High pressure pre-treatment of Moringa oleifera seed kernels prior to aqueous enzymatic oil extraction

High pressure processing (HPP) was applied as a pre-treatment on Moringa oleifera (MO) kernels, for the first time, prior to aqueous enzymatic extraction (AEE) of the MO oil, and the effect of this pre-treatment is reported in terms of the free oil recovery and the nature of the cream emulsions formed. The HPP pre-treatments (50–250 MPa, 20–60 °C, 10–60 min) generally resulted in higher free oil recoveries and thinner emulsion layers from ground-sieved kernels than the whole kernels. Optimization of the HPP parameters indicated linear increment in free oil recovery with increase in temperature and time, but not the pressure level. Without the pre-boiling step in the AEE process, the use of HPP pre-treatment at 50 MPa and 60 °C for 35 min resulted in approximately 73% (w/w) free oil recovery with thinner emulsion layer than the use of AEE alone. These findings highlighted the ability of HPP in altering the MO protein structure into a form of less emulsifying functional properties, thus further de-emulsification method may not be necessary.Industrial relevanceHigh pressure processing (HPP) applications are increasing in the food industry. High pressure application allows the use of relatively lower temperatures in processes, in order to achieve comparable outcomes of higher temperature processing. This study explores the application of HPP on Moringa oleifera (MO) kernels prior to aqueous enzymatic extraction (AEE) of oil. In general, the main disadvantage of AEE is its lower oil recovery in comparison with solvent extraction, which is attributed to the formation of a relatively stable cream emulsion after extraction. This study shows that the thickness of the creamy emulsion can be significantly reduced, and oil recoveries improved, by subjecting the kernels to HPP prior to extraction. The improvement in recoveries did not depend strongly on the level of high pressure applied, but downstream processes for free oil separation and recovery were considerably simplified.     

Chemical,functional and nutritional properties of wet dehulled niger (Guizotia abyssinica Cass.) seed flour

Niger seeds were dehulled using hot lye treatment. Dehulling of niger seeds increased the protein and fat contents from 24 to 35 and 31–53 g/100 g and decreased the crude fiber from 16.9 to 2.2 g/100 g, respectively. The defatted flour prepared from dehulled niger seeds was evaluated for chemical, functional and nutritional properties and compared to the undehulled flour. The protein content of the dehulled flour increased from 44 to 63 g/100 g. Dehulling resulted in inactivation of trypsin inhibitor activity. The dehulled flour had higher water and fat absorption capacities. However, the nitrogen solubility, emulsification capacity and foaming properties decreased. Chemical score of the dehulled flour was higher; threonine was the first limiting amino acid followed by lysine and isolecuine. The in vitro digestibility of the protein increased due to dehulling (85.5%) compared to that of undehulled flour (76%). The calculated nutritional indices, essential amino acid index, biological value, nutritional index and C-PER, were higher in dehulled flour compared to undehulled flour. The available lysine content appeared to be unchanged.     

Optimization of the enzymatic treatment during aqueous oil extraction from sunflower seeds

Partially dehulled sunflower seeds were subjected to a hydrolytic treatment with cellulases during aqueous processing for oil and protein extraction. Sub-optimal extraction conditions (particle size and separation technology) were established in order to appreciate the potential improvement caused by the enzymatic treatment and to select the best operational conditions. The effects of three operational variables (extraction–treatment time, water/seeds ratio and enzyme/seed ratio) were studied on three objective functions (the extent of hydrolysis reaction, the oil extraction yield and the percent polyphenolics removal). After 2 h of enzymatic treatment–extraction a practical optimum in the range 7.5–8 g water g⁻¹ seeds and 1.25–1.4 g enzyme 100 g⁻¹ seeds could be defined. Under these conditions the oil extractability and the polyphenolics removal are improved by more than 30 and 80%, respectively.     

