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     

Evaluation of starch analysis methods for feed samples

The objectives of this work were to evaluate the efficacies of commercial starch analyses and of starch analysis extraction and gelatinisation procedures. In Study 1, accuracy and specificity of commercially available starch analyses were evaluated with six co‐operating laboratories (five commercial, one university). Results from 11 test samples showed three laboratories with recoveries of purified starch of 92 g kg⁻¹ or less. Three and four laboratories had inflated values when samples contained glucose or sucrose, respectively. Analyses appeared to have good specificity for glucose. Incompleteness of starch detection and interference by non‐starch carbohydrates can affect commercially available analyses. In Study 2, extraction with 80:20 ethanol/water (v/v; 80EtOH) or 90:10 ethanol/water (v/v; 90EtOH) to remove low‐molecular‐weight carbohydrates, and gelatinisation with heat, alkali (KOH), 6 M urea or 8 M urea were evaluated. Extraction with 80EtOH or 90EtOH reduced interference from non‐starch carbohydrates. Gelatinisation with heat was adequate for good recoveries of starch glucose for both control (non‐extracted) and 80EtOH‐extracted samples; gelatinisation with alkali was required for 90EtOH‐extracted samples. Recoveries of pure starch samples were greatest with no extraction and heat gelatinisation. 80EtOH extraction with heat gelatinisation appears to be an adequate preparation method when removal of low‐molecular‐weight carbohydrates is desired. © 2000 Society of Chemical Industry     

Effects of time/temperature treatments on potato (Solanum tuberosum) starch: a comparison of isolated starch and starch in situ

Previously, time/temperature treatments of starch have been performed mainly on starch/water systems. In this study the same time/temperature treatments were applied to starch/water systems and to potato starch in situ. Two potato varieties (Solanum tuberosum cultivars Asterix and Bintje) were used. The effect of time/temperature treatments on gelatinisation behaviour was evaluated using differential scanning calorimetry (DSC). A blanching process was simulated by heating samples to 74 °C and then cooling them to 6 °C. A DSC scan showed that starch was completely gelatinised after this treatment. Retrogradation of amylopectin increased during storage at 6 °C from 0 to 24 h after blanching. Annealing of starch, with the aim of altering cooking properties, was performed by heating samples to temperatures below the gelatinisation onset temperature. Treating samples at 50 °C for 24 h caused a shift in gelatinisation onset temperature of 11–12 °C for isolated starch and 7–11 °C for in situ samples. The extent of the annealing effect depended on the difference between onset and annealing temperatures, and prolonged treatment time increased the effect. Starch/water systems and tissue samples behaved similarly when exposed to time/temperature treatments. The most apparent difference was the shift of gelatinisation to higher temperatures in tissue samples. Copyright © 2003 Society of Chemical Industry     

Gelatinisation Characteristics of Cassava Starch Settled in the Presence of Different Chemicals

Addition of chemicals during the extraction of cassava starch for enhancing the settling rate, whiteness and compactness of the settled starch is an accepted commercial practice. The effect of addition of selected chemicals such as acids (sulphuric and hydrochloric acids), bleaching and oxidising agents (sodium metabisulphite and sodium hypochlorite) and alum during settling on the thermal and pasting properties of the cassava starch was examined. Treatment with sulphuric acid produced a noticeable increase in all DSC gelatinisation parameters, viz. onset gelatinisation temperature (T_o), temperature at peak minimum (T_p) and end temperature (T_e), with increasing concentration of acid, while only a marginal shift could be obtained even at higher concentration of hydrochloric acid. However, no major effect resulted from treatment with sodium metabisulphite, sodium hypochlorite and alum. The gelatinisation enthalpy was hardly affected by the treatments. An exception was hydrochloric acid, which brought about a perceptible decrease in enthalpy at higher concentrations indicating that starch crystallinity is influenced to a small extent by hydrochloric acid. Pasting characteristics studied using a Rapid Visco Analyser showed that sulphuric acid, even at the lowest concentration (5 mM), considerably affected the structural characteristics of cassava starch, while hydrochloric acid induced similar effect only at higher concentrations. Alum reduced the paste viscosity while the bleaching agents (sodium metabisulphite and sodium hypochlorite) were not so effective in modifying the starch viscosity characteristics.     

