Textural and Microstructural Changes in Frozen Stored Sardine Mince Gels

The freezing of sardine mince gels produced slight alterations in texture, microstructure and degree of chemical aggregation of proteins, irrespective of freezing temperature (– 18°C or – 40°C). The most noticeable changes took place during frozen storage 3 mo, particularly in gels frozen at – 18°C which were strongly affected by storage temperature (– 12°C or – 18°C), unlike those frozen at – 40°C. Better gel integrity was found in those frozen at – 40°C, where cavities were more numerous, but smaller and more evenly distributed than in gels frozen at – 18°C.     

High pressure-induced tapioca starch gels: physico-chemical characterization and stability

Gelatinization of tapioca starch (25% dry basis) was induced by high hydrostatic pressure processing (HPP) at 600 MPa under different time and temperature regimes (30 °C for 10, 20 and 30 min; 50 °C for 10 min; 80 °C for 10 min). Textural, thermal and structural properties of the gels were studied and their stability was evaluated after 28 days of refrigerated (4 °C) and frozen (−18 °C) storage. Thermally induced gels (90 ± 1 °C, 20 min, gel-T) were used as controls. HPP resulted in the formation of harder gels than thermal processing (more significantly at lower processing temperatures) partially preserving the granular structure of the native starch. Longer HPP treatments caused only a slight decrease in hardness that was significant only at longer processing times (30 min). DSC thermograms of high pressure-induced samples showed a more asymmetrical ice-melting peak than that of thermally induced gels. Asymmetry of the peak of HP treated samples was more pronounced in samples processed at lower than at higher temperature. A different starch–water and/or starch/starch interaction may be hypothesized. During storage, all samples became stiffer and the amylopectin recrystallization increased, more extensively in thermally induced than in HPP samples where a stronger starch–starch and/or starch/water interactions may have hindered the recrystallization process.     

Changes in Electrophoretic Patterns of Gadoid and Non-gadoid Fish Muscle during Frozen Storage

Sodium dodecyl sulfate polyacrylamidc gel electrophoresis of fish muscle during frozen storage showed that a crosslinked protein of 280,000 daltons formed with gadoids, whereas this band did not occur with non-gadoid fish species. For cod, 20 days at -7°C are needed for the crosslink to appear, whereas for whiting only 3 days arc needed. Formaldehyde (FA) may be responsible for the crosslinking. Adding ascorbic acid to cod mince prior to freezing accelerated dimcthylamine and FA formation during frozen storage and accelerated the formation of the crosslinked protein, while leaving cod fillets on ice for 10 days prior to freezing, reduced the Instron hardness and the crosslinked protein did not appear with 50 days of frozen storage at -7°C.     

Effect of temperature fluctuations during frozen storage on the quality of potato tissue (cv. Monalisa)

 Results are presented on the effect of different ranges of temperature fluctuation (–24 to –18°C, –18 to –12°C, –12 to –6°C, –24 to –12°C and –18 to –6°C) on the compression, shear and tension parameters of packed and unpacked frozen potato tissue. The initial temperature, duration and number (2, 4, 8, 16, 24 and 32) of fluctuations were varied. The highest parameter values occurred in samples subjected to fluctuations between –24°C and –18°C, and the lowest values in the range –18 to –6°C. The mechanical strength of the frozen tissue decreased with an increase in the number of fluctuations and in most cases was lower in the packed samples. Moisture loss was greatest in the –18 to –6°C range for pre-packed samples. Changes in the maximum compression force, as a measure mechanical damage, showed the greatest level of significance. Received: 17 June 1997     

Effect of temperature fluctuations during frozen storage on the quality of potato tissue (cv. Monalisa)

 Results are presented on the effect of different ranges of temperature fluctuation (–24 to –18°C, –18 to –12°C, –12 to –6°C, –24 to –12°C and –18 to –6°C) on the compression, shear and tension parameters of packed and unpacked frozen potato tissue. The initial temperature, duration and number (2, 4, 8, 16, 24 and 32) of fluctuations were varied. The highest parameter values occurred in samples subjected to fluctuations between –24°C and –18°C, and the lowest values in the range –18 to –6°C. The mechanical strength of the frozen tissue decreased with an increase in the number of fluctuations and in most cases was lower in the packed samples. Moisture loss was greatest in the –18 to –6°C range for pre-packed samples. Changes in the maximum compression force, as a measure mechanical damage, showed the greatest level of significance. Received: 17 June 1997     

