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.     

Frozen Carrots Texture and Pectic Compotients as Affected by Low-Temperature-Blanching and Quick Freezing

Carrots preheated for 2 hr at 60°C and then cooked became firmer than raw or cooked carrots. After preheating, the amount of high methoxyl pectin decreased, and low methoxyl pectin increased. Firmness of carrots decreased through freezing then thawing, but preheated carrots retained firmer texture than those blanched in boiling water. Quick-freezing resulted in better texture than slow-freezing. Loss in texture was accompanied by release of pectin. Slow-freezing accelerated release of pectin as compared to quick-freezing. Preheated carrots were slower in release of pectin. The degree of esterification of pectin substances in raw carrots decreased during preheating, freezing and thawing. Cell damage in quick frozen carrots was slight. Optimum preheating occurred with 30 min at 60°C or 5 min at 70°C. Preheating and then quick freezing were effective in improving texture of frozen carrots.     

High-Pressure-Freezing Effects on Textural Quality of Carrots

Raw or 3 min blanched carrots were pressurized for 45 min at ?18°C ～–20°C and then thawed at 20°C. When carrots were frozen at 100Mpa (ice I), firmness decreased and strain increased. Textural values of carrots pressurized at 200MPa (liquid), 340MPa (ice III), 400MPa (ice V) at ca. –20°C were acceptable. When pressure was increased above 500MPa, the strain increased. Release of pectin and histological damage in carrots pressurized at 200, 340 and 400MPa were less than carrots frozen at 100 and 700MPa (ice VI). After pressurization at 200 and 340MPa at —20°C, carrots were stored in a freezer (–30°C). Firmness decreased and strain increased, but textural values were higher and histological structure were more intact than those frozen at –30°C (0.1MPa) then stored. Thus, high-pressure-freezing at 200, 340 and 400MPa appeared to be effective in improving both the texture and histological structure of frozen carrots.     

Structural and Textural Quality of Kinu-Tofu Frozen-then-Thawed at High-Pressure

To determine effects of high-pressure thawing on quality of high-pressure frozen tofu, kinu-tofu (soybean curd) was frozen 90 min at ca ?20°C at 100 MPa (ice I), 200 MPa (liquid phase), 340 MPa (ice III), 400, 500 or 600 MPa (ice V), then thawed at the same pressure. Texture and structure of this tofu (D) were compared with high-pressure-frozen tofu thawed at atmospheric pressure (A: 90 min frozen; B: 90 min frozen then 2 days at ?30°C; C: 160 min frozen). When tofu was frozen at 200- 500 MPa, ice crystals were largest to smallest in B > A and C > D; pore size of D was the same as untreated tofu. Results indicated ice crystals never grew when frozen at 200–500 MPa. Growth occurred during reduction of pressure at ca ?20°C, frozen storage or while thawing at atmospheric pressure due to phase transition.     

Pressure-shift freezing and its influence on texture,colour, microstructure and rehydration behaviour of potato cubes

Temperature changes during pressure-shift freezing (400 MPa) of potato cubes and its effects on the drip loss (weight and conductivity), texture (shear and compression tests), colour (L, a, b values), drying behaviour, rehydration properties (water uptake, texture after rehydration) and visible cell damage after thawing (micrographs) were investigated and compared with conventional freezing (0.1 MPa, -30 °C), subsequent frozen storage (-18 °C) or pressure treatment (400 MPa) at +15 :C. Pressure-shift freezing resulted in increased crystallization rates compared to conventional freezing at -30 °C. Crystallization and cooling to ?8 =C took 2.5 min during and after pressure release versus 17 min at atmospheric pressure. Drip loss was reduced from 12.0 to 10.8g/100g. Water uptake during 10 min of rehydration (93.9g/100g compared to 77.4g/100g and incomplete rehydration) and texture values were improved. Browning after thawing or after fluidized bed drying was reduced (increased a value, lower L value), suggesting partial enzyme inactivation during pressure treatment. Differences in colour and texture to the untreated controls were smaller after pressure-shift freezing than after conventional freezing. Cooling to ?30 °C after pressure-shift freezing did not significantly affect the results, whereas subsequent frozen storage at ?18 °C resulted in quality deterioration, as observed after frozen storage of conventionally frozen samples. The improved preservation of cell structure was demonstrated using scanning electron microscopy.     

