 nm, possibly due to the different oxidation states of the haem proteins in the muscles.     

Relevance of season and nucleotide catabolism on changes in fillet quality during chilled storage of raw Atlantic salmon (Salmo salar L.)

Farmed 5–6 kg Atlantic salmon were pre-rigor filleted, vacuum packed and subsequently analysed after 1, 9 and 13 days of storage at 4 °C. The study was repeated in February, April, August and October. The conversion of hypoxanthine (Hx) showed the highest seasonal variation among the nucleotide metabolites, with an inverse relationship with sea temperature at harvesting (R² = 0.95–0.96). The Hx content was inversely related to fresh odour and flavour (R² = 0.81–0.83), but positively to tenderness (R² = 0.87). Hence, these results suggest that salmon reared in seawater of 11–15 °C (August–October) maintain a superior sensory quality for a longer period post-mortem than salmon reared at 6–8 °C (February–April). The colour intensity increased from days 1 to 9 post-mortem, probably due to rigor contraction. The highest increase in drip loss was observed in October and the lowest in April. It is proposed that seawater temperature significantly influences the storage life of raw salmon, and that Hx is a valuable biomarker for sensory quality.     

A study of the ice crystal sizes of red muscle of pre-rigor Atlantic salmon (Salmo salar) fillets during superchilled storage

Pre-rigor salmon fillets were superchilled in an impingement freezer and stored at −1.7 ± 0.3 °C for 29 days. The objective of this work was to study the ice crystal sizes in red muscle of pre-rigor salmon fillets that were partially frozen at fast (−30 °C, 227 W/m² K, 2.1 min) which is referred to as process F and slow (−20 °C, 153 W/m² K, 4.2 min) which is referred to as process S during superchilled storage. It was observed that the size of intracellular ice crystals in pre-rigor muscles at faster superchilling rate was significantly (p < 0.05) smaller than that at slower superchilling rate. The size of ice crystals formed in pre-rigor muscle was significant (p < 0.05) smaller than that formed in post-rigor muscle. It was also observed that the size of intracellular ice crystals formed in pre-rigor red muscles was significant smaller than that in white muscle. In addition, a large number of small ice crystals are formed within the muscle during partial freezing of pre-rigor muscle compared to post-rigor muscle. Future research should focus on tests of the quality parameters separately in red and white muscles (pre- and post-rigor) during superchilled storage of food products in order to understand more about their characteristics (quality and shelf life).     

Detection of frozen-thawed salmon (Salmo salar) by a rapid low-cost method

The aim of this study was to evaluate a rapid low-cost system based on impedance spectroscopy as an alternative method to differentiate between fresh and frozen-thawed salmon. Samples of fresh salmon and others submitted to freezing at −18 °C or to 2 freezing cycles, kept in frozen storage for different times, were analysed. In general, no significant differences in moisture, total volatile basic nitrogen, pH, texture parameters, K₁ value, or microbial counts between the different samples were observed. This revealed that the freezing process, storage time or number of freezing cycles did not affect the physico-chemical parameters of fish samples, except for water holding capacity, which was significantly lower in all frozen samples compared with fresh salmon. The results showed that impedance spectroscopy was unable to differentiate between different storage times under frozen conditions; however, this technique could be a useful tool to detect fish submitted to freezing process.     

Authentication of Atlantic salmon (Salmo salar) using real-time PCR

A real-time PCR assay based on LNA TaqMan probe technology was developed for the detection and identification of Atlantic salmon (Salmo salar). Among the advantages it is worth highlighting simplicity, rapidity, highest potential for automation and minor risk of contamination of this technique. The TaqMan real-time PCR is the currently most suitable method for screening, allowing the detection of fraudulent or unintentional mislabelling of this species. The method can be applied to all kind of products, fresh, frozen and processed products, including those undergoing intensive processes of transformation.     

The effects of carbon monoxide on Atlantic salmon (Salmo salar L.)