Kinetics of softening of potato tissue by temperature fluctuations in frozen storage

 Pre-packed and unpacked potato tissues were frozen, subjected to temperature fluctuations and then thawed. Temperature fluctuations ranged from –24  °C to –18  °C and from –18  °C to –6  °C. The number of fluctuacions ranged from 0 (that is to say, only freezing and thawing processes) to 32 at each above fluctuation range, simulating practical frozen storage conditions. Compression, shear and tension tests were carried out to measure the extent of structural damage caused to the potato tissue. Plots of log (rheological parameters and moisture content) versus number of temperature fluctuations showed two distinct regions; the first was a rectilinear plot with a steep negative slope up to four fluctuations. The second was also a rectilinear plot with a shallow negative slope beyond four fluctuations. For higher number of fluctuations, most of rheological parameters reached a value almost constant. These two-stage softening rate curves are consistent with the biphasic model and qualitatively similar to those for thermal softening of the vegetables. This study shows that two substrates S_a and S_b may be involved in providing firmness to potato tissue in freezing and frozen storage conditions. By analogy with earlier works, the term "frozen storage firmness" can be proposed to describe the amount of firmness that is resistant to degradation by freezing with temperature fluctuations during frozen storage and final thawing of the product. Received: 30 April 1999     

Effects of Hydrolysates from Silver Carp (Hypophthalmichthys molitrix) Scales on Rancidity Stability and Gel Properties of Fish Products

This study aimed to evaluate the effectiveness of hydrolysates, which were obtained from the scales of silver carp (Hypophthalmichthys molitrix) by papain, flavourzyme, and Alcalase 2.4 L, as natural antioxidants in silver carp mince and surimi gels during storage at 4 °C. The hydrolysates that possess greater in vitro antioxidant activities (DPPH radical-scavenging activity, Fe²⁺-chelating activity, and reducing power), including hydrolysates catalyzed by papain at 10 min (HP), flavourzyme at 5 min (HF), and Alcalase 2.4 L at 5 min (HA), were chosen as additives. Color, cooking loss, conjugated dienes (CDs), thiobarbituric acid reactive substances (TBARS), fatty acids, and sensory scores of mince were measured on days 0, 2, 4, 6, and 8 during 4 °C storage; additionally, whiteness, breaking force, deformation, gel strength, and sensory score of surimi gels were measured on days 1, 3, 5, 7, 9, and 11 during 4 °C storage. The results indicate that HA was conducive to lowering the cooking loss of mince and that HF significantly (P?<?0.05) reduced the CDs value of mince. For surimi gels, HF improved whiteness, deformation, and gel strength. Hence, HF could serve as a natural antioxidant during early oxidation and improve gel formation of silver carp products.     

Original article: Gel properties of red tilapia surimi: effects of setting condition,fish freshness and frozen storage

This study aimed to determine effects of setting condition, fish freshness and storage time of frozen surimi on properties of red tilapia surimi gel. To investigate the effect of setting condition, a combination of eight setting temperatures (35–70 °C) and four setting times (30–120 min) was used. Maximum breaking force, deformation and gel strength were obtained after the gel had been set at 40 °C for 90 or 120 min. Setting at 65 °C resulted in the lowest obtained gel strength, because of proteolytic degradation of myosin heavy chain. Increasing storage time of raw fish material in ice caused a significant decrease in gel strength of the resultant surimi gel (P < 0.05). Gels produced from surimi kept in frozen storage for up to 9 months also exhibited reduced gel strength, with a concomitant increase in the expressible drip, with increasing storage time (P < 0.05).     

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.     

Determining Washing Conditions During the Preparation of Frozen Surimi from Surubí (Pseudoplatystome Coruscans) Using Response Surface Methodology

The effect of process temperature (2 to 18 °C), time (1 to 7 min/ cycle), and water‐mince ratio (2:1 to 8:1) on the quality attributes of surubí (Pseudoplatystoma coruscans) surimi was studied using Response Surface Methodology (RSM). Conditions were identified that allowed to achieve 25% of extracted proteins and a moisture content of 79%, compatible with an acceptable quality of surimi gel. The verification of the prediction models was acceptable. Two cryoprotectant mixtures (sucrose‐sorbitol and maltodextrin‐sorbitol) were also evaluated, with regard to the freezing and frozen storage and the functional quality of the gels. Freezing proved to be an aggressive method, and the 2 mixtures tested showed to be efficient for 6 months of frozen storage.     

