Influence of acetylation on physicochemical, functional and thermal properties of potato and cassava starches

Starches were isolated from cassava (Manihot esculenta) and potato (Solanum tuberosum) tubers. They were further modified by acetylation. The physicochemical, functional and thermal properties of native and modified starches, prepared using acetic anhydride at different times (10 and 20 min) were compared. Potato starch (Sipiera/20) showed higher acetyl percentage and degree of substitution values than cassava (2425/20) starch when acetylated for 20 min. Proximate analysis revealed that the acetylated starches retained more moisture than the native ones. Above 75 °C, acetylation improved the water binding capacity of the native cassava starch; the same trend was observed for potato starch from 60 to 90 °C after acetylation. The X-ray powder diffraction patterns derived from acetylated potato starches were similar to its native form, which was expected as B-type pattern; the same trend was observed for modified cassava starch. However the modified starches showed increased crystalline index.     

Effect of low and high acetylation degree in the morphological, physicochemical and structural characteristics of barley starch

Barley starch was acetylated at two levels (low degree: LD (0.9), and high degree: HD (2.7)) substitution and the morphological, physicochemical and structural of the resultant acetylated barley starch were determined. The acetylated barley starches presented the signal at 1226 cm⁻¹ that corresponds to the C-O stretching of acetyl groups. The morphological study showed fusion of starch granules in the acetylated starch with HD. This effect was evident in the pasting test, because the viscoamylograph profile of HD starch showed the absence in peak viscosity, viscosity breakdown and viscosity setback. The peak gelatinization was similar for native and LD and decrease in the HD acetylated starch. The gelatinization enthalpy value showed difference among the samples, indicating that the loss of the ordered double helices more than the crystallinity loss was higher in the HD acetylated barley starch. In the retrogradation test, acetylation affected both retrogradation and enthalpy value, because acetylated barley starch with HD substitution at three storage days had 3.2 j/g and with LD 4.8 j/g. The molecular weight and z-average radius of gyration values decreased due to the acetylation process, indicating depolymerization of starch components as it was evidenced by the increase in short chains level in the acetylated samples.     

Functional properties and retrogradation behaviour of native and chemically modified starch of mucuna bean (Mucuna pruriens)

Mucuna bean (Mucuna pruriens) starch was isolated and subjected to chemical modification by oxidation and acetylation. The proximate analysis of the non‐starch components of the native starch on a dry weight basis was 92 g kg^?1 moisture, 5 g kg^?1 ash, 2 g kg^?1 fat, 7 g kg^?1 crude fibre and 19 g kg^?1 protein. Chemical modification reduced the values for all the non‐starch components except the moisture level. For all the samples, swelling power and solubility increased as the temperature increased in the range 50–90 °C. The swelling power of mucuna native starch (MNS) and mucuna acetylated starch (MAS) increased with increasing acidity and alkalinity, while that of mucuna oxidised starch (MOS) only increased with increasing pH in the acidic range. The maximal solubility of all the starches was observed at pH 12. All the starch samples absorbed more oil than water. The lowest gelation concentration followed the trend MAS < MNS < MOS. Chemical modification reduced the gelatinisation temperature (Tp), while peak viscosity (Pv), hot paste viscosity (Hv) and cold paste viscosity (Cv) decreased after oxidation but increased following acetylation. The setback tendency of the native starch was reduced significantly after chemical modification. However, the breakdown value of MNS, 65 BU (Brabender units), was lower than that of MOS (78 BU) but higher than that of MAS (40 BU). Differential scanning calorimetry studies of gelatinisation and retrogradation revealed that chemical modification reduced the onset temperature (T_o), peak temperature (T_p) and conclusion temperature (T_c). Oxidation and acetylation reduced the gelatinisation and retrogradation enthalpies of the native starch. The enthalpy of retrogradation of the starches increased as the length of storage increased. Copyright © 2003 Society of Chemical Industry     

Myrosma cannifolia,chemical composition and physicochemical properties of the extracted starch

