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.     

Effect of blanching,drying, freezing and storage on degradation of β-carotene in different fruits

Since biologically active carotenoids play a significant role in metabolism and because of the fact that its stability can be affected by various factors decomposition degree of β-carotene of various kinds of fruits after drying, freezing, blanching as well as after drying and freezing of blanched fruits has been researched in order to prolong their consumption time-limit. The β-carotene content was determined by means of the spectrophotometric method measuring adsorbance intensity at 450 nm. The results of investigation reveal that the decomposition degree of β-carotene increases significantly with storage time. Depending on the kind of fruits, treatment and storage time it ranged from 6.10% to 68.74%. No significant differences have been found after a longer storage between blanched and non-blanched fruits, either dried or frozen.     

Effect of high-pressure induced ice I/ice III-transition on the texture and microstructure of fresh and pretreated carrots and strawberries

The effect of pressure treatments at −25 °C between 150 and 300 MPa, indicated as high-pressure induced crystallization (HPIC) processes if formation of ice III occurs during pressurization, on the texture and structure of frozen strawberries and carrots were studied. The formation of ice III, which has been proven to inactivate the microbial load of a frozen food, occurred when pressure was increased to 250 MPa or higher. Volume changes related to the formation of ice III affected the cell wall integrity of infused frozen strawberries and caused a 42–46% reduction of the fruit’s hardness. These textural and structural changes were not affected by the pressure holding time (30 s versus 10 min), and thus by partial thawing during the pressure holding time, and were absent in frozen fruits treated at pressures lower than 250 MPa. The structure and texture of frozen carrots were respectively not and only slightly altered during high-pressure–low-temperature (HP–LT) treatments at all pressure levels studied. However, if carrots were blanched (30 min at 60 °C, 2 min at 90 °C and a combination of both) prior to freezing, structural damages during pretreatment and freezing made the tissue, in terms of both structural and textural quality, unsuitable for a post-freezing HP–LT treatment. These observations should be taken in mind when analyzing the possibilities of HPIC processes as a tool for post-freezing microbial reduction when applied to tissue based systems.     

The effects of antifreeze proteins on chilled and frozen meat

The effects of cryoprotectant proteins, trivially termed ‘antifreeze proteins’, from the Antarctic Cod and the Winter Flounder were assessed in meat during chilling and freezing. In light-microscopy studies, bovine muscle (Sternomandibularis) samples were soaked in phosphate buffered saline with and without 0·1 mg/ml antifreeze protein. Samples were then held frozen (−20°C) or chilled (2°C) for 3 days. Samples were freeze-substituted, embedded in resin and sectioned. With antifreeze protein present, transverse sections of frozen samples had many small intracellular spaces, probably representing ice crystals. Frozen controls had much larger intracellular single spaces. Antifreeze protein had no effect on chilled samples.

Similarly treated samples were examined by scanning electron microscopy using a cryostage attachment. Chilled ovine muscle samples (Peroneus longus) were soaked for various periods (0–7 days) in 0·9% saline containing various concentrations of antifreeze proteins (0–1 mg/ml). Samples were then held frozen (−20°C) or chilled (2°C) for 5 or 7 days. With frozen samples, antifreeze proteins reduced the size of ice crystals, compared to the control. This effect depended upon the concentration used and the period of soaking before the samples were frozen, but was independent of source. Antifreeze proteins had no effect on chilled samples.     

Effects of freezing, thawing and storage on some quality factors for portion-size beef cuts

Portion-size beef cuts packaged in oxygen impermeable plastic bags were used to study the effects of rates of freezing and thawing, and storage time and temperature on drip and cooking losses, shear force, destruction of glutathione and accumulation of protein-breakdown products in meat. Portions weighing 150 g or over and frozen in an air-blast at −30°C gave lower losses of drip and lower amounts of nitrogenous constituents in drip than samples weighing less than 150 g or samples frozen in cardboard boxes in still air at −18°C. Freezing and thawing or frozen storage had no significant effect on shear force of meat frozen after ageing. During frozen storage, the destruction of glutathione and accumulation of protein-breakdown products increased, depending directly on storage temperature and time. The results show that a test based on these two biochemical changes would be suitable for assessing the quality of frozen beef.     

Calpains from thaw rigor muscle

Pre-rigor beef M. Longissimus lumborum and diaphragma were frozen at −70 °C and thawed at different temperatures and the activities of extracted calpains and the toughness of heated meat compared with those in chilled muscle.

