Effect of added calcium chloride on the physicochemical and rheological properties of aqueous mixtures of sodium caseinate/sodium alginate and respective oil-in-water emulsions

Changes induced by addition of calcium chloride in particle size distribution and electrokinetic potential were determined in sodium caseinate/sodium alginate mixtures dissolved in water or acetate buffer at ambient temperature. Rheological properties of aqueous mixtures and respective oil-in-water emulsions (30% oil w/w) were evaluated using a low-stress rheometer. Stability and particle diameter of emulsions were measured. Caseinate and alginate solutions were negatively charged and showed negative electrokinetic potential; however values of mixtures were between those of the values for the individual hydrocolloids. When calcium ions were added the electrokinetic potential diminished while the negative charge was preserved. Aqueous mixtures of caseinate and alginate showed average particles size between of those of caseinate or alginate samples. We observed low viscosity values and Newtonian behavior for both caseinate (1 and 2%) and alginate (0.1%). Addition of 5 mM CaCl₂ to alginate solutions induced shear-thinning behavior as well as the development of viscoelasticity. Both the viscosity and the elastic modulus of these polysaccharide solutions were attenuated by the presence of protein or dispersed oil in mixtures or emulsions, respectively. High average particle diameter of emulsions prepared was obtained (close to 10 μm), however, stability of emulsions was possible only with the addition of CaCl₂ to the mixtures, in both water and acetate buffer. In these cases elastic behavior predominated to viscosity in the formation of emulsions, confirming the prevalence of aqueous phase rheology on emulsions.     

Effects of xanthan gum on physicochemical properties and stability of corn oil-in-water emulsions stabilized by polyoxyethylene (20) sorbitan monooleate

The influence of added xanthan gum on rheological and dispersion characteristics and stability of concentrated (50% w/w) corn oil-in-water emulsions, stabilized with 5% (percentage on oil amount) polyoxyethylene (20) sorbitan monooleate (Tween 80), have been investigated. Emulsion with no xanthan indicated coalescence and poor creaming stability. All emulsions, with and without xanthan, showed shear-thinning flow behavior. Addition of xanthan protected emulsions from coalescence during 15 days of storage. Increase in xanthan concentration led to decrease in droplet average radius and creaming index, and increase in elastic properties of emulsions. Decrease in the emulsions flow behavior indexes, which suggested the extent of non-Newtonian behavior of emulsions, was influenced by increase in xanthan concentration. Above 0.04% of xanthan concentration, G′ and G″ values indicated formation of weak gels. Gel structure existence arises from droplet network association, due to depletion flocculation. Standard deviation of emulsions droplet size mean diameter decreased while concentration of added xanthan increased.     

Concentrated O/W emulsions formulated by binary and ternary mixtures of sodium caseinate,xanthan and guar gums: rheological properties,microstructure, and stability

Food Science and Biotechnology - The effects of xanthan gum (XG) (0, 0.3, 0.6 wt%), guar gum (GG) (0, 0.3, 0.6 wt%) and XG:GG mixtures (0.3–0.3, 0.3–0.6, 0.6–0.3 and 0.6–0.6...     

黄原胶对酪蛋白酸钠乳状液稳定性的影响

研究了一定pH条件下,黄原胶浓度及剪切稀化效应对酪蛋白酸钠乳状液稳定性的影响。结果表明,在酸性条件下,黄原胶无法抑制酪蛋白的变性沉淀,乳液在制备之初,即产生严重絮凝。在中性和弱碱性条件下,黄原胶在一定浓度范围内,诱发了乳状液的排斥絮凝;体系的pH显著影响了乳状液的稳定性,pH6条件下,较低的黄原胶浓度(0.2wt%)便可赋予乳状液良好的稳定性。均质过程大大降低了黄原胶的粘度,导致乳状液的稳定性下降,与添加未经均质处理的黄原胶相比,添加量增大近一倍,才能获得稳定的乳状液。     

