DISPERSION STATE OF PROTEIN-STABILIZED EMULSIONS

The stability of concentrated benzene-in-water emulsions emulsified by bovine serum albumin (BSA) in the presence of various concentrations of sodium chloride has been measured in the light of the coalescence kinetics. On the acid and alkaline sides of the isoelectric point of BSA (pH 4.9), the rate of coalescence between globules decreased and approached that at the isoelectric point of BSA with increasing concentrations of sodium chloride. In these systems, the interfacial tension at the benzene/aqueous BSA solution interface, and the globule size distribution in the emulsions, reached the values observed at the isoelectric point when the concentration of sodium chloride was above about 50 mM. The role of the adsorbed film of BSA on the surface of dispersed globules is considered in relation to the dissociation state of the BSA molecules.     

Composition of interfacial layers in complex food emulsions before and after aeration: effect of egg to milk protein ratio

Whipped emulsions were prepared at pilot scale from fresh milk, whole egg, and other ingredients, for example, sugars and stabilizers (starch, polysaccharides). Egg content was varied: 4 recipes were studied differing in their egg to milk protein ratio (0, 0.25, 0.38, and 0.68). Protein and fat contents were kept constant by adjusting the recipes with skim-milk powder and fresh cream. Emulsions were prepared by high-pressure homogenization and whipped on a pilot plant. Particle-size distribution determined by laser-light scattering showed an extensive aggregation of fat globules in both mix and whipped emulsions, regardless of recipe. Amount of protein adsorbed at the oil-water interface and protein composition of adsorbed layer were determined after isolation of fat globules. Protein load is strongly increased by the presence of egg in formula. Values obtained for the whipped emulsions were dramatically lower than those obtained for the mix by a factor of 2 to 3. Sodium dodecyl sulfate-PAGE indicated a preferential adsorption of egg proteins over milk proteins at the oil-water interface, regardless of recipe. This phenomenon was more marked in aerated than in unaerated emulsions, showing evidence for desorption of some milk proteins during whipping. Egg proteins stabilize mainly the fat globule surface and ensure emulsion stability before whipping. Air bubble size distribution in whipped emulsions was measured after 15 d storage. When the egg to milk protein ratio is decreased to 0.25, large air cells appear in whipped emulsions during storage, indicating mousse destabilization. The present work allows linking the protein composition of adsorbed layers at the fat globule surface to mousse formula and mousse stability.     

瓜尔豆胶对搅打稀奶油的搅打性能的影响

研究了不同浓度的瓜尔豆胶对搅打稀奶油乳状液的表观黏度、脂肪球粒度、脂肪球界面蛋白浓度、脂肪球部分聚结率、泡沫硬度和搅打起泡率的影响。结果表明，瓜尔豆胶对搅打稀奶油乳状液的表观黏度影响非常显著；瓜尔豆胶浓度过高或过低，都会使得解冻后的乳状液粒径变大；瓜尔豆胶的质量分数越高，脂肪球部分聚结速度越快，泡沫硬度也越大；搅打起泡率随着瓜尔豆胶质量分数增大而降低。     

Functional characterization of protein stabilized emulsions: Emulsifying behaviour of proteins in a valve homogenizer

Protein stabilised emulsions have been prepared in a valve homogeniser incorporated into a recirculating emulsification system, where the power input and number of passes have been varied. The food proteins studied were a soy-bean protein isolate, a whey protein concentrate (WPC) and a sodium caseinate. The emulsions obtained were characterized in terms of particle size distribution and amount of protein adsorbed on to the fat surface (protein load). Generally, the final fat surface area of the emulsions obtained increases more as a function of power input than as a function of number of passes. Distribution width, c_s, decreases mostly with increasing power supply and number of passes, but at the highest power input c_s increases. The protein load on the fat globules is largely determined by the fat surface area and by the type of protein adsorbed. The soy proteins give a high protein load and the caseinates give a low protein adsorption at small fat surface areas created. This relation is reversed at large surface areas of the fat globules. The relation between percentage protein adsorbed from bulk as a function of surface area suggests that the caseinates mainly cover the newly created interface by adsorption from the bulk, whereas the soy proteins fulfil this task mostly by spreading at the interface. Salt addition to 0.2M-NaCl enhances protein adsorption at the fat globule interface in the case of soy protein and caseinate, but for the whey proteins protein load is higher in distilled water.     

