Effect of Molar Substitution on Rheological Properties of Hydroxypropylated Rice Starch Pastes

The steady and dynamic shear rheological properties of hydroxypropylated rice starch pastes (5%, w/w) were evaluated at different molar substitution (MS, 0.030‐0.142). The swelling power (35.5‐52.8 g/g) and solubility (8.19‐10.7%) values of the hydroxyproylated rice starches were higher than those of native rice starch (26.6 g/g and 7.78%) and increased with an increase in MS. The hydroxypropylated starch pastes at 25°C showed a pronounced shear‐thinning behavior (n = 0.33‐0.40) with Casson yield stress (σ_oc = 15.9‐31.7 Pa). The consistency index (K) and yield stress (σ_oc) values of the hydroxypropylated starch pastes were lower than those of the native starch, and increased progressively with an increase in MS. The apparent viscosity (η_a,500) obeyed the Arrhenius temperature relationship over the temperature range of 10‐55°C; the activation energies (E_a) of the hydroxypropylated starch pastes were in the range of 14.8‐18.5 kJ/mol, i.e. higher than that (14.1 kJ/mol) of the native starch. Storage (G′) and loss moduli (G′′) of hydroxypropylated starch pastes increased with an increase in MS, while tan δ (G′′/G′) values decreased, indicating that G′ rose more strongly than G′′ with increased MS.     

Physicochemical properties of high amylose rice starches purified from Korean cultivars

The physicochemical and pasting properties of high amylose rice starches isolated using alkaline steeping method from different Korean rice cultivars, Goamy2 and Goamy, and from imported Thai rice were examined. The protein and lipid contents of the Goamy2 starch were higher than those of the other two starches. The amylose and total dietary fiber contents were ranged from 31.4 to 36.8% and from 6.3 to 8.6%, respectively. Total dietary fiber was positively correlated to amylose content. Water binding capacity was higher in the Goamy2 starch (172.2%) than in the Goamy and Thai rice starches (112.7–115.6%). The swelling power of the Goamy2 starch showed lower values, but its value at 95°C was similar to others because of its rapid increment at 85°C. The granular size of Goamy2 starch was widely distributed compared to those of others. The Goamy2 starch showed a high initial pasting temperature (92.0°C) and low breakdown and setback viscosities. The Goamy and Thai rice starch granules were polygonal‐shaped with A‐type crystals, whereas the Goamy2 starch granules were round‐shaped with B‐type crystals. Goamy and Goamy2 starches showed a single endotherm at 60.8 and 76.0°C for peak temperature and 10.0 and 11.5 J/g for gelatinization enthalpies, respectively. The Thai rice starch presented an endotherm with a shoulder peak at 68.3°C (75.3°C for the main peak) and a gelatinization enthalpy of 12.4 J/g.     

Development and Physicochemical Characterization of New Resistant Citrate Starch from Different Corn Starches

Resistant starch has drawn broad interest for both potential health benefits and functional properties. In this study, a technology was developed to increase resistant starch content of corn starch using esterification with citric acid at elevated temperature. Waxy corn, normal corn and high‐amylose corn starches were used as model starches. Citric acid (40% of starch dry weight) was reacted with corn starch at different temperatures (120–150°C) for different reaction times (3–9 h). The effect of reaction conditions on resistant starch content in the citrate corn starch was investigated. When conducting the reaction at 140°C for 7 h, the highest resistant starch content was found in waxy corn citrate starch (87.5%) with the highest degree of substitution (DS, 0.16) of all starches. High‐amylose corn starch had 86.4% resistant starch content and 0.14 DS, and normal corn starch had 78.8% resistant starch and 0.12 DS. The physicochemical properties of these citrate starches were characterized using various analytical techniques. In the presence of excess water upon heating, citrate starch made from waxy corn starch had no peak in the DSC thermogram, and small peaks were found for normal corn starch (0.4 J/g) and Hylon VII starch (3.0 J/g) in the thermograms. This indicates that citrate substitution changes granule properties. There are no retrogradation peaks in the thermograms when starch was reheated after 2 weeks storage at 5°C. All the citrate starches showed no peaks in RVA pasting curves, indicating citrate substitution changes the pasting properties of corn starch as well. Moreover, citrate starch from waxy corn is more thermally stable than the other citrate starches.     

