Microbiological, physicochemical and organoleptic changes in dry-salted olives of Thassos variety stored under different modified atmospheres at 4 and 20 °C

Microbiological, physico-chemical and organoleptic changes were studied in dry-salted olives, cv. Thassos, stored under different atmospheres (100% carbon dioxide and nitrogen, 40% CO₂/30%O₂/30%N₂ and air) at 4 and 20 °C for 180 days. The initial microbial flora comprised of yeasts, no lactic acid bacteria, enterobacteria, pseudomonads or Staphylococcus aureus were detected, as the low water activity/high salt content does not favour their growth. At 4 °C, the population of yeasts declined steadily throughout storage but to a different extent depending on the gaseous atmospheres. At 20 °C, there was an initial decline in yeast counts in all samples followed by a steady increase until the end of the storage period. The CO₂ atmosphere was most effective at keeping the number of yeasts low at both storage temperatures. All gas atmospheres prevented fungal growth at both temperatures apart from the samples stored in air. The pH, a_w and salt content of the olives did not change significantly throughout the storage period. The prevailing yeast species was the salt tolerant Candida famata . The organoleptic characteristics did not differ significantly among differently treated olives. However, increased rancidity and reduced fruit colour was observed in the samples stored at 20 °C.     

Shelf Life and Microbial Quality of Fresh-cut Mango Cubes Stored in High CO2 Atmospheres

ABSTRACT: Fresh-cut'Carabao'and'Nam Dokmai'mango cubes were stored in air or in high CO₂ atmospheres (3%, 5%, and 10%) at 5 °C and 13 °C. Freshly sliced'Carabao'mango cubes had a lower respiration rate and total bacterial count and higher L-ascorbic acid content and firmness than'Nam Dokmai'mango cubes. The shelf life of fresh-cut mango, based on browning discoloration and water-soaked appearance, was 6 d at 5 °C and 4 d at 13 °C for'Carabao'and 2 d at 5 °C and less than 1 d at 13 °C for'Nam Dokmai'. High CO₂ atmospheres retarded the development of water-soaked'Carabao'cubes at 5 °C and 13 °C and'Nam Dokmai'cubes at 5 °C. Texture of'Carabao'cubes was enhanced by high CO₂, but ethanol and L-ascorbic acid contents were not affected at 5 °C and 13 °C. Total bacterial count was lower in'Carabao'cubes than in'Nam Dokmai'cubes during storage at both temperatures, and a 10% CO₂ only reduced the bacterial count on'Carabao'and'Nam Dokmai'cubes stored at 13 °C. Bacterial flora in'Nam Dokmai'mango cubes consisted mostly of Gram-negative rods assigned primarily to phytopathogenic bacteria such as Pantoea agglomerans and Burkholderia cepacia . The genera of bacteria isolated from cubes stored in 10% CO₂ were similar to those from cubes on the initial day.     

The Effects of Residual Oxygen on the Storage Life of Retail-Ready Fresh Beef Steaks Masterpackaged Under a CO2 Atmosphere

ABSTRACT:  Retail-packed rump ( Gluteus medius , GM) and striploins ( Longissiumus dorsi, LD) steaks were masterpackaged under carbon dioxide (CO₂) and stored at 1 °C ± 1 °C for 14, 28, 35, and 42 d. A commercial oxygen (O₂) scavenger (ATCO HV1000®, Standa Industrie, Caen, France) was used in the masterpacks to achieve an O₂-free atmosphere. Similar packages without the O₂ scavengers were also prepared. At each storage time, 2 masterpacks of each treatment were opened and the retail trays were placed in a display case at 4 °C ± 2 °C for 1 and 48 h for microbiological and sensorial evaluations. The low growth rate of aerobic psychrotrophic flora on the stored beefsteaks demonstrated the bacteriostatic effect of CO₂ during storage. The maximum level of psychrotrophic aerobic bacteria reached during storage was approximately 10⁶ CFU/g. The steaks stored in masterpacks with scavengers bloomed to the desirable red color associated with freshly cut meat in the display case for all of the storage periods, except in the case of GM steaks, which showed a cycle of transient discoloration. GM and LD steaks were well accepted (65% and 82%, respectively) after 42 d under CO₂ at 1 °C ± 1 °C. The GM and LD steaks stored without the O₂ scavenger showed variable fractions of discoloration that significantly detracted from the appearance of the samples.     