Impacts of Low and Ultra-Low Temperature Freezing on Retrogradation Properties of Rice Amylopectin During Storage

Amylopectin retrogradation is a serious problem in starch-based ready meals. In the current research, rice amylopectin was frozen by low temperature (−20, −30, and −60°C) and ultra-low temperature (−100°C), and then stored at 4°C for 21 days or at −18°C for up to 5 months to evaluate the retrogradation properties. Amylopectin retrogradation enthalpy of rice was determined by a differential scanning calorimetry. The results showed that low temperature and ultra-low temperature freezing can effectively retard amylopectin retrogradation during the freezing process and during frozen storage (−18°C) for at least 5 months. However, rice amylopectin still retrograded after the freezing process during chill storage at 4°C. The methods of low and ultra-low temperature freezing combined with frozen storage might be potentially very useful for food industry to produce high quality starch-based ready to eat meals.     

Improvement of Gelling Properties of Lizardfish Mince as Influenced by Microbial Transglutaminase and Fish Freshness

ABSTRACT:  The effects of microbial transglutaminase (MTGase) at different levels (0 to 0.8 units/g sample) on the properties of gels from lizardfish ( Saurida undosquamis ) mince set at 25 °C for 2 h or 40 °C for 30 min prior to heating at 90 °C for 20 min were studied. Breaking force and deformation of gels increased with increasing MTGase amount added ( P < 0.05). At the same MTGase level used, gels with the prior setting at 40 °C for 30 min showed a higher breaking force compared with those subjected to prior setting at 25 °C for 2 h ( P < 0.05). Sodium dodecyl sulfate-polyacrylamide gel electrophoretic study revealed that myosin heavy chain (MHC) underwent polymerization to a higher extent in the presence of MTGase. Regardless of setting condition, microstructure of gel added with MTGase was finer with a smaller void compared with that of gel without MTGase. Therefore, setting temperature affected the property of gels added with MTGase. Gel properties of mince obtained from lizardfish stored in ice for different times (0 to 10 d) with and without MTGase at a level 0.6 units/g were determined. Irrespective of MTGase addition, breaking force and deformation of all gels decreased as the storage time of lizardfish increased ( P < 0.05). The addition of MTGase was able to increase both breaking force and deformation of the resulting gel produced from lizardfish kept in ice for all storage times used. Therefore, both freshness and MTGase addition had the direct impact on gel properties of lizardfish mince.     

Principal component analysis to study the effect of temperature fluctuations during storage of frozen potato

 The effects of temperature fluctuation ranges, number of fluctuations carried out, and packaging during frozen storage on the texture of potato tissue in terms of compression, shear, and tension rheological parameters were assessed through data generated according to a factorial design using principal component analysis (PCA). Five ranges of fluctuation (–24  °C to –18  °C, –18  °C to –12  °C, –12  °C to –6  °C, –24  °C to –12  °C and –18  °C to –6  °C) applied 2, 4, 8, 16, 24, and up to 32 times on unpacked and pre-packed frozen potatoes, were considered. The controls were unpacked and prepacked frozen tissues thawed immediately without undergoing any fluctuation. In addition, several geometrical, technological, and chemical parameters were determined. PCA showed that maximum shear force, F_s was the best rheological parameter for differentiation of the structural damage and softening occurring in the tissue at each treatment, which was closely related to its duration, TT _d . PCA did not permit complete discrimination between the five fluctuation ranges, but it clearly separated samples subjected to –18  °C/–6   °C from those subjected to –24  °C/–18  °C. Frozen samples undergoing up to four fluctuations formed a separate cluster from those undergoing a higher number. Analysis also clearly separated unpacked from pre-packed samples in response to slower freezing rates reached in the latter. Received: 17 December 1999     

Frozen Storage of Unwashed Cod (Gadus morhua) Frame Mince with and without Kidney Tissue

Removal of kidney material was essential for a higher quality cod frame mince. The removal of kidney tissue before deboning eliminated typical “chemical” and “petroleum” type flavors and resulted in a white, less red, and higher quality unwashed frame mince. Those samples without kidney tissue had good frozen storage stability, (particularly at -40°C) and could be used as an ingredient in apropriate meat products. The length of iced storage of frames or whole cod had little effect on frame mince quality during frozen storage.     

