Effect of phosphorylation of the maize starch on thermal generation of stable and short‐living radicals

Effect of hydrolysis, phosphorylation and treatment with high hydrostatic pressure on thermal generation of stable and short‐living radicals in maize starch was studied by X‐ray diffraction (XRD), electron paramagnetic resonance (EPR) spectroscopy, differential scanning calorimetry and polarized light microscopy. Phosphorus was introduced into maize starch as mono‐ and distarch phosphates. XRD indicated localization of phosphate groups in amorphous part of the granule whereas calorimetric data suggested some cross‐linking of the distarch phosphates. Stable and short‐living radicals with unpaired electron localized at carbon atom were generated in all investigated samples in the temperature range commonly used for processing food. The number of detected short‐living radicals, stabilized by a spin trap, is of two orders of magnitude greater than that of the stable radical species. Hydrolysis and phosphorylation strongly increase the number of stable radicals while pretreatment of the starch with high hydrostatic pressure diminishes their amount. The EPR spectra of stable radicals consist of two components, single line and another one with hyperfine structure, indicating interaction of unpaired electron with neighboring hydrogen atom. The EPR spectra of the spin trap adducts with short‐living radicals contain three components from species differing in their dynamic properties depending on localization in zones of various degree of crystallinity.     

Effect of acid hydrolysis on rheological and thermal characteristics of lentil starch slurry

A comparative rheological and thermal study was carried out between acid hydrolyzed and unhydrolyzed (control) lentil starch dispersions (25-33.3 g starch per 100 g water) as function of temperature. After acid hydrolysis, the peak gelatinization temperature (T_p) shifted to higher temperature than the corresponding starch without hydrolysis whereas the gelatinization enthalpy remained unaffected by hydrolysis. The starch gelatinization kinetics was evaluated by a non-isothermal technique as function of elastic modulus (G′) and G′ vs. time (t) data up to the gelatinization peak value was considered for rate estimation. A 2nd-order reaction kinetics described well the starch gelatinization process and the process activation energy was ranged between 241 and 434 kJ/mol. Acid hydrolysis strongly affected the rheological properties by lowering gel strength compared to unhydrolyzed starch. The creep analysis further revealed that starch gel was significantly affected by hydrolysis and exhibited less resistant to the stress. A 4-parameters Burgers model well-described creep curves and supported oscillatory rheological data.     

Color degradation kinetics of pineapple puree during thermal processing

Improvement of color, as a quality attribute of processed pineapple puree, has been made possible by the increase in knowledge of kinetic of color change. The kinetics of color degradation of pineapple puree were investigated during heat treatment at 70-110 °C in order to cover the temperature range that used in preheat and sterilization of commercial aseptic pineapple puree. Color changes associated with heat-treated puree were monitored using Hunter colorimeter (L, a, b, total color difference—ΔE) and Browning index (A₄₂₀). The changes in L and b values fitted well to the first-order kinetic model while ΔE, a value, and Browning index followed the zero-order kinetic. The dependence of the rate constant on temperature was represented by an Arrhenius equation. The results suggested that ΔE and lightness, based on activation energy, were the most sensitive measures of color change at temperature range 70-90 and 95-110 °C, respectively.     

Effect of ground corn steeping on starch properties

Pasting and thermal properties, and microstructure of starch from ground corn (GS) steeped at 52 °C in sulphurous acid solution (0.20%) at different steep times (8, 16, 24, 32 and 40 h) were investigated. The isolated starch obtained by wet milling was characterised by determining pasting properties in Rapid Visco Analyser (RVA), retrogradation enthalpy in differential scanning calorimetry (DSC), and microstructure of granules in light (LM) and scanning electron microscopy (SEM). Milling before steeping and long steep time caused reduction in peak, hot paste, cool paste, breakdown and setback viscosities. Steep time provoked an increase in the retrogradation temperatures (onset and peak), whereas no significant differences were found in retrogradation enthalpy. Microstructure characteristics analysed by SEM showed many cracks and cavities on surface in samples steeped 8 h, whereas samples steeped 40 h showed a great alteration and disruption of their inner layer. LM with polarised light confirmed that starches retained birefringence with several differences depending on the steep time. The use of ground kernels allowed a better steep solution–endosperm interaction, which caused changes in rheological, thermal and microstructural starch characteristics.     

Physicochemical,crystallinity, pasting and thermal properties of heat‐moisture‐treated pinhão starch

The effect of heat‐moisture treatment (HMT) on the properties of pinhão starches under different moisture and heat conditions was investigated. The starches were adjusted to 15, 20 and 25% moisture levels and heated to 100, 110 and 120°C for 1 h. The X‐ray diffractograms, swelling power, solubility, gel hardness, pasting properties and thermal properties of the native and HMT pinhão starches were evaluated. Compared to native starch, there was an increase in the X‐ray intensity and gel hardness of HMT starches, with the exception of the 25% moisture‐treated and 120°C heat‐treated starch. HMT reduced the swelling power and solubility of the pinhão starches when compared to native starch. There was an increase in the pasting temperature, final viscosity and setback and a decrease in the peak viscosity and breakdown of HMT pinhão starches compared to native starch. HMT increases the gelatinisation temperature of native pinhão starch and reduces gelatinisation enthalpy.     