Mathematical modelling of O2 consumption and CO2 production rates of whole mushrooms accounting for the effect of temperature and gas composition

Investigation of respiration rate of fresh produce, under different gas composition and temperatures, and respective mathematical modelling is central for the modified atmosphere packaging design. This work investigates the effect of temperature (4, 8, 12, 16, 20 °C) and gas composition (O₂ between 3 to 21% and CO₂ between 0 to 15%) on respiration rate of whole mushrooms. Oxygen and carbon dioxide respiration rates increased significantly (3–4 fold) as the temperature elevated from 4 to 20 °C and were in the range of 13.23 ± 3.12 to 102.41 ± 2.132 mL kg⁻¹ h⁻¹) and 14.33 ± 1.56 to 97.02 ± 2.51 mL kg⁻¹ h⁻¹) respectively. Low O₂ and high CO₂ levels reduced O₂ consumption and CO₂ production rates of whole mushrooms on average by a circa 47–60% at all temperatures as compared to the respiration rate at ambient air. Mathematical models were developed for RO₂ and RCO₂, by combining the Arrhenius and Michaelis–Menten uncompetitive equations. These models predicted well, O₂ consumption and CO₂ production rates of whole mushrooms as a function of both temperature and gas composition.     

Microbiological, physicochemical and organoleptic changes of shredded carrots stored under modified storage

The effect of initial head spaces of air, 4.9% CO₂/2.1% O₂/93% N₂ and 5% CO₂/95% N₂ on the microbial flora of shredded carrots was studied at 4 and 10°C. The microbial flora of shredded carrots comprised lactic acid bacteria, pseudomonads and yeasts. Lactic acid bacteria were the predominant organisms in all samples. The pH dropped during the storage of carrots and this was more pronounced at 10°C. The concentration of different organic acids such as lactic, acetic, tartaric, citric and succinic increased in all samples stored under modified atmosphere packaging conditions at both temperatures. The spoilage of carrots stored under 5% CO₂/95% N₂ was delayed, as indicated by the changes in their texture, colour and odour, compared with those samples stored under air or 4.9% CO₂/2.1% O₂/93% N₂.     

Effect of controlled atmospheres on maintaining quality of persimmon fruit cv. "Rojo Brillante"

ABSTRACT:  Astringent "Rojo Brillante" persimmon fruits were stored in air or in 2 different controlled atmospheres: 10% CO₂+ 90% N₂ (CA1) or 97 % N₂+ air (CA2) for up 50 d at 15 °C. After different periods, the fruit were treated with 95% CO₂ for 24 h at 20 °C in order to remove astringency, and then transferred to 20 °C in air free of CO₂ for 5 d to simulate shelf life. Other fruits were directly transferred to shelf life without being submitted to deastringency treatment. Storage under CA2 allowed storability of persimmon "Rojo Brillante" during 30 d at 15 °C, maintaining commercial firmness. Moreover, CA2 had an effect on removing astringency when fruits were stored for 30 d at 15 °C, or after 20 d following to shelf life. As consequence, deastringency treatment could be avoided when the fruits were previously stored under this controlled atmosphere.     

EFFECTS OF LOW CONCENTRATIONS OF H2O2 ON LIPID OXIDATION AND OF STORAGE AND pH ON NONHEME IRON CONTENT OF RAW BEEF MUSCLE

Ground beef samples were prepared from semimembranosus muscles, and beef muscle residue devoid of heme pigments was prepared by repeated washing of the ground muscle with distilled-deionized water. When ground muscle, or muscle residue samples treated with metmyoglobin-H₂O₂ (4 mg metmyoglobin/g muscle residue; 1:0.1 to 1:1 for molar ratio of metmyoglobin to H₂O²) were stored at 4°C for 0 or 6 days, no changes in nonheme iron content were observed. Similarly, nonheme iron content of stored samples was not affected by pH (5.5, 6.0 or 6.5). While metmyoglobin-H₂O² added to water-extracted beef muscle residue catalyzed the oxidation of the indigenous lipids, treatment of the residue with H₂O² alone had no effect on the oxidation.     

