RHEOLOGICAL PROPERTIES OF MIXED GELS

The rheological properties of carrageenan/gelatin and agar/gelatin mixed gels were investigated by measuring the rupture properties, the texture parameters and the dynamic viscoelasticities. fie melting point, transparency and syneresis of these gels were measured in order to obtain the relationship with the rheological properties. The physical properties of the two mixed gels were slightly different. The agar/gelatin mixed gels generally showed the hindered effect of gelatin. The brittleness of agar gel disappeared on mixing with gelatin. It then became a flexible, cohesive and transparent gel. Carrageenan/gelatin mixed gels showed a decrease in the values of almost all of the mechanical properties when compared with carrageenan gels. However, the rupture properties of the C0.5 mixed gel were much higher than those of simple carrageenan gels.     

MECHANICAL PROPERTIES OF TWO-PHASE DISPERSE AGAR/GELATIN MIXED GELS

Agar/gelatin mixed gels with the same composition but with a different two-phase disperse structure were prepared and their mechanical properties compared. The agar/gelatin mixture was first kept at temperature above the gelling temperature of gelatin but below that of agar and stirred for the selected period, before cooling it below the gelling temperature of gelatin. For the low rupture stress system the agar concentration was 0.7% (w/w), while the gelatin concentration was 4.5% (w/w) to achieve the same rupture stress as the agar gel. The mixing temperatures selected were 20 and 37C. For the high rupture stress system, the agar and gelatin concentration was 2.8 and 10.4% (w/w), respectively, to achieve the same rupture stress. The mixing temperatures selected were 37 and 40C. The both mixed gels prepared by this method consisted of a dispersed phase of agar and a continuous phase of gelatin. The rupture stress of the mixed gels decreased as the content of the dispersed phase increased. The rupture stress had a tendency to be lower as the size of the dispersed particles increased. These results suggest that the interface between the dispersed phase and the continuous phase plays an important role as Griffith's crack, with the rupture of mixed gels occurring from that place.     

Studies on “sugar-reactivity” of agars extracted from some Indian agarophytes

Sugar reactivity was observed within the sugar–agar complexes in presence of sucrose and glucose with agars of Indian agarophytes viz. Gelidiella acerosa, Gracilaria edulis, Gracilaria crassa and Gelidium pusillum. The sugar reactivity was more pronounced in presence of sucrose than glucose. Oxoid agar was used as the reference material. Control agar gel contained 1.12% agar (w/w) in water. Sucrose–agar and glucose–agar gels in water consisted of 50% (w/w) sucrose and 50% (w/w) glucose, respectively along with 1.12% (w/w) agars of the four seaweeds mentioned above. Addition of sucrose resulted in increase (ca. 25–45%) in gel strength; increase (2–3 °C) in gelling and melting temperatures was observed in the gels prepared with agars from all the agarophytes and Oxoid agar. On the other hand, addition of glucose resulted in increase (19–34%) in the gel strength and gelling and melting temperatures of the agar gels of Oxoid as well as of all other agars decrease (2–3 °C). Maximum sugar reactivity was observed with the 50% level of sucrose and glucose in agar gels. Rheological and thermogravimetric characteristics of these gel samples were studied. The latter showed two patterns e.g. control agar gel of Oxoid agar was thermally less stable than the four control agar samples studied; in sugar–agar gel samples it followed a reverse pattern. To our knowledge, this is the first report of “sugar reactivity” of agar of Indian agarophytes. Sugar reactivity of agar in presence of glucose is also reported for the first time. The results of this study will be useful in bioprospecting as well as in exploring new applications.     

Rheological and physico‐chemical properties of gelatin extracted from the skin of a few species of freshwater carp

The physico‐chemical and rheological properties of gelatin from the skins of three different freshwater carp species, namely Catla catla, (catla) Cirrhinus mrigala (mrigal) and Labeo rohita (rohu), have been assessed and compared with that of gelatin from porcine skin. The average solids yield from the three species of carp varied in the range of 11.8–14.1%. The amino acid profile showed that the porcine gelatin had a higher proportion of imino acids and glycine than carp skins gelatin. The average molecular weight of carp skins gelatin as determined using a gel filtration technique was 233 kDa, while that of porcine skin gelatin was 282 kDa. The gelling temperature of carp skins gelatin was in the range of 6–15.7 °C, and the melting temperature was 17.9–23.7 °C as determined using a controlled stress rheometer. A higher gelling and melting temperature was observed for porcine skin gelatin.     