Characterisation of fish oil emulsions stabilised by sodium caseinate

Fish oil emulsions varying in sodium caseinate concentration (25% w/w oil and 0.1–1.0% w/w protein, giving oil-to-protein ratios of 250–25) were investigated in terms of their creaming stability, rheological properties, the mobility of oil droplets and the oil/protein interaction at the interface. The presence of excessive protein in an emulsion (i.e., at 1% w/w) caused the aggregation of oil droplets through depletion flocculation, resulting in low creaming stability and high low-shear viscosity. At a lower protein concentration (0.1% w/w), when protein was limited, the emulsion droplets were stabilised by bridging flocculation and showed good stability to creaming. Shear-thinning behaviour was observed for both flocculated emulsions. A reduction in the low-shear viscosity and a Newtonian flow was obtained for the emulsion containing an intermediate concentration of protein (0.25% w/w). At this concentration, there was relatively little excess unadsorbed protein in the continuous phase; thus the emulsion was most stable to creaming. NMR was used to characterise these emulsion systems without dilution. Shorter T₂ values (by low-field ¹H NMR), for the emulsions containing both high (1% w/w) and low (0.1% w/w) amounts of protein, indicated increased restricted mobility of oils, caused by depletion or bridging flocculation. The line broadening in oil signals in the high-field NMR spectra (¹H, ¹³C) indicated increased interaction between oil molecules and proteins at the interface with increasing protein concentration in emulsions. In addition, ³¹P NMR spectra, which reflect the mobility of the casein component only, showed increased line broadening, with reduction in protein content due to the relatively higher proportion of the protein being adsorbed to the interface of the oil droplets, compared to that in the continuous phase (i.e., as the oil-to-protein ratio was increased). The T₂ values of resonances of the individual groups on oil molecules, obtained using high-field ¹H NMR, reflected their different environments within the oil droplet.     

Oil-in-water emulsions stabilized by sodium caseinate: Influence of pH,high-pressure homogenization and locust bean gum addition

The effect of pH, addition of a thickening agent (locust bean gum) or high-pressure homogenization on the stability of oil-in-water emulsions added by sodium caseinate (Na-CN) was evaluated. For this purpose, emulsions were characterized by visual analysis, microstructure and rheological measurements. Most of the systems were not stable, showing phase separation a few minutes after emulsion preparation. However, creaming behavior was largely affected by the pH, homogenization pressure or locust bean gum (LBG) concentration. The most stable systems were obtained for emulsions homogenized at high pressure, containing an increased amount of LBG or with pH values close to the isoelectric point (pI) of sodium caseinate, which was attributed to the size reduction of the droplets, the higher viscosity of continuous phase and the emulsion gelation (elastic network formation), respectively. All the studied mechanisms were efficient to decrease the molecular mobility, which slowed down the phase separation of the emulsions. In addition, the use of sodium caseinate was also essential to stabilize the emulsions, since it promoted the electrostatic repulsive interactions between droplets.     

Interactions between pig gastric mucin and sodium caseinate in solutions and in emulsions

The interactions between pig gastric mucin (PGM) and sodium caseinate (Cas) were studied in solutions and in Cas-stabilized emulsions with respect to the ratio of the two components and the pH (1–7) with an emphasis on pH cycling, using absorbance, zeta potential, light scattering, creaming and microscopy measurements. In solutions, pH-reversible interactions were observed at pH 3 or lower, down to pH 1. Zeta potential measurements suggest that interactions are electrostatic in nature at pH 3, while the negligible charge of PGM allows for some attractive interactions with positively charged Cas at pH 1. Caseinate-stabilized oil-in-water emulsions are stable toward coalescence at pH 1 and pH 7; some coalescence is observed at pH 3. Addition of PGM results in flocculation, either due to depletion (pH 7), or due to bridging flocculation and Cas–PGM interactions similar to those observed in solution (pH 1 and pH 3). The flocculation is reversible, as is shown in pH cycling at pH 1 to pH 7, then to pH 1. Overall, the above can be of interest as an examination of the fate of emulsions in pH transitions and cycling in the human gastrointestinal tract.     

