Quality changes of ready-to-eat ginseng chicken porridge during storage at 25°C

Ready-to-eat (RTE) ginseng chicken porridge was heated in a retort with an F-value of 4.0 after being packaged in a gas-tight plastic tray (PP/EVOH/PP) with top film (PET/PA/CPP). Various quality changes were investigated during the storage for 28weeks at 25°C. Over the storage period, microorganisms were not detected above 1.0 log cfu/cm(2) (detection limit). The viscosity increased sharply from 775 to 2025cp for initial 4weeks and increased steadily until 16weeks, with a slight reduction thereafter. During the 28weeks of storage, the ratio of residual oxygen and pH decreased from 10.8% and 6.49 to 5.7% and 6.05, while retrogradation degree increased from 0% to 55.9%. Hunter L(?), b(?), and ΔE values increased until 20weeks and remained for the rest of storage. Based on sensory, microbiological and physicochemical evaluations, the RTE ginseng chicken porridge could be marketable for at least 24weeks at 25°C.     

Determination of biogenic amines in fresh unpacked and vacuum-packed beef during storage at 4°C

Biogenic amines, putrescine, cadaverine, and histamine were determined in unpacked and vacuum-packed beef; during storage at 4°C for 12 and 35 days, respectively, under the same conditions. Analysis by High Performance Liquid Chromatography in both kind of samples, showed variation of cadaverine and histamine with an increasing tendency to a definite increase of putrescine. In unpacked samples, maximum mean contents for each amine reached 10.4, 5.2 μg/g for putrescine and cadaverine, respectively (12th day) and 2.2 μg/g for histamine (5th day). The total amine content reached 16.5 μg/g (12th day). After 8 days of storage, organoleptic fall-off began and, on the 12th day, all samples were disqualified. In vacuum packs, amine levels increased after 19 days. Maximum levels were determined for putrescine on the 35th day (36.3 μg/g), for cadaverine on the 26th day (28.9 μg/g) and for histamine on the 35th day (19.0 μg/g). Although the vacuum-packed beef was organoleptically acceptable up to 35 days, the total amine levels were greater than 5 μg/g after the 12th day, indicating a leveling off of quality.     

Quality changes and shelf life of imported vacuum-packaged beef chuck during storage at 0°C

The objective of this study was to investigate differences in adipose tissue fatty acid composition among stress genotypes as well as to determine relationships of those fatty acids with performance, carcass and meat quality traits. Haplotypic analysis of parents and offspring was employed to assign 48 pigs to three stress genotypes of swine. Individual fatty acid profiles were determined on subcutaneous backfat. Stress genotype had a significant effect on the proportions of C14:0 (P<0.05), C16:0 (P<0.10), C16:1 (P<0.05) and C18:0 (P<0.05) fatty acids. After adjusting for stress and gender, there was a negative correlation between backfat thickness and essential fatty acids (linoleic and linolenic) (P<0.001). In contrast, the correlation of loin muscle area with C18:2 (P<0.01) and C18:3 (P<0.001) was positive. The degree of fat firmness was negatively correlated to the proportion of total unsaturated fatty acids (P<0.01). No significant correlations were observed between fatty acid contents and lean meat quality traits.     

Quality changes of ready-to-eat ginseng chicken porridge during storage at 25 °C

Ready-to-eat (RTE) ginseng chicken porridge was heated in a retort with an F-value of 4.0 after being packaged in a gas-tight plastic tray (PP/EVOH/PP) with top film (PET/PA/CPP). Various quality changes were investigated during the storage for 28 weeks at 25 °C. Over the storage period, microorganisms were not detected above 1.0 log cfu/cm² (detection limit). The viscosity increased sharply from 775 to 2025 cp for initial 4 weeks and increased steadily until 16 weeks, with a slight reduction thereafter. During the 28 weeks of storage, the ratio of residual oxygen and pH decreased from 10.8% and 6.49 to 5.7% and 6.05, while retrogradation degree increased from 0% to 55.9%. Hunter L^⁎, b^⁎, and ΔE values increased until 20 weeks and remained for the rest of storage. Based on sensory, microbiological and physicochemical evaluations, the RTE ginseng chicken porridge could be marketable for at least 24 weeks at 25 °C.     

