Variation of composition and functional properties of gum from six Canadian flaxseed (Linum usitatissimum L.) cultivars

Flaxseed gum (FG) was prepared from six Canadian flaxseed (Linum usitatissimum L.) cultivars. Yield, neutral sugar content, acidic sugar content and protein content varied significantly among cultivar FG extracts. Zeta potential (?16.4 to ?27.4 mV) and rheological properties of solution were cultivar dependent. Solutions prepared with CDC Glas FG had the highest viscosity (2.984 Pa?s), while CDC Sorrel produced the lowest (0.048 Pa?s). FG solutions exhibited pseudoplastic shear‐thinning behaviour. Viscosity of FG solution increased with concentration, while viscosity and pseudoplasticity decreased with increased temperature. NaCl addition decreased solution viscosity while adding sucrose increased viscosity. FG solutions prepared from Flanders and CDC Sorrel had the highest and lowest emulsion activity index, respectively, while solutions of CDC Arras and CDC Bethune FG had the lowest and highest emulsion stability, respectively. Findings presented here provide information that could enable greater utilisation in food, cosmetic and pharmaceutical industries as thickeners and/or emulsifiers.     

Fractionation and physicochemical characterization of peach gum polysaccharides

One kind of Chinese peach gum was fractionated by different solvent extraction (water followed by alkaline solutions). Chemical analysis showed peach gum polysaccharides were acidic arabinogalactans, mainly composed of arabinose (∼50%), galactose (∼37%) and uronic acid (13–14%), with the molecular weight of ∼4.60 × 10⁶ g/mol according to high performance size exclusion chromatography (HPSEC) analysis. Peach gum solution exhibited typical shear thinning flow behavior properties, K (consistency index) values increased while n (flow index) values decreased with the increasing of concentration. Dynamic sweep tests showed that moduli of peach gum solutions were highly dependent on frequency, concentration and temperature. Water extractable fraction was able to form gel network when concentration was higher than 4%. Alkaline extracted peach gum gave weaker rheological responses, such as lower viscosity at same concentration when compared to the water extractable fraction. Two alkaline extractable fractions exhibited similar intrinsic viscosities of 21.18 dl/g (0.1 M NaOH extractable, AE01) and 21.76 dl/g (0.5 M NaOH extractable, AE05), respectively, while water extractable fraction (WE) formed aggregate in water at low concentration. All fractions extracted from peach gum exudates showed better emulsion capacity and stability than gum arabic and fenugreek, which could be used in food industry to replace or partially replace gum arabic.     

Influence of selected hydrocolloids on triticale starch rheological properties

The aim of the study was to define the influence of selected nonstarch polysaccharides (guar gum, xanthan gum and arabic gum) on several rheological properties of triticale starch pastes/gels, at constant polysaccharide concentration (6.5 g/100 g). These included pasting characteristics, flow curves at 50 °C and mechanical spectra at 25 °C. It was found that the presence of a gum in a system modified the rheological properties of triticale starch gels/pastes, depending on the type and concentration of the gums. In the case of guar and xanthan gums, higher pasting viscosity was observed and the shear stress was increased compared with native starch. The presence of guar gum reduced the degree of thixotropy hysteresis, negative values for this being found for systems with xanthan in spite of their shear‐thinning behaviour. Systems containing arabic gum displayed lower values of pasting and flow viscosity. The type and concentration of gums added to the polysaccharide influenced the viscoelastic properties of the gels.     

Rheological properties of whey protein isolate stabilized emulsions with pectin and guar gum

Dynamic oscillatory and steady-shear rheological tests were carried out to evaluate the rheological properties of whey protein isolate (WPI) stabilized emulsions with and without hydrocolloids (pectin and guar gum) at pH 7.0. Viscosity and also consistency index of emulsions increased with hydrocolloid concentration. At γ = 20 s⁻¹, the value of viscosity of the emulsion with 0.5% (w/v) pectin was about fivefold higher than that of the emulsion without pectin. Flow curves were analyzed using power law model through a fitting procedure. Flow behaviour index of all emulsions except for containing 0.5% (w/v) guar gum was approximately in the range of 0.9–1.0, which corresponds to near-Newtonian behaviour. The shear thinning behaviour of emulsions containing 0.5% (w/w) guar gum was confirmed by flow behaviour index, n, of 0.396. Both storage (G′) and loss modulus (G″) increased with an increase in frequency. Emulsions behaved like a liquid with G″ > G′ at lower frequencies; and like an elastic solid with G′ > G″ at higher frequencies. Effect of guar gum was more pronounced on dynamic properties. Phase angle values decreased from 89 to <10° with increasing frequency and indicated the viscoelasticity of WPI-stabilized emulsions with and without pectin/guar gum.     