Cross-linking proteins by laccase: Effects on the droplet size and rheology of emulsions stabilized by sodium caseinate

The aim of this work was to evaluate the influence of laccase and ferulic acid on the characteristics of oil-in-water emulsions stabilized by sodium caseinate at different pH (3, 5 and 7). Emulsions were prepared by high pressure homogenization of soybean oil with sodium caseinate solution containing varied concentrations of laccase (0, 1 and 5 mg/mL) and ferulic acid (5 and 10 mM). Laccase treatment and pH exerted a strong influence on the properties with a consequent effect on stability, structure and rheology of emulsions stabilized by Na-caseinate. At pH 7, O/W emulsions were kinetically stable due to the negative protein charge which enabled electrostatic repulsion between oil droplets resulting in an emulsion with small droplet size, low viscosity, pseudoplasticity and viscoelastic properties. The laccase treatment led to emulsions showing shear-thinning behavior as a result of a more structured system. O/W emulsions at pH 5 and 3 showed phase separation due to the proximity to protein pI, but the laccase treatment improved their stability of emulsions especially at pH 3. At pH 3, the addition of ferulic acid and laccase produced emulsions with larger droplet size but with narrower droplet size distribution, increased viscosity, pseudoplasticity and viscoelastic properties (gel-like behavior). Comparing laccase treatments, the combined addition of laccase and ferulic acid generally produced emulsions with lower stability (pH 5), larger droplet size (pH 3, 5 and 7) and higher pseudoplasticity (pH 5 and 7) than emulsion with only ferulic acid. The results suggested that the cross-linking of proteins by laccase and ferulic acid improved protein emulsifying properties by changing functional mechanisms of the protein on emulsion structure and rheology, showing that sodium caseinate can be successfully used in acid products when treated with laccase.     

The increased viability of probiotic Lactobacillus salivarius NRRL B-30514 encapsulated in emulsions with multiple lipid-protein-pectin layers

Probiotics have demonstrated various health benefits but have poor stability to sustain food processing and storage conditions, as well as after ingestion. Biopolymer beads are commonly studied to encapsulate probiotic cells to improve their stability, but the millimeter-dimension of these beads may not meet the quality requirement of food products. The aim of this study was to enhance the viability of Lactobacillus salivarius NRRL B-30514 by encapsulation in emulsion droplets with multiple lipid-protein-pectin layers. Spray-dried L. salivarius was suspended in melted anhydrous milk fat that was then emulsified in a neutral aqueous phase with whey protein isolate or sodium caseinate to prepare primary solid/oil/water (S/O/W) emulsions. Subsequently, pectin was electrostatically deposited onto the droplet surface at pH 3.0 to form secondary emulsions. The encapsulation efficiency was up to 90%. After 20-day storage at 4 °C, the viable cell counts of bacteria in secondary emulsions at pH 3.0 and primary emulsions at 7.0 were 3 log higher than the respective free cell controls. After heating at 63 °C for 30 min, free L. salivarius was inactivated to be undetectable, while about 2.0 log CFU/mL was observed for primary (at pH 7.0) and secondary (at pH 3.0) emulsion treatments. Additionally, a 5 log-CFU/g-powder reduction was observed after spray drying free L. salivarius, while a 2 log CFU/g reduction was observed for emulsion treatments with capsules smaller than 20 μm. Furthermore, cross-linking the secondary emulsion with calcium enhanced the viability of L. salivarius after the simulated gastric and intestinal digestions. Therefore, the studied S/O/W emulsion systems may be used to improve the viability of probiotics during processing, storage, and gastrointestinal digestion.     

