Preservation of spinach by isochoric (constant volume) freezing

Efforts are currently directed towards improving the quality of vegetables after freezing and thawing. One of the methods under investigation is isochoric freezing. In this study, we evaluated isochoric freezing for preserving the quality of baby-leaf spinach. We compared the properties of thawed spinach frozen to −4°C in an isochoric system with those of fresh spinach, thawed spinach frozen to −4°C in an isobaric system and thawed spinach that were commercially frozen. Spinach leaves frozen under isobaric conditions lost mass and thickness, making them softer and translucent. They also lost much of their nutrient content. In comparison, isochoric freezing maintained cell integrity and turgidity. Thawed leaves remained crunchy with characteristics similar to fresh leaves. Isochoric freezing also preserved nutritional content better than isobaric freezing, although significant nutrient losses still occurred.     

Preservation of sweet cherry by isochoric (constant volume) freezing

Due to the perishable nature of fruits and the importance of reducing food waste, an effective preservation technique is required to prolong the shelf life and maintain the physical and nutritional properties of seasonal fruits. In this study, we evaluated isochoric freezing for preserving the quality of sweet cherries. We examined the physical characteristics and nutritional values of thawed cherries frozen to −4 °C or −7 °C in an isochoric system and compared them with those of fresh cherries, thawed cherries that were individually quick frozen and thawed cherries frozen to −4 °C or −7 °C in an isobaric system. We found that isochoric freezing decreased the drip loss and better preserved the color, texture, structure, ascorbic acid, phenolic and antioxidant content of frozen cherries, thereby proving their potential in frozen fruit applications.     

Behavior of Escherichia coli O157:H7 and Listeria monocytogenes in Tryptic soy broth subjected to various low temperature treatments

The inactivation and injury of Escherichia coli O157:H7 and Listeria monocytogenes in Tryptic soy broth stored at −5, −18 and −28°C were studied. Regardless of storage temperature, viable populations of E. coli O157:H7 and L. monocytogenes determined with TSA (uninjured and injured cells) or TSAB (uninjured cells), decreased as the storage time increased. However, the least surviving population of both test organisms was noted when stored at −18°C followed by those stored at −28 and −5°C. The viable populations of E. coli O157:H7 determined either with TSA or TSAB, was reduced most drastically during the first day of storage then decreased slowly thereafter. Viable populations of L. monocytogenes declined slightly and gradually during the entire storage period. Furthermore, E. coli O157:H7 was found more susceptible to the freezing storage than L. monocytogenes. After 21-day storage at −18°C, population reduction of E. coli O157:H7 determined with TSA was ca 1.72 log CFU/ml. On the other hand, a population reduction of only 0.64 log CFU/ml was noted with L. monocytogenes. Besides, the surviving population of E. coli O157:H7 contained a larger proportion of injured cells than L. monocytogenes.     

Effects of sodium hypochlorite and acidified sodium chlorite on the morphological,microbiological, and sensory qualities of selected vegetables

The effects of washing with sodium hypochlorite (NaClO) and acidified sodium chlorite (ASC) on the reduction of various pathogens contaminated produce, as well as the change in sensory qualities during storage and morphological characteristics of the surface of the washed produce, including cherry tomato, cucumber, and carrot were evaluated. Produce was inoculated with Bacillus cereus, B. cereus spore, Campylobacter jejuni, Salmonella Typhimurium, and Listeria monocytogenes and then washed with 100, 150, or 200 ppm NaClO and stored for 11 days at 4°C. The produce contaminated with S. Typhimurium or L. monocytogenes was also washed with 100 ppm NaClO containing 5% acetic acid and 500 ppm ASC. The greatest washing efficacy was observed in B. cereus, followed by S. Typhimurium, L. monocytogenes, and C. jejuni. NaClO with 5% acetic acid was significantly (p<0.05) more effective than 500 ppm ASC at S. Typhimurium, but not at L. monocytogenes, regardless of the types of produce, while ASC was the most effective sanitizer for L. monocytogenes in cucumber. Scanning electron microscopy showed that washing with NaClO removed the pathogens, but also part of the wax layer from the surface, which might affect sensory qualities of the produce during storage.     