Temperature-dependent complexation between sodium caseinate and gum arabic

Complex formation between sodium caseinate and gum arabic as a function of temperature was investigated using dynamic light scattering, fluorescence and NMR. At neutral pH, the turbidity and the particle size increased when sodium caseinate and gum arabic mixtures were heated in situ at temperatures above a critical temperature. The increases in turbidity and particle size were reversible. This effect was considered to be due to hydrophobic interactions, leading to the formation of a complex between sodium caseinate and gum arabic. ¹H NMR spectroscopy showed that ANS, which bound to caseinate at low temperatures in caseinate solution or a caseinate-gum arabic mixture, was released at high temperatures upon formation of a caseinate or caseinate-gum arabic complex. This supported changes observed in the fluorescence of 8-anilino-1-naphthalene sulfonate upon binding to caseinate, which decreased at high temperatures for caseinate alone or when sodium caseinate was mixed with gum arabic. Light-scattering (turbidity) and dynamic light-scattering studies show that the temperature-dependent complexation between sodium caseinate and gum arabic was sensitive to the mass ratio of protein to gum arabic (greater complexation at a 1:5 ratio than a 1:1 ratio) and the pH (maximum complexation at pH 6.5).     

The effects of xanthan conformation and sucrose concentration on the rheological properties of acidified sodium caseinate–xanthan gels

Xanthan solution transitions caused by annealing at different temperatures were studied by oscillatory rheology. The rheological behaviour of solutions evaluated at 10 °C showed different irreversible xanthan transitions, depending on the annealing temperature. The effect of xanthan conformation and caseinate, xanthan and sucrose concentrations on the mechanical and stress relaxation properties of acidified dairy gels were also investigated. Xanthan transitions produced different structural characteristics in mixed gels, as observed by their relaxation time and residual stress. The amount of sucrose played an important role in the network formation of gels and on the final elasticity. Intermediate concentrations of sucrose yielded gels that were finer than those obtained with low sucrose content, whereas at high amounts of this co-solute, the gels became more fragile. This quadratic effect of sucrose occurred at lower sucrose contents than in protein–sucrose or polysaccharide–sucrose systems. The mechanical properties at equilibrium were affected only by the strength of the interactions between caseinate and xanthan.     

Interfacial composition and stability of emulsions made with mixtures of commercial sodium caseinate and whey protein concentrate

The interfacial composition and the stability of oil-in-water emulsion droplets (30% soya oil, pH 7.0) made with mixtures of sodium caseinate and whey protein concentrate (WPC) (1:1 by protein weight) at various total protein concentrations were examined. The average volume-surface diameter (d₃₂) and the total surface protein concentration of emulsion droplets were similar to those of emulsions made with both sodium caseinate alone and WPC alone. Whey proteins were adsorbed in preference to caseins at low protein concentrations (<3%), whereas caseins were adsorbed in preference to whey proteins at high protein concentrations. The creaming stability of the emulsions decreased markedly as the total protein concentration of the system was increased above 2% (sodium caseinate >1%). This was attributed to depletion flocculation caused by the sodium caseinate in these emulsions. Whey proteins did not retard this instability in the emulsions made with mixtures of sodium caseinate and WPC.     

Impact of chemical composition of xanthan and acacia gums on the emulsification and stability of oil-in-water emulsions

Xanthan gum (GX) and acacia gum (GA) are widely employed in food industry, indeed xanthan gum is used for its thickening properties of aqueous solutions and acacia gum for its emulsifying ability. The present work aims to study the effect of GX–GA mixtures on the stability of oil-in-water (o/w) emulsions; attention is particularly focused on the impact of the chemical structure of each gum. Emulsion stability has been evaluated by monitoring the evolution of droplet size and viscometric properties over time when submitted to accelerated ageing conditions. On the one hand results show that the higher the ArabinoGalactanProtein (AGP) content the more stable the emulsion as observed when GA is used alone. On the other hand, we proved, unexpectedly, that the most viscous aqueous phase does not exhibit the best emulsion stability. Besides, we clearly evidenced the presence of specific interactions between GX and GA in both emulsion and aqueous solution, these interactions being governed by the gums chemical composition.     