Influence of emulsifier type on in vitro digestibility of lipid droplets by pancreatic lipase

The objective of this study was to investigate the influence of interfacial composition on the in vitro digestion of emulsified lipids coated by various emulsifiers by pancreatic lipase. Sodium caseinate, whey protein isolate (WPI), lecithin and Tween 20 were used to prepare corn oil-in-water emulsions (3 wt% oil). Pancreatic lipase (1.6 mg/mL) and/or bile extract (5.0 mg/mL) were added to each emulsion and the particle charge, droplet aggregation, microstructure and free fatty acids released were measured. In the absence of bile extract, the amount of free fatty acids released per unit volume of emulsion was much lower for lipid droplets coated by Tween 20 (13 ± 16 μmol ml⁻¹) than those coated by lecithin (75 ± 20 μmol ml⁻¹), sodium caseinate (220 ± 24 μmol ml⁻¹) or WPI (212 ± 6 μmol ml⁻¹). In the presence of bile extract, there was an appreciable increase in the amount of free fatty acids released in all the emulsions, with the most appreciable effects being observed in the Tween 20-stabilized emulsions. The stability of the emulsions to droplet flocculation and coalescence during hydrolysis was also strongly dependent on emulsifier type, with the WPI emulsions being the least stable and the Tween 20 emulsions being the most stable. Our results suggest that the access of pancreatic lipase to emulsified fats decreases in the following order: proteins (caseinate and WPI) > phospholipids (lecithin) > non-ionic surfactants (Tween 20). These results may have important consequences for the design of foods with either increased or decreased lipid bioavailability.     

Stability and release properties of double-emulsions stabilised by caseinate–dextran conjugates

The subject of the present paper was to investigate the possibility of stabilising water-in-oil-in-water emulsions (W/O/W) by using sodium caseinate (SC)–dextran (Dex) conjugates in order to influence the release of vitamin B₁₂ from the inner water phase (W₁) to the outer aqueous phase (W₂).To prepare the conjugate the SC was combined with Dex (M_r 250,000 or 500,000 g/mol) and incubated at 60 °C and a humidity of 79% for 8 h.The double emulsions, with encapsulated vitamin B₁₂, were prepared using a two-step emulsification technique. Whereas different amounts of polyglycerin polyricinoleate (PGPR, E476) were the hydrophobic emulsifier, the conjugate and the SC alone were used as the hydrophilic emulsifiers. The investigations comprised the determination of the particle size distribution of the W/O/W emulsion and measurement of the amount of vitamin B₁₂ migration from W₁- to the W₂-phase during the second stage of emulsion preparation and after heating or pH changing of emulsion.The water-containing oil droplets of the W/O/W emulsions were smaller and distributed more narrowly using SC–Dex conjugate as emulsifier instead of pure protein. Under acidic conditions, the conjugate-containing emulsions were more coalescence stable than the emulsions with SC, and the vitamin B₁₂ release from the inner W₁-phase was significantly decreased.     

Physical stability of emulsion encapsulated in alginate microgel particles by the impinging aerosol technique

Emulsion filled alginate microgel particles can be applied as carrier systems for lipophilic actives in pharmaceutical and food formulations. In this study, the effects of oil concentration, emulsifier type and oil droplet size on the physical stability of emulsions encapsulated in calcium alginate microgel particles (20–80 μm) produced by a continuous impinging aerosol technique were studied. Oil emulsions emulsified by using either sodium caseinate (SCN) or Tween 80 were encapsulated at different oil concentrations (32.55, 66.66 and 76.68% w/w of total solids content). The emulsions were analysed before and after encapsulation for changes in emulsion size distribution during storage, and compared to unencapsulated emulsions. The size distribution of encapsulated fine emulsion (mean size ~ 0.20 μm) shifted to a larger size distribution range during encapsulation possibly due to the contraction effect of the microgel particles. Coarse emulsion droplets (mean size ~ 18 μm) underwent a size reduction during encapsulation due to the shearing effect of the atomizing nozzle. However, no further size changes in the encapsulated emulsion were detected over four weeks. The type of emulsifier used and emulsion concentration did not significantly affect the emulsion stability. The results suggest that the rigid gel matrix is an effective method for stabilising lipid emulsions and can be used as a carrier for functional ingredients.     

