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.     

Cover Caption

September Online Cover : Cryo-scanning electron microscopy images of potato parenchyma tissue microstructures before and after freezing for 4 weeks under different freezing methods, and photographs of fresh and thawed potatoes frozen for different periods of time under isochoric, isobaric, or individually quick frozen conditions, from “Effect of isochoric freezing on quality aspects of minimally processed potatoes” by Cristina Bilbao-Sainz, Yuanheng Zhao, Gary Takeoka, Tina Williams, Delilah Wood, Bor-Sen Chiou, Matthew J. Powell-Palm, Vivian C.H. Wu, Boris Rubinsky, and Tara McHugh. p. 2656.     

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     

Viability of Listeria monocytogenes and Salmonella Typhimurium after isochoric freezing

Isochoric freezing, different from isobaric (conventional) freezing, allows for storage below freezing temperatures without significant damage from ice formation. While several types of tissues have been successfully stored in sub-zero isochoric conditions, it is unknown how isochoric freezing affects pathogenic microorganisms. Thus, the objective of this study was to investigate the survival of Salmonella Typhimurium and Listeria monocytogenes at below freezing storage (<0°C) in isochoric conditions. Tested conditions included storage at −4, −7, and −15°C for 24 hr and at −15°C for 1, 2, 3, 6, 12, and 24 hr. A comparison of bacterial survival during isobaric freezing was included with every trial. Additionally, bacterial cells were examined for morphological damage using transmission electron and field-emission scanning electron microscopes. Isochoric freezing at −15°C for 24 hr reduced both species of bacteria down to unrecoverable levels and maximum efficacy achieved after the 6 hr timepoint for L. monocytogenes and the 12 hr timepoint for S. Typhimurium. When viewed using electron microscopy, S. Typhimurium cells were noticeably disfigured with regions of cytosol separated from the cell wall. The results of this study demonstrate that isochoric freezing is capable of substantial levels of pathogen reduction. Unlike conventional nonthermal interventions, isochoric freezing does not require additional devices such as elevated pressure machines or pulsed electric fields and can be achieved with simple, inexpensive, rigid closed volume containers such as household freezers or commercial cold storage facilities.     

Studies on freezing of partially dehydrated spinach

Spinach (Spinacea oleracea) was dehydrated at 70 °C, partially dehydrated frozen (dried to its critical moisture ratio and frozen at ?20 °C) and frozen at ?20 °C. Results indicated that the time required for spinach dehydration was 7 h. Thus, the moisture ratio was 10.1 and 0.054 for the fresh and dried spinach, respectively. The critical moisture ratio during dehydration process was 2.20 after 2.65 h of drying time. Reducing sugars, free amino nitrogen, ash, iron and magnesium were slightly decreased in the partially dehydrated frozen spinach relative to the fresh samples. Dehydration markedly degraded the total chlorophyll, chlorophyll a, chlorophyll b, carotenoides and ascorbic acid whereas the freezing of partially-dehydrated spinach and freezing process were less effective. On the other hand, freezing of partially dehydrated spinach increased phaeophytin. There were no changes in pH-values of studied preserved samples. Freezing of partially dehydrated spinach improved the reconstitution of product at 100 °C and at room temperature (25 °C) comparing to dehydration. The drip loss of frozen spinach was 16.4% after 105 min of thawing time. Cooked fresh and frozen spinach were better in colour, flavour, texture, appearance and shape and over-all acceptability than that of dehydrated cooked one. Moreover, freezing of partially dehydrated spinach improved the aforementioned properties.     

