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     

Effect of γ‐radiation and microwave heating of wheat grain on some starch properties in irradiated grain as well as in grain of the next generation crops

Grains of the Polish winter wheat variety Begra were subjected to γ‐radiation (grain harvested in 1996) within the dose range of 0.05–10 kGy and microwave heating (grain harvested in 1997) from 28°C to 98°C. Later the grains were divided into two parts, the first was used for direct analyses after treatment. The second part was sown on the experimental fields. The obtained crop was described as the first generation and divided into two parts. One part was destined to determination of starch properties and the second part was sown in order to obtain the second generation crop. The same pattern was conducted in order to achieve the third generation crop. γ‐Irradiation directly applied on the wheat grain reduced statistically significant falling number values and gelatinisation enthalpy (ΔH) of the grain treated by 5 and 10 kGy. Calculated linear regression correlation coefficient between the falling number values and the gelatinisation enthalpy was equal to 0.94 (p ? 0.001) and showed that these two starch characteristics are well correlated in the case of directly irradiated wheat grain. The falling number values, peak temperatures (T_p) and gelatinisation enthalpy (ΔH), in three generations of wheat grain crop studied, did not show any statistically significant differences as a result of indirect effect of γ‐irradiation. Microwave direct heating of wheat grain to 98°C caused a statistically significant increase in the falling number value and decrease in starch gelatinisation power expressed by the enthalpy of gelatinisation (ΔH). The statistically significant changes in the falling number values, slight changes in the peak temperatures (T_p) and enthalpy of gelatinisation (ΔH) were found in all three generation crops as an indirect effect of microwave heating.     

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.     

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).     

Gelatinisation properties of native and annealed potato starches

The relationship between the gelatinisation parameters of native and annealed starches extracted from ten different potato varieties grown at the same site at the same time was studied. The objective was to identify how native gelatinisation temperatures and enthalpies impacted on annealed starch gelatinisation parameters. Prior to ANN, the initial onset (T_o), peak (T_p) and conclusion (T_c) gelatinisation temperatures ranged from 58.71 to 62.45, 62.52 to 66.05 and 68.67 to 72.27°C, respectively, which increased to 66.15 to 69.12, 70.22 to 72.30 and 76.21 to 77.44°C, respectively, post ANN. Overall, the greater the initial gelatinisation temperatures the smaller the increment (ΔGT) post ANN. Comparable enthalpy values pre‐ and post‐ANN were 15.13 to 18.37 and 15.76 to 18.37 J/g, respectively. These data indicate that the more ‘perfect’ the crystallites were before ANN the less they could be enhanced by the ANN process and that against a constant background of α‐glucan structure, the pattern (rate) of starch deposition might be the primary differentiator of starch architecture across the varieties.     

Physicochemical,crystalline, and thermal properties of native and enzyme hydrolyzed Pueraria lobata (Willd.) Ohwi and Pueraria thomsonii Benth. starches

Starches isolated from the bulbs of Pueraria lobata (Willd.) Ohwi (PLO) and Pueraria thomsonii Benth. (PTB) were hydrolysed by glucoamylase for different lengths of time (2, 4, 8, 12, and 24 h). The hydrolysis results were compared by scanning electron microscope (SEM), X‐ray power diffractometer (XRD), and differential scanning calorimetry (DSC). The SEM results revealed that both of the PLO and PTB starches showed the same hydrolysis mechanism, which indicated that the glucoamylase primarily attacking the exterior of starch granules and then the interior. The results of XRD revealed the crystalline type of PTB starch changed from C‐type to A‐type with crystallinity reducing from 43.5 to 20.9% during the hydrolysis. Unlike PTB starch, the PLO starch did not show marked changes in crystalline style but lower degree of crystallinity was obtained from 32.4 to 13.7% during the hydrolysis. All the XRD results demonstrated that B‐type polymorph was preferentially degraded than A‐type polymorph in the C‐type starch. The DSC results revealed that both of the PLO and PTB starches showed decreased enthalpy of gelatinization (ΔH_gel) and gelatinization temperature range (R)‐value after hydrolysis, while the gelatinization temperature (T_p) indicated different tendency, initially ranging from 68.6 to 64.3°C and then increasing to 67.8°C for PLO starch. While for PTB starch, the T_p‐value showed progressive reduction from 85.4 to 74.3°C during the whole process.     