Influence of the Heating Rate on the Pasting Properties of Various Flours

Viscoamylographic tests were carried out on six commercial flour samples, three wheat flours (WF), two semolinas (S) and one rice flour (RF), using the Brabender Micro Visco‐Amylo‐Graph (MVA). The slurries were subjected to a definite temperature profile (30°C‐95°C, 95°C×30 min, 95°C‐50°C, 50°C×30 min), stirring at 250 min⁻¹ and using a 300 cm·g_f cartridge and recording the viscosity (in Brabender Units, BU) as a function of temperature and time. The aim of this work was to evaluate the influence of different heating rates (1.5, 3.0, 5.0, 7.5, 10.0°C/min) on the pasting properties of the various flours. The peak viscosity of WFs and Ss increased when high heating rates were applied, while the RF showed similar pasting properties independently of the heating rate. These behaviours were mainly ascribed to the different molecular organisation of the starch granules, responsible of different swelling and gelatinising extents, and also to a different kinetic of alpha‐amylase inactivation according to the heating rate applied. The key role of the alpha‐amylase activity in controlling the pasting viscosity of the different samples was demonstrated by the viscoamylographic test performed in the presence of silver nitrate as enzyme inhibitor.     

Pasting Properties of Non‐waxy Rice Starch‐Hydrocolloid Mixtures

The swelling and pasting properties of non‐waxy rice starch‐hydrocolloid mixtures were investigated using commercial and laboratory‐generated hydrocolloids. The swelling power of the rice starch‐hydrocolloid mixtures was generally depressed at low concentration of hydrocolloids (0–0.05%), but increased directly with increasing hydrocolloid concentrations (0.05–0.1%). In gellan gum dispersion, the swelling power at 100°C was higher than that of control. The rice starch‐hydrocolloids mixtures showed shear‐thinning flow behavior (n = 0.26–0.49). Hydrocolloids except the exopolysaccharide from S. chungbukensis (EPS‐CB) increased apparent viscosity and consistency index (K) of rice starch dispersions, but decreased the n value. Hydrocolloids enhanced the trough and final viscosity of rice starch dispersions but EPS‐CB reduced the viscosity of rice starch pastes. Hydrocolloids lowered peak viscosity but addition of guar gum resulted in high peak viscosity, apparent viscosity, and consistency index of rice starch dispersions. Total setback viscosity appeared to be not affected by hydrocolloids at low concentration (0.05%). The hot and cold paste of the starch‐gellan gum mixture exhibited the highest viscosity values in the Brookfield viscometer.     

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.     

Steady and Dynamic Shear Rheology of Rice Starch‐Galactomannan Mixtures

Rheological properties of rice starch‐galactomannan mixtures (5%, w/w) at different concentrations (0, 0.2, 0.4, 0.6 and 0.8%, w/w) of guar gum and locust bean gum (LBG) were investigated in steady and dynamic shear. Rice starch‐galactomannan mixtures showed high shear‐thinning flow behaviors with high Casson yield stress. Consistency index (K), apparent viscosity (η_a,100) and yield stress (σ_oc) increased with the increase in gum concentration. Over the temperature range of 20–65°C, the effect of temperature on apparent viscosity (η_a,100) was described by the Arrhenius equation. The activation energy values (E_a = 4.82–9.48 kJ/mol) of rice starch‐galactomannan mixtures (0.2–0.8% gum concentration) were much lower than that (E_a = 12.8 kJ/mol) of rice starch dispersion with no added gum. E_a values of rice starch‐LBG mixtures were lower in comparison to rice starch‐guar gum mixtures. Storage (G′) and loss (G′′) moduli of rice starch‐galactomannan mixtures increased with the increase in frequency (ω), while complex viscosity (η*) decreased. The magnitudes of G′ and G′′ increased with the increase in gum concentration. Dynamic rheological data of ln (G′, G′′) versus ln frequency (ω) of rice starch‐galactomannan mixtures have positive slopes with G′ greater than G′′ over most of the frequency range, indicating that their dynamic rheological behavior seems to be a weak gel‐like behavior.     