Influence of environmental stresses on the physicochemical stability of orange oil bilayer emulsions coated by lactoferrin–soybean soluble polysaccharides and lactoferrin–beet pectin

Based on layer-by-layer electrostatic deposition, orange oil bilayer emulsions stabilized with lactoferrin (LF)–soybean soluble polysaccharides (SSPS) and lactoferrin (LF)–beet pectin (BP) were prepared. The effect of environmental stresses (ionic strength, pH, freeze–thaw and light) on the physicochemical stability of primary and secondary emulsions was investigated. In the absence of anionic polysaccharides, orange oil emulsion was highly unstable and aggregated at pH 7–9 and NaCl of 0.1–0.5 M. The droplets in LF–SSPS coated emulsion were stable against aggregation at pH range of 3–10 and NaCl concentration less than 0.3 M, while the droplets in LF–BP coated emulsion were stable against aggregation at pH 4–9 and NaCl concentrations of 0–0.5 M. All the primary and secondary emulsions showed the instability after the freeze–thaw treatment and the stability could be improved in the presence of maltodextrin. During the light exposure (0.35 W/m², 45 °C) for 8 h, the bilayer emulsions could protect key volatile compounds (decanal, octanal and geranial) from the oxidation compared with the primary emulsions. These results suggested that the layer-by-layer electrostatic deposition could improve the stability of LF-coated emulsion to environmental stresses.     

Sensory odour profiling and physical characteristics of edible oil blends during frying

Edible oil blends containing 80 parts of mustard oil (MO) or groundnut oil (GNO) or sunflower oil (SNO) and 20 parts of sesame oil (SO) or refined red palm oil (RPO) or rice bran oil (RBO) were studied to determine the changes in their physical and sensory characteristics during deep fat frying. Odour evaluation by the trained sensory panel revealed that successive fryings subdued the intensity of typical odour notes of the oil blends. Intensity of sulphury, pungent and vinegar (sour) notes of MO, nutty and sweet notes of GNO, sweet and seedy notes of SNO, seedy and earthy notes of SO, husk-like note of RPO and beany and branny notes of RBO decreased significantly by end of the 7th frying. Apparent viscosity of the oil blends increased on successive frying. Colour measured in CIE system indicated that the dominant parameters were a+ (redness) in RPO blends, b+ (yellowness) in blend containing SO or MO and a− (greenness) in RBO blends. The redness component decreased and yellowness increased with successive frying in SNO + RPO blend and GNO and RBO blend, respectively. Applying principal component analysis (PCA) to the data showed seggregation of various oil blends as distinct groups exhibiting their typical and characteristic attributes. PCA also revealed the pathway of change of oils during different frying cycles. MO and blend of MO + RPO were characterised by sulphury, pungent, harsh odour notes and red colour; GNO occupied a quadrant with fresh-oil-like, green and sweet notes, and SNO was characterised by fresh-oil-like, seedy odour and yellow colour. Addition of SO increased earthy note and lightness value, while blends containing RBO had distinct yellow colour, increased heated note and higher apparent viscosity.     

Encapsulation of flaxseed oil within native and modified lentil protein-based microcapsules

The physical properties of lentil protein-based maltodextrin microcapsules with entrapped flaxseed oil was investigated using native (n-LPI) and pre-treated (heated, un-hydrolyzed (u-LPI); and heated, hydrolyzed (h-LPI)) lentil proteins and as a function of oil load (10, 20 and 30% of total solids). Specifically, the moisture, water activity, surface oil and entrapment efficiency (EE) were assessed, along with droplet size and emulsion morphology of all formulations. Moisture (< 6%) and water activity (< 0.2) of all capsules were characteristics of dried powder ingredients. Light microscopy imaging of the emulsions, revealed that the h-LPI had slightly larger oil droplets than the n-LPI and u-LPI, which both appeared similar. Findings were confirmed by light scattering, where droplet sizes were 6.7, 4.2 and 4.2 μm for the h-LPI, u-LPI and n-LPI stabilized emulsions, respectively. Overall capsules prepared from h-LPI showed significantly higher surface oil and lower EE than both the n-LPI and u-LPI materials. Furthermore, as the oil content increased, overall surface oil became higher and EE became lower. Based on testing, capsules prepared using n-LPI with 10% oil loading was found to have the lowest surface oil content (~ 3.7%) and highest EE (~ 62.8%) for all formulations, and was subjected to an oxidative storage stability test over a 30 d period vs. free oil. The encapsulation process proved to be effective at lowering the production of primary and secondary oxidative products than free oil.     