Fresh muscle contained about 14 μg of μ-calpain/g and was unaffected by freezing, but was reduced after thawing. Rapid thawing at 30 °C for 20 min reduced the μ-calpain to 14%. When cooked from the frozen state, extensive shortening occurred and tender meat was obtained.

By storing at −3 °C for 1 day, thaw-shortening was prevented, but tougher meat obtained. The μ-calpain decreased to 70% whilst the m-calpain was unaffected. Toughness decreased after further storage at −3 °C, as did the μ-calpain. The latter changes were similar to those during development of rigor mortis and ageing of non-shortened meat stored at 4 °C. Variation in calpain activity, rather than in sarcomere length, are likely to be the cause of toughness variation in thaw rigor muscle.     

The extractable β-carotene content of Guku (Bidens pilosa) leaves after cooking, drying and storage

Summary  The β-carotene content of young tender leaves of Guku (Bidens pilosa ) was found to be 64 μg g^-1 in fresh samples. The extractable β-carotene content of Guku leaves boiled for 20 min was 31% greater than that in leaves blanched for 1 min. Boiling for up to 60 min resulted in a 6% decrease of β-carotene compared with the concentration in blanched leaves. Drying in the sun and in the shade resulted in losses of β-carotene of 92% and 93% respectively. After 6 days of refrigeration of unblanched leaves, about 38% of the β-carotene was lost. There was no appreciable change in the levels of β-carotene after the blanched leaves had been kept frozen at -18C for 5 weeks. Blanched mature leaves had 62% more β-carotene than young leaves.     

Relationship between heat transfer parameters and the characteristic damage variables for the freezing of beef

One of the most suitable parameters for relating the freezing rate to the volume of drip produced during the thawing of meat is the characteristic time, defined as the time necessary to reduce the temperature of the sample from −1·1°C (initial freezing point in beef) to −7°C (80% of the water frozen).

However, as the freezing of beef in factories takes place with important temperature gradients, distributions of these characteristic times must be expected along the pieces of frozen meat.

In order to relate these characteristic time distributions to heat transfer parameters under industrial freezing conditions, a mathematical model which simulates the freezing of beef is developed in this paper.

The model establishes the heat transfer equations with simultaneous change of phase, taking into account the dependence of the thermal properties with the ice content and considering the anisotropy of the thermal conductivity according to the direction of the fibres.

Boundary conditions include the possibility of thermal resistances in the refrigerated interphase.

The model developed was compared with laboratory experiments performed under factory freezing conditions and showed a satisfactory agreement between theory and experiment.     

Conventional freezing plus high pressure-low temperature treatment: Physical properties, microbial quality and storage stability of beef meat

Meat high-hydrostatic pressure treatment causes severe decolouration, preventing its commercialisation due to consumer rejection. Novel procedures involving product freezing plus low-temperature pressure processing are here investigated. Room temperature (20 °C) pressurisation (650 MPa/10 min) and air blast freezing (−30 °C) are compared to air blast freezing plus high pressure at subzero temperature (−35 °C) in terms of drip loss, expressible moisture, shear force, colour, microbial quality and storage stability of fresh and salt-added beef samples (Longissimus dorsi muscle). The latter treatment induced solid water transitions among ice phases. Fresh beef high pressure treatment (650 MPa/20 °C/10 min) increased significantly expressible moisture while it decreased in pressurised (650 MPa/−35 °C/10 min) frozen beef. Salt addition reduced high pressure-induced water loss. Treatments studied did not change fresh or salt-added samples shear force. Frozen beef pressurised at low temperature showed L, a and b values after thawing close to fresh samples. However, these samples in frozen state, presented chromatic parameters similar to unfrozen beef pressurised at room temperature. Apparently, freezing protects meat against pressure colour deterioration, fresh colour being recovered after thawing. High pressure processing (20 °C or −35 °C) was very effective reducing aerobic total (2-log₁₀ cycles) and lactic acid bacteria counts (2.4-log₁₀ cycles), in fresh and salt-added samples. Frozen + pressurised beef stored at −18 °C during 45 days recovered its original colour after thawing, similarly to just-treated samples while their counts remain below detection limits during storage.     

Effect of β-carotene on vitamin A light stability in fortified milk

The effect of incorporation of β-carotene into the carrier system on the light stability of all-trans retinyl palmitate in fortified skim milk was investigated. Skim milk was fortified with all-trans retinyl palmitate using corn oil with and without added β-carotene as the vitamin carrier. Two levels of β-carotene were used, one similar to, the other half the concentration of vitamin A in the carrier system. After homogenization and pasteurization, fortified milk samples were exposed to fluorescent light (1614 lx) at 4°C in glass tubes.