Interactions and gel strength of mixed myofibrillar with soy protein, 7S globulin and enzyme-hydrolyzed soy proteins

The mixed protein gels were prepared adding soy protein isolate (SPI), 7S globulin, enzyme-hydrolyzed soy proteins, 10- to 100-kDa ultrafiltration fraction and 0.5- to 10-kDa ultrafiltration fraction to myofibril protein isolate (MPI) gels, and five chemical interactions namely nonspecific associations, ionic bonds, hydrogen bonds, hydrophobic interactions and disulfide bonds in these gels were investigated by means of determining gel solubility within 20–75 °C. Furthermore, correlations between gel strength and different chemical interactions were evaluated statistically by Pearson’s correlation test. The gels with 0.5- to 10-kDa fraction presented the biggest gel strength below 60 °C, and the gels with SPI had better gel strength above 65 °C. At different endpoint temperatures, nonspecific associations decreased in order of MPI mixed with 0.5- to 10-kDa fraction, 10- to 100-kDa fraction, enzyme-hydrolyzed soy proteins, 7S globulin and SPI. Gels with ultrafiltration fractions had higher ionic bonds. Hydrogen bonds fluctuated in small scale below 55 °C and reduced at higher temperature. Hydrophobic interactions increased to maximum before decreasing slowly as the temperature went on. In short, both hydrophobic interactions and ionic bonds had significantly positive correlation with gel strength for mixed gels with enzyme-hydrolyzed soy proteins, whereas for the other four mixed gels, it was hydrophobic interactions and nonspecific associations.     

Frozen storage of high-pressure- and heat-induced gels of blue whiting (Micromesistius poutassou) muscle: rheological, chemical and ultrastructure studies

This paper examines the influence of frozen storage over 34 weeks on the rheological properties as well as the chemical and microstructural characteristics of gels made from muscle of blue whiting (Micromesistius poutassou) subjected to different gelling treatments entailing three combinations of pressure, temperature and time: 200 MPa, <10°C, 10 min (lot L), 375 MPa, 38°C, 20 min (lot H) and atmospheric pressure, 37°C, 30 min and then 90°C, 50 min (lot T). Freezing at –40°C caused certain changes in rheological parameters. In heat-induced gels, breaking deformation, elasticity and cohesiveness increased. Of the high-pressure-induced gels, breaking force increased and cohesiveness decreased in the gel formed at lower pressures, while the only change in the gel formed at higher pressure was some loss of elasticity. There was a general fall in water holding capacity (WHC) values. Lightness remained stable. In terms of protein solubility, there was an increase in covalent bonds in lot L. As for the ultrastructure, all gels matrixes were more disorganized as a result of freezing. In the course of frozen storage, the greatest changes in rheological parameters generally took place during the first 8 weeks, and in all the gels there was a decrease in WHC. In the heat-induced gel the changes were less marked over the storage period compared with those in the high-pressure-induced gels, but the heat-induced gel was more brittle and did not maintain maximum folding test scores. Covalent bonds increased and hydrophobic interactions decreased in all lots. The general appearance of the structure of gel T remained more homogeneous, while the pressurized gels exhibited more and larger cavities.     

Gel-forming ability of small scale mud carp (Cirrhiana microlepis) unwashed and washed mince as related to endogenous proteinases and transglutaminase activities

Gel-forming ability of small scale mud carp (Cirrhiana microlepis) mince and washed mince was investigated with respect to their proteinase and transglutaminase (TGase) activities. Proteinases in sarcoplasmic fluid showed the optimum activity at 65 °C and pH 9, whereas autolytic activity was maximum at 70 °C and pH 10, indicating the presence of heat-stable alkaline proteinases. When mince was washed with three volumes of water twice, TGase and proteinases were mainly removed in the first washing cycle, resulting in a decreased autolytic activity of washed mince. Breaking force of the single washed mince gels was greater than the twice washed mince and the unwashed mince gels (p<0.05). Pre-incubation of mince pastes at 40 °C for 1 h prior to cooking (90 °C/30 min) increased breaking force of all samples, particularly the single washed mince (p<0.05). This coincided with an increase of higher molecular weight polymers observed on SDS-PAGE. Washing did not completely eliminate proteinases as it was evident by an increased trichloroacetic acid (TCA)-soluble oligopeptides of washed gels pre-incubated at 55 °C. Whiteness values of washed mince gels were greater than that of mince gels.     