Effect of Freezing of Beef on Subsequent Postmortem Aging and Shear Force

Seventy-two steaks were used to determine effects of freezing postrigor muscle on aging of meat and shear force. Steaks were removed from each carcass 24 hr postmortem and aged at 2°C for 2 or 6 days; or frozen at ? 30°C for 27 days, thawed 24 hr and aged 2 or 6 days at 2°C. After aging, steaks were cooked and shear force determinations made. Aging of meat reduced shear force values; however, meat aged after freezing had lower (P < 0.03) shear force values than meat aged before freezing. Meat cooked after freezing had greater (P < 0.05) cooking losses. Freezing enhances the aging process and improves shear values of meat.     

Freezing and Thawing Conditions Affect the Gel Stability of Different Varieties of Rice Flour

The freeze‐thaw stabilities of three different rice flour gels (amylose rice flour with 28% amylose, Jasmine rice flour with 18% amylose and waxy rice flour with 5% amylose) were studied by first freezing at –18 °C for 22 h and subsequent thawing in a water bath at 30 °C, 60 °C and 90 °C, or by boiling in a microwave oven. The freeze‐thaw stability was determined for five cycles. Starch gels thawed at higher temperature exhibited a lower syneresis value (percent of water separation) than those thawed at lower temperature. Amylose rice flour gels gave the highest syneresis values (especially at the first cycle). The Jasmine rice flour gels gave a higher syneresis value than the waxy rice flour gel. Except for freezing by storage at –18 °C and thawing at 30 °C, there was no separation of water at any cycle when waxy rice flour gel was thawed at any temperature, irrespectively of the freezing methods used. Cryogenic Quick Freezing (CQF) followed by storage at –18 °C and then thawing (by boiling or by incubation at any other temperatures) gave lower syneresis values than all comparable samples frozen by storage at –18 °C. The order of syneresis values for the three types of rice flour was waxy rice flour < Jasmine rice flour < amylose rice flour. The syneresis values and the appearance of starch gels, which had gone through the freeze‐ thaw process, suggested that the order of freeze‐thaw stability of gels for the three types of rice flour was waxy > Jasmine > amylose rice flour.     

Histological Changes in High-Pressure-Frozen Carrots

Histological changes in carrots frozen using a computer-programmed high pressure pilot unit for food processing were examined by light microscope. When raw carrots were frozen at 50 MPa, – 15°C; 100 MPa, –15°C; 150 MPa, –25°C; 200 MPa, –28°C, they were extremely damaged due to volume expansion by the formation of ice I. Conversely, carrots pressurized at 100 MPa, – 10°C (between liquid phase and ice I) and 200 MPa at –20°C (liquid phase) were not damaged because they were frozen rapidly during pressure reduction. They were not damaged even after pressurizing-then-immersing in LN₂. Carrots frozen at 240 MPa, –28°C and at 280 MPa, –25°C, were also not damaged, although ice III formed. The structure of carrots frozen at 400 MPa, –20°C (ice V) was comparatively intact. When carrots were preheated at 60°C for 30 min and frozen at 100 MPa, –15°C or at 400 MPa, –20°C, damage was reduced further.     

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     

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.     

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.     

Air thawing of beef quarters

An experimental study of thawing beef hind and forequarters of different weights in air has been made with respect to thawing time, weight loss, appearance and changes in bacterial numbers. From the experimental results a mathematical model and a computer programme have been developed to predict thawing times of quarters under other thawing conditions. Percentage weight losses varied from 1.2 when thawing at 5°C to 2.4 at 30°C. The appearance of quarters thawed at 5 and 10°C was satisfactory for normal use while a darkening of the lean and a drying out of thin sections made those thawed at 20 and 30°C only suitable for processing. The mean bacterial counts (expressed in logio/cm²) were always below 4.75 on quarters thawed at 5°C but they increased as the temperature of the thawing media was raised, means in excess of 7.0 being recorded on hindquarters thawed at 30°C.     

Freezing, thawing and cooking effects on quality profile assessment of green beans (cv. Win)

