Browsing by Author "Srinivasan, Magesh"
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- ItemEmulsifying properties of sodium caseinate : a thesis presented in partial fulfilment of the requirements for the degree of Master of Technology in Food Technology at Massey University(Massey University, 1995) Srinivasan, MageshThe main objectives of this study were to determine the influence of compositional and processing parameters on: (i) the protein surface coverage and protein surface composition and (ii) the creaming stability, for emulsions stabilized by sodium caseinate. Emulsions were usually prepared from 2.5% (w /w) protein solution and 30% soya oil. In some cases, emulsions were made with varying concentrations of caseinate or soya oil. The mixture was usually homogenized at 102/34 bar at 55°C and in some cases the mixture was homogenized at varying Pressures. Surface coverage of protein in freshly prepared emulsions was determined from analysis of the aqueous phase, using Kjeldahl. SDS-PAGE was used to identify the unadsorbed protein components in the aqueous phase. As the concentration of caseinate was increased from 0.5 to 7.5% (w/w) the protein load increased; the protein load attained a plateau value of 1.3 mg/m2 when the caseinate concentration was in the range 2 - 4% (w/w). Further increases in caseinate concentration markedly increased the protein load with a value of 3.55 mg/m2 at 7.5% caseinate concentration. At low concentrations of caseinate (below 2%), β-casein adsorbed at the surface of oil droplets in preference to other caseins while at higher concentrations of caseinate, no distinct preference of any caseins was observed. As the fat concentration was increased from 5 to 20% (w /w), the protein load decreased from - 9.9 to 3.7 mg/m2, but further increases in fat concentration caused only slight decreases in the protein load. At high fat concentration (50%) β-casein was adsorbed in preference to other caseins. As the homogenization pressure was increased from 34 to 340 bars, the protein load decreased from ~ 2.2 mg/m2 to ~ 1.5 mg/m2. β-Casein was preferentially adsorbed at the surface in emulsions homogenized at pressures above 204 Bar. Variations in the pH of sodium caseinate solution prior to emulsification from 5.0 to 8.5 caused a slight decrease in the protein load (from ~ 1.8 to 1.6 mg/m2). However, the sodium caseinate solutions adjusted to pH 2.0 or 3.0 prior to emulsification showed considerably greater protein loads (~ 2.7 mg/m2). There was no preferential adsorption of any of the caseins in different pH emulsions. Addition of calcium chloride to sodium caseinate solutions above 0.08% w /w, resulted in large casein particles/aggregates which subsequently adsorbed on to the oil surface resulting in higher protein loads (~ 5.8 mg/m2). Addition of calcium chloride increased the adsorption of αs-casein at the interface. The protein loads of different emulsions prepared from sodium caseinate manufactured under different processing conditions deceased in the order of freeze-dried laboratory made sodium caseinate (α 2.1 mg/m2) > sodium caseinates made under mild manufacturing conditions (α 1.4 mg/m2) > sodium caseinate manufactured under normal conditions (α 1.2 mg/m2) = freeze dried sodium caseinate manufactured under severe heat treatments (α 1.2 mg/m2) = spray dried sodium caseinate manufactured under severe heat treatment (α 1.2 mg/m2) = commercially made sodium caseinate (α 1.2 mg/m2). β-Casein was preferentially adsorbed in freeze-dried laboratory made sodium caseinates and sodium caseinate made under mild manufacturing conditions. There was no significant preferential adsorption for the other sodium caseinates. A stability tube was designed to study the extent of creaming under gravity at 20°C for 24 hours in these sodium caseinate-stabilized emulsions. The results were expressed as stability rating, defined as per cent change in fat in lower aqueous phase after creaming. In general, the stability rating increased with an increase in caseinate concentration. Emulsions containing caseinate concentrations of 4 and 5% (w/w) showed little fat separation under these conditions. The stability rating also increased with an increase in fat concentration in the emulsions indicating that high fat emulsions were more stable than emulsions containing low fat concentrations. As expected the stability rating increased with increase in homogenization pressure (i.e., decrease in oil droplet diameter). Emulsions prepared from sodium caseinate solutions, adjusted to pH 2.0 and 3.0, were found to be more stable than those prepared at pH 6.0, 7.0 and 8.5. Addition of calcium chloride to the sodium caseinate solution at 0.02 and 0.04% (w/w) had no effect on the stability rating of emulsions, but further additions of calcium chloride caused a marked increase in stability rating with no visible fat separation. Variations in the processing conditions (i.e. pasteurization temperatures, cooking temperatures, washing temperatures) during the manufacture of sodium caseinate had no significant effect on the stability of emulsions.