Differential scanning calorimetry: gelatinisation of sago starch in the presence of sucrose and sodium chloride

The effect of sucrose and sodium chloride (NaCl) on sago starch gelatinisation was investigated by differential scanning calorimetry (DSC). The gelatinisation of starch in the presence of low levels of water and high levels of sucrose was studied. The gelatinisation temperature was found to increase in the presence of sucrose, whereas the gelatinisation enthalpy was unaffected. The gelatinisation temperature range was not as broad in the presence of sucrose as without sucrose. Furthermore, the shape of the gelatinisation endotherm was changed by the addition of sucrose. The double endotherm obtained in limited water–starch systems was changed into a single endotherm, similar to the endotherm obtained in excess water–starch systems at higher temperature. DSC was also used to examine the effects of water and NaCl content on the phase transitions of sago starch. Samples were adjusted to starch–water weight ratios of 2:3 and 3:2 in NaCl concentrations from 1 to 5 M . The gelatinisation temperature of sago starch increased and then decreased as the NaCl concentration increased. NaCl created similar effects on the endotherms with excess water content and on the first endotherm with limited water content. © 1999 Society of Chemical Industry     

Measurement of electrical conductivity,differential scanning calorimetry and viscosity of starch and flour suspensions during gelatinisation process

Electrical conductivity measurements were applied to analyse the gelatinisation process of 12 starch or flour suspensions. The electrical conductivity of starch suspensions was found to increase upon gelatinisation because of the release of ions from starch granules. The initiation temperature of ion release, T_i, correlated well with the onset temperature in the DSC thermogram (R = 0.868), while the completion temperature of ion release, T_f, correlated with the temperature at the start of viscosity increase (R = 0.865). Thus T_i and T_f corresponded to the beginning and ending temperatures of gelatinisation respectively. The electrical conductivity measurement will be used as an on‐line technique to monitor the whole process of starch gelatinisation. © 2001 Society of Chemical Industry     

Effect of miniemulsion cross‐linking and ultrasonication on properties of banana starch

Miniemulsion technique has been widely used to prepare cross‐linked starch microsphere for food application. The objective of this study was to examine the effect of miniemulsion and ultrasonic treatment on the morphological, physicochemical and thermal properties of banana starch. Results showed that the miniemulsion cross‐linked banana starch (MCBS) exhibited lower swelling power (SP) and solubility (S) but higher gelatinisation enthalpy (ΔH_gel) than native banana starch. Ultrasonic treatment conditions (amplitude and time) did not show any significant difference in SP and ΔH_gel of MCBS. Ultrasonicated MCBS showed rough surfaces and slight fragmentations without any change in particle size. At gelatinisation temperature (80 °C), the SP and S of MCBS were higher than those at 29 °C. Moreover, MCBS with ultrasonic treatment showed a lower range in the gelatinisation temperature (ΔT) than untreated. The FT‐IR spectrums revealed that MCBS were fully cross‐linked and had high extent of hydrogen bonding.     

Effects of different components in skim milk on high-pressure-induced gelatinisation of waxy rice starch and normal rice starch

The gelatinisation of starch in skim milk required higher pressures than did the gelatinisation of starch in water. This study examined the effects of various milk components on the pressure-induced gelatinisation of waxy rice starch and normal rice starch, in order to understand the differences between the gelatinisation characteristics of starch in skim milk and starch in water. Gelatinisation was retarded in skim milk, which was attributed to the effects of soluble milk minerals and lactose. The presence of these components may reduce the plasticising ability of the suspension medium. Direct interactions between the milk components and starch molecules may also contribute to retarded gelatinisation. Milk proteins (casein and whey protein) did not affect the degree of pressure-induced gelatinisation at the concentrations of these components in skim milk, at 10% total solids.     

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.     

Effect of varying starch properties and mashing conditions on wort sugar profiles

The aim of this research was to investigate the relationship between starch composition in barley and its malted counterpart alongside malt enzyme activity and determine how these factors contribute to the fermentable sugar profile of wort. Two Australian malting barley varieties, Commander and Gairdner, were sourced from eight growing locations alongside a commercial sample of each. For barley and malt, total starch and gelatinisation temperature were taken, and for malt, α‐ and β‐amylase activities were measured. Samples were mashed using two mashing profiles (infusion and Congress) and the subsequent wort sugar composition and other quality measures (colour, original gravity, soluble nitrogen) were tested. Variety had no significant (<0.05) effect on any barley, malt, enzyme or wort characteristics. However, growing location impacted gelatinisation temperature, colour, malt protein content and original gravity. The gelatinisation temperature in malt samples was higher, by ~0.8°C, than in the equivalent barley sample. Several malt samples, even with protein contents <12.0%, had gelatinisation temperature >65°C. The fermentable sugars measured in the malt prior to mashing showed a higher proportion of maltose than glucose or maltotriose. In addition, there were significant differences in the amount of sugar produced by each mashing method with the high temperature infusion producing a higher amount of sugar and proportionally more maltose. There is scope for further research on the effect of genetics and growing environment on gelatinisation temperature, mash performance and fermentable sugar development. Routinely measuring gelatinisation temperature and providing this information on malt specification sheets could help brewers optimise performance. © 2019 The Institute of Brewing & Distilling     

