Influence of type,concentration and flow behaviour of hydrocolloid solutions on aroma perception

The effects of the addition of two hydrocolloids—locust bean (LBG) and xanthan gums—at two concentrations (0.2 and 0.5%, w/v) on the intensity of the aroma of limonene and of isopentyl acetate solutions was studied using the pairwise ranking test. Previously, the rheological behaviour of the studied gums was analysed, finding that while LBG solutions were slightly pseudoplastic at the lower concentration and more so at the higher one, the xanthan solutions were clearly pseudoplastic at both concentrations. Addition of 0.2% LBG did not alter the limonene aroma intensity perceived, but on adding 0.5% LBG, above the coil overlap concentration (c*), the decrease in aroma intensity was significant. Addition of xanthan gum at any concentration did not modify the limonene aroma intensity perceived by judges, which can be attributed to the low value of c* for solutions of this gum. No difference in isopentyl acetate aroma was found among samples.     

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.     

Rheological study of xanthan and locust bean gum interaction in dilute solution

An oscillatory capillary rheometer was used to investigate visco-elastic properties of xanthan and locust bean gum (LBG) blends in dilute solution. Gums were evaluated for intrinsic viscosity and the elastic component. Molecular conformation of the complex of xanthan–LBG was assessed by the power law and the Huggins equations. A 60% xanthan–40% LBG blend exhibited the strongest attraction between xanthan and LBG molecules as evidenced by a greater intrinsic viscosity, the polymer miscibility coefficient α, the elastic component, and a positive Huggins coefficient K_m. The power-law model was successfully applied to predict the molecular conformation of xanthan and LBG alone in dilute solution and was exhibited as rod-like and random coil conformation. The power-law coefficient b increased as the LBG fraction increased in the blends, suggesting a more flexible xanthan–LBG complex dependent on LBG.     

Viscosity of guar gum and xanthan/guar gum mixture solutions

The viscosity of diluted guar gum solutions and the viscosity of xanthan and guar gum mixture solutions have been studied. Guar gum solutions showed pseudoplastic behaviour. Apparent viscosity increased with gum concentration and decreased with the temperature at which viscosity was measured. A maximum in the plot of viscosity versus increasing dissolution temperature was observed at 60 °C. This behaviour was related to differences in molecular structure of the polymers solved at different temperatures. Mixtures of xanthan and guar gum showed a higher combined viscosity than that occurring in each separate gum. This synergistic interaction was affected by the gum ratio in the mixture and dissolution temperature of both gums. The effect of polysaccharide concentration (1.0, 1.5 and 2.0 kg m⁻³), xanthan/guar gum ratio (1/5, 4/2, 3/3, 4/2 and 5/1) and dissolution temperature (25, 40, 60 and 80 °C for both gums) on the viscosity of solutions of mixtures were studied. The highest viscosities were observed when 2.0 kg m⁻³ gum concentration was used together with a ratio of xanthan/guar gum of 3/3 (w/w) and dissolution temperature of 40 and 80 °C for xanthan and guar gum, respectively. © 2000 Society of Chemical Industry     

Rheology and modelling of aqueous gum solutions commonly used in the food industry

Rheological properties of solutions prepared using xanthan (XG), locust bean (LBG) or sodium carboxymethyl cellulose (CMC) gums, and their binary mixtures were studied. The influence of shear rate, total gum content, measurement time and temperature on the apparent viscosity was investigated. In the binary mixtures, the presence of different gum ratios at several total gum content was also analysed. XG solutions were always the most stable, providing high viscosity values which rose notably with increasing gum content. XG/LBG and CMC/XG mixtures depicted high values of viscosity for very low gum amounts. Viscosity did not change with measurement time in mixtures containing XG, whereas varied with measurement temperature. This variation was lower for samples with larger total gum content. The viscosity was also modified when different gum ratios were tested. A mathematical model was proposed to evaluate the combined effect of temperature, concentration and shear rate on the apparent viscosity.     