Effects of cationization on DSC thermal profiles,pasting and emulsifying properties of sago starch

Cationic sago starches were prepared using an aqueous alkaline process with different levels of cationic reagent 3‐chloro‐2‐hydroxypropyltrimethylammonium chloride (0.01–0.10 M ), sodium hydroxide (0.03–0.86 M ) and reaction temperature (30–62 °C). The degree of substitution (DS), reaction efficiency, thermal and pasting properties of cationic sago starches were analysed. Emulsifying and fat binding properties of native sago starch, cationized sago starch and commercial chitosan were compared at two different pH values (4 and 7). Degree of substitution increased with an increase in concentration of cationic reagent or NaOH, or reaction temperature. The reaction efficiency was proportional to the concentration of NaOH and reaction temperature but inversely proportional to the cationic reagent concentration. The highest DS and reaction efficiency achieved was 0.06 and 79%, respectively. The pasting temperature and gelatinization enthalpy of cationic starch (DS 0.06) were lower compared with native sago starch. Cationization increased the peak viscosity and breakdown of the starch paste but decreased the setback. The presence of cationic groups significantly increased emulsion stability, emulsion viscosity and fat binding capacity of sago starch. However, the cationic sago starch was still inferior to chitosan, which showed the highest emulsion stability, emulsion viscosity and fat binding capacity. There was no significant difference between the surface tension values of native and cationic sago starch and chitosan. The influence of pH on emulsifying properties was not significant. The emulsion stability of the cationic sago starch improved due to an increase in viscosity and fat binding capacity but not its surface active property. Copyright © 2004 Society of Chemical Industry     

Crystallinity and Rheological Properties of Pregelatinized Rice Starches Differing in Amylose Content

Three rice starches with different amylose contents (Glutinous: 1.4%, Jasmine: 15.0% and Chiang: 20.2%) were pregelatinized in a double drum dryer at 110, 117 and 123°C. Starch crystallinity was determined by X‐ray diffractometry and Fourier transform infrared (FTIR) spectrometry. Rheological properties were assessed by a Rapid Visco Analyser (RVA) and rheometer. Pregelatinized starches obtained from Glutinous (PGS) and Jasmine rice (PJS) gave an RVA pasting profile with cold peak viscosity. At drum temperature 110°C, PGS and PJS showed X‐ray patterns that were indicative of amorphous structures. However, pregelatinized Chiang rice starch (PCS) exhibited RVA hot peak viscosity and the presence of an amylose‐lipid complex with remaining granule structure. The PCS had a lower water absorption index (WAI) and water solubility index (WSI) than PJS and PGS. After pregelatinization at increased drum temperature (117, 123°C), the PGS had a lower WAI, whereas PCS showed an opposite trend indicating lower degree of granule disruption. In addition, the cold peak viscosity of PGS and PJS decreased with increasing drum temperature. For all drum temperatures, the apparent viscosity at 25°C for PGS and PJS decreased with increasing shear rate, indicating shear‐thinning behavior.     

Effects of Cationization on Functional Properties of Pea and Corn Starches

Amylography, scanning electron microscopy and storage tests demonstrated that native pea starches were highly resistant to granule disintegration during heating in dilute slurries, resulting in low hot paste viscosity, high retrogradation and syneresis. Cationization at degrees of substitution of 0.02 to 0.05 reduced the pasting and gelatinization temperatures, increased peak viscosities and set-back on cooling but eliminated syneresis after storage at 4°C and − 15°C. The principal effects of cationization were to promote rapid granule dispersion at low pasting temperatures, yielding a molecular dispersion of amylose and amylopectin on heating to 95°C. On cooling, the gel structures were firm and the cationic groups controlled the realignment of starch chains during low temperature storage.     

