Quality assessment of wild European eel (Anguilla anguilla) stored in ice

The quality assessment of wild European eel (Anguilla anguilla) stored in ice and in boxes without ice (3 ± 1 °C) was investigated by the sensory analysis, levels of nucleotide breakdown products and biogenic amines for up to 19 days. Sensory analysis was assessed using the Tasmanian Food Research Unit Scheme. K and related values (K_i, G, P, H and F_r) were used as freshness indicators. Linear regressions (r²) obtained from K, K_i, G, P, H and F_r were 0.95, 0.96, 0.83, 0.96, 0.99 and 0.96, respectively, for eel stored in ice whereas, for eel kept in boxes without ice, the values were 0.86, 0.86, 0.96, 0.91, 0.98 and 0.86, respectively. When eel stored in ice and in boxes without ice were considered at the limit of acceptability by assessors at ∼12–14 days and ∼5–7 days, respectively, the average K, K_i and P values were ∼70–85%, H values were ∼60% and F_r values were ∼10% for both storage conditions. The level of histamine exceeded the legal limit (5 mg/100 g fish) in eel stored without ice after 6–7 days and, in ice, after 13–14 days of storage, at which time eels were rejected by the sensory panel. The concentrations of biogenic amines were higher in eel stored in boxes without ice than in eel kept in ice. The levels of histamine in the muscle of eel kept in boxes without ice and in ice increased to the maximum levels of 17.9 mg/100 g on day 12 and 12.6 mg/100 g on day 19, respectively.     

Evaluation of an ozone–slurry ice combined refrigeration system for the storage of farmed turbot (Psetta maxima)

The use of ozonised slurry ice was investigated as a new refrigeration system for the storage of farmed turbot (Psetta maxima). With this purpose in mind, an ozone generator device was coupled to a slurry ice system working subzero at −1.5 °C. The ozone concentration was adjusted to a redox potential of 700 mV, and the slurry ice biphasic mixture was prepared at a 40% ice/60% water ratio and 3.3% salinity. Certain biochemical parameters indicative of fish freshness, such as the rate of nucleotide degradation or TMA-N formation, were not significantly affected by the presence of ozone in the slurry ice mixture. However, storage in ozonised slurry ice significantly slowed down the mechanisms responsible for lipid hydrolysis and lipid oxidation in farmed turbot. Storage in ozonised slurry ice also led to significantly (p < 0.05) lower counts of both total aerobes and psychrotrophic bacteria in both turbot muscle and skin, as compared with the control batch stored without ozone. Sensory analyses confirmed an extended shelf life of turbot specimens stored in ozonised slurry ice; these maintaining “A” sensory quality up to day 14, while the counterpart batch stored in slurry ice kept this quality only up to day 7. The combination of ozone and slurry ice may be recommended for the chilling and storage of farmed turbot with a view to extending its shelf-life.     

Biochemical changes and quality loss during chilled storage of farmed turbot (Psetta maxima)

Changes in three of the major biochemical components – nucleotides, lipids and proteins – related to quality loss in farmed turbot, were determined during 29 days of iced storage; results were complemented with sensory analysis. Nucleotide degradation, as estimated by the K value, underwent a gradual increase until day 19, in agreement with the loss of freshness observed for the sensory scores (high quality: days 0–2; good quality: days 3–14; fair quality: days 15–19). After day 19, the fish was judged unacceptable and the K value did not show differences until the end of storage. Lipid hydrolysis and oxidation occurred at slow rates, free fatty acid contents and the peroxide value being below 20.0 g kg⁻¹ lipids and 4.00 meq active oxygen kg⁻¹ lipids, respectively, during the whole storage. The content of fluorescent compounds did not increase significantly until day 19, when a sharp increase was detected. The electrophoretic protein profiles of turbot muscle did not point to any major protein degradation event or any significant change in protein during storage. However, a new band, corresponding to 22 kDa, could be observed at day 2 in the low-ionic strength buffer extract, whose concentration seemed to increase at days 9 and 14 and was present until the end of the chilled storage. The results obtained in this work indicate slow and gradual biochemical changes and long shelf life and good quality times (19 and 14 days, respectively) for iced turbot; these long times would be very profitable when turbot commercialisation is carried out in places distant from production farms.     

