Abstract:The aim of the present study was to investigate the ability of partially hydrolysed whey proteins to microencapsulate fish oil. Microcapsules were produced by spray-drying emulsions composed of fish oil, glucose syrup (DE38) and b-lactoglobulin or hydrolysates thereof prepared using bovine trypsin or alcalase. Hydrolysis did not negatively affect encapsulation performance during spray-drying and microencapsulation efficiency was very high for all samples (99 AE 0.5%). However, enzymatic hydrolysis resulted in … Show more
“…After 2.5 h of extraction at room temperature, the sample was centrifuged (5000 g, 20 °C for 30 minutes) followed by lyophilisation of the supernatant. Enzymatic hydrolysis was conducted as described by Tamm, et al (2015) with modifications. In brief, PPC was dissolved in distilled water and the pH value adjusted (0.1 M HCl / 1 M HCl).…”
Section: Pea Protein Concentrate (Ppc) Preparation and Hydrolysismentioning
With regard to applications in dispersed systems (i.e. emulsions), improving the poor solubility of pea protein in the pH-range applicable to foods (pH 3 to pH 7) is a prerequisite. To achieve this, a pea protein concentrate was produced on a lab scale using alkaline extraction and subsequent enzymatic hydrolysis to degrees of 2 and 4%. Solubility was improved and interfacial properties were influenced. All samples led to the formation of emulsions but displayed a tendency towards wider oil-droplet size distributions at pH close to the isoelectric point. Using microscopy, this increase could be attributed to the formation of aggregates, which in turn can be ascribed to lack of repulsion caused by the low absolute values of ζpotentials. The same lack of repulsion led to stronger and more elastic interfacial films at pH 4 and 5 than at pH 7. Moreover, film strength increased significantly with increasing degree of hydrolysis. Dilatational experiments imply that hydrolysis enhances in-plane structural rearrangements. Thus, it is concluded that tryptic hydrolysis has the potential to improve the overall stability of emulsions.
“…After 2.5 h of extraction at room temperature, the sample was centrifuged (5000 g, 20 °C for 30 minutes) followed by lyophilisation of the supernatant. Enzymatic hydrolysis was conducted as described by Tamm, et al (2015) with modifications. In brief, PPC was dissolved in distilled water and the pH value adjusted (0.1 M HCl / 1 M HCl).…”
Section: Pea Protein Concentrate (Ppc) Preparation and Hydrolysismentioning
With regard to applications in dispersed systems (i.e. emulsions), improving the poor solubility of pea protein in the pH-range applicable to foods (pH 3 to pH 7) is a prerequisite. To achieve this, a pea protein concentrate was produced on a lab scale using alkaline extraction and subsequent enzymatic hydrolysis to degrees of 2 and 4%. Solubility was improved and interfacial properties were influenced. All samples led to the formation of emulsions but displayed a tendency towards wider oil-droplet size distributions at pH close to the isoelectric point. Using microscopy, this increase could be attributed to the formation of aggregates, which in turn can be ascribed to lack of repulsion caused by the low absolute values of ζpotentials. The same lack of repulsion led to stronger and more elastic interfacial films at pH 4 and 5 than at pH 7. Moreover, film strength increased significantly with increasing degree of hydrolysis. Dilatational experiments imply that hydrolysis enhances in-plane structural rearrangements. Thus, it is concluded that tryptic hydrolysis has the potential to improve the overall stability of emulsions.
“…Most studies evaluated the antioxidant activity of the hydrolysates/peptides in vitro using different methods such as DPPH scavenging activity, reducing power, ABTS scavenging activity, Fe 2C chelating activity, b-carotene bleaching preventing activity, linoleic acid autoxidation inhibition activity (Chalamaiah et al, 2012). Some studies also investigated the ability of the hydrolysates/peptides to inhibit lipid oxidation in real food systems such fish oil in water emulsions Ghelichi et al, 2017) or fish oil microcapsules (Tamm et al, 2015;Morales-Medina et al, 2016). Finally, only a few works are devoted to studying the antioxidant activity of peptides in cell-based and in vivo systems (Chakrabarti et al, 2014).…”
Production of peptides with various effects from proteins of different sources continues to receive academic attention. Researchers of different disciplines are putting increasing efforts to produce bioactive and functional peptides from different sources such as plants, animals, and food industry by-products. The aim of this review is to introduce production methods of hydrolysates and peptides and provide a comprehensive overview of their bioactivity in terms of their effects on immune, cardiovascular, nervous, and gastrointestinal systems. Moreover, functional and antioxidant properties of hydrolysates and isolated peptides are reviewed. Finally, industrial and commercial applications of bioactive peptides including their use in nutrition and production of pharmaceuticals and nutraceuticals are discussed.
“…The parent emulsions and reconstituted emulsions presented values of the 90th percentile below 2 µm ( Table 1), indicating that the WPH efficiently stabilized the oil droplets by maintaining the structural integrity of the oil/water interface prior, during and after the microencapsulation process [16]. Despite the lack of surface-active properties of the encapsulating agents used, the results show significant differences (p < 0.05) for the ODSD of the parent emulsions prior to drying, which are mainly attributed to minor differences in pressure adjustments in the homogenizer.…”
Section: Oil Droplet Size Distribution (Odsd) Of Emulsionsmentioning
confidence: 99%
“…Nevertheless, the protective effect of WPH on the reduction of lipid oxidation in the microcapsules was not investigated in any of the latter studies. More recently, Tamm et al [16] produced fish oil-loaded microencapsulates using glucose syrup as the wall material in the presence of unmodified or hydrolyzed β-lactoglobulin (β-LG). The unmodified and hydrolyzed proteins were used as a film-forming material around the oil droplets.…”
The influence of the carbohydrate-based wall matrix (glucose syrup, GS, and maltodextrin, MD21) and the storage temperature (4 °C or 25 °C) on the oxidative stability of microencapsulated fish oil was studied. The microcapsules (ca. 13 wt% oil load) were produced by spray-drying emulsions stabilized with whey protein hydrolysate (WPH), achieving high encapsulation efficiencies (>97%). Both encapsulating materials showed an increase in the oxidation rate with the storage temperature. The GS-based microcapsules presented the highest oxidative stability regardless of the storage temperature with a peroxide value (PV) of 3.49 ± 0.25 meq O2/kg oil and a content of 1-penten-3-ol of 48.06 ± 9.57 ng/g oil after six weeks of storage at 4 °C. Moreover, low-fat mayonnaise enriched with GS-based microcapsules loaded with fish oil and containing WPH as a film-forming material (M-GS) presented higher oxidative stability after one month of storage when compared to low-fat mayonnaise enriched with either a 5 wt% fish oil-in-water emulsion stabilized with WPH or neat fish oil. This was attributed to a higher protective effect of the carbohydrate wall once the microcapsules were incorporated into the mayonnaise matrix.
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