不同黏度多糖阿拉伯胶和瓜尔胶对肌原纤维蛋白乳化性质的影响

选取两种分子质量相近、黏度相差较大的天然高分子多糖阿拉伯胶（arabic gum,AG）和瓜尔胶（guar gum,GG）分别与肌原纤维蛋白（myofibrillarprotein,MP）进行复合,研究不同多糖添加量（0.1%～0.5%）对MP-多糖复合物乳液性质的影响规律。结果表明,AG和GG均可以显著改善MP的乳化性质,其中AG对乳化活性的改善效果较好,而GG更有利于乳液的稳定性。随着多糖质量分数增加,乳化活性指数和稳定性指数均呈先升高后降低趋势,AG和GG添加量分别为0.3%和0.2%时,乳化活性指数和稳定性指数达到最大值。界面蛋白含量测定结果显示,AG和GG均会导致界面蛋白含量下降,尤其是GG的作用更明显。随着AG和GG添加量增加,乳液粒径逐渐减小,且尺寸分布更加均一,添加量超过0.3%后,GG组乳液出现少量絮凝现象。同一添加量下,GG组乳液粒径明显小于AG组。流变学分析证实,所有乳液均为假塑性流体,表现出弱凝胶性质。AG添加量较少（≤0.3%）时会降低乳液黏度,并明显提高乳液的储能模量,而GG的添加使乳液表观黏度和储能模量均显著提高,与AG相比,高黏度GG制备的乳液拥有更高的...     

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.     

低钠条件下超声处理对鸡肉肌原纤维蛋白乳液稳定性的影响

低钠条件下肌原纤维蛋白（myofibrillar protein,MP）作为乳化剂制备的乳液稳定性差,本实验采用高强度超声波（high intensity ultrasound,HIU）（频率20 kHz、功率450 W）对低钠条件下（0.15 mol/L NaCl）MP进行不同时间（0、3、6、9、12 min）处理,测定处理后MP乳液乳化活性指数（emulsifying activity index,EAI）、乳液稳定性指数（emulsion stability index,ESI）、Turbiscan稳定性指数（turbiscan stability index,TSI）和平均粒径等,并进行微观结构观察和流变性分析等,研究低钠条件下超声处理对鸡肉MP乳化特性及其乳液稳定性和流变性能的影响。结果表明：与对照组相比,随着超声处理时间延长,MP的EAI和ESI显著增加（P＜0.05）,MP制备乳液的TSI和粒径随着超声处理时间的延长明显减小,且乳液液滴分布均匀,乳液Zeta-电位的绝对值显著增加（P＜0.05）。乳液的流变学特性分析结果表明超声波明显提高了MP乳液的黏弹性。MP乳液的油-水界面张力分析结果显示超声处理有效增强了MP的移动性,使界面张力迅速降低,同时超声处理显著增加了MP乳液吸附蛋白相对含量（P＜0.05）,这表明超声处理MP有助于稳定乳液。通过冷场扫描电子显微镜观察进一步证实了超声处理12 min MP制备的乳液液滴体积最小。综上,超声波能够有效提高低钠条件下MP的乳液稳定性,本实验可为超声处理在减盐乳化型肉制品中的应用提供理论参考。     

Mangosteen Oil-In-Water Emulsions: Rheology, Creaming, and Microstructural Characteristics during Storage

The rheological properties and physical stability of mangosteen (Garcinia mangostana L.) extract in oil-in-water (MIO/W) emulsions were investigated. Rheological study on the emulsions exhibited Newtonian flow behavior. The 20?wt.% emulsion showed higher apparent viscosity than 10?wt.% MIO/W sample. The effects of salt (NaCl) concentration (0, 50, 100, and 200?mM) and heat treatment (70?°C) on the stability of the emulsions were also examined. Heat (70?°C)- and NaCl (100 and 200?mM)-treated emulsions showed creaming and droplet aggregation on storage for a period of 60?days. The 10?wt.% MIO/W emulsions stored at 4?°C showed a homogeneous distribution of oil droplets with good stability to creaming and viscosity independent of shear stress (i.e., a Newtonian liquid).     