A comparative study on viscosity behavior of water‐soluble chemically modified guar gum derivatives with different functional lateral groups

A comparative study was carried out on the viscosity behavior of three new water‐soluble chemically modified guar gum derivatives with different functional lateral groups, including O‐carboxymethyl‐O‐hydroxypropyl guar gum (CMHPG), with anionic character, O‐2‐hydroxy‐3‐(trimethylammonio)propyl guar gum (HTPG), with cationic character, and O‐carboxymethyl‐O‐2‐hydroxy‐3‐(trimethylammonio)propyl guar (CMHTPG), with amphoteric character. It was found that the shear rate, concentration, temperature, added salt and surfactant affected the viscosity properties of these new guar gum derivatives in aqueous solutions. Regardless of the functional lateral groups, all sample solutions behaved as non‐Newtonian shear‐thinning fluids, and their viscosity increased with the increase in their concentration but decreased with the increase in temperature. Aqueous CMHTPG solution had the strongest shear‐thinning property, and aqueous CMHPG solution investigated had the greatest viscous flow activation energy. In contrast to cationic HTPG or anionic CMHPG, amphoteric CMHTPG had an enhanced viscosity property in aqueous salt solutions, exhibiting an unusual anti‐polyelectrolyte viscosity behavior. The addition of sodium dodecylsulfate was found to result in a decrease in the viscosity of aqueous HTPG solution and an increase in the viscosity of aqueous CMHPG solution or CMHTPG solution. Copyright © 2005 Society of Chemical Industry     

Steady and dynamic shear rheological properties of extrusion modified fenugreek gum solutions

This study investigated the rheological properties of extrusion modified fenugreek gum solutions (0.5, 1.0, 1.5, and 2.0%, w/v) under steady and dynamic shear conditions. Fenugreek gum was extruded in a twin-screw extruder without an exit die to minimize a decrease in molecular weight of fenugreek gum during extrusion process. Both of the steady and dynamic shear rheological tests revealed that extrusion process did not substantially influence the steady and dynamic shear properties of the gum. The power law model was applied to describe the flow behavior of the extruded gum solutions. The extrusion modified fenugreek gum solutions exhibited a shearthinning flow behavior at 25°C, and the values of consistency index (K) and apparent viscosity (η_a,100) increased with an increase in the gum concentration. The magnitudes of storage modulus (G′) and loss modulus (G″) for the extrusion modified fenugreek gum solutions increased with increasing frequency (ω) and with increasing gum concentration.     

Rheological properties and gel strength of Phaseolus lunatus protein/carboxymethylated flamboyant gum systems

The rheological behaviour and gel strength of hydrocolloid mixture systems (HMSs) of carboxymethylated flamboyant gum (CFG) with protein hydrolysates (PHs) of Phaseolus lunatus were examined to evaluate the influence of the protein/polysaccharide ratio (2:1 and 3:1), pH (3 and 9) and concentration of solids, according to a 2³ factorial design. The protein concentrate of P. lunatus was hydrolysed with pepsin–pancreatin enzymes. The flow curve results were fitted to the Ostwald–de Waele model. The flow behaviour index (0.66–0.78) for all conditions studied was indicative of the shear‐thinning behaviour. For the HMS, the consistency index (k) values ranged from 0.4 Pa sⁿ to 1.2 Pa sⁿ. The analyses of variance showed that the ratio of PH/CFG and pH were the main variables that had significant effect on k values (P < 0.05). Only PH system presented a weak gel‐like viscoelastic behaviour. Both functional properties were affected by the protein degree of hydrolysis (DH).     

Effect of gum arabic on the surface tension and surface dilational rheology of trisiloxane surfactant

The surface tension and surface dilational properties of trisiloxane surfactant silwet408, gum arabic, and their mixed solutions are reported. The dilational rheological properties are measured by means of oscillating drop method. The influences of dilational frequency, bulk concentration and aging time on dilational rheology properties have been investigated. The adsorption films of silwet408 behave elastic in nature at low bulk concentration. With increasing concentration, the dilational modulus becomes more frequency dependent and reaches a maximum value. The addition of 1 wt% gum arabic has no remarkable influence on the silwet408 films since the adsorption ability of silwet408 is much better than that of gum arabic. However, the maximum of dilational modulus and dilational elasticity are shifted toward a higher concentration, which has been correlated with the decreased molecular exchange in the presence of 1 wt% gum arabic.     