Less light degradation of all-trans retinyl palmitate occurred in samples containing added β-carotene in the carrier systems compared to samples without added β-carotene. The β-carotene content of fortified milk samples showed only a slight decrease over the four-day period of exposure.     

Rapid freezing, frozen storage and the tenderness of lamb

Cold-shortening in pre-rigor lamb can be prevented by freezing carcasses very rapidly in less than four hours. Thaw-shortening can also be prevented by storing the carcasses for a period (> 10 days) in the frozen state (− 12°C). By this simple combination of rapid freezing and frozen storage, the hazard of toughness development from cold- and thaw-shortenings is avoided.     

Supercooling capacity of Tineola bisselliella (Hummel) (Lepidoptera: Tineidae): Its implication for disinfestation

The variations in weight, water content and supercooling point (SCP) were studied in Tineola bisselliella at different stages in its development.

The egg, with a fresh weight of 0.037 mg and a water content of 314% of the dry weight, is the stage most resistant to freezing with an SCP of −23 °C. The young larva (second instar), with a fresh weight of 2.5 mg and a water content of 145% of the dry weight, is the least resistant stage with an SCP of −13 °C. Despite the large differences in weights and water contents between males and females, they have the same SCP value of −19 °C.

Because of the large individual variations observed in this species, it appears necessary to treat infested materials with a temperature lower than or equal to −29 °C to destroy all stages of development promptly.     

Definition of the optimum freezing rate-1. Investigation of structure and ultrastructure of beef M. longissimus dorsi frozen at different freezing rates

The influence of freezing rate on location, shape and size of ice crystals formed during freezing of beef M. longissimus dorsi, as well as its influence on ultrastructure, were investigated. Muscle samples were frozen at different rates: 0·22 cm/h and 0·39 cm/h (cooling agent was chilled air), and 3·33 cm/h, 3.95 cm/h, 4·92 cm/h and 5·66 cm/h (cooling agent was liquid carbon dioxide which expanded in the sucking-pipe of the tunnel freezer).

It was found that by slow freezing (freezing rates 0·22 cm/h and 0·39 cm/h) 30·00 μm). An increase in the freezing rate was followed by a change in ice crystal location. In this case they had also been formed intracellularly. The number of crystals increased while their size decreased.

The most intensive fibre damage was found in samples frozen at a rate of 0·22 cm/h, and the least in samples frozen at a rate of 3·95 cm/h with a freezing temperature of −50°C.     

Effect of freezing and canning on the content of selected vitamins and pigments in seeds of two grass pea (Lathyrus sativus L.) cultivars at the not fully mature stage

Seeds of the grass pea (Lathyrus sativus L.) cultivars Derek and Krab, with a dry matter content of about 33%, were used for freezing and for canning. The content of vitamins C, B1, and B2 and of carotenoids, beta-carotene, and chlorophylls was determined in raw and blanched material, in frozen products after 6-month storage before and after cooking to consumption consistency, and in canned products after 6-month storage. In comparison with the cultivar Krab, raw seeds of Derek contained 45% more vitamin C, 14% more total chlorophylls, 13% less thiamine (vitamin B1), and 7% less riboflavin (vitamin B2). The level of carotenoids was similar. Blanching of seeds led to a statistically significant decrease only in the content of vitamin C. Freezing and frozen storage significantly lowered the level of vitamin C and chlorophylls. The cooking of frozen seeds and the production of canned products and their storage resulted in a statistically verified reduction in the content of components analysed in all the samples. Greater losses were found in products prepared from seeds of the cv. Krab. After cooking, frozen seeds contained more of all the analysed components than the canned products.     