Atlantic salmon were exposed to carbon monoxide (CO) before the fish were percussively killed and gill cut. The fish were compared against a control group treated identically, without CO. Salmon exposed to CO expressed no adverse reactions and were easily stunned by percussion. CO-treated salmon had an earlier onset of rigor mortis and a faster decrease in muscle pH than the control group. No significant difference in drip loss was found between salmon treated with CO and the control. A significantly deeper red colour of both gills and fillets of CO-treated salmon was observed 10 days post mortem. Significantly higher levels of plasma lactate and potassium were found in CO-treated salmon compared to control, as well as a lower level of pCO₂. Exposure to CO did not increase plasma cortisol, sodium, haematocrit or glucose; however, lactate was high. Exposure of salmon or other fish to CO could improve quality and welfare when slaughtered.     

High-pressure processing and water-holding capacity of fresh and cold-smoked salmon (Salmo salar)

The influence of high pressure on the water-holding capacity (WHC) of fresh and cold-smoked salmon (CSS) was investigated up to a pressure level of 200 MPa at room temperature for 10- and 20-min periods. Changes in moisture content and WHC were determined by two methods, namely filter paper and spin-spin relaxation proton nuclear magnetic resonance. Both pressure (p<0.05) and process time (p<0.05) had significant effects on the moisture content of CSS, but not on fresh Atlantic salmon. Fresh salmon had less WHC than smoked salmon and a pressure of 150 MPa for 10 min caused a 2% increase in WHC of smoked salmon (p<0.001). The spin-spin proton relaxation (T₂) values were heavily affected by high pressure in both the samples, with substantial effects seen in CSS. At 150 MPa, both fresh and smoked fish behaved differently with respect to T₂ values compared with other pressure levels used.     

VIS/NIR spectroscopy for non-destructive freshness assessment of Atlantic salmon (Salmo salar L.) fillets

Visible/near-infrared spectroscopy has been evaluated for use in freshness prediction and frozen-thawed classification of farmed Atlantic salmon fillets, where fresh samples were stored as whole fish in ice. A handheld interactance probe for performing rapid measurements of single fillets and an imaging spectrometer for online analysis at an industrial speed of one fillet per second, have been used. Freshness as storage days in ice is predicted with an accuracy of 2.4 days for individual fillets, whereas frozen-thawed salmon fillets are completely separated from fresh fillets. The prediction results are comparable to previous results using the Quality Index Method with trained panelists. The region between 605 and 735 nm, which excludes interference by carotenoids and water, is appropriate for both frozen-thawed classification and freshness prediction of salmon fillets. The results indicate that the spectral changes are explained mainly by oxidation of heme proteins during the freeze–thaw cycle and during chilled storage in ice.     

Relevance of calpain and calpastatin activity for texture in super-chilled and ice-stored Atlantic salmon (Salmo salar L.) fillets

The aim of the present experiment was to measure the protease activities in ice-stored and super-chilled Atlantic salmon (Salmo salar) fillets, and the effect on texture. Pre-rigour fillets of Atlantic salmon were either super-chilled to a core temperature of −1.5 °C or directly chilled on ice prior to 144 h of ice storage. A significantly higher calpain activity was detected in the super-chilled fillets at 6 h post-treatment compared to the ice-stored fillets and followed by a significant decrease below its initial level, while the calpastatin activity was significantly lower for the super-chilled fillets at all time points. The cathepsin B + L and B activities increased significantly with time post-treatment; however, no significant differences were observed at any time points between the two treatments. For the ice stored fillets, the cathepsin L activity decreased significantly from 6 to 24 h post-treatment and thereafter increased significantly to 144 h post-treatment. There was also a significantly lower cathepsin L activity in the super-chilled fillets at 0 h post-treatment. No significant difference in breaking force was detected; however, a significant difference in maximum compression (F_max) was detected at 24 h post-treatment with lower F_max in the super-chilled fillets. This experiment showed that super-chilling had a significant effect on the protease activities and the ATP degradation in salmon fillets. The observed difference in F_max may be a result of these observed differences, and may indicate a softening of the super-chilled salmon muscle at 24 h post-treatment.     

