Chitosan and Protein Coatings Affect Yield, Moisture Loss, and Lipid Oxidation of Pink Salmon (Oncorhynchus gorbuscha) Fillets During Frozen Storage

The effects of chitosan (CH1 = 1% and CH2 = 2% solution), egg albumin (EA), soy protein concentrate (SPC), pink salmon protein powder (PSP), and arrowtooth flounder protein powder (AFP) as edible coatings on quality of skinless pink salmon fillets were evaluated during 3 mo frozen storage. Coating with 2% chitosan (CH2) resulted in significantly higher yield than coating with PSP and AFP. The thaw yield of salmon fillets coated with CH2 was higher than those of the control and fillets coated with AFP. The noncoated, CH1‐, and CH2‐coated fillets had similar drip loss (0.4% to 1.2%), which was lower than those observed for PSP‐ and AFP‐coated fillets. All fillet samples had similar cook yield (84.2% to 88.8%). The fillet coated with CH1, CH2, SPC, and EA had significantly higher (P < 0.05) moisture content after thawing than the control noncoated fillets. Coating with CH1 and CH2 was effective in reducing about 50% relative moisture loss compared with the control noncoated fillets. Chitosan (CH1 and CH2) and SPC delayed lipid oxidation. There were no significant (P > 0.05) effects of coating on a*, b*, and whiteness values for cooked fillets after 3 mo frozen storage.     

Functional, Nutritional, and Rheological Properties of Protein Powders from Arrowtooth Flounder and their Application in Mayonnaise

ABSTRACT: Arrowtooth flounder soluble protein powder (AFSP) and arrowtooth flounder insoluble protein powder (AFISP) were evaluated for their functional, nutritional, and rheological properties. AFSP and AFISP contained 80% and 79% protein and 5.9% and 14.9% fat, respectively. Yield of AFSP (8.6%) was less than AFISP (13.1%). AFSP and AFISP had desirable essential amino acid and mineral contents. Emulsion stability of AFSP was greater than AFISP. Fat and water absorptions (mL/g protein) were 5.2 and 1.8 for AFSP, respectively, and 3.3 and 4.2 for AFISP Mayonnaises made from AFSP had greater emulsion stability than mayonnaise made from AFISP. Mayonnaises from both AFSP and AFISP possessed pseudoplastic and viscoelastic characteristics.     

Physicochemical Properties of Microencapsulated ω‐3 Salmon Oil with Egg White Powder

The objective of this study was to produce microencapsulated omega(ω)‐3 fatty acids (PUFAs) fortified egg white (EW) powders and to characterize their nutritional and physical properties. Stable emulsions (E‐SO‐EW) containing 3.43 (g/100 g) salmon oil (SO), 56.21 (g/100 g) EW, and 40.36 (g/100 g) water and a control (E‐EW) containing EW and water were prepared. E‐SO‐EW and E‐EW were separately spray dried at 130, 140, and 150 °C inlet air temperatures. This resulted in 3 microencapsulated SO fortified EW powders (SO‐EW), and 3 dried EW powders (DEW). The powders were analyzed for microencapsulation efficiency (ME), color, fatty acids methyl esters, protein, fat, moisture, ash, amino acids, minerals, microstructure, and particle size. The EPA and DHA content of SO and the ME of the powders were not affected by the inlet air temperature. The crude protein content of SO‐EW powders was approximately 24 (g/100 g) lower than dried EW powders. Leucine was the most abundant essential amino acid found in all the powders. Most of the powders’ median particle size ranged from 15 to 30 μm. The study demonstrated that microencapsulated ω‐3 salmon oil with high quality EW protein can be produced by spray drying.     

Comparisons of Chemical and Physical Properties of Catfish Oils Prepared from Different Extracting Processes

ABSTRACT:  Four different catfish oil extraction processes were used to extract oil from catfish viscera: process CF1 involved a mixture of ground catfish viscera and water, no heat treatment, and centrifugation; process CF2 involved ground catfish viscera (no added water), heat treatment, and centrifugation; process CF3 involved a mixture of ground catfish viscera and water, heat treatment, and centrifugation; process CF4 involved ground catfish viscera, enzymatic hydrolysis, and centrifugation. Chemical and physical properties of the resulting of catfish oils were evaluated. The CF4 process recovered significantly higher amounts of crude oil from catfish viscera than the other 3 extraction methods. The CF4 oil contained a higher percent of free fatty acid and peroxide values than CF1, CF2, and CF3 oils. Oleic acid in catfish oil was the predominant fatty acid accounting for about 50% of total fatty acids. Weight loss of oils increased with increasing temperatures between 250 and 500 °C. All the catfish oil samples melted around −32 °C regardless of the extraction methods. The flow behavior index of all the oil samples was less than 1, which indicated that the catfish oils exhibited non-Newtonian fluid behavior. The apparent viscosity at −5 and 0 °C was significantly higher ( P  < 0.05) than those at 5, 10, 15, 20, 25, and 30 °C. The average magnitude of activation energy for apparent viscosity of the oil was higher for CF2 than CF1, CF3, and CF4.     

Development of cantaloupe (Cucumis melo) juice powders using spray drying technology

Cantaloupes are a good source of carotenoids and vitamin C. Cantaloupe fruit juice powder containing vitamin C and β-carotene can be produced by spray drying. The objective of this study was to develop cantaloupe fruit juice (CJ) powder and to evaluate its nutritional and physical properties. Fresh cantaloupe fruits purchased from a local store were diced and juiced. CJ with 10% maltodextrin (MD) added was spray dried at inlet temperatures of 170, 180 and/or 190 °C. Three spray dried cantaloupe powders, including CJ dried with MD at 170 °C (CJP1), CJ dried with MD at 180 °C (CJP2), CJ dried with MD at 190 °C (CJP3) were analyzed for moisture, water activity, vitamin C, β-carotene, dissolution, and microstructure. The actual production rate of the cantaloupe juice powders was lower than the estimated production rate. CJP1 had (p < 0.05) higher moisture content and water activity than CJP2, and CJP3. Vitamin C content (mg/100 g, dry solids) was significantly (p < 0.05) higher in CJP1 (136.36 ± 5.84) than CJP2 (91.85 ± 5.23) and CJP3 (78.30 ± 1.96). The powder produced at inlet temperatures 170 °C had higher β-carotene content (μg/g) than that produced at 180 and 190 °C.     