Effect of antibacterial treatments and natural chemicals on the quality and safety of marinated raw crab paste during storage at −20°C

The effects of antibacterial treatments and several natural chemicals on the quality and safety of crab paste during storage at −20°C were investigated. All antibacterial treatments significantly reduced the bacterial total viable count (TVC) of swimming crabs, with sodium hypochlorite (NaClO) combined with ultrasonic cleaning having the best effects. Four chemicals significantly inhibited the increase in TVC, pH, and the accumulation of total volatile basic nitrogen (TVB-N) compared to controls, and their combined treatment had synergistic effects. The L ₉(3 ⁴) orthogonal experiment showed that the optimum combination was A₁B₃C₃D₂ (i.e., 0.1 g kg⁻¹ nisin, 0.4 g kg⁻¹ ε-polylysine hydrochloride, 0.3 g kg⁻¹ tea polyphenol, and 0.5 g kg⁻¹ citric acid). The TVC, TVB-N concentration, and pH in A₁B₃C₃D₃-treated samples remained far below the maximum acceptable limit for good-quality marinated, raw, aquatic animal product after 12 months of frozen storage at −20°C. Furthermore, the combined treatment (A₁B₃C₃D₃) significantly inhibited the reproduction of foodborne pathogenic bacteria and spoilage bacteria. The antibacterial treatments and natural chemicals reduced foodborne pathogenic bacteria and inhibited microbial spoilage, and therefore maintained the quality and safety of crab paste during frozen storage. Antibacterial treatments and natural chemicals could be commercially utilized to maintain the quality and safety of crab paste.     

Functional properties of raw and cooked pork patties with added irradiated, freeze-dried green tea leaf extract powder during storage at 4 °C

Functional and sensory properties of raw and cooked pork patties with added irradiated freeze-dried green tea leaf extract powder were studied. Components of green tea were extracted by 70% ethanol, and the extract was irradiated to obtain a bright color. The irradiated green tea extract was freeze-dried and the powdered sample (0.1%) was added to the pork patties (Trt C). Pork patties without any ingredient (Trt A) and with nonirradiated, freeze-dried green tea extract powder (Trt B) were also prepared for comparison. Lipid oxidation, radical scavenging effect, color, and sensory properties of pork patties with treatments were analyzed at 5-day intervals for 15 days with storage at 4?°C. The lipid oxidation had a lower (P<0.05) and radical scavenging effect was greater (P<0.05) in the raw and cooked pork patties with added Trt B and Trt C, than those of Trt A (control). The pork patties with Trt B and Trt C had a higher Hunter color a*-value and less cooking loss than that of Trt A. Sensory panelists preferred the odor of the raw pork patties and color of the cooked pork patties of Trt C (P<0.05). Generally, no significant difference between Trt B and Trt C was found. Therefore, irradiated, freeze-dried green tea extract powder can be used for producing functionally-improved meat products.     

Effect of Eryngium caeruleum essential oil on microbial and sensory quality of minced fish and fate of Listeria monocytogenes during the storage at 4°C

The present study investigated in vitro antimicrobial activity of Eryngium caeruleum essential oil (EEO) against five foodborne pathogenic bacteria based on microdilution and disk diffusion methods. Moreover, its effects on specific spoilage microorganisms, inoculated Listeria monocytogenes, and its sensory changes in minced fish were evaluated during 12 days of storage at refrigeration temperature. The results showed that Staphylococcus aureus and Escherichia coli were the most sensitive and the most resistant bacteria with a minimum inhibitory concentration of 0.125 and 1 mg/ml, as well as inhibition zones of 15.66 and 11.66 mm, respectively. Regarding the antimicrobial effect of EEO on the microbial profile and inoculated L. monocytogenes, treating with 0.4% EEO caused a significant decrease in the studied microorganisms when compared to the control group (p < 0.05). In addition, considering the sensory evaluation, the best scores were observed for the samples treated with 0.2% and 0.4% EEO. However, none of the groups obtained acceptable scores until the final day of storage except for the color attribute. In general, sensory evaluation and its correlation with microbial counting indicated that the treatment with 0.4% EEO was able to preserve the microbial quality of the minced fish at refrigeration temperature without any undesirable sensory effects.     