Effect of microwave vacuum drying and hot air drying on the physicochemical properties of durian flour

Unripe durian cv. Monthong was subjected to microwave vacuum drying (MVD) at 1200, 1600 and 2200 W and hot air drying (HAD) at 40, 50 and 60 °C to produce durian flour. Drying rate of MVD and HAD was 0.34–0.58 kg water kg dry solid^?1 min^?1 and 0.02–0.06 kg water kg dry solid^?1 min^?1, respectively. An increase in drying rate by either increasing hot air temperature or increasing microwave power decreased the degree of crystallinity from 21.95% to 2.31% and from 7.72% to 4.05%, respectively. Moreover, the increased drying rate caused a decrease in endothermic enthalpy (ΔH_gel) and pasting properties. Starch content of the durian flour was 41.40–47.03%. The starch granule morphology of durian flour was disrupted which indicated gelatinisation of flour during drying. Due to a short drying process, the MVD flour had less a*‐value (P ≤ 0.05) than the HAD flour.     

A comparison between the properties of seed,starch, flour and protein separated from chemically hardened and normal kidney beans

The physicochemical, functional and thermal properties of starch, flour and protein isolates obtained from chemically hardened kidney beans were evaluated. A rapid chemical hardening procedure (soaking in acetate buffer, pH = 4.0, 37 °C, 6 h) was used to produce hardened kidney beans. Chemical hardening altered physicochemical, cooking, hydrating and textural properties of beans to a significant level (P < 0.05). Soaked and cooked chemically hardened beans had a higher value for different textural parameters than their normal counterparts. Chemical hardening increased cooking time (from 49 to 123 min) of beans and decreased swelling power and solubility of starch. The turbidity value of gelatinized starch suspensions from chemically hardened beans was significantly lower than that from normal beans. Chemical hardening of beans caused significant increase in transition temperatures (T_o, T_p, T_c) and enthalpy of gelatinization (ΔH_gel) of both starch and flour. Chemically hardened bean starch showed significantly higher pasting temperature (94.9 °C) as compared to normal bean starch (83.2 °C). Flour and protein isolate from chemically hardened beans showed significantly lower water absorption, oil absorption, foaming capacity and gelling ability than those from normal beans. The onset temperature (T_m), peak denaturation temperature (T_d) and heat of transition or enthalpy (ΔH) of protein isolate from hardened and normal beans did not differ significantly. Copyright © 2007 Society of Chemical Industry     

Effects of cross‐linking on the rheological and thermal properties of sweet potato starch

Sweet potato starches were modified with three different concentrations of phosphorus oxychloride (POCl₃) (0.01, 0.02, and 0.03%, based on dry weight of starch) as a cross‐linking agent. The effects of crosslinking on rheological and thermal properties of sweet potato starch (SPS) pastes were evaluated. Cross‐linking considerably reduced the swelling power, consistency index (K), apparent viscosity (η_a), and yield stress (σ_oc) values of SPS, which significantly decreased with increase in POCl₃ concentration. The gelatinization temperature (T_p) and enthalpy (ΔH) values of the cross‐linked SPS, which were determined using differential scanning calorimetry, were higher than those of native SPS. Storage modulus (G′), loss modulus (G″), and complex viscosity (η*) of the cross‐linked SPS pastes determined using small deformation oscillatory rheometry, were higher than native starch, and they also decreased with increase in POCl₃ concentration from 0.01 to 0.03%. The tan δ (ratio of G″/G′) values (0.15–0.19) of the cross‐linked SPS samples were much lower than that (0.37) of the native SPS, indicating that the elastic properties of the SPS pastes were strongly influenced by modifications from cross‐linking. Finally, Cox–Merz plots showed that η* was much higher than η_a for the cross‐linked SPS pastes.     