Freezing/defrosting/frying of sardine fillets. Influence of slow and quick defrosting on protein quality

The effect of sequential freezing/defrosting/frying on protein quality is not well known. With this in mind, fillets of fresh sardine were stored frozen, then thawed, either conventionally at 4 °C in a refrigerator or with the use of a microwave oven, and subsequently deep‐fried. Proximate and amino acid compositions, protein solubility in sodium dodecyl sulphate/β‐mercaptoethanol (SDS/β‐ME), total ? SH group content and amino acid chemical score were determined. The lowest protein concentration was observed in frozen/4 °C‐thawed sardines (CR), whilst the lowest fat content was found in both fresh/fried sardines (F) and 4 °C‐thawed/fried sardines (CF). Every step of each process studied caused a decrease in cyst(e)ine; the most important loss was recorded in CF samples and in frozen sardines fried without defrosting (Fro‐F). The lowest solubility in SDS/β‐ME and the lowest total ? SH group content were observed for Fro‐F samples and microwave‐thawed/fried sardines (MF). On the other hand, the lowest chemical score was found for Fro‐F, CF and MF samples. Although weight loss and proximate composition seemed to change less when defrosting sardine fillets using a microwave oven rather than at 4 °C, the results for SDS/β‐ME solubility and total ? SH group content suggest that a slow defrosting process (refrigerator at 4 °C) is preferable to a much quicker process (microwave oven) for thawing frozen sardine fillets before frying. Copyright © 2003 Society of Chemical Industry     

Synthesis and degradation of adenosine triphosphate in cod (Gadus morhua) at subzero temperatures

This study has demonstrated that the extraction step is very important when analysing ATP and its degradation products. An important factor is whether the sample is fresh, frozen or thawed when homogenised since thawing of the sample will lead to rapid loss of ATP. During frozen storage it was found that ATP in cod (Gadus morhua) was stable at −40 °C in small samples for at least 12 weeks. At −20 °C it was found that ATP content increases initially and thereafter falls. It was demonstrated that degradation of ATP in small samples occurs faster at 0 °C than at −2 and −5 °C. Furthermore, it was found that in whole cod ATP could be synthesised at a significant rate at −7 °C. © 1999 Society of Chemical Industry     

Synergistic mechanism of steam blanching and freezing conditions on the texture of frozen yellow peaches based on macroscopic and microscopic properties

Freezing and blanching are essential processing steps in the production of frozen yellow peaches, inevitably leading to texture softening of the fruit. In this study, the synergistic mechanism of stem blanching, freezing conditions (−20°C, −40°C, −80°C, and liquid nitrogen [−173°C]), and sample sizes (cubes, slices, and half peaches) on macroscopic properties of texture, cellular structure, and ice crystal size distribution of frozen yellow peaches were measured. Blanching enhanced the heat and mass transfer rates in the subsequent freezing process. For nonblanched samples, cell membrane integrity was lost at any freezing rate, causing a significant reduction in textural quality. Slow freezing further exacerbated the texture softening, while the ultra-rapid freezing caused structural rupture. For blanched samples, the half peaches softened the most. The water holding capacity and fracture stress were not significantly affected by changes in freezing rate, although the ice crystal size distribution was more susceptible to the freezing rate. Peach cubes that had undergone blanching and rapid freezing (−80°C) experienced 4% less drip loss than nonblanched samples. However, blanching softened yellow peaches more than any freezing conditions. The implementation of uniform and shorter duration blanching, along with rapid freezing, has been proven to be more effective in preserving the texture of frozen yellow peaches. Optimization of the blanching process may be more important than increasing the freezing rate to improve the textural quality of frozen yellow peaches.     

A comparison of the vitamin C content of fresh and frozen vegetables

This study, using vitamin C (ascorbic acid) as ‘marker’, allowed a direct comparison of the nutritional quality of fresh vegetables at various stages of distribution and storage, with the same vegetable commercially quick-frozen and stored deep frozen for up to 12 months. The nutrient status of frozen peas and broccoli was similar to that of the typical market-purchased vegetable and was superior to peas that have been stored in-home for several days. Fresh peas and broccoli retained their quality for up to 14 days when stored under chill conditions. The nutrient status of frozen whole green beans and frozen carrots, with no loss on freezing, was similar to the fresh vegetable at harvest. Frozen spinach also compared reasonably well with the harvested fresh vegetable and was clearly superior to all market produce.     

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.     