Application of multi-component biopolymer layers to improve the freeze–thaw stability of oil-in-water emulsions: β-Lactoglobulin–ι-carrageenan–gelatin

This study examines the influence of interfacial composition on the freeze–thaw stability of oil-in-water emulsions. Three 5% w/w oil-in-water emulsions (5 mM phosphate buffer, pH 6.0) were prepared using the layer-by-layer electrostatic deposition method that had different interfacial compositions: (i) primary emulsion (β-Lg); secondary emulsion (β-Lg–ι-carrageenan); (iii) tertiary emulsion (β-Lg–ι-carrageenan–gelatin). The primary, secondary and tertiary emulsions were subjected to from one to three freeze–thaw cycles (−20 °C for 22 h, +40 °C for 2 h) in the absence or presence of sucrose (10% w/w), and then their stability was assessed by ζ-potential, particle size, microstructure and creaming stability measurements. In the absence of sucrose, the primary and secondary emulsions were highly unstable to droplet aggregation and creaming after three freeze–thaw cycles, whereas the tertiary emulsion was stable, which was attributed to the relatively thick biopolymer layer surrounding the oil droplets. In the presence of 10% w/w sucrose, all of the emulsions were much more stable, which can be attributed to the ability of sucrose to increase the amount of non-frozen aqueous phase in the emulsions. The interfacial engineering technology used in the study could therefore lead to the creation of food emulsions with improved stability to freezing and thawing.     

Effects of freezing on the pigment content in green beans and padrón peppers

 The amounts of chlorophylls a and b, β-carotene and lutein in green beans, blanched green beans and Padrón peppers, all frozen at −22 °C, were monitored over 12 months by reverse-phase, gradient HPLC (C18 column, visible detection). In unblanched beans, these amounts of the pigments decreased considerably during month 1, but were generally stable during the next 11 months (β-carotene content decreased further in month 2 before stabilizing). Similar results were obtained for blanched beans, but decreases were offset by increases due to blanching (carotenoids) and lipoxygenase deactivation (β-carotene), or enhanced by blanching-induced decreases (chlorophylls). In contrast, the amounts of pigments in frozen Padrón peppers fluctuated around more or less constant values over the 12 months. Freezing in bags sealed under vacuum lead to moderate decreases in chlorophyll a in Padrón peppers and in β-carotene in blanched green beans. Received: 22 July 1996 / Revised version: 4 December 1996     

Definition of the optimal freezing rate-2. Investigation of the physico-chemical properties of beef M. longissimus dorsi frozen at different freezing rates

The influence of freezing rate on weight loss during the freezing, thawing and cooking, on water-binding capacity, on sensory and other physico-chemical properties of beef M. longissimus dorsi was investigated. The changes in myofibrillar proteins in muscle samples frozen at different freezing rates were also investigated.

The greatest weight losses during the freezing, thawing and cooking were registered at slow freezing procedures (freezing rate of 0·22 cm/h and 0·29 cm/h), when the meat was tougher and less soft. The solubility of myofibrillar proteins was least from those muscles frozen at such freezing rates.

The freezing of samples at freezing rates of 3·33 cm/h and 3·95 cm/h had less influence on their physico-chemical characteristics. The solubility of the myofibrillar proteins from such samples was greatest, and the cooked samples were the most tender.

From analysis of the results it was concluded that optimal conditions for meat freezing seem to be those when the average freezing rate is 2–5 cm/h.     

Effects of blanching and sulphur dioxide on ascorbic acid and pigments of frozen capsicums

The frozen storage of capsicum tissue for 1 year at −12°C resulted in appreciable losses (from 10 to 58%) of ascorbic acid dependent upon the cultivar and the extent of tissue blanching. Ascorbic acid retention was maximal, but retention of chlorophyll a was minimal and pH dependent, in frozen blanched tissue which accordingly showed a greater increase in pheophytin formation. Sulphite treatment of unblanched tissue maintained acceptable colour through retardation of degradative interconversion and isomerization reactions of chlorophyll and carotenoid pigments during frozen storage.     

Nitrites, nitrates and N-nitrosoamines in Estonian cured meat products: Intake by Estonian children and adolescents

The contents of nitrate, nitrite and N-nitrosoamines in commercial cured meat products on the Estonian market were determined for 2000-01 and 2003-04 as part of the Estonian food safety monitoring programme and the Estonian Science Foundation grant research activities. The maximum permitted levels of residual nitrites and nitrates were not exceeded in the samples analysed. However, a great variation in the content of nitrate, nitrite and N-nitrosoamines was found for all the products. The concentrations of these compounds in domestic cured meat products showed a decrease from year to year. The mean intake of nitrate, nitrite and N-nitrosoamines by Estonian children (n = 346) from cured meat products was calculated on the basis of individual intake data. The mean daily intake of nitrates was 1.7 mg, that of nitrites was 0.83 mg and that of N-nitrosoamines was 0.073 µg. In the 2000-01 study, the calculated nitrite intake exceeded the acceptable daily intake by up to 140% for 1-6-year-old children and up to 105% in 2003-04.