Effects of protein concentration and oil-phase volume fraction on the stability and rheology of menhaden oil-in-water emulsions stabilized by whey protein isolate with xanthan gum

The influences of protein concentration (0.2, 1, 2 wt%) and oil-phase volume fraction (5%, 20%, 40% v/v) on emulsion stability and rheological properties were investigated in whey protein isolate (WPI)-stabilized oil-in-water emulsions containing 0.2 wt% xanthan gum (XG). The data of droplet size, surface charge, creaming index, oxidative stability, and emulsion rheology were obtained. The results showed that increasing WPI concentration significantly affected droplet size, surface charge, and oxidative stability, but had little effect on creaming stability and emulsion rheology. At 0.2 wt% WPI, increasing oil-phase volume fraction greatly increased droplet size but no significant effect on surface charge. At 1 or 2 wt% WPI, increasing oil-phase volume fraction had less influence on droplet size but led to surface charge more negative. Increasing oil-phase volume fraction facilitated the inhibition of lipid oxidation. Meanwhile, oil-phase volume fraction played a dominant role in creaming stability and emulsion viscosity. The rheological data indicated the emulsions may undergo a behavior transition from an entropic polymer gel to an enthalpic particle gel when oil-phase volume fraction increased from 20% to 40% v/v.     

Flaxseed gums and their adsorption on whey protein-stabilized oil-in-water emulsions

The effect of the addition of flaxseed gum on the physicochemical properties of whey protein-stabilized (WPI) oil-in-water emulsions at pH 3.5 was investigated. Two different varieties (Emerson and McDuff) were tested at concentrations ranging from 0% to 0.33% (w/v), by measuring droplet size, ζ-potential, phase separation behavior, microstructure and apparent viscosity. With addition of flaxseed gum the ζ-potential of the droplets decreased from around +30 mV to a negative value (−10 mV) at concentrations >0.2%. These results indicated that the negatively charged polysaccharide fraction from flaxseed interacted with the protein adsorbed at the interface. An increase in apparent particle size was also noted with increasing flaxseed concentration, with destabilization becoming visually evident at concentrations higher than 0.1% (w/v). Microscopy, rheological data and size distribution analysis demonstrated for the first time that flaxseed gum interacts with protein-stabilized oil droplets at low pH, causing bridging flocculation. No significant differences were noted between flaxseed gums extracted from the Emerson and McDuff varieties. This research demonstrated that the electrostatic interactions between flaxseed gums and protein-stabilized emulsions need to be controlled when designing novel acidic beverages containing these polysaccharides.     

黄原胶与魔芋胶混胶黏度的影响因素研究

黄原胶和魔芋胶都是非凝胶多糖，二者在一定条件下共混可以出现强烈的协同效应。本文研究当黄原胶和魔芋胶以5／5的配比共混，总浓度为1％，温度，柠檬酸，蔗糖和功能型甜味对混胶多糖黏度的影响。结果表明：升高温度使混胶的黏度降低；当柠檬酸的使用量大于0．2％时，混胶的黏度下降；40℃时甜味剂的加入使得混胶的黏度升高。     

Influence of emulsifier type on freeze-thaw stability of hydrogenated palm oil-in-water emulsions

The influence of emulsifier type (Tween 20, whey protein isolate, casein) on the physical properties of 20 wt% hydrogenated palm oil-in-water emulsions after crystallization of (i) the oil phase only or (ii) both the oil and water phases has been examined. Emulsion stability was assessed by differential scanning calorimetry measurements of fat destabilization after cool–heat cycles, and by measurements of mean particle size, oiling off, and gravitational separation after isothermal storage (−20 to 37 °C). Tween 20-stabilized emulsions showed appreciable fat destabilization at temperatures where the oil phase was partially crystalline, which was attributed to partial coalescence. Protein-stabilized emulsions were stable under these conditions, which was mainly attributed to the relatively thick interfacial membranes surrounding the droplets. When both oil and water phases crystallized, there was complete destabilization of Tween 20- and casein-stabilized emulsions, and extensive destabilization of whey protein-stabilized emulsions, which was attributed to ice crystallization. The results of this study could facilitate the development of frozen food products with improved properties.     

Effect of xanthan gum on the physical properties and textural characteristics of whipped cream

Xanthan gum was used as thickening agent to prepare whipped cream in this work. A dose-dependent effect was observed on the average particle size (d_3,2) of whipped cream. At each xanthan gum level (0.025–0.125%) used, whipping time also showed a positive effect on the average particle size. With the increase of xanthan gum level or whipping time, the partial coalescence of fat in the whipped cream increased gradually. However, xanthan gum level showed no significant effect on the overrun of whipped cream. The textural characteristics of whipped cream were also investigated and the results indicated that a positive correlation was found between xanthan gum level and firmness, cohesiveness or viscosity of whipped cream. A different tendency was detected for consistency. The consistency of whipped cream increased with the increase of xanthan gum level to 0.100%, thereafter decreased.     