Fate of Aflatoxin M1 during Manufacture and Storage of Feta Cheese

ABSTRACT:  The effect of feta cheese manufacture on aflatoxin M₁ (AFM₁) content was studied using an enzyme immunoassay technique. Feta cheese was made from milk spiked with 1 and 2 μg AFM₁ per kilogram milk. Pasteurization at 63 °C for 30 min caused <10% destruction of AFM₁. During cheese making, the remaining AFM₁ in milk was partitioned between curd and whey with two-thirds retained in the curd and one-third going into the whey. Cheeses were then stored for 2 mo in 8%, 10%, and 12% brine solutions at 6 and 18 °C. There was a 22% to 27% reduction of AFM₁ during the first 10 d of storage, with slightly more loss as salt concentration increased and when the cheese was stored at 18 °C. Further storage caused only slight decrease in AFM₁ and after 30 d of brining there was no difference in AFM₁ content of the cheese based upon salt concentration of the brine. At 18 °C, no further losses of AFM₁ occurred after 30 d, and at 6 °C, there was continued slight decrease in AFM₁ levels until 50 d. After 60 d of brining, there was a total loss of 25% and 29% of the AFM₁ originally present for cheese brined at 6 and 18 °C, respectively. Thus, the combination of pasteurization, conversion of milk into feta cheese, and at least 50 d storage of cheese in brine caused a total loss of about 50% of the AFM₁ originally present in the raw milk.     

Portable Electronic Nose for Detection of Spoiling Alaska Pink Salmon (Oncorhynchus gorbuscha)

ABSTRACT:  The ability of a portable hand-held electronic nose (EN) in detecting spoilage of whole Alaska pink salmon ( Oncorhynchus gorbuscha ) stored at 14 °C and in slush ice (1 °C) was investigated. Fish were sampled daily at 14 °C for up to 3 d, while fish stored in slush ice were sampled at various intervals up to 16 d. Sensory evaluations indicated that fish were rejected at day 3 when stored at 14 °C and at day 12 when stored in slush ice. Aerobic bacteria counts for fish skin at 14 °C ranged from 3.4 log₁₀ colony-forming units (CFU)/cm² (day 0) to 4.8 log₁₀ CFU/cm² (day 3) and for fish stored in slush ice ranged from 3.4 log₁₀ CFU/cm² (day 0) to 5.5 log₁₀ CFU/cm² (day 16). The correct classification rate using forward stepwise general discriminate analysis was 85% and 92% for EN analysis of belly cavity volatiles for fish held at 14 °C and in slush ice, respectively. A predictive model may be developed for spoilage of whole Alaska pink salmon by analyzing belly cavity odors using the EN.     

Influence of oxygen concentration and temperature on respiratory characteristics of fresh-cut green onion

The characteristics of the respiration rates in precut green onion, as influenced by oxygen levels and temperature, were examined to provide design factors for modified atmosphere packaging (MAP). Fresh-cut green onions ( Allium fistulosum L.) were prepared and sealed, with and without a CO₂ absorbent, in gas-tight glass containers that had initially been purged with air or a gas mixture (O₂ 9%/N₂ balance). The containers were stored at different temperatures (0, 10, 20 °C). At 10 °C, the maximum O₂ uptake rate (V_m) and the O₂ concentration at half-maximum (K_m) uptake rate were 30.95 mL kg⁻¹ h⁻¹ and 1.63%, respectively. Regardless of temperature, the lower O₂ limit was estimated to be about 1.0% O₂ on the basis of respiratory quotient (RQ) increase. Respiration of cut green onion was dependent on O₂ concentration as well as temperature, as shown by applying the Michaelis–Menten type model and the Arrhenius equation. However, the presence of CO₂ had little effect on O₂ uptake of cut green onion at relatively high O₂ concentrations (≤20%).     

