瓜尔豆胶对大豆分离蛋白乳浊液稳定性的影响

研究了不同pH值条件下瓜尔豆胶对大豆分离蛋白乳浊液乳析稳定性和絮凝稳定性的影响。研究结果表明 ,在瓜尔豆胶浓度低于 0 0 4%时 ,随着瓜尔豆胶浓度的增加 ,乳浊液的稳定性逐渐增加。当多糖浓度高于 0 0 4%时 ,液滴发生排斥絮凝 ,体系的稳定性急剧下降 ,更高浓度的瓜尔豆胶因与乳浊液液滴间的热力学不相容性而导致体系发生各向同性和各向异性相分离。     

甲基纤维素对大豆分离蛋白乳浊液稳定性影响的研究

本文研究了甲基纤维素对大豆分离蛋白乳浊液稳定性的影响。研究结果表明，在低浓度时，甲基纤维素增加了体系的稳定性，对NaCl引起的液滴絮凝也有很好的抑制作用。而高浓度的甲基纤维素导致pH6．5和7．0的体系同时发生乳析和蛋白质沉积现象。其作用机理可能是，在低浓度时甲基纤维素吸附到液滴蛋白质层的外围形成次级保护层，增加了体系的稳定性，而高浓度时则可能置换出液滴的蛋白质吸附层。     

亲水性胶体在乳制品工业中的应用

<正> 亲水性胶体是指水溶性多糖,其作用是使多糖分散体系具有黏度和形成凝胶的能力。根据原料来源,亲水性胶体可分为:生物胶(黄原胶、葡聚糖、结冷胶)、植物胶(刺槐豆胶、瓜尔豆胶)、植物渗出液(阿拉伯胶、黄耆胶)、海藻胶(卡拉胶、琼胶)、纤维素及衍生物(纤维素、羧甲基纤维素(钠))、淀粉及其衍生物、动物胶(明胶)、果胶。 在乳制品工业中被广泛应用的亲水性胶体主要有刺槐豆胶、瓜尔豆胶、果胶和卡拉胶。主要作用是保护体系中的蛋白质以耐受加工中     

魔芋葡甘聚糖与瓜尔豆胶协同相互作用及其凝胶化研究

魔芋葡甘聚糖(也称魔芋胶)与瓜尔豆胶均为非凝胶多糖，但二者共按一定比例共混可以得到凝胶，这是多糖分子间相互作用的结果．当总糖浓度为1％，魔芋胶与瓜尔豆胶的共混比例为60／40，制备温度为80℃，体系盐离子(Ca^2 )浓度为0．1mol／L时可得到协同相互作用的最大值，从FT-IR谱图上分析了两种多糖分子间相互作用的机理。     

Sorbet制造中乳化稳定剂的选择

本文确定了Sorbet的生产工艺，并重点研究了卡拉胶、瓜尔豆胶、海藻酸钠、羰甲基纤维素钠、三聚甘油单硬脂酸酯等乳化稳定剂对Sorbet膨胀率、抗融性的影响。     

魔芋葡甘聚糖与瓜尔豆胶协同相互作用及其凝胶化研究

魔芋葡甘聚糖( 也称魔芋胶)与瓜尔豆胶均为非凝胶多糖,但二者共按一定比例共混可以得到凝胶,这是多糖分子间相互作用的结果。当总糖浓度为 1%,魔芋胶与瓜尔豆胶的共混比例为 60/40,制备温度为 80OC,体系盐离子(Ca2 )浓度为 0.1mol/L时可得到协同相互作用的最大值,从 FT-IR 谱图上分析了两种多糖分子间相互作用的机理。     

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。     

质构仪分析法在常用增稠剂对乳制品品质评价中的应用

利用质构仪研究了卡拉胶、瓜尔豆胶、羟甲基纤维素钠(CMC)、黄原胶对乳制品质构的影响。分析发现,卡拉胶、CMC可以在一定程度上改善乳制品的质构,同时使得乳制品保水性得到改善。添加瓜尔豆胶、黄原胶的乳制品其硬度、黏附性、内聚性和弹性均不同程度的降低,同时造成乳制品的保水性下降,不仅没有改变乳制品的品质特性,反而使其品质劣化。就上述4种增稠剂而言,从改变乳制品品质上看,卡拉胶、羟甲基纤维素钠(CMC)可以作为改善乳制品的增稠剂而运用于乳制品行业。     