Comparative study of Pickering emulsions stabilised by starch particles from different botanical origins

Starch botanical origin is a key factor for the characteristics of Pickering emulsion. Starches with different sizes from rice (2.9–7.6 µm), waxy corn (9.3–25.0 µm), wheat (11.4–33.7 µm) and potato (24.4–54.1 µm) were esterified by octenyl succinic anhydride. The modified starch particles were used as stabilisers to produce oil-in-water Pickering emulsions. The physical stability, microstructures and rheological properties of different emulsions were compared. Results indicated that the emulsion stabilised with rice starch particles had the minimum droplet size of 83.6 µm and best physical stability during 30 days of storage. Moreover, starch particle size was negatively correlated with emulsion stability (P < 0.05). The particles (3.85% of the emulsion, w/w) built up wall-like structures around oil droplets, which prevented them from freely moving. All emulsions showed pseudoplastic fluid behaviours and presented gel properties, but elastic modulus (G′) and loss modulus (G″) were mainly affected by starch botanical origins.     

声流效应对大豆分离蛋白超声乳化效果研究

目的 研究不同超声功率（0、28、47、69、88、109 W）作用下声流效应对大豆分离蛋白(soy protein isolate, SPI)乳化效果的影响。方法 将声流效应形成机制与有限元方法相结合,对声场内的声流现象进行仿真计算,获取不同超声功率下的声流速度场分布,探究超声空化场分布特性。通过大豆分离蛋白超声乳化实验,对不同功率条件下声流效应产生的空化作用效果进行验证,利用激光粒度分析仪、紫外可见分光光度计、旋转流变仪测量大豆分离蛋白乳化液的粒径、乳化活性、乳化稳定性、表观粘度。结果 增大超声功率可使沿反应器轴向区域相同位置处声流速度值增大,声流效应增强,显著提高(P<0.05)超声空化空间分布范围。声流作用下,对大豆分离蛋白乳化液进行超声处理可显著降低(P<0.05)乳化液平均粒径和粒径分布,提高(P<0.05)乳化活性、乳化稳定性和表观粘度。超声功率为88 W时,乳化效果最佳。结论 超声功率为88 W所产生的声流效应对大豆分离蛋白乳化液的乳化效果影响最为显著,研究成果可为超声乳化的优化研究提供可行的方法。     

Influence of different β-glucans on the physical and rheological properties of egg yolk stabilized oil-in-water emulsions

The objective of this study was to obtain additional information on the influence of different β-glucan preparations, i.e. curdlan (CL), barley (BG), oat (OG), and yeast (YG) β-glucans, on the physical and rheological properties of egg yolk stabilized oil-in-water emulsions containing 20% oil. The emulsion without β-glucan (REF) was also prepared as a reference. Addition of CL and OG increased emulsion oil droplet sizes, whereas BG and YG showed no effect. Emulsion microstructures revealed that β-glucans induced flocculation of the oil droplet in the following order: CL > BG ≈ OG > YG. Dynamic oscillatory shear tests indicated that all emulsions exhibited weak gel-like characteristics which were enhanced by β-glucans addition as evidenced by an increase in G′ and a decrease in tan δ values. Flow tests showed that β-glucans enhanced thixotropy and yield stress of the emulsions. Stability tests demonstrated that β-glucans addition improved creaming stability of the emulsions during storage possibly due to an increase in viscosity of the continuous phase and/or a formation of a three-dimensional droplet network. CL exhibited the most pronounced effects on the aforementioned properties of emulsions compared to the other β-glucans tested. YG gave emulsion with higher viscoelastic properties and yield stress but lower stability than those made with BG or OG, indicating complex relationship between rheology and stability of these emulsion systems.     

Influence of Ultrasonication Parameters on Physical Characteristics of Olive Oil Model Emulsions Containing Xanthan

Ultrasonic emulsification of 20-wt.% o/w emulsions (pH 3.8) containing a food-grade emulsifier (whey protein isolate, WPI, 2.7 wt.%) and xanthan gum (XG, 0.25 wt.%) was performed. Time and amplitude of ultrasonic treatment changed in order to evaluate their influence on emulsion droplet size, viscosity, and stability (by multiple light scattering (MLS) profiles) during cold storage (10 days at 5 °C). Ultrasonic treatment duration changed from 1 to 4 min at constant amplitude of 70 %. Considering the amplitude, intervals of 40, 60, 80, and 100 % were chosen, for a constant time of 1 min. Similarly, time and amplitude conditions were used to treat solutions of XG of 1 wt.% and evaluate their influence on viscosity and how that was related to the stability of the emulsion. Increase in sonication time from 1 to 4 min led to a significant oil droplet size decrease from 1.14 to 0.89 μm (median droplet diameter). The viscosity of emulsions and XG solutions was highly influenced and considerably decreased with sonication time applied. At those conditions, an increase of backscattering was observed from 58.9 to 72.7 % after 10 days of storage, meaning that more stable emulsions, thinner and of smaller oil droplet size were produced. A similar trend was observed when the amplitude was increased, but droplet size and creaming were always greater than those noticed by changing the sonication time. However, the rate of viscosity, droplet size, and stability change was greater by increasing the amplitude rather than by changing the sonication time.     

