Fine Structure,Thermal and Viscoelastic Properties of Starches Separated from Indica Rice Cultivars

Starches were separated from indica rice cultivars (PR‐113, Basmati‐370, Basmati‐386, PR‐115, IR‐64, and PR‐103) and evaluated using gel permeation chromatography (GPC), X‐ray diffraction, differential scanning calorimetry (DSC) and dynamic viscoelasticity . Debranching of starch with isoamylase and subsequent fractionation by GPC revealed 9.7–28.3% apparent amylose content, 3.7–5.0% intermediate fraction (mixture of short amylose and long side‐chains of amylopectin), 20.6–26.6% long side‐chains of amylopectin and 45.8–59.4% short side‐chains of amylopectin). IR‐64 starch with the highest crystallinity had the highest gelatinization temperatures and enthalpy, T_o, T_p, T_c, and ΔH_gel being 71.8, 75.9, 82.4°C and 5.1 J/g, respectively, whereas PR‐113 starch with lower crystallinity showed the lowest gelatinization temperatures (T_o, T_p, T_c, of 60.8, 65.7 and 72.2°C, respectively). Basmati‐386 starch exhibited two endotherms during heating, the first and second endotherm being associated with the melting of crystallites and amylose‐lipid complexes, respectively. T_o, T_p, T_c and ΔH_gel of the second endotherm of Basmati‐386 starch were 99.0, 100.1, 101.1°C and 2.0 J/g, respectively. During cooling, Basmati‐386 also showed an exotherm at a peak temperature of 87°C. PR‐113 starch with the highest amylose content and the lowest content of short side‐chains of amylopectin had the highest peak storage modulus (G′= 1.6×10⁴ Pa). The granules of PR‐113 starch were the least disintegrated after heating. The effects of heating starch suspensions at different temperatures (92°C, 130°C and 170°C) on intrinsic viscosity [η], transmittance and viscoelasticity were also studied to evaluate the extent of breakdown of the molecular structure. The intrinsic viscosity of starch suspensions heated at 92, 130 and 170°C ranged between 103–114, 96–110 and 28–93 mL/g. Transmittance value of starches cooked at 92°C decreased with increase in storage duration. All starches except PR103, cooked at 130°C also showed decrease in transmittance during storage, however, at lower rate. PR103 starch heated at 130°C did not show any change in transmittance up to a storage time of 48 h. The changes in viscoelasticity of starch pastes cooked at different temperatures during cooling and reheating were also evaluated. G′ and G′′ increased with decrease in temperature during cooling cycle. Starches heated at 130°C with apparent amylose content ≤ 21.2% showed an improvement in G′ and G′′ in comparison to the corresponding starches heated at 92°C, this improvement was observed to be higher in starches with lower amylose content. All starches heated at 170°C had a higher proportion of breakdown in molecular structure as indicated by lower G′ and G′′ than the same starches heated at 130 and 92°C.     

On the gelation of Vicia faba protein in dependence on the acetylation degree

Using the method of mathematical planning of experiments and taking the shear modulus of the gels as an equivalent of the gelation degree, the conditions of the thermal denaturation at the maximum shear modulus were found to be T_D ≈? 100 °C and t_D ≈? 60 min for the non-acetylated Vicia faba protein and T_D ≈? 100 °C and t_D ≈? 40 min for the acetylated Vicia faba protein. On these conditions the dependence of the shear modulus (G) on the protein concentration (C) is expressed by exponential functions G = α C4.3 and G = α C5.0, respectively. By an increasing acetylation of the Vicia faba protein the shear modulus, the thickness of the many-line chains, and the net density of gels are increased; the same is valid for the shear modulus and the masking of disulfide groups by an increasing concentration of non-acetylated and acetylated Vicia faba proteins.     

Rheological, Thermal and Microstructural Properties of Whey Protein-Cassava Starch Gels

Mixed gels of cassava starch (CS) and a whey protein isolate (WPI), obtained by heating solutions of 10% total solids, pH 5.75 to 85°C, were characterized as a function of the starch fraction, θ_s, by axial compression, small-amplitude oscillatory rheometry, differential scanning calorimetry (DSC) and scanning electron microscopy (SEM). Gelation did not occur for θ_s > 0.7. In the range 0<θ_s < 0.4 mixed gels showed higher mechanical (E, elastic modulus) and rheological (G′, storage modulus) properties than pure gels, with maximum values for θ_s= 0.2–0.3. Viscoelastic measurements as a function of time showed that gels containing higher levels of WPI developed a larger G. Blends of both biopolymers showed independent thermal transitions in DSC measurements, related to gelatinization and denaturation. Microstructure of a mixed gel formed at θ_s= 0.2 showed a continuous matrix formed by strands of WPI particle aggregates and an independent CS phase.     