大豆蛋白-瓜尔豆胶水解物Maillard反应共聚物的乳化特性研究

研究了不同水解时间的瓜尔豆胶对蛋白质-多糖Maillard反应共聚物的乳化特性的影响及不同水相条件下共聚物与酪朊酸钠乳化特性的差异。研究表明,瓜尔豆胶的酸水解时间对大豆分离蛋白-多糖共聚物的乳化活性和乳化稳定性都有明显的影响。水解40min的瓜尔豆胶与大豆分离蛋白反应10 d的共聚物具有优良的乳化性能;在0.3mol/L NaCl和pH 4.0的酸性条件下,共聚物的乳化活性和乳化稳定性都明显高于商品乳化剂酪朊酸钠;在90℃热处理60 min后其乳化活性和乳化稳定性仍接近未经热处理时的酪朊酸钠的乳化活性和稳定性。该共聚物作为安全高效的天然高分子食品乳化剂具有广阔的应用前景。     

复合膳食纤维素的结构及物性研究

采用大豆纤维素为基料,水溶性天然植物胶——瓜尔豆胶、果胶为辅料复合后,制备一种兼有水溶性和非水溶性双重特性的复合膳食纤维素。测定复合膳食纤雏素的粘度和表面张力,并对复合膳食纤维素体系进行扫描电镜观察后发现,大豆纤维素与瓜尔豆胶复合物的粘度和表面张力较两种单一成分均有明显提高,且复合物可调和成为以瓜尔豆胶溶胶为基体、大豆纤维素颗粒均匀镶嵌其间的稳定体系。大豆纤维素与果胶复合物的上述指标也有提高,但体系不稳定。     

Effect of Xanthan Gum Upon the Rheology and Stability of Oil-Water Emulsions

Soyabean oil-water emulsions were studied. In oil-water emulsions (up to 60% oil) xanthan is essential to prevent creaming. A yield stress arises primarily from the polysaccharide liquid crystalline structure. In concentrated systems where the oil droplets interact strongly there is a significant contribution to the yield stress arising from the need to modify individual droplet shapes when shear is applied to the system. Studies of droplet sizes suggest that the xanthan gum can also modify the equilibrium droplet size by lowering the oil-water interfacial tension.     

The potential of electrospraying for hydrophobic film coating on foods

There is a continuous need for thinner edible coatings with excellent barrier properties, and this requires new application methods. Electrospraying is known to yield fine droplets of size down to 20 μm, giving the potential of very thin and even coatings. A single electrospraying nozzle was used to characterise droplet formation and investigate the formation of thin films on well-defined surfaces. The experimental droplet size was successfully described as a function of operational parameters and liquid properties using scaling relations. The influence of operating parameters as nozzle height and electrostatic potential were evaluated as well.Thin film deposition was experimentally investigated for sunflower oil electro-sprayed on a highly conductive (aluminium) and insulating target surface (Parafilm). For both aluminium foil and Parafilm the droplet deposition was found to be random. For aluminium foil, being a conductive target, this was expected as repellence between droplets on the surface and new droplets is low, due to charge leakage to the ground. For Parafilm, droplet repellence appeared so large that droplets deposited on larger empty spots or were even pushed away from the surface. To evaluate the film formation performance, Monte Carlo simulations were carried out, and it was found that the method is a useful tool to characterise droplet deposition and film formation characteristics.     

Modifications in stability and structure of whey protein-coated o/w emulsions by interacting chitosan and gum arabic mixed dispersions

The influence of chitosan and gum arabic mixtures on the behaviour of o/w emulsions has been investigated at pH = 3.0. The emulsion behaviour, properties and microstructure were found to be greatly dependent on the precise gum arabic to chitosan ratio. Mixing of gum arabic with chitosan leads to the formation of coacervates of a size dependent on their ratio. Incorporation of low gum arabic to chitosan weight ratios into whey protein-coated emulsions causes depletion flocculation and gravity-induced phase separation. Increasing the polysaccharide weight ratio further, a droplet network with a rather high viscosity (at low shear stress) is generated, which prevents or even inhibits phase separation. At even higher gum arabic to chitosan ratios, the emulsion droplets were immobilised into clusters of an insoluble ternary matrix. Although the emulsion droplet charge had the same sign as that of the coacervates, clusters of oil droplets in a ternary matrix were generated. A mechanism to explain the behaviour of the whey protein-stabilised o/w emulsions is described on the basis of confocal and phase contrast microscopic observations, rheological data, zeta potential measurements, particle size analysis and visual assessment of the macroscopic phase separation events.     