Gelatinization and retrogradation characteristics of wheat (Rosella) starch

The non-Newtonian behavior and elastic modulus of wheat (Rosella) starch solutions after preparation, and storage at 25 °C and 4 °C for 24 h were measured with a rheogoniometer. The flow curves of wheat starch showed plastic behavior above 4.0% solution. After storage at 4 °C in 4.0% solution, elastic modulus increased at low temperature and showed a constant value with increase in temperature. Elastic modulus increased upon addition of urea (4.0 M) at low temperature and remained constant up to 60 °C. Elastic modulus of Rosella also increased in 0.05 M NaOH solution after storage. Rheological characteristics of Rosella starch differed from those of rice starches. This might be caused by difference in structure of amylopectin and large amount of amylose content on starch.     

The influence of flaxseed gum on the retrogradation of maize starch

The influence of flaxseed gum (FG) on the retrogradation of maize starch (MS) was investigated in this study. Based on the results of rapid visco‐analyzer (RVA), differential scanning calorimetry (DSC), X‐ray diffraction (XRD), Low field nuclear magnetic resonance (LF‐NMR) and scanning electron microscopy (SEM), FG has a retardation effect on the retrogradation of MS. With the addition increasing, the more significant the retardation effect was observed (P < 0.05). However, when the concentration of FG was up to 0.4%, the change of retrogradation ratio showed no significant difference (P > 0.05). FG could wrap around starch granules, suppress the recrystallisation of amylose and amylopectin, increase the water mobility and decrease the water loss. In summary, the overall results suggested that FG could be used as a natural inhibitor of the retrogradation of starch in food industry.     

Viscosity of solutions of xanthan/locust bean gum mixtures

Xanthan and locust bean gums are polysaccharides able to produce aqueous solutions with high viscosity and non‐Newtonian behaviour. When these solutions are mixed a dramatic increase on viscosity is observed, much greater than the combined viscosity of the separated polysaccharide solutions. In this work the influences of different variables on the viscosity of solutions of mixtures of xanthan/locust bean gum have been studied. Total polysaccharide concentration, xanthan and locust bean ratio on mixture and temperature at which the gum was dissolved (dissolution temperature) for both xanthan and locust bean gums have been considered. Under these different operational mixture conditions shear rate and time have also been considered to describe the rheological behaviour of the solutions studied. The high viscosity increase observed in these mixtures is due to the interaction between xanthan gum and locust bean gum molecules. This interaction takes place between the side chains of xanthan and the backbone of the locust bean gum. Both xanthan molecule conformation in solution – tertiary structure – and locust bean gum structure show great influence on the final viscosity of the solution mixtures. Xanthan conformation changes with temperature, going from ordered structures to disordered or chaotic ones. Locust bean gum composition changes with dissolution temperature, showing a dissolved galactose/mannose ratio reduction when temperature increases, ie the smooth regions – zones without galactose radicals – are predominantly dissolved. The highest viscosity was obtained for the solution mixture with a total polysaccharide concentration of 1.5 kg m⁻³ and a xanthan/locust ratio of 2:4 (w/w) and when xanthan gum and locust bean gum were dissolved at 40°C and 80°C, respectively. © 1999 Society of Chemical Industry     

Influence of various levels of flaxseed gum addition on the water-holding capacities of heat-induced porcine myofibrillar protein

Abstract: As a food hydrocolloid, flaxseed gum (FG) can significantly increase the water‐holding capacity (WHC) of food, which is important to both yield and texture of related products. The main purpose of this study is to examine the WHC increase by FG in a meat product and the mechanism of the interactions between proteins and polysaccharides when FG is added into porcine myofibrillar protein (PMP). Increasing the FG concentration caused a significant increase in WHC (P < 0.001). Scanning electron micrographs (SEM) showed that WHC in the protein gel network was related to gel microstructure. Distributed analysis of the T₂ relaxation revealed that addition of FG significantly decreased water mobility of porcine myofibrillar protein (PMP) (P < 0.05). The Fourier transform infrared spectroscopy (FT‐IR) analysis suggested that the FG adding strengthened electrostatic attraction of PMP system. Improvement of WHC in heat‐induced PMP by FG is concentration dependent and achieved by a finer gel network, lower relaxation time, and stronger electrostatic attraction. Practical Application: Flaxseed gum (FG) addition significantly increased water holding capacity (WHC) of porcine myofibrillar protein (PMP). In addition, the improvement of WHC in heat‐induced PMP by FG was concentration dependent and achieved by a finer gel network, lower relaxation time, and stronger electrostatic attraction. Thus, FG has potential for use in meat products.     