Influence of temperature,calcium and sucrose concentration on viscoelastic properties of Prosopis chilensis seed gum and nopal mucilage dispersions

Viscoelastic properties of two nontraditional hydrocolloid dispersions were evaluated. Prosopis chilensis seed gum was evaluated based on temperature (5–80 °C) and added CaCl₂ (0.07%), whereas nopal mucilage was evaluated based on temperature (5–80 °C) and sucrose concentration (0–20%). Viscoelasticity was tested by the small strain oscillatory shear test; storage modulus (G′), loss modulus (G″) and tan δ were reported. Prosopis chilensis and nopal dispersions behaved as weak gels (G’ > G’’) regardless of experimental condition. Raising temperature from 20 to 80 °C significantly increased G’. The gel structure was strengthened by adding CaCl₂ and G’ increased at 40 °C. The sucrose effect depended on concentration and temperature; at low sucrose concentrations, G’ modulus increased regardless of temperature level, but at high concentrations, it decreased at temperatures >40 °C. In conclusion, nopal and Prosopis chilensis dispersions show weak gel structure regardless of experimental condition. G′ increases as temperature increases, and these dispersions could be suitable for food applications requiring heat tolerance.     

DSC Determination of Glass Transition Temperature on Sea Bass (Dicentrarchus labrax) Muscle: Effect of High-Pressure Processing

Differential scanning calorimetric determination of glass transition temperature in the freeze-concentrated matrix ( T_\textg^\text￠ T_{\text{g}}^{\text{'}} ) of sea bass muscle was optimized. Conventional and modulated differential scanning calorimetry (DSC) techniques (using diverse cooling/heating rate and modulation parameters) and effect of an annealing step (−30, −20, or −15°C, 30min) were assayed. Transition was more evident using conventional DSC assays, cooling/heating rate: 10°C/min, annealing step at –20°C. A T_\textg^\text￠ T_{\text{g}}^{\text{'}} value of –15.2 ± 0.3°C was observed for sea bass fresh muscle. This method was chosen for T_\textg^\text￠ T_{\text{g}}^{\text{'}} determination on high-pressure (HP) treated and pressure shift freezing (PSF)—stored at –20°C—sea bass muscle. Thus, in both cases, transition at –15°C was less evident as a function of the pressure level applied, being very difficult to detect after treatment at 400 and 600MPa. It was observed that T_\textg^\text￠ T_{\text{g}}^{\text{'}} values were shifted to slightly higher temperatures (around 1°C higher) after HP treatment at 400 and 600MPa. The present work constituted a first approach to the study on the effect of HP on the glass transition of a complex food matrix, giving useful information about stability of the frozen food.     

Dynamic rheological measurements on heat-induced myosin gels: An evaluation of the method's suitability for the filamentous gels

Formation of bovine myosin gels (10 mg ml^?1) by heat treatment at pH 6 and an ionic strength of 0.24 M has been monitored by using the Bohlin Rheometer System in the oscillatory mode. Rheological thermograms were determined with a general repeatability of about 2% for a given suspension. A pronounced maximum and an accompanying minimum in storage modulus (G′) were found at about 50 and 55°C, respectively. The thermograms for the loss modulus (G″) and the phase angle (δ) displayed complex behaviour as well, suggesting a multitransition process. Presumably, denaturational events in parts of the molecule are responsible for the complex rheology observed. This complexity is not related to trivial wall slippage as data obtained from cells with different gap sizes were highly reproducible and consistent with other measurements. A decrease in heating rate from 2.5 to 0.1°C min^?1 had a large effect on G′; it increased from 905 to 1600 N m^?2 for gels at 75°C. The phase angle was also affected by the heating rate, especially at about 55°C. The effect of increasing the strain from 0.003 to about 0.1 was significant in two temperature regions; G′ at temperatures higher than 65°C and δ at temperatures lower than 54°C increased with increasing strain.     