Influence of pH on linear viscoelasticity and droplet size distribution of highly concentrated O/W crayfish flour-based emulsions

In the present work, the influence of pH on stability of oil-in-water (O/W; 75 wt%/25 wt%) emulsions stabilized by crayfish flour (CF) has been studied. CF (containing ca. 65 wt%) showed poor functionality in a wade range of pH, which inhibits formation of stable emulsions. An indirect procedure has been developed in order to obtain emulsion at a broad pH range, including isoelectric point (pI) value. The emulsions have been characterized by means of linear dynamic viscoelasticity and droplet size distribution (DSD) analysis. These emulsions present a behaviour characteristic of highly concentrated emulsions with a well-developed plateau region. The most unfavourable DSD and linear viscoelastic results correspond to the pI. A significant improvement takes place as the pH value departs from the pI. An exception for linear viscoelasticity results have been found at pH 10, which is close to the pI for rod segments of myofibrillar proteins. Stability of these emulsions has been studied by following the evolution of DSD and linear viscoelastic parameters along time. The poorer results in emulsion stability correspond to pH values close to the pI, at which the increase in droplet size or uniformity parameter as well as the decrease in the plateau modulus become more pronounced. Conversely, the stability significantly improves as the pH departs from pI.     

Ability of whey protein isolate and/or fish gelatin to inhibit physical separation and lipid oxidation in fish oil-in-water beverage emulsion

The effect of pH on the capability of whey protein isolate (WPI) and fish gelatin (FG), alone and in conjugation, to form and stabilize fish oil-in-water emulsions was examined. Using layer-by-layer interfacial deposition technique for WPI–FG conjugate, a total of 1% protein was used to prepare 10% fish oil emulsions. The droplets size distributions and electrical charge, surface protein concentration, flow and dynamic rheological properties and physiochemical stability of emulsions were characterize at two different pH of 3.4 and 6.8 which were selected based on the ranges of citrus and milk beverages pHs, respectively. Emulsions prepared with WPI–FG conjugate had superior physiochemical stability compare to the emulsions prepared with individual proteins. Higher rate of coalescence was associated with reduction in net charge and consequent decrease of the repulsion between coated oil droplets due to the proximity of pH to the isoelectric point of proteins. The noteworthy shear thinning viscosity, as an indication of flocculation onset, was associated with whey protein stabilized fish oil emulsion prepared at pH of 3.4 and gelatin stabilized fish oil emulsion made at pH of 6.8. At pH 3.4, it appeared that lower surface charge and higher surface area of WPI stabilized emulsions promoted lipid oxidation and production of hexanal.     

油脂用量对搅打稀奶油的搅打性能和品质的影响

研究了油脂用量对搅打稀奶油的粒度分布、脂肪部分聚结、液相蛋白质浓度、搅打起泡率、质构特性、感官品质和稳定时间的影响。研究表明:随着油脂用量增加,冷却后乳浊液脂肪球粒径增大;搅打过程中脂肪部分聚结速度和脂肪球粒径d4,3均随油脂用量增加而增大,且脂肪部分聚结率与脂肪球粒径d4,3有很好的相关性;液相蛋白质浓度和搅打起泡率降低;搅打稀奶油的质构特性值增加;稳定时间呈先增后减趋势,当油脂用量为23%时,搅打稀奶油的稳定时间最长达到2.7h;搅打稀奶油的感官品质以油脂用量为20%最好,综合考虑,油脂最佳用量范围是20%-23%。     

Candelilla Wax Emulsion, Preparation and Stability

Wax in water emulsions were prepared with candelilla wax using a modified conventional method of high pressure homogenization for foods. The resulting emulsions were compared to coconut oil-in-water emulsions. A model based on spectra absorbance analysis was used to evaluate creaming rates of wax-in-water emulsions as well as coconut oil-in-water emulsions, prepared at different homogenization pressures. It showed creaming rates for wax-in-water emulsion were lower than for oil-in-water emulsion. Wax-in-water emulsions prepared at 4100 kPa produced suspended globules of 1.89 μmin size; emulsions prepared at higher homogenization pressures produced smaller average particle sizes, i.e., 0.66 μm at 27560 kPa.     