Characterization of gelation time and texture of gelatin and gelatin–polysaccharide mixed gels

The effects of cooling rate, holding temperature, pH and polysaccharide concentration on gelation characteristics of gelatin and gelatin–polysaccharide mixtures were investigated using a mechanical rheometer which monitored the evolution of G′ and G″. At low holding temperatures of 0 and 4 °C, elastic gelatin gels were formed whereas a higher holding temperature of 10 °C produced less elastic gels. At slow cooling rates of 1 and 2 °C/min, gelling was observed during the cooling phase in which the temperature was decreased from room temperature to the holding temperature. On the other hand, at higher cooling rates of 4 and 8 °C/min, no gelation was observed during the cooling phase. Good gelling behavior similar to that of commercial Strawberry Jell-O^® Gelatin Dessert was observed for mixtures of 1.5 and 15 g sucrose in 100 ml 0.01 M citrate buffer containing 0.0029–0.0066 g low-acyl gellan. Also, these mixed gels were stronger than Strawberry Jell-O^® Gelatin Desserts as evidenced by higher G′ and gel strength values. At a very low gellan content of 0.0029 g, increasing pH from 4.2 to 4.4 led to a decrease in the temperature at the onset of gelation, G′ at the end of cooling, holding and melting as well as an increase in gel strength. The gelation time was found to decrease to about 40 min for gelatin/sucrose dispersions in the presence of 0.0029 g gellan at pH 4.2 whereas the corresponding time at pH 4.4 was higher (79 min). In general, the gelation time of gelatin/sucrose dispersions decreased by a factor of 2 to 3 in the presence of low-acyl gellan. The addition of low-acyl gellan resulted in an increase in the gelation rate constant from 157.4 to 291 Pa. There was an optimum low-acyl gellan content for minimum gelation time, this optimum being pH dependent. Addition of guar gum also led to a decrease in gelation time to 73 min with a corresponding increase in the gelation rate constant to 211 Pa/min though these values were not sensitive to guar gum content in the range of 0.008–0.05 g. The melting temperature of gelatin/sucrose/gellan as well as gelatin/sucrose/guar mixtures did not differ significantly from that of pure gelatin or Strawberry Jell-O^® Gelatin Desserts. At pH 4.2, the melting rate constant was highest at a low-acyl gellan content of 0.0029 g whereas the rate constant was insensitive to low-acyl gellan content at pH 4.4. Addition of guar did not seem to affect the melting temperature or the melting rate constant.     

Characterization of gellan/gelatin mixed solutions and gels

The physico-chemical properties of gellan/gelatin mixed solutions and gels were examined at five different ratios of gellan to gelatin (100:0 (I), 80:20 (II), 60:40 (III), 40:60 (IV), 20:80 (V)) and four different NaCl levels (0–300 mmol/l). All mixed solutions exhibited the shear-thinning behavior, which decreased with increasing gelatin proportion, temperature, and NaCl level. Synergism on G′ was observed in mixed solution III and IV depending on NaCl level. Hardness of mixed gel decreased with increasing gelatin proportion and cohesiveness increased up to the gellan to gelatin ratio of 40–60 and then decreased. For gellan dominant gels, maximum hardness and cohesiveness were observed at NaCl level of 150 mmol/l. Increasing gelatin proportion caused an increase in gel turbidity at lower NaCl levels and a decrease in gel turbidity at higher NaCl levels. In general, WHC increased with increasing gelatin proportion and decreasing NaCl level. Color holding capacity significantly increased with increasing gelatin proportion. Flavor holding capacity increased by adding gelatin and then linearly decreased with increasing gelatin proportion. Therefore, this study suggests that there is an optimum NaCl concentration and gellan to gelatin ratio to enhance the physico-chemical properties of gellan/gelatin mixed solutions and gels.     

