Quality changes in chilled Norway lobster (Nephrops norvegicus) tail meat and the effects of delayed icing

The quality deterioration of Norway lobster (Nephrops norvegicus) tail meat was monitored during ice storage. The K‐value started at 0.7% and reached a value of 39.7% on day 14. Muscle pH followed a sigmoidal pattern that reached a plateau on day 6. Bacterial load and trimethylamine (TMA) increased only after a lag phase to reach considerable levels by day 14 (5.3 log cfu and 10.2 mg (100 g)^?1, respectively). These analytical data were compared with sensory data. Principal component analysis (PCA) indicated that laboratory measures were correlated positively with the smell strength of cooked product (increasingly strong) and negatively with the smell character of raw and cooked product (sour‐ammoniacal in raw and neutral in cooked products), flavour and aftertaste (both increasingly bland–bitter). The effects of icing delays on the quality of tail meat were also evaluated. Changes in K‐values, microbial load, muscle pH and TMA indicated that the delay to icing should be no more than 4 h (at 16 °C) to ensure that quality is not compromised during subsequent post‐harvest storage.     

Nutritional quality of red shrimp,Aristeus antennatus (Risso), pink shrimp,Parapenaeus longirostris (Lucas), and Norway lobster,Nephrops norvegicus (Linnaeus)

The proximate composition, amino acid and fatty acid profiles, lipid classes and cholesterol and glycogen contents were determined in the edible part of red shrimp, Aristeus antennatus (Risso), pink shrimp, Parapenaeus longirostris (Lucas), and Norway lobster, Nephrops norvegicus (Linnaeus), in two distinct periods of the year. The proximate composition did not vary significantly between species or between periods of sampling. Significant differences in glycogen content were obtained between winter and summer; the lowest values were attained in winter (1.2, 1.1 and 1.0% wet weight for red shrimp, pink shrimp and Norway lobster respectively). With the exception of Norway lobster, an opposite trend was obtained for cholesterol content, ie lower values in summer (60.8 and 57.8 mg per 100 g wet weight for red shrimp and pink shrimp respectively). The major essential amino acids (EAA) were arginine, lysine and leucine and the limiting amino acid was methionine in all three crustacean species. The most important non‐essential amino acids (NEAA) were glutamic acid, aspartic acid, proline and glycine. In respect to lipid classes, phospholipids and free cholesterol predominated. The major fatty acids were 16:0, 18:1n‐9, 20:5n‐3 and 22:6n‐3. The polyunsaturated fraction was dominant (42.1–48.4%), followed by the monounsaturated (26.3–34.6%) and saturated (22.9–27.4%) fatty acids. In conclusion, the nutritional quality of these shellfish species is similar, they are valuable protein and lipid sources for the human diet and are adequate elements of the traditional Portuguese diet. Copyright © 2003 Society of Chemical Industry     

Identification of Irradiated Norway Lobster (Nephrops norvegicus) Using Electron Spin Resonance (ESR) Spectroscopy and Estimation of Applied Dose Using Re-irradiation: Results of an In-House Blind Trial

An in-house blind trial on Norway lobster (Nephrops norvegicus) was carried out in which 72 coded samples were correctly identified. The samples were either left unirradiated or had been given doses of 1·03, 2·39 or 3·40 kGy and stored for 0, 7 or 14 days at 1°C. Using re-irradiation, the doses received by the samples identified as irradiated were determined with either linear, quadratic or asymptotic equations being fitted to the data. The most successful estimates of absorbed dose were obtained using a quadratic fit, with average values of 1·71, 2·98 and 3·45 kGy being calculated. © 1997 SCI.     

Characterization of phenoloxidase activity of carapace and viscera from cephalothorax of Norway lobster (Nephrops norvegicus)

The characterization of phenoloxidase activity was performed in both carapace and viscera extracts of Norway lobster. Phenoloxidase activity rose with increasing temperature up to 60 °C. The carapace enzymatic extract showed the highest themostability, retaining about 80% of maximum activity at 45 °C and 40% at 65 °C. On the other hand, both enzymatic extracts showed a single peak activity at neutral-slightly alkaline pH and were quite resistant to inactivation at alkaline pH (pH > 8), but phenoloxidase activity became unstable at pH lower than 5.5. The enzymatic extract obtained from viscera showed a higher affinity for catechol (K_M 5.97 mM) than carapace extract (K_M 19.40 mM). Both mono- and diphenoloxidase activities were found in carapace and viscera. Polyphenoloxidase and converted-hemocyanin into PPO-like enzyme could be the main responsible for these activities.     