Myrosma cannifolia Lf (Maranthaceae) is a tuber‐producing plant which is native to Apure State in Venezuela and is consumed by the Pumé Amerindians of the region. Its chemical composition and physical characteristics were determined. The chemical, physicochemical, morphometric characteristics and rheological properties of starch isolated from Myrosma were studied. The starch yield was 438.6 g kg ⁻¹ (DW). Starch granules were oval, elliptical, irregular and polyhedric, with granules of 9.5–21.25 μm wide and 9.6–19.05 μm long. Scanning electron micrographs revealed the presence of smooth surfaces. The starch showed a characteristic ‘A‐pattern’ of cereal starches by X‐ray diffraction, with zones of high crystallinity. The amylographic study showed a rapid gelatinisation with high stability during heating and cooling cycles. The starch might be a potential ingredient for food products manufactured using different temperatures during processing. © 1999 Society of Chemical Industry     

Effect of Acetylation on Some Properties of Corn and Potato Starches

Corn starch and starches separated from different potato cultivars were acetylated to evaluate the effect of plant source on the physicochemical, morphological, thermal, rheological, textural and retrogradation properties of the starches. Corn starch showed a lower degree of acetylation than potato starches under similar experimental conditions. The degree of acetylation for different potato starches also differed significantly. Morphological examination revealed that the granules of acetylated Kufri Chandermukhi and Kufri Sindhuri starches tended to appear as fused and less smooth than native starch granules. Acetylation of corn and potato starches decreased the transition temperatures and enthalpy of gelatinization and increased swelling power and light transmittance. However, the change in these was greater in the potato starches with higher percentage of small sized granules. Acetylated starches showed higher peak G', G'' and lower tan δ than their counterpart native starches during heating. Among the starches from different cultivars, the change in the rheological parameters after acetylation differed to a significant extent. The retrogradation was observed to be negligible in the acetylated cooked starch pastes. Results implied that the change in functional properties of starches with acetylation depends on source and granule morphology of native starch.     

Influence of prior acid treatment on physicochemical and structural properties of acetylated sorghum starch

Influence of prior acid treatment on acetylation of starch isolated from an Indian sorghum cultivar was investigated. The starch was acid thinned (AT) using 0.1, 0.5, and 1 M HCl for 1.5 h and then acetylated (Ac) with acetic anhydride (8% w/w). The acid thinning and subsequent acetylation appeared to reduce the percentage acetylation as indicated by degree of substitution. Ac‐AT starches exhibited significantly different physicochemical, thermal, pasting, and gel textural properties from those of AT and Ac starches. Starches after dual modification showed higher solubility, lower AM content, gelatinization temperatures, retrogradation, peak viscosity, and gel hardness than native starch. Enthalpy and range of gelatinization were observed to be higher in dual modified starches than native starch. However, no significant changes in granule morphology or crystalline pattern of Ac‐AT starches were observed compared with native starch.     

Morphological,Thermal, Pasting,and Rheological Properties of Barley Starch and Their Blends

Native barley starch, as well as its blends with corn, wheat, and rice starch at different ratios of 75:25, 50:50, 25:75 were examined in terms of morphology, thermal, pasting, rheological, and retrogradation properties. Amylose content varied between 10.9–41.4% in rice, corn, wheat, and barley while it ranged from 18.02–38.40% in blends of barley starch with rice, corn, and wheat. A rapid visco analyzer showed that barley starch and its blends having low amylose content exhibited higher peak viscosity, breakdown, and setback than the high-amylose-containing starches and their blends. Amylose content was found to be negatively correlated with swelling power while it exhibited nonlinear relationship with solubility index. The transmittance of starch suspension stored at 4°C decreased during storage up to 6 days. Barley starch granules were largest (<110 μm) in size followed by wheat (<30 μm), corn (<25μm) and rice (<20μm) starches. Gelatinization temperatures (To, Tp, Tc) and enthalpies of gelatinization (ΔHgel) of starches from different sources also differed significantly. Corn and rice starches showed higher transition temperatures in general than those from wheat and barley; however, they showed higher ΔHgel values. Barley starch showed a higher tendency towards retrogradation than the cereal starches. Barley starch showed highest peak G′, G″ and lower tan Ð than corn, rice and wheat starches during the heating cycle. This study showed that the magnitude of changes in their properties during blending depends on the amylase content and morphological characteristics.     