Effect of mungbean [Vigna radiata (L.) Wilczek] protein isolates on the microbial transglutaminase‐mediated porcine myofibrillar protein gels at various salt concentrations

This study was performed to investigate the effects of mungbean protein isolates (MPI) as a meat/water binder on the MTGase‐mediated porcine myofibrillar protein (MP) gels at 0.15, 0.3, and 0.45 m salt concentrations. The general property of MP gel was evaluated by pH, cooking loss (CL) (%) and gel strength (gf). Protein–protein interactions among MPI, MTGase, and MP during cooking were also assessed using gel electrophoresis, thermal analysis and microstructure. When salt content was reduced, gel CL (%; P < 0.05) was increased while pH and gel strength (gf) values were decreased (P < 0.05). Addition of MTGase to MP increased pH, CL (%), and gel strength (gf) values, while co‐addition of MTGase and MPI induced synergistic effects on the MP gel strength (gf; ≥0.3 m salt concentration; P < 0.05). In scanning electron micrograph images, increase of salt concentrations made MP gels more swollen and interwoven or conglomerated, regardless of treatment. In conclusion, addition of MPI and MTGase strengthened gel‐forming ability and improved cooking yield of MP gel at salt concentration (≥0.3 m ).     

RHEOLOGICAL PROPERTIES OF AQUEOUS AGAROSE-GELATIN GELS

Melting temperatures were determined for 1-5% agarose gels, 7.5-40% gelatin gels and mixed gels of different concentrations of the two hydro-colloids. The dynamic viscoclastic constants were also quantified at 0.05 HZ for mixed gels containing 0.5% agarose and 2.5–20% gelatin.
In single component gels, the melting temperature increased with hydrocolloid concentration. The melting temperature of gelatin gels was lower than that of agarose gels (22–31°C vs 69–80°C) and less concentration dependent. The melting temperature of mixed gels was more similar to that of agarose gels at low (2.5–6.25%) gelatin concentrations and more similar to that of gelatin gels at high (7.5–20%) gelatin concentrations. The storage modulus decreased with increasing temperature indicating that the thermal rupturing of the noncovalent crosslinks in the gels was stronger than the entropic behavior of the network. The temperature dependence of the storage modulus and of the dynamic viscosity increased with gelatin concentration. Based on these results and on the determination of the activation energy it is concluded that, in mixed agarose/gelatin gels, the two species form individual networks which interfere with one another at high concentrations.     

Characteristics and functional properties of gelatin from seabass skin as influenced by defatting

Gelatins from nondefatted and defatted seabass skins were characterised and evaluated for their functional properties in comparison with commercial fish skin gelatin. All gelatins contained α₁‐ and α₂‐chains as the predominant components and showed a high imino acid content (199–201 residues/1000 residues). All gelatins had a relative solubility greater than 90% in the wide pH ranges (1–10). Foaming properties of all gelatins increased with increasing concentrations (1–3%, w/v). Gelatin from defatted skin had higher foam expansion and stability than that extracted from nondefatted skin. Emulsion containing gelatin from defatted skin had smaller oil droplet size (d₃₂, d₄₃), compared with that having gelatin from nondefatted skin (P < 0.05). After 10 days of storage at room temperature (28–30 °C), emulsion stabilised by gelatin from defatted skin showed the higher stability as indicated by the lower increases in d₃₂ and d₄₃, and lower flocculation factor and coalescence index. Coincidentally, emulsion stabilised by gelatin from defatted skin had higher zeta potential than that containing gelatin from nondefatted skin. Thus, defatting of seabass skin directly affected characteristics and functional properties of resulting gelatin.     