Correlation between astaxanthin amount and a* value in fresh Atlantic salmon (Salmo salar) muscle during different irradiation doses

The amount of astaxanthin and a* value changes in fresh Atlantic salmon light and dark muscle during cold storage was studied for different e-beam doses (0, 1, 1.5, 2 and 3 kGy). Astaxanthin (mg/kg muscle) and a* value decreased with increasing irradiation dose for both fresh light and dark muscle. The level of irradiation dose gave high correlation between a* value and amount of astaxanthin. The reason for the change in colour or decrease in a* value of Atlantic salmon during irradiation could be due to the destruction of astaxanthin. The amount of astaxanthin and a* value of 1 kGy treated salmon fillets were not significantly different (p > 0.05) from that of the control but significantly different (p < 0.05) from other irradiation treatments. The colour (a* value) of salmon muscle was related to the content of astaxanthin, which decreased as irradiation increased. The amount of astaxanthin in light muscle was three to five times greater than dark muscle. This study demonstrated that irradiating salmon fillets at 1 kGy, can be successfully used and leads to no significant change in colour and amount of astaxanthin.     

Angiotensin I-converting enzyme inhibitory activity of low-molecular-weight peptides from Atlantic salmon (Salmo salar L.) skin

Collagen extracted from Atlantic salmon (Salmo salar L.) skin (which is normally discarded in the process of manufacture) was hydrolyzed with Alcalase and papain, and treated by multistage separation. The salmon skin collagen peptides (SSCP) obtained had high protein content (91.20 ± 1.03%) and low molecular weights, 90.79% of which were less than 1000 Da. SSCP was then separated by reversed-phase high performance liquid chromatography. Eleven major fractions were collected and their angiotensin I-converting enzyme (ACE) inhibitory activity was assayed. Fractions 5 and 7 displaying higher ACE inhibitory activity were subjected to mass spectrometer to identify the ACE inhibitory peptides. A total of eleven peptide sequences were identified, and two dipeptides, Ala-Pro and Val-Arg, were selected for further ACE inhibitory activity analysis. The ACE inhibitory activities of Ala-Pro (IC₅₀ = 0.060 ± 0.001 mg/ml) and Val-Arg (IC₅₀ = 0.332 ± 0.005 mg/ml) were found to be approximately 20- and 4-fold higher than that of SSCP (1.165 ± 0.087 mg/ml), respectively.     

Whey protein-based coatings on frozen Atlantic salmon (Salmo salar): Influence of the plasticiser and the moment of coating on quality preservation

The effects of different whey protein concentrate coating formulations (with or without glycerol or sorbitol in two proportions) on frozen Atlantic salmon quality parameters were evaluated. The influence of the moment of coating application (before or after freezing) was also studied. The coating application after freezing increased the thaw yield, decreased the drip loss, and modified colour parameters of frozen and thawed fillets, in comparison with application before freezing. The moment of coating also influenced the colour of cooked fish fillets. The type of plasticiser affects the colour of thawed and cooked samples, but not the colour of frozen samples. The protein coatings delayed lipid oxidation of salmon fillets, providing better protection against it than water glazing, and this effect was more pronounced when glycerol instead of sorbitol was used in the coating formulation.     

Effect of slaughter weight and breed on instrumental and sensory meat quality of suckling kids

The effects of breed and slaughter weight on chemical composition, fatty acid groups, texture, and sensory characteristics of meat of 141 suckling male kids from 5 Spanish breeds were studied. There was a decrease in texture and lightness and hue angle with the increase of the slaughter weight. Fatty acid composition was correlated with the intramuscular fat content. All the breeds except MO had values of n-6/n-3 ratio below 4, which is the healthy limit recommended, and a low atherogenic index as well as a low intramuscular fat content. A multivariate analysis discriminated light kid, which had the most tender and juicy meat, from heavy kid which had more intense kid and milk odours. Blanca Andaluza and Pirenaica had most tender and juicy meat. The effect of slaughter weight on meat traits should be considered separately for each breed to find the most appropriate meat according to consumers preferences.     