Development of chilling injury symptoms in stored tomato fruit (Lycopersicon esculentum Mill)

Mature-green tomato fruit cv Calypso were stored at 5, 7,12 or 19^oC for 0, 3, 9, 12 or 21 days, ripened at 19^oC for 3 or 6 days and analysed for surface colour (a_L/b_L ratio), firmness, and tissue disorganisation in chill-damaged (pitted) and adjacent unpitted tissues. Manifestation of cell disorganisation and death was evident in pitted tissues. Alternaria spp, Stemphylium spp, Penicillium spp and Aureobasidium spp were isolated from pitted tissues. Fruit stored for either 9 or 12 days at 5 or 7°C subsequently ripened to an acceptable colour, but longer storage times inhibited satisfactory colour development. After storage at 12 or 19°C, fruit surface colour improved progressively with time. Loss of fruit firmness was highest at 19°C but decreased with increasing temperature from 5 to 12°C, showing biphasic maxima firmness loss on days 9 and 21. Surface pits occurred at the stem end and in the equatorial region of the fruit. Fruits were also stored at 7, 12 or 19°C for 10 or 20 days and then ripened at 19°C for 10 days before evaluation of visible defects; these were greatest at 7°C followed by 19°C and were lowest at 12°C.     

Improvement of the commercial quality of chilled Norway lobster (Nephrops norvegicus) stored in slurry ice: Effects of a preliminary treatment with an antimelanosic agent on enzymatic browning

The use of slurry ice is gaining increasing importance as an advanced method for the hygienic and efficient chilling and sub-zero storage of aquatic food products. In this work, this technology was applied as a novel technique for the chilling and storage of Norway lobster (Nephrops norvegicus) – a crustacean species of high-commercial value – under refrigeration conditions at −1.5 °C. In addition, the effects of a preliminary treatment with 0.5% Na HSO₃ on surface browning were evaluated and compared with the results obtained in control batches not subjected to such treatment. The processing of lobster in slurry ice significantly (p < 0.05) slowed down microbial spoilage, as determined by the counts of aerobes, psychrotrophs, proteolytic bacteria, and lactose-fermenting Enterobacteriaceae, and by the formation of volatile amines. Likewise, the autolytic breakdown mechanisms – as determined by the K value – were also significantly (p < 0.05) inhibited in the slurry ice batch. Remarkably, preliminary treatment with 0.5% sodium metabisulphite permitted better maintenance of the parameters involved in sensory quality – especially as regards the aspect of the carapace – as compared with non-treated batches, and allowed a shelf life of 9 days without surpassing the 150 mg/kg legal limit established for this food additive. On contrast, the non-treated batch stored in slurry ice exhibited a shelf life of 5 days. The combination of technological treatments proposed in this work – preliminary antimelanosic treatment and storage in slurry ice – may be successfully applied to other fresh and frozen shellfish species with a view to extending shelf life and to avoiding the legal and toxicological problems derived from current abuse of such antimelanosic agents to prevent shellfish browning.     

Microbial spoilage analysis and its effect on chemical changes and shelf‐life of Norway lobster (Nephrops norvegicus) stored in air at various temperatures

Microbial activity and spoilage of Norway lobster (Nephrops norvegicus) from Greek temperate waters, stored in air at 20, 5 and 0 °C was assessed. Microbial spoilage population, Total Volatile‐Base Nitrogen (TVB‐N), Trimethylamine‐Nitrogen (TMA‐N), pH and organoleptic changes were determined. Shelf‐life of Norway lobster stored at 20, 5 and 0 °C was 24, 72 and 96 h respectively. The product was spoiled due to the development of TVB‐N and melanosis of the carapace, as TVB‐N was apparent from the early stages of storage and correlated very well with microbial growth and shelf‐life. Pseudomonas sp. was the predominant spoilage bacterium. Product rejection coincided with TVB‐N levels of 330–400 mg kg^?1 and Pseudomonas sp. population level of about 5 × 10⁵ cfu g^?1. Pseudomonas sp. and TVB‐N are presumably the Specific Spoilage Organism and the Chemical Spoilage Index of the product.     