Heat-induced gel formation of a protein-rich extract from the microalga Chlorella sorokiniana

Microalgae proteins are an underutilized biomass source for foods with unknown technofunctionalities. Heat-induced gel formation was used in this study to investigate the gelation properties of a protein-rich extract from the microalga Chlorella sorokiniana. Gel formation was achieved at a minimum protein concentration of 9.9 g/100 mL and a temperature of 61 °C was necessary to produce a stable gel network. Small-amplitude oscillatory shear measurements revealed that a weak gel was formed with tan δ > 0.1, which was also evident during backward extrusion measurements. The elasticity of the gels increased when the final T_set was increased and a maximum gel elasticity was obtained at T_set = 80 °C and a heating rate of 1 °C min⁻¹. Increasing the heating rate to 5 and 15 °C min⁻¹ negatively affected the gel strength. Additionally, increasing the ionic-strength and increasing or decreasing the pH negatively affected the gel network, which was related to a change in electrostatic interactions. The results obtained showed that it is possible to produce protein gels from water-soluble protein-rich extracts from Chlorella sorokiniana, which may simplify application of protein extracts from this microalga in foods.     

Thermal gelation of globulin from Phaseolus angularis (red bean)

The heat-induced gelation properties of red bean globulin (RBG) were studied under the influence of salts and several protein structure perturbants. The viscoelastic properties of the gels were evaluated by small amplitude oscillatory tests and creep experiments. Gel structure developed progressively when a protein dispersion (≈10% w/v) was heated from 25 to 95 °C, and both the storage modulus (G′) and loss modulus (G″) increased rapidly during cooling. The addition of NaCl at lower concentrations led to increases in G′ and G″ values, with decreased creep compliance, suggesting higher viscoelasticity. At higher salt concentrations, viscoelasticity was decreased, and the optimum NaCl concentration to produce maximum gel rigidity was 0.2 M. Sodium dodecyl sulfate and urea caused more pronounced reduction of the gel moduli than dithiothreitol and N-ethylmaleimide. The data suggest that hydrophobic interactions and hydrogen bonding play an important role in heat-induced gelation, while electrostatic interactions and a balance of attractive–repulsive forces are also important. The gels formed at 95 °C exhibited a homogenous microstructure with extensive cross-links and sheet-like network structures.     

Whey protein concentrate/λ-carrageenan systems: Effect of processing parameters on the dynamics of gelation and gel properties

The thermal characteristics, dynamics of gelation and gel properties of commercial whey protein concentrate (WPC), WPC/λ-carrageenan (λ-C) mixtures (M) and WPC/λ-C spray-dried mixtures (DM) have been characterized. In a second stage, the effect of the gelling variables (T, pH, total solid content) on gelation and textural properties of DM was evaluated through a Doehlert uniform shell design.The presence of λ-C either in mixtures (M) or in DM promoted the WPC gelation at lower concentration (8%). M showed higher rates of formation and better gel properties (higher hardness, adhesiveness, springiness and cohesiveness) than DM.Nevertheless, when the effects of pH (6.0–7.0), heating temperature (75–90 °C) and total solid content (12–20 wt%) on gelation dynamics and gel properties of DM were studied, gels with a wide range of rheological and textural properties were obtained. While pH did not affect the gelation dynamics, it had some effect on rheological and textural properties. Total solid content and heating temperature were the most important variables for the dynamics of gelation (gelation rate (1/t_gel), gelation temperature (T_gel), rate constant of gel structure development (k_G), elastic modulus after cooling (G′_c) and textural parameters (hardness, springiness and cohesiveness).     

A NEW TECHNIQUE FOR EVALUATING FLUID-TO-PARTICLE HEAT TRANSFER COEFFICIENTS UNDER TUBE-FLOW CONDITIONS INVOLVING PARTICLE OSCILLATORY MOTION