SWEETNESS PERCEPTION IN RELATION TO SOME TEXTURAL CHARACTERISTICS OF HYDROCOLLOID GELS

The apparent sweetness of five different hydrocolloid gels prepared with equal amounts of sodium Sucaryl varied significantly (P < 0.01) when tested in a multiple paired arrangement by seven trained judges. Results from four replications consistently showed sweetness to be the greatest in carrageenan gels and the least in cornstarch gels. It was intermediate in low methoxyl pectin, agar and gelatin gels. Concentrations of gelling agents were selected to produce gels comparable in hardness. Characterization of mechanical textural properties with the GF-Zenken Texturometer showed that gels of cornstarch and gelatin were more cohesive, springy, chewy and gummy than those of agar, low methoxyl pectin and carrageenan (P < 0.01). These findings suggested that gels which take more effort to disintegrate limit taste perception. Multiple regression analyses showed that the measured mechanical textural parameters accounted for 52.3% of the variability in sweetness scores suggesting that other characteristics may also play a role. Inspection of correlation coefficients of sweetness with single textural parameters showed no one characteristic as a dominating influence over sweetness.     

Structural Relaxation of Salmon Gelatin Films in the Glassy State

Mechanical relaxation of glassy carbohydrates has been reported extensively in the literature; however, little work is available on protein-based systems. This study deals with the structural relaxation of salmon (Salmo salar) gelatin in the glassy state. Skin gelatin was obtained by an acid–alkaline extraction method. Molecular weight (M _w) was determined by capillary viscometry. Films prepared by casting (7% w/v) were equilibrated to a moisture content of ~18.4% (db). The glass transition temperature (T _g) and enthalpic relaxation were determined by differential scanning calorimetry (DSC). Mechanical properties were assessed using a texture analyzer at constant temperature and moisture content. DSC showed a T _g ~34°C, and the selected storage temperature (T _a ) was 29°C (T _g − T _a = 5°C). The films were aged for 0, 4, 8, 16, and 40 h. Viscometry produced values of M _w ~90.2 kDa. The stress relaxation was modeled by the Kohlrausch–Wlliams–Watts (KWW) equation, reporting an increase in relaxation time (τ ₀) as the ageing time increased (τ ₀ ~6.41E + 03 s for 0 h; τ ₀ ~9.01E + 05 s for 40 h). β parameter was smaller for the aged films, indicating a spread of relaxation times. The derivative of KWW equation (dφ/dt) indicated a more rapid relaxation in a fresh sample compared with aged films. DSC showed an excess in enthalpy (ΔH) on the aged samples due to the non-equilibrium state of the matrix. ΔH increased with ageing time with values of ΔH ~2.42 J/g for the films aged for 40 h. This work demonstrated molecular relaxation process of gelatin in the glassy state, which must be taken into account if this material is used as a structure forming matrix.     

Gelation properties of goose liver protein recovered by isoelectric solubilisation/precipitation process

Isoelectric solubilisation/precipitation (ISP) process was applied to goose liver (GL) for protein extraction. The gelation properties of proteins extracted by acid processes (ACP, pH 2.0, 2.5 and 3.0) and alkaline processes (ALP, pH 11.0, 11.5 and 12.0) were estimated, where the unextracted ground GL was set as the control. Nearly 58.39~79.00% of GL proteins were recovered by ISP treatments. High molecular weight (100~250 kDa) proteins were found to be partially hydrolysed by ACP, while few changes in proteins occurred during ALP. As evidenced by rheological and textural measurements, ALP proteins formed gels with high elasticity and superior texture, whereas ACP proteins had inferior gelation properties. Moreover, ALP proteins were able to form a highly interconnected and homogeneous three‐dimensional microstructure. Predominantly, gels produced by 11.0 had optimal texture and the lowest cooking loss (P < 0.05). These results suggested that the ISP process (ALP) is a potential method to improve the economic value of GL.     