Effect of freezing/thawing conditions and long‐term frozen storage on the quality of mashed potatoes

The effects of freezing temperature (−80, −40 or −24 °C) and thawing mode (microwave or overnight at 4 °C) on quality parameters of mashed potatoes made from tubers (cv Kennebec) and from potato flakes were examined, as was the effect of long‐term frozen storage on the quality of mashed potatoes. Mashed potatoes were tested for texture profile analysis (TPA) and cone penetration, oscillatory and steady rheometry, colour, dry matter, Brix and sensory analyses. In natural mashed potatoes, TPA hardness and oscillatory parameters showed that processing resulted in a softer product than the fresh control. The parameters were lower in the samples thawed at 4 °C than in those thawed by microwave at all the freezing temperatures used, which may be ascribed to gelatinisation of the starch released from damaged cells. Differences from the freshly prepared product decreased when the samples were frozen at −80 °C and thawed by microwave. No difference was found in sensory acceptability between samples frozen at −80 and −40 °C, which probably reflects the panellists' mixed preferences for air‐thawed versus microwave‐thawed samples. Increasing the time in frozen storage led to a natural mash with a firmer texture, higher L*/b* value and Brix; nonetheless, panellists found the samples at 0, 3 and 12 months of frozen storage equally acceptable. In commercial mash, penetration and oscillatory parameters showed that processing made for a firmer product than the fresh control, probably owing to retrogradation of gelatinised starch. Thawing mode had a significant effect on parameters, which were lower in the samples thawed at 4 °C. The structure and quality of commercial mash was more detrimentally affected by freezing and, therefore, we would not recommend either freezing or frozen storage of this mashed potato in the used conditions. Natural mash made from Kennebec potatoes should be frozen quickly and thawed by microwave in the conditions described to obtain a product more similar to that freshly made. If the samples are frozen by air blasting at −40 °C, the product can withstand frozen storage for one year. Copyright © 2005 Society of Chemical Industry     

Changes in Microflora and Other Characteristics of Vacuum-packaged Pork Loins irradiated at 3.0 kGy

Effects of 3.0-kGy irradiation on microflora and other attributes of fresh, vacuum-packaged pork loins were examined during storage (2–4°C, 98 days) and mishandling (24–25°C, 24 and 48 hr). Shelf life of pork chops from irradiated loins was determined at 5°C. Irradiated loins kept at 2–4°C tested negative for Salmonella spp., Campylobacter spp., Clostridium perfringens and Staphylococcus aureus. Yersinia spp. was detected in pork chops held at 5°C; this organism, C. perfringens and Aeromonas spp. were present in abused samples. In two irradiated samples Listeria monocytogenes was found. Irradiation reduced aerobic, anaerobic and Aeromonas spp. counts; lactobacilli were least affected. Chemical spoilage began after 91 days at 2–4°C. With irradiation, TBA values were unaffected but Hunter a color values increased.     

Fate of Listeria monocytogenes During Freezing and Frozen Storage

A cell suspension of Listeria monocytogenes was frozen 30 min at ?18°C, or 10 min in liquid nitrogen (LN) at ?198°C. Solidification required 15 min at ?18°C and ca. 1 min at ?198°C. Freezing and storage 1 month in phosphate buffer (PB) at ?18°C caused 87% death and 79% injury. These were 54 and 45%, respectively, for cells in Tryptose Broth (TB) at ?18°C. Freezing and storage 1 month in LN caused no death or injury of cells suspended in PB, whereas some injury and death occurred in TB. Freezing at ?198°C followed by storage 1 month at ?18°C resulted in 60% death and 36% injury in PB, and 61 and 44.2%, in TB. Repeated freezing and thawing caused more death/injury than did a single freeze-thaw cycle.     

Inhibitor‐Assisted High‐Pressure Inactivation of Bacteria in Skim Milk

The combined inactivation effects of high hydrostatic pressure (HHP) and antimicrobial compounds (potassium sorbate and ε‐polylysine [ε‐PL]) on 4 different bacterial strains present in skim milk and the effect of these treatments on milk quality were investigated in this study. HHP treatment at 500 MPa for 5 min reduced the populations of Escherichia coli, Salmonella enterica Typhimurium, Listeria monocytogenes, and Staphylococcus aureus from 6.5 log colony‐forming units (CFUs) or higher to less than 1 log CFU/mL. Compared to HHP alone, HHP with potassium or ε‐PL resulted in significantly higher reductions in the bacterial counts. After 5 min of treatment with HHP (500 MPa) and ε‐PL (2 mg/mL), no growth of E. coli, S. enterica Typhimurium, or L. monocytogenes in skim milk was observed during 15 d of refrigerated storage (4 ± 1 °C). Scanning electron microscopy analysis revealed that the synergistic treatments caused more serious damage to the bacterial cell walls. Quality assessments of the treated samples indicated that the combined treatments did not influence the color, the turbidity, the concentrations of –SH group of the proteins, or the in vitro digestion patterns of the milk. This study demonstrates that HHP with potassium or ε‐PL may be useful in the processing of milk or milk‐containing foods.     