Thermal degradation kinetics of anthocyanin and visual colour of plum puree

Thermal degradation kinetics of anthocyanin and visual colour (tristimulus L, a and b values) of plum puree were studied at selected temperatures (50–90 °C) for a residence time of 20 min. Results indicated that the thermal degradation of anthocyanin, tristimulus colour a value (representing redness) and L×a×b value (representing total colour) followed first-order reaction kinetics. The activation energy values for anthocyanin, red colour and total colour were 37.48, 25.86 and 30.68 kJ/mol respectively. Higher activation energy signified higher thermal sensitivity of anthocyanin during heat processing of plum puree. A linear relationship described well the variation of total visual colour (L×a×b) with anthocyanin content of plum puree during thermal processing.     

Effect of high‐pressure microfluidization on the structure of cassava starch granule

Microfluidization has been applied to modify starch granules. The study was conducted to investigate the effect of microfluidization on the structure and thermal properties of cassava starch–water suspension (20% w/w). The means of optical microscopy, SEM, FTIR spectroscopy, XRD, and DSC were applied to analyze the changes in microstructure, crystallinity, and thermal property. Microscopy observations revealed that native starch granules were oval, round, and truncated in shape. After the microfluidization treatment, a bigger starch granule was partially gelatinized, and a gel‐like structure was formed on a granular surface. No significant difference in XRD patterns of the samples were observed and all samples exhibited A‐type allomorph. Crystallinity decreased with the pressure. Sample treated at 150 MPa contains 17.1% crystalline glucan polymer, lower than that of native granules which have crystallinity of about 25.8%. A lower crystallinity means poor order of crystalline glucan polymer structure in starch granules. The disruption of crystalline order within the granule was also observed by FTIR measurement. Thermal analysis using DSC indicated that the microfluidization treatment brought about a significant decrease of melting enthalpy. The gelatinization enthalpy was 12.0 and 3.0 J/g for the native sample and samples treated under the 150 MPa, respectively. The results indicate that high‐pressure microfluidization process induced the gelatinization of cassava starch, which is evaluated by a percentage of the degree of gelatinization, due to a pronounced decrease with increasing microfluidizing pressure.     

Effect of acid‐ethanol treatment followed by ball milling on structural and physicochemical characteristics of cassava starch

Structural and physicochemical characteristics of cassava starch treated with 0.36% HCl in anhydrous ethanol during 1 and 12 h at 30, 40, and 50°C followed by ball milling for 1 h were analyzed. Average yield of acid‐ethanol starches reached 98% independent of the treatment conditions. Solubility of acid‐ethanol starches increased with reaction temperature and time, but it did not change after ball milling. Granule average size reduced with chemical treatment from 25.2 to 20.0 µm after 12 h at 50°C. Ball milling decreased the granule average diameter of the native starch and those chemically treated at 30°C/1 h or 40°C/1 h, but it did not alter the starches treated for 12 h, independent of temperature. From scanning electron microscopy (SEM), starch granules presented round shape and after modification at 50°C/12 h, before and after ball milling, showed a rough and exfoliated surface. Some granules were deformed, suggesting partial gelatinization that was more intense after milling. Starch crystallinity increased as temperature and time of chemical treatment were increased, while amylose content, intrinsic, and pasting viscosities decreased. Gelatinization temperatures increased for all chemical starches. The findings can be related to the preferential destruction of amorphous areas in the granules, which are composed of amylose and amylopectin. After ball milling, the starch crystallinity decreased, amylose content, intrinsic, and pasting viscosities kept unchanged and gelatinization temperatures and enthalpy reduced. Ball milling on native and chemical starches caused the increase of amorphous areas with consequent weakening and decreasing of crystalline areas by breaking of hydrogen bonds within the granules.     

Influence of manufacturing conditions on thermo‐physical properties of ripened experimental Emmental‐type cheese and comparison with commercial Emmental cheese

Experimental Emmental cheese was produced at pilot plant scale with varied process conditions, and the ripened cheeses were analysed in terms of thermo‐physical properties. The amount of propionic acid and the temperature at tan δ_max ( loss factor) were significantly influenced by varied process parameters. Experimental cheeses were compared to commercial Emmental cheese by the application of principal component analysis. Commercial Emmental cheese was clearly discriminated from experimental Emmental cheese mainly due to the melting behaviour. The results allow the establishment of a small‐scale process for Emmental cheese production to promote product development on a time and cost‐saving level.     

湿热处理玉米淀粉对酶敏感性研究

该研究以玉米淀粉为原料,用湿热处理方法对淀粉进行改性。以改性后其对淀粉酶敏感性为指标,通过正交试验得到最佳工艺参数为:淀粉水分含量32%(W/W),湿热处理温度120℃,作用时间5.5h,此处理条件对酶敏感性提高8.13%。     

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.