Properties of Alaska Pollock Skin Gelatin: A Comparison with Tilapia and Pork Skin Gelatins

ABSTRACT:  The objective of this work was to compare the physiochemical and rheological properties of Alaska pollock skin gelatin (AG) to those obtained for tilapia and pork skin gelatins. Results were also obtained for some mixed gels containing AG and pork skin gelatin, or AG and tilapia gelatin. AG contained about 7% hydroxyproline (Hyp), which was lower than that of tilapia (∼11%) or pork skin gelatin (∼13%). Most of the protein fractions in AG were α chain, β chain, and other oligomers. The gel strength of AG was 98 gram-force at 10 °C, and increased at a greater rate than other gelatins with decreasing temperature. The gel melting point of AG was the lowest with the oil-drop method, while the viscosity of AG was the highest of the samples studied. The rheological properties of gelatins were determined using small amplitude oscillatory shear testing. G' was nearly independent of frequency for most of the gelatin gels, but AG gels showed a slight dependence on G' and a minimum in G". G' was found to be a power law function of concentration for all gelatins used: G'= k × Cⁿ. In rheological measurements, AG also showed the lowest gel melting temperature and sharpest melting region. Increasing gelatin concentration resulted in a higher melting temperature and a broader melting region for all gelatin gels. For both the AG-pork and AG-tilapia mixed gels, the gel melting temperatures decreased and melting regions narrowed as the AG fraction was increased.     

A comparative study on different concentration methods of extracts obtained from two raspberries (Rubus idaeus L.) cultivars: evaluation of anthocyanins and phenolics contents and antioxidant activity

The effects of conventional (CV) and microwave (MW) heating on total soluble solid (TSS) content, total anthocyanin content (TAC), total phenolic content (TPC) and antioxidant activity of raspberry juice obtained from two cultivars of Amol (AM) and Siyahkal (SK) were scrutinised. Antioxidant activity of the juices was measured by 2,2 diphenyl‐1‐picrylhydrazyl (DPPH) radical scavenging capacity and expressed as EC₅₀ value. In the both methods, the concentration rate constant for the juices was significantly decreased by increasing operational pressure from 12 to 100 kPa (P < 0.05). A first‐order reaction kinetic model was successfully fitted for the degradation of monomeric anthocyanins at all operating pressures. The results also showed that thermal treatment of MW compared CV in both SK and AM cultivars caused a lower decrease in the TAC, TPC and antioxidant activity. Moreover, the changes in trend of the antioxidant activities due to the thermal treatment were positively correlated with the TPC (r = 0.74, P < 0.05) and TAC (r = 0.61, P < 0.05).     

Effect of salt content on gelation of normal and wooden breast myopathy chicken pectoralis major meat batters

This study investigated the effects of salt content (0–4%) on water holding capacity (WHC), textural characteristics, rheological properties, and microstructure of cooked normal (NOR) and wooden breast (WB) chicken meat batters. Results indicated with 0–2% salt addition, the WB batters had significantly lower WHC and storage modulus (G’) compared with the NORs (P < 0.05). However, these differences were eliminated when salt contents were increased to 3% or 4%. In addition, the NORs formed more regular and pored networks than the WBs (0–2%). Salt level significantly affected the textural properties of both batter types (P < 0.05). The hardness of the WB batters was lower than NORs at all NaCl levels (P < 0.05). Overall, compared with NORs, the WB batters showed inferior gelation properties at salt contents of 0–2%, while increasing salt content to 3–4% can improve the WHC and microstructure of gels.     

Structural properties of single and mixed milk/soya protein systems

Single-component gels were prepared by cold-setting aqueous preparations of thermally processed milk and soya proteins. Small deformation mechanical measurements on soya protein samples showed a strong elastic response (G′) even at the hydration temperature (50°C). Both proteins produced an initial monotonie increase in G′ on cooling, followed by a relatively constant modulus during a subsequent time sweep at the setting temperature (5°C). Networks were fully reversible on heating; the milk protein gels melting out completely at temperatures >60°C, whereas the soya protein gels maintained significant structure even at the highest accessible temperature (95°C). The lack of thermal hysteresis or of sharp, cooperative melting was also confirmed by differential scanning calorimetry. Further investigation of the macromolecular properties of the gels, comprising G′ dependence as a function of frequency of oscillation and creep experiments, suggests that gels remain stable within the time scale of the measurements (90 min). Finally, under increasing amplitude of oscillation, networks withstood structural breakdown up to strain levels of ~70%; behaviour anticipated for biopolymer gels. Mixed gels were studied using a fixed amount of milk protein (10% w/w) with soya protein concentrations from 6 (minimum gelling requirement) to 16% w/w (solubility limit). Comparison of melting profiles (G′ vs. T) for the phase separated systems with those obtained for the individual components indicated phase-inversion from a milk protein continuous network to a soya continuous system at a soya protein concentration of ~11%. Analysis of solvent partition between the constituent phases utilized classical theory of network deswelling for polymer combinations below the phase inversion point and phase equilibria treatment for the soya continuous network with milk protein inclusions. In the case of equilibrium separation of the two components, results were expressed in terms of a single adjustable parameter, p (the ratio of solvent to polymer in one phase divided by the corresponding ratio in the other phase), indicating a soya hydrophilicity of ~1.25 times that of milk protein.     