Emulsifying properties of lactose-amines in oil-in-water emulsions

Lactose-amines were synthesized with hexadecyl-amide and lactose via the Maillard reaction and their emulsion stabilization properties were investigated. Lactose-amines were synthesized using two different constant heating (4 and 8 h) and two different heating/cooling cycles (12 and 24 h). Each lactose-amine sample was used as an emulsifier in 20:80 ratio oil-in-water emulsions at four different concentrations (0.01%, 0.05%, 0.1%, and 1%). Emulsion stability was monitored by measuring the oil droplet sizes and the extent of destabilization via clarification over 5 days. At 1% concentrations, emulsions prepared with lactose-amines synthesized for 4, 12, and 24 h were as stable as the whey protein positive control emulsion. The 8 h lactose-amine sample resulted in a less stable emulsion. We assume the difference is related to the amount of heat this sample was exposed to during synthesis, with extensive heat leading to advanced Maillard products, which possessed reduced emulsification properties.     

Physical characteristics of submicron emulsions upon partial displacement of whey protein by a small molecular weight surfactant and pectin addition

O/W emulsions (6 wt.% olive oil) were prepared at pH 3.3 using different WPI:Tween 20 weight ratios (1:0, 3:1, 1:1, 1:3, 0:1) at 1 wt.% total concentration. The emulsion droplet size was found to decrease with an increase in Tween 20. A minimum droplet size of d_3,2 300 nm was found for Tween systems alone, similar to that found (360 nm) for a 1:1 WPI:Tween 20 combination (p < 0.05). This specific composition showed a value for the interfacial tension close to that of Tween 20 alone. However, the emulsions presented low stability regardless of the WPI:Tween 20 ratio. To increase their stability, pectin was added, in various concentrations (0.2, 0.4 and 0.6 wt.%), using the Layer by Layer technique. In the presence of pectin, the ζ-potential of the oil droplets became negative; indicating that negatively charged pectin was absorbed onto the positively-charged droplet surface forming a secondary layer. The additional layer resulted in a wide range of emulsion stability. For all pectin concentrations, the 1:1 ratio of WPI:Tween 20 showed the highest stability. In most emulsions, extensive aggregation of oil droplets was observed, and their viscosity increased. Insufficient amounts of pectin to form the secondary layers led to bridging flocculation phenomena of oppositely charged pectin and proteins, leading to aggregation of the oil droplets. The higher the concentration of pectin, the greater the stability of the emulsion due to higher viscosity. All in all, the addition of a second layer consisting of pectin can be used to increase the stability of an emulsion containing emulsion droplets in the sub-micron range.     

Effect of germination on the chemical,functional and pasting properties of flour from brown and yellow varieties of tigernut (Cyperus esculentus)

The chemical, functional and pasting properties of flours processed from germinated (0, 24, 48 and 72 h) brown and yellow varieties of tigernut (Cyperus esculentus) seed was studied. Germination decreased carbohydrate (60.50–53.60%) and fat (60.50–53.60%) while protein and ash increased from 8.23% to 12.40% and 3.28% to 4.26%, respectively. In addition, functional properties such as foaming, emulsion, water and oil absorption capacities increased from 7.75% to 12.91%, 14.32–20.25 ml oil/g sample, 2.56–6.97 g water/g sample and 1.14–1.78 g oil/g sample, respectively, with germination. Least gelation of flour samples were improved as a result of germination process. Conversely, bulk density decreased with germination time (0.58–0.50 g/cm³). Trough, peak viscosity, break down, final viscosity, peak time and pasting temperature values were in the range (120.96–203.04 RVU), (145.28–228.11 RVU), (7.85–14.32 RVU), (180.62–324.73 RVU), (5.01.83–6.00 min) and (63.85–65.47 °C), respectively. Our results suggest that the incorporation of germinated tigernut flours may help in enhancing protein calorie delivery with improved functionality in complementary food formulations and baked products.     