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 properties and in vitro digestibility of flours and starches from taro cultivated in different regions of Thailand

This research aimed to study physicochemical properties and in vitro digestibility of flours and starches from taro cultivated in different regions of Thailand, that is, Kanchanaburi (KB), Chiang Mai (CM), Phetchaburi (PB) and Saraburi (SB). Taro starches were extracted from taro flours using either water or alkaline extraction. The taro flours had significantly (P ≤ 0.05) larger particle size, higher pasting and gelatinisation temperatures, and resistant starch content but lower total starch content, whiteness (L* value), paste viscosities and clarity than their corresponding extracted starches. All the taro starches exhibited polygonal and irregular granules and gave A-type X-ray diffraction pattern. The alkaline-extracted taro starches had significantly (P ≤ 0.05) higher extraction yield, total starch content, L* value, pasting and gelatinisation temperatures, and paste clarity but lower granular size, amylose content, resistant starch content, paste viscosities and relative crystallinity than their water-extracted counterparts.     

Degree of Gelatinisation of Cooked Rice

A method for determining degree of gelatinisation of rice starch or rice flour, based on the amylose/iodine blue value after dispersion in alkali, has been developed. The method can be used to follow the course of cooking of rice under different conditions, and has been checked against a novel infrared technique for relating degree of gelatinisation to the phenomenon of hydrogen bonding.     

Development and Testing of Methods to Screen Chickpea Flour for Starch Characteristics

Rapid screening methodology has been developed for assessing the chemical composition and the gelatinisation and pasting properties of starch using flour from chickpea seeds. The methodology allows samples to be assessed using a minimal amount of sample and for starch information to be interpreted in the presence of other components present in the flour. The starch content of the flour and the amylose content of the starch was determined by modifying existing kit-based methods (Megazyme International Ltd). Using the Differential Scanning Calorimeter (DSC), starch gelatinisation characteristics can be assessed based on temperature of gelatinisation (T_p), specific heat capacity (Cp^sp ) and half width of transition (½ΔT). Pasting properties could be assessed using the Rapid Visco Analyser (RVA), based on the determination of onset temperature for the RVA profile (T \displaystyle _o^{RVA} ), T_p − T \displaystyle _o^{RVA} and final viscosity (FV) values. The developed methodology was tested using a range of chickpea samples. No significant variation was found between the samples for starch content or for the proportion of amylose/amylopectin in the various starches. Significant variation was found in the starch properties of two of the samples, while the variation between the remaining samples was very small.     

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     

Effects of psyllium and cellulose fibres on thermal,structural, and in vitro digestion behaviour of wheat starch

The study investigated the effects of adding different types of fibre (psyllium and cellulose) on in vitro digestion behaviour of wheat starch with its thermal and structural properties. Psyllium and cellulose fibres interfered with the wheat starch differently. Psyllium fibre hindered starch gelatinisation, restricted the loss of starch crystallinity, and decreased the accessibility of enzymes to starch. In contrast, cellulose fibre had no significant effect on gelatinisation and loss of crystallinity but limited the digestive enzyme mobility. The impact of psyllium was more pronounced than cellulose on reducing starch digestibility. Rapidly digestible starch fractions of the cooked starch reduced from between 57.90 ± 0.60–69.72 ± 0.46 (% in starch) to between 28.06 ± 0.36–46.34 ± 1.10 (% in starch) and 53.23 ± 0.36–66.71 ± 0.24 (% in starch) for psyllium and cellulose fibre, respectively. This information could be helpful to design foods containing starch with reduced digestibility for a healthy diet.     

