Glass transition behaviour of fructose

The glass transition temperature and the second transition (the endothermic change between the glass transition and melting temperatures) of fructose were studied. The thermal history strongly affected both transitions of fructose. Storage for 10 days at 22 °C increased the dynamic glass transition temperature from 16 to 25 °C and decreased the second transition of fructose from 110 to 98 °C in the first differential scanning calorimetric (DSC) scan. The amplitude of the second transition increased slightly with storage time and reached 260% of the first transition for vacuum oven dried samples. The effect of thermal history on the glass transition temperature of fructose can be removed by scanning the sample in a DSC to 130 °C. The effects of water content, glucose and sucrose on the two transitions were also investigated.     

Influence of storage time and temperature on lipid deterioration during cod (Gadus morhua) and haddock (Melanogrammus aeglefinus) frozen storage

Lean fish deterioration during frozen storage (−30 and −10 °C) for up to 1 year was studied by the assessment of lipid changes. Comparison between a formaldehyde (FA)-forming species (cod) and a non-FA-forming one (haddock) was carried out. Lipid damages were measured on the basis of free fatty acids (FFA), peroxide value (PV), thiobarbituric acid index (TBA-i) and fluorescent compounds. In both species at −30 °C, most lipid damage indices showed significant correlations with the storage time. However, at −10 °C, only the FFA and fluorescence detections provided significant correlations with the storage time. Comparison between the fish species showed higher lipid oxidation (PV and TBA-i) and hydrolysis (FFA content) in haddock than in cod at −10 °C; however, a higher fluorescence development was observed in cod at the same temperature. At −30 °C, little differences in lipid damage indices were detected between the two species. © 1999 Society of Chemical Industry     

Thermal Properties of Proteins in Chicken Broiler Tissues

The thermal behavior of breast and thigh muscles, blood and skin tissues of chicken broilers was evaluated by differential scanning calorimetry (DSC). Onset temperature of transition (T_o), maximum thermal transition (T_max) temperatures, and denaturation enthalpy (ΔH) were evaluated. Breast muscle exhibited a complex thermogram with five endothermic transitions at 57°C, 63°C, 67°C, 73°C, and 78°C at a heating rate of 10°C/min. Thigh muscle exhibited only three major transitions at 60°C, 66°C, and 76°C. Thermal curves of isolated protein fractions indicated that the thermal transitions in muscle corresponded to the denaturation of myosin, sarcoplasmic proteins, collagen and F-actin. An increase in the heating rate from 1.0° to 40°C/min significantly elevated the onset temperature of transition and major transition temperatures, as well as the enthalpy of denaturation. Enthalpy of the muscle system heated to various end-point temperatures, cooled and reheated, showed that myosin was completely denatured at 60°C, sarcoplasmic proteins at 70°C and actin at 80°C.     

Phase Transitions of Amorphous Sucrose and Frozen Sucrose Solutions

Amorphous sucrose showed typical thermal transitions of amorphous materials. The temperatures of those transitions, glass transition, crystallization and melting, decreased with increasing moisture content. The glass transition temperature of dry amorphous sucrose at 57°C was decreased to -46°C as the sucrose was plasticized with excess water. That value remained constant due to maximal freeze-concentration with 72-73% sucrose in the unfrozen matrix which showed ice melting at -34°C. Concentrated solutions may become supercooled resulting in partial freeze-concentration with resultant lowering of glass transition temperature.     

Effects of frozen storage temperature on the quality and oxidative stability of bigeye tuna flesh after light salting

Effects of frozen storage temperature on the quality and oxidative stability of lightly salted tuna were investigated. The bright and vivid colour became totally brown after 4 weeks at −20 °C and 8 weeks at −30 °C, where the a^*/b^* value decreased from 1.35 to 0.38 and 0.58, respectively. Discoloration and lipid oxidation occurred concurrently in lightly salted tuna flesh, and it was speculated that the oxidation of oxymyoglobin to metmyoglobin exacerbated lipid oxidation and vice versa. Storage at −40 °C or lower temperatures effectively suppressed the discoloration and maintained the high water-holding capacity and unique textural properties of lightly salted flesh. It was attributed to the reduction in the conformational changes and particularly hydrophobic interactions among proteins, protecting the myoglobin from oxidative damages during frozen storage. Considering the quality maintenance and energy savings, storage at −40 °C was appropriate for lightly salted tuna flesh.     

