Production of reduced-calorie grape juice jelly with gellan, xanthan and locust bean gums: sensory and objective analysis of texture

 The production of reduced-calorie grape juice jellies with gellan, xanthan and locust bean gums (LBG) was studied. Twenty formulations of grape juice jelly were prepared according to a second-order composite rotatable design (with six central points). Response surface methodology (RSM) was used to optimise jelly formulation using as independent variables: total sugar content, ranging from 14 to 46°Brix; and total gum concentration ranging from 0.30 to 0.70% (w/v), with the proportion of gums in the mixture xanthan:LBG:gellan ranging from 5:5:90 up to 45:45:10. The processing temperature used was 90°C for complete solubilisation of gums. The dependent variables were objective measures of texture and a parameter obtained from sensory analysis, the overall balance (B), which represents the overall evaluation of the jelly. The resulting polynomial equation (R ² = 0.929) revealed that a jelly produced with white grape juice, total sugar with sucrose equal to 39.3°Brix, and, 0.54% (w/v) of total gum added in the proportions of: 1:1:1.7 (gellan:xanthan:LBG) had a maximum value of B. The sensory-optimised jelly was objectively characterised for texture and the model was tested. The texture characteristics, i.e. gel hardness, cohesiveness and springiness, were found to be similar to those of a reference product, a previously developed reduced-calorie grape juice jelly with low methoxyl pectin. Received: 12 June 1997 / Revised version: 21 August 1997     

Sweetening power of aspartame in hydrocolloids gels: Influence of texture

Equivalent sweetness of aspartame relative to two sucrose concentrations (10% and 20% w/w) were determined in water and in hydrocolloids gels. The influence of the texture of three hydrocolloids gelled systems—gellan gum, κ-carrageenan, and κ-carrageenan/locust bean gum (LBG)—at two gums concentrations (0.3% and 1.2% w/w) on the equivalent sweetness of aspartame were then studied. For the three gelled systems, the increase in hydrocolloid concentration produced a significant increase in the true rupture stress and in the deformability modulus values. For both κ-carrageenan and mixed gels the true rupture strain values increased when increasing hydrocolloid concentration while for gellan gels, decreased. For the same hydrocolloid concentrations the κ-carrageenan/LBG gels showed the largest strain at rupture and gellan gels the smallest (most brittle). For both soft (0.3% gum) and hard (1.2% gum) gellan gels and κ-carrageenan gels, the concentrations of aspartame needed to deliver a sweetness intensity equivalent to that of gels with 10% sucrose (0.079–0.087% w/w) were similar to those obtained for aqueous solutions (0.084% w/v). For hard κ-carrageenan/LBG gels the corresponding concentration of aspartame was slightly lower. For all gelled systems the concentrations of aspartame needed to deliver a sweetness intensity equivalent to that of gels with 20% sucrose were higher for soft gels than for hard gels.     

Effect of substitution of aspartame for sucrose on instrumental texture profile of hydrocolloids gelled systems

The effect of substituting aspartame (0.04–0.16% w/w) for sucrose (5–25% w/w) on the instrumental texture profile of three hydrocolloid gelled systems: -carrageenan, gellan gum and -carrageenan/locust bean gum at three different concentrations (0.3, 0.75 and 1.2% w/w) was studied. In gellan gels hardness and chewiness increased with sucrose concentration but not so in either -carrageenan or -carrageenan/LBG gels where no changes in these parameters were detected. Addition of sucrose also produced a small but significant increase in cohesiveness in gellan gels. The effect of sucrose concentration on all texture parameters of gellan gels was higher as gellan concentration increased. Aspartame addition did not affect TPA parameters. TPA results obtained for aspartame gels did not differ from those corresponding to the unsweetened gels considered here. Summarising the above information it can be said that substituting aspartame for sucrose in this type of sweetened gel changed the textural properties and that the changes produced depended on the hydrocolloid type and concentration and on the sucrose concentration replaced.     

Effect of addition of sucrose and aspartame on the compression resistance of hydrocolloids gels

The effect of adding sucrose (5–25% w/w) and aspartame (0.04–0.16% w/w) on the compression resistance of three hydrocolloid gelled systems: κ‐carrageenan, gellan gum and κ‐carrageenan/locust bean gum at three different concentrations (0.3, 0.75 and 1.2% w/w) was studied. Sucrose addition increased true rupture stress in the three‐gelled systems, this effect being stronger in gellan gels. The deformability modulus increased with sucrose concentration in gellan gels, but not in the other systems. Rupture stress and deformability modulus increased with the addition of sucrose only in the harder gels (0.75 and 1.2% w/w). The effect of sucrose addition on the true rupture strain was significant but, in general, not important, mainly for lower gum concentrations. Aspartame addition did not affect the compression parameters.     