Studies on the morphological,thermal and rheological properties of starch separated from some Indian potato cultivars

The starches separated from five different Indian potato cultivars (Kufri Chandermukhi, Kufri Badshah, Kufri Jyoti, Kufri Sindhuri and S1) were investigated for morphological, thermal, rheological, turbidity and water-binding properties. The starch separated from all the five potato cultivars had a granule size ranging between 15–20 μm and 20–45 μm. The shape of starch granules varied from oval to irregular or cuboidal. Starch isolated from cv. Kufri Badshah had largest irregular or cubiodal granules while starch from cv. Kufri Chandermukhi had small and oval granules. The transition temperatures and enthalpy of gelatinization (ΔH_gel) were determined using differential scanning calorimetry (DSC). The enthalpy of retrogradation (ΔH_ret) of gelatinized starch was also determined after 14 days of storage at 4°C using DSC. Kufri Chandermukhi starch showed the lowest ΔH_gel and ΔH_ret while Kufri Badshah starch showed the highest values. ΔH_gel and ΔH_ret values of 12.55 J/g and 6.42J/g, respectively, for Kufri Chandermukhi starch against 13.85 J/g and 8.61 J/g, respectively, for Kufri Bhadshah starch were observed. Rheological properties of starches from different potato cultivars, measured using the Dynamic Rheometer during heating and cooling, also differed significantly. The starch from cv. Kufri Badshah showed the highest peak G′ and G″ and lowest tan δ. The starches having higher peak G′(G′ at gelatinization temperature) showed higher breakdown in G′ and vice versa. The turbidity of gelatinized aqueous starch suspensions from all potato cultivars increased with increase in storage period. Starches with low water binding capacity had higher G′ and G″ and lower tan δ values.     

Functional and tableting properties of acetylated and oxidised finger millet (Eleusine coracana) starch

The functional and tableting properties of native (NaFM) and chemically modified (by acetylation, AcFM; and oxidation, OxFM) finger millet starches were investigated. The tablet formation properties of the starches were assessed by Heckel and Kawakita analysis. The swelling power and solubility of the starch increased with increase in temperature with AcFM having the highest swelling power, while OxFM had the highest solubility. X‐ray diffractometry showed that the starches had the characteristic ‘A’ pattern with strong peaks at 3.78, 4.37, 4.87, and 5.17 Å. Chemical modification causes rupture of some starch granules as revealed by the Scanning Electron Micrograph. Chemical modification also leads to improved gelatinisation profile, with reduction in ΔH_gel from 9.64 J/g (NaFM) to 3.88 J/g (AcFM) and 8.76 J/g (OxFM). The bulk density and Hausner's ratio increased after chemical modification of the starch. Chemical modification reduced the mean yield pressure, P_y (Heckel analysis) but increased the deformability P_k (Kawakita analysis) of the starch compacts. Chemical modification also increased the crushing and tensile strength of the starch compacts, but lowered its disintegration time and friability.     

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.     

Comparison of the physicochemical and functional properties of Aconitum carmichaeli and Aconiti lateralis Preparata starches

Aconitum, an important toxic traditional Chinese medicine, has been widely used in clinical practice. Owing to its toxicity, it should be processed before application. Aconiti lateralis Preparata (ALP) is one of the most important commercial processed products of Aconitum. The object of this work is to study the physicochemical and functional properties of Aconitum and ALP starches. The results revealed that AM content changed, transforming from 37.5 to 27.5% after processing. The shape of Aconitum starch granules also changed from spherical or oval with sizes of 5–15 µm to irregular and polygonal with sizes of 30–60 µm. The crystallinity of Aconitum decreased from 38.7 to 23.0% after processing. The transition temperatures (T_o, T_p and T_c) and enthalpy of gelatinization (ΔH_gel) were determined using DSC. T_o, T_p and T_c decreased from 52.9 to 48.6, 66.9 to 58.9, and 82.2 to 69.3°C, respectively. Aconitum starch showed higher ΔH_gel values (1.6 J/g), while the ALP starch showed lower values (0.4 J/g).     

