Antimicrobial chitosan-lysozyme (CL) films and coatings for enhancing microbial safety of mozzarella cheese

ABSTRACT:  This study investigated the antimicrobial activities of chitosan-lysozyme (CL) composite films and coatings against tested microorganisms inoculated onto the surface of Mozzarella cheese. CL film-forming solutions (FFS) with a pH of 4.4 to 4.5 were prepared by incorporating 0% or 60% lysozyme (per dry weight of chitosan) into chitosan FFS with or without a pH adjustment to 5.2. Sliced cheese was subjected to 3 CL package applications: film, lamination on a multilayer coextruded film, and coating. Cheese was inoculated with Listeria monocytogenes , Escherichia coli , or Pseudomonas fluorescens at 10⁴ CFU/g, or with mold and yeast at 10² CFU/g. Inoculated cheese was individually vacuum packaged and stored at 10 °C for sampling at 1, 7, and 14 d for bacteria, and at 10, 20, and 30 d for fungi. Inoculated bacteria survived but failed to multiply in untreated cheese during storage. Treated cheese received 0.43‐ to 1.25‐, 0.40‐ to 1.40‐, and 0.32- to 1.35-log reductions in E . coli , P. fluorescens , and L . monocytogenes , respectively. Incorporation of 60% lysozyme in chitosan FFS showed greater antimicrobial effect than chitosan alone on P. fluorescens and L . monocytogenes . The pH adjustment only affected the antimicrobial activity on L . monocytogenes , with lower pH (unadjusted) showing greater antimicrobial effect than pH 5.2. Mold and yeast increased to 10⁵ CFU/g in untreated cheese after 30 d storage. Growth of mold was completely inhibited in cheese packaged with CL films, while 0.24‐ to 1.90‐ and 0.06‐ to 0.50-log reductions in mold populations were observed in cheese packaged with CL-laminated films and coatings, respectively. All CL packaging applications resulted in 0.01- to 0.64-log reduction in yeast populations.     

Effect of Molecular Weight,Acid, and Plasticizer on the Physicochemical and Antibacterial Properties of β‐Chitosan Based Films

Abstract: Effects of chitosan molecular weight (1815 and 366 kDa), type of acid (1% acetic, formic, and propionic acid, or 0.5% lactic acid) and plasticizer (0, 25% glycerol or sorbital w/w chitosan) on the mechanical, water barrier, and antibacterial properties of β‐chitosan films were investigated. Tensile strength (TS) of high molecular weight (Hw) films was 53% higher than that of low molecular weight (Lw) ones, acetate, and propionate films had the highest TS (43 and 40 MPa) among tested acids, and plasticizer‐reduced film TS 34%. Film elongation at break (EL) was higher in Hw films than in Lw ones, in which formate and acetate films were the highest (9% and 8%, respectively), and plasticizer increased the film EL 128%. Molecular weight of chitosan did not influence water vapor permeability (WVP) of the films. Acetate and propionate films had lower WVP than other acid types of films, and plasticizer increased film WVP about 35%. No difference was found between glycerol and sorbitol films in terms of film mechanical and water barrier properties. Lw β‐chitosan films showed significant antibacterial activity against E. coli and L. innocua. This study demonstrated that β‐chitosan films are compatible to α‐chitosan films in physicochemical properties and antibacterial activity, yet with simple sample preparation. Practical Application: β‐chitosan based edible films at molecular weight of about 300 kDa showed great antibacterial activity against Gram‐positive and Gram‐negative bacteria. The films have similar mechanical and water barrier properties to α‐chitosan based films at the similar molecular weight, but simple sample preparation procedures and more attractive color. The release of active chitosan fragment from the film matrix acts as an antibacterial agent, making β‐chitosan films suitable as intelligent food wraps or coatings for a wide range of food products to control moisture loss and prevent surface bacterial growth.     

Heat Curing of Soy Protein Films at Atmospheric and Sub-atmospheric Conditions

ABSTRACT: The effect of heat curing at atmospheric or subatmospheric conditions on selected properties (moisture content, water vapor permeability (WVP), color, tensile strength (TS), elongation (E), and total soluble matter (TSM) content) of cast soy protein isolate films was investigated. Films were heat cured at 85 °C for 6, 12, 18, or 24 h at absolute pressures of 101.3, 81.32, or 61.32 kPa. Heat-cured films had increased (P < 0.05) TS and decreased (P < 0.05) WVP and E compared to control, unheated films. Heat treatment under vacuum reduced the WVP of films faster than heat curing at atmospheric pressure. High TS values, low E values, and low TSM values were also reached within short heating time under vacuum. However, vacuum treatment increased the size and number of cavities in cured films as evidenced by scanning electron micrographs.     

Effects of gelatin origin,bovine-hide and tuna-skin,on the properties of compound gelatin–chitosan films

With the purpose to improve the physico-chemical performance of plain gelatin and chitosan films, compound gelatin–chitosan films were prepared. The effect of the gelatin origin (commercial bovine-hide gelatin and laboratory-made tuna-skin gelatin) on the physico-chemical properties of films was studied. The dynamic viscoelastic properties (elastic modulus G′, viscous modulus, G″ and phase angle) of the film-forming solutions upon cooling and subsequent heating revealed that the interactions between gelatin and chitosan were stronger in the blends made with tuna-skin gelatin than in the blends made with bovine-hide gelatin. As a result, the fish gelatin–chitosan films were more water resistant (∼18% water solubility for tuna vs 30% for bovine) and more deformable (∼68% breaking deformation for tuna vs 11% for bovine) than the bovine gelatin–chitosan films. The breaking strength of gelatin–chitosan films, whatever the gelatin origin, was higher than that of plain gelatin films. Bovine gelatin–chitosan films showed a significant lower water vapour permeability (WVP) than the corresponding plain films, whereas tuna gelatin–chitosan ones were only significantly less permeable than plain chitosan film. Complex gelatin–chitosan films behaved at room temperature as rubbery semicrystalline materials. In spite of gelatin–chitosan interactions, all the chitosan-containing films exhibited antimicrobial activity against Staphylococcus aureus, a relevant food poisoning. Mixing gelatin and chitosan may be a means to improve the physico-chemical performance of gelatin and chitosan plain films, especially when using fish gelatin, without altering the antimicrobial properties.     

Properties of Chitosan Films as a Function of pH and Solvent Type

ABSTRACT: Two different deacetylated chitosans were dissolved in formic, acetic, lactic, or propionic acid to prepare chitosan films. The pH values of the film-forming solutions were adjusted to 3, 4, and 5. Water vapor permeability (WVP), tensile strength (TS), elongation (E), and total soluble matter (TSM) were significantly ( P < 0.05) affected by acid type, pH, and degree of deacetylation (DA). Low DA (LDA) chitosan films had lower WVP and TSM, higher TS compared with high DA (HDA) chitosan films. The E values were not affected by DA. As pH increased, WVP and TSM of chitosan films tended to increase while TS decreased significantly ( P