Quality of giant freshwater prawn (Macrobrachium rosenbergii) during the storage at −18°C as affected by different methods of freezing

This study investigated the effects of liquid nitrogen quick-freezing, ?35°C air-blast freezing, and ?18°C refrigerator direct-freezing on quality retention of frozen giant freshwater prawns using various indicators: microscopic structure, physicochemical, texture, and color properties. The results showed that the shelf lives of prawns treated with liquid nitrogen quick-freezing, ?35°C air-blast freezing, and ?18°C refrigerator direct-freezing were about 20, 12, and 8 weeks, respectively, in terms of total volatile basic nitrogen content and K-value. Meanwhile, liquid nitrogen quick-freezing could effectively improve texture property of frozen giant freshwater prawn. These findings confirm that liquid nitrogen quick-freezing is a promising method to extend the shelf life of frozen prawns.     

Metabolomes of the psychrotolerant bacterium Listeria monocytogenes 10403S grown at 37 °C and 8 °C

Listeria monocytogenes is a food-borne pathogen with the ability to grow at refrigeration temperatures. Knowledge of the mechanisms involved in low temperature growth is incomplete and here we report the results of a metabolomics investigation of this. The small molecule contents of L. monocytogenes 10403S grown at 37 °C and 8 °C were compared by gas chromatography/mass spectrometry (GC/MS). Over 500 peaks were detected in both 37 °C and 8 °C-grown cells, and 103 were identified. Of the identified metabolites, the concentrations of 56 metabolites were increased (P < 0.05), while the concentrations of 8 metabolites were decreased at low temperature. Metabolites increasing in concentration at 8 °C included amino acids, sugars, organic acids, urea cycle intermediates, polyamines, and different compatible solutes. A principal component analysis (PCA) was used to visualize and compare the matrix containing the data in 6 samples, and this clearly identified the 37 °C and 8 °C metabolomes as different. The results indicated that an increase in solute concentrations in the cytoplasm was associated with low temperature adaptation, which may be a response to chill stress with the effect of lowering the freezing point of intracellular water and decreasing ice crystal formation.     

Survival of Listeria monocytogenes introduced as a post-aging contaminant during storage of low-salt Cheddar cheese at 4, 10, and 21°C

Traditional aged Cheddar cheese does not support Listeria monocytogenes growth and, in fact, gradual inactivation of the organism occurs during storage due to intrinsic characteristics of Cheddar cheese, such as presence of starter cultures, salt content, and acidity. However, consuming high-salt (sodium) levels is a health concern and the dairy industry is responding by creating reduced-salt cheeses. The microbiological stability of low-salt cheese has not been well documented. This study examined the survival of L. monocytogenes in low-salt compared with regular-salt Cheddar cheese at 2 pH levels stored at 4, 10, and 21°C. Cheddar cheeses were formulated at 0.7% and 1.8% NaCl (wt/wt) with both low and high pH and aged for 10 wk, resulting in 4 treatments: 0.7% NaCl and pH 5.1 (low salt and low pH); 0.7% NaCl and pH 5.5 (low salt and high pH); 1.8% NaCl and pH 5.8 (standard salt and high pH); and 1.8% NaCl and pH 5.3 (standard salt and low pH). Each treatment was comminuted and inoculated with a 5-strain cocktail of L. monocytogenes at a target level of 3.5 log cfu/g, then divided and incubated at 4, 10, and 21°C. Survival or growth of L. monocytogenes was monitored for up to 90, 90, and 30 d, respectively. Listeria monocytogenes decreased by 0.14 to 1.48 log cfu/g in all treatments. At the end of incubation at a given temperature, no significant difference existed in L. monocytogenes survival between the low and standard salt treatments at either low or high pH. Listeria monocytogenes counts decreased gradually regardless of a continuous increase in pH (end pH of 5.3 to 6.9) of low-salt treatments at all study temperatures. This study demonstrated that post-aging inoculation of L. monocytogenes into low-salt (0.7%, wt/wt) Cheddar cheeses at an initial pH of 5.1 to 5.5 does not support growth at 4, 10, and 21°C up to 90, 90, and 30 d, respectively. As none of the treatments demonstrated more than a 1.5 log reduction in L. monocytogenes counts, the need for good sanitation practices to prevent post-manufacturing cross contamination remains.     