- ItemFormation and stability of oil-in-water emulsions : a thesis presented in partial fulfilment of the requirements for the degree of Doctor of Philosophy in Food Technology at Massey University(Massey University, 1998) Srinivasan, Magesh; Srinivasan, MageshThe main objective of this study was to gain a better understanding of the formation, stability and microstructure of oil-in-water emulsions stabilized by commercial sodium (ALANATE 180) and calcium caseinates (ALANATE 380). The study also determined the effects of heat treatment and NaCI addition on the formation and stability of these emulsions. Emulsions were prepared using various concentrations of sodium or calcium caseinate solutions (0.5 to 5.0%) and 30% soya oil. Surface protein coverage (mg/m2) in freshly prepared emulsions was determined from analysis of the aqueous phase after centrifugation of emulsions at 45,000 g for 40 minutes, using the Kjeldahl method. SDS-PAGE was used to identify the adsorbed protein components in the cream phase. Creaming stability was determined after storage of emulsions for 24 hours at 20°C by a low speed centrifugation method. The microstructure of these emulsions was determined using confocal laser scanning microscopy. The aggregation state of caseins in sodium and calcium caseinate solutions was determined by successive centrifugation, gel permeation chromatography and multi-angle laser light scattering techniques. For emulsions stabilized with sodium caseinate, the surface protein concentration increased gradually with protein concentration up to 3%, but the increase was much smaller at higher concentrations. By comparison, the surface protein coverage in emulsions stabilized with calcium caseinate showed an almost linear increase with protein concentration (0.5 to 5.0%). At all protein concentrations, the surface protein coverage of emulsions stabilized with calcium caseinate was higher than that of sodium caseinate emulsions. β-Casein was adsorbed in preference to other caseins in emulsions made using ≤ 2.0% sodium caseinate, but αs-casein (αs1- + αs2-) appeared to adsorb in preference to other caseins when emulsions were made using > 2.0% sodium caseinate. In calcium caseinate-stabilized emulsions, αs-casein was found to adsorb in preference to other caseins at all protein concentrations used. Heat treatment (121°C for 15 min) of sodium caseinate emulsions or heat treatment of sodium caseinate solutions prior to emulsion formation, at all caseinate concentrations, resulted in an increase in surface protein coverage and altered the proportions of individual caseins at the droplet surface. The surface protein coverage of emulsions formed with calcium caseinate solutions increased markedly when the emulsions were heated (121°C for 15 min) or when calcium caseinate solutions were heated prior to emulsion formation. The preferential adsorption of αs-casein, observed in the unheated calcium caseinate emulsions, diminished after heating, which was due to polymerization of αs-casein during heating and/or degradation of this casein. In sodium caseinate emulsions, the surface protein coverage and the composition of emulsion droplets were influenced by the presence of NaCl prior to emulsion formation. The surface protein coverage in emulsions made with 1 and 3% sodium caseinate increased with an increase in NaCl concentration up to 40 mM, with a large increase in the adsorption of αs-casein at the droplet surface. Addition of NaCl beyond 40 mM had no further effects on surface coverage and composition. Similar trends were observed when NaCl was added to the emulsions after they were formed. By contrast, in calcium caseinate emulsions, the surface protein coverage decreased with increase in NaCl concentration up to 40 mM, but with further increase in NaCl concentration the surface protein coverage increased slightly. In these emulsions, the composition of the interface remained largely unafffected by NaCl addition; αs-casein was adsorbed in preference to other caseins. Creaming stability of calcium caseinate emulsions, after storage at 20°C for 24 hours, increased with an increase in protein concentration. However, the creaming stability of sodium caseinate emulsions decreased markedly as the protein concentration was increased above 2%. This decrease in stability was attributed to the reversible flocculation arising from a 'depletion flocculation' mechanism. This flocculation in turn resulted in enhanced creaming at high caseinate concentrations. In sodium caseinate emulsions, the appearance of the droplets in the confocal micrographs was dependent on the concentration of protein used for making emulsions. Emulsions formed with low concentrations of sodium caseinate (0.5 and 1.0%) appeared to be homogenous with no sign of flocculation. However the emulsions made with > 2% sodium caseinate showed some irregular flocs, which appeared to be forming a network structure at higher concentrations of protein. In contrast, confocal micrographs of emulsions formed with calcium caseinate at all protein concentrations showed individual droplets. The creaming stability of these emulsions improved, when the emulsions were heated or when emulsions were made using heated sodium or calcium caseinate solutions. The presence of 200 mM NaCl prior to emulsion formation resulted in improved creaming stability and a reduced degree of flocculation.