One of the critical parameters for the modelling of particle temperature profiles in continuous processing of particulate foods in a carrier liquid is the fluid-to-particle heat transfer coefficient between the fluid and the particles (h_fp). A laboratory scale apparatus was fabricated to evaluate h_fp under conditions imparting particle oscillatory motion while being heated in a model holding tube. Spherical particles (d = 12.7 × 10^?3m) with centrally located fine-wire flexible thermocouples (d = 7.62 × 10^?5 m) were suspended from the upper mid-section of a curved glass tube (ID = 50.8 × 10^?3 m) to provide lateral movement of the particle as the tube was subjected to an oscillatory motion. A variable speed reversible motor, in conjunction with an electronic circuit board, was used to control the frequency and amplitude of the tube thereby keeping the particle in continuous motion. Time-temperature data were gathered continuously from the time the particle-mounted oscillatory unit, set at room temperature for the desired amplitude and frequency, was transferred to a heated sucrose solution (0, 30 and 50% w/w) at 70 or 90C. The h_fp values were calculated from the evaluated heat rate index, f_h, at three particle velocities (0.09, 0.16 and 0.26 m/s) under three oscillatory amplitudes (90, 180 and 270°). The h_fp values increased with amplitude of oscillation and particle velocity, and decreased with the sucrose concentration. The h_fp values associated with the fixed particles were higher than those for particles which were free to move.     

High-pressure homogenisation of raw bovine milk. Effects on fat globule size distribution and microbial inactivation

Whole raw milk was processed using a 15 L h⁻¹ homogeniser with a high-pressure (HP) valve immediately followed by a cooling heat exchanger. The influence of homogenisation pressure (100–300 MPa) and milk inlet temperature T_in (4°C, 14°C or 24°C) on milk temperature T₂ at the HP valve outlet, on fat globule size distribution and on the reduction of the endogenous flora were investigated. The T_in values of 4–24°C led to milk temperatures of 14–33°C before the HP valve, mainly because of compression heating. High T_in and/or homogenisation pressure decreased the fat globule size. At 200 MPa, the d_4.3 diameter of fat globules decreased from 3.8±0.2 (control milk) to 0.80±0.08 μm, 0.65±0.10 or 0.37±0.07 μm at T_in=4, 14°C or 24°C, respectively. A second homogenisation pass at 200 MPa (T_in=4°C, 14°C or 24°C) further decreased d_4.3 diameters to about 0.2 μm and narrowed the size distribution. At all T_in tested, an homogenisation pressure of 300 MPa induced clusters of fat globules, easily dissociated with SDS, and probably formed by sharing protein constituents adsorbed at the fat globule surface. The total endogenous flora of raw milk was reduced by more than 1 log cycle, provided homogenisation pressure was ⩾200 MPa at T_in=24°C (T₂∼60°C), 250 MPa at T_in=14°C (T₂∼62°C), or 300 MPa at T_in=4°C (T₂∼65°C). At all T_in tested, a second pass through the HP valve (200 MPa) doubled the inactivation ratio of the total flora. Microbial patterns of raw milk were also affected; Gram-negative bacteria were less resistant than Gram-positive bacteria.     

Formation of starch spherulites: Role of amylose content and thermal events

Commercial maize starches and potato starches of two cultivars differing in physicochemical composition (granule size distribution; amylose to amylopectin ratio) and crystallinity were heated to 180 °C and then cooled by fast quench using a differential scanning calorimeter (DSC), in order to produce spherulitic starch morphologies. Among the raw maize starches, waxy maize starch had highest relative crystallinity (49%) whereas a lowest crystallinity of 33–39% was calculated for high-amylose maize starches. Potato starches showed a relative crystallinity of 50%. The temperatures and enthalpies of gelatinisation and melting varied among all the starches. High-amylose maize starches showed higher transition temperatures of gelatinisation (T_gel), whereas waxy maize starch had lowest T_gel and enthalpy of gelatinisation (ΔH_gel). Similarly, a considerable variation in parameters related with crystalline melting (T_m1, T_m2 and ΔH_m1, ΔH_m2) was observed for different starches. The superheated gels of different starches treated using DSC were subjected to polarised microscopy, to confirm the formation of spherulites. Both the high-amylose starch gels showed the presence of spherulites exhibiting birefringence and a weak crystalline pattern. No birefringence was observed for waxy maize starch gel, while potato starch gels had some birefringence. The particle size distribution of high-amylose maize starch gels analysed through Zetasizer showed the sizes of spherulitic particles fall in the range of 300 nm–900 nm. The scanning electron micrographs of the dried high-amylose maize starch gels showed the presence of round spherulites consisting of several aggregated spherulitic particles. Amylose content and melting of crystallites during heating play an important role during recrystallisation of amylose (spherulite morphologies).     