Results are presented of the effect of freezing followed by thawing (air and water immersion, both at environmental temperature) and cooking (traditional boiling in a covered pot) on quality profile (in terms of objective texture, colour, chlorophylls and pheophytins and sensory attributes) and structure of green beans (cv. Win). Freezing was carried out at three different rates by forced convection with liquid nitrogen vapour. Kramer shear cell (KSC) and Warner–Bratzler (WB) tests were used for objective assessment of the texture. The highest parameter values occurred in beans frozen at the highest rate and air-thawed at the slowest rate. Also, minimum alteration of the rheological behaviour of cooked beans was achieved by freezing at the highest rate. The best parameter for assessing the texture of frozen green beans after thawing and cooking was the Warner–Bratzler slope (S _WB). Coefficients of softening estimated for S _WB in the thawed beans showed that the texture of the beans frozen at −24 °C was almost four and almost five times softer than that of the beans frozen at −70 °C, for air and water thawing respectively. Frozen and thawed green beans were darker than fresh control, whereas freezing prior to cooking produced lighter-coloured beans than direct cooking. The freezing rate affected colour parameters differently depending on the process that followed. When beans were thawed, increasing the freezing rate produced lighter-coloured beans, whereas when beans were cooked, increasing the rate produced darker-coloured beans. No difference was found in sensory assessments between cooked samples frozen at −24 °C, −35 °C and −70 °C, which probably reflects the panellists' mixed preferences for quickly and slowly frozen samples. Scanning electron microscopy (SEM) revealed different degrees of mechanical damage to tissue structure, which accounted for the rheological behaviour of the beans.     

Growth of Salmonella serovars, Escherichia coli O157:H7, and Staphylococcus aureus during thawing of whole chicken and retail ground beef portions at 22 and 30 degrees C

Food regulatory agencies advise against thawing frozen meat and poultry at room temperature. In this study, whole chickens (1,670 g) and ground beef (453 and 1,359 g) were inoculated with Salmonella serovars, Escherichia coli O157:H7, and Staphylococcus aureus on the surface (all products) and in the center (ground beef). After freezing at -20 degrees C for 24 h, products were thawed at 22 or 30 degrees C for 9 h. Pathogen growth was predicted using product time and temperature data and growth values from the U.S. Department of Agriculture Agricultural Research Service Pathogen Modeling Program 7.0 predictive models of pathogen growth. No pathogen growth was predicted for whole chicken or 1,359 g of ground beef thawed at 30 degrees C or 453 g of ground beef thawed at 22 degrees C. Growth (< or = 5 generations) was predicted for 453 g of ground beef at 30 degrees C. Inoculation study data corroborated the predictions. No growth occurred on whole chickens or 1,359-g portions of ground beef thawed at 30 degrees C for 9 h. Pathogen numbers increased an average of 0.2 to 0.5 log on the surface of 453-g ground beef portions thawed for 9 h at 22 or 30 degrees C. Our results suggest that thawing > or = 1,670 g of whole chicken at < or = 30 degrees C for < or = 9 h and thawing >453 g ground beef portions at < or = 22 degrees C for < or = 9 h are not particularly hazardous practices. Thawing smaller portions at higher temperatures and/or for longer times cannot be recommended, however. Use of values derived from the Pathogen Modeling Program 7.0 model provided realistic predictions of pathogen growth during thawing of frozen ground beef and chicken.     

Differentiation of fresh and frozen/thawed fish, European sea bass (Dicentrarchus labrax), gilthead seabream (Sparus aurata), cod (Gadus morhua) and salmon (Salmo salar), using volatile compounds by SPME/GC/MS

BACKGROUND: A simple method based on solid phase microextraction/gas chromatography/mass spectrometry (SPME/GC/MS) was applied for studying the volatile profiles of whole fish samples of European sea bass (Dicentrarchus labrax) and gilthead seabream (Sparus aurata) and fillets of cod (Gadus morhua) and salmon (Salmo salar) during frozen storage in order to be able to differentiate a fresh product from one that has been frozen. Analysis of volatile compounds was performed on these two product types, fresh and after freezing/thawing following storage at ? 20 °C for 30 and 90 days. RESULTS: More than a hundred volatile compounds were found by SPME/GC/MS. Statistical processing by principal component analysis and ascending hierarchical classification was used to classify the samples into categories and verify the possibility of separating fresh samples from those that had been frozen and thawed. The compounds to be used as differentiators were identified. Four compounds were common to all species: dimethyl sulfide, 3‐methylbutanal, ethyl acetate and 2‐methylbutanal. Not only were they found in larger quantities after thawing but they also increased with the duration of storage at ? 20 °C. CONCLUSION: These four compounds can therefore be considered as potential markers of differentiation between a fresh product and one that has been frozen. Copyright © 2012 Society of Chemical Industry     