Chemical and sensory changes in haddock and herring stored under modified atmosphere

The effectiveness of storage in atmospheres with increased proportions of CO₂ to extend the shelf-life of haddock and herring was examined. Using a 40: 30: 30/CO₂: O₂: N₂ atmosphere with haddock no useful extension of shelf-life was achieved at +5°C and only limited extension at 0°C. A more useful extension of shelf-life at 0°C was obtained by storing haddock in a 60: 20: 2O/CO₂: O₂: N₂ atmosphere and with herring in a 60:40/CO₂::N₂: atmosphere. Total volatile bases (TVB) and hypoxanthine values (Hx) correlated with the cooked flavour. There were no significant differences in drip-loss between the modified atmosphere packaging (MAP) stored samples and the controls. Peroxide values (PV) in herring were lower in MAP stored samples. Whole haddock and whole herring were found to have a longer shelf-life when stored in MAP at 0°C than when stored as fillets.     

Development of Biogenic Amines in Yellowfin Tuna (Thunnus albacares): Effect of Storage and Correlation with Decarboxylase-Positive Bacterial Flora

ABSTRACT: The effects of storage at 0,4,10, and 22°C for 0,1,3,5, and 9 d on the quality of yellowfin tuna fillets as determined by microbiological assessment, development of some biogenic amines, and sensory analysis were studied. Tuna fillets stored at 22 °C for 3 d, 10 °C for 5 d, and 4 °C for 9 d were rated unacceptable for consumption. Those stored at 22 °C for 3 d had total aerobic bacterial count of > 8 log₁₀ CFU/g, a histamine-producing bacterial population of 7 log₁₀ CFU/g, and 832 ppm of histamine, 35.8 ppm of putrescine, and 147 ppm of cadaverine. A comparison of the capillary electrophoresis, AOAC fluorometric method, and gas chromatography showed a very good correlation (r² > 0.99) among these 3 methods for histamine quantitation in tuna samples. Morganella morganii, Enterobacter agglomerans, Enterobacter intermedium, Pseudomonas fluorescens, Proteins vulgaris , and Serratia liquefaciens were the decarboxylase-positive bacterial species isolated by using the Niven's medium and identified during storage, which were responsible for histamine production in test tuna fillets.     

Effects of gas atmosphere, antimicrobial dip and temperature on the fate of Listeria innocua and Listeria monocytogenes on minimally processed lettuce

The growth and survival of inoculated strains of Listeria innocua and L. monocytogenes on minimally processed lettuce were studied. The effects of package atmospheres (lettuce sealed within packages after flushing with 100% N₂ or without flushing with N₂, lettuce sealed within perforated packages), antimicrobial dips (100 p.p.m. chlorine solution for 5 min, 1% citric acid solution for 5 min) and storage temperatures (3°C and 8°C) were investigated. Populations of L. innocua and L. monocytogenes on undipped lettuce stored at 3°C gradually decreased (by 1–1.5 log cycles) during a 14 day storage period. By contrast counts on lettuce stored at 8°C did not change significantly ( P > 0.05). Flushing packages of lettuce with 100% N₂ followed by storage at 8°C resulted in a significant increase ( P < 0.05, by 2–3 log cycles) in L. innocua and L. monocytogenes counts during storage. L. innocua , strain NCTC 11288, behaviour was similar to that of L. monocytogenes (strains ATCC, 19114 and NCTC 11994) under these storage temperatures and atmospheres. Using L. innocua as a model for L. monocytogenes , it was found that dipping lettuce in a chlorine or citric acid solution followed by storage at 8°C resulted in a significant increase ( P < 0.05, by 2 log cycles) in L. innocua populations compared with undipped samples. It is concluded that N₂ flushing or use of antimicrobial dips combined with storage at 8°C, both enhanced the survival and growth of Listeria populations on shredded lettuce.     

