Influence of sucrose on thermal and pasting properties of tapioca starch and xanthan gum mixtures

Sugars and hydrocolloids are used in starch-based product formulations during processing for improving the final quality of foods. Effect of sucrose (0–30%) on thermal and pasting properties of 5% w/w tapioca starch (TS) – xanthan gum (Xan) mixtures was investigated using differential scanning calorimeter (DSC), rapid visco-analyser (RVA) and rheometer. Sucrose increased gelatinization temperatures and enthalpies of TS and TS/Xan dispersions. RVA pasting temperatures, peak viscosity, final viscosity, breakdown and setback values of TS/Xan mixtures increased with increasing sucrose concentration (p < 0.05). Addition of sucrose in all TS/Xan pastes increased the rate of viscosity breakdown during RVA heating under constant shear and temperature. Setback values of TS/Xan pastes increased with sucrose addition but decreased significantly with increasing Xan content. Xan enhanced thermal stability of steady shear viscosities to TS pastes with and without sucrose. Linear regression from pasting profile revealed a good relationship for predicting final viscosity. These results could facilitate the development of TS-based products with improved thermal and pasting properties.     

Influence of xyloglucan on gelatinization and retrogradation of tapioca starch

Dynamic and steady shear rheometry and differential scanning calorimetry (DSC) were used to investigate effects of xyloglucan (XG) on gelatinization and retrogradation of tapioca starch (TS). The viscosity of TS/XG pastes immediately after gelatinization increased with increasing XG content at the total polysaccharide concentration of 3.5%. Gelatinized TS alone showed pseudoplastic flow at low shear rates and dilatant behavior at higher shear rates (about >1 s⁻¹), while mixtures with XG did not show dilatancy. Mechanical spectra of TS pastes containing XG were more liquid-like than those of TS pastes without XG. XG provides shear stability to the TS during storage. Increases in dynamic moduli during storage at 5 °C were suppressed in the presence of XG. In contrast, the retrogradation ratio determined based on DSC increased more rapidly in the presence of XG. These results suggest that XG forms a continuous liquid phase in a mixture to impart better mechanical stability during storage but to accelerate re-ordering of starch polysaccharides by effectively reducing the amount of water available for starch.     

Effect of heating–cooling on rheological properties of tapioca starch paste with and without xanthan gum

The effect of xanthan gum (Xan) on pasting and gelatinization behavior of tapioca starch (TS) was investigated. Rheological measurements of TS/Xan mixtures with 5% w/w total polysaccharide concentration at different mixing ratios (10/0, 9.5/0.5, 9/1 and 8.5/1.5) were performed to understand the pasting and gelatinization behavior of TS with and without Xan on heating–cooling cycle using a Rapid Visco Analyzer (RVA) and conventional rheometers. Xan increased storage modulus (G′) and loss modulus (G″) of TS dispersions during gelatinization process. Pastes of TS/Xan tended to be more solid-like, i.e., G′ larger than G″, with increasing Xan. The G′ of TS/Xan paste increased when kept at 10 °C indicating the network formation. Pasting temperatures, peak viscosity, final viscosity and breakdown values of TS increased with increasing Xan content but the opposite result was observed in setback value from RVA measurement. Temperature dependence of steady shear viscosity became less pronounced with increasing Xan content on both cooling and reheating indicating that Xan made the mixture more thermally stable. All the results suggest that the sample preparation and measuring conditions influence the rheological properties of TS/Xan mixtures, which should be taken into account in food application.     

Thermal and rheological properties of tapioca starch gels with and without xanthan gum under cold storage

Changes in the thermal and rheological properties of tapioca starch (TS) with and without xanthan gum (Xan) (total polysaccharide concentration = 25% w/w) were investigated using a differential scanning calorimeter, Rheolograph Gel and Texture Analyser. The gelatinization temperatures of TS shifted to higher values with the Xan concentration. Xan enhanced the retrogradation of TS during the initial stage of storage but retarded the process for a further storage time at 5 °C. The onset temperature of all reheated TS/Xan gels decreased with increasing storage time indicating thermally unstable structure formation after a longer storage time. Storage Young’s moduli (E′) of the TS and TS/Xan gels stored at 5 °C increased with increasing storage time. The E′ values became more temperature dependent with storage time due to the weak cross-linkage of amylopectin molecules in the gels but became less dependent in the system containing Xan. TS/Xan gels kept for 14 days showed lower Young’s moduli than TS gels from the compression test confirming retardation of the retrogradation process by Xan. The results suggested that Xan could retard the retrogradation of TS gels for longer storage times.     