High-Resolution NMR and Magnetic Resonance Imaging (MRI) Studies on Fresh and Frozen Cod ( Gadus morhua) and Haddock (Melanogrammus aeglefinus)

Changes in the fish muscle from cod ( Gadus morhua ) and haddock ( Melanogrammus aeglefinus ) were investigated by high-resolution NMR and magnetic resonance imaging (MRI). Water- and salt-soluble extracts from fish stored at −20°C and −30°C were analysed by high-resolution proton NMR and enabled the identification of metabolites including trimethylamine oxide, trimethylamine (TMA) and dimethylamine. It was not possible to detect formaldehyde by NMR either in the stored fish samples or in spiked water or salt extracts even at high levels of formaldehyde addition, probably due to polymerisation. Systematic and controlled storage trials indicated the presence of dimethylamine at around 9 months for samples stored at −20°C, whereas no changes were detected at the control storage temperature of −30°C. A comparison of cod and haddock fillets stored for 1 year at −20 and −30°C confirmed the production of dimethylamine only in cod stored at −20°C. It was interesting to note that ‘fresh’ cod and haddock samples purchased from a local supermarket showed high levels of TMA indicating a breakdown of trimethylamine oxide to TMA by bacteria. TMA was not detected in the fish fillets especially obtained for the storage trials. MRI of fresh cod and fish stored at −8 and −30°C indicated that the fish half stored at −8°C exhibited dense lines or arches which are indicative of gaps in the tissue due to possible breakdown of the connective tissue. The images of fish stored at −30°C did not indicate any differences compared with the fresh fish. MRI also showed the presence of frozen and unfrozen areas in the fish non-destructively.     

Thermal Transitions of Actomyosin and Surimi Prepared from Atlantic Croaker as Studied by Differential Scanning Calorimetry

Differential scanning calorimetry (DSC) was used to investigate thermal transitions of fish mince (surimi) and actomyosin from croaker. Three endothermic peaks were observed in DSC thermograms of surimi. After addition of salt, transition temperatures shifted to lower temperatures. Preheating samples containing 3% salt at various temperatures showed that 40°C heating caused the first peak to disappear, and preheating at temperatures higher than 50°C caused virtual disappearance of all transition peaks. Low temperature storage (4°C) of samples caused no significant change in thermograms of salted or unsalted surimi over a 5-day storage period. Evidence suggests that changes of fish protein during low temperature “setting” are different from those occurring during high temperature “setting.”     

Glass Transition Values of Muscle Tissue

Reports of glass transition (Tg') values for frozen muscle tissue are not common and reported values are mostly much lower than would be expected. Tg’ values for muscle tissue and isolated proteins were studied using differential scanning calorimetry. Apparent Tg's of mackerel, cod and beef were similar (ca ?11 to ?13°C) and substantially higher than most published values (?15 to ?77°C for tuna and beef), but in accord with expectations for substances of high molecular weight. Dialyzed insoluble and soluble protein fractions from mackerel yielded apparent Tg’ values (ca ?7°C) that were similar, with both being higher than those for whole muscle. Apparent Tg’ values of ca ?7°C were determined for aqueous samples of gelatin and collagen, but none was detected for zein.     

Modification of glass transition temperature through carbohydrates addition and anthocyanin and soluble phenol stability of frozen blueberry juices

To evaluate the influence of carbohydrate addition on anthocyanin and soluble phenol stability, blueberry juices were added with 20% (wt/wt) of maltose, sorbitol and a mixture (1:1) of glucose and fructose. A juice without addition of carbohydrates was used as a control. The juices were frozen and stored up to six months at −10, −20 and −30 °C. The transition temperatures T_m^′ correlated with those of the added sugars. The glass transition was shifted to higher temperatures by addition of maltose and no significant changes in the transition temperatures were noticed with storage time. Anthocyanin and soluble phenol changes were mainly influenced by storage temperature and storage time: the lower the temperature, the shorter the storage time, the lower the changes. Sugar addition had no influence on anthocyanin content.     

Thermal Activation of Actomyosin Mg-ATPases from Ordinary and Dark Muscles of Tuna and Sardine

Changes in activities of actomyosin, acto-heavy meromyosin (acto-HMM), and acto-subfragment-I (acto-S-I) ATPases from tuna and sardine due to heat treatment (20°, 25°, 30°, 35°, 40°C) were compared for ordinary muscle and dark muscle. Activation of ordinary muscle actomyosin Mg-ATPases was more than doubled for tuna and tripled for sardine by heating at 35°C, while activation of dark muscle actomyosin was not observed at any temperature. The occurrence of thermal activation corresponded to a rapid loss of the EDTA-ATPase activity. Activation of hybrid actomyosins from dark and ordinary muscles was dependent upon myosin. For acto-HMM and acto-S-I thermal activation was not observed. The role of myosin tail fragments in thermal activation is discussed.     