Effect of heat treatment on the properties of soy protein‐stabilised emulsions

The effect of heat treatment on the properties of soy protein‐stabilised emulsions was investigated. Emulsions were prepared with unheated and heat‐treated soy protein (NSP and HSP) dispersions. Heating on soy protein dispersions at 95 °C for 30 min resulted in smaller average oil droplet size, lower tendency for oil droplet flocculation, higher protein adsorption and lower viscosity. The properties of emulsions were significantly influenced by the protein concentration. The sodium dodecyl sulphate–polyacrylamide gel electrophoresis (SDS–PAGE) profiles showed that the heat treatment on soy protein dispersions increased the protein adsorption at O/W interface. The viscosity of all samples at low shear rate was inversely proportional to the d₃₂, suggesting a positive relation to the total interfacial area per unit volume. Emulsions showed shear‐thinning behaviour. The relaxation time was found to increase with aqueous phase viscosity determined by the Cross viscosity model.     

Rheology and microstructure of myofibrillar protein-plant lipid composite gels: Effect of emulsion droplet size and membrane type

Composite gels were prepared from 2% myofibrillar protein (MP) with 10% imbedded pre-emulsified plant oils (olive and peanut) of various particle sizes at 0.6 M NaCl, pH 6.2. Dynamic rheological testing upon temperature sweeping (20-70 °C at 2 °C/min) showed substantial increases in G′ (elastic modulus) of MP sols/gels with the addition of emulsions, and the G′ increases were inversely related to the emulsion droplet size. Furthermore, gels containing emulsified olive oil had a greater (P < 0.05) hardness than those containing emulsified peanut oil. Regardless of oil types, MP-coated oil droplets exhibited stronger reinforcement of MP gels than Tween 80-stablized oil droplets; the latter composite gels had considerable syneresis. Light microscopy with paraffin sectioning revealed a stable gel structure when filled with protein-coated oil droplets, compared to gels with Tween 80-treated emulsions that showed coalesced oil droplets. These results suggest that rheological characteristics, hardness, texture, and water-holding capacity of MP gels were influenced by type of oils, the nature of the interfacial membrane, and the size of emulsion droplets.     

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.     

Oleosomes from Buriti (Mauritia flexuosa L. f.): Extraction,characterization and stability study

This study proposes a new strategy for extracting lipids from Buriti fruit in the form of oleosomes (OB) using an alkaline extraction medium and also evaluates the stability of OB under different pH conditions. The extracted oleosomes were evaluated under three pH conditions (2, 4.5 and 7) and showed sizes between 14.33 ± 0.03 and 16.44 ± 0.08 μm. Their zeta potential values varied with increasing pH (from 2 to 9), with an isoelectric point between pH 2.0 and 3.0. Proteins associated with oleosomes were observed between 14 and 29 kDa. The stability of the oleosome emulsions was confirmed by measuring the droplet size (D_3,2) which showed constant values during 28 days of storage. The Turbiscan stability index (TSI) also corroborates the stability of these emulsions in the same storage period. Furthermore, the carotenoid content in the oleosome emulsions was more stable than the carotenoids in bulk Buriti oil during 28 days of storage.     

椰子油纳米乳液制备工艺优化及其稳定性分析

为制备较为稳定的椰子油乳液,将酪蛋白酸钠(Sodium caseinate,SC)和黄原胶(Xanthan gum,XG)复合作为乳化剂,椰子油为油相,采用超声方法制备椰子油乳液。以平均粒径、Zeta-电位、离心稳定性及浊度等为考察指标,通过单因素实验筛选出超声功率、超声时间、油相质量分数和水相pH的合理研究范围。以平均粒径为响应值,用Box-Behnken响应面法对超声功率、超声时间和水相pH做进一步优化实验并对制备的乳液进行稳定性实验。结果表明,最佳制备工艺参数为:超声功率为480 W,超声时间为18 min,水相pH为7,所得椰子油纳米乳液的平均粒径为304.5±13.2 nm。所制备的椰子油纳米乳液在热处理温度40～90℃,pH6～8,离子浓度0～0.5 mol/L条件下具有良好的稳定性,且经3次冻融循环后乳液保持稳定,为构建用于食品加工的高稳定性椰子油乳液提供了理论支持。     