The pasting behaviour and freeze–thaw stability of native starch and native starch–xanthan gum pastes

The pasting properties, gelatinization profiles and freeze–thaw stability of natural waxy maize starches, pasted in the presence of xanthan gum (XG) and resistant starch, were evaluated using a Rapid Visco Analyser, together with turbidimetric analysis. Freeze–thaw stability was determined for four cycles over a 4 weeks period. The final viscosity of the pastes was unaffected by the addition of resistant starch (RS) whereas XG additions increased final viscosity. Addition of mixtures of combinations of XG and RS increased the peak viscosity of the starch pastes. Freeze–thaw stability (as estimated by the final viscosity of the pastes during a series of four freeze–thaw cycles) was improved with the addition of XG.     

Microstructure of acid–induced skim milk–locust bean gum–xanthan gels

The microstructure of acid skim milk gels (14% w/w milk protein low heat powder) with or without addition of locust bean gum (LBG), xanthan gum (XG) and LBG/XG blends was determined by transmission electron microscopy (TEM), phase-contrast light microscopy (PCLM) and scanning electron microscopy (SEM). Three polysaccharide concentrations (0.001%, 0.02% and 0.1%, w/w) were used for binary mixtures. In the case of ternary mixtures, three LBG/XG weight ratios were used (4/16, 11/9 and 16/4) at 0.02% total polysaccharide concentration. Control acid skim milk gels were structured by a homogeneous network of casein particles (0.1–0.7 μm in diameter) and clusters immobilizing whey in small pores (1–5 μm in diameter). Filamentous structures and small aggregates were observed at the surface of casein particles. Low concentration of LBG or XG (0.001% w/w) did not affect markedly the microstructure of acid skim milk gels. Conversely, LBG or XG at 0.02 or 0.1% concentration and LBG/XG blends at the three ratios selected had a great influence on the gel microstructure. Although the size and surface structure of the casein particles were not modified by the presence of polysaccharides, the primary casein network appeared very compact with a decrease of pore size and a large increase in the porosity of the network at the supramolecular level (sponge-like morphology). The effect is stronger for gels containing LBG and XG used at higher concentration and less apparent for gels containing LBG/XG blends. Skim milk/XG gels were highly organized into fibrous structures whereas skim milk/LBG gels were more heterogeneous. These structures were discussed in the light of volume-exclusion effects (demixing) and specific interactions between casein micelles and polysaccharides. At the three weight ratios, skim milk/LBG/XG gels displayed both jagged “coral-like”, “veil-like” and filamentous structures. These structures could originate from a secondary network constituted by the known LBG/XG synergistic interactions.     

Pasting,rheological properties and gelatinization kinetics of tapioca starch with sucrose or glucose

Effects of sugars (sucrose and glucose) on the pasting, rheological and thermal properties of tapioca starch (TS) were studied. Rapid visco-analyser (RVA) and differential scanning calorimetry (DSC) showed that pasting and gelatinization temperature of TS increased with increased sugar concentration in the order of sucrose > glucose. Peak, breakdown, final and setback viscosities tended to increase with increased sugar content. Rheological parameters calculated from Herschley–Bulkley model showed sugar addition increased the yield stress and consistency coefficient, while decreased the thixotropy of TS gels. Loss tangent determined from dynamic viscoelastic tests revealed that sugars increased the solid-like characteristics of TS gels. Kinetics analysis showed E_a raised and rate constants declined in the presence of sugars, suggesting the same sugar effect as the experiments of RVA and DSC. And thus kinetics analysis could provide new evidences for the influence of sugars on starch gelatinization.     