Survival of Salmonella serovars introduced as a post-aging contaminant during storage of low-salt Cheddar cheese at 4, 10, and 21 °C

The microbiological stability of low-salt cheese has not been well documented. This study examined the survival of Salmonella in low-salt compared to regular salt Cheddar cheese with 2 pH levels. Cheddar cheeses were formulated at 0.7% and 1.8% NaCl (wt/wt) with both low and high-pH and aged for 12 wk resulting in four treatments: 0.7% NaCl and pH 5.1 (low-salt and low-pH); 0.7% NaCl and pH 5.5 (low-salt and high-pH); 1.8% NaCl and pH 5.7 (standard-salt and high-pH); and 1.8% NaCl and pH 5.3 (standard-salt and low-pH). Each treatment was comminuted and inoculated with a 5-serovar cocktail of Salmonella at a target level of 4 log CFU/g, then divided and incubated at 4, 10 and 21 °C for up to 90, 90, and 30 d, respectively. Salmonella counts decreased by 2.8 to 3.9 log CFU/g in all treatments. In the initial period of survival study, standard-salt treatments exhibited significantly lower Salmonella counts compared to low-salt treatments. The pH levels did not exhibit obvious significant effect in the Salmonella survival in low-salt treatments. Salmonella counts declined gradually regardless of a continuous increase in pH (end pH of 5.3 to 5.9) of low-salt treatments at all study temperatures. Salmonella counts were reduced faster at 21 °C storage. Although there were significant reductions in Salmonella counts, the treatments demonstrated survival of Salmonella for up to 90 d when stored at 4 or 10 °C and for up to 30 d at 21 °C, the need for good sanitation practices to prevent postmanufacturing cross contamination remains. PRACTICAL APPLICATION: Low-salt aged Cheddar cheese could not support the growth of inoculated Salmonella and in fact gradual reduction in Salmonella count occurred during storage. Besides being nutritionally better, low or reduced salt Cheddar are safe as their full salt counterparts and that salt may only be a minor food safety hurdle regarding the post-aging contamination and growth of Salmonella. However, the treatments could not demonstrate complete destruction of Salmonella for up to 90 d when stored at 4 or 10 °C and for up to 30 d at 21 °C, the need for good sanitation practices to prevent postmanufacturing cross-contamination remains.     

Effect of low-dosage electron beam irradiation on antioxidant activities of navel oranges during storage at a low temperature of 3°C

Food Science and Biotechnology - Effects of low-dosage electron beam irradiation on antioxidant activities of Navel oranges during storage at a low temperature of 3°C were studied. Oranges...     

The fate of Escherichia coli O157 : H7 in Myzithra,Anthotyros, and Manouri whey cheeses during storage at 2 and 12°C

Myzithra, Anthotyros and Manouri whey cheeses were inoculated the day after production withEscherichia coli O157 : H7 at concentrations of approx. 1·8×10⁶cfu g⁻¹, and stored at 2 and 12°C for 30 and 20 days, respectively. The pH of the whey cheeses decreased from an initial value of approx. 6·20 to 5·83 or 5·60 (Myzithra) 5·75 or 5·20 (Anthotyros) and 5·80 or 5·30 (Manouri) by the end of the corresponding storage periods at 2 and 12°C, respectively. Escherichia coli O157 : H7 populations in the whey cheeses at the end of the 12°C storage period, had grown with an increase of approx. 1·3 log₁₀cfu g⁻¹. E. coli O157 : H7 populations in whey cheeses at the end of the 2°C storage period did not grow and decreased, with an approx. 2·5 log₁₀cfu g⁻¹reduction. Results showed that E. coli O157 : H7 can grow at 12°C and survive at 2°C storage in Myzithra, Anthotyros and Manouri whey cheeses, and therefore post-manufacturing contamination with this pathogen must be avoided by employing hygienic control programmes such as HACCP.     

Quality and shelf life evaluation of emulsion and restructured buffalo meat nuggets at cold storage (4±1°C)

The study was aimed at comparing the physico-chemical characteristics and texture profile of emulsion and restructured buffalo meat nuggets (BMN) and assessing their shelf life at refrigeration temperature (4±1°C). The stability of restructured batter was significantly lower than that of the emulsion form. Emulsion nuggets (EN) had significantly higher product yield, fat content and calories while restructured nuggets (RN) had significantly higher moisture and protein contents. Texture profile analysis revealed that RN had significantly higher cohesiveness, gumminess, chewiness and shear force values. Differences in TBARS values for emulsion and restructured nuggets were not significant at any particular storage time. Throughout storage, counts for mesophilic, psychrotrophic and coliforms did not exceed log(10)3.09 and 3.44cfu/g, log(10)2.23 and 2.11cfu/g, log(10)1.30 and 1.30cfu/g for emulsion and restructured buffalo meat nuggets, respectively. In spite of a higher overall acceptance for EN initially, panelists rated them considerably lower compared to RN during subsequent storage. Buffalo meat nuggets were acceptable for at least 20 days in cold storage (4±1°C) under aerobic conditions in polypropylene bags.     

Effect of chemical dips on unchilled fresh beef inoculated with E. coli, S. aureus, S. faecalis and Cl. perfringens and Stored at 30°C and 20°C

The antimicrobial effect of three chemical dips (A: potassium sorbate, 20g; sodium acetate, 5g; sodium chloride, 5g; water, 100 ml. B: potassium sorbate, 20g; sodium acetate, 5g; sodium chloride, 5g; propylene glycol, 20 ml; glycerol, 10 ml; water, 70 ml and 0·5N NaOH to pH 10. C: potassium sorbate, 10 g; sodium acetate, 10 g; sodium citrate, 10g; sodium chloride, 5g; water, 100 ml and 0·5N NaOH to pH 10) on unchilled f resh beef samples inoculated with E. coli, S. aureus, S. faecalis and Cl. perfringens and stored at 30°C and 20 °C was investigated. Treatments had produced a significant (P < 0·01) inhibitory effect on all the organisms inoculated, with a reduction of about 3 to 5 log units compared with the control. pH changes were comparable with the control at 5°C. No significant differences were found between the treatments and shelf life could be extended up to 44 h at 30°C and 68 h at 20°C whilst, in the control, visual spoilage and high bacterial counts were observed by 20h at 30°C and by 20 to 32h at 20°C. Treatment C, containing potassium sorbate at a low level (10%), was considered better than treatments A and B since potassium sorbate at higher levels had produced slight off-odours without a greater inhibitory effect.     

Field study on the microbiological quality of pickles in brine and survival of Salmonella Typhimurium and Listeria monocytogenes during storage at 4 °C

The aim of this study was to assess the microbiological quality and the ability of Listeria monocytogenes and Salmonella enterica serovar Typhimurium strains to survive during storage at 4 °C of all available brand names of brined pickles and some in-bulk ones, in the district of Athens. None of the samples could be characterized as heavily contaminated. The microbial populations detected could be due to inadequacy of packaging, regarding the ones available in-bulk and improper thermal treatment in the case of the canned ones. Moreover, the ability of both pathogens to survive for 5 days at 4 °C, in some products, has been exhibited.