黄原胶的特性、生产及应用进展

黄原胶是Xanthomnas.sp分泌的胞外水溶性多糖,由于其有突出的高粘性和水溶性、独特的流变特性、优良的温度稳定性和pH稳定性、极好的兼容性以及安全环保等特性,已被广泛于石油开采、食品工业、纺织和化妆品等诸多行业。主要综述了黄原胶的分子结构、分子特性、生产以及应用的研究进展。     

Effect of gums on the multi-scale characteristics and 3D printing performance of potato starch gel

This research investigated the multi-scale characteristics of potato starch gel (PSG) with different addition ratios of xanthan gum (XG) and locust bean gum (LBG). These characteristics are closely related and had significant impacts on 3D printing performance. Both xanthan gum and locust bean gum were able to increase the apparent viscosity, storage modulus (G′) and loss modulus (G″) of the blended gel system to varying degrees. Large amplitude oscillation shear (LAOS) was used to detect slight rheological differences led by microstructure changes. The critical strain values of the blended gel system rose as the addition ratio of locust bean gum increased. At the same time, the elastic and viscous Lissajous curves could characterize the viscoelastic changes under large strains. Fourier transforms infrared spectroscopy (FT-IR) illustrated that locust bean gum could strengthen the hydrogen bonds so that the gel had stronger mechanical properties compared with the addition of xanthan gum. Scanning electron microscopy (SEM) could observe the changes in the microstructure of the blended gel systems with addition of different addition ratios of gums. From the perspectives of 3D printing results and data analysis, the appropriate amount of xanthan gum improved the fineness and fluidity of the gels by virtue of its lubricating and coating characteristics, while the locust bean gum enabled them to have stronger shape retention abilities and better performances of resisting compressed deformation.     

Viscosity of solutions of xanthan/locust bean gum mixtures

Xanthan and locust bean gums are polysaccharides able to produce aqueous solutions with high viscosity and non‐Newtonian behaviour. When these solutions are mixed a dramatic increase on viscosity is observed, much greater than the combined viscosity of the separated polysaccharide solutions. In this work the influences of different variables on the viscosity of solutions of mixtures of xanthan/locust bean gum have been studied. Total polysaccharide concentration, xanthan and locust bean ratio on mixture and temperature at which the gum was dissolved (dissolution temperature) for both xanthan and locust bean gums have been considered. Under these different operational mixture conditions shear rate and time have also been considered to describe the rheological behaviour of the solutions studied. The high viscosity increase observed in these mixtures is due to the interaction between xanthan gum and locust bean gum molecules. This interaction takes place between the side chains of xanthan and the backbone of the locust bean gum. Both xanthan molecule conformation in solution – tertiary structure – and locust bean gum structure show great influence on the final viscosity of the solution mixtures. Xanthan conformation changes with temperature, going from ordered structures to disordered or chaotic ones. Locust bean gum composition changes with dissolution temperature, showing a dissolved galactose/mannose ratio reduction when temperature increases, ie the smooth regions – zones without galactose radicals – are predominantly dissolved. The highest viscosity was obtained for the solution mixture with a total polysaccharide concentration of 1.5 kg m⁻³ and a xanthan/locust ratio of 2:4 (w/w) and when xanthan gum and locust bean gum were dissolved at 40°C and 80°C, respectively. © 1999 Society of Chemical Industry     

Response surface methodology and multivariate analysis of equilibrium headspace concentration of orange beverage emulsion as function of emulsion composition and structure