Physicochemical Properties of Whey Protein-Stabilized Emulsions as affected by Heating and Ionic Strength

Corn oil-in-water emulsions (19.6 wt%; d₃₂～ 0.6 μm) stabilized by 2 wt% whey protein isolate (WPI) were prepared with a range of pH (3–7) and salt concentrations (0–100 mM NaCl). These emulsions were heated between 30 and 90°C and their particle size distribution, rheological properties and susceptibility to creaming measured. Emulsions had a paste-like texture around the isoelectric point of WPI (～φ 5) at all temperatures, but tended to remain fluid-like at pH >6 or <4. Heating caused flocculation in pH 7 emulsions between 70 and 80°C (especially at high salt concentrations), but had little effect on pH 3 emulsions. Flocculation increased emulsion viscosity and creaming. Results were interpreted in terms of colloidal interactions between droplets.     

κ-卡拉胶影响大豆分离蛋白乳浊液稳定性的研究

研究了卡拉胶对大豆分离蛋白乳浊液粒度分布、乳析率和离心沉淀率的影响,在此基础上分析了静置过程中乳浊液粒径与乳析率、离心沉淀率之间相关性,结果表明:乳浊液粒径随卡拉胶浓度由小到大依次为0.03%<空白样<0.06%<0.09%;而体系的表观粘度随卡拉胶浓度的增大而升高;静置过程中乳浊液顶部粒径d3,2与乳析率有较好的相关性;乳浊液底部d3,2与离心沉淀率有很好的相关性。进一步分析了其可能的作用机理:卡拉胶低浓度时,卡拉胶分子被吸附到液滴的蛋白质正电荷区域,增加了液滴间的静电排斥,从而增加了体系的絮凝稳定性;随着卡拉胶浓度增大,卡拉胶会引起体系排斥絮凝。     

Turbidity of Beverages with Citrus Oil Clouding Agent

Basic principles of light scattering were used to predict turbidity in cloudy beverages for monodisperse and polydisperse systems of suspended citrus oil globules. Predicted values for specific turbidity agreed well with experimental values for diluted citrus oil-in-water beverage cloud emulsions. Citrus oil-in-water cloud emulsions were prepared with a pressure homogenizer at different pressures (4.1–27.56 kPa). Size distributions obtained for the emulsions fit the long-normal distribution and the distribution curves became more narrow as pressure of homogenization increased.     

pH-dependent emulsifying properties of pea [Pisum sativum (L.)] proteins

Emulsifying properties of two partially purified legumin and vicilin (PL and PV) and protein isolate (PPI) from dry pea seeds at various pH values (3.0, 5.0, 7.0 and 9.0) were investigated. The tested emulsion characteristics included droplet size, flocculation and coalescence indices (FI and CI), creaming index, as well as interfacial protein adsorption. Some physicochemical properties of these proteins, e.g., free sulfhydryl and disulfide bond contents, protein solubility (PS), surface hydrophobicity (H_o) and thermal stability (and denaturation), were also characterized. The results indicated that emulsifying ability and emulsion stability of various pea proteins considerably varied with the preparation process, protein composition and pH. Overall, all the pea proteins exhibited least emulsifying ability at pH 5.0 (around isoelectric point), and concomitantly, the resultant emulsions were most unstable against coalescence and creaming. The emulsifying ability of these proteins at pH 3.0 was generally better than that at neutral or alkali pH values, and among all the three proteins, PL exhibited highest emulsifying ability at this pH. The flocculated state and size of droplets in fresh emulsions did not directly affect stability of these emulsions against flocculation and coalescence (upon 24 h of storage), and even creaming (up to 7 days). Interestingly, the PL and PV exhibited much better creaming stability than PPI, at pH deviating from the pI. The emulsifying properties of these proteins were not only related to their PS and H_o, but also associated with the protein adsorption and nature (e.g., viscoelasticity) of interfacial protein films. These results can greatly extend the knowledge for understanding the emulsifying properties of pea proteins, especially the pH dependence of emulsion characteristics.     

