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.     

Effects of Alcalase/Protease N treatments on rice starch isolation and their effects on its properties

The effects of different protease treatments on rice starches and their properties were studied. The rice starches produced from protease N exhibited higher pasting viscosities than those produced from alcalase. The hot pastes of the starches produced from protease N also showed higher elastic moduli, zero-order Newtonian viscosities and yield stresses than those produced from alcalase. No differences were found in the crystalline pattern, thermal properties, granules appearance, and average molecular weight (M_w) of the rice starches between the two protease treatments. But the M_w of the pasted starch produced from protease N was higher than that produced from alcalase. When additional protease was added to the isolated starches and the mixture pasted, the M_w of the starches pasted with added alcalase was significant lower than that of the starches pasted with added protease N. The reduction in molecular weight suggested that alcalase had modified the starch molecules during pasting.     

Relationship between monolayer and multilayer water contents,and involvement in gelatinization of baked starch products

Water sorption was investigated using a gravimetric technique to determine the involvement of water in gelatinization for baked starch products. The water isotherm could be described well using both the GAB and the Smith equations. Baked products with higher GAB monolayer water content (M₀C) could be made from dough with higher water content. In addition, M₀C was found to be correlated with both the Smith parameters w_b and w′, whereas the multilayer water content (MC) was reflected more in w′ than w_b. Although the desorption process maintains more water than adsorption, the ratio of M₀C to MC was constant irrespective of sorption process. Both M₀C and MC showed good correlations with the gelatinization parameters, but the correlations were weaker in the case of adsorption. Therefore, gelatinization may reflect water desorption characteristics, suggesting that hydration is incomplete in the adsorption process and new binding sites of water would be involved to a greater extent in gelatinization.     

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.     

Gelatinization and Pasting Properties of Waxy and Non‐waxy Rice Starches

Gelatinization and pasting properties of diverse rice types grown in two locations were examined by differential scanning calorimetry (DSC) and rotational rheometry, respectively. The data were compared to previously reported molecular starch properties for these samples: specifically, amylose content, starch molecular weight (M_w), and amylopectin side‐chain‐length distributions. Significant correlations were observed between amylose content, starch M_w, and the weight degree of polymerization of the long side chains of amylopectin F₁(DP_w) and many of the gelatinization and pasting properties measured. Higher amylose content corresponded with increased gelatinization onset (T_o) and peak temperatures (T_p), pasting onset and peak temperatures, and decreased peak and trough viscosity. Starch M_w correlated negatively with T_o, T_p, pasting onset, and peak temperature and positively with peak, trough, final, and breakdown viscosity. Amylopectin with DP_w 59‐78 of F₁(DP_w) correlated with increased T_o, T_p, pasting onset and peak temperature, and decreased peak, trough, final and breakdown viscosity. Pasting properties were also somewhat related to DP_w 21 of shorter side chains of amylopectin (F₂(DP_w)). Significant correlations between F₂(DP_w) and peak, final, and breakdown viscosity were observed (r = −0.447*, −0.391*, −0.388*, peak, final, and breakdown viscosity, respectively).     

Impact of Thermal and Chemical Pretreatments on Physicochemical,Rheological, and Functional Properties of Sweet Potato (Ipomea batatas Lam) Flour

The impact of thermal and chemical pretreatments on the physicochemical, rheological, and functional properties of sweet potato flour was investigated. The chemical pretreatment consisted in dipping peeled sweet potatoes in 1 % (w/v) calcium chloride (CaCl₂), while the thermal pretreatment was achieved by blanching them in tap water at 90 °C for 1 min. Composition in flour moisture, protein, fat, non-reducing sugars, and starch was determined using standard methods. Particle size, color, gelatinization, and rheological properties were analyzed. The water absorption index (WAI) and water solubility index (WSI), as well as the swelling capacity (SC) and sorption isotherms, were determined. The reducing sugar content of sweet potato flour was slightly higher in CaCl₂-pretreated (SSPCaCl₂) samples than that in blanched (SSPB) and control (SSP) samples. However, the lightness of the SSPB sample was lower than that of the SSPCaCl₂ and SSP samples. SSPCaCl₂ sample had the higher value of enthalpy of gelatinization and elasticity modulus G′. The SC was higher in blanched samples. A slight increase in the constant of water binding energy (C _BET) was observed after the CaCl₂ treatment and a marked increase for the blanched sample. Owing to the differences induced by blanching and CaCl₂ pretreatments, CaCl₂-pretreated flour samples are more suitable for bread-making processes and can also be used in food formulations.     