Kinetics of Lipid Oxidation and Degradation of Flaxseed Oil Containing Crawfish (<Emphasis Type="Italic">Procambarus clarkii</Emphasis>) Astaxanthin

Flaxseed oil (FO) containing crawfish (Procambarus clarkii) astaxanthin (FOA) was evaluated for lipid oxidation and astaxanthin degradation. The FOA was analyzed for astaxanthin content, free fatty acids (FFA), peroxide value (PV), fatty acid methyl esters (FAMEs) profile, and color. The amount of extractable astaxanthin in the crawfish byproducts was 3.02 mg/100 g of crawfish byproducts. FOA and FO had a similar alpha-linolenic acid (ALA) content (on a weight% basis). The FO was lighter and more yellow in color than FOA. The oxidation rate of FOA was lower than that of FO. When FO and FOA were heated to 30 °C, both oils exhibited minimal lipid oxidation with increasing heating time, whereas FO, when heated to 40, 50, 60 °C, had a higher lipid oxidation rate than FOA with increasing the heating time from 0 to 4 h. Astaxanthin was an effective antioxidant agent in FO when it was heated from 30 to 60 °C. The degradation of astaxanthin in FOA could be described by first order reaction kinetics. Astaxanthin was stable in flaxseed oil at 30 and 40 °C, while its stability decreased significantly at 50 and 60 °C. The rate of astaxanthin degradation in FOA was significantly influenced by temperature.     

Effects of enzymatically-extracted purple rice bran fiber as a protectant of L. plantarum NRRL B-4496 during freezing,freeze drying,and storage

This study investigated purple rice bran fiber (PRF) as a protectant for Lactobacillus plantarum NRRL B-4496 (LP) during freezing, freeze drying and storage. PRF was enzymatically extracted from purple rice bran. L. plantarum NRRL B-4496 was grown in MRS broth, centrifuged, and immobilized on PRF suspension. LP cells immobilized on PRF (LP-PRF) and free LP cell (control) samples were frozen in either air blast (AF) or cryogenic freezing (CF) before freeze drying. Freeze-dried (FLP) samples were stored either at room temperature or at refrigerated temperature. For either freezing method, PRF protected cells had less than one log reduction of viable cells while the control had reductions greater than six logs after freeze drying. The log reductions of viable LP cells protected with PRF after freeze drying and 12 weeks storage at 4° C for AF and CF treatments were 0.7 and 1.3 log cycle, respectively. The viable LP-PRF cell count for CF was significantly lower than for AF after 12 weeks at room temperature. PRF improved LP survival in both AF and CF samples in bile. This study demonstrated that freezing methods affected LP viability during storage and that PRF could protect at both refrigerated and room temperatures.     

Purifying salmon oil using adsorption,neutralization, and a combined neutralization and adsorption process

The performance of activated earth and/or chitosan as an adsorbent to remove free fatty acids (FFA) and peroxides from the unpurified salmon oil was evaluated. The unpurified salmon oil was purified using three methods included activated earth adsorption process, neutralization process, and combined neutralization and activated earth adsorption processes. The purified salmon oil samples were evaluated for free fatty acids (FFA), peroxide values (PV), minerals, color, tocopherols, moisture content, insoluble impurities, and water activity. Neither chitosan nor the activated earth adsorption process was effective in removing FFA from the salmon oil. Neutralized oil had a higher intraparticular diffusion coefficient than the unpurified salmon oil for adsorbing peroxides. FFA of unpurified salmon oil was 3.5% and was significantly reduced (P < 0.05) to 0.12% by neutralization. No significant reduction of tocopherols content of the oil was observed in any of the three purification processes. After the adsorption processes, PV of neutralized oil had decreased from 4.75 to 2.90 mmol/kg. All three purification processes increased the lightness (L^∗) and decreased the redness (a^∗) and reduced mineral, insoluble impurities, moisture content, and water activity of the salmon oil. This study demonstrated that the combined process was more effective in reducing FFA, peroxides, and moisture content than either the activated earth adsorption or neutralization purification process alone.     

Microwave-assisted catfish liver oil extraction and FA analysis

FA profiles of catfish liver oils were analyzed after microwave-assisted (without solvent extraction) and/or conventional (with solvent extraction) preparation methods. Microwave heating of the smaples was performed at 100, 80, 60, or 40% power at 1,000 W and 2,450 MHz, each for 80, 60, 40, or 20 s. Significant differences in the content of recovered FA were observed among the microwave-heated samples, except for C20∶0 and C20∶4. Recovery of C16∶0, C20∶0, and C20∶4 from the samples analyzed by the microwave-assisted method was lower than that of the samples analyzed by the conventional method. Much greater recovery was observed for C18∶1, C18∶2, and C22∶6; however, the recovery was not different from or was only slightly lower than that of the conventional method when microwave heating was set at 40% power for 20 s. This was also observed for the total unsaturated or saturated FA. Compared to other microwave treatments, heating at 100% power for 80 s yielded the greatest recovery of C14∶0, C18∶0, C18∶1, C18∶2, C18∶3, C20∶1, C20∶2, and C22∶6.