Partial purification and characterization of proteases from Norway lobster (Nephrops norvegicus) and their role in the phenolase activation process

Proteolytic activity in Norway lobster (Nephrops norvegicus) was studied. An improved separation and partial purification of the three proteases (designated as proteases I, II and III) was achieved from Norway lobster heads by a combination of acetone precipitation and DEAE-Sepharose CL-6B column chromatography.The purification achieved was 63-, 25- and 217-fold at pH 8.2, and 40-, 25- and 160-fold at pH 6.4 for protease I, II and III, respectively.With casein as substrate, protease III was most active at pH 8.2, whilst proteases I and II showed activity over a wide range of pH.Protease III was characterized as an alkaline Zn-serine protease as it was strongly inhibited by PMSF, soybean trypsin inhibitor, Co²⁺, Mn²⁺ and 1–10 phenanthroline. Protease I was strongly inhibited by p-benzoquinone, iodo-acetamide, heavy metals (Ag⁺, Cu²⁺) and 1–10 phenanthroline and was thus characterized as a Zn-thiol protease. Protease II was also inhibited by the same inhibitors as protease I (but to a lesser extent) and was characterized as a thiol protease.The molecular weights were determined to be 22.5, 45 and 42.5 kDa (with activity at 18 kDa) for proteases I, II and III, respectively.It was found that protease III activates phenolase at pH 8.2, whilst proteases II and I can activate phenolase at both pH 6.7 and 8.2.     

Effect of chill storage under different icing conditions on sensory and physical properties of canned farmed salmon (Oncorhynchus kisutch)

This work focuses the sensory and physical properties of canned farmed coho salmon (Oncorhynchus kisutch); the effect of flake ice and slurry ice as previous slaughter and chilling conditions was studied. Hydrolytic chemical changes related to sensory and physical properties were also evaluated in canned salmon. Thermal treatment led to a canned muscle showing higher firmness, lower cohesivity and colour changes (higher L* and b* values; lower a* values); filling oils showed higher turbidity scores and lower L*, a* and b* values than starting oil. Additionally, oxidised and putrid odour development in canned muscle and filling oil was low. However, previous icing condition and time (up to 9 days) provided no changes in canned muscle and filling oil, except for an increasing oxidised odour and turbidity in filling oil with chilling time. Meantime, free fatty acid formation and K value were markedly affected by previous icing system and time.     

Structural changes,chemical composition and antioxidant activity of cherry tomato fruits (cv. Micro‐Tom) stored under optimal and chilling conditions

BACKGROUND: Cherry tomato fruits cv. Micro‐Tom, a model plant for tomato genetics, were analysed in order to determine the main structural and chemical changes under optimal and chilling storage conditions. The comparison of Micro‐Tom to standard tomato cultivars will give an insight into suitability of this dwarf cultivar as a model for studying the influence of low‐temperature conditions on tomato fruits. RESULTS: During chilling, fruit tissue was progressively destroyed due to the collapse of the deep layers of the pericarp. Chilling lowered the typical tomato kinetics of ripening in sugars (glucose, fructose, sucrose), organic acids (tartaric, malic, citric, ascorbic and succinic) and the antioxidants phenol and lycopene, while carotenoid synthesis seemed to be blocked. Glutathione level was elevated and the activity of ROS scavenging enzymes was altered. Essentially, Micro‐Tom fruits showed a quality evolution that was similar to that described for standard tomato cultivars. CONCLUSION: The cherry tomato cultivar Micro‐Tom could be used as a model for studying the influence of low temperature on biochemical and structural changes taking place during chilling injury conditions. Copyright © 2009 Society of Chemical Industry     

Sensory,microbial and chemical effects of a slurry ice system on horse mackerel (Trachurus trachurus)

Slurry ice, a biphasic system consisting of small spherical ice crystals surrounded by seawater, was evaluated in parallel with flake ice for the storage of horse mackerel (Trachurus trachurus). Storage in slurry ice led to a significant enhancement of shelf life (5 days for flake ice to 15 days for slurry ice), better control of pH and lower counts of total aerobes and proteolytic and lipolytic bacteria, these reaching an average difference between batches of 2, 1.43 and 1.98 log units respectively after 8 days of storage. Storage in slurry ice also involved a significantly slower formation of total volatile basic nitrogen and trimethylamine after 8 days of storage. Staphylococcus xylosus and Proteus penneri were identified as the leading proteolytic and lipolytic organisms in horse mackerel muscle. Storage of horse mackerel in slurry ice enhances the shelf life of this medium‐fat fish species through better maintenance of sensory and microbiological quality. Copyright © 2004 Society of Chemical Industry     