单液滴干燥过程中载体组分对植物乳杆菌的保护作用

喷雾干燥是目前制备益生菌微胶囊最常用的方法,而研究喷雾干燥塔内液滴的干燥历程有一定的难度。本试验中采用单液滴干燥(SDD)技术模拟喷雾干燥条件,以不同DE值糖浆和不同熔点棕榈油包埋植物乳杆菌,研究90℃和110℃两种干燥条件下对植物乳杆菌的保护作用。研究结果表明,两种干燥条件下含高熔点棕榈油的液滴中植物乳杆菌的存活率均高于低熔点棕榈油的液滴。扫描电镜观察到干燥后的单液滴颗粒表面均无游离的植物乳杆菌。结合液滴干燥过程中水分含量变化推断糖浆的DE值越高越利于表面结构的稳定。对液滴干燥参数以及乳状液的热稳定分析表明,植物乳杆菌的存活率主要与液滴温度有关,棕榈油的熔点越高在干燥过程中吸收的热就越多,从使植物乳杆菌的存活率越高。     

Emulsifying properties of gelatin conjugated to pectin under alkaline conditions

Gelatin–pectin mixed solution incubated under mild alkaline conditions for a period of 4 h exhibited an improvement of emulsion stability in terms of both droplet coalescence and serum separation. Application of SDS–PAGE provided evidence for gelatin–pectin hybrid formation possibly due to amide bonds between the lysine group residues of protein and the esterified carboxyl groups of the polysaccharide. The superior stabilizing properties of the heat‐treated protein–polysaccharide conjugate is attributed to the enhancement of the repulsive steric forces operating between emulsion oil droplets, as a result of conjugate adsorption through their protein moiety. Copyright © 2004 Society of Chemical Industry     

Oil globule microstructure of protein/polysaccharide or protein/protein bilayer emulsions at various pH

The microstructure of oil droplets of bi-layer emulsions was studied as a function of pH (i.e. 7, 5, and 3) using scanning electron microscopy. The bi-layer emulsions consisted of a primary emulsion: 5 wt% soybean oil (SBO) in a 1% protein (nonfat dry milk) aqueous solution. The secondary layer was ι-carrageenan, high- (HMp), low (LMp)-methoxyl pectin, or gelatin. The secondary emulsions consisted of 2.5% SBO, 0.5% protein, and 0.2% polysaccharide or protein. Gelatin secondary emulsions were stable at pH 7 with defined droplets and became unstable at pH 5 and 3. The destabilization mechanisms for these emulsions at pH 5 and 3 were different as observed with the SEM: at pH 5 there is complete aggregation of protein due to their proximity to the isoelectric point; and at pH 3 the droplets are perfectly separated, suggesting that at this pH, when the net charge is positive, the destabilization is mainly due to depletion flocculation. HMp secondary emulsions shift from being stable (individual droplets) at pH 3 to being unstable at pH 7 where an extensive webbing is observed between the droplets at this pH value. The ι-carrageenan secondary emulsions are stable at each pH and the individual droplet microstructure is minimally altered as the pH changes. LMp secondary emulsions shift from being stable at pH 7 with individual droplets observed in the SEM micrographs to being unstable at pH 3 where extensive webbing is observed in the SEM micrographs.     

EFFECTS OF OIL DROPLETS ON PHYSICAL AND SENSORY PROPERTIES OF O/W EMULSION AGAR GEL

Effects of oil droplets in an agar gel matrix were investigated by mechanical analyses and sensory evaluation. The results for compressive and puncture properties were expressed in terms of relative values. All compressive properties; stress, strain and compressive energy of emulsion gels, as obtained by compression tests, decreased with both increases of oil droplet size and oil volume fraction. The stress, strain and energy of the emulsion gels obtained by puncture tests did not change with an increase in oil droplet size. Results of sensory evaluation showed that the sample containing small oil droplets was harder than that with large oil droplets. On the other hand, the large oil droplet sample was oilier than that with small oil droplets. The sensory evaluations for hardness and oiliness of emulsion gels did not exhibit significant relations to most of the properties of mechanical analyses.     