Study on retrogradation of maize starch–flaxseed gum mixture under various storage temperatures

This study aimed to investigate the effect of flaxseed gum (FG) on the retrogradation of maize starch (MS) gels under different storage temperatures. In this work, MS‐FG gels with 0–0.4% FG were stored under different temperatures (–20, 4 and 20 °C). Under all storage temperatures, the addition of FG inhibited the retrogradation process of MS, suppressed the recrystallisation of starch molecules, reduced the water loss of starch gels and improved the texture of the gels. Among the three storage temperatures, ?20 °C could almost stop the starch retrogradation but leading it results in the hardest gel texture. The retrogradation of MS‐FG gels stored under 4 °C was most serious with the fastest rate of recrystallisation. When stored at 20 °C, the gels had a retrogradation degree that was lower than when they were stored at 4 °C and also had the softest texture.     

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     

Effects of some anionic polysaccharides on the gelatinization and retrogradation behaviors of wheat starch: Soybean-soluble polysaccharide and gum arabic

Gelatinization and retrogradation behaviors of wheat starch were investigated in an aqueous system in the presence or absence of some anionic polysaccharides, soybean-soluble polysaccharide (SSPS), and gum arabic (GA). Weight-average molecular weight was almost equivalent between SSPS and GA, while z-average root-mean-square radius of gyration of GA was ca. twice as large as that of SSPS. The addition of each polysaccharide (0.1–1 w/v%) decreased the peak viscosity of the composite system (starch concentration: 5% or 13%) during gelatinization, and this effect of SSPS was greater than that of GA at the higher starch concentration. It also shifted the onset of viscosity increase to lower temperatures at the higher starch concentration, but no difference was seen in this effect between SSPS and GA. The addition of each polysaccharide (0.1–1%) decreased the amount of amylose leached during gelatinization, and this effect of SSPS was generally greater than that of GA. It hardly altered, on the other hand, the average particle diameter of the starch granules after gelatinization. “Starch ghosts” were less frequently observed microscopically in the presence of each polysaccharide, which appeared to exist around the surface of the starch granules to inhibit amylose leaching. The addition of each polysaccharide (0.5%) increased the rate constants, representing short-term (24 h) retrogradation of starch (5%). It also decreased the saturated dynamic storage modulus of the composite system after storage at 4 °C for 24 h, and this effect of SSPS was greater than that of GA with larger amount of syneresis generated. The results were discussed mainly in relation to the phase arrangement between starch components and each polysaccharide.     

Effects of pectin and guar gum on creaming stability, microstructure and rheology of egg yolk plasma-stabilized emulsions

The influence of pectin and guar gum on the creaming stability, microstructure and rheological properties of 1.0% (w/v) egg yolk plasma (EYP)-stabilized 25.0% (v/v) soybean oil-in-water emulsions was studied at pH 7.0. Addition of pectin/guar gum decreased creaming percentage, and no creaming was detected in the presence of 0.5% (w/v) pectin/guar gum as a result of increasing viscosity. At the end of 10 h, creaming percentage decreased from 61 to 57% with the addition of 0.05% (w/v) guar gum and to 39% with the addition of 0.2% (w/v) guar gum. Microscopic observations represented the droplet aggregation arising from the presence of nonabsorbing biopolymers. At \mathop g^. \mathop \gamma \limits^{.}  = 10 s⁻¹, a tenfold increase in viscosity was observed in the presence of 0.5% (w/v) guar gum compared to the presence of 0.1% guar gum due to the thickening effect of polysaccharide. Increasing gum concentrations enhanced the viscosity and hence the consistency index. All emulsions, except for those containing 0.5% (w/v) guar gum, reflect the near-Newtonian behaviour with flow behaviour index, n, of 0.9–1.0. All emulsions exhibited a liquid-like behaviour at low frequencies (<7.0 Hz) where G″ values were higher than G′. Both G′ and G″ showed a frequency dependency and these two moduli crossed each other at higher frequencies (>7.0 Hz), G′ became greater than G″ and the system behaved like an elastic solid. Addition of pectin at all levels cause no significant change in G′ and G″ values, whereas addition of guar gum, especially at a concentration of 0.5% (w/v), significantly improved these values.     