Mobility and redistribution of waters within bighead carp (Aristichthys nobilis) heat-induced myosin gels

Water-holding capacity is closely related to gel microstructure, and is a very important quality trait in surimi and surimi product. The changes in the secondary structure, gel microstructure, and the migration of water in bighead carp (Aristichthys nobilis) myosin gel induced by different temperatures (50–90°C) were investigated. The α-helical structure of myosin decreased at temperatures of 40°C or higher. The fractal dimension of the gels increased at 40, 50, and 60°C, but decreased at temperatures over 60°C. The pore size of the gels increased with temperatures up to 50°C, decreased at 60°C, and then increased with temperatures up to 90°C again. The transverse relaxation times also varied; T₂₁ remained constant at temperatures over 40°C; T₂₂ decreased at temperatures lower than 50°C, increased at 60°C, and then decreased with temperatures up to 90°C; and T₂₃ increased at temperatures lower than 50°C and then remained constant until 90°C. Principal component analysis showed that the proportion of T₂₂ water (PT₂₂) was inversely correlated with the unfolding of myosin, whereas directly correlated with the pore size. The proportion of T₂₃ water (PT₂₃) was positively correlated with the fractal dimensions of the gels, whereas negatively correlated with the pore size. The migration of the secondary layer of water was mainly caused by hydrophobic force and the physical space formed by the myosin backbone, and the migration of water within the third layer was mainly caused by capillary pressure. Therefore, the mobility and redistribution of waters depend on the water retention mechanism, which is determined by the physical structure of gels. This study provides further information about the relationship between the NMR data, gel microstructure, water mobility, and distribution.     

The effect of pH and calcium ion on rheological behaviour of β‐lactoglobulin‐basil seed gum mixed gels

Effect of pH (4.5–7.5) and Ca²⁺ (0.01–0.5 m ) on gelation of single and mixed systems of 10% β‐lactoglobulin (BLG) and 1% basil seed gum (BSG) was investigated. The gelling point of BLG and BSG gels was strongly pH‐dependent, and stiffer gels formed at higher pH. The BLG gels were formed upon heating to 90 °C and reinforced on cooling to 20 °C; however, the gelation of BSG occurred at temperatures below 70 °C. By increasing Ca²⁺ concentration, storage modulus of BLG and BSG gels were increased, although pH had a greater effect than Ca²⁺. In contrast, mixed systems showed two distinct types of behaviour: BLG gel formation and BSG network, suggesting that phase‐separated gels were formed. In addition, higher strength was obtained for BLG‐BSG mixture at higher Ca²⁺ concentration.     

Synergistic interaction of <Emphasis Type="Italic">Auricularia auricula</Emphasis>-<Emphasis Type="Italic">judae</Emphasis> polysaccharide with yam starch: effects on physicochemical properties and in vitro starch digestibility

Thermal stable polysaccharides from Auricularia auricula-judae (AP) have unique molecularstructures and multiple bioactivities. The effects of AP on the physicochemical properties and in vitro starch digestibility of yam starch (YS) were studied. The addition of AP induced a significant increase in the swelling power, solubility, mean volume diameter and adhesiveness as well as a dramatic decrease in the hardness and gumminess (p?<?0.05). AP showed a strong suppressive effect on in vitro starch digestibility. Higher modulus (G′, G″) and stiffness parameters (A_α), and lower order of relaxation function (α), were observed in oscillatory rheological measurements, indicating that the gels were more elastic-like and had higher pseudoplasticity in the presence of AP. Furthermore, AP remarkably decreased the syneresis and storage modulus (G′), and also retarded the retrogradation process of YS gel at 4°C, revealing a synergistic interaction between AP and YS, which could also be demonstrated by scanning electron microscopy.     

Effect of cross‐linking on some properties of potato (Solanum tuberosum L.) starches

Starches separated from different potato cultivars were modified using two different cross‐linking agents: epichlorohydrin (EPI) and phosphoryl chloride (POCl₃) at different concentrations (1.0 and 2.0 g kg^?1 POCl₃; 2.5, 5.0 and 10 g kg^?1 EPI). Differential scanning calorimetry, rheological and retrogradation measurements were performed to characterise the influence of cross‐linking on the properties of potato starches. Cross‐linking considerably reduced swelling power, solubility, water‐binding capacity and paste clarity. The decrease became greater as the reagent concentration increased. The starches treated with 1.0 g kg^?1 POCl₃ exhibited exceptionally higher swelling power than their counterpart native starches. Neither cross‐linking agent caused any change in morphology of the starch granules. Studies on the phase transitions associated with the gelatinisation showed significantly higher values for the onset temperature (T_o), peak temperature (T_p), conclusion temperature (T_c) and enthalpy of gelatinisation (ΔH_gel) for the cross‐linked starches than the native starches. Starches treated with both the reagents showed lower peak storage modulus (G′) and loss modulus (G″) than their native counterparts. The tendency of the starch pastes towards retrogradation increased considerably with increases in storage duration. However, the starches treated with 1 g kg^?1 POCl₃ exhibited much lower syneresis than the other cross‐linked starches. Copyright © 2006 Society of Chemical Industry     