OXALACETATE SYNTHESIS IN APPLES AND BANANAS AT LOW TEMPERATURES

¹⁴CO₂ was applied to apples and bananas that were stored at various temperatures and the incorporation of ¹⁴C into oxalacetate was determined. Apples that were susceptible to internal breakdown showed an initial decrease in incorporation as the storage temperature was reduced but incorporation then increased at temperatures below 10°C (Jonathan) or 5°C (Twenty Ounce). Apples that were not susceptible to breakdown (Delicious and Granny Smith) showed no incorporation at any temperature. Green bananas showed a minimum incorporation at 10°C but in ripe bananas, incorporation markedly increased at all temperatures less than 20°C. The respiration rate of the apple varieties at 20°C was found to be higher in fruit that were more susceptible to breakdown whereas at O°C the higher rates of respiration were from fruit less susceptible to the disorder.     

Shelf life of Turkish whey cheese (Lor) under modified atmosphere packaging

In this study, the shelf life of Lor cheese stored under different atmosphere compositions was assessed and compared. Lor cheeses were held in four different atmospheres containing: vacuum packaging (VP), 40% CO₂/60% N₂, 60% CO₂/40% N₂ and 70% CO₂/30% N₂ (modified atmosphere packaging). Control cheeses were stored in air. All cheese samples were kept in the refrigerator at 4°C for 45 days and investigated for physicochemical, microbiological and sensory properties. The acidity index value was significantly higher ( P  < 0.05) in the control and vacuum packaged samples than in those stored for the same period under CO₂. Microbiological results showed that modified atmosphere packaging delayed microbial growth compared with air and VP samples. Of the three modified atmospheres, gas mixtures 60% and 70% CO₂ were the most effective for inhibition of growth of micro-organisms. Sensory evaluation (odour and taste) results showed that Lor cheese packaged under modified atmosphere packaging (60% CO₂/40% N₂ and 70% CO₂/30% N₂ ) retained good characteristics for 45 days of storage, while vacuum and control samples were sensorily unacceptable after 10 days of storage.     

Some effects of modified-atmosphere packaging and vacuum packaging in combination with antioxidants on quality and storage life of chilled potato strips

A modified-atmosphere packaging system for chilled fresh potato strips, which rapidly produced oxygen levels < 3%, was identified. This system enclosed the strips within 25 μ low density polyethylene film heat sealed to a fibre tray lined with Surlyn-PVdC-Surlyn, and the package flushed with an initial atmosphere of 5% O₂, 10% CO₂. An equilibrium-modified atmosphere of 3–4% CO₂, 1–2% O₂ was established after 3 days' storage at 5°C. This modified-atmosphere package, used in combination with dipping of potato strips in a 10% ascorbic acid solution, inhibited enzymatic discoloration for 1 week at 5°C. Vacuum packaging within a Surlyn/PVdC-coated polyester film, with or without dipping in ascorbic acid solution, inhibited discoloration of chilled potato strips stored at 5°C for at least 2 weeks.     

Controlled atmosphere storage to decrease physiological disorders in nectarines

'Fantasia', 'Flavortop', and 'Flamekist' nectarines were examined for their response to controlled atmosphere (CA) storage. All three cultivars stored well for up to 6 weeks at 0°C in an atmosphere of 10% O₂+ 10% CO₂, while some but not all the cultivars also stored well in 2% O₂+ 5% CO₂ or 10% O₂+ 5% CO₂. The physiological storage disorders of internal breakdown and reddening were almost completely absent in nectarines kept in 10% O₂+ 10% CO₂. When 'Flamekist' nectarines from two harvests were stored in 10% O₂+ 10% CO₂ atmosphere for 6 or 8 weeks at 0°C, the fruit from the first harvest was of better quality after post-storage ripening. Although this controlled atmosphere prevented internal breakdown and reddening, after extended storage fruit did not develop the increased soluble solids content or extractable juice during post-storage ripening that occurred in non-stored fruit. Therefore, while preventing storage disorders, CA does not reduce the loss of ripening ability occurring during nectarine storage.     