Freshness assessment of cultured sea bream (Sparus aurata) by chemical,physical and sensory methods

The quality changes of cultured sea bream (Sparus aurata) stored in ice for a period of up to 23 days were determined by K and related values, sensory assessment and texture by texturometer. Sensory schemes, based on the Tasmanian Food Research Unit (TFRU) scheme for raw fish and on the Torry scheme for cooked fish were modified to be appropriate for whole cultured sea bream, according to the trained panellists’ perceptions, during the storage period in ice. The TFRU sensory score of fish showed good agreement with K value and texture results throughout the storage period. The limit for acceptability of cultured sea bream stored in ice was about 17–18 days. Generally, K, K_i and G values had good correlation with the degree of freshness and can be used as freshness indicators.     

Sensory,microbiological and chemical assessment of the freshness of red mullet (Mullus barbatus) and goldband goatfish (Upeneus moluccensis) during storage in ice

The shelf life of red mullet and goldband goatfish during ice storage were studied in terms of sensory, microbiological and chemical changes. The sensory acceptability limit was 8 days for goldband goatfish (Upeneus moluccensis) and 11 days for red mullet (Mullus barbatus) stored in ice. The TVC level was correlated with sensory assessment. The TVC exceeded 7 log cfu g⁻¹ after 8 days for goldband goatfish, and 11 days for red mullet. At the end of storage period, pH, TVB-N, TBA, FFA and PV for red mullet were 7.84, 47.19 mg/100 g, 0.69 mg MA kg⁻¹, 1.17% oleic acid and 1.58 meq O₂/kg and for goldband goatfish they were 7.53, 43.97 mg/100 g, 0.74 mg MA kg⁻¹, 1.62% oleic acid and 1.68 meq O₂/kg, respectively. In red mullet, agmatine, serotonin, histamine and dopamine became the dominant amines, reaching 7.30, 5.97, 2.52 and 2.31 mg/100 g, respectively. Also the dominant amines for goldband goatfish were 4.37, 3.88, 3.38 and 2.00 mg/100 g for histamine, agmatine, dopamine and putrescine, respectively.     

Nucleotide degradation and biogenic amine formation of wild white grouper (Epinephelus aeneus) stored in ice and at chill temperature (4 °C)

Sensory (cooked and uncooked), chemical (proximate composition, TVB-N, nucleotide degradation products and biogenic amines) and microbiological quality (TVC and total coliform) changes were investigated during storage of ungutted white grouper kept in ice and at chill temperature (4 °C). According to the sensory assessment, the shelf life of white grouper was 16 days in ice and 4 days for fish stored at chill temperature. TVB-N values increased with storage time. Amines found in white grouper stored in ice were TMA, putrescine, cadaverine, 2-phenylethylamine, dopamine, agmatine, tryptamine and serotonin. Histamine, spermine, spermidine were never detected with either storage condition. The acceptability limit in terms of microbial count was exceeded at 8 days in ice and at 4 days for fish stored at chill temperature. Total coliform count was 2.8 log₁₀ cfu/ml at 1 day and reached 10⁵ cfu/ml for both storage conditions.     

Quality Assessment of Tiger Tooth Croaker (Otolithes ruber) During Ice Storage

Quality and shelf life of tiger tooth croaker (Otolithes ruber) during 19 days of iced storage were investigated in terms of sensory, chemical (total volatile basic nitrogen (TVB-N), thiobarbituric values (TBA), peroxide value (PV), free fatty acid (FFA), and pH) and microbiological (total viable count, TVC and total psychrotrophic count. TPC) aspects. Acceptability quality of Tiger tooth croaker determined by panelists was 15–17 days. Limiting factors for acceptability were eye, gills, peritoneum, smell of gills and abdominal cavity, internal organs and flesh. Bacterial loads in samples were higher than limiting level (3 × 10⁶ CFU g^?1) between 15–17 days of ice storage. Of the chemical indicators of spoilage, the initial value of pH was 6.71 and increased to 7.35 at the end of storage. TVB-N content was 15.31mg N/100g on day 0 and reached to 36.52 on day 19. The acceptability of tiger tooth croaker decreased as FFA, PV and TBA values increased (P < 0.05). The release of FFA increased from an initial value of 4.15 (expressed as % of oleic acid) to a final value of 12.75 during the storage period. The initial PV value was 11.69 meq/kg and it increased to 50.75 meq/kg on day 12 and then started to decrease to 35.82 meq/kg at the end of storage period. The initial and final values of TBA were 0.83 and 3.75, respectively.     