Influence of Gluten and Gum Additives and Cryogenic Treatment on Some Properties and Morphology of Wheat Starch Complex Gels

The influence of gums (guar and xanthan) and gluten additives on the physicochemical properties and structural features of wheat starch gels (8%, w/w) subjected to cryogenic treatment at various temperatures (−9°C, −20°C, −40°C) was studied. Shear modulus and breaking stress of the gels were measured, the gels' morphology was studied with optical microscopy and the local mobility of water in the gels was determined with ESR. The total concentration of polysaccharide additives did not exceed 1% (w/w), and a 65:35 (w/w) mixture of guar and xanthan gums proved to be the optimal additive, which caused a noticeable increase in rigidity and strength of the resulting complex gels. Shear modulus and breaking stress of the gels decreased with lowering the temperature of the cryogenic treatment. The heterogeneous morphology of thin sections of the gel samples was revealed via optical microscopy. ESR studies showed that the local mobility of water was much lower in the gels than in pure water.     

Effect of Low Temperature Sonication on Orange Juice Quality Parameters using Response Surface Methodology

Freshly squeezed orange juice samples were sonicated at a constant frequency of 20 kHz for a range of processing temperatures (10–30 °C), amplitude levels (40–100%) and time (2–10 min) with pulse durations of 5 s on and 5 s off. Hunter colour values (L*, a* and b*), pH, ^oBrix, titratable acidity, cloud, non-enzymatic browning and ascorbic acid content were measured. Response surface methodology (RSM) based upon a three-factor, three-level Box–Behnken experimental design was used to determine the effect of independent variables. Under process conditions used in this study, no significant difference (p < 0.05) in pH, ^oBrix or titratable acidity was observed. Model predictions developed for Hunter colour values, cloud value, non-enzymatic browning and ascorbic acid content were closely correlated (R ² > 0.92) to experimental data. Box–Behnken design and RSM was demonstrated to be an effective technique to model the effect of sonication on juice quality while minimising the number of experiments required.     

Compression resistance,sweetener's diffusion and sweetness of hydrocolloids gels

The effects of the type and concentration of two hydrocolloids—κ-carrageenan and gellan gum—and of the type and concentration of two sweeteners—sucrose and aspartame—on the gel resistance to compression, on the sweetener diffusion and on the intensity of the gel sweetness and the relationships between the gel physical properties and their perceived sweetness were studied. The gels true rupture stress increased with hydrocolloid concentration, this increase being higher for gellan gels. Gellan gels showed lower true rupture strain values, which in contrast with carrageenan gels, decreased on increasing hydrocolloid concentration. The addition of sucrose produced a bigger increase in gel strength at the higher hydrocolloid concentration. The main effect detected on the sweeteners’ diffusion constant was the higher value observed in low concentration (3 g L⁻¹) κ-carrageenan gels. Gellan gels were perceived as sweeter than κ-carrageenan gels. The decrease in sweetness due to an increase in hydrocolloid concentration was greater in gellan than in carrageenan gels. Variations in sweetener concentration, true rupture strain, and deformability modulus values explained 93% of the variability in sweetness for gels with sucrose and 94% for gels with aspartame.     

Interactions between milk proteins and gellan gum in acidified gels

The mechanical properties, microstructure and water holding capacity of systems formed from whey protein concentrate (0–3% WPC w/w), sodium caseinate (0–2% w/w), and gellan gum (0.1–0.3% w/w) in the coil or helix conformational state (Coil/Helix), were investigated. This polymer combination resulted in bi-polymeric or tri-polymeric systems, which were slowly acidified to pH 4.0 by the addition of GDL in order to favor electrostatic protein–polysaccharide interactions. The properties of the tri-polymeric systems differed considerably from the bi-polymeric ones. At high polymer concentrations the WPC-gellan samples showed incompatibility and microphase separation, which resulted in weaker and less deformable gels. However, in systems with coil gellan the incompatibility was less intense, which was attributed to the formation of electrostatic complexes between the protein and the polysaccharide during the mixing process. In caseinate–gellan systems, complex formation was observed and an increase in the gel mechanical properties as the caseinate concentration rose, although the water holding capacity decreased at higher gellan concentrations. The caseinate–gellan coacervate was not visualized in the tri-polymeric systems and the incompatibility between the biopolymers was intensified, although the mechanical properties were considerably higher than in the bi-polymeric gels.     