Study of emulsions stabilized with Phaseolus vulgaris or Phaseolus coccineus with the addition of Arabic gum, locust bean gum and xanthan gum

The properties of o/w emulsions stabilized with 1%w/v common bean (Phaseolus vulgaris L.), V or scarlet runner bean (P. coccineus L.), Coc extracted by isoelectric precipitation or ultrafiltration, at pH 7.0 and 5.5, with the addition of Arabic gum, locust bean gum, xanthan gum and a mixture of xanthan gum–locust bean gum (0.1 %w/v and 0.25 %w/v) are studied. The stability of emulsions was evaluated on the basis of oil droplet size, creaming, viscosity and protein adsorption measurements. The addition of Arabic gum, caused an increase in D[4,3] values and a decrease in the amount of protein adsorbed at the interface. The addition of locust bean gum in some emulsions reduced the amount of protein adsorbed. The addition of xanthan and to a less extend of the polysaccharide mixture, promoted a decrease in D[4,3]. So, emulsion stability was affected by the polysaccharide nature. Differences were also observed with respect to the protein nature, the method of its preparation and emulsion's pH. All polysaccharides enhanced the emulsions viscosity with xanthan and xanthan–locust bean gum exhibiting the higher values. V isolates and isoelectricaly precipitated isolates of both V, Coc showed higher viscosity values. The stability was enhanced by the increase of the viscosity of the continuous phase and the creation of a network, which prevents the oil droplets from coalescence.     

The rheological behaviour of low fat soy‐based salad dressing

Low fat soy‐based salad dressings were formulated with different oil levels (3%, 13% and 23%) and emulsifiers (whey protein concentrate, soy‐lecithin and sodium caseinate) using either blender or ultra‐turrax (UT) homogeniser. Results showed that the rheological behaviour of these samples were highly dependent on the oil content, emulsifiers and blending methods. The UT method produced samples with better viscosity and have droplet size of 2–100 μm. Samples containing higher oil level have higher viscosity, smaller droplet size, larger G′ and G″ values. All samples show a shear‐thinning effect and larger G′ than G″, indicating the elastic nature of the samples. A quantity Q(t)% was applied to estimate the elasticity and the values were found to be in the range 22.8–85.2%. G′ and G″ were found to decrease with increased temperature. However, tan δ increased slightly with temperature; the values ranged from 0.2 to 0.4 at 5 °C to 0.3–0.5 at 25 °C. Current results demonstrated that the formulated samples have good stability compared with commercial products.     

RHEOLOGICAL PROPERTIES OF OIL-IN-WATER EMULSIONS FORMED WITH MILK PROTEIN CONCENTRATE

The rheology and the microstructure of emulsions stabilized with milk protein concentrate (MPC) were investigated using different MPC and oil concentrations. Steady‐shear tests showed that the emulsions were Newtonian at low oil concentrations (<20 wt%), whereas they were pseudoplastic and thixotropic at high oil concentrations (>20 wt%). Dynamic rheological measurements demonstrated that these emulsions behaved as weak gels, as indicated by relatively high values of G′ to G″. The rheological behavior of these emulsions was consistent with bridging flocculation mechanisms, whereby more than one droplet is shared by adsorbed casein aggregates/micelles. This was confirmed by confocal microscopy, which showed that these emulsions were aggregated.     

EFFECTS OF ADDED WEIGHTING AGENT AND XANTHAN GUM ON STABILITY AND RHEOLOGICAL PROPERTIES OF BEVERAGE CLOUD EMULSIONS FORMULATED USING MODIFIED STARCH