Effect of Aqueous Ethanol Cationization on Functional Properties of Normal and Waxy Starches

Cationic starch ethers of normal and waxy corn, normal and waxy barley and normal pea starch were prepared by an aqueous alcoholic process for evaluation of their functional properties as compared to the native starch controls. The native starches exhibited a wide range in average granule size (10–21 μm diameter), amylose content (0–34%) and swelling power (13–31). Cationization to degrees of substitution (DS) of 0.030–0.035 with 3-chloro-2-hydroxypropyltrimethylammonium chloride resulted in marked increases in swelling power of all starches, with little corresponding increases in starch solubility. Cationization also decreased the onset of endothermic transitions and pasting temperatures quite substantially, and promoted the development of sharp peak viscosities in the amylographs of all normal and waxy starches, including that of pea starch. Final cold viscosities of the cationic starches exhibited positive setbacks, and the cooked starch gels, after storage for 7 days at 4°C and −15°C, showed no syneresis. All cationic starches except for waxy corn were more susceptible to α-amylase hydrolysis than native control starches. The general improvement in functional properties, especially in the waxy corn, waxy barley and pea starches, due to the aqueous alcoholic-alkaline cationization process would greatly enhance their industrial applications.     

Pasting,Thermal, Hydration,and Functional Properties of Annealed and Heat-Moisture Treated Starch of Sword Bean (Canavalia gladiata)

The effects of annealing (ANN) and heat-moisture treatments (HMT) on the physicochemical and functional properties of Sword bean starches were investigated. The pasting properties differ significantly among the starches, with peak viscosity ranging from 399.17 RVU to 438.33 RVU; however, all the starches exhibited ‘Type C’ class with restricted swelling. The HMT starches had the highest gelatinization temperature, while change in enthalpy of gelatinization, ΔH_gel of the native starch, was higher (13.82 J/g) than that of the modified starches (1.39–6.74 J/g). The solubility and swelling power of all the starches increased as the temperature increased. The oil and water absorption capacity of the starches ranges between 3.24–3.91 g/g and 2.42–3.35 g/g, respectively. HMT (at 25 and 30% moisture level) changes the X-ray diffraction pattern of the starch from Type ‘B’ to Type ‘C’. The Scanning electron micrograph results revealed the starch granules with smooth ellipsoids and indentation in their centre, hydrothermal modification showed little effect on the morphology and size of the granules. Hydrothermal modification improved the physicochemical and functional properties of the starch without destroying the granule of the starch.     

Molecular and physicochemical characterisation of starches from yam,cocoyam, cassava,sweet potato and ginger produced in the Ivory Coast

Granule sizes, macromolecular features and thermal and pasting properties of starches from seven tropical sources (Florido, Kponan and Esculenta yams, cocoyam, cassava, sweet potato and ginger) were compared with those of several well‐known cereal, legume and tuber starches. The aim of the study was to characterise some non‐conventional starches with a view to possibly marketing them. Amylose content varied from 148 mg g^?1 in Esculenta starch to 354 mg g^?1 in smooth pea starch. For total starches, weight‐average molar mass (M?_w) ranged between 0.94 × 10⁸ and 1.80 × 10⁸ g mol^?1 for potato and normal maize starches respectively. Gyration radius (R?_G) varied from 157 nm for ginger starch to 209 nm for normal maize starch. Gelatinisation enthalpy (ΔH) ranged between 9.8 and 20.7 J g^?1 for wheat and Florido starches respectively. Gelatinisation peak temperature (T_g) varied from 58.1 °C for wheat starch to 87.3 °C for ginger starch. Native starch granule mean diameter ranged between 5.1 and 44.5 µm for Esculenta and potato starches respectively. Cassava and potato starches had the highest swelling power and dispersed volume fraction at all treatment temperatures, while ginger starch had the lowest. Cocoyam starch had the highest and ginger starch the lowest solubility at 85 and 95 °C. Cassava starch was the most stable under cold storage conditions. Roots and tubers such as ginger and cassava produced in the Ivory Coast are new sources of starches with very interesting properties. Thus these starches could be isolated on an industrial level in order to market them. Copyright © 2007 Society of Chemical Industry     

Functional and dynamic rheological properties of acetylated starches from two cultivars of cassava