Polymer and Ion Concentration Effects on Gellan Gel Strength and Strain

Failure stresses and strains were measured in compressive, tensile and torsional modes on gellan gels at four polymer (0.6–1.8% w/v) and seven Ca⁺⁺ (1.5–60 mM) concentrations. Shear stresses at failure were equal in all three testing modes and proportional to gellan content. Low calcium gels increased linearly in strength with Ca⁺⁺ concentration until it reached a level of about 0.5 calcium ions per repeat tetrasaccharide unit of gellan gum polymer. Gel strength decreased linearly with Ca⁺⁺ at higher concentrations. Low calcium gels were extensible with failure strains decreasing as the logarithm of Ca⁺⁺; whereas high calcium gels were brittle and failed at a constant strain, the value of which was twice as high in compression and torsion as in tension.     

Influence of pH and added gums on the properties of konjac flour gels

The gel strength and texture of konjac gel and mixed gels of konjac and various gums were measured after gelation at various concentrations of alkali. A selection of different alkaline reagents was used. Regardless of alkali concentration, increasing konjac levels caused a decrease in pH but an increase in hardness and strength of konjac/gellan gum mixed gels. The highest gel strength and hardness were given by mixed konjac/gellan gum gels using sodium carbonate as the gelling medium. Under similar gelling conditions, the addition of gellan gum resulted in the greatest gel hardness. Of the gums examined, a possible synergistic effect on konjac/gellan gum mixed gel texture was observed.     

Use of High-Intensity Ultrasound and UV-C Light to Inactivate Some Microorganisms in Fruit Juices

Novel technologies that involve non-thermal processes have been investigated in the last two decades as full or partial alternatives to conventional heat treatment. The main objective of this study was to evaluate the survival of single or strain cocktail of Escherichia coli, Saccharomyces cerevisiae, and a yeast cocktail in orange (pH 3.5; 9° Brix) and/or apple (pH 3.1; 12° Brix) juices and in 0.1% w/w peptone water processed by two non-thermal techniques: high-intensity ultrasound (USc) and/or short-wave ultraviolet radiation (UV-C). USc treatments (20 kHz, 95 μm-wave amplitude) were performed using a stainless steel continuous flow cell with a 13-mm probe (0.2 L/min; 40°C). The UV-C device consisted of a 90-cm long UV-C-lamp (100 W) placed inside a glass tube leaving an annular flow space (0.2 L/min; 40°C). Inoculated systems were recirculated through simultaneous or consecutive USc and UV-C devices and samples were taken at preset time intervals. Microbial populations were monitored by plate count technique. In peptone water and apple juice, UV-C radiation provoked higher E. coli ATCC 35218 inactivation than USc treatment. E. coli ATCC 35218 and its cocktail were more sensitive than S. cerevisiae KE162 and the cocktail of yeasts. UV-C efficiency was highly dependent on media nature. The poor single effect of UV-C light in orange juice was enhanced by the combination with USc. Combined treatment was more effective in simultaneous rather than in a series of USc − UV-C arrangement.     

The Impact of Thermosonication and Pulsed Electric Fields on Staphylococcus aureus Inactivation and Selected Quality Parameters in Orange Juice

The effect of thermosonication (TS) and pulsed electric fields (PEF) on inactivation of Staphylococcus aureus (SST 2.4) and selected quality aspects in orange juice was investigated. Conventional pasteurization (HTST, 94 °C for 26 s) was used as a control. TS (10 min at 55 °C) applied in combination with PEF (40 kV/cm for 150 μs) resulted in a comparable inactivation of S. aureus to that achieved by conventional HTST. TS/PEF did not affect the pH, conductivity, or °Brix and had a milder impact on the juice color than thermal treatment. Furthermore, the non-enzymatic browning index was significantly affected by HTST (P < 0.05) but not by TS and PEF. Ascorbic acid retention was almost complete after TS and PEF (96.0%), but it was substantially lower (P < 0.05) after HTST (80.5%). Residual activity of pectin methyl esterase (PME) decreased as PEF field strength and treatment time increased; however, applying TS and PEF in combination left a greater residual PME activity than HTST (12.9 vs 5.0%, respectively).     