Effect of gutting on microbiological,chemical, and sensory properties of aquacultured sea bass (Dicentrarchus labrax) stored in ice

The effect of gutting on microbiological, chemical, and sensory properties of aqua-cultured sea bass (Dicentrarchus labrax) stored in ice was studied. Pseudomonads and H₂S-producing bacteria (including Shewanella putrefaciens) were the dominant bacteria at the end of the 16-day storage period in ice for both whole ungutted and gutted sea bass. Brochothrix thermosphacta and Enterobacteriaceae were also found in the spoilage microflora of ungutted and gutted sea bass but their counts were always less than those of Pseudomonads and H₂S-producing bacteria. Bacterial counts of whole ungutted sea bass were always higher than those obtained for gutted sea bass samples. Mesophilic counts for gutted and ungutted fish exceeded 7 log cfu g⁻¹ after 9 and 15 days of ice storage, respectively. Of the chemical indicators of spoilage, TMA values of ungutted sea bass increased very slowly whereas for gutted samples higher values were obtained reaching a final value of 0.73 and 4.39 mg N 100 g⁻¹, respectively (day 16). TVB-N values showed no significant increase for whole ungutted sea bass during storage reaching a value of 27.7 mg N 100 g⁻¹ (day 16) whereas for gutted fish 36.9 mg N 100 g⁻¹ was recorded. TBA values remained low for ungutted sea bass samples until day 16 of storage, whereas for gutted fish were variable. Of the chemical indices used, none proved useful means of monitoring early ungutted and gutted sea bass freshness in ice. Sensory assessment using the EC freshness scale gave a grade E for up to 5 days for the ungutted sea bass, a grade A for a further 2 days and a grade B for an additional 4 days, after which sea bass was graded as C (unfit). Gutted sea bass was given a grade E for up to 3 days, a grade A for the 4–7th days, and a grade B for the 8–10th days of storage, whereas on day 11 it was graded as unfit. Acceptability scores for odor, taste and texture of cooked ungutted and gutted sea bass decreased with time of storage. Results of this study indicate that the shelf-life of whole ungutted and gutted sea bass stored in ice as determined by the overall acceptability sensory scores and microbiological data is 13 and 8 days, respectively.     

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.     

Effects of slaughtering methods on sensory,chemical and microbiological quality of rainbow trout (<Emphasis Type="Italic">Onchorynchus mykiss</Emphasis>) stored in ice and MAP

The effects of slaughtering methods (percussive stunning and death in ice slurry) on the quality of rainbow trout stored in ice and modified atmosphere packing (MAP) (40% CO₂, 30% N₂ and 30% O₂) were investigated in terms of sensory, chemical and microbiological analysis. Sensory analysis showed that the demerit points of fish slaughtered by percussive stunning were higher than those slaughtered by the ice slurry method, but there were no significant differences in demerit points (P>0.05). In addition, the rate of increase in demerit points in fish in MAP was significantly (P>0.05) higher at 6 and 10 days of storage than that in fish in ice for each slaughter method, which was due to increased drip, the appearance of slime and the odour of the fish in MAP packing. The mean K values of rainbow trout slaughtered by percussive stunning in this study were significantly lower (P<0.05) than those of trout slaughtered according to the ice slurry method. The level of biogenic amines, regardless of the slaughter method, showed a similar trend (P>0.05), but higher concentrations of biogenic amines were found for the ice slurry slaughter method and for fish stored in ice. There were no significant differences (P>0.05) in total viable count of fish stored in ice and MAP, regardless of the different slaughter methods used. However, fish packed in MAP showed reduction in bacterial counts compared to fish held in ice throughout study. The results of this study showed that slaughter by percussive stunning improved the quality of trout compared to the ice slurry method.     