Rheological properties of rice–locust bean gum gels from different rice varieties

Pasting and gelatinization behavior of rice gels from Japonica (Ariete, Euro), Indica (Gladio, Suriname) and waxy (Glutinous) varieties were analyzed. These varieties differ widely in amylose contents and differential scanning calorimetry (DSC) gelatinization temperatures. Besides, the effect of locust bean gum (LBG) addition and the impact of successive viscoanalyser multiple-heating–cooling and freezing–thawing cycles on the gels pasting viscosities (peak-η_peak, trough-η_min, final-η_final), viscoelasticity by oscillatory rheometry and syneresis were evaluated.     

Gelling properties of gelatin–xanthan gum systems with high levels of co-solutes

The effects of moisture content, xanthan gum (XG) addition and glucose syrup (GS):sucrose ratio on elastic (G′) and viscous (G″) moduli during in situ gelation and on large deformation rheological properties of cured gels were investigated. An increase in both moduli of the samples with XG addition indicates network structure being strengthened. All gel samples exhibited distinct fracture. An increase in GS:sucrose ratio led to a decrease in fracture stress and an increase in fracture strain, implying more flexible polymer network. Decreasing moisture content may lead to phase separation between sugar-rich and polymer-rich phases to form stronger connection within the network structure. Textural characteristics of samples analyzed using a texture map, indicated that increasing GS:sucrose ratio rendered the sample texture more rubbery when the samples contained XG. We also related factors affecting the gelling mechanisms in terms of T_g measured by different techniques including DMA and modulated DSC.     

Chemometric Analysis of the Gelatinization and Pasting Properties of Long‐grain Rice Starches in Relation to Fine Structure

Chemometric tests were carried out to better understand the multidimensional facet of starch fine structure‐relationship concerning gelatinization and pasting properties. With Ward's hierarchical cluster analysis 20 long‐grain rice starch samples were sorted out into three clusters based on similarities in functional properties, particularly, paste peak (PV) and final viscosity (FV). The three clusters (arbitrarily named Clusters A, B, and C) exhibited a pasting profile trend of PV<FV, PV˜FV, and PV>FV, respectively. Cluster A samples were also lower in peak temperature, range and enthalpy of gelatinization, and swelling power. These attributes were associated with higher amylose content (AM), β‐amylolysis limit, and percentage of B1 chains (DP13‐24), but lower amylopectin weight‐average molar mass (M_w) and percentage of A chains (DP6‐12). A 5‐variable linear discriminant function correctly predicted 85% of the Ward's cluster membership of the individual cultivars. The discriminant function included the variables A, B1, and B2 (DP25‐36) chains, average chain length (ACL), and gyration radius (R_z). Fine structure variance was fully explained by a total of nine principal components, with the first three components cumulatively accounting for 74%. The leading variables included in the three rotated components pertained to amylopectin chain length distribution (A, B2, and B3+ or DP≥37 chains, and ACL) and amylopectin molar mass (M_w, R_z, and polydispersity). AM and M_w were loaded most frequently in the 4‐variable, best‐fit linear regression models for predicting gelatinization and pasting properties. A combination of at least two fine structure variables controls the functionality of rice starch.     

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.     

Effects of Gelatinization and Gel Storage Conditions on the Formation of Canna Resistant Starch

The effects of gelatinization and gel storage conditions on the formation of canna resistant starch (RS) were investigated. Starch slurries (10%, dwb) were autoclaved at 121?°C for 30, 60, and 120?min. The gels obtained were subsequently stored at different temperatures (4?°C, 30?°C, and 100?°C) and times (0, 1, 3, 5, and 7?days). Analyses of the RS content in gelatinized starch samples in comparison with that in granular starch showed that the RS fraction in granular starch was very high (97.3% w/w); however, nearly all of the RS was thermally unstable, as indicated by a great reduction in RS content (to 1.9% w/w) after cooking at 100?°C for 20?min. The RS contents in gelatinized starch samples were 12.0?C15.9% w/w, which were reduced to 7.9?C10.8% w/w after cooking. Storage of gels resulted in a significant increase in the amount of the thermally stable RS fraction, e.g., a thermally stable RS content of 16.8% w/w was found in the gel sample gelatinized for 120?min and stored at 4?°C for 3?days. This indicated that the ordered structures of the RS portion were tightened under the storage conditions. The gelatinization temperature of canna starch was 72.2?°C, whereas the RS products exhibited two melting temperature ranges, 51.1?C76.3?°C and 163.1?C165.1?°C, indicating that the newly formed crystals were very strong.     