Rheological characterization and activation energy values of binary mixtures of gellan

The present study determined the flow behavior and activation energy of high (HA) and low (LA) acyl gellan dispersions (0.2%) and their mixtures as a function of preparation temperature (25 and 90 °C) and of the presence or absence of Ca²⁺ (30 mM). Heated gellan mixtures containing calcium were acidified with δ-gluconolactone to obtain gels and determine linear viscoelasticity using the Kelvin–Voigt model. The studied dispersions showed non-Newtonian shear-thinning behavior. HA dispersions (with and without Ca²⁺) showed the highest activation energy values, 88.60 and 51.18 kJ/mol. Whereas, LA dispersions showed the lowest activation energy values, 3.73 and 9.19 kJ/mol. With respect to the rheological studies, it was observed that the relationships between HA and LA gellan did not affect the recovery percentages because similar values were obtained (86.90–90.00%), and this behavior along with the mean viscosity values obtained in the gel mixtures could indicate that the hydrogen bond formation between both gellan helix (HA, LA) is possible. These results can contribute to possible industrial applications of gellans in the development of new alimentary products.     

Extraction of capsaicinoids from chillies (Capsicum frutescens L.) and paprika (Capsicum annuum L.) using supercritical fluids and organic solvents

 Supercritical fluid extraction (SFE) with subsequent HPLC analysis was performed in order to determine the amount of capsaicinoids in paprika and chillie powder samples. The extraction yields obtained by SFE were compared to those obtained by organic solvent extraction and were found to be comparable or slightly lower. The advantages of SFE are shorter extraction times, less sample preparation needed prior to HPLC analysis and fewer interfering peaks in the chromatograms. In addition, the SFE method developed (extraction temperature=80 ^°C, density= 0.75 g/ml, modifier=20 μl water) was shown to be suitable for analysis of capsaicinoids (capsaicin, dihydrocapsaicin, nordihydrocapsaicin) that are present over a wide range of concentrations (10–1400 μg/g) in the samples. Received: 12 July 1996/Revised version: 26 August 1996     

Biogenic amines in dry sausages during shelf-life storage

 Supercritical fluid extraction (SFE) with subsequent HPLC analysis was performed in order to determine the amount of capsaicinoids in paprika and chillie powder samples. The extraction yields obtained by SFE were compared to those obtained by organic solvent extraction and were found to be comparable or slightly lower. The advantages of SFE are shorter extraction times, less sample preparation needed prior to HPLC analysis and fewer interfering peaks in the chromatograms. In addition, the SFE method developed (extraction temperature=80 ^°C, density= 0.75 g/ml, modifier=20 μl water) was shown to be suitable for analysis of capsaicinoids (capsaicin, dihydrocapsaicin, nordihydrocapsaicin) that are present over a wide range of concentrations (10–1400 μg/g) in the samples. Received: 12 July 1996/Revised version: 26 August 1996     

Ultraviolet Treatment of Orange Juice to Inactivate <Emphasis Type="Italic">E. coli</Emphasis> O157:H7 as Affected by Native Microflora

The effect of yeast concentration on ultraviolet (UV) inactivation of five strains of Escherichia coli O157:H7 from different sources, inoculated both individually and simultaneously in orange juice, was analyzed and mathematically modeled. The presence of yeast cells in orange juice decreases the performance of UV radiation on E. coli inactivation. UV absorption coefficients in the juice increased with increasing yeast concentration, and higher UV doses were necessary to inactivate bacterial strains. UV intensities of I = 3.00 ± 0.3 mW/cm² and exposure times (t) between 0 and 10 min were applied; radiation doses (energy, E = I × t) ranging between 0 and 2 J/cm² were measured using a UV digital radiometer. All the tested individual strains showed higher resistance to the treatment when UV radiation was applied at 4 °C in comparison to 20 °C. UV inactivation of E. coli O157:H7 individual strain was satisfactory fitted with a first order kinetic model. A linear relationship was found between UV absorptivities and D values (radiation doses required to decrease microbial population by 90%) for each strain. The dose required to reach 5-log reduction for the most unfavorable conditions that is the most UV resistant strain, and maximum background yeast concentration was 2.19 J/cm² at 4 °C (corresponding to 11 min of UV treatment) and 2.09 J/cm² at 20 °C (corresponding to 10.55 min of UV treatment). When a cocktail of strains was inoculated in orange juice, the logistic equation was the best model that fits the experimental results due to the deviation from the log-linear kinetics. The UV resistance between strain cocktail and single strain were mathematically compared. Slopes of the decline curves for strain cocktail at high UV doses were lower than the slopes of the log-linear equation calculated for the individual strains, even for the most resistant one. Therefore, microbial inactivation tests using a cocktail of strains are particularly important to determine the performance of the UV inactivation treatment.     