The influence of emulsion composition (i.e. Arabic gum, xanthan gum and, orange oil) and structural emulsion properties (i.e. average droplet size and apparent viscosity) on equilibrium headspace concentration of beverage emulsions was investigated. Increase in average droplet size led to increase the equilibrium headspace concentration of more hydrophilic volatile compounds (i.e. lower log P) such as ethyl acetate and octanal, but decrease in more hydrophobic volatile compounds such as 3-carene, myrcene and limonene. In most cases, apparent viscosity had significant positive effect on equilibrium headspace concentration. Principle component analysis (PCA) score discriminated the beverage emulsions containing the same orange oil content but different contents of emulsifiers in different classes, thus indicating the significant (p < 0.05) effect of emulsifier fraction on equilibrium headspace concentration. Beverage emulsion containing 22.2% (w/w) Arabic gum, 0.52% (w/w) xanthan gum and 14.21% (w/w) orange oil was estimated to provide the highest equilibrium headspace concentration.     

Viscosity of galactomannans during high temperature processing: influence of degradation and solubilisation

The rheological properties of guar gum (GG) and locust bean gum (LBG), in response to high temperature treatments, were measured using a rheometer equipped with a high pressure cell. This has allowed the viscosity to be assessed at temperatures above 100°C and as the polymer suspension is heated from 20 to 121°C and then cooled back to ambient temperature to simulate a food sterilisation cycle. Activation energies for depolymerisation estimated from viscosity changes with time at a series of constant temperatures were estimated as 63 kJ/mol for GG and 98, 104, 110 kJ/mol for three different samples of LBG. A model was developed to interpret the viscosity change through the simulated sterilisation cycle. This took into account the degradation of the polysaccharide and the change in viscosity due to thermal motion. Estimations of molecular weight changes during the heating process suggest that GG is more susceptible to thermal degradation than LBG. It is suggested that this is due to the greater ability of the latter to associate in solution.     

Influence of non-starch polysaccharides on the in vitro digestibility and viscosity of starch suspensions

The effects of adding non-starch polysaccharides (xanthan gum, guar gum, konjac glucomannan, and pectin) on the starch digestibility and viscosity of raw starch suspensions in a mixed system were determined. Each type of polysaccharide was added to high-amylose corn starch suspensions at defined concentrations. High-amylose rice starch suspensions mixed with xanthan and guar gum were prepared for comparison. The extent of starch digestibility was determined by an in vitro method, and the glucose diffusibility from the dialysis tube in the presence of polysaccharides was measured. The added polysaccharides were observed to decrease the starch digestibility in a mixed system. When compared at the same concentration, xanthan gum showed the most pronounced suppressive effect on starch digestibility and glucose diffusibility from the dialysis tube. The addition of polysaccharides increased the viscosity of the starch suspension. Significant relations were found between the extent of starch digestibility and the apparent viscosity at low shear rate.     

Rheological study of xanthan and locust bean gum interaction in dilute solution: Effect of salt

An oscillatory capillary rheometer was used to investigate the effects of NaCl, KCl, and CaCl₂ on visco-elastic properties of xanthan and locust bean gum (LBG) blends in dilute solution. Gums were evaluated for intrinsic viscosity and elastic component. Molecular conformation of the xanthan–LBG complex was assessed by the power-law and Huggins equations. Addition of any of the three salts reduced significantly the intrinsic viscosity and elastic component of the gum blends, with a pronounced effect from divalent ions, compared with monovalent ions. The 60% xanthan–40% LBG blend exhibited the strongest attraction between xanthan and LBG. For the three salts, the attraction weakened when 5-mM salt was added and vanished with the addition of 50-mM salt. The strongest attraction between xanthan and LBG molecules was also evidenced by a positive Huggins miscibility coefficient K_m, and a positive attraction–repulsion coefficient α. With addition of 50 mM of any of the three salts, the coefficient α became negative, suggesting a strong repulsion between the two gums. The power-law coefficient b increased as salt concentration and LBG fraction increased in the blends for the three salts, suggesting a more flexible xanthan–LBG complex dependent on salt concentrations and LBG.     