Temperature and pH as factors influencing droplet size distribution and linear viscoelasticity of O/W emulsions stabilised by soy and gluten proteins

The influence of pH and two post-emulsification treatments (pH modification and thermal cycles) over linear dynamic viscoelasticity and droplet size distribution, DSD, of O/W emulsions (75% oil) stabilized either by soy protein isolate, SPI, or wheat gluten, WG were studied in the present work. Rheological properties and droplet size of fresh emulsions showed an important dependence on pH as a consequence of the role of electrostatic interactions, not being possible to obtain a stable emulsion for pH values close to the protein isoelectric point, pI, (4–5 for SPI and 6 for WG). In order to overcome this inconvenient, an alternative emulsification procedure, basically consisting in a modification of pH after emulsification (indirect emulsification), was successfully developed. Emulsions obtained after this post-emulsification treatment, showed higher elastic (G′) and loss (G″) moduli and also larger oil droplets than fresh emulsions prepared at the same pH. Moreover, the application of upward/downward temperature cycles from 20 to 70 °C to emulsions directly prepared at a pH yielded to significantly higher values of the rheological functions when compared to those found for fresh emulsions. Accordingly, both post-emulsification treatments lead to apparent enhancements in emulsion rheology and microstructure, which is indicative of a good potential to improve long-term emulsion stability.     

Influence of pH and CaCl2 on the stability of dilute whey protein stabilized emulsions

The influence of pH and CaCl₂ on the physical stability of dilute oil-in-water emulsions stabilized by whey protein isolate has been studied. The particle size, zeta potential and creaming stability of 0.05 wt% soy bean oil-in-water emulsions (d ≈ 0.53 μm) were measured with varying pH (3 to 7) and CaCl₂ concentration (0 to 20 μM). In the absence of CaCl₂ extensive droplet aggregation occurred around the isoelectric point of the whey proteins (4 < pH < 6) because of their low electrical charge, which led to creaming instability. Droplet aggregation occurred at higher pH when CaCl₂ was added to the emulsions. The minimum concentration of CaCl₂ required to promote aggregation increased as the pH increased. Aggregation was induced in the presence of CaCl₂ probably because of the reduction in electrostatic repulsion between droplets, caused by binding of counter ions to droplet surfaces and electrostatic screening effects.     

Physicochemical properties of dry-heated soy protein isolate–dextran mixtures

Soy protein isolate–dextran mixtures were incubated for up to three weeks and an improvement of their ability to stabilize emulsions against creaming, giving emulsions with lower droplet size, at pH values near the protein isoelectric point, was observed. Analysis of the adsorbed protein fraction indicated that the protein–polysaccharide hybrid can adsorb, together with the other mixture constituents, at the interface, during emulsion formation and in this way may contribute to droplet stabilization by enhancing repulsive steric forces by interpenetrating neighbouring droplets and polysaccharide chains.     

Effect of Emulsion Droplet Size on Foaming Properties of Milk Fat Emulsions

Foamability and foam stability of dairy-based emulsions, as a function of emulsion droplet size ranging from micron- to nanometre-scale, were investigated. Fat phase (10 % w/w of anhydrous milk fat, stearin or olein fraction) was mixed with 2 % w/w protein solution (sodium caseinate or whey protein concentrate) and homogenised at 3, 10 and 35 MPa to obtain emulsions having particle sizes of about 1.20, 0.60 and 0.20 μm, respectively. The emulsions were cooled down and aged at 4 °C for 48 h to promote crystallisation. No fat coalescence was observed in any of the emulsions, as particle size distribution remained the same upon aging and whipping. It was shown that the smaller the particle size, the higher was the apparent viscosity and the lower was the solid fat content. Higher solid fat content tended to yield better foamability and foam stability. Destabilisation of air cells happened fastest with nanosized fat particles, resulting in shorter half-life of foam.     