Changes in texture,microstructure and nutritional quality of carrot slices during blanching and freezing

Thermal processing of vegetables has pronounced effects on the cell structure, often lowering the final textural properties of the product. In order to investigate the effect of thermal processing on carrot, slices were subjected to different blanching and freezing treatments before frozen storage. Microwave-, steam- or water-blanched material was frozen and then stored at −24 °C. Steam-blanched carrots were subjected to blast freezing or cryogenic freezing at different temperatures before frozen storage. The influence of these process conditions on the texture (maximum load and slope), microstructure, dry matter, sugars, carotene and drip loss was investigated. Microwave blanching differed from the other blanching methods by resulting in a heterogenic cell structure. The content of dry matter, carotene and sucrose was higher following microwave blanching. Blast freezing resulted in low maximum load which seemed to be caused by major tissue damage. Concerning cryogenic freezing, lowering the temperature from −30 °C to −70 °C resulted in better preservation of the native microstructure together with an increase in maximum load, which was most pronounced after one month of storage. No significant effect was observed when lowering the temperature from −30 °C to −70 °C for any of the other measured parameters. © 1999 Society of Chemical Industry     

Packaging Film Permeability in Conjunction with Sodium Nitrite, Potassium Sorbate or Lactic Acid Starter Culture for Control of Clostridium sporogenes (PA3679) Growth in Sliced Bologna

A sliced bologna was prepared and inoculated with Clostridium sporogenes (PA3679), packaged in films ranging in oxygen permeability from 0.1 cc/m²/24 hr to 120 cc/m²/24 hr and stored at 5°C, 15°C or 25°C. Subsequent bologna preparations included either 156 ppm sodium nitrite, 0.26% potassium sorbate or a lactic acid starter culture. Water activity, pH, TBA number and PA3679 counts were monitored during 28 days of storage. TBA numbers increased in packages with over 60 cc/m²/24 hr permeability but PA3679 counts did not change as a function of packaging film. Nitrite and sorbate were equally effective as inhibitors. At 15°C and 25°C, the lactic acid culture allowed the least PA3679 growth. Oxygen permeability did not alter any inhibitory effects even when increased TBA numbers resulted from using an oxygen-permeable film.     

Effects of Freezing Rate, Frozen Storage Temperature and Storage Time on Tenderness Values of Beef Patties

All-beef and soy-extended patties were frozen to ?18°C in either 24, 48, 72 or 96 hr and stored at ?23°, ?18° or ?7°C for 6, 9, 12, 18 or 24 months. Freezing produced considerable reductions in both sensory and instrumental measures of tenderness with the effects being greater for the slower freezing rates. Thus, just after freezing, and prior to storage, tenderness was found to be higher in patties subjected to faster freezing compared to slower rates of freezing. Storage at ?7°C reduced sensory scores for tenderness and increased stress in relation to strain during shearing. Extending patties with soy reduced the effects of freezing rate, storage temperature and storage time on tenderness.     

Growth of Listeria monocytogenes Inoculated in Waste Fluids from Clean-up of a Meat Grinder

The potential of waste fluids from clean-up of a meat grinder to support growth (8°C and 35°C) of artificially inoculated Listeria monocytogenes Scott A was examined. Estimated generation times were 10.1 and 2.3 hr at 8°C, and 8.9 and 2.2 hr at 35°C for a fluid collected during rinsing of the meat grinder and a fluid collected from the floor drain, respectively. A sanitizer fluid (25 ppm titratable iodine), collected after sanitation of the grinder, inactivated the inoculated cells. Thus, waste fluids may support growth of L. monocytogenes in meat processing facilities, but frequent sanitation should inactivate the pathogen.     

Control of Listeria monocytogenes in Vacuum-Packaged Pre-Peeled Potatoes

Growth of Listeria monocytogenes on the surface of fresh peeled potatoes, treated with sulfite or a commercial browning inhibitor (CBI), packaged under vacuum and stored at 4,15 and 28°C was determined. At 4°C, L. monocytogenes did not grow in all treated potatoes even after 21 days. At 15°C, L. monocytogenes grew to 7 log₁₀ CFU/g within 12 days in the potatoes treated with sulfite or CBI. At 28°C, L. monocytogenes population was greater than 3 log₁₀ CFU/g by 24 h in all samples regardless of treatment. Sulfites or a CBI appeared to provide a measure of safety in pre-peeled potatoes packaged under vacuum when kept at proper refrigeration temperatures.     