Changes in flour gelatinisation of trifoliate yam (Dioscorea dumetorum) tubers after harvest

BACKGROUND: Changes in the properties of starch during postharvest hardening of trifoliate yam (Dioscorea dumetorum) tubers need to be investigated. In this work the starch gelatinisation kinetics of D. dumetorum cv. Yellow stored under prevailing tropical ambient conditions (0.98–2.32 kg vapour per 100 m³ airflow) for 0, 2, 7, 14, 21 and 28 days was studied using a 3 × 5 factorial experiment with three cooking temperature (75, 85 and 95 °C) and five cooking times (0, 5, 10, 20 and 40 min). Samples were also evaluated for starch properties and gelatinisation temperature. RESULTS: Storage of D. dumetorum tubers caused starch damage. However, the starch gelatinisation temperature was between 70 and 75 °C irrespective of the tuber storage duration. The starch gelatinisation reaction followed first‐order kinetics defined by the relationship ln(1 ? α) = ? k_Gt. The gelatinisation rate was significantly influenced (P≤0.05) by cooking temperature and increased with tuber storage duration. The activation energy also increased with tuber storage duration. CONCLUSION: Although the gelatinisation temperature of D. dumetorum starch was not influenced by tuber storage, the starch gelatinisation process was affected by tuber storage duration, since tuber storage involved a greater need of energy for starch gelatinisation, which may be an effect of the postharvest hardening phenomenon. Copyright © 2008 Society of Chemical Industry     

Genetic diversity in the physicochemical properties of waxy rice (Oryza sativa L) starch

The genetic diversity in the physicochemical properties of starches from 56 waxy rice (Oryza sativa L) genotypes (34 of indica and 22 of japonica) was studied. The parameters included thermal and retrogradation properties tested by differential scanning calorimetry (DSC), pasting viscosity tested by rapid viscoanalyser (RVA), and flour swelling volume (FSV). Wide diversity was found in all the parameters. According to their gelatinisation temperature (GT), the waxy rice genotypes could be divided into two groups, a high‐GT group and a low‐GT group. A total of 15 genotypes were identified as high‐GT, all belonging to the indica subspecies. There was about a 5 °C difference within each group and a 10 °C difference between groups. Many parameters were correlated with each other in all 56 waxy rices, but some correlations were also consistent and significant when comparing the high‐GT group and the low‐GT group separately. For example, hot paste viscosity (HPV) was positively correlated with onset temperature (T_o) and enthalpy of gelatinisation (ΔH_g). The results suggested that initial screening in waxy rice breeding programmes for varieties with desirable starch properties for specific food uses could be efficiently accomplished using pasting profiles from the RVA. Copyright © 2004 Society of Chemical Industry     

Chemical and Physical Characterisation of Grain Tef [Eragrostis tef (Zucc.) Trotter] Starch Granule Composition

Chemical and physical properties of starch granules isolated from five grain tef (Eragrostis tef) varieties were characterised and compared with those of maize starch. Endogenous starch lipids extracted with hot water‐saturated n‐butanol and total starch lipids extracted with n‐hexane after HCl hydrolysis were 7.8 mg/g (mean) and 8.9 mg/g (mean), respectively, slightly lower than in the maize starch granules. The starch phosphorus content (0.65 mg/g) was higher than that of maize starch but virtually the same as reported for rice starch. The starch granule‐swelling factor was lower than that of maize starch and extent of amylose leaching was higher. The starch X‐ray diffraction pattern was characteristic of A type starch with a mean crystallinity of 37%, apparently lower than the crystallinity of maize starch and more similar to that reported for rice and sorghum starches. The starch DSC gelatinisation temperature was high, like for other tropical cereals; T_o, T_p, T_c and ΔH were in the range 63.8—65.4, 70.2—71.3, 81.3—81.5 °C and 2.28—7.22 J/g, respectively. The lower swelling, apparently lower percentage crystallinity and lower DSC gelatinisation endotherms than maize starch suggest that the proportion of long amylopectin A chains in tef starch is smaller than in maize starch.     