Ultrasonication retains more milk fat globule membrane proteins compared to equivalent shear-homogenization

Ultrasonication, like common shear homogenization, can reduce the milk fat globule size and may change the milk fat globule membrane (MFGM). This work compared the effect of ultrasonication to equivalent shear homogenization on MFGM proteins and lipid-derived volatile components. Results showed that treating milk with ultrasound at 35 kJ/L would realize a similar size distribution of the milk fat globules as shear-homogenization at 20 MPa. Proteomics analysis revealed that in total 192 MFGM proteins were identified and quantified and a number of these proteins were lost after both treatments; however, more MFGM proteins remained after ultrasonication than after shear-homogenization. SDS-PAGE results showed that milk plasma proteins, and especially caseins, were absorbed on the milk fat globules after both treatments. In addition, the amount of the volatile free fatty acids increased after both treatments.Industrial relevance: Ultrasonication, as an innovative food processing technology, in comparison to traditional homogenization, was shown to equally efficiently decrease the MFG size, but lead to less damage to native MFGM proteins, which may be due to its longer homogenization time window. These results increased knowledge on the biochemical changes of milk fat globules after their size reduction and showed that ultrasonication could be used as a novel approach to improve dairy product quality.     

Influence of gastric digestive reaction on subsequent in vitro intestinal digestion of sodium caseinate-stabilized emulsions

In this study, in vitro intestinal lipid digestion and the physicochemical and microstructural changes of sodium caseinate-stabilized emulsions were examined after the emulsions had been digested in a model simulated gastric fluid containing pepsin for different times. The average size, size distribution, microstructure, proteolysis of interfacial proteins and lipolysis of the emulsion droplets were monitored as a function of digestion time. The emulsion droplets underwent extensive droplet flocculation, with some coalescence together with proteolysis of interfacial proteins, in simulated gastric fluid, resulting in changes in the droplet size and the microstructure of the emulsions. In general, digestion in simulated gastric fluid containing pepsin accelerated coalescence of the emulsion droplets during subsequent digestion in simulated intestinal fluid containing pancreatic lipase. However, the changes in the size, the microstructure and the proteolysis of the interfacial proteins of the emulsions under gastric conditions did not influence the rate and the extent of lipid digestion in the subsequent intestinal environment.     

Chemical and structural characterisation of almond oil bodies and bovine milk fat globules

Lipids in almonds are present as oil bodies in the nut. These oil bodies are surrounded by a membrane of proteins and phospholipids and are a delivery vehicle of energy in the form of triglycerides, similarly to the more studied bovine milk fat globule membrane. Chemical, physical and microscopic analyses revealed major differences in the composition and structure of almond oil bodies and bovine milk fat globules. The lipids of both natural emulsions differed in degree of unsaturation, chain length, and class. The almond oil body membrane does not contain any cholesterol or sphingomyelin unlike the bovine milk fat globule membrane. Therefore, the phospholipid distribution at the surface of the oil bodies did not present any liquid-ordered domains. The membranes, a monolayer around almond oil bodies and a trilayer around bovine fat globules, may affect the stability of the lipid droplets in a food matrix and the way the lipids are digested.     

Effect of pH and Ionic Strength on the Physicochemical Properties of Coconut Milk Emulsions

ABSTRACT:  Coconut milk (16% to 17% fat, 1.8% to 2% protein) was extracted from coconut ( Cocos nucifera L.) endosperm and diluted in buffer to produce natural oil-in-water emulsions (10 wt% oil). The effect of pH (3 to 7) and NaCl (0 to 200 mM) on the properties and stability, namely, mean particle size, ζ-potential, viscosity, microstructure, and creaming stability, of the natural coconut milk emulsions was investigated. At pH values close to the isoelectric point (IEP) of the coconut proteins (pH 3.5 to 4) and in the absence of NaCl, coconut milk flocculated, but did not coalesce. Flocculation corresponded to low surface charges and was accompanied by an increase in emulsion viscosity. Adding up to 200 mM NaCl to those flocculated emulsions did not change the apparent degree of flocculation. Coconut milk emulsion at pH 6 was negatively charged and not flocculated. Upon addition of salt, the ζ-potential decreased from –16 to –6 mV (at 200 mM NaCl) but this was not sufficient to induce flocculation in coconut milk emulsions. At low pH (< IEP), the positively charged droplets of coconut milk emulsions only flocculated when the NaCl concentration exceeded 50 mM, as the ζ-potential approached zero.