Stability of beverage emulsion is measured by the rate at which the emulsion creams, flocculates or coalesces, and is generally dependent on rheology of water phase, difference in specific gravities of the two phases and droplet size/distribution of the emulsion. The effects of weighting agents (sucrose acetate isobutyrate and brominated vegetable oil) and xanthan gum on modified starch‐based emulsions were evaluated in this study. Emulsion was formed by addition of 9% coconut oil, in the presence or absence of weighting agents, into the water phase containing modified starch at 10, 12 or 14% without or with the addition of 0.3% xanthan gum. Stabilities of emulsions were evaluated both in the concentrated form used for storage and dilute form used in beverages. The addition of xanthan gum into the water phase decreased the flow behavior index (n) from 0.88 down to 0.31 and increased elastic modulus (G′) over 20 times at elevated frequency (ω = 50 rad/s) and elevated the stability of the emulsion. The xanthan gum‐added emulsion had smaller particle size and demonstrated 14 and 5 times slower phase separation compared to the emulsions without or with the addition of weighting agents, respectively. When the elastic modulus was larger than the viscous modulus (G′ > G″), the emulsions demonstrated greater stability. In dilute beverage solutions, creaming was observed in the absence of xanthan gum.     

豌豆分离蛋白-羧甲基纤维素纳静电复合物在乳液中的应用研究

为改善豌豆分离蛋白(PPI)在酸性乳液体系中的应用特性,采用阴离子多糖-羧甲基纤维素钠(CMC)与PPI在酸性条件下形成的静电复合物稳定O/W型乳液。首先研究了3% PPI溶液的溶解度、表面疏水性随CMC浓度(0~0.5%)的变化,在此基础上,分析了PPI-CMC静电复合物对乳液ζ-电位、粒径、粘度、乳析稳定性指数及微观结构的影响。结果表明:在pH4.5条件下,随着CMC浓度由0增加至0.5%,乳状液滴表面负电性不断增强,当CMC浓度≥0.4%时,PPI乳液稳定性明显提高,液滴分散均匀,絮凝程度明显降低,在4 ℃下存放一周,未发现明显分层。因此,通过调控PPI-CMC相互作用可有效改善PPI在酸性乳液体系中的应用特性,研究成果有望为高豌豆蛋白酸性乳品和饮料的开发提供参考。     

Stability and rheology of concentrated O/W emulsions based on soybean oil/palm kernel olein blends

Droplet size distribution and rheological properties of egg yolk-stabilized emulsions were studied before and after storage (25 °C, 30 days). The dispersed phase (70%) of the emulsions was based on soybean oil (SBO) and 10–40% palm kernel olein (PKO) replacements of SBO. Replacement of PKO resulted in a significant increase in droplet mean diameters and a decrease in rheological properties of the emulsions. All emulsion exhibited a gel-like characteristic with storage modulus higher than loss modulus and tan δ greater than 0.3. Significant increase (p < 0.05) was found for droplet mean diameters and rheological properties of the emulsions after storage. Emulsion with fully SBO and the highest PKO replacement (40%) were found to be the most unstable, which was ascribed to a strong flocculation. With 10–30% PKO replacements, the emulsions displayed a better stability after storage, most probably promoted by significant content of short-medium chain fatty acids in PKO.     

Emulsifying properties of β-lactoglobulin and Quillaja bark saponin mixtures: Effects of number of homogenization passes,pH, and NaCl concentration

The effects of number of homogenization passes, pH, and NaCl concentration on the formation and stability of oil-in-water emulsions comprising a mixture of a biosurfactant (Quillaja bark saponin) and a globular protein (β-lactoglobulin) were investigated. The emulsions were characterized as to visual appearance, droplet size, droplet surface charge, and rheology. The emulsions obtained by different conditions (4, 6, or 8 passes; pH 7, 8, or 9; and 0, 100, or 200 mmol L^?1 of NaCl) were polydisperse, presented relatively small average droplet sizes (z-average < 323 nm) as well as negative droplet charge (between –20 and –79.6 mV) in all evaluated conditions. Regardless of the number of homogenization passes, the emulsions exhibited low apparent viscosity and pseudoplastic behavior with small yield stress. Viscoelastic behavior was also observed, thus the emulsions were characterized as weak gels. Four homogenization passes were enough to obtain small droplets in the evaluated conditions. Droplet size was not significantly affected by NaCl concentration and pH (p > 0.05). On the other hand, the absolute ζ-potential values significantly decreased and increased upon increased NaCl content and pH, respectively. Regardless of the tested conditions, all emulsions had good stability against phase separation and droplet aggregation, since no significant changes in average droplet size were observed throughout storage (p > 0.05). In the presence of NaCl, in which droplet charge significantly decreased, emulsion was also stable. Thus, we can conclude that electrostatic repulsion as well as steric repulsion was responsible for stabilization.