Spraying of 4-hexylresorcinol based formulations to prevent enzymatic browning in Norway lobsters (Nephrops norvegicus) during chilled storage

A comparison was made of the effects on melanosis development in Norway lobsters (Nephrops norvegicus) of treatment by dusting with a commercial sulphite-based product and of spraying with a formulation containing 4-hexylresorcinol (0.1% and 0.05%), in combination with organic acids and chelating agents. The following tests were performed during chilled storage: polyphenol oxidase (PPO) activity, melanosis score, colour parameters, tyrosine and tyramine content, as the main substrate of PPO. Differences among treatments were evaluated by means of statistical analyses (ANOVA, principal components and discriminant analyses). All formulations diminished PPO activity during storage successfully. The melanosis score was higher in sulphite-treated Norway lobsters, and a formulation with 0.05% 4-hexylresorcinol was enough to prevent the appearance of melanosis for 12 days. The tyrosine content decreased during storage, but the tyramine content was insignificant. Formulations with 4-hexylresorcinol improved the appearance of Norway lobsters, in comparison with the commercial sulphite-based product.     

The function of endogenous cathepsin in quality deterioration of grass carp (Ctenopharyngodon idella) fillets stored in chilling conditions

Changes of textural properties and cathepsin activity of grass carp fillets during storage in superchilling (?1.5 ± 0.2 °C) and ice (0.2 ± 0.1 °C) was investigated, and the function of cathepsin in quality deterioration of grass carp fillets was discussed. Results showed that shear force of superchilled and ice‐stored fillets decreased by 50% and 55% after 6 days of storage, respectively. The cathepsin activies in different fractions changed significantly during storage at both conditions. Cathepsin B, B+L activities in sarcoplasma, myofibrillar and heavy mitochondrial fraction significantly increased during the early 3 days postmortem, accompanied by remarkable reduction of corresponding activity in lysosome. Cathepsin D activity in sarcoplasma and myofibrillar significantly increased during 6 days of storage with corresponding decrease in lysosome and heavy mitochondria. Correlation analysis showed that changes of shear force of grass carp fillets were significantly correlated with integration of cathepsin B, D and B+L throughout storage time (r² > 0.94). As derived from the first‐order exponential decay model, the enzyme efficiencies (k_a) of cathepsin B and B+L were more than twofold higher than those of cathepsin D, suggesting the major role of cathepsin B and B+L in textural deterioration of grass carp fillets in chilling storage.     

Effects of gutting and ungutting on microbiological, chemical, and sensory properties of aquacultured sea bream (Sparus aurata) and sea bass (Dicentrarchus labrax) stored in ice

The effect of gutting and ungutting on microbiological, chemical, and sensory properties of aqua-cultured sea bream (Sparus aurata) and sea bass (Dicentrarchus labrax) stored in ice were studied. The total viable mesophilic and psychrophilic bacterial counts increased throughout the storage period of gutted and ungutted sea bream and sea bass. The mesophilic counts reached 8.19 log cfu/g for ungutted sea bream and 7.93 log cfu/g for ungutted sea bass after 14 days of storage. The mesophilic counts reached 8.89 log cfu/g for gutted sea bream and 8.16 log cfu/g for gutted sea bass after 14 days of storage. On day 14 of storage the psychrophilic counts of ungutted sea bream and sea bass were 8.24 log cfu/g and 8.03 log cfu/g, respectively, and for gutted sea bream and sea bass were 8.93 and 8.22, respectively. At the end of the storage period of 14 days, TVB-N, TBA, and TMA-N values of ungutted sea bass were determined as 50.13 +/- 0.25 mg/100 g, 2.66 +/- 0.06 mg malonaldehit/kg, 9.86 +/- 0.01 mg/100 g respectively. TVB-N, TBA, and TMA-N values of ungutted sea bream reached 55.90 +/- 0.36 mg/100g, 2.51 +/- 0.21 mg malonaldehit/kg, 9.79 +/- 0.01 mg/100 g on day 14 respectively. And also at the end of the storage period of 14 days, TVB-N, TBA, and TMA-N values of gutted sea bass were determined as 48.00 +/- 0.26 mg/100 g, 2.48 +/- 0.03 mg malonaldehit/kg, 8.71 +/- 0.06 mg/100 g respectively. TVB-N, TBA, and TMA-N values of gutted sea bream reached 49.66 +/- 0.77 mg/100g, 2.64 +/- 0.07 mg malonaldehit/kg, 8.97 +/- 0.01 mg/100 g on day 14 respectively. The result of this study indicates that the shelf-life of whole ungutted sea bass and sea bream stored in ice as determined by the overal acceptibility sensory scores, chemical quality, and microbiological results show us that the fish were spoilt on day 14. Each chemical, sensory, and microbiological result for sea bream showed us that there was a correlation and similarity and on day 14 it was spoilt.     