Effect of modified Acacia gum (SUPER GUM™) on the stabilization of coconut o/w emulsions

Two modified Acacia gums, the already tested SUPER GUM? EM2 and the new EM10, were used as combined emulsifiers and stabilizers in coconut oil model emulsions. The properties of gum solutions as well as those of the emulsions were examined. The gum solutions were completely mechanically stable during high-pressure homogenization; therefore, the gum could be added to the emulsion prior to high-pressure treatment. The emulsions were prepared by a small-scale rotor-stator process and by high-pressure homogenization, respectively. Droplet size, stability and rheological properties of the emulsions were examined. As expected, the high-pressure process was very effective. The emulsions made with both modified gums had a droplet size below 1 μm and were completely stable for at least 7 weeks at up to 30 °C. The new SUPER GUM? EM10 was more efficient as an emulsifier than EM2; the droplet size distribution was more homogenous. All emulsions proved to be low-viscous and nearly Newtonian liquids. It can be concluded that the emulsion stability was mainly a result of the excellent emulsifying properties and not of an additional thickening effect of the gums. The modified Acacia gums can be recommended as an emulsifier and stabilizer for application in different food products, preferably in low-viscous emulsions such as coconut milk drinks or other beverages.     

Rheological properties of model dairy emulsions as affected by high pressure homogenization

The aim of this work was to evaluate the effect of different homogenization pressures on the rheological properties of model dairy emulsions. Solutions of sodium caseinate and whey protein concentrate at 2% + 1% and 2% + 2% (w/v) were emulsified with milk fat at the final contents of 5%, 8% and 15% (w/v). Raw and pasteurized emulsions were subjected to conventional (15/3 MPa) and high pressure (97/3 MPa and 147/3 MPa) homogenization. Differences in viscosity were observed according to fat content, protein ratio, heat treatment and pressure homogenization conditions. Gel networks formed in 8% and 15% fat content emulsions after pasteurization and high pressure homogenization. Gel strength was mostly affected by protein and fat contents.Dynamic high pressure may be used to produce emulsion gels with modulated structures which could be exploited low fat formulations.Industrial relevanceTexture influences people's acceptance of food and may be more important than the flavor in some products. Gelation of emulsions was observed after pasteurization and high pressure homogenization treatments, depending on fat and protein contents. Dynamic high pressure may be an alternative tool to improve viscoelastic properties and mouth feel of emulsions by providing a weak gel structure in the system. These characteristics can be exploited for low fat and low additive formulations.     

Fat mimetic capacity of Chlorella vulgaris biomass in oil-in-water food emulsions stabilized by pea protein

Vegetable proteins proved to be good emulsifiers for food emulsions with dietetic advantages. The use of these emulsions as carriers for healthy ingredients, such as colourings, with antioxidant and other beneficial properties, is an interesting subject.In this work, the capacity of the biomass of the microalga Chlorella vulgaris (which has been widely used as a food supplement) as a fat mimetic, and its emulsifier ability, was evaluated. Pea protein emulsions with C. vulgaris addition (both green and orange – carotenogenic) were prepared at different protein and oil contents. The rheological properties of the respective food emulsions were measured in terms of the viscoelastic properties and steady state flow behaviour and texture properties. It was observed that the two microalgal forms evidenced a fat mimetic capacity in these emulsions, the performance of the green stage of this C. vulgaris organism was significantly (p < 0.05) better than the orange stage.     