MECHANICAL PROPERTIES OF WEAK LOCUST BEAN GUM (LBG) GELS UNDER CONTROLLED RAPID FREEZE-THAWING

Locust bean gum (LBG) solutions and gels were studied in compression, and stress-relaxation was monitored by an Instron universal testing machine (UTM). The strength of the formed gels under freeze-thaw treatment was dependent upon the freezing and thawing rates and the temperature of freezing. LBG solution which froze at a rate of 50C/min was stiffer than those samples which froze at a rate of 1C/min. LBG solution thawed at a rate of 1C/min was stiffer than those samples which were thawed at 10C/min. Very high freezing rates may reduce the size of the formed ice crystals (less disturbance to network formation), while slow thawing may induce the favored gelation. LBG solutions frozen to -60C were stiffer than those frozen to -20C. A short holding time (up to 90 min) at the freezing temperature did not influence the strength of the cryogels. These parameters are important in building products which require a priori knowledge of their texture.     

Impact of frozen storage on polyacetylene content, texture and colour in carrots disks

This study investigated the effect of freezing method (slow or blast freezing) with or without blanching during storage at −20 °C on the levels of three polyacetylenes, falcarinol (FaOH), falcarindiol (FaDOH), falcarindiol-3-acetate (FaDOAc) in carrot disks. The quality of the carrot disks was also assessed using instrumental texture and colour measurements. Blast frozen carrot disks retained higher amounts of polyacetylenes compared to their slow frozen counterparts. Whilst the levels of retention of total polyacetylenes was higher in unblanched than blanched disks prior to freezing there was a sharp decrease in the levels of polyacetylenes in unblanched frozen carrots during the storage period for 60 days at −20 °C. FaDOH was observed to be the most susceptible to degradation during frozen storage of unblanched carrot disks, followed by FaOH and FaDOAc. The changes in the level of polyacetylenes during storage were adequately described by using Weibull model. The texture and colour were also found to decrease during frozen storage compared to fresh carrots.     

Cell Disruption in Broiler Breast Muscle Related to Freezing Time

SUMMARY— Cell disruption, resulting from different freezing times, was evaluated by studying the composition and amount of drip obtained from broiler breast muscles after freezing and thawing. The degree of cell disruption was estimated after measuring the amount of drip released and by total solids, nitrogen and deoxyribonucleic acid (DNA) concentration of the drip. Initial drip release was noted approximately 5% hr after the frozen meat was placed in a refrigerator at 16°C, and collections were made through the 18th hr. Degree of cell disruption was not uniformly related to changes in freezing times of 0.5 to 1,494 min. In general, increased freezing time resulted in greater cell disruption; however, several exceptions were noted. Cell disruption was relatively severe for tissues frozen in 18 to 35, 87, and 252 min, and relatively low for tissues frozen in times of 1 to 18 min, 132 to 22.5 min, and longer than 1,044 min. All frozen and thawed muscles had higher contents of total solids, nitrogen and DNA than unfrozen controls.     

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.     

Use of β-hydroxyacyl-CoA-dehydrogenase (HADH) activity to differentiate frozen from unfrozen fish and shellfish

 Further work on an enzymic method to differentiate frozen from unfrozen fish and shellfish is reported. The method is based on the release of the β-hydroxyacyl-CoA-dehydrogenase (HADH) from mitochondria during freezing. Enzymic activity was evaluated in fresh and frozen thawed samples from sole (Solea solea), sea bream (Pagellus centrodontus), hake (Merluccius merluccius), gilt headed bream (Sparus aurata), sea bass (Dicentrarchus labrax), salmon (Salmo salar), prawn (Penaeus japonicus) and Norwegian lobster (Nephrops norvegicus). Changes in the HADH activity of fresh and frozen thawed samples were compared after freezing at –196  °C for 15 min. Two values were obtained: U (by dividing: HADH activity of samples frozen at –196  °C, then thawed/HADH activity of unfrozen samples) and F (by dividing: HADH activity of samples frozen at –18  °C, thawed, then frozen at –196  °C /HADH activity of samples frozen at –18  °C, then thawed). Statistical analysis showed significant differences (P≤0.05) between both quotients for gilt headed bream, salmon, sea bream, sole and prawn, and an arbitrary limit was set at 2 to differentiate frozen thawed from unfrozen samples. The application of this limit made it possible to discriminate the unfrozen from the frozen thawed state of around 90% of the total samples analysed. Best results were obtained for prawn (100% of samples differentiated). In the present paper, a laboratory routine is proposed based on the comparison of the HADH activity of a sample analysed straight away and that of a sample frozen at –196  °C and then thawed. The reported method is simple and fast. The entire laboratory procedure can be performed in 45 min. Received: 20 July 1998 / Revised version: 2 November 1998