Comparison of starches separated from different Dioscorea bulbifera Linn. cultivars

The physico‐chemical, morphological, thermal, and crystal properties of the starches separated from three different rhizomes of Dioscorea bulbifera Linn. (D.BLH, Hubei; D.BLG1, Guangxitianlin; D.BLG2, Guangxiyulin) were studied and compared. A light microscopic technique was applied in order to quantify the integrity and shape of the starch granules after isolation. Amylose contents of different cultivars were in the range of 12.18–14.34%. Moisture content, ash content, swelling power, solubility, water‐binding capacity, and protein content of starches also differed significantly. The three different D. bulbifera starches all showed a typical C‐type pattern with crystallinity 45.36, 27.10, and 53.04%, corresponding to D.BLH, D.BLG1, and D.BLG2, respectively. The starch separated from the three starches above showed gelatinization range of 10.09, 11.55, and 7.26°C, corresponding to D.BLH, D.BLG1, and D.BLG2. The enthalpy of gelatinization (ΔH_gel) ranged from 1.28 to 3.11 J/g. Correlation analysis displayed that amylose content and relative crystallinity values were important in determining thermal starches.     

Physicochemical and structural characteristics of cross‐linked banana starch using three cross‐linking reagents

Banana starch was cross‐linked using different cross‐linking reagents, phosphoryl chloride (POCl₃), sodium trimetaphosphate (STMP), and epichlorohydrin (ECH), under alkaline conditions. The reaction conditions were selected to produce similar pasting profiles. The effects of the different cross‐linking reagents on the physicochemical and structural characteristics of cross‐linked starches were evaluated. The microscopy study did not show difference on the surface of the granules. Slight decrease in the peak temperature and enthalpy were found in the cross‐linked banana starch. The chemical groups introduced in the starch molecules by the diverse reagents promoted the re‐association of starch chains during storage. The rheological analysis of all starch dispersion at 10% (flow curves) showed a non‐Newtonian shear‐thinning; pastes obtained were time‐independent, suggesting an important contribution of the continuous phase. Structural study showed that the cross‐linked STMP‐starch had the lowest level of amylose and the ratio short/long amylopectin chains. The three reagents used for cross‐linking presented different action mode on starch granule and its components.     

Characterisation of starches separated from sorghum cultivars grown in India

Starches from 15 Indian sorghum cultivars were separated and evaluated for physicochemical, morphological, thermal, retrogradation, pasting and textural properties. The morphological characterisation revealed the presence of irregular-polyhedral as well as spherical shaped granules. A wide variation in amylose content ranging from 11.2% to 28.5% was observed. Thermal, retrogradation, pasting and textural characteristics also showed significant differences amongst all the starch cultivars. Principal component analysis was carried out to extract five principal components that could explain 75% of the total variance. The first two principal components PC1 (T_o, T_p, T_c and ΔH_gel) and PC2 (amylose content, range of gelatinisation, PHI and pasting and textural properties) could explain a cumulative variance of 44%, indicating the importance of amylose, thermal and textural properties on the sorghum starch functionality.     

Physicochemical,Thermal, Morphological and Pasting Properties of Starches from some Indian Black Gram (Phaseolus mungo L.) Cultivars

The starches separated from thirteen different black gram cultivars were investigated for physicochemical, thermal, morphological and pasting properties. Amylose content, swelling power, solubility and water binding capacity of starches ranged between 30.2–34.6%, 16.0–22.3 g/g, 14.8–17.3% and 73.5–84.5%, respectively. The diameter of starch granules, measured using a laser‐light scattering particle‐size analyzer, varied from 12.8 to 14.3 μm in all black gram starches. The shape of starch granules varied from oval to elliptical. The transition temperatures (T_o, T_p and T_c) and enthalpy of gelatinization (ΔH_gel) determined using differential scanning calorimetry, ranged between 66.1–71.3, 71.0–76.2, 75.9–80.4°C and 6.7–9.4 J/g, respectively. Pasting properties of starches measured using the Rapid Visco Analyser (RVA) also differed significantly. Pasting temperature, peak viscosity, trough, breakdown, final viscosity and setback were between 75.8–80.3°C, 422–514, 180–311, 134–212, 400–439 and 102–151 Rapid Visco Units (RVU), respectively. Turbidity values of gelatinized starch pastes increased during refrigerated storage. The relationships between different properties were also determined using Pearson correlation coefficients. Amylose content showed a positive correlation with swelling power, turbidity and granule diameter. Swelling power showed a negative correlation with solubility and setback. T_o, T_p and T_c showed positive correlation with turbidity, pasting temperature and were negatively correlated to peak and breakdown viscosity.