Effect of high‐pressure treatments prior to cooking on gelling properties of unwashed protein from barramundi (Lates calcarifer) minced muscle

Heat‐induced gelling properties of barramundi minced muscle with 1.5% and 2% added salt were assessed after application of pressures at 300, 400 and 500 MPa at 4 °C (initial temperature) for 10 min and subsequent cooking at 90 °C for 30 min. Whiteness, gel‐forming ability, water‐holding capacity, hardness and springiness of the barramundi gels increased as applied pressure and salt concentration increased. At 2% salt concentration, high‐pressure treatment results in barramundi gels with higher gel strength, mechanical properties and smoother texture as compared to conventional heat‐induced gels (0.1 MPa, 90 °C for 30). At a reduced salt concentration (1.5%) and pressure ≥ 400 MPa, the quality (gel strength, water‐holding capacity, hardness and springiness) of pressurised cooked gels is comparable to those heat‐induced gels with 2% added salt, but the microstructure is smoother. Scanning electron microscope images of pressurised cooked gels showed dense and compact network with smoother surface than those of heat‐only‐induced gels. Thus, application of high‐pressure treatment prior to cooking could be an effective method to enable reduced salt concentration in barramundi gels.     

Comparison of the properties of gels derived from cod surimi and from unwashed and once-washed cod mince

Surimi is a washed and stabilized fish mince with valuable gel-forming properties. However the preparation process is wasteful and a modified process, with less washing, was investigated. The properties of the gels (cooked at 40°C for 30 min followed by 90°C for 40 min) were assessed by instrumental and sensory methods. Gels prepared from surimi were soft and very flexible; gels from unwashed fresh cod mince were firmer and less elastic, but still gave a maximum score on the folding test. A single wash made the gels firmer and slightly more elastic than those from unwashed mince. Gels from unwashed mince of frozen cod were firmer than surimi-derived gels, and were the most brittle. Sensory assessment of the gels found no difference in firmness between the different washing procedures and small differences in elasticity and toughness. The addition of starch (fish: starch, 100:5, w/w) increased the firmness and sensory toughness of each derived gel, and reduced the elasticity in the mouth of non-surimi gels. The colour of gels derived directly from fish was off-white, compared with the white surimi-derived gels. The colour of the former darkened during frozen storage, but lightened again after thawing.     

Texture and structure of pressure-shift-frozen agar gel with high visco-elasticity

To determine the effects of sucrose and high-pressure-freezing, two kinds of agar gel were compared; A gel with high visco-elasticity and B gel, an ordinary dessert gel. Both agar gels with 0, 5, 10 or 20% sucrose were frozen at 0.1–686 MPa and −20 °C. They were frozen during pressurization, and exothermic peaks were detected at 0.1, 100, 600 and 686 MPa and −20 °C (freezing). However, at 200 MPa, they did not freeze but froze with released pressure (pressure-shift-freezing). Thus, the amount of syneresis from gel pressure-shift-frozen at 200 MPa was smaller than that from gel frozen at other pressures. Also, amount of syneresis from A was smaller than B. In addition, compared to control gels, the appearance of 0% sucrose–agar gels frozen at 0.1, 100, 600 and 686 MPa differed greatly due to syneresis and a volumetric shrinkage of the gel. It was apparent that the rupture stress of the gels decreased, strain and size of ice crystals increased and quality declined. Conversely, due to quick freezing, the texture and structure of both A and B pressure-shift-frozen at 200 MPa were better than the other pressure-treated gels and gels frozen in freezers (−20, −30 or −80 °C) at atmospheric pressure. Consequently, pressure-shift-freezing was more effective. However, texture, structure and syneresis of A were somewhat better than that of B. It was found that the addition of sucrose to the gel was effective in improving the quality of frozen agar gels.