Effects of the methods of pre-treatment before freezing on the retention of chlorophylls in frozen leaf vegetables prepared for consumption

The investigation included kale, New Zealand spinach and spinach. The evaluation covered the raw material; the raw material after blanching; the raw material after cooking; and frozen products prepared for consumption after 0, 4, 8 and 12 months of refrigerated storage. Both the traditional method of freezing (blanching before freezing) and the modified method of freezing (cooked before freezing) were used in the experiment, as well as two storage temperatures, T = −20 °C and T = −30 °C. The content of chlorophylls in fresh kale was four times that in New Zealand spinach and 1.5 times that in spinach. With the exception of New Zealand spinach, blanching and cooking significantly reduced the content of chlorophylls. In kale products prepared for consumption, the content of chlorophylls decreased in each successive stage of the investigation. In products of New Zealand spinach and spinach, the losses were usually not significant. After 12 months of refrigerated storage, frozen kale products prepared for consumption retained 52–65% of total chlorophylls compared with the content in the raw material; products of New Zealand spinach and spinach retained 66–71%. In kale and New Zealand spinach, the content of chlorophyll a decreased more rapidly than that of chlorophyll b, while in spinach the converse was true. The kale products obtained using the modified method contained more chlorophylls, while in the two spinach species their content was lower. The lower storage temperature resulted in a higher retention of chlorophylls in vegetables.     

Influence of vegetable shortening and emulsifiers on the unfrozen water content and textural properties of frozen French bread dough

The influence of vegetable shortening (VS) and emulsifiers (calcium stearoyl-2-lactylate (CSL) and polysorbate 80 (PS80)) on frozen French bread dough has been studied. Eight formulations without yeast were used with different quantities of VS, CSL and PS80. Dough was prepared by mixing all ingredients in a dough mixer at two speeds. The fresh dough was divided into 60 g pieces and molded. Fresh dough samples were also collected for water content and textural analyses. The dough pieces were packed, frozen in a freezer at −30°C and stored at −18°C up to 56 days. After 2, 7, 21, 28 and 56 days of frozen storage, samples were removed from the freezer, thawed at ambient temperature and textural analyses were conducted.The enthalpy of freezable water on fresh bread dough was determined by Differential Scanning Calorimetry (DSC) at the heating rate of 3°C/min, temperature range of −40°C to 20°C. The value of unfrozen water was 0.30–0.34 g H₂O/g solids and additives used during the storage up to 56 days significantly affected the textural properties of frozen dough.     

Programmed Freezing Affects Texture, Pectic Composition and Electron Microscopic Structures of Carrots

Raw and blanched carrots (3 min, boiling water) were frozen at ?2°C, ?3°C, ?4°C or ?5°C/min (final ?20°C or ?50°C) then thawed at 20°C or 100°C. Firmness of thawed raw carrots was: ?5°C > ?4°C > ?3°C > ?2°C/min. Effect of freezing rate on blanched carrots was less than that on raw carrots, but firmness of thawed carrots was not affected by final temperature of freezing. When raw carrots were thawed at 20°C, high methoxyl pectin decreased. Pectin decrease in blanched carrots caused by freezing was greater than that in frozen raw carrots. Effects of slow-freezing, programmed-freezing (slow + quick + slow) and quick-freezing showed quick freezing (—5°C/min) best for texture. As freezing rate decreased, drip increased. A wide difference among experimental samples in fine structure was revealed by cryo-scanning electron microscopy.     

Effect of freezing conditions and storage on ice crystal and drip volume in turbot (Scophthalmus maximus): Evaluation of pressure shift freezing vs. air-blast freezing

Turbot fillets were frozen either by pressure shift freezing (PSF, 140 MPa, −14°C) or by air-blast freezing (ABF), and then stored at −20°C for 75 days. Smaller and more regular intracellular ice crystals were observed in fillets frozen by PSF compared with air-blast frozen ones. Ice crystals area in PSF samples was approximately 10 times smaller than that of ABF samples, on average. The PSF process reduced thawing drip compared with air-blast freezing. Conversely to this classical freezing process, the storage time did not adversely influence the thawing drip of PSF samples. In addition, PSF appeared to reduce cooking drip after 45 days of storage at −20°C. Differential scanning calorimetry analysis showed a significant reduction of the total enthalpy of denaturation for the pressure shift frozen samples compared to fresh and conventional frozen samples. Besides, a new melting transition appeared on the thermogram of PSF samples at approximately +40°C.     