Extraction,Physicochemical and Compaction Properties of Tacca Starch — a Potential Pharmaceutical Excipient

Some physicochemical properties of tacca starch (Tacca leontopetaloides, Taccaceae) have been examined and the results compared to those of maize and potato starches. Tacca starch was found to have a higher amylose content than maize starch but a lower content than potato starch. The starch granules were small (average particle size 3.5 μm) relative to maize and potato starches and were predominantly polyhedral with edges. The gelatinisation characteristics except from the temperature were similar to those of maize starch but much higher than those of potato starch. Tacca starch had relatively higher swelling power and solubility than the other starches. Its features in the formation of compacts (tablets) were comparable to those of maize starch with tacca starch being more resistant to deformation.     

Effects of oligosaccharides on phase transition temperatures and rheological characteristics of waxy rice starch dispersion

BACKGROUND: The creation of starch‐based foods incorporated with functional ingredients such as probiotics is of great current interest in the food industry. This study aimed to investigate the effects of prebiotic oligosaccharides on the phase transition temperatures and rheological characteristics of waxy rice starch dispersions. Four oligosaccharides were applied to the rice starch dispersions: chitooligosaccharides, fructooligosaccharides, isomaltooligosaccharides and xylooligosaccharides. RESULTS: The addition of 125 g kg^?1 oligosaccharides elevated the onset and peak temperatures for gelatinisation of 200–400 g kg^?1 waxy rice starch dispersions. The temperature of the storage modulus (G′) for gelatinisation increased markedly on adding fructooligosaccharides to 200–300 g kg^?1 waxy rice starch. For gelatinisation of 300 g kg^?1 rice starch dispersion the effectiveness of the oligosaccharides in changing the above parameters was as follows: chitooligosaccharides > fructooligosaccharides > isomaltooligosaccharides > xylooligosaccharides. Moreover, their effectiveness was dependent on the amylose content, as illustrated by comparing waxy and non‐waxy rice starches (amylose contents 9–256 g kg^?1). Importantly, the logarithmic G′₉₅ change was linearly and negatively correlated with amylose content. CONCLUSION: The results suggest that oligosaccharide‐containing rice starch dispersions may potentially be used for the formulation of oligosaccharide‐containing starchy functional foods owing to the rheological changes of these starch dispersions. Copyright © 2011 Society of Chemical Industry     

Effect of gelatinisation on slowly digestible starch and resistant starch of heat-moisture treated and chemically modified canna starches

The effects of gelatinisation on slowly digestible (SDS) and resistant starch (RS) of native and modified canna starches were investigated. Starch slurries (10% w/w) were gelatinised at 100 °C for 5, 10, 20 and 40 min using a rapid visco analyzer (RVA). Significant change in the degree of gelatinisation (DG) values of all starch samples was observed during the initial 10 min of gelatinisation; after that the DG values increased gradually with gelatinisation time. The RS contents in all gelatinised starches decreased with increasing gelatinisation time, while the SDS values fluctuated. Chemical modification affected DG values as well as RS/SDS contents. The RS contents in 10% (w/w) acetylated, hydroxypropylated, octenyl succinylated and cross-linked canna starches gelatinised at 100 °C for 40 min were 26.6%, 32.0%, 45.3% and 19.8%, respectively, which were higher than that of the native starch (12.4%). Canna starch modified by crosslinking had the highest SDS content when gelatinised for 20-40 min. Modification of canna starch by heat-moisture treatment resulted in a lower content of RS for all treated samples. However, the Vt-HMT25 (canna starch containing moisture content of 25% during heat treatment) when gelatinised for 5-20 min contained a higher amount of SDS, compared to unmodified starch. The most effective modification method for RS and SDS formation was octenyl succinylation, where the sum of RS and SDS approached that of Novelose260.     

Resistant starch and thermal,morphological and textural properties of heat‐moisture treated rice starches with high‐, medium‐ and low‐amylose content

This study investigated the effects of heat‐moisture treatment (HMT) on the resistant starch content and thermal, morphological, and textural properties of rice starches with high‐, medium‐ and low‐amylose content. The starches were adjusted to 15, 20 and 25% moisture levels and heated at 110°C for 1 h. The HMT increased the resistant starch content in all of the rice starches. HMT increased the onset temperature and the gelatinisation temperature range (T_finish–T_onset) and decreased the enthalpy of gelatinisation of rice starches with different amylose contents. This reduction increased with the increase in the moisture content of HMT. The morphology of rice starch granules was altered with the HMT; the granules presented more agglomerated surface. The HMT affected the textural parameters of rice starches; the high‐ and low‐amylose rice starches subjected to 15 and 20% HMT possessed higher gel hardness.