Effect of substitution of aspartame for sucrose on instrumental texture profile of hydrocolloids gelled systems

The effect of substituting aspartame (0.04–0.16% w/w) for sucrose (5–25% w/w) on the instrumental texture profile of three hydrocolloid gelled systems: -carrageenan, gellan gum and -carrageenan/locust bean gum at three different concentrations (0.3, 0.75 and 1.2% w/w) was studied. In gellan gels hardness and chewiness increased with sucrose concentration but not so in either -carrageenan or -carrageenan/LBG gels where no changes in these parameters were detected. Addition of sucrose also produced a small but significant increase in cohesiveness in gellan gels. The effect of sucrose concentration on all texture parameters of gellan gels was higher as gellan concentration increased. Aspartame addition did not affect TPA parameters. TPA results obtained for aspartame gels did not differ from those corresponding to the unsweetened gels considered here. Summarising the above information it can be said that substituting aspartame for sucrose in this type of sweetened gel changed the textural properties and that the changes produced depended on the hydrocolloid type and concentration and on the sucrose concentration replaced.     

Gelatinization and rheological properties of rice starch/xanthan mixtures: Effects of molecular weight of xanthan and different salts

Effects of molecular weight (M_w) of xanthan (XG) and salts (0.1 M NaCl or CaCl₂) on the pasting, thermal, and rheological properties of rice starch (RS) were studied. A series of five XG samples, having various M_w, was prepared by homogenization of native XG solutions in the presence or absence of salts. The presence of salts greatly reduced the intrinsic viscosities, [η], of all XG solutions. Rapid visco-analysis (RVA) data showed that XG addition increased the peak, breakdown, final, and setback viscosities of RS, either in the presence or absence of salts, whereas the pasting temperatures were unaffected. Differential scanning calorimetry (DSC) demonstrated that the gelatinization temperatures of RS were unaffected by XG addition but slightly increased by CaCl₂ addition, whereas the gelatinization enthalpies (ΔH) were significantly decreased by additions of XG and salts. Dynamic shear data revealed weak gel-like behaviour in all paste samples in which their rigidity was decreased by XG addition. Flow tests showed that all pastes exhibited time-dependent shear-thinning (thixotropic) with yield stress behaviour in which the hysteresis loop areas were significantly decreased by XG addition, whereas the other rheological parameters varied differently among the samples, with and without added salt. In general, the effects of XG addition on the pasting and rheological properties of RS were more pronounced with increasing M_w of XG and these effects depended on salts added.     

Gellan gum/cassava starch mixtures in water systems and in milk systems

Cassava starch is an important ingredient in various foods. However, when processed, it develops some properties that are unsuitable for many industrial applications, such as unstable viscosity and excessive cohesiveness. To reduce those disadvantages, one alternative is a mixture of starch with hydrocolloids. The aim of this study was to evaluate the effect of 0:05, 0.1, 0.2, or 0.3% w/v gellan gum on the physical properties of pastes and gels of cassava starch in water and in milk systems. Differential scanning calorimetry (DSC), pasting properties, the texture profile, and the microstructure of gels were studied. The addition of gellan gum dispersions to the water system (WS) and the milk system (MS) gave rise to pastes with higher viscosity and, in the case of MS, with lower thermal and shear stability (higher breakdown). The addition of gellan gum had a greater textural effect on the MS, in which the addition of gellan at concentrations of 0.1 and 0.3% increased adhesiveness and decreased springiness of gels. Microscopy revealed a more uniform gel structure in the MS compared with the WS. Starch gelatinization temperatures were higher in MS than in WS.     

Steady and Dynamic Shear Rheology of Fucoidan‐Buckwheat Starch Mixtures

Rheological properties of fucoidan (F) and buckwheat starch (B) mixtures (3% or 6%) at different blending ratios of fucoidans (0, 0.1, 0.2, 0.5 and 1.0%) were investigated in steady and dynamic shear. Steady shear viscosity measurement revealed that aqueous pastes of the BF blends (3%, w/v) had a pseudoplastic and shear‐thinning behavior with flow behavior index (n) values of 0.61–0.68. The substitution of starch with fucoidan polymers significantly lowered the apparent viscosities compared with the pure starch paste and, when mixed with less than 0.5% of fucoidan, the viscosities of the pastes were even lower than those of the starch pastes at the corresponding starch concentrations. According to dynamic viscoelastic measurement performed at 6% total carbohydrate concentration, buckwheat starch mixtures behaved like weak gels and the BF blends containing less than 0.5% fucoidan had considerably lower storage (G') and loss (G') moduli than the starch paste at the corresponding starch concentrations. However, the magnitude of G' increased with fucoidan concentrations over 0.5%, suggesting that a concentration of fucoidans > 0.5% might enhance the formations of three‐dimensional networks and crosslinking of the starch samples, probably because of the mutual exclusion between starch and fucoidan polymers through the phase separation process. This study indicates that it is possible to obtain the BF blends having various rheological properties by changing the concentration of fucoidan polymers.     