Meat quality comparison between fresh and frozen/thawed ostrich M. iliofibularis

A pairwise comparison of the meat quality between fresh and frozen/thawed Musculus iliofibularis was conducted. Thirty-two (16 left; 16 right) muscles were collected and allocated to two treatments: fresh and frozen/thawed. Frozen vacuum-packed samples were stored for 1 month at -20°C before thawing. The fresh samples had higher pH (P<0.05), water binding capacity (P<0.05), CIE L* (P<0.0001), CIE a* (P<0.05) and Chroma values (P<0.05) than the frozen/thawed samples, indicating the fresh samples were bright red in appearance and had minimal exudate. The frozen/thawed samples lost 5.09±0.21% moisture during thawing and had a greater drip loss (P<0.0001) and shear force (P<0.001). No differences were obtained with regard to cooking loss, CIE b*, hue and TBARS. Protein oxidation (mM carbonyls/mg protein) was lower (P<0.05) in the frozen/thawed samples, which was attributed to the higher (P<0.0001) protein concentration negating the higher (P<0.001) carbonyl content. Industrial freezing and thawing regimes negatively affected the quality of ostrich meat.     

Novel assistive technologies for efficient freezing of pork based on high voltage electric field and static magnetic field: A comparative study

To enhance the freezing rate and thawed product quality of pork tenderloin, an experimental study was conducted using the high voltage electric field and static magnetic field separately during freezing. Pork tenderloin pieces were frozen at −20 °C under several high voltage electric fields (10 kV/m (HVEF1), 30 kV/m (HVEF3), 50 kV/m (HVEF5)) and magnetic fields of 2 mT (MF2), 4 mT (MF4), 6 mT (MF6) and 8 mT (MF8). The effects of different methods on freezing rate, ice crystal size as well as the distribution, and product quality after thawing were investigated. The freezing time of pork tenderloin was reduced by 40.04% and 37.81% respectively, under the optimal electric and magnetic field conditions tested. The thawing loss decreased from 5.7% of conventional freezing to 1.7% of HVEF1 and 2.4% of MF2, respectively. In addition, both high-voltage electric field freezing and magnetic field freezing can better maintain the moisture state in the sample. The results for color and pH confirmed that the thawed product quality using HVEF1 and MF2 was superior to that obtained under other conditions. The myofibrillar protein in the thawed products obtained from HVEF1 and MF2 treatments was also found to be thermally more stable. It is noteworthy that the HVEF1 treated sample has the highest umami signal and the lowest salty signal. Considering the enhanced freezing efficiency and improved quality, application of HVEF1 is recommended as a viable strategy to produce high-quality frozen pork tenderloin.Industrial relevanceThe slow freezing rate of frozen meat products and serious deterioration of product quality are the key problems. Therefore, improving the efficiency of freezing is desirable. This study provides ideas for pork preservation. It caters to the need of industrial production of meat product where better efficiency freezing process is highly desirable, and the findings of this study is beneficial to the meat processing industry.     