Microbiological,chemical and sensory assessment of iced whole and filleted aquacultured rainbow trout

The effect of filleting on microbiological, chemical, and sensory properties of aquacultured freshwater trout (Onchorynchus mykiss) stored in ice was studied. Pseudomonads, H₂S-producing bacteria (including Shewanella putrefaciens) and Brochothrix thermosphacta were the dominant bacteria while, Enterobacteriaceae in lower counts were also found in the spoilage microflora of whole ungutted and filleted trout over an 18-day storage period in ice. Bacterial counts of whole ungutted trout were always lower than those obtained for filleted trout samples. Mesophilic counts for filleted and ungutted fish exceeded 7 log cfu/cm² after 10 and 18 days of ice storage, respectively. Of the chemical indicators of spoilage, trimethylamine (TMA) values of ungutted trout increased very slowly whereas for filleted samples higher values were obtained reaching a final value of 4.29 and 6.38 mg N/100 g, respectively (day 18). Total volatile basic nitrogen (TVB-N) values showed no significant increase for whole ungutted trout during storage reaching a value of 20.16 mg N/100 g (day 18) whereas for filleted fish a respective value of 26.06 mg N/100 g was recorded. Thiobarbituric acid (TBA) values of ungutted trout increased very slowly whereas for filleted samples higher values were obtained reaching a final value of 16.21 and 19.41 μg MA/g, respectively (day 18). Of the chemical indices used, none proved useful means of monitoring early freshness for ungutted and filleted trout freshness in ice. Sensory assessment using the EC freshness scale gave a grade E for up to 6 days for the ungutted trout, a grade A for a further 3 days and a grade B for an additional 6 days, after which trout was graded as C (unfit). Acceptability scores for odor, taste and texture of cooked ungutted and filleted trout decreased with time of storage. Results of this study indicated that the shelf-life of whole ungutted and filleted trout stored in ice as determined by sensorial and microbiological data is 15–16 and 10–12 days, respectively.     

Effects of storage in slurry ice on the microbial,chemical and sensory quality and on the shelf life of farmed turbot (Psetta maxima)

The application of slurry ice, a binary mixture of small spherical ice crystals surrounded by seawater at subzero temperature, is a potentially new preservation method for farmed turbot (Psetta maxima), a flat fish species of increasing commercial interest. Comparative biochemical, microbiological and sensory analyses were carried on turbot specimens stored in either slurry ice or flake ice for up to 40 days. The results obtained in the sensory analysis correlated well with the observed chemical and microbial changes. Storage of turbot in slurry ice resulted in a slowing-down of the nucleotide degradation pathway and lipid oxidation mechanisms. A good stabilisation of the high molecular weight protein fraction of turbot muscle was also achieved as a consequence of storage in slurry ice. A slower production of both trimethylamine and total volatile bases was also observed. Likewise, low levels of total aerobes, anaerobes, coliforms, and proteolytic bacteria were attained. The application of slurry ice to farmed turbot is advisable to achieve better quality maintenance during storage and distribution.     

The effects of partial replacement of fish meal by vegetable protein sources in the diet of rainbow trout (Onchorynchus mykiss) on post mortem spoilage of fillets

Five test diets were formulated with decreasing levels of fish meal (up to 50%) replaced by alternative protein sources. Rainbow trout were fed the experimental diets for 12 weeks.The effects of feed ingredients on spoilage of Oncorhynchus mykiss in ice and under MAP/ice (40% CO₂, 30% N₂ and 30% O₂) were investigated in terms of sensory, chemical and microbiological analyses. The results showed that the trout in MAP/ice was rejected at 14 days, after sensory analysis, due to excessive drip, whereas trout in ice were found to be acceptable even after 14 days of storage. However, cooked trout fillets, under both storage conditions, were rejected at 17 days. Fish in ice produced higher K values and higher concentrations of biogenic amines during the storage period of 17 days than the fish in MAP/ice. Bacteria grew more quickly in rainbow trout kept in ice than in MAP/ice. MAP/ice storage extended the shelf life of rainbow trout by approximately 2 days compared to ice storage alone in terms of microbiological analyses.     

Oxidation of linoleic acid as a marker for shelf life of corn flour

The objective of this study was to measure the oxidation of linoleic acid of nixtamalised corn masa (NCM) during an accelerated shelf life study at high temperature (45–85 °C), and 0.45 a_w for 180 days. Linoleic acid (LA) was present at 55.1%, followed by oleic acid (26.9%), as measured by gas chromatography. The propagation of lipid oxidation, measured by anisidine value, reached its peak 2–5 days after the peroxide value had passed over its maximum value. At this time, flour showed at least a 10% reduction of LA; but, at the end of storage only 10% of LA remained. The autocatalytic oxidation of linoleic acid in NCM was temperature-dependent, with Q₁₀ = 1.4. The index of quality loss for corn flour stored at 55 °C was 0.48% per day; under these conditions 50% of its quality decreased in only 104 days. Mathematical modelling estimates a shelf life of 84 days for corn masa (<6 meq/kg peroxide) stored at 25 °C.     