The starches derived from two different cultivars of cassava were modified with acetic anhydride. The increase in swelling power and solubility of the cassava starch (CS) pastes treated with different acetic anhydride concentration could be attributed to easier hydration, resulting from reduction of interaction between starch chains due to the substitution. The transition temperatures (T_o, T_p and T_c) and enthalpy of gelatinisation (ΔH) of acetylated CS, were determined. The values were lower than those of native starches. Rheological properties of CS pastes (5% w/w) as a function of the degree of substitution were evaluated in dynamic shear force measurements. Magnitude of storage modulus (G′), loss modulus (G′′) and complex viscosity (Eta*) of acetylated CS pastes were determined also. Dynamic moduli (G′, G′′ and Eta*) values of acetylated sweet cultivar pastes were generally higher than those of native starch whereas the acetylated samples of the bitter cultivar were lower than those of native starch. The magnitudes of G′ were greater than those of G′′ and Eta* at all frequencies (ω). The fact that all the tan δ (ratio G′′/G′) values (0.7–0.48 and 0.25–0.44) were less than one is an indication that the samples are more elastic than viscous. The acetylated starches could find promising industrial uses in food products like Lemon curd and Mayonnaise and other non‐food applications.     

Physicochemical properties of acetylated starches from some Indian kidney bean (Phaseolus vulgaris L.) cultivars

Starches separated from four kidney bean cultivars were modified by acetylation to reduce retrogradation and increase gel stability and compared with respective native starches (data of native starch reported by Wani et al., 2010 ). Acetylation was carried out by treating starches with 0.04 and 0.08 g of acetic anhydride per gram of starch dry weight basis (dwb) at 25 °C and pH between 8.0 and 8.5. The extent of acetylation increased proportionally with the concentration of acetic anhydride used. The pasting curves of 10.7% starch determined by Rapid Visco Analyzer at 160 rpm showed that acetylation decreased the setback viscosity values by 0.64–34.58% and pasting temperature by 4.4–9.2 °C when compared with the native starch. Differential scanning calorimetry observations also revealed significant (P ≤ 0.05) decrease in gelatinisation temperature of acetylated starches than the corresponding native starches. Hardness of starch gels varied between 14.3 and 44.0 g, which was significantly (P ≤ 0.05) lower than the corresponding native starch gels.     

Turmeric powder and starch: selected physical, physicochemical, and microstructural properties

Turmeric powder and its starch were characterized for physical, physicochemical, and microstructural characteristics. X-ray diffractogram indicated that turmeric starch to be of B type. Dried and cured-dried turmeric powder samples showed higher water-holding capacity (3.62 and 4.78 g/g, respectively) compared to isolated starch (1.07 g/g) at 30 °C. Non-Newtonian shear-thinning characteristics were observed with turmeric powder dispersion containing 10% (w/w) solids. A power law model fitted well to correlate the shear-rate and shear-stress data (r= 0.993 to 0.999, P≤ 0.01) for both samples. Apparent viscosities of isolated turmeric starch and cured-dried turmeric powder dispersion containing 10% (w/w) solids were 1.29 ± 0.03 and 7.57 ± 0.39 mPa s, respectively. Microstructure of starch particles showed a smooth flat outer surface. The approximate length and breadth of isolated elliptical starches were 25 and 10 μm while the thickness was about 5 μm. PRACTICAL APPLICATION: Isolation and characterization of starch from an unconventional source like turmeric rhizome indicate a potential application as a functional ingredient in foods and pharmaceutical industries including agglomerated products.     

Effect of phosphoric acid treatment on physicochemical,functional, and structural properties of starch extracted from yam (Dioscorea rotundata)