Interference of sodium caseinate in the TBARS assay

One of the most common methods of measuring lipid oxidation in foods is the quantification of malonaldehyde by reaction with 2-thiobarbituric acid (TBA) in the so called TBA-reactive substances (TBARS) assay. Different variants of the TBARS assay include those in which the food sample reacts directly with the TBA reagent and those that involve collection of a distillate from the food before reaction with TBA. Interference of sodium caseinate (NaCas) in a TBARS assay involving direct reaction of TBA with a food sample was observed while exploring the possible retardation of lipid oxidation in sliced turkey meat coated with a NaCas-containing edible film. This short report shows the extent of interference encountered and illustrates the importance of validating the TBA method for particular applications.     

酪朊酸钠的酶解及分离分析

利用复合蛋白酶水解酪朊酸钠制备营养性酪蛋白小分子肽，对水解的工艺参数，小分子肽的得率变化及酶解液溶解性进行了系统的研究，并对酶解产物进行了SDS-PAGE电泳实验和氨基酸组成分析。     

Oleogel production based on binary and ternary mixtures of sodium caseinate,xanthan gum,and guar gum: Optimization of hydrocolloids concentration and drying method

We report the optimization of oleogel formulation based on sodium caseinate (CN, 0–4 g/100 g), xanthan gum (XG, 0–1 g/100 g), guar gum (GG, 0–1 g/100 g), and drying method (freeze and oven drier) using response surface methodology to achieve the desired oil binding capacity, textural, and rheological attributes. All the selected responses were successfully fitted by a quadratic model with determination coefficient values higher than .95 with the exception of firmness values which was fitted by linear model. There were considerable increases in all the responses for the samples containing ternary mixtures of protein-gum (CN:XG:GG) as well as binary mixtures (CN:GG and CN:XG) compared to samples containing protein or gums alone due to the synergistic effect of CN and gums on formation of highly ordered and strong gel network. Regression modeling demonstrated that freeze drying method led to significantly greater structure recovery values than those of oven drying method. The best formulation was the freeze dried oleogel containing 4 g/100 g CN, 0.43 g/100 g XG, and 0.98 g/100 g GG. Results showed that fabrication of oleogels with at least 94.5 g/100 g sunflower oil and characteristics similar to industrial shortening is feasible.     

Improvement of stability of oil-in-water emulsions containing caseinate-coated droplets by addition of sodium alginate

ABSTRACT:  The potential of sodium alginate for improving the stability of emulsions containing caseinate-coated droplets was investigated. One wt% corn oil-in-water emulsions containing anionic caseinate-coated droplets (0.15 wt% sodium caseinate) and anionic sodium alginate (0 to 1 wt%) were prepared at pH 7. The pH of these emulsions was then adjusted to 3.5, so that the anionic alginate molecules adsorbed to the cationic caseinate-coated droplets. Extensive droplet aggregation occurred when there was insufficient alginate to completely saturate the droplet surfaces due to bridging flocculation, and when the nonadsorbed alginate concentration was high enough to induce depletion flocculation. Emulsions with relatively small particle sizes could be formed over a range of alginate concentrations (0.1 to 0.4 wt%). The influence of pHs (3 to 7) and sodium chloride (0 to 500 mM) on the properties of primary (0 wt% alginate) and secondary (0.15 wt% alginate) emulsions was studied. Alginate adsorbed to the droplet surfaces at pHs 3, 4, and 5, but not at pHs 6 and 7, due to electrostatic attraction between anionic groups on the alginate and cationic groups on the adsorbed caseinate. Secondary emulsions had better stability than primary emulsions at pH values near caseinate's isoelectric point (pHs 4 and 5). In addition, secondary emulsions were stable up to higher ionic strengths (< 300 mM) than primary emulsions (<50 mM). The controlled electrostatic deposition method utilized in this study could be used to extend the range of application of dairy protein emulsifiers in the food industry.