Physicochemical characteristics of inulins obtained from Jerusalem artichoke (Helianthus tuberosus L.)

The physicochemical characteristics (thermal stability, glass transition temperature and degree of crystallinity) of inulins, obtained from the tubers of four varieties Jerusalem artichoke (Helianthus tuberosus L.) grown in Bulgaria—Energina, Verona, Topstar and Spindel, were investigated. The inulins obtained had molecular weight from 4,882 to 5,600 Da (degree of polymerization around 30 fructose units). The experimental data from differential scanning calorimetry showed that the glass transition temperature of inulins is between 51 °C and 55 °C. It was found that the first transition (due to evaporation of the unbound water) starts from 77 to 80 °C. The second transition phase started between 152 and 158 °C, and it determines the limit of inulin thermal stability. The data from differential thermal analysis confirmed the results of differential scanning calorimetry with slight differences in the starting temperatures and durations of the phase transitions. X-ray analysis showed that the degree of crystallinity of inulins is very low (except for Spindel inulin—21%).     

A DSC determination of phase transitions and liquid fraction in fish oils and mixtures of triacylglycerides

The thermal phase transitions of 18 pure triacylglycerides (TAGs) and four fish oils were investigated using differential scanning calorimetry (DSC) and modulated DSC (MDSC) in the temperature range from − 150 to 80 °C. The dependence between the heat of fusions and the melting temperatures was determined for pure TAGs, and a regression equation was obtained. A liquid fraction in TAG mixtures and fish oils was determined by the partial integration of melting peaks enhanced by the regression equation. The method was considered to be beneficial for fish oils, because several pure TAGs did not show crystallization. These “unfreezable” TAGs were composited by polyunsaturated fatty acids with three or more double bonds. They showed a glass transition in the temperature range between − 113.9 and − 105.6 °C. The fish oils melted in the range between − 92.6 and 23 °C. The heat of melting was measured to be between 31.5 and 41.8 J g^− 1. The oils had a significant share of liquid fraction (between 40.0 and 58.0%) at temperatures down to − 110.0 °C when the glass transition appeared.     

The influence of storage temperature and storage time on color stability,retail properties and case-life of retail-ready beef

Steaks from three different muscles were either vacuum or carbon dioxide packed and stored for up to 24 weeks at three different storage temperatures (−1.5, 2, or 5 °C). Following storage, they were displayed for up to 30 h. CIE color coordinates, the oxidative states of myoglobin and pH were measured and muscle color, surface discoloration, retail appearance, and odor were evaluated prior to storage and during display (0, 1, 2, 4, 6, 24 and 30 h), and/or immediately prior to and following display. Prior to display, pH was negatively related to duration of storage, and samples stored at −1.5 °C had the highest and samples stored at 5 °C, had the lowest pH. Perception of muscle color was influenced by duration of storage and display, but lower storage temperatures appeared to produce a stabilizing effect. Both lightness of muscle color and deoxymyoglobin content were apparently not influenced by storage temperature or duration of storage or display. Both oxymyoglobin (OMB) and redness, as defined by CIE a* values, were lost progressively during storage and display, but this loss was progressively lower as storage temperature decreased. Yellowness of muscle color, as defined by CIE b* values, generally decreased as storage was prolonged, and this decrease was observed more quickly at higher storage temperatures. Surprisingly, b* values were not related to duration of display. Both surface discoloration and metmyoglobin (MMB) content increased progressively during storage and display. Samples stored at 5 °C displayed the most surface discoloration, while samples stored at −1.5 °C contained the least MMB and displayed the least surface discoloration. Retail appearance deteriorated progressively during storage in all samples stored at 2 and 5 °C and in samples stored at −1.5 °C, which were displayed for at least 24 h. Retail appearance also deteriorated progressively during display in samples stored at −1.5 and 2 °C for three weeks or longer and in samples stored at 5 °C for 0 to 15 and 24 weeks. In unstored samples, samples to be stored at −1.5 °C generally received the lowest retail appearance scores, but after prolonged storage and display, samples stored at −1.5 °C received higher retail appearance scores than samples stored at 5 °C, particularly when samples were stored for 12 weeks or longer and displayed for 1 h or more. Odor deteriorated progressively during storage when measured both prior to display and after 30 h of display. In samples stored for three weeks or longer, samples stored at −1.5 °C generally received the lowest odor scores and were perceived to have the least prevalent off-odors. Samples stored at −1.5 °C maintained a retail case-life of 30 h, when stored for up to 17 weeks, while samples stored at 2 and 5 °C maintained a retail case-life of 30 h, when stored for only eight and seven weeks, respectively. Consequently, storage life can be more than doubled by storage at subzero temperatures (−1.5 °C).     