This work was designed to elucidate selected physicochemical, functional, and structural properties of native and modified yam (Dioscorea rotundata) starch. The isolated starch was chemically modified using 5, 10, 15, 20, and 25% phosphoric acid solution at 50°C for 1 h, and yield, swelling power, gelation, water holding capacity, paste clarity, blue value, and amylose and amylopectin content of the native and modified yam starch were determined. Structural changes in the native and starch modified with 25% phosphoric acid were evaluated using Fourier transform infrared spectroscopy and optical microscopy. The result showed that the yield, swelling power, water holding capacity, paste clarity, blue value and amylose and amylopectin content of native yam starch was 33.38% (217 g), 3.84 g/g, 1.0 v/g, 10%, 0.52 and 25.96, respectively, whereas gelation study of the native and modified starch indicated that native starch was viscous and modified starch firm. However, yield, swelling power, water holding capacity, paste clarity, blue value, and amylose content of modified yam starch reduced in a dose dependent manner with phosphoric acid. The reduction in the values of the various functional properties could be associated with the effect of phosphoric acid on the starch granular structure. The result of Fourier transform infrared spectroscopy and optical microscopy revealed that the yam starch was modified by phosphoric acid with changes in functional groups spectra such as –OH stretch (3177 cm^?1), H₂O absorbed (1644 cm^?1) (amorphous region), C-H stretch (2923 cm^?1), CH₂O (1253 cm^?1), and C-O-C (1078 cm^?1) when compared to native starch. The morphology of native and modified yam starch granules ranged from oval to eliptical. However, modified starch granules were rough in surface. In conclusion, the characterized physicochemical and functional properties and structure exhibited by native and modified yam starch indicated that, yam could be a cheap and valuable source of starch for industrial application.     

Quinoa (Chenopodium quinoa) Starch — Physico-chemical Properties and Functional Characteristics

Starch was isolated from quinoa (Chenopodium quinoa) for a study of physico-chemical properties, functional characteristics and a comparison with starches from wheat, barley, wild rice, amaranth and potatoes. Quinoa starch granules range in size from 0.6 to 2.0 μm and are found within the cells of the seed as single entities or as compound structures of spherical or oblong aggregates. Quinoa starch exhibited a higher Amylograph viscosity, a greater waterbinding capacity and a greater swelling power compared to wheat- or barley starch. The gelatinization temperature range of quinoa starch was slightly higher than that of wheat- or barley starch. Amylose content was lower. As a thickening agent for fillings, quinoa starch performed better than other starches in the study. However, breads and cakes baked with quinoa starch were of poor quality. Volumes were lower, the grain non-uniform with thick cell walls and the texture dense and compact. The overall performance of quinoa starch in baked goods was similar to that of other non-cereal starches (amaranth- and potato starch).     

Properties of starch from root tuber of Stephania epigaea in comparison with potato and maize starches

The dry root tuber of Stephania epigaea contained 36.5% starch, indicating a good starch source. In this study, starch was isolated from S. epigaea. Its morphology, physicochemical, and functional properties were investigated and compared with potato and maize starches. S. epigaea starch had small spherical granules with centric hila and large ellipsoidal granules with eccentric hila, and granule sizes varied from 7 to 40 μm. The starch had 33.9% amylose content and B-type crystallinity. The gelatinization onset, peak, and final temperatures were 59.4, 62.3, and 66.2°C, respectively, and were lower than those of potato and maize starches, but the enthalpy (16.3 J/g) was higher than that of potato and maize starches. The peak, hot, final, and breakdown viscosities were 2227, 1623, 2149, and 594 dPa s, respectively, and were significantly higher than those of maize starch and lower than those of potato starch. S. epigaea starch was more susceptible to amylase hydrolysis and in vitro digestion than potato starch and less than maize starch. This study would be useful for the applications of starch from S. epigaea in the food and non-food industries.     

Physicochemical,Morphological, Thermal and Pasting Properties of Starches Isolated from Rice Cultivars Grown in India