Effect of polysaccharides with different ionic charge on the rheological,microstructural and textural properties of acid milk gels

The effects of addition of polysaccharides with different ionic charge on rheology, microstructure, texture and water holding capacity (WHC) of acid milk gels were studied and compared to that of gelatin addition. Similar to gelatin, starch (neutral) and xanthan gum (anionic) did not prevent milk gelation in the first 30 min of the acidification stage, even at high concentrations, and the typical casein network in acid milk gels could still be seen from electron micrographs; gelling and melting of these hydrocolloids were observed during the cooling and heating stages at specific concentrations. On the other hand, two neutral polysaccharides, guar gum (≥ 0.05%) and locust bean gum [LBG] (≥ 0.1%) inhibited milk gelation from the beginning of the acidification stage; the microstructure of the gel was modified greatly and no gelling/melting was observed during the cooling or heating stages. Another anionic polysaccharide, carrageenan, induced earlier milk gelation at low concentration (≤ 0.05%), but inhibited gelation entirely at high concentration (0.2%); inflections at ~ 27 °C and 21 °C were also observed during the cooling and heating stages at 0.05% concentration. The gel microstructure was not changed greatly, but showed smaller particle size at a carrageenan concentration of 0.05% than control sample. None of the polysaccharides showed as much improvement in WHC of the milk gels as gelatin did. Hence, xanthan and starch were found to be closer to gelatin in their effect on acid milk gels compared to guar gum, LBG and carrageenan.     

Rheological characterisation of yolk-based gels and Staphylococcus growth

Model yolk-based (10% v/v) gels with different concentrations of κ-carrageenan (0–2% w/w) were characterised employing rheological measurements, textural analysis and scanning electron microscopy. Additionally, the effect of the microstructure of the model gels on the growth rate of Staphylococcus was also evaluated. In all cases, the nature of the gel was dominated by the elastic component, specifically, 1.5, 1.75 and 2% κ-carrageenan samples can be described as ‘true gels’ (tan δ < 0.1). Maximum strength of the interactions between rheological units (A) was observed with 1.75% κ-carrageenan (4.74 ± 0.38 kPa), which indicates that the strength of interactions was determined not only by κ-carrageenan concentration, but also by the amount of yolk. Finally, an inverse linear correlation was found between the maximum specific growth rate of Staphylococcus and rheological data (R² > 0.99).     

Physiochemical and nutritional characteristics,bioaccessibility and sensory acceptance of baked crackers containing broccoli co-products

The effects of the inclusion of broccoli co-products into crackers on the bioaccessibility as well as their overall physical and nutritional quality were evaluated. Crackers were formulated using a 12.5 or 15.0% flour substitution level. Broccoli-containing crackers presented higher specific volume and spread ratio and lower weight and specific volume than control crackers (P < 0.05). Crackers containing broccoli co-products showed an increased green hue and a higher colour intensity (P < 0.05). Incorporation of broccoli co-products into crackers significantly increased the total phenolic content and antioxidant capacity (P < 0.05). A simulated gastrointestinal digestion suggested that the amount of phenolic and antioxidant compounds released during digestion might be higher than what could be expected from common water-organic extracts. The incorporation of broccoli co-products into baked crackers would not only reduce the amount of food discarded as waste but also promote health and open novel commercial opportunities to food processors.