Effect of high pressure processing and cooking treatment on the quality of Atlantic salmon

The effect of high pressure treatment (HPP) (150 MPa and 300 MPa for 15 min) and cooking on quality of Atlantic salmon based on microbial activity, lipid oxidation, fatty acid profile, colour and texture during 6 days of storage was studied. High pressure and cooking significantly (p < 0.05) reduced microbial growth. The 300 MPa treatment and cooking showed higher L∗ and b∗ values but lower a∗ values for dark muscle compared to control and samples treated at 150 MPa. An increase in pressure resulted in an increase in hardness, gumminess and chewiness parameters, and a decrease in adhesiveness compared to control and cooked samples. Whereas cooking and 150 MPa led to similar oxidation development as control in dark muscle, the 300 MPa treatment effectively reduced the samples susceptibility to oxidation. Fatty acid profile of cooked Atlantic salmon dark muscle showed significantly (p < 0.05) lower amounts of total saturated, n−3 Polyunsaturated fatty acids (PUFA) and n−6 PUFA and significantly (p < 0.05) higher amounts of monoenes than HPP treated samples during the entire storage period. However, the most important finding of this study was that there was no significant (p > 0.05) difference between control and HPP treated samples in terms of total saturated, monoenes, n−3 PUFA and n−6 PUFA fatty acid profile. This demonstrates that HPP is a very mild process in terms of its effect on fatty acids.     

Effect of freezing on the physicochemical, textural and sensorial characteristics of salmon (Salmo salar) smoked with a liquid smoke flavouring

This study reports the effect of different refrigeration/freezing treatments on the physicochemical, textural and sensorial properties of farmed Atlantic salmon (Salmo salar) treated with a commercial liquid smoke flavouring. Observations were made on three groups of fillets - group RFS: salted, smoked and stored at 4 °C; group BFS: frozen at −25 °C for 24 h, thawed, salted, smoked and stored at 4 °C; and group AFS: salted, smoked and frozen at −25 °C for 24 h and stored at −18 °C - over a period of 45 days. Scores (on a scale of 1-9) were provided for different sensorial attributes by a panel of 10 trained tasters. Sixty percent of the panellists consistently preferred the AFS fillets. The maximum shelf life associated with each treatment was defined as the last sampling day on which a mean score of ≤5 was awarded for the fillet sensorial attributes by ≥50% of the panellists. Freezing the salmon for 24 h before smoking (BFS) did not increase its shelf life (30 days) over that of refrigerated smoked salmon (RFS). In addition, the former treatment had a negative effect on the adhesiveness, cohesiveness, smoke odour intensity and colour intensity of the flesh. However, maintaining the fish frozen at −18 °C (AFS) increased its shelf life (>45 days) and invested the flesh with greater firmness, cohesiveness and colour intensity.     

Effects of processing on detection and quantification of the parvalbumin gene in Atlantic salmon (Salmo salar)

Consumption of Atlantic salmon is a common cause of fish allergies with parvalbumin (Sal s1) being the major allergen. The presence of DNA encoding Sal s1 indicates the presence of Atlantic salmon in food. Using real-time polymerase chain reaction (PCR), the effects of food processing on the ability to detect and quantify the Sal s1 gene were determined. The method was specific for salmon and did not cross-react with 53 other species. Baking and pressure cooking caused a 5–100-fold decrease in detectable copies of the Sal s1 gene. Despite a 98% reduction in detectable copies following pressure cooking for 60 min, the relative standard deviation (RSD) between replicates was 20% and the response was 100-fold grater than the lowest copy number of Sal s1 reliably detected by the assay. Despite efforts to develop a quantitative assay, the PCR assay was qualitative. It is impossible to predict the effects of food matrices not included in this study, some of which may affect the reliability of the assay. Analyses of raw and pressure cooked salmon using a commercial PCR kit indicated comparable results to the PCR assay.     

Protein expression and enzymatic activities in normal and soft textured Atlantic salmon (Salmo salar) muscle

Soft textured Atlantic salmon is a sporadic and occasionally very severe problem for the farming and processing industries. The firm and soft fillets examined in this work differed in their gelatinase activities, cross-reactivity with anti-ubiquitin and anti-cathepsin L antibodies, as well as in the in-gel α-chymotryptic peptide maps of electrophoretically isolated myosin heavy chain (MHC) bands. The immunodetections of actin, α-actinin, MHC, and the MALDI TOF MS peptide mass fingerprinting of electrophoretically isolated MHCs only showed minor differences between samples. Other analyses revealed merely individual differences. These results seem to indicate a higher level of gelatinase activation, ubiquitination and cathepsin L cross-reacting material in softer muscle. These results would be consistent with a myopathy, but also with what could be expected in the skeletal muscle of healthy salmonid fish during a normal period of hyperplastic growth.