Effect of freezing rate and frozen storage on starch–sucrose–hydrocolloid systems

Model food systems based on starch (100 g kg⁻¹), sucrose (150 g kg⁻¹) and water (750 g kg⁻¹) with and without the addition of a low proportion of hydrocolloid (xanthan gum, guar gum or sodium alginate) were gelatinised, frozen at different rates and stored to analyse textural changes by oscillatory rheometry. Differential scanning calorimetry (DSC) was used to analyse gelatinisation, amylopectin retrogradation and glass transition temperatures. Sucrose had a significant effect on the increase in the gelatinisation temperature as well as on the decrease observed in glass transition values. The onset temperature of the second step of the glass transition, corresponding to the heat capacity change close to ice melting (denoted Tg_im in the present work), ranged between −23.0 and −22.2 °C. Rheological viscoelastic tests showed an increase in the dynamic moduli G* and G ′ after slow freezing and during storage at −19 °C (T > Tg_im) in starch–sucrose systems that is related to sponge formation due to amylose retrogradation. DSC studies confirmed that also amylopectin retrogradation occurs during storage; however, samples containing gums did not develop the spongy appearance. Storage at the usual commercial temperatures (close to −18 °C, slightly above Tg_im) affects the quality of aqueous starch–sucrose pastes without gums owing to amylose and amylopectin retrogradation. However, when hydrocolloids are included in the formulations, the usual storage conditions allow the maintenance of acceptable textural attributes. © 2000 Society of Chemical Industry     

A DSC study on the effects of various maltodextrins and sucrose on protein changes in frozen‐stored minced blue whiting muscle

A DSC heat denaturation study on the effects of various maltodextrins and sucrose on protein changes in minced blue whiting muscle during frozen storage at −10 and −20 °C was carried out. All maltodextrins slowed down the decreases in the denaturation enthalpies (ΔH_d) ascribed to myosin and actin, making evident a noticeable effectiveness against protein denaturation, especially at −20 °C. Sucrose was as effective as maltodextrins at −20 °C, but was the least effective treatment at −10 °C. Significant correlations between both ΔH_ds and either protein solubility or formaldehyde production were found at each storage temperature. A low protein sensitivity to the small amounts of formaldehyde produced during the first weeks of storage and errors associated with the determination of enthalpies led to poorer correlations at −20 °C. Maximum denaturation temperatures (T_max) correlated with protein solubility only at −20 °C. No clear relationship between either T_max and the effectiveness of cryostabilisation was found, as T_max also depends on the effectiveness of the treatments against the thermal denaturation of proteins. © 2001 Society of Chemical Industry     

Glass transition of pomegranate skin,as analyzed by thermal,mechanical, and nuclear magnetic resonance methods

Glass transition of pomegranate skin was measured by thermal, mechanical, and magnetic resonance techniques. Differential scanning calorimetry thermogram showed a shift (i.e., onset glass transition at 20°C) followed by an endothermic peak (i.e., solids-melting peak at 165°C and enthalpy 140 kJ/kg). Overlapping of the glass transition and melting was observed in the differential scanning calorimetry thermogram; however, more sensitive modulated differential scanning calorimetry allowed to separate two transitions (i.e., glass transition from reversible and melting from non-reversible thermograms). The onset of mechanical glass-rubber transition from differential mechanical thermal analysis was observed at 122°C with a shift in the storage modulus (E′); however, the onset of liquid-like or entangled-reaction dominating transition was observed at 70°C (i.e., onset peak in loss modulus, E′′) and peak at 184°C. In addition onset peak in tan δ was observed at 113°C and peak at 201°C. Spin–spin (T₂ relaxation) and spin-lattice (T₁ relaxation) relaxations in time domain nuclear magnetic resonance was modeled by two-exponential relaxation curve (i.e., rigid and flexible domains). T₂ relaxation showed maximum peak with an onset at 40°C with maximum peak at 150°C. Rigid domain of T₁ relaxation showed a minimum peak onset at 40°C and a minimum peak at 120°C, whereas flexible component showed an onset at 20°C and a minimum peak at 160°C.     