Thermal Destruction of Listeria monocytogenes in a Meat Slurry and in Ground Beef

Thermal destruction of Listeria monocytogenes cells was determined in phosphate buffer, a meat slurry (20% ground beef/80% water) and in ground beef. D-values at 60°C, 65°C and 70°C in phosphate buffer, and in the meat slurry were 0.63, 0.29 and 0.15, and 2.54, 0.75 and 0.23 min, respectively. Heating of ground beef (80% lean) in a 75°C water bath to 50°C, 60°C or 65°C required 6.2, 8.4 and 10.6 min, respectively, and resulted in 0.2-0.9, 1.6-3.4 and 4.4-6.1 log reductions in L. monocytogenes cells, from the initial inoculation level of 8.08 log CFU/g. Viable cells were also detected after cold (21 days) or selective enrichment (24 hr) in eight out of nine samples of ground beef inoculated with 7.84-8.08 log CFU/g and cooked to 70°C.     

Growth or Survival of Listeria monocytogenes in Ready-to-Eat Meat Products and Combination Deli Salads During Refrigerated Storage

Growth or survival of Listeria monocytogenes in cold‐smoked salmon; sliced, cooked ham; sliced, roasted turkey; shrimp salad; and coleslaw obtained at retail supermarkets stored at 5 °C, 7 °C, or 10 °C (41 °F, 45 °F, or 50 °F, respectively) for up to 14 d was evaluated. Cold‐smoked salmon, ham, and turkey were obtained in case‐ready, vacuum packages. All food products were stored aerobically to reflect additional handling within the retail supermarket. Cold‐smoked salmon, ham, and turkey supported the growth of L. monocytogenes at all 3 storage temperatures. Fitted growth curves of initial populations (about 3 log₁₀ colony‐forming units [CFU]/g) in cold‐smoked salmon, ham, and turkey stored at 5 °C achieved maximal growth rates of 0.29, 0.45, and 0.42 log₁₀ CFU/g growth per day, respectively. Storage at 10 °C increased the estimated maximal growth rate of the pathogen by 0.56 to 1.08 log₁₀ CFU/ g growth per day compared with storage at 5 °C. A decline in populations of L. monocytogenes was observed in shrimp salad and coleslaw, and the rate of decline was influenced by storage temperature. Retention of viability was higher in shrimp salad than in coleslaw, where populations fell 1.2, 1.8, and 2.5 log₁₀ CFU/g at 5 °C, 7 °C, and 10 °C, respectively, after 14 d of storage. Inability of shrimp salad and coleslaw to support the growth of L. monocytogenes may be attributed to the acidic pH (4.8 and 4.5, respectively) of the formulations used in this study. Results show that the behavior of L. monocytogenes in potentially hazardous ready‐to‐eat foods is dependent upon the composition of individual food products as well as storage temperature.     

Comparison of air freezing,liquid immersion freezing and pressure shift freezing on freezing time and quality of snakehead (Channa Argus) fillets

The objective of this study was to investigate the freezing time and quality differences in Snakehead fillets frozen by pressure shift freezing (PSF), conventional air freezing (AF) and liquid immersion freezing (LIF) at −20 °C, −40 °C and − 60 °C, respectively. The results showed that liquid immersion freezing at −60 °C maintained the quality best, with a freezing time of 3.62 min and the cross sectional area of 209.11 um². Air freezing at −20 °C had the longest freezing time (184.58 min) and the largest cross sectional area (4470.79 um²), and lowest hardness and springiness of the fillets. Pressure shift freezing did not demonstrate the well established advantages of maintaining better product quality found in similar technique with some other foods. The samples of pressure shift freezing also had higher thawing loss and free water ratio after thawing. Therefore, the liquid immersion freezing at lower temperatures was demonstrated to better maintain the quality of frozen products and held significant potential for commercial application.Industrial relevanceFreezing is a widely used method for extending the shelf life of aquatic products, but some freezing methods, especially the slower ones, often lead to the decrease in the quality and commercial value of frozen products during storage. This paper explored the comparison of industrially used freezing techniques (air freezing and liquid immersion freezing) with the novel pressure shift freezing technique. Liquid immersion freezing at −60 °C was found to be the preferred freezing method for Snakehead fillets, which maintained better frozen product quality, with a simple freezing process and low cost.     