不同条件对胖大海胶表观黏度的影响

以胖大海胶研究对象,研究pH、钙离子浓度、不同阳离子、蔗糖及其他胶体对胖大海胶黏度的影响。结果表明:pH偏高或偏低、阳离子存在均使胶体溶液表观黏度下降;随着蔗糖浓度增加,溶液表观黏度逐渐增大;胖大海胶与瓜尔豆胶复合后胶体溶液黏度大于原胶体的黏度,而与黄原胶、海藻酸钠、琼脂复合则小于原胶体黏度。     

Rheological interactions between Lallemantia royleana seed extract and selected food hydrocolloids

BACKGROUND: Lallemantia royleana (Balangu) is a mucilaginous endemic plant which is grown in different regions of world. The flow behaviour of Balangu seed extract (BSE) and its mixture with xanthan, guar and locust bean gums at 1:3, 1:1 and 3:1 ratios, in addition to control samples (0% BSE), were evaluated. To describe the rheological properties of samples, the power law model was fitted on apparent viscosity–shear rate data. To evaluate the interaction between BSE and selected hydrocolloids in dilute solutions, the relative viscosity was also investigated. RESULTS: There was no significant difference between the consistency coefficient of guar and locust bean solutions and their blends substituted with 250 g kg^?1 BSE. The BSE–xanthan mixture at 1:3 and 1:1 ratios had consistency index equal to xanthan solution. BSE–locust bean gum at all ratios, BSE–xanthan at 1:3 ratio and BSE–guar gum at 1:1 and 3:1 ratios indicated relative viscosity lower than values calculated assuming no interaction. The intrinsic viscosity value of BSE was determined 3.50 dL g^?1. CONCLUSION: The apparent viscosities of BSE, selected hydrocolloids and their blends were the same at a shear rate of 293 s^?1 and the commercial gums can be substituted by 250 g kg^?1 and 500 g kg^?1 BSE. Copyright © 2011 Society of Chemical Industry     

黄原胶和魔芋胶抑制碱诱导鸭蛋清凝胶的高温液化

本研究分别将黄原胶和魔芋胶添加至鸭蛋清中制备碱诱导凝胶,以探究亲水胶体对凝胶高温液化的抑制作用,结果表明:与对照组相比,添加亲水胶后的蛋清凝胶黏度、储能模量和损耗模量增大明显(p<0.05),褐变强度增加了7.99%和33.21%;当黄原胶和魔芋胶的浓度由0.50%增加至1.50%,凝胶硬度值提高49.60%和119.56%,穿刺强度提高20.59%和78.42%,持水性提高1.02%和9.47%,且添加黄原胶的蛋清凝胶硬度、穿刺强度和持水性均显著大于魔芋胶(p<0.05)。两种胶的浓度均为1.00%时,蛋清凝胶的感官评分最高。两种亲水胶的加入会改变蛋白质的二级结构及凝胶内部的分子间作用力:黄原胶量的增加显著降低了离子相互作用(p<0.05),无规则卷曲减少了41.23%,α-螺旋增加了81.29%;魔芋胶量的增加显著降低了疏水相互作用(p<0.05),β-折叠减少了34.97%,无规则卷曲和α-螺旋分别增加了68.97%和70.37%;氢键和二硫键均随两种胶浓度的增加而增强。综上所述,添加黄原胶和魔芋胶均能抑制碱诱导蛋清凝胶在高温处理过程中的液化现象,且加入黄原胶所形成的凝胶质构特性和持水性优于魔芋胶,而魔芋胶对于凝胶褐变强度的影响大于黄原胶。     

Effect of medium molecular weight xanthan gum in rheology and stability of oil‐in‐water emulsion stabilized with legume proteins