Rheological Properties of Rice Starch Dispersions in Dimethyl Sulfoxide

The steady and dynamic shear rheological properties of rice starches dispersed in dimethyl sulfoxide (DMSO) solution (90% DMSO‐10% water) were evaluated at various concentrations (7, 8, 9 and 10%, w/w). Rice starch dispersions in DMSO solution at 25°C showed a shear‐thinning flow behavior (n=0.44–0.60) and their consistency index (K) and apparent viscosity (η_a,100) increased with the increase in concentration. The apparent viscosity over the temperature range of 25–70°C obeyed the Arrhenius temperature relationship, indicating that the magnitudes of activation energy (E_a) were in the range of 11.7–12.7 kJ/mol. The Carreau model provided better fit on the shear rate‐apparent viscosity data than the Cross model. Dynamic frequency sweep test showed that both storage modulus (G′) and loss modulus (G′′) of rice starch dispersions increased with the increase in concentration. G′′ showed a higher dependence on frequency (ω) compared to G′ due to the higher G′′ slopes. All rice starch dispersions showed the plateau of G′ at high frequencies. Intrinsic viscosity of rice starch dispersions in DMSO was 104.1 mL/g.     

Some Properties of Starch Isolated from Radix Cynanchi bungei

The physicochemical and scanning electron micrograph characteristics of Radix Cynanchi bungei (RCb) starch were investigated. RCb starch presented an apparent amylose content of 20.1%, less than that of potato starch (23.6%), with a granule size ranging from 5 to 15 μm with round, spherical and polygonal shapes and B‐type X‐ray diffraction pattern. The RVA pasting properties of RCb starch were similar to those of potato starch, with pasting temperature of 60.8°C, lower than that of potato starch (64.3°C). The gelatinization parameters of RCb starch were found to be 55.9°C (T_o), 60.0°C (T_p), 66.6°C (T_C) and 13.2 J/g (ΔH) while those of potato starch were 58.9°C, 63.5°C, 68.6°C and 13.2 J/g. Both RCb and potato starch pastes behaved as high shear‐thinning liquids. RCb starch pastes had lower apparent viscosity than potato starch pastes at the same shear rate.     

Rheology of Rice Starch‐Sucrose Composites

The effect of sucrose at different concentrations (0, 10, 20 and 30%) on rheological properties of rice starch pastes (5% w/w) was investigated in steady and dynamic shear. The steady shear properties of rice starch‐sucrose composites were determined from rheological parameters for power law and Casson flow models. At 25°C all the starch‐sucrose composites exhibited a shear‐thinning flow behavior (n=0.25–0.44). The presence of sucrose resulted in the decrease in consistency index (K), apparent viscosity (η_a,100) and yield stress (σ_oc). Dynamic frequency sweeps at 25°C indicated that starch‐sucrose composites exhibited weak gel‐like behavior with storage moduli (G′) higher than loss moduli (G′′). G′ and G′′ values decreased with the increase in sucrose concentration. The dynamic (η*) and steady‐shear (η_a) viscosities at various sucrose concentrations did not follow the Cox‐Merz superposition rule. G′ values as a function of aging time (10 h) at 4°C showed a pseudoplateau region at long aging times. In general, the values of G′ and G′′ in rice starch‐sucrose composites were reduced in the presence of sucrose and depended on sucrose concentration.     