Effects of Hot Rehydration in the Presence of Hydrogen Peroxide on Microbial Quality, Texture, Color, and Antioxidant Activity of Cold-stored Intermediate-moisture Sun-dried Figs

ABSTRACT: Pectin methylesterase (PME) causes considerable softening in intermediate-moisture (IM) figs rehydrated at 30°C and cold stored at 28% to 29% moisture content. Rehydration of figs at 80°C for 16 min inactivated PME partially (25–30%), but this did not prevent the softening over 3 mo of cold storage. Also, heating did not reduce the microbial load of figs significantly and increased their browning. In contrast, rehydration of figs 1st in 2.5% H₂O₂ at 80°C for 8 min and then in water at 80°C for 8 min reduced the microbial load of IM figs significantly, turned their brown color to yellow-light brown, and maintained their desired textural properties. The residual H₂O₂ in IM figs decomposed in 3 or 1.5 wk by the in situ catalase or by application of the iron (II) sulfate-ascorbic acid residue elimination method, respectively. Hot rehydration did not affect the antioxidant activity of IM figs, but treatment of figs with H₂O₂ increased their antioxidant activity slightly. These results indicate that the hot rehydration of figs in the presence of H₂O₂ and cold storage may be applied to obtain safe and SO₂-free light-colored IM fig products.     

Improved Sanitizing Treatments for Fresh Tomatoes

ABSTRACT:  Fresh tomatoes repeatedly have been associated with major outbreaks of salmonellosis; however, efforts to disinfect them with chlorine or other sanitizing agents have had only mixed success. Our objective was to determine whether hydrogen peroxide (H₂O₂) treatments would be more efficacious than conventional methods in disinfecting tomatoes containing human pathogens and, at the same time, be noninjurious to quality. Tomatoes were dip inoculated with Escherichia coli NRRL B-766 or a Salmonella cocktail and then held for 0, 24, or 48 h at 4 or 24 °C prior to treatment. Treatments included 200 ppm chlorine (Cl₂) at 20 °C for 3 min, water at 20 °C for 3 min or at 60 °C for 2 min, 1% H₂O₂ at 20 °C for 15 min or at 60 °C for 2 min, and 5% H₂O₂ at 60 °C for 2, 3, or 5 min. In tomatoes held 48 h postinoculation, the chlorine treatment was only marginally more effective than an equivalent water rinse in reducing the target bacterial population, while the hot water and 1% H₂O₂ treatments achieved reductions no greater than 1.3 logs. However, application of 5% H₂O₂ at 60 °C resulted in larger reductions. Efficacy of all treatments decreased as the time interval between inoculation and treatment increased. Greater reductions could not be achieved with 5% H₂O₂ at 60 °C by increasing the contact time or addition of surfactants, and these treatments caused some quality loss.     

Temperature-Sensitive Microcapsules Containing Lactoferrin and Their Action Against Carnobacterium viridans on Bologna

ABSTRACT:  Lactoferrin (LF) was encapsulated in 2 types of emulsion to protect it from contact with agents like divalent cations, which interfere with its antimicrobial activity. First, paste-like microcapsules were prepared as water-in-oil (W₁/O) emulsions from mixtures of 20% w/v LF in distilled water, 20% w/v LF in 3% w/v sodium lactate or in 20 mM sodium bicarbonate, which were emulsified with an oil mixture of 22% butter fat plus 78% corn oil and 0.1% polyglycerol polyricinoleate. Second, freeze-dried double emulsion (W₁/O/W₂), powdered microcapsules were produced following emulsification of paste-like microcapsules in an external aqueous phase (W₂) consisting of a denatured whey protein isolate (WPI) solution. The release of LF from the W₁/O microcapsules was dependent on temperature and NaCl concentration. LF was not released from the W₁/O emulsion at <5.5 °C. Its release was greater from W₁/O microcapsules when suspended in 5% aqueous NaCl than in water at ≥10 °C, whereas LF release from freeze-dried microcapsules was not controlled by temperature change. Paste-like microcapsules were incorporated in edible WPI packaging film to test the antimicrobial activity of LF against a meat spoilage organism Carnobacterium viridans . The film was applied to the surface of bologna after its inoculation with the organism and stored under vacuum at 4 or 10 °C for 28 d. The growth of C. viridans was delayed at both temperatures and microencapsulated LF had greater antimicrobial activity than when unencapsulated. The temperature-sensitive property of the W₁/O microcapsules was reduced when they were incorporated into a WPI film.