Freshness assessment of ray fish stored in ice by biochemical,chemical and physical methods

Ray fish were caught, filleted, and stored in ice. Fillets were analysed for 18 days to determine the chemical, biochemical and physical changes and their relation to the muscle eating quality. Trimethylamine (TMA-N), total volatile bases (TVB-N), ATP content and breakdown products, K value, pH, texture, water-holding capacity (WHC) and colour changes were monitored. At the beginning of the study, the ray fish muscle showed a low concentration of ATP and a high value of inosine 5′-monophosphate (IMP). Regarding to the signs of freshness and deterioration, K value presented an exponential increase (r2 = 0.95) with an initial value of 4.7% and a final value of 47.5%. Furthermore, the TBV-N and TMA-N significantly increased (P < 0.05) during the storage in ice. As for the physical analysis whereas the texture changed (P < 0.05); pH and the WHC were not affected (P < 0.05). The overall results of this study indicated that the edible quality of ray fish muscle was maintained during at least 15 days of ice storage.     

Shelf Life Assessment of Modified Atmosphere Packaged Turbot (Psetta maxima) Fillets: Evaluation of Microbial, Physical and Chemical Quality Parameters

Quality and safety of turbot fillets under modified atmosphere packaging (MAP) were assessed by microbial (total viable counts), physical (drip loss, pH, colour CIE Lab) and chemical parameters (total volatile basic nitrogen (TVBN), trimethylamine nitrogen (TMAN), biogenic amine contents). Three different atmospheres (MAP 1, 10/40/50 % O₂/CO₂/N₂; MAP 2, 10/60/30 % O₂/CO₂/N₂; MAP 3, 10/80/10 % O₂/CO₂/N₂) were tested. Packaged turbot fillets were stored at 2?±?1 °C and monitored over 30 days, at intervals of 5 days. Fillets from the control group, packaged with air (AIR), were the first to present signs of degradation reaching rejection threshold values for all evaluated parameters. In MAP fillets, total bacterial count was lower than 10⁶ cfu/g for a longer period. After 10 days of storage, MAP and AIR fillets showed significant differences (p?<?0.05) on the values of TVBN, TMAN and biogenic amines. MAP fillets presented a higher drip loss, and fillets in AIR became more yellowish (upper b* values) while those in MAP looked whitish for an increased period (upper L* values). All microbial, chemical and physical traits revealed the protective effect of the different MAP studied, especially those with a higher percentage of CO₂. MAP application added, at least, 5 days to shelf life of turbot fillets.     

Quality assessment of gutted wild sea bass (Dicentrarchus Labrax) stored in ice, cling film and aluminium foil

The effects of aluminium foil and cling film on microbiological, chemical and sensory changes in wild sea bass (Dicentrarchus labrax) stored at chill temperature (4 °C) were studied. A quality assessment of wild sea bass stored in ice, in boxes without ice, wrapped in aluminium foil (WAF) and wrapped in cling film (WCF) at 4 °C was performed by monitoring sensory quality, nucleotide breakdown products, total volatile base nitrogen (TVB-N), and total viable counts (TVCs). The observed organoleptic shelf-life of sea bass was found to be 16 days in ice, 4 days in boxes without ice, 8 days in aluminium foil and 8 days in cling film. Demerit points did not differ significantly (P>0.05) between WCF fish and WAF fish. The nucleotide degradation pattern was found to be similar for all storage conditions except for inosine and hypoxanthine contents, which decreased after 12 days of storage for WAF and WCF. The content of TVB-N for all storage conditions showed similar tendencies until 12 days storage but reached the highest level (41.6 mg TVB-N 100 g^–1 flesh) for fish stored in WAF and WCF. No significant differences (P>0.05) were found in TVB-N concentrations within the treatments during the early stages of the storage period. Bacteria grew most quickly in the sea bass kept in boxes without ice, followed by those kept WAF, WCF and in ice. Significant differences (P<0.05) in TVC were observed amongst the treatments, especially between fish stored in boxes without ice and fish stored in ice     