Steady and Dynamic Shear Rheology of Rice Starch‐Galactomannan Mixtures

Rheological properties of rice starch‐galactomannan mixtures (5%, w/w) at different concentrations (0, 0.2, 0.4, 0.6 and 0.8%, w/w) of guar gum and locust bean gum (LBG) were investigated in steady and dynamic shear. Rice starch‐galactomannan mixtures showed high shear‐thinning flow behaviors with high Casson yield stress. Consistency index (K), apparent viscosity (η_a,100) and yield stress (σ_oc) increased with the increase in gum concentration. Over the temperature range of 20–65°C, the effect of temperature on apparent viscosity (η_a,100) was described by the Arrhenius equation. The activation energy values (E_a = 4.82–9.48 kJ/mol) of rice starch‐galactomannan mixtures (0.2–0.8% gum concentration) were much lower than that (E_a = 12.8 kJ/mol) of rice starch dispersion with no added gum. E_a values of rice starch‐LBG mixtures were lower in comparison to rice starch‐guar gum mixtures. Storage (G′) and loss (G′′) moduli of rice starch‐galactomannan mixtures increased with the increase in frequency (ω), while complex viscosity (η*) decreased. The magnitudes of G′ and G′′ increased with the increase in gum concentration. Dynamic rheological data of ln (G′, G′′) versus ln frequency (ω) of rice starch‐galactomannan mixtures have positive slopes with G′ greater than G′′ over most of the frequency range, indicating that their dynamic rheological behavior seems to be a weak gel‐like behavior.     

Rheological behaviour of tamarind seed gum in aqueous solutions

Tamarind seed gum as seed polysaccharide from Tamarindus indica L. has been characterized for physicochemical and rheological properties in the present work. The structural analysis determined the presence of glucose:xylose:galactose in a molar ratio of 2.61:1.43:1.The Huggins and Kraemer plots obtained by capillary viscometry gave an intrinsic viscosity of 4.7 dl g⁻¹ and the viscosity average molecular mass was calculated to be 9.18 × 10⁵ g mol⁻¹ using the Mark-Houwink relationship. The steady shear and dynamic viscoelasticity properties of tamarind seed gum in aqueous solutions at different concentrations were investigated at 20 °C using a Haake Rheometer RS75. The tamarind seed gum solutions clearly exhibited shear-thinning flow behaviour at high shear rate and Newtonian region occurred at low shear rate range, however, at higher concentrations, pronounced shear thinning was observed. The value of zero shear viscosity (η₀) was estimated by fitting Cross and Carreau models. The specific viscosity at zero shear rate (η_sp0) was plotted against the coil overlap parameter (C[η]) and the slopes of the lines in the dilute and semi-dilute regions were found to be ∼2.2 and 4.3, respectively. The value of the critical concentration (C^∗) was about 4.23/[η]. While, the mechanical spectra in the linear viscoelastic region of tamarind seed gum solutions showed the typical shape for macromolecular solutions. Plots of η versus γ and η^∗ versus ω were superimposable and hence obey the Cox-Merz rule.     

Complex coacervates obtained from interaction egg yolk lipoprotein and polysaccharides

Protein–polysaccharide coacervates formation was evaluated under influence of pH (3.0, 4.0, 6.5, 8.5 and 10.0), temperature (10, 20, 30, 40 and 50 °C) and polysaccharide mass (0.025, 0.033 and 0.050 g). It was possible to observe that solutions with lower turbidity values were found in pH band 3.0 to 4.0. Statistical analysis of turbidity data have shown that for all polymers pH was meaningful in coacervate formation, although for some, besides pH, temperature and polymer concentration could also influence significantly (p < 0,05) in coacervate formation. Encapsulates morphology made by coacervation was directly linked to the kind of polymer used and its interactional degree. Dehydrated coacervates have presented heterogeneous morphology, different from their original structures.     

Extraction and physicochemical characterisation of polysaccharide gum from Yanang (Tiliacora triandra) leaves

Yanang (Tiliacora triandra) is a vegetable used in many cuisines of the northeast of Thailand and Lao People’s Democratic Republic. This paper reports the optimised extraction and some physicochemical characteristics of polysaccharide gum from Yanang leaves. The optimised extraction condition was at the leaf:water ratio of 1:6.6, 85 °C, and 100 min extraction time. The major monosaccharide constituent of Yanang gum was xylose, together with substantial amounts of other neutral sugars. The FT-IR spectra of Yanang gum were similar to that of xylan. Yanang gum exhibited shear-thinning flow behaviour and the extent of shear-thinning was concentration dependent. The mechanical spectra of Yanang gum at low concentration (0.5%) were typical of semi-diluted to concentrated solutions. However, with increasing concentration, the solution behaved like a weak gel.