Proton spin–spin relaxation time of peel and flesh of navel orange varieties exposed to freezing temperature

Proton spin–spin relaxation times (T₂) of peel (albedo and flavedo) and juice sacs (flesh segments) of navel oranges were measured at 10 MHz using a Bruker Minispec PC 110 NMR spectrometer. The oranges were subjected to chilling (5 °C) and freezing (−7 °C) temperatures for 20 h and warmed to room temperature before peeling for T₂ measurements. The exposure to chilling or freezing temperature did not affect the T₂ values of peel, but freezing caused an appreciable decrease (∼15%) in the T₂ values of flesh segments of the varieties of navel oranges studied. When the peel was exposed to −20 °C, the T₂ showed a drastic reduction suggesting that the peel did not freeze at −7 °C. The possible cause of reduction in the T₂ values when exposed to freezing temperature may be damage to the juice sac membrane and leakage of juice out of the sac. The difference in the T₂ values between juice sacs of freeze-affected and normal oranges can potentially be used for detection of freeze-damaged fruits. Copyright © 2005 Society of Chemical Industry     

Survival and growth of foodborne pathogens in minimally processed vegetables at 4 and 15 °C

Abstract: We conducted this study to investigate the survival and growth of pathogens on fresh vegetables stored at 4 and 15 °C. Vegetables (romaine lettuce, iceberg lettuce, perilla leaves, and sprouts) were inoculated with 4 pathogens (Salmonella enterica serovar Typhimurium, Staphylococcus aureus, Listeria monocytogenes, and Escherichia coli O157:H7) and stored at 2 different temperatures for different periods of time (3, 6, 9, 12, and 15 d at 4 °C and 1, 2, 3, 5, and 7 d at 15 °C). Populations of the 4 pathogens tended to increase on all vegetables stored at 15 °C for 7 d. Populations of E. coli O157:H7 and S. Typhimurium increased significantly, by approximately 2 log₁₀CFU/g, on loose and head lettuce stored at 15 °C for 1 d. No significant differences were observed in the growth of different pathogens on vegetables stored at 4 °C for 15 d. E. coli O157:H7 did not survive on sprouts stored at 15 or 4 °C. The survival and growth of food pathogens on fresh vegetables were very different depending on the pathogen type and storage temperature. Practical Application: Survivals and growth of pathogens on various vegetables at 4 and 15 °C were observed in this study. Survivals and growth of pathogens on vegetables were different depending on the pathogen type and storage temperature. Therefore, vegetables should be stored under refrigerated conditions (below 4 °C) prior to consumption. This recommendation may vary depending on the type of vegetable.     

Practical application of bacteriophage in food manufacturing facilities for the control of Listeria sp.

Listeria monocytogenes is a foodborne pathogen with the ability to persist and form biofilm matrices in processing environments of food manufacturing facilities. Bacteriophages are bacterial viruses with host specific lethality. Published research on the application of phage to control Listeria sp. in manufacturing environments is limited. In this study, we have assessed the capacity of bacteriophage P100 (Listex™) to reduce incidence of Listeria sp. in the ready-to-eat (RTE) environment of refrigerated (4°C) and ambient (20°C) temperature facilities using two different application strategies. A moderate application applied as a single treatment every 24 hr over three days (2 × 10⁷ PFU/ml) and an intensified application applied once every 6 hr over a 24 hr period (1 × 10⁸ PFU/ml). Environmental nonfood contact surface (NFCS) samples were collected and analyzed for the presence of Listeria sp. before and after treatment. When the moderate treatment protocol was applied the incidence of positives decreased from 51.3 to 17.5% in the 4°C environment and from 67.5 to 23.1% in the 20°C production area. For the intensified phage treatment method, the initial positive rate in the 4°C environment ranged from 5 to 47.5%, with an overall 43% reduction in Listeria sp. In the 20°C facility, initial environmental Listeria sp. ranged from 15 to 50%, with an overall reduction of 32% after treatment with phage P100. Data indicate the application of Listeria specific phage P100 in RTE food production environments by either the moderate or intensified application method can reduce incidence and be considered an additional intervention strategy for controlling this pathogen on NFCS.     

Freezing Qualities of Raw Ovine Milk for Further Processing

Raw whole ovine (sheep) milk was frozen at −15°C and −27°C and microbiological and physico-chemical properties were evaluated periodically. Total bacteria decreased at a faster rate in milk stored at −15 than at −27°C. Acid degree values for milk stored at −15°C were significantly higher than that stored at _27°C. Samples stored at −15°C exhibited protein destabilization after 6 mo of storage, while those stored at −27°C were stable throughout the 12-mo storage period.Frozen ovine milk was evaluated in several products including cheese, yogurt, and whey protein concentrates. Products produced from milk frozen at −27°C exhibited good sensory and functional characteristics. Ovine whey showed a higher proportion of β-lactoglobulin, about the same proportion of α-lactalbumin and lower proportions of serum albumin and immunoglobulin than bovine whey. Ovine whey protein concentrate showed significantly better foam overrun, foam stability, and gel strength than bovine or caprine whey protein concentrates.