Utilisation of pectin coating to enhance spray-dry stability of pea protein-stabilised oil-in-water emulsions

In this study, development of pea (Pisum sativum) protein stabilised dry and reconstituted emulsions is presented. Dry emulsions were prepared by spray-drying liquid emulsions in a laboratory spray-dryer. The effect of drying on the physical stability of oil-in-water emulsions containing pea protein-coated and pea protein/pectin-coated oil droplets has been studied. Oil-in-water emulsions (5 wt.% Miglyol 812 N, 0.25 wt.% pea protein, 11% maltodextrin, pH 2.4) were prepared that contained 0 (primary emulsion) or 0.2 wt.% pectin (secondary emulsion). The emulsions were then subjected to spray-drying and reconstitution (pH 2.4). The stability of the emulsions to dry processing was then analysed using oil droplet size, microstructure, Zeta potential, and creaming measurements. Obtained results showed that the secondary emulsions had better stability to droplet aggregation after drying than primary emulsions. To interpret these results, we propound that pectin, an anionic polysaccharide, formed a less charged protective layer around the protein interfacial film surrounding the oil droplets that improved their stability to spray-drying mainly by increasing steric effects.     

Deformation and fracture of emulsion-filled gels: Effect of gelling agent concentration and oil droplet size

The effect of the ratio between the modulus of the oil droplets and that of the gel matrix (varied by changing gelling agent concentration and oil droplet size) on the large deformation properties of gelatine, κ-carrageenan and whey protein isolate (WPI) gels was studied at different compression speeds. The effect of gelling agent concentration and oil droplet size on strain-dependency of modulus and viscoelastic properties was also studied. An increase in the concentration of gelling agent resulted in denser gels with more bonds between structural elements. This induced an increase of both Young's modulus and fracture stress for all gels. With increasing gelling agent concentration, polymer gels (gelatine and κ-carrageenan) became less strain-hardening, and the particle gels (WPI) even became strain-softening. The effect of a decrease in the oil droplet size on the Young's modulus was generally according to the Van der Poel theory, unless when the oil droplets were aggregated. Moreover, a decrease in oil droplet size induced a decrease of the fracture strain in gels with non-aggregated bound droplets. The extent of these changes was shown to depend on the gelling agent concentration. The effect of a decrease of the oil droplet size on other fracture parameters and in other gel systems was minor. With decreasing oil droplet size gelatine gels with unbound droplets and WPI gels became more viscous and less elastic.     

Impact of dietary fiber coatings on behavior of protein-stabilized lipid droplets under simulated gastrointestinal conditions

Multilayer emulsions containing lipid droplets coated by lactoferrin (LF) - anionic polysaccharide layers have improved resistance to environmental stresses (such as pH, salt, and temperature), but their behavior within the gastrointestinal tract (GIT) is currently unknown. The objective of this research was therefore to monitor changes in the physicochemical properties and digestibility of these systems under simulated GIT conditions. Primary emulsions (5% corn oil, 0.5% LF) were prepared using a high-pressure homogenizer. Secondary emulsions (5% corn oil, 0.5% LF, 0.5% polysaccharide) were prepared by incorporating alginate, low methoxyl pectin (LMP) or high methoxyl pectin (HMP) into primary emulsions. Emulsions were then subjected to simulated gastric fluid (SGF) and simulated intestinal fluid (SIF) conditions in sequence. LF, LF-LMP and LF-HMP emulsions were stable to droplet aggregation in the stomach but aggregated in the small intestine, whereas LF-alginate emulsions aggregated in both the stomach and small intestine. The presence of a dietary fiber coating around the initial lipid droplets had little influence on the total extent of lipid digestion in SIF, but LF-alginate emulsions had a slower initial digestion rate than the other emulsions. These results suggest that the dietary fiber coatings may become detached in the small intestine, or that they were permeable to digestive enzymes. Pepsin was found to have little influence on the physical stability or digestibility of the emulsions. The knowledge obtained from this study is important for the design of delivery systems for encapsulation and release of lipophilic bioactive ingredients.