Glass Transition of Tuna Flesh at Low Temperature and Effects of Salt and Moisture

Glass transition of fresh red meat of bigeye tuna (Thunnnas obesus) and its filtrate occurred between —71°C and —68°C, independent of cooling rate from 1 K/min up to 50 K/min. Glass transition at low temperature appeared to occur in the liquid part. Neither dilution nor concentration of the filtrate affected the glass transition temperature (Tg) but the solute concentration of the freeze concentrated phase (Cg) was affected. Addition of salt to the filtrate caused a decrease of ～20 K in Tg. Results suggested the possibility of qualitative improvement in quality of fish by lowering the storage temperature by 15 K below the present storage temperature (—55°C).     

Corn Starch-Xanthan Gum Interaction and Its Effect on the Stability During Storage of Frozen Gelatinized Suspension

The knowledge of starch pastes behavior during frozen storage becomes necessary to understand more complex systems (e.g. sauces, dressings and desserts) The effect of sub-zero storage on the quality attributes of corn starch pastes (10% w/w) with and without xanthan gum (0.3% w/w) was analyzed. Pastes were frozen at different rates (0.3 to 270cm/h) and stored at −5, −10 and −20°C. Exudate production (syneresis) and rheological behavior were studied by means of capillary suction and rotational viscometry respectively. Ice recrystallization was analyzed by indirect microscopic observations using isothermal freeze fixation and amylopectin retrogradation by differential scanning calorimetry (DSC). Samples stored at −5°C (glass transition temperature) or higher temperatures were under the rubbery state evidenced by starch recrystallization. This state favored molecular mobility leading to deteriorative changes (like spongy structure formation related to amylose retrogradation). At lower storage temperatures (−10 and −20°C) under the glassy state, starch retrogradation was not detected and deteriorative changes can be related to ice recrystallization. The addition of xanthan gum minimized amylose retrogradation, syneresis and rheological changes, however, its presence did not prevent ice recrystallization nor amylopectin retrogradation.     

Storage of spinach juice agglomerates: Physical,flow, structural,and thermal properties

The objective of this study was to investigate how the various storage temperatures affected the physical properties, flow characteristics, microstructure, and glass transition temperature of spinach juice agglomerates. For this purpose, spray-dried spinach juice powders were processed to agglomerates by using a modified fluidized bed dryer (1.6 m/s airflow rate, 60°C drying air temperature, 20 min processing time, and with different binder solutions containing agents as maltodextrin, gum Arabic, and whey powder isolate). The analyses were carried out every month throughout 6 months while the spinach juice agglomerates were stored at temperatures of 4, 20, and 35°C. The results revealed that over the storage time, the moisture content and water activity values of the agglomerates were generally under 11% and 0.6, respectively. The color values generally showed a decreasing trend depending on the storage time. The solubility times of the samples stored at 4°C were longer than those of stored at other storage temperatures. The SJA-GA had the lowest HR and CI values and thus the best flowability properties during all storage times. There was no detectable change in the structures of SJA stored at 20°C according to the storage time. Throughout the storage time, it was discovered that the glass transition temperature of all spinach juice agglomerates was remarkably similar. Overall, the investigation revealed that storage at 35°C for 6 months might be suitable because it delivered the intended outcomes such as greater flowability and cohesiveness, and shorter wettability and solubility times.     

TEMPERATURE ACCLIMATION OF ATLANTIC COD (GADUS MORHUA) AND ITS INFLUENCE ON FREEZING POINT AND BIOCHEMICAL DAMAGE OF POSTMORTEM MUSCLE DURING STORAGE AT 0° and -3°C

The freezing point of muscle fluid from Newfoundland Atlantic cod held at ambient sea water temperature was as low as - 1.30°C in March and as high as - 0.80°C in July. Muscle fluid from cod held live at 0°C for 3 weeks had a freezing point of - 1.02°C in contrast to a muscle fluid freezing point of - 0.90°C for cod acclimated at 10°C prior to sacrifice. Muscle fluid from cold acclimated cod exhibited 0.40°C thermal hysteresis indicating freezing point depression was influenced by antifreeze substances. The following indices of deterioration were measured in muscle sections stored at 0°C or - 3°C for 21 days: extractable protein (EP), free drip (FD), extracellular area (EA), trimethylamineoxide (TMAO), trimethylamine (TMA), dimethylamine (DMA), free amino acids (AA), and pH. Muscle sections at the anterior end of fillets, from myotomes 9–20, prepared using aseptic technique and treated with antibiotic showed less evidence of biochemical deterioration: (a) when stored at - 3°C compared to 0°C with respect to EP, AA, EA; (b) when prepared from fish acclimated at 0°C compared to at 10°C and stored at 0°C or - 3°C with respect to EP, EA, FD, AA. Negligible changes in pH, TMA and DMA occurred during 21 days storage at either temperature. TMAO decreased more during storage at-3°C than at 0°C.