Physicochemical characteristics and gelation properties of collagen superfine powder from swine skin: the effects of preheating treatment

Following different preheating treatments (60 °C for 20 min; 80 °C for 20 min; or 120 °C for 10 min, referred as T₁, T₂ and T₃), edible collagen superfine powder (CSP) from swine skin was prepared by superfine grinding method. The CSPs showed a preheating‐dependent decrease in the D₅₀, with different degrees of hydrolysis (9.51–31.05%). A significant effect of preheating on rheological properties of the CSP aqueous dispersions at pH 4–9 was observed, wherein T₂ had the biggest viscosity and water holding capacity. All the 5% CSP dispersions were transformed into stable cold‐set gels after heating at 50–90 °C for 20 min, with insignificant differences in strength. These attributes were consistent with microstructures of the CSP gels detected by scanning electron microscope.     

Gelation behaviour and rheological properties of acid-induced soy protein-stabilized emulsion gels

The protein concentration dependence on the rheological properties of acid-induced gels formed with unheated and heated soy protein-stabilized emulsions (UHSPE and HSPE) was investigated at different acidification temperatures. Pre-heat treatment on soy protein solutions resulted in a higher storage modulus (G′) and a shorter gelation time (t_gel) of acid-induced emulsion gels. A maximum in tan δ was observed in the UHSPE gels but no maximum was detected in the HSPE gels. Increasing the acidification temperature decreased the G′ and t_gel. The dependence of the G′ on the protein concentration (c) can be scaled with a power law: G′ ∼ c^A. The exponent (A) increased with pre-heat treatment and acidification temperature. The experimental data.fitted the fractal scaling model (G′ ∼ φ^A) and the simple time- scaling model above very well for the acid-induced soy protein-stabilized HSPE gels with varying oil volume fraction. The large deformation and fracture properties were significantly affected by soy protein concentration, pre-heat treatment, acidification temperature and volume fraction of oil droplets (p < 0.05).     

Measurement of dynamic rheology during cooling of honey-invert sugar mixtures by small-deformation oscillatory rheometry

Dynamic rheological properties of honeys in the presence of invert sugar at different levels (0, 10, 20, 30, and 40%) were evaluated by small-deformation oscillatory measurements of dynamic moduli (G′ and G″) during cooling from 0 to ?14°C. The storage modulus (G′) and loss modulus (G″) thermograms of honey during cooling showed more pronounced G″ values when compared to G’, indicating that the presence of invert sugar in honey reduced G″. Such a reduction in G″ can be taken as a good indicator for the adulteration of honey with invert sugar. Therefore, dynamic rheometry for small-deformation oscillatory measurement in the cooling process at sub-zero temperatures appears to be a useful method for detecting the effect of invert sugar adulteration on the structural properties of honey.     

Physicochemical,morphological, and thermal properties of starches separated from bulbs of four Chinese lily cultivars

The starches separated from bulbs of four different lily cultivars (Lanzhou, Pinglu, Yixing‐1, and Yixing‐2) were investigated for physicochemical, morphological, crystalline, and thermal properties. AM content of lily bulbs starches from different cultivars ranged from 19.46 to 25.17%. The swelling power of starches ranged between 14.4 and 21.3 g/g, and the solubility ranged from 8.92 and 16.6% at the temperature of 85°C. Four cultivars of lily starches paste had excellent transparency and the transmittance value of Lanzhou lily as high as 54.7%. The transmittance of the gelatinized aqueous starch suspensions, from all lily cultivars, decreased with increase in storage period. The shape of starch granules varied from triangular to cylindrical and XRD of four lily starches all showed B‐type pattern. The transition temperatures and enthalpy of gelatinization (ΔH_gel) were determined using DSC. T_p varied from 62.52 to 65.25°C. Pinglu lily starch showed the highest ΔH_gel and gelatinization range (T_c–T_o) index among starches from four different lily cultivars.