Physicochemical, morphological, thermal, and pasting properties of starches, isolated from basmati (HBC-19 and Bas-370) and non-basmati (Jaya, a coarse cultivar; P-44 and HKR-120, the medium cultivars and Sharbati, fine cultivar) rice cultivars grown in India were studied. The amylose content of starches from different cultivars ranged from 2.25 (Jaya) to 22.21 g/100 g of starch (HBC-19). Jaya, HKR-120, and P-44 cultivars showed soft gel consistency as 84, 73, and 69 mm, respectively, whereas Sharbati, Bas-370 and HBC-19 cultivars showed medium gel consistency as 54, 53, and 58 mm, respectively. Swelling power (at 95°C) indicated a significant positive correlation with amylopectin content (r = 0.828, p < 0.05) and gel consistency (r = 0.983, p < 0.01). Turbidity had a highly significant positive correlation with solubility (r = 0.919, p < 0.01) and amylose content (r = 0.945, p < 0.01). Starch form Jaya cultivar showed the presence of smallest size granules (2.4–5.7 μm) with an average size of 3.96 μm, whereas Bas-370 showed the presence of largest size granules (3.3–6.7 μm) with an average size of 5.0 μm. The transition temperatures, enthalpy of gelatinization (ΔH_gel), peak height index (PHI) and gelatinization range were determined using differential scanning calorimetry (DSC). The starch from Sharbati cultivar showed highest onset temperature (T_o), peak temperature (T_p), conclusion temperature (T_c), enthalpy of gelatinization and peak height index (PHI) of 68.8°C, 73.2°C, 79.0°C, 11.56 J/g and 2.63 respectively. Pasting temperature of rice starches varied from 68.9°C (Jaya) to 74.5°C (Sharbati). The peak viscosities observed were in the range of 2223 to 3297 cP, lowest for HBC-19 starch and highest for Jaya starch.     

Isolation of Velvet Bean (Mucuna pruriens) Starch: Physicochemical and Functional Properties

The velvet bean (Mucuna pruriens) is an excellent potential starch source as it contains approximately 52 % of this carbohydrate. The physicochemical and functional properties of velvet bean starch were evaluated and compared to those of other starches. The chemical composition was: moisture 10.78 %; solid matter: protein 0.71 %; fiber 0.54 %; ash 0.28 %; fat 0.40 %; starch 98.1 %; and phosphorus 0.015 %. Amylose content was higher (39.21 %) than in tuber and cereal starches but similar to other legume starches. Average granule size was 23.6 μm, granules having an oval shape. Paste properties were: gelatinization temperature, 74.82 °C; gelatinization temperature range, 70—80 °C; and alkali number, 3.22. Gels produced with velvet bean starch were firmer than those produced with corn starch, and had a higher degree of retrogradation, even at high concentrations. At 90 °C, solubility was 16.2 % and swelling power was 16.17 g of water/g of starch. Given these properties, velvet bean starch has potential applications in food products requiring high temperature processing, such as jams, jellies and canned products.     

Spectral analysis and physical properties of benzylated starch

A‐ and B‐wheat starch (in native or acetylated form) and potato starch (slightly acetylated) were subjected to benzylation with benzylchloride in various reaction conditions and at various reaction times (40–100°C, 1–90 h). Modified and original starches were characterized by elemental analysis and spectroscopic methods (FT‐IR and 1H NMR). The semicrystalline or amorphous character was indicated by X‐ray powder (XRD) patterns. Rheological properties of benzyl starch of DS ∼ 1 were measured by small amplitude oscillation shear rheology (SAOS) using the rheometer Haake Rheostress RS 80. The results indicated predominantly elastic behavior because the storage modulus was higher than the loss modulus over the whole frequency range; it corresponded to a true gel. The storage and loss moduli increased with increasing frequency while the tangent of phase did not change and was approximately δ = 40°.     

Indigestible Starch of P. lunatus Obtained by Pyroconversion: Changes in Physicochemical Properties

Lima bean (Phaseolus lunatus) starch was modified using pyroconversion to produce non‐digestible starch and the functional properties of the pyrodextrinized starches were evaluated. Reaction conditions included: starch/2.2 M HCl ratio (80:1 and 160:1, w/v); temperature (90°C and 110°C) and reaction time (1 and 3 h). “In vitro” indigestible starch and color difference (ΔE) were determined and used as response variables. The optimum product was recovered from native starch treated with a 160:1 starch/HCl ratio, at 90°C for 1 h, which produced modified starches containing 49.5% indigestible starch and ΔE of 18.86. Starch pyrodextrinization decreased the amount of enzymatically available starch through formation of atypical glycosidic bonds that are not digested by the amylases and maltooligosaccharidases in the small intestine of humans. Compared to the P. lunatus native starch, the pyrodextrinized starch exhibited increased paste and gel clarity (52.7%T), solubility (88.7%), and swelling power (26 g water/g starch), a higher gelatinization temperature range (72.5–89.8°C) and lower viscosity. This process can be considered a promising treatment for production of resistant starch (RS) from P. lunatus.