Xanthan gum is a water‐soluble extracellular polysaccharide that has gained widespread commercial use because of its strong pseudoplasticity and tolerance to high ionic strength, which bring unique rheological properties to solutions. This study compares and evaluates the emulsifying properties of oil‐in‐water (30:70 v/v) emulsions stabilized with lupin and soya protein isolates and medium molecular weight xanthan gum. The protein was obtained by an isoelectric precipitation method and the polysaccharide was produced by Xanthomonas campestris ATCC 1395 in batch culture in a laboratory fermenter (LBG medium) without pH control. The addition of xanthan gum in the emulsion formulation enhances emulsion stability through the phenomenon of thermodynamic incompatibility with the legume protein, resulting in an increase of the adsorbed protein at the interface. The emulsion stability is also enhanced by a network structure built by the polysaccharide in the bulk phase. Copyright © 2005 Society of Chemical Industry     

盐及非盐物质对常用低浓度食品胶溶液粘度影响的研究

对饮料生产中常用的食品胶－黄原胶、海藻酸钠、瓜尔胶和琼脂在低浓度水相体系中外加盐（阴、阳离子）、乙醇、蔗糖及柠檬酸对溶液粘度的影响作了探讨性研究,结果表明四种胶溶液（０．１０％黄原胶、０．３０％海藻酸钠、０．２５％瓜尔胶、０．１０％琼脂）中、瓜尔胶溶液对盐的耐受性最好,即大多数阴阳离子都不会对其粘度产生影响,而常用金属盐阳离子及Ｃｌ＾－、ＳＯ３＾２－对黄原胶溶液粘度的影响与阴阳离子对海藻酸钠和琼脂     

Conformational Role of Xanthan in its Interaction with Locust Bean Gum

ABSTRACT: Texture analysis and Ubbelohde capillary viscometry were used to investigate the effects of chain conformational changes of xanthan or deacetylated xanthan on its interaction with locust bean gum (LBG). The stability of xanthan helical structure or xanthan chain flexibility played a critical role in interacting with LBG. Destabilization of xanthan helical structure by deacetylation and heating facilitated the intermolecular binding between xanthan and LBG. Xanthan conformational change was noted in the presence of LBG, even when its helical structure was stabilized by salt. However, this conformational change was not observed for deacetylated xanthan, presuming deacetylated xanthan was in the exact conformation to bind LBG.     

海藻酸钠和黄原胶糊料粘弹性行为的研究

通过稳态剪切和小幅振荡剪切应力扫描试验,研究了海藻酸钠和黄原胶糊料的粘弹性能.结果表明:与海藻酸钠相比,黄原胶在低用量、低剪切速率下就具有高粘度,表现出显著的假塑型流体"剪切变稀"特征.海藻酸钠以粘性效应为主,表现出较多的类液态特征,而黄原胶以弹性效应为主,表现出较多的类固态特征.随着剪切应力的增加,海藻酸钠的粘弹性能比较稳定,损耗模量始终大于储能模量,损耗角大于45°,主要表现出粘性行为;黄原胶的粘弹性能经历了由高弹性向粘性转变的突变区,在突变之前其储能模量大于损耗模量,损耗角小于45°,表现出很显著的弹性行为.     

黄原胶对壳聚糖精油复合膜的性能及精油释放的影响

为探究黄原胶对壳聚糖精油复合膜性能和精油释放的影响,本文利用流延法制备了不同配比的黄原胶-壳聚糖-精油复合膜,并测定膜的物理性能、精油释放和微观结构等指标。结果表明:当黄原胶的添加量在低于50%的范围内,膜的水溶性随黄原胶添加量的增加逐渐升高,含水量、膨胀程度以及断裂伸长率逐渐下降,然而黄原胶的添加量对膜的抗拉强度无显著性影响。添加黄原胶明显增加了精油在食品模拟物中的释放速率,从不同食品模拟物的释放速率来看,由快到慢依次为水包油乳状液和含酒精食品的模拟物、蒸馏水、脂肪食品模拟物;微观结构显示黄原胶影响了膜的内部结构,使膜的横截面出现较大的颗粒,形成不连续的结构特征,该研究为开发应用精油控释型薄膜提供了理论依据。