Physicochemical characteristics of rice starch supplemented with dietary fibre

Various dietary fibres (DF) from rice flours of Taichung Sen 10 (TCS10) and Tainung 67 (TNu67) rice cultivars were isolated while their roles in governing the pasting and the rheological properties of the rice starch were examined. The addition of DF (at 5 wt.% on dry starch basis), most notably from TCS10 cultivar generally caused significant increases in swelling power and pasting viscosities of 10 wt.% rice starch dispersions. Furthermore, the addition of DF was found to improve the rheological parameters of the 10 wt.% rice starch gel. Nuclear magnetic resonance (NMR) relaxation measurements revealed that the water mobility of starch gel was decreased with the addition of DF. The statistically significant factors were concluded to be arabinoxylan-related compositions for the increments of pasting and rheological characteristics, meanwhile the swelling power and setback viscosity mainly depend on β-glucan compositions and arabinose-to-xylose molar ratio (R_AX).     

Thermal and rheological properties of tapioca starch and xyloglucan mixtures in the presence of sucrose

The influence of sucrose on thermal and rheological properties of tapioca starch (TS)–tamarind seed xyloglucan (XG) mixtures was investigated. Rapid visco-analysis profiles of 5% w/w TS/XG dispersions at different mixing ratios revealed that peak and final viscosities increased with increasing sucrose and XG contents. Loss tangent of each mixing ratio of TS/XG pastes determined from dynamic rheometry exhibited a lower value with increasing sucrose, suggesting solid-like properties contributed from the dissolved sucrose in the systems. Gelatinization temperatures of 25% w/w TS/XG at mixing ratios of 10/0 and 9/1 increased with increasing sucrose content whereas the gelatinization enthalpy of pastes increased in the presence of high sucrose concentration. Sucrose increased the stiffness and hardness of the 25% w/w TS/XG gels (mixing ratios of 10/0, 9.5/0.5 and 9/1) from the compression test. These results suggest that sucrose delays the gelatinization of TS and XG mixtures and strengthens the gels by increasing the elastic component.     

Physicochemical and Gelatinization Properties of Starches Separated from Various Rice Cultivars

Morphological, viscoelastic, hydration, pasting, and thermal properties of starches separated from 10 different rice cultivars were investigated. Upon gelatinization, the G′ values of the rice starch pastes ranged from 37.4 to 2057 Pa at 25 °C, and remarkably, the magnitude depended on the starch varieties. The rheological behavior during gelatinization upon heating brought out differences in onset in G′ and degree of steepness. The cultivar with high amylose content (Goami) showed the lowest critical strain (γ_c), whereas the cultivars with low amylose content (Boseokchal and Shinseonchal) possessed the highest γ_c. The amylose content in rice starches affected their pasting properties; the sample possessing the highest amylose content showed the highest final viscosity and setback value, whereas waxy starch samples displayed low final viscosity and setback value. The onset gelatinization temperatures of the starches from 10 rice cultivars ranged between 57.9 and 64.4 °C. The amylose content was fairly correlated to hydration and pasting properties of rice starches but did not correlate well with viscoelastic and thermal characteristics. The combined analysis of hydration, pasting, viscoelastic, and thermal data of the rice starches is useful in fully understanding their behavior and in addressing the processability for food applications.     

Rheological behavior of functional sugar-free guava preserves: Effect of the addition of salts

The addition of salts to carrageenan and locust bean gum gels functions to improve the characteristics of texture, thereby increasing gel strength. This effect is widely studied in gels of model systems but is studied to a lesser extent in complex systems, such as fruit preserves. The objective of this study was to evaluate the effect of adding salts on the rheological behavior of functional sugar-free guava preserves, as well as to correlate the rheological parameters. To this end, three types of texture properties were analyzed (texture profile, stress relaxation and uniaxial compression) in functional sugar-free guava preserves prepared with different concentrations of KCl and CaCl₂ salt. The analyses were performed with a texturometer (Stable Micro Systems, Model TA - XT2i), and the parameters were analyzed using a Scott-Knott test at 5% probability, principal components analysis and Pearson correlation. CaCl₂ was more effective for improving the characteristics of texture, especially gel strength (concentration near the F3: 0.33%), whereas KCl addition degraded gel strength. In the analysis of test relaxation, the Maxwell model parameters provided better discrimination between samples than the Peleg model parameters. Positive and negative correlations were observed, and the parameters of hardness, adhesiveness and elastic modulus ideal (E₁) were the most correlated with other rheological parameters.     

Structural and rheological properties of xanthan gum/lysozyme system induced by in situ acidification

Structural and rheological properties of xanthan gum/lysozyme (XG/Ly) system induced by electrostatic interaction through in situ acidification were investigated. The two biopolymers transited from co-solubility state to form soluble complexes, and finally produced tenuous network as the pH further decreased. The fluorescent images indicated that the network was cross-linked of XG chains by Ly, liking a polymerization process which resulted in the sol-gel transition by electrostatic interactions. High Ly content could accelerate the phase transition at the same pH condition, while XG played a contrary role. XG addition could enhance the thermal stability of Ly. The phase transition was also illustrated by ζ-potential at different pHs. The boundary parameters were determined to distinguish the phase transition regions. At the pH higher than pH_φ, the negatively liked XG and Ly were in co-soluble state. They formed soluble complexes at the pH between pH_φ and pH_g, and gel was obtained with net microstructure as the pH continuously decreased (lower than pH_g). The paper provides practical parameters that may be applicable in controlling the structure, texture, and stability of polysaccharide/protein system, as well as in food and medicinal application with various purposes.     