Protein changes in shrimp (Metapenaeus ensis) frozen stored at different temperatures and the relation to water-holding capacity

To study the effects of freezing temperature on muscle proteins, shrimp (Metapenaeus ensis) were frozen stored at either −18 or −60 °C up to 90 and 210 days. Shrimp frozen at −18 °C had higher thawing and compression loss and poor myofibril water-holding capacity compared with those frozen at −60 °C. In terms of protein characteristics, shrimp frozen at −18 °C had higher levels of carbonyls and reduced sulphhydryls. Moreover, the shrimp frozen at −18 °C had higher surface hydrophobicity and reduced Ca²⁺-ATPase activity, indicating increased protein denaturation. Proteomics revealed that seventy-five proteins were classified as differentially abundant proteins (DAPs) following freezing. There were sixty-four DAPs in the F18-CON comparison group (shrimp frozen at −18 °C vs. control) and thirty-two DAPs in the F60-CON comparison group (shrimp frozen at −60 °C vs. control), suggesting that freezing at −18 °C results in more DAPs than freezing at −60 °C. A comparison between F18 and F60 revealed that ribosomal proteins (L44, L7a) and heat shock protein 21 were downregulated in F18. These results increase our understanding of the variable quality associated with shrimp frozen at different temperatures.     

Effect of pretreatment and conditions and period of storage on some quality indices of frozen chive (Allium schoenoprasum L.)

Chive leaves for freezing contained 13.9 g dry matter, 133 mg vitamin C, 4.7 mg β carotene, 121 mg chlorophylls (a+b), 40.4 mg nitrates, and 0.19 mg nitrites in 100 g of edible parts. Blanching of the raw material before freezing reduced the level of dry matter by 22%, vitamin C 29%, β carotene 20%, chlorophylls 21%, and nitrates 26%, while that of nitrites increased three times. Freezing and 12-month storage of frozen material caused further losses in the analysed constituents except dry matter. Losses were distinctly higher on freezing non-blanched chive, a further enhancement of losses being observed with a storage temperature at −20°C. After a 12-month storage of frozen chive, the preserved content of vitamin C ranged from 11 to 66%, β carotene 37 to 65%, chlorophylls 65 to 75%, and nitrates 58 to 81%. If the blanching is omitted and the storage temperature is −20°C, a good preservation of vitamin C is not possible even for a period of 3 months. In contrast, the pretreatment of blanching ensures its good preservation at −20°C and at −30°C, and also yields a very good conservation of all the constituents analysed.     

Changes in optical and mechanical properties during osmodehydrofreezing of kiwi fruit

The influence of osmotic dehydration and freezing–thawing on optical (colour and translucency) and mechanical properties of kiwi slices were analysed. Osmotic treatments were carried out in sucrose solutions up till the soluble solids in kiwi fruit reached 30 °Brix, both at atmospheric pressure (OD) and by applying a vacuum pulse (PVOD). Analyses were carried out on fresh and dehydrated samples before and after frozen storage (at −18 °C for 1 and 30 days). Reflexion spectra (400–700 nm) were measured to obtain the Kubelka–Munk coefficients and CIE-L*a*b* colour co-ordinates. Mechanical properties were analysed through the compression test. A transparency gain was observed in PVOD treated samples and in frozen–thawed samples, which implied a reduction in product clarity and chrome. Colour hue did not change notably, due to either osmotic treatments or freezing. Samples treated with 45 °Brix osmotic solution at atmospheric pressure were the best preserved in mechanical properties after freezing–thawing.     

The effect of low-temperature blanching on the quality of fresh and frozen/thawed mashed potatoes

The effect of low‐temperature blanching (LTB) prior to cooking on colour, textural, firmness and oscillatory parameters, sensory attributes and overall acceptability of either fresh or frozen/thawed mashed potatoes was studied using response surface methodology (RSM) to establish the optimum temperature and time for blanching in both types of mashed potatoes. A central composite rotatable design was used to study the effects of variation in levels of blanching temperature (57.93–72.07 °C) and time (15.86–44.14 min) on the quality parameters. Stationary points showing maximum thickening had critical temperatures (approximately 67–69 °C) and times (approximately 26–30 min) in the ranges of temperature and time used for each independent variable for both fresh and frozen/thawed mashed potato. Results showed a high correlation between structural reinforcement and overall acceptability under optimum experimental blanching conditions. This demonstrates the potential of this experimental approach in terms of tailoring physical properties to predetermined levels in order to meet consumer preferences in mashed potatoes, and of altering the changes that occur after freezing and thawing.