Microbiological and physicochemical properties of red claw crayfish (Cherax quadricarinatus) stored in different package systems at 2 degrees C

ABSTRACT:  This study compared 3 package systems for their influence on the stability of shell-on red claw crayfish tail meat stored at 2 °C for 14 d. Modified atmosphere packaging (MAP, with 80% CO₂/10% O₂/10% N₂) suppressed ( P < 0.05) the growth of aerobic bacteria and coliforms when compared with aerobic packaging using polyvinylchloride (PVCP) and vacuum packaging (VP). MAP and VP tended to retard lipid oxidation, inhibited Ca-ATPase activity change, but produced more intense protein denatuation when compared with PVCP. The MAP packaging enhanced proteolysis and resulted in more ( P < 0.05) cooking losses and a higher ( P < 0.05) shear force than VP and PVCP for samples stored for 6 and 14 d ( P < 0.05). Sensory panel results were in general agreement with the physicochemical changes, suggesting that the specific package systems had a significant impact on the quality of refrigerated red claw crayfish raw meat.     

Evaluation of sampling units and sampling plans for adults of Cryptolestes ferrugineus (Coleoptea: Laemophloeidae) in stored wheat under different temperatures, moisture contents, and adult densities

Development and evaluation of optimum size and number of sample units is required for cost-effective management of stored grain beetles. In this study, we evaluated the sampling parameters and accuracy of insect density detection and estimation, developed the optimum size and number of sample units, and conducted a feasibility study of the insect detection and density estimation. The measured insect densities in 92% of random samples were less than the introduced insect densities and 67.4 ± 10.8% of random samples did not contain adults when the introduced insect density was 0.1 A/kg (adult/kg). If the random sampling technique was used and 15% of the stored wheat bulk was sampled, 72% of determined means of insect densities of the sampling sets were lower than the introduced insect densities. Increasing the size of sample units did not improve the accuracy of the estimation of insect densities; however, it did considerably increase the probability of insect detection when insect densities were lower than 1.0 A/kg. We recommend at least 7 kg per sample unit for insect detection (especially when insect densities < 0.1 A/kg) and the optimum number of sample units with 15 kg grain per unit should be >24 for a fixed precision of 0.35 when insect densities < 0.1 A/kg. This might be a challenge for grain storage practice. Therefore, using sampling technique to estimate insect densities and detect insects at low insect densities (<0.1 A/kg) might not be practicable.     

A wild strain of Plodia interpunctella (Hübner) (Lepidoptera: Pyralidae) from farm-stored maize in South Carolina: Development under different temperature, moisture, and dietary conditions

The purpose of this study was to determine the duration of immature development and survivorship of Plodia interpunctella (Hübner) on maize over a range of temperatures and grain moisture contents encountered in maize stored on farms in the southeastern states (USA). Laboratory cultures were established with moths collected from farm-stored maize in South Carolina and maintained on cracked maize at 30 °C and 60% r.h. The incubation period and percentage hatch of eggs was determined at 18 combinations of temperature and r.h. Hatch was <1% at 15 and 40 °C. In the range 20-35 °C, percentage hatch declined as temperature increased, and the mean incubation period ranged from 3.1 to 8.5 d. Neither percentage hatch nor incubation period were affected by r.h. between 43% and 76%. The relationship between mean developmental period (oviposition to adult eclosion) and temperature was well described by a quadratic polynomial that predicted a decline from 67.6 to 30.1 d as temperature increased from 20 to 31.1 °C, followed by an increase to 38.5 d as temperature increased further to 35 °C. The results suggest a lower temperature threshold for development near 15 °C and an upper limit slightly greater than 35 °C. Moisture content had a significant effect on developmental period at all the temperatures studied, but the pattern of variation with moisture depended upon the temperature.