Effect of different β-glucans on the gelatinisation and retrogradation of rice starch

Four β-glucan preparations, i.e., curdlan (CL), oat (OG), barley (BG) and yeast (YG) β-glucans, were compared for their effects on the gelatinisation and retrogradation of rice starch (RS). Rapid visco-analysis (RVA) showed that addition of any of these β-glucans significantly increased the peak, breakdown, final, and setback viscosities of RS, whereas the pasting temperatures were significantly decreased by OG or CL addition, but were unaffected by BG or YG addition. Differential scanning calorimetry (DSC) demonstrated that all the β-glucans had a negligible effect on the onset (T_o), peak (T_p), and conclusion (T_c) temperatures but slightly decreased the gelatinisation enthalpy (△H₁) of RS. Storage of all the gels at 4 °C resulted in a marked decrease in the T_o, T_p, T_c, and melting enthalpy (△H₂) values. The retrogradation ratio (△H₂/△H₁) and the phase transition temperature range (T_c–T_o) of all the gels increased with storage time. Dynamic viscoelastic measurements revealed weak gel-like behaviour of all the gels, in which their storage modulus (G′) increased and their loss tangent (tan δ) decreased during storage. Steady flow tests illustrated time-dependent shear-thinning (thixotropic) behaviour of all the gels. The hysteresis loop area and the gel hardness increased with storage time. However, the rate and extent of retrogradation and the rheological and textural changes of the RS gels were reduced by addition of any of these β-glucans. The extent of the aforementioned effects differed among the different β-glucan preparations, generally in the order OG ≈ BG > CL ≈ YG.     

The effect of electrostatic interactions on pasting properties of potato starch/xanthan gum combinations

The effects of electrostatic interactions on pasting properties of potato starch (PS)/xanthan gum (XG) combinations were investigated. The RVA peak viscosity of combinations was decreased firstly and then increased with the adding of XG. The analysis and regression model performance of RVA measurement showed that there was the relationship between pasting properties of combinations and XG concentrations. Electrostatic repulsions between native potato starch or anionic modified potato starches (AP) and XG could be present by decreasing peak viscosity, but the pasting temperatures showed increasing trend. However, electrostatic attractions between cationic modified potato starch (CP) and XG showed the opposite effect. Negative zeta potential determination for combinations (− 54.6 mv) was higher than PS (− 35.2 mv) illustrated that combinations had more electronegativity and stability, in addition a phase-separated microstructure was exhibited in the combinations determined by Zeta potential results. SEM micrographs presented that XG film attached to the surface of PS granules, which inhibited the starch granules destruction and leaching of amylase. The electrostatic repulsion leaded to more stability of the three dimensional network structures of combinations. The strong electrostatic interactions between PS and XG were found to play an important role on the pasting properties of the combinations.     

Effects of methylcellulose,xanthan gum and carboxymethylcellulose on thermal properties of batter systems formulated with different flour combinations

The functionalities of hydrocolloid–flour mixtures in terms of the thermal properties of their resulting batter systems were investigated, and the effects of different thermal processes such as cooking–freezing–thawing (CFT) and freezing–cooking (FC) on thermal properties of the various batter systems were determined in this study. Differential scanning calorimetry (DSC) was used to determine thermal property parameters including gelatinization temperature (T_G), total enthalpies of gelatinization (ΔH_G), glass transition temperature (T_g), melting peak temperature (T_m), and total melting enthalpies (ΔH_m). The different thermal processes did not significantly affect either T_G or ΔH_G of batter systems, but they influenced the glass transition behavior and the ΔH_m of batter systems. The thermal processes also showed different effects on the batter systems containing different hydrocolloids such as methylcellulose (MC), carboxymethylcellulose (CMC), and xanthan gum (XG). The hydrocolloids shifted T_G upwards, depressed T_g, and increased T_m of batters. The effect of these hydrocolloids on glass transition temperature was more pronounced in raw samples (FC process) than in cooked samples and increased with increasing levels of CMC and MC used in the formulations. Batters with MC showed increased ΔH_m for all the thermal processes. CMC only showed significant effect on ΔH_m for cooked samples (CFT process). MC and CMC showed more pronounced effects on T_g for raw uncooked rice- and corn flour-based batters than on raw uncooked wheat flour-based batters. However, this special effect was not obvious in the batters containing 0.2% XG.     

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.