Ultra-High Pressure Homogenization enhances physicochemical properties of soy protein isolate-stabilized emulsions

The effect of Ultra-High Pressure Homogenization (UHPH, 100–300 MPa) on the physicochemical properties of oil-in-water emulsions prepared with 4.0% (w/v) of soy protein isolate (SPI) and soybean oil (10 and 20%, v/v) was studied and compared to emulsions treated by conventional homogenization (CH, 15 MPa). CH emulsions were prepared with non-heated and heated (95 °C for 15 min) SPI dispersions. Emulsions were characterized by particle size determination with laser diffraction, rheological properties using a rotational rheometer by applying measurements of flow curve and by transmission electron microscopy. The variation on particle size and creaming was assessed by Turbiscan® analysis, and visual observation of the emulsions was also carried out. UHPH emulsions showed much smaller d_3.2 values and greater physical stability than CH emulsions. The thermal treatment of SPI prior CH process did not improve physical stability properties. In addition, emulsions containing 20% of oil exhibited greater physical stability compared to emulsions containing 10% of oil. Particularly, UHPH emulsions treated at 100 and 200 MPa with 20% of oil were the most stable due to low particle size values (d_3.2 and Span), greater viscosity and partial protein denaturation. These results address the physical stability improvement of protein isolate-stabilized emulsions by using the emerging UHPH technology.     

The effect of pectin concentration and degree of methyl-esterification on the in vitro bioaccessibility of β-carotene-enriched emulsions

Soluble fibers, like pectin, are known to influence the physicochemical processes during the digestion of dietary fat and may therefore affect the absorption of lipophilic micronutrients such as carotenoids. The objective of the current work was to investigate whether the pectin concentration and degree of methyl-esterification (DM) influence the bioaccessibility of carotenoids loaded in the oil phase of oil-in-water emulsions. The in vitro β-carotene bioaccessibility was determined for different oil-in-water emulsions in which 1 or 2% citrus pectin with a DM of 99%, 66% and 14% was present. Results show that pectin concentration and DM influence the initial emulsion properties. The most stable emulsions with the smallest oil droplets (D(v,0.9) of 15–16 μm) were obtained when medium or high methyl-esterified pectin was present in a 2% concentration while gel-like pectin structures (D(v,0.9) of 114 μm), entrapping oil droplets, were observed in the case where low methyl-esterified pectin was present in the aqueous emulsion phase. During in vitro stomach digestion, these gel-like structures, entrapping β-carotene loaded oil droplets, significantly enlarged (D(v,0.9) of 738 μm), whereas the emulsion structure could be preserved when the medium or high methyl-esterified pectin was present. Initial emulsion viscosity differences, due to pectin concentration and especially due to pectin DM, largely disappeared during in vitro digestion, but were still significant after the stomach digestion phase. The observed differences in emulsion structure before and during in vitro digestion only resulted in a significant difference between emulsions containing low methyl-esterified pectin (β-carotene bioaccessibility of 33–37%) and medium/high methyl-esterified pectin (β-carotene bioaccessibility of 56–62%).     

Characterization and acid-induced gelation of butter oil emulsions produced from heated whey protein dispersions

Whey protein isolate was dispersed at 4% or 8% (w/v) and heated at neutral pH to produce protein polymers. Butter oil, up to 20%, was homogenized in heated whey protein dispersions at pressure ranging from 10 to 120 MPa. Emulsion gelation was induced by acidification with glucono-δ-lactone. Whey protein polymers produced finely dispersed emulsions with fat droplet diameter ranging from 340 to 900 nm. Homogenization pressure was the main factor influencing droplet size. At low fat volume fraction, the emulsions exhibited Newtonian behaviour. As fat content increased, shear thinning behaviour developed as a result of depletion flocculation. Emulsion consistency index increased with protein and fat concentrations. Increasing homogenization pressure had no effect on Newtonian emulsions but promoted flocculation and significantly increased the consistency of high fat emulsions. Protein concentration was the main factor explaining emulsion gel hardness and syneresis. Syneresis decreased with increasing fat content in the gel.