Use of Iodine as a Tool to Understand Wheat Starch Pasting Properties

The ability of iodine to bind amylose has been used to understand a variety of structural and functional aspects of starch in food systems. In this study, the changes in starch granule swelling, polymer leaching and their relationship to pasting properties was investigated by adding iodine to the starch slurry at either room temperature or 95°C. The objective of the study was to investigate the contribution of leached and solubilized starch polymers on the pasting behavior of wheat starch. The addition of very small amounts of iodine (0.1%, dry basis, db) at room temperature increased peak and final pasting viscosities as compared to when no iodine was added. Further increases in iodine concentration resulted in a decrease in peak and final pasting viscosities. The amount of iodine required to completely inhibit granule swelling was more than that required to minimize amylose leaching from the granule. Adding increasing amounts of iodine at 95°C to the starch slurry resulted in the gradual decrease in peak and final pasting viscosities. The contrasting effects of iodine on paste viscosity behavior when added at room temperature or at 95°C suggest that the contribution of extra‐granular amylose on the setback viscosity is minimal and a larger proportion of amylose is retained in the intragranular spaces.     

Study on physicochemical characteristics of waxy potato starch in comparison with other waxy starches

The physicochemical properties of wx potato, wx corn, and wx rice starches were examined and compared. wx potato starch displayed the B‐type XRD pattern, whereas wx rice and wx corn displayed the A‐type. Shapes of wx potato starch were oval or slightly round, wx corn and wx rice starch granules were polygonal. AM contents of the three starches were between 1.0 and 1.5%. Rapid viscosity analyzer data showed initial pasting temperatures of wx potato, wx corn, and wx rice starches as 69.6, 75.4, and 76.8°C, respectively, peak viscosity, breakdown, and setback of wx potato starch were 2114, 1084, and 4 mPa s. Using DSC, onset temperature of gelatinization of wx potato starch was 5.5–7.2°C higher than those of wx rice and wx corn starches. The thermal enthalpies of the starches studied in our laboratory were in the range of 0.2268–1.9900 J/g with decreasing order of wx potato > wx corn > wx rice starch.     

Changes in rheological properties of hydroxypropyl potato starch pastes during freeze—thaw treatments. III. Effect of cooking conditions and concentration of the starch paste

The effects of different cooking conditions and concentrations on the freeze-thaw stability of hydroxypropyl potato starch (molar substitution 0·125) paste were investigated by dynamic rheological measurements and syneresis determination. The cooking conditions of the starch were chosen by taking the starch pastes at peak consistency (SP/Peak), at half breakdown consistency (SP/HB), after being held at 95°C for 15 min (SP/95°C) and after the whole pasting cycle (SP/25°C) in the Brabender Amylograph. The concentration effect was studied with the starch pastes after a whole pasting cycle at 35, 50 and 65 g kg^?1. Depending on cooking conditions and concentration, the rheological responses in changes of complex modulus (G*) and phase angle () of the starch pastes, with regard to the number of freeze-thaw cycles, differed considerably. This indicated that the starch pastes had undergone various structural changes during freeze-thaw treatments. With an increased extent of pasting, and with an increased starch concentration, the rheological responses indicative of the destabilisation process of the starch pastes were, in general, delayed. The number of freeze-thaw cycles required for the appearance of a peak in G*, related to the first syneresis, was one, two, five and six for SP/Peak, SP/HB, SP/95°C and SP/25°C, respectively. For the starch pastes at 35, 50 and 65 g kg^?1, it was four, six and seven cycles, respectively. Based on these rheological data, it was suggested that the amount of inter-mingled amylose and amylopectin in the dispersion of hydroxypropyl starch paste is the main controlling factor, which plays a critical role in the rheological response as well as in the syneresis.     

Physicochemical Properties of Sweet Potato Flour and Starch as Affected by Blanching and Processing

The effects of blanching on physicochemical properties of flours and starches prepared from two varieties of sweet potatoes (Mun‐Kai and Negro) were studied and compared. The pasting temperature and peak viscosity of starches, respectively, were 74 and 80 °C and 381 and 433 RVU. The pasting temperature (74.0‐94.8 °C) of flours was greater than that of starch, depending on the variety and blanching process. However, the peak viscosity (ca. 103‐120 RVU) of flours was lower than that of the corresponding starches. Partial gelatinization of starch granules was observed as a result of a 1‐min blanching. Composition of starch and flour was found to affect swelling power and solubility. The starch content of starches, flours from unblanched sweet potato and flours from 1‐min blanched sweet potatoes were 97; 66.3 and 74.9; as well as 36.6 and 40.4%, respectively. Amylose content of flours and starches varied from 17.2‐20.8%.     