The effects of fermentation on the thermostability of the yellow-orange pigments extracted from cactus pear (Opuntia ficus-indica)

 Cactus pear (Opuntia ficus-indica) juice with a total soluble solids content of 15.94 °Brix was fermented using the wine yeast Saccharomyces cerevisiae. A 94.54% conversion of fermentable sugar was achieved with an ethanol production of 55.3 ml/l. The pigment degradation was found to be 17% at the end of the time allowed for fermentation. However, the fermentation had actually ceased due to depletion of fermentable sugars after 12 h, a point at which only 9.4% pigment degradation was observed and there was no further total soluble solids degradation. The thermal stability of the yellow-orange pigment of the fermented juice was determined as a function of temperature at pH 5.0. The kinetic experiments were carried out at three different temperatures, 50, 70 and 90  °C. For a pseudo-first order thermal degradation rate the reaction rate constants were determined to be 0.0066, 0.0206 and 0.1244 min^–1 for temperatures of 50, 75 and 90  °C, respectively. The activation energy was calculated as 15.71 kcal mole^–1. The fermentation process did not affect the thermostability of the pigment extract. Received: 10 January 2000 / Revised version: 31 March 2000     

Viscosity of guar gum and xanthan/guar gum mixture solutions

The viscosity of diluted guar gum solutions and the viscosity of xanthan and guar gum mixture solutions have been studied. Guar gum solutions showed pseudoplastic behaviour. Apparent viscosity increased with gum concentration and decreased with the temperature at which viscosity was measured. A maximum in the plot of viscosity versus increasing dissolution temperature was observed at 60 °C. This behaviour was related to differences in molecular structure of the polymers solved at different temperatures. Mixtures of xanthan and guar gum showed a higher combined viscosity than that occurring in each separate gum. This synergistic interaction was affected by the gum ratio in the mixture and dissolution temperature of both gums. The effect of polysaccharide concentration (1.0, 1.5 and 2.0 kg m⁻³), xanthan/guar gum ratio (1/5, 4/2, 3/3, 4/2 and 5/1) and dissolution temperature (25, 40, 60 and 80 °C for both gums) on the viscosity of solutions of mixtures were studied. The highest viscosities were observed when 2.0 kg m⁻³ gum concentration was used together with a ratio of xanthan/guar gum of 3/3 (w/w) and dissolution temperature of 40 and 80 °C for xanthan and guar gum, respectively. © 2000 Society of Chemical Industry     

Maltase activity and dough rising ability of baker’s yeasts obtained at different growth conditions during the maturation stage

 The effects of temperature, pH and dissolved oxygen (DO) at the final production stage on the quality of baker’s yeast were studied. It was noted that an increase of temperature above 37 °C worsened dough-rising ability; nevertheless, at the same time, a good value of maltase activity – 26.0 nmol⋅min^-1⋅mg^-1 was found. Dough-rising ability and maltase activity are strongly influenced by pH. The highest maltase activity, 68 nmol⋅min^-1⋅mg^-1, was obtained at pH 6.0, which improves the dough-rising ability to 55 cm³ CO₂. The concentration of DO affects the fermentation activity of the strain Saccharomyces cerevisiae 3: the metabolism became oxido-fermentative at less than 40% DO and maltase activity and dough-rising ability increased up to 43.5 nmol⋅min^-1⋅mg^-1 and 56 cm³, respectively. The results indicate that dough-rising ability and maltase activity increased as the temperature increased, and as the concentration of DO decreased. A direct correlation between maltase activity and dough-rising ability was found. Received: 24 October 1996     

Determination of Free Arginine, Glutamine, and β-alanine in Nutritional Products and Dietary Supplements

A method for the determination of free arginine, glutamine, and β-alanine in nutritional products and dietary supplements is described. The amino acids are derivatized with the fluorescent tag 9-fluorenylmethoxycarbonyl (FMOC), and the derivatives are then determined by reversed phase HPLC. Method suitability was defined by experimental assessments of linearity (R ² > 0.999), precision (day-to-day RSD ≤ 1.0%), accuracy (spike recoveries=98.7%–101.8%, n = 18), and selectivity (baseline resolution from the other common amino acids). The method provides for an accurate and precise quantification of the three amino acids, when present at concentrations >0.2% (w/w) in nutritional products and dietary supplements. Assessments of free l-glutamine stability in three different reconstituted powder products, as performed by the method, found recoveries >97% through 24 h at room temperature.