Effect of select parameters on the properties of edible film from water-soluble fish proteins in surimi wash-water

Edible film from water-soluble fish proteins were developed by casting film solution on leveled trays and effects of pH (9.5, 10.0 and 10.5), heating temperature (60, 70 and 80 °C), and heating time (10, 20 and 30 min) of the film solution on various film properties were determined using Response Surface Methodology (RSM). The impact of pH and heating temperature of film solution was more significant, overall, on the film's properties than heating time. Contour plots of tensile strength and elongation at break was highest at pH of 10.0 at 70 °C (2.75-3.02 MPa) but low in elongation at break (6.35-9.16%), while water vapor permeability and oxygen permeability were at their lowest (58.55-65.96 g mm/m² d kPa and 351.33-624.18 cm³ μm/m² d kPa). There was a direct correlation between the films’ and proteins’ solubility on one hand, and heating temperature of film solution on the other, which reversed with change in pH of film solution. Film color was darker and more yellowish with increase in the pH of film solution.     

Preparation and properties of rice starch–chitosan blend biodegradable film

Biodegradable blend films from rice starch–chitosan were developed by casting film-solution on leveled trays. The influence of the ratio of starch and chitosan (2:1, 1.5:1, 1:1, and 0.5:1) on the mechanical properties, water barrier properties, and miscibility of biodegradable blend films was investigated. The biodegradable blend film from rice starch–chitosan showed an increase in tensile strength (TS), water vapor permeability (WVP), lighter color and yellowness and a decreasing elongation at the break (E), and film solubility (FS) after incorporation of chitosan. The introduction of chitosan increased the crystalline peak structure of starch film; however, too high chitosan concentration yielded phase separation between starch and chitosan. The amino group band of the chitosan molecule in the FTIR spectrum shifted from 1541.15 cm⁻¹ in the chitosan film to 1621.96 cm⁻¹ in the biodegradable blend films. These results pointed out that there was a molecular miscibility between these two components. The properties of rice starch–chitosan biodegradable blend film and selected biopolymer and synthetic polymer films were compared; the results demonstrated that rice starch–chitosan biodegradable blend film had mechanical properties similar to the other chitosan films. However, the water vapor permeability of rice starch–chitosan biodegradable blend film was characterized by relatively lower water vapor permeability than chitosan films but higher than polyolefin.     

Effect of citric acid,PVOH, and starch ratio on the properties of cross-linked poly(vinyl alcohol)/starch adhesives

The properties of tapioca starch adhesives were improved by cross-linking and the cross-linked adhesive compared with pure tapioca starch and poly(vinyl alcohol) adhesives. The effect of starch ratio, type of PVOH, and adding citric acid were important factors on the cross-linked adhesives. Wood adhesives made from cross-linked PVOH/starch were prepared by PVOH and tapioca starch, using hexamethoxymethyl melamine (HMMM) and citric acid (CA) as a cross-linking agent and catalyst, respectively. The effect of CA, PVOH/starch ratio, and type of PVOH such as medium (M PVOH) and high molecular weight (H PVOH) were investigated. The condition of the cross-linking reaction was 175?°C for 15?min. The structural properties of cross-linked adhesive were investigated by FT-IR spectroscopy. The results were confirmed in terms of thermal properties with a differential scanning calorimeter (DSC) and the shear strength of the adhesive. The cross-linked adhesive resulted in the increase of T _g and showed good blend compatibility with all of the cross-linked adhesives. The adhesive strength significantly increased when using CA as a catalyst in the cross-linking reaction. The optimum contents of the cross-linked PVOH/starch adhesives were 1:1.8 for M PVOH and 1:0.5 for H PVOH.     

Properties and antimicrobial activity of edible films incorporated with kiam wood (Cotyleobium lanceotatum) extract

The antimicrobial properties of wood extracts are well known; however their application to edible films is limited. In this study, the minimum bactericidal concentration (MBC) of kiam wood extract was established as 300 mg/L at which bacterial growth was completely inhibited. The antimicrobial properties of hydroxypropyl methylcellulose (HPMC) films containing 1-5 fold of MBC of kiam wood extract were tested against Escherichia coli O175:H7, Staphylococcus aureus and Listeria monocytogenes. The edible films containing kiam wood extract exhibited more effective impact on the growth reduction of L. monocytogenes than S. aureus and E. coli (p < 0.05). The use of kiam wood extract at 1 and 2 fold of MBC incorporated into edible HPMC films did not exhibit any antimicrobial activity. However, the inhibitory effect of edible HPMC films containing kiam wood extract was observed at 3, 4 and 5 fold of MBC. The greatest zone of inhibition was observed at 5 fold of MBC incorporated in edible HPMC films. Tensile strength and elongation at break significantly decreased with the incorporation of kiam wood extract, whereas water vapor permeability and film solubility increased. The color of edible films became darker and more reddish-yellowish as well as having a lower transparency as the level of kiam wood extract was increased. Kiam wood extract incorporated in edible film provided the films with a rougher surface than pure edible film. Our results pointed out that the incorporation of kiam wood extract as a natural antibacterial agent has potential for use in extending the shelf life of food products.     

Recovery and characterization of proteins precipitated from surimi wash-water

The objectives of this study were testing the methodology involved in the recovery of water-soluble proteins from surimi wash-water (SWW) by shifting the pH and organic solvent use, and characterization of the recovered proteins. Water-soluble proteins were recovered from three successive washes in a surimi process; these were: 1.23 ± 0.08, 0.64 ± 0.06 and 0.54 ± 0.05 mg/mL for wash stages I (WS-I), II (WS-II) and III (WS-III), respectively. For WS-I, most of the recovered proteins had a molecular weight (MW) between 23.2 and 71.6 kDa with some traces having less than 23.2 kDa. WS-II and III also had MW between 23.2 and 71.6 kDa; however, at a lower amount. Maximum precipitation from surimi wash-water was obtained at pH 3.5 (66.3 g protein/100 ml SWW). Percentage of precipitation was directly related to temperature. Increasing the organic solvent concentration (10-60 g ethanol/100 g SWW) yielded greater precipitation. The highest precipitation (65.0 g protein/100 mL SWW) was obtained with ethanol concentration of 60 g/100 g SWW. Reaction time for pH shift and organic solvent had little or no significant effect (p > 0.05) on percentage of precipitation. Minimum solubility of recovered proteins occurred around pH 3.5 and 60 g/100 g of ethanol, an increase in temperature decreased protein solubility.