Gelatinization and pasting properties of rice starch modified with 2‐octen–1‐ylsuccinic anhydride

Rice starch was modified with various levels of 2‐octen‐1‐ylsuccinic anhydride (OSA). Treatments with OSA at 3, 5, and 10% resulted in starch derivatives with 0.016, 0.033, and 0.070 degrees of substitution (DS( respectively. Thermovisco properties of the derivatives were investigated by differential scanning calorimetry (DSC) and rapid visco analysis (RVA). Water content in the sample was found to have a significant effect on the characteristics of the DSC endotherm. Pasting properties of the OSA‐starch and the effect of pH and salt on the RVA profiles were also studied. In general, with increased OSA‐modification, the starch derivatives swelled and gelatinized at lower temperatures to achieve higher viscosities. Specifically, based on DSC analysis at 80% water, the peak temperature of gelatinization decreased from 68.5 to 63.2°C as the OSA modification increased in DS from 0 (intact starch) to 0.070. On the other hand, RVA results indicate that, for samples undergoing similar increase in OSA modification, the pasting temperature decreased from 88.7 to 51.5°C and the peak viscosity increased from 668 to 6822 cP.     

Chemical and Physical Properties of Kiwifruit (Actinidia deliciosa) Starch

Chemical and physical properties of kiwifruit (Actinidia deliciosa var. ‘Hayward’) starch were studied. Kiwifruit starch granules were compound, irregular or dome‐shaped with diameters predominantly 4–5 µm or 7–9 µm. Kiwifruit starch exhibited B‐type X‐ray diffraction pattern, an apparent amylose content of 43.1% and absolute amylose content of 18.8%. Kiwifruit amylopectins, relative to other starches, had low weight‐average molecular weight (7.4×10⁷), and gyration radius (200 nm). Average amylopectin branch chain‐length was long (DP 28.6). Onset and peak gelatinization temperatures were 68.9°C and 73.0°C, respectively, and gelatinization enthalpy was high (18.5 J/g). Amylose‐lipid thermal transition was observed. Starch retrograded for 7 d at 4°C had a very high peak melting temperature (60.7°C). Peak (250 RVU), final (238 RVU) and setback (94 RVU) viscosity of 8% kiwifruit starch paste was high relative to other starches and pasting temperature (69.7°C) was marginally higher than onset gelatinization temperature. High paste viscosities and low pasting temperature could give kiwifruit starch some advantages over many cereal starches.     

Physicochemical properties,digestibility and expected glycaemic index of high amylose rice differing in length-width ratio in Sri Lanka

Gelatinization, pasting, digestibility and estimated glycaemic index of six high amylose rice varieties differing in length/width ratio were studied. Amylose content ranged narrowly (27.8–29.1%). Resistant starch content ranged from 0.44% to 1.4%. In contrast to gelatinisation enthalpy, gelatinisation temperature (GT) ranged narrowly (76.7–77.4 °C). For all rice varieties, melting temperature of amylose-lipid complex I and II was around 99 °C and 110 °C, respectively. The enthalpy of amylose-lipid complex I and II ranged between 0.18–0.87 and 0.23–0.55, respectively. Expected in vitro glycaemic index (GI) of all tested varieties was similar (88.2–92.4). The results showed that the size of the rice grain (length/width) and resistant starch content had no apparent impact on the GI of high amylose rice. The dominant factors determining the digestibility and glycaemic response of the tested high amylose rice varieties seemed to be amylose content and the GT. Besides the pasting temperature, other pasting properties varied significantly but were not correlated to starch digestibility and estimated GI among the six rice varieties. Thus, RVA pasting properties, except for pasting temperature, may not be good predictors for the GI of these high amylose rice.