Hydrolysis and oxidation of European eel oil during frozen storage for 48 weeks

The quality assessment of the wild European eel (Anguilla anguilla) stored at −20 °C was assessed by sensory, chemical (total volatile basic nitrogen (TVB-N), peroxide value (PV), free fatty acid (FFA), thiobarbituric values (TBA) and pH) methods. The sensory analysis of showed that European eels were acceptable by panellists and can be stored for more than 48 weeks at −20 °C. No effects of frozen storage were observed on the proximate composition of eel. The level of TVB-N showed fluctuations (7.09–14.72 mg TVB-N/100 g) during frozen storage period, thus TVB-N could not be used as an indicator of frozen eel quality. FFA, PV and TBA values showed fluctuations during frozen storage period but remained low at the end of storage period, PV reached to the maximum level of 13.20±1.73 meq/kg, which did not exceed the maximum recommended value for human consumption (20 meq/kg). The release of FFA slightly increased (P>0.05) from the initial value of 0.88 to 2.14 (expressed as % of oleic acid) until 32 weeks of frozen storage while TBA increased from the initial value of 0.085 mg MA/kg to maximum level of 0.7696 mg MA/kg after week 40. After that, their values decreased to 1.82 and 0.5577 at week 48, respectively. This study showed that off-flavour and off-odour was not detected and frozen European eels were still acceptable by panellists and can be stored for more than 48 weeks at −20 °C.     

Effects of aluminium foil and cling film on biogenic amines and nucleotide degradation products in gutted sea bream stored at 2±1 °C

Biogenic amines and nucleotide degradation products of sea bream stored in ice, wrapped in aluminium foil (WAF) and in cling film (WCF) at 2±1 °C were investigated by using a rapid HPLC method. Results obtained from this study showed that for household purposes packing fish in different materials has a little effect on the biogenic amines formation and nucleotide degradation products. The highest decrease of IMP content was observed for sea bream in WAF, followed by WCF. INO values showed a fluctuation and remained below the levels of 5.5 μmol/g for all storage conditions. Hx value constantly increased with the storage time during chilled storage. For all of the storage condition, K and Ki value increased linearly with storage time. At the end of the storage period, K, Ki, H and G value reached 60–76%, 65–81%, 30–54% and 89–173%, respectively. Among biogenic amines, (trimetylamine) TMA, putrescine, cadaverine, spermidine, spermine, tryptamine, tyramine, β-phenylalanine and histamine were detected during storage period. TMA and putrescine were observed to increase linearly during storage period. Histamine production was only found at the end of storage period. The highest histamine values for fish wrapped in aluminium foil were 6.4 mg/100 g and fish wrapped in cling film was 4.6 mg/100 g.     

Relation of biogenic amines to microbial and sensory changes of precooked chicken meat stored aerobically and under modified atmosphere packaging at 4 °C

The formation of biogenic amines and their correlation to microflora and sensory characteristics of a precooked chicken meat product stored aerobically and under modified atmosphere packaging (MAP) (30% CO₂, 70% N₂) was studied. Putrescine was the main amine formed both in aerobically and MA-packaged chicken samples. For the rest of the biogenic amines, including tyramine, histamine, and cadaverine, a stepwise increase was recorded throughout the 23-day storage period under the above packaging conditions. Spermidine was found in higher amounts, as compared to spermine in both aerobically and MA-packaged chicken samples at 4 °C. Formation of these amines in precooked chicken stored either aerobically or under a 30% CO₂, 70% N₂ atmosphere followed an inconsistent trend during the entire storage period at 4 °C. Agmatine, β-phenyl-ethylamine, and tryptamine were not detected in precooked chicken. Of the bacterial groups monitored, lactic acid bacteria (LAB) became the dominant bacteria after day 8 of storage under MAP while LAB were the dominant population of natural microflora of precooked chicken stored both aerobically or under MAP, reaching 7.5 and 8.0 log cfu/g, respectively, on day 23 of refrigerated storage. Enterobacteriaceae populations in chicken meat were below the detection limit (<1 log cfu/g) by pour plating throughout the 23-day storage period, irrespective of packaging conditions. Based on sensory data, after ca. 8 days for the precooked chicken meat stored aerobically and after 12 days under MAP (time to reach initial decomposition stage, score of 2) the putrescine and tyramine content of chicken samples were ca. 14–19 and 1.4 mg/kg, values that may be proposed as the limit for spoilage initiation of precooked chicken meat (respective TVC for both aerobically and MA-packaged chicken meat were ca. 6.5 log cfu/g).