低酰基结冷胶-果胶复配体系的性能

利用质构仪和流变仪对低酰基结冷胶(low acyl gellan,LA)和果胶复配体系的胶体质构和流变性能进行研究。考察不同种类离子(Ca~(2+)、K~+)、离子浓度(0、2、4、6、8、10、20、40 mmol/L)以及LA和果胶不同质量比(100:0、75:25、50:50、25:75)对复配体系质构特性的影响。结果表明,随着离子浓度的增加破坏应力先增大,当达到临界值后开始减小,二价离子(Ca~(2+))的作用效果要强于一价离子(K~+)。复配胶破坏应力随LA比例降低先增加后减少,质量比在75:25时具有显著协同效应。复配体系的黏度随剪切速率增大而减小;当剪切速率相同时,黏度随LA比例的增加而增加,离子种类和浓度对复配体系黏度的影响与质构特性一致。随着温度的升高,复配体系黏度减小,在相同温度条件下,结冷胶与果胶质量比75:25时,体系的黏度最大。储能模量G’大于相应质量比损耗模量G",且G’和G"随LA比例的增加而增大,说明体系的黏性和弹性随LA比例增加而变大。     

Effect of sucrose on rheological properties of xanthan gum-locust bean gum mixtures

Food Science and Biotechnology - The effect of sucrose (0, 10, 20, 30, and 40%) on flow and dynamic rheological properties of xanthan gum (XG) mixed with locust bean gum (LBG) at different mixing...     

A DIFFERENTIAL SCANNING CALORIMETRIC (DSC) STUDY ON the EFFECTS of ANNEALING and SUGARS-EMULSIFIERS ON GELATINIZATION of SAGO STARCH (Metroxylon sagu)

This study investigated the effects of annealing, at different temperatures (45–70C), times (0–24 h) and water:starch ratios (0.6/1–4/1), on the DSC thermal properties profiles associated with gelatinization temperatures of sago starch-water mixtures. the effects of sugars-emulsifiers and of starch mixtures and their interactions were also investigated. DSC data showed an increased gelatinization temperature and enthalpy and a narrower gelatinization tempera ture range (T_m-T_o) after annealing of sago starch; the extent of these changes was inversely proportional to the degree of crystallinizy of the native starch. For sago starch, the G transition occurring at about 66–69C and the M1 transition occurring at about 75C in excess water became broader and shifted to higher temperatures as the water content was decreased. the effects on the gelatinization temperature and H, of the addition of sugars-emulsifiers to the starch- water mixture, were observed by comparison with the starch-water results. Sucrose raised the gelatinization temperature by about 6–7C more than did glucose, for sago starch. Emulsifiers (sucrose ester and polysorbate-60), in the presence of sucrose or glucose, did not affect the gelatinization temperature.     

不同种类甘薯淀粉混合对其物化特性及粉条品质的影响

以不同混合比例(100:0、75:25、50:50、25:75、0:100)的商薯19和广薯87淀粉为研究对象,分析其结构、物化特性及粉条品质特性等。结果表明,不同比例混合淀粉的基本成分、粒径及官能团结构表现为两种淀粉的加合效应;商薯19淀粉的糊化特性高于广薯87淀粉,低比例(≤50%)广薯87淀粉与商薯19淀粉的交互作用提高了混合淀粉的糊化特性,而高比例(>50%)广薯87淀粉的添加则对糊化特性产生拮抗作用;两种淀粉之间的拮抗作用降低了混合淀粉的溶解度,高比例(>50%)广薯87淀粉的添加对膨胀势的增加有协同效应;商薯19淀粉的起始温度与热焓值高于广薯87淀粉,二者之间的交互作用提高了混合淀粉的起始温度,降低了混合淀粉的热焓值。同时,混合淀粉的糊化特性和起始温度与粉条的品质特性呈正相关关系,因此可将上述因子作为淀粉混合的评价指标,指导粉条生产。     

Rheological behaviour of uncross-linked and cross-linked gelatinised waxy maize starch with pectin gels

Rheological characterisation of uncross-linked (UPS) and cross-linked (CPS) waxy maize starch with pectin was conducted to determine the influence of pectin on the properties of the starch. The viscoelastic behaviour of 5% (w/v) gel systems containing UPS and CPS polysaccharides at 25 °C was evaluated by small angle deformation oscillation rheometry. Viscoelasticity measurements of the cross-linked polysaccharides indicated that the elastic component increased after cross-linking. Among all gels studied, the properties of the CPS mixtures (ratios 2:3 and 3:2) showed quite high storage (G′) and loss (G″) moduli (compared with gels of other ratios), indicating that gels of these two particular ratios had the greatest degree of elasticity and were very well structured. The results suggest that cross-linking between starch and pectin molecules can give rise to novel rheological properties.     

Proton NMR and Dielectric Measurements on Sucrose Filled Agar Gels and Starch Pastes

Low-field proton NMR and high-frequency dielectric measurements were performed on sucrose-filled agar gels of 0 to 1.2g sucrose/g water and starch pastes of concentrations between 0.2 and lg starch/ g water. The dielectric constant decreased linearly with increasing concentration for both. The dielectric loss of sucrose-filled agar gels showed two regions, first increasing and then decreasing with concentration. The dielectric loss data for starch pastes showed a constant value close to that of pure water throughout the concentration range. Dielectric data were related to hydration models derived from proton NMR measurements.     

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.     

Limonene encapsulation in freeze-drying of gum Arabic-sucrose-gelatin systems

Encapsulation of limonene in freeze-drying of various matrices consisting of gum Arabic, sucrose and gelatin was studied. Retention of limonene in freeze-drying was observed by measuring absorbance at 252 nm using a spectrophotometer. Two different levels of limonene, in the weight ratios (w/w) of 9:1 and 8.5:1.5 (total solids (TS):limonene) were studied. Highest amount of limonene (75.3±0.3% of initially added amount) in the emulsions homogenised at 25 MPa (4 MPa in second stage) followed by freeze-drying, was retained in a matrix consisting of gum Arabic, in the ratio of 9:1 (w/w). A mixture consisting of gelatin-sucrose-gum Arabic in the w/w ratio of 0.66:0.17:0.17 retained highest amount (71.8±0.1% of initially added amount) of limonene in the ratio (w/w) of 8.5:1.5 (TS:limonene). A matrix consisting of gum Arabic-sucrose-gelatin (1:1:1 w/w/w) with added limonene at a ratio (w/w) of 9:1 (TS:limonene), was used to study the effects of ultra high-pressure homogenisation (50-250 MPa) on limonene encapsulation in freeze-drying. Highest amount (84% of initially added amount) of limonene was retained in the emulsions homogenised at a pressure of 100 MPa. Electron micrograph of freeze-dried matrix of gum Arabic-sucrose-gelatin in the weight ratio of 1:1:1 suggested that it possessed a flake like structure, which was free of dents and shrinkage. A mixture consisting of gum Arabic-sucrose-gelatin is an efficient encapsulant for limonene encapsulation by freeze-drying.     

Highly acetylated pectin from cacao pod husks (Theobroma cacao L.) forms gel

A pectin (OP) obtained from cacao pod husk with a high acetyl content, which is a structural feature that could disturb the pectins' gel formation, was able to form gels at low pH and a high sucrose content. Pectin gels (1.32% GalA equivalent, w/w) were prepared at pH 2.5–3.3 in the presence of 60% sucrose (w/w). Rheological analyses were performed to determine the optimal pH for further studies. Next, the OP samples were prepared at pH 2.7 in concentrations ranging from 0.33 to 1.98% GalA (w/w) with 60% sucrose (w/w) and subjected to rheological analysis. Dynamic oscillatory experiments at 25 °C indicated the presence of gels for all of the analysed concentrations. Measurements of the elastic (G′) and viscous (G″) moduli at 25 °C also indicated that increasing the pectin concentration resulted in stronger gels. Rotational experiments revealed a shear-thinning behaviour in which the apparent viscosities of the samples increased as the concentration increased. Although the OP had a high degree of acetylation, this pectin was able to form gels, which suggests its potential for use as a gelling and thickening additive.