Physiological and quality changes of fresh-cut pineapple treated with antibrowning agents

The physiological responses of pineapple slices to antibrowning agents have been studied. Slices were immersed for 2 min in solutions of isoascorbic acid (IAA) 0.1 mol/l, ascorbic acid (AA) 0.05 mol/l or acetyl cysteine (AC) 0.05 mol/l, packaged in polystyrene trays, prior to storage for up to 14 days at 10°C. The use of these antibrowning agents reduced browning and decay of pineapple slices significantly. These treatments also reduced changes in L^* and b^* values as well as firmness loss. Changes of in-package atmosphere did not adversely affect quality of slices. Slices treated with 0.1 mol/l IAA had the best visual appearance and were more acceptable compared with the control slices. The best results were obtained using IAA, followed by AC and AA. Organoleptic attributes were not affected and no off-flavors were detected in the treated slices. We conclude that pineapple slices can be maintained in good condition for up 14 days at 10°C following treatment with antibrowning agents.     

The inhibitory potential of feed supplementation with rosemary and/or α-tocopheryl acetate on microbial growth and lipid oxidation of turkey breast during refrigerated storage

Twenty-four 12-week-old female turkeys divided into four equal groups were fed a basal diet (CONT) or basal diet supplemented with 300 mg α-tocopheryl acetate/kg (TOC), or 5 g rosemary/kg (ROS5), or 10 g rosemary/kg (ROS10), for 4 weeks. Following slaughter, fillets from breast were stored at 4 °C in the dark for 12 days, and lipid oxidation was assessed on the basis of the malondialdehyde formed, whereas microbial growth on the basis of total viable counts (TVC), lactic acid bacteria (LAB), Enterobacteriaceae (ENB) and psychrotrophic (PSY) bacteria. Results showed that incorporation of dried rosemary in turkey diets delayed lipid oxidation in raw breast meat during refrigerated storage. Dietary rosemary at the level of 1 g/100 g was significantly (P<0.05) more effective in delaying lipid oxidation compared to 0.5 g/100 g but inferior to the dietary supplementation of 300 mg α-tocopheryl acetate/kg. TVC, LAB, ENB and PSY bacterial counts were all significantly increased (P<0.05) in breast samples of all groups throughout the refrigerated storage. The TOC and CONT groups presented TVC, LAB, ENB and PSY counts that did not differ (P>0.05) among each other, during the whole storage period. However, the rosemary-supplemented groups presented bacterial counts that were significantly lower (P<0.05) than the CONT and TOC groups, at day 2 of storage period and thereafter. During this period, the ROS5 group presented TVC, LAB, ENB and PSY counts that were significantly higher (P<0.05) than the ROS10 group.     

Antioxidant action of ganghwayakssuk (Artemisia princeps Pamp.) in combination with ascorbic acid to increase the shelf life in raw and deep fried chicken nuggets

Raw and deep fried chicken nuggets containing various levels of ganghwayakssuk ethanolic extract (GE) in combination with ascorbic acid (Aa) were evaluated for shelf-life during refrigerated storage (4 °C). The pH and color (lightness, redness, and yellowness) values of raw and deep fried samples were significantly affected by the addition of GE (P < 0.05). All antioxidant combinations except for Aa + GE 0.01 were effective at delaying lipid oxidation (CD, POV, and TBARS) when compared to the control or Aa. Raw samples with GE 0.2 and Aa + GE 0.1 exhibited lower bacterial populations during storage. The sensory characteristics (color, juiciness, flavor, tenderness, and overall acceptability) did not differ significantly in all deep fried chicken nugget samples, except color, whereas storage time had a significant effect (P < 0.05). The results suggest the possibility of utilizing raw and deep fried chicken nuggets with a mixture of ganghwayakssuk and ascorbic acid for the increase of shelf-life and quality.     

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.     

Effect of high-pressure processing on reduction of Listeria monocytogenes in packaged Queso Fresco

The effect of high-hydrostatic-pressure processing (HPP) on the survival of a 5-strain rifampicin-resistant cocktail of Listeria monocytogenes in Queso Fresco (QF) was evaluated as a postpackaging intervention. Queso Fresco was made using pasteurized, homogenized milk, and was starter-free and not pressed. In phase 1, QF slices (12.7 × 7.6 × 1 cm), weighing from 52 to 66 g, were surface inoculated with L. monocytogenes (ca. 5.0 log₁₀ cfu/g) and individually double vacuum packaged. The slices were then warmed to either 20 or 40°C and HPP treated at 200, 400, and 600 MPa for hold times of 5, 10, 15, or 20 min. Treatment at 600 MPa was most effective in reducing L. monocytogenes to below the detection level of 0.91 log₁₀ cfu/g at all hold times and temperatures. High-hydrostatic-pressure processing at 40°C, 400 MPa, and hold time ≥15 min was effective but resulted in wheying-off and textural changes. In phase 2, L. monocytogenes was inoculated either on the slices (ca. 5.0 log₁₀ cfu/g; ON) or in the curds (ca. 7.0 log₁₀ cfu/g; IN) before the cheese block was formed and sliced. The slices were treated at 20°C and 600 MPa at hold times of 3, 10, and 20 min, and then stored at 4 and 10°C for 60 d. For both treatments, L. monocytogenes became less resistant to pressure as hold time increased, with greater percentages of injured cells at 3 and 10 min than at 20 min, at which the lethality of the process increased. For the IN treatment, with hold times of 3 and 10 min, growth of L. monocytogenes increased the first week of storage, but was delayed for 1 wk, with a hold time of 20 min. Longer lag times in growth of L. monocytogenes during storage at 4°C were observed for the ON treatment at hold times of 10 and 20 min, indicating that the IN treatment may have provided a more protective environment with less injury to the cells than the ON treatment. Similarly, HPP treatment for 10 min followed by storage at 4°C was the best method for suppressing the growth of the endogenous microflora with bacterial counts remaining below the level of detection for 2 out of the 3 QF samples for up to 84 d. Lag times in growth were not observed during storage of QF at 10°C. Although HPP reduced L. monocytogenes immediately after processing, a second preservation technique is necessary to control growth of L. monocytogenes during cold storage. However, the results also showed that HPP would be effective for slowing the growth of microorganisms that can shorten the shelf life of QF.     

A comparison between E-beam irradiation and high pressure treatment for cold-smoked salmon sanitation: microbiological aspects

The effectiveness of electron beam irradiation and high pressure treatment for the sanitation of cold-smoked salmon from two points of view, microbial safety and shelf-life extension, was compared. From the response of L. monocytogenes INIA H66a to irradiation, a D value of 0.51 kGy was calculated. For samples stored at 5 °C, 1.5 kGy would be sufficient to attain a Food Safety Objective (FSO) of 2 log₁₀cfu/g L. monocytogenes for a 35-day shelf-life, whereas 3 kGy would be needed in the case of a temperature abuse (5 °C + 8 °C). Pressurization at 450 MPa for 5 min was considered to be an insufficient treatment, since the FSO of 2 log₁₀cfu/g L. monocytogenes was only attained for a shelf-life of 21 days at 5 °C. However, treatment at 450 MPa for 10 min achieved this FSO for samples held during 35 days at 5 °C, or during 21 days under temperature abuse (5 °C + 8 °C) conditions. Irradiation at 2 kGy kept the microbial population of smoked salmon below 6 log₁₀cfu/g after 35 days at 5 °C, with negligible or very light changes in its odor. Pressurization at 450 MPa for 5 min also kept the microbial population below 6 log₁₀cfu/g after 35 days at 5 °C and did not alter odor, but affected negatively the visual aspect of smoked salmon.     

Efficacy of washing with hydrogen peroxide followed by aerosolized antimicrobials as a novel sanitizing process to inactivate Escherichia coli O157:H7 on baby spinach

Aerosolization was investigated as a potential way to apply allyl isothiocyanate (AIT), hydrogen peroxide (H₂O₂), acetic acid (AA) and lactic acid (LA) on fresh baby spinach to control Escherichia coli O157:H7 during refrigeration storage. In this study, baby spinach leaves were dip-inoculated with E. coli O157:H7 to a level of 6 log CFU/g and stored at 4 °C for 24 h before treatment. Antimicrobials were atomized into fog-like micro-particles by an ultrasonic nebulizer and routed into a jar and a scale-up model system where samples were treated. Samples were stored at 4 °C for up to 10 days before the survival of the cells was determined. A 2-min treatment with 5% AIT resulted in a > 5-log reduction of E. coli O157:H7 on spinach after 2 days refrigeration regardless if the samples were pre-washed or not; however, this treatment impaired the sensory quality of leaves. Addition of LA to AIT improved the antimicrobial efficacy of AIT. In the jar system, washing with 3% H₂O₂ followed by a 2-min treatment of 2.5% LA + 1% AIT or 2.5% LA + 2% AIT reduced E. coli O157:H7 population by 4.7 and > 5 log CFU/g, respectively, after 10 days refrigeration. In the scale-up system, up to 4-log reduction of bacterial population was achieved for the same treatments without causing noticeable adverse effect on the appearance of leaves. Thus, this study demonstrates the potential of aerosolized AIT + LA as a new post-washing intervention strategy to control E. coli O157:H7 on baby spinach during refrigeration storage.     

Effects of some commercial additives on the quality of sucuk (Turkish dry-fermented sausage)

The effects of some commercial additives on the quality of sucuk (Turkish dry-fermented sausage) were investigated during the ripening and storage periods. Microbial, chemical and sensory changes were followed for 15 days of ripening and 36 days of storage. Aerobic plate count (APC) increased (P < 0.05) from 5.19 to 6.09 log CFU/g during the first 10 days of ripening and afterwards decreased (P < 0.05) to 3.69 log CFU/g. APC and lactic acid bacteria (LAB) changed significantly (P < 0.05) with time and additives. LAB increased (P < 0.05) from 4.62 log CFU/g to about 5.47 log CFU/g during the first 10 days of the ripening period and decreased to 1.79 log CFU/g at the end of storage. Control sucuk without additives had the highest level of mould and yeast counts (5.09 log CFU/g). TBARS values increased gradually (P < 0.05) from 0.61 to 1.73 mg/kg and tyramine concentrations varied from 56.8 to 419 mg/kg. Control sucuk was found to have the lowest overall sensory quality (P < 0.05), and nitrate/nitrite concentration increased (P < 0.05) the overall sensory quality of the sausages. Pearson’s correlation test indicated that there was a link (P < 0.01) between the overall sensory quality and pH, TBARS values, mould and yeast counts, and putrescine concentration.     

Ascorbic acid degradation kinetics of sonicated orange juice during storage and comparison with thermally pasteurised juice

Ascorbic acid degradation kinetics of sonicated orange juice during storage were determined and compared to thermally pasteurised samples. Acoustic energy densities (AED) ranging from 0.30 to 0.81 W/mL and treatment times of 2-10 min were investigated. The degradation kinetics of sonicated samples followed first-order kinetics (R² ≥ 0.91) during processing. During storage ascorbic acid degradation of sonicated samples followed the Weibull model (R² ≥ 0.97) with β values ranging from 0.662 to 0.697. Comparatively, first-order degradation kinetics were observed during storage for thermally pasteurised (R² = 0.98) and control samples (R² = 0.96). Increased shelf life based on ascorbic acid retention was found for sonicated samples compared to thermally pasteurised samples. Predicted shelf life for sonicated orange juice ranged from 27 to 33 days compared to 19 days for thermally pasteurised juice during storage at 10 °C. These results indicate that sonication results in enhanced retention of ascorbic acid in orange juice during storage compared to thermal processing.     

Isolation of hesperidin from peels of thinned Citrus unshiu fruits by microwave-assisted extraction

Simultaneous extraction by microwave-irradiation and crystallisation were performed in the same pot of solvent of 70% (v/v) aqueous ethanol for isolation of hesperidin from thinned immature fruit peels of Citrus unshiu as refining of Citrus waste biomass. The hesperidin content in immature fruits peels was about 3.2-fold higher than that of mature fruit. After microwave-assisted extraction (MAE), the yield of hesperidin reached 58.6 mg/g, which was comparable to the amount obtained after extraction using DMSO:methanol (1:1, v/v) as a solvent for 30 min at room temperature. Heating temperature and time for isolation of hesperidin crystallites were optimised as 140 °C and 8 min by using response surface methodology. Under this optimal condition, 86.8% (47.7 mg/g) of total hesperidin was isolable by MAE and low-temperature storage (5 °C, 24 h).     

Effect of high pressure processing on the quality of squid (Todarodes pacificus) during refrigerated storage

The influence of high pressure processing (HPP) on the inhibition of trimethylamine-N-oxide demethylase (TMAOase) activity and off-odour production in squid treated at 300 MPa for 20 min was investigated during 12 days of refrigerated storage. TMAOase activity of raw squid (21.5 nkat/g) was significantly decreased to approximately 5 nkat/g after 20 min of HPP. The production of dimethylamine (DMA) in HPP-treated squid for 20 min was significantly decreased to 0.31 μmol/g after 12 days of storage. The decrease in DMA was correlated with the decrease in TMAOase activity. At 300 MPa, the number of total aerobic bacteria in squid was reduced by 1.26 log units after 20 min of HPP. The HPP-treated samples effectively reduced the amount of trimethylamine (TMA). Therefore, the HPP could be used as a promising alternative technology to retard the quality deterioration of squid by inhibiting TMAOase activity and microbial growth.     

Characterization of E- and Z-ajoene obtained from different varieties of garlics

Synthesised E- and Z-ajoene were used to determine their amounts in food oils containing various fresh garlics. The best yield of E-ajoene (172.0 μg/g of garlic) and Z-ajoene (476.0 μg/g of garlic) was obtained from freshly prepared Japanese garlic with rice oil which was heated at 80 °C. Determination of E- and Z-ajoene from soybean oil containing 15% Japanese garlic samples prepared at 80 °C for 0.5 h gave the amount of E-ajoene (170.0 μg/g of garlic) and Z-ajoene (127.0 μg/g of garlic). After 9-month storage, 54.0% E- and 11.0% Z-ajoene remained in Japanese garlic with rice oil. Ajoene (0.1 mM) in ethyl acetate was incubated under UV-light (253.7 nm) for 3 days, 81.7% E- and 56.9% Z-ajoene remained. 4.3% and 0.5% E- and Z-ajoene remained when ajoene (0.1 mM in ethyl acetate) was incubated at 100 °C.     

Combined Vacuum Impregnation and Electron‐Beam Irradiation Treatment to Extend the Storage Life of Sliced White Button Mushrooms (Agaricus bisporus)

This study assessed the application of an antibrowning solution using vacuum impregnation (VI) and then electron‐beam irradiation as a means to extend the shelf life of sliced white button mushrooms (Agaricus bisporus). A preliminary study helped to determine the best antibrowning solution and VI process parameters. Mushroom slices were impregnated with 2 g/100 g ascorbic acid + 1 g/100 g calcium lactate; 2 g/100 g citric acid + 1 g/100 g calcium lactate; 1 g/100 g chitosan + 1 g/100 g calcium lactate; and 1 g/100 g calcium lactate at different vacuum pressures and times and atmospheric restoration times. Selection of the antibrowning solution and VI parameters was based on texture and color of the mushroom slices. Next, the slices were irradiated at 1 kGy using a 1.35‐MeV e‐beam accelerator. Physicochemical, sensory, and microbial quality of mushrooms was monitored for 15 d at 4 °C. The best impregnation process in this study was 2 g/100 g ascorbic acid and 1 g/100 g calcium lactate at 50 mm Hg for 5 min and an atmospheric restoration time of 5 min. The control (untreated) samples suffered structural losses throughout storage. Only the vacuum impregnated‐irradiated samples had acceptable color by the end of storage. Sensory panelists consistently preferred the samples produced with VI and irradiation because exposure to ionizing radiation inhibited growth of spoilage microorganisms.     

Antioxidant activity of Spirulina platensis extracts by supercritical carbon dioxide extraction

Supercritical CO₂ extraction of antioxidants from Spirulina platensis was optimized using response surface methodology. About 10.26 g/kg of extracts from S. platensis could be obtained under the optimum conditions of 48 °C at 20 MPa over a 4 h period. The antioxidant activity of the extracts prepared under the optimized condition, determined by linoleic acid peroxidation inhibition method, was lower compared with BHT and Trolox, but significantly higher than α-tocopherol in 300 min and became similar to α-tocopherol after that. The components of the extracts were further analyzed, and the results showed that the extracts contained 85.1 g/kg of flavonoids, 77.8 g/kg of β-carotene, 113.2 g/kg of vitamin A and 3.4 g/kg of α-tocopherol, which may contribute greatly to their high antioxidant activity. The main fatty acids in the extracts were palmitic acid (35.32%), linolenic acid (21.66%) and linoleic acid (20.58%).     

Stability of lipids and fatty acids in frozen and gamma irradiated Patagonian toothfish (Dissostichus eleginoides) from the Southwestern Atlantic

Patagonian toothfish were captured in the Southwestern Atlantic Ocean (FAO Zone N° 41). The fatty acid profile of total lipids and the triacylglycerol and phospholipid content of control and irradiated samples (1 and 5 kGy) stored at −18 °C were analyzed at 0 and 293 days post irradiation. The fatty acids are mainly monounsaturated acids (47 g/100 g total fatty acids), the most abundant one being oleic acid (18:1 n-9). This is followed in order of abundance by saturated fatty acids (26 g/100 g total fatty acids), consisting mainly of palmitic acid (16:0). Polyunsaturated fatty acids were less abundant (17 g/100 g total fatty acids) and consisted mainly of eicosapentaeonic (20:5 n-3) and docosahexaenoic (22:6 n-3) acids. Triacylglycerol content was 563.07 mg/mL oil, whereas phospholipids were 11.21 mg/mL oil. Gamma irradiation did not significantly affect the fatty acid profile or triacylglycerol and phospholipid content of P. toothfish stored for 293 days at −18 °C. The results suggest that the species exhibits a marked stability when subjected to irradiation and prolonged storage in the frozen state.     

Influence of casein-based microencapsulation on freeze-drying and storage of probiotic cells

The influence of microencapsulation in casein-based microcapsules produced by enzymatic gelation with transglutaminase on the viability of two probiotic strains, which differ in their sensitivity against dehydration, Lactobacillus F19 and Bifidobacterium Bb12 during freeze-drying and subsequent storage was investigated. Water activities after drying did not differ between free and encapsulated samples in all cases. However, Lactobacillus F19 survived in significantly higher numbers in the encapsulated state, compared to free cells (protein-cell-mixture). Storage conditions were varied in terms of relative humidity (11%/33%) and temperature (4 °C/25 °C). Encapsulation improved the survival of Bifidobacterium Bb12 during storage for up to 90 days under all tested conditions. Further co-encapsulation of prebiotic resistant starch corns negatively influenced the physical barrier of the protein matrix, hence leading to a reduction of the protective effect. In the case of Lactobacillus F19 no encapsulation-related protective effect was found during storage.     

Osmotic dehydration of Aloe vera (Aloe barbadensis Miller)

Aloe vera possess immunomodulatory, anti-inflammatory, antibacteria effects and wound and burn healing properties, but it is a very unstable product due to its high water content. Osmotic dehydration can be used to obtain stable products from aloe. In this work the effect of osmotic dehydration (OD) on Aloe vera (Aloe barbadensis Miller) leaves was studied. Peeled and unpeeled Aloe vera slices (15 × 50 mm), were immersed in sucrose solutions at 35, 50 and 65 °Brix at 25 and 40 °C. Moisture, effective diffusion coefficients and mass fluxes (water loss, solids gained and weight reduction) were determined. Osmotic dehydration experiments were conducted at atmospheric pressure. The best conditions for the OD of Aloe slices with the highest effect on diffusivity were obtained using a temperature of 40 °C for peeled samples. The analysis of the effect of temperature on mass transfer kinetics showed that unpeeled samples were more effected than peeled samples.     

Antinutritional factors changes occurring in trifoliate yam (Dioscorea dumetorum) tubers after harvest

Studies were conducted on the changes in antinutritional factors occurring during the storage of Dioscorea dumetorum (cv. Yellow) yam tubers. The tubers were harvested and stored under prevailing tropical ambient conditions (19–28 °C, 60–85% RH) for 0, 2, 5, 7, 14, 21, 28, 42 and 56 days. The samples were evaluated for total phenols, tannins, phytic acid, α-amylase inhibitors, trypsin inhibitors and oxalates. Results showed that, during storage, total phenols and tannin contents decreased by approximately 22–28% after 56 days of harvest, due to the hardening phenomenon and sprouting. Phytate and α-amylase inhibitor levels declined, respectively, from 690–416 mg/100 g and 1013–659 AIU/g, while oxalates and trypsin inhibitor contents increased during the first week of storage (days 0–7) and, after this period, they started to decrease progressively. Since sprouting of most tubers was observed after 28 days of storage, the results suggest that post-harvest hardening and sprouting influence antinutritional composition of D. dumetorum tubers.     

Microbial, physical and sensory properties of yogurt supplemented with lentil flour

In this study, skim milk (9.5% w/v solid content) was supplemented with 1-3% (w/v) lentil flour or skim milk powder, inoculated with a yogurt culture, fermented and stored at 4 °C. Acid production during the fermentation, microbial growth, physical properties (pH, syneresis, and color), rheological properties (dynamic oscillation temperature sweep test at 4-50 °C), during 28 days of refrigerated storage and also sensory properties (flavor, mouth feel, overall acceptance and color) after production, were studied. Milk supplementation with 1-3% lentil flour enhanced acid production during fermentation, but the microbial population (CFU) of both S. thermophilus and L. delbrueckii subsp. bulgaricus were in the same range in all lentil flour and skim milk powder supplemented yogurts. The average pH of samples decreased from 4.5 to 4.1 after 28 days storage. Syneresis in 1-2% lentil flour supplemented yogurts was significantly higher than all other samples; however, greater lentil supplementation (3%) resulted in the lowest syneresis during the 28 days storage. With respect to color, “a” and “L” values did not significantly differ in all samples and remained constant after 28 days whereas “b” value increased as a result of lentil supplementation. Yogurt with 3% lentil flour showed higher storage (G') and loss (G?) moduli in comparison with samples supplemented with 1-3% skim milk powder and the non-supplemented control yogurt. Storage modulus (G') was higher than loss modulus (G?) in all samples and at all temperatures between 4 and 50 °C and they showed a hysteresis loop over this temperature range when the samples were heated and cooled. 1-2% lentil flour supplemented yogurt showed comparable sensory properties in comparison with 1-2% skim milk powder supplemented yogurt and the control sample.     

Combined antimicrobial effect of oregano essential oil and caprylic acid in minced beef

Oregano essential oil (OEO) and caprylic acid (CA) are highly aromatic natural antimicrobials with limited individual application in food. We proved their combined additive effect when used in meat. Application of 0.5% CA and 0.2% OEO (v/w) with 0.1% of citric acid in vacuum packed minced beef inoculated with Listeria monocytogenes at a concentration of 5 log cells/g reduced counts of lactic acid bacteria by 1.5 log CFU/g and counts of psychrotrophic bacteria and L. monocytogenes by more than 2.5 log CFU/g at the end of storage at 3 °C for 10 days. In sensory evaluation the samples with OEO showed during the whole experiment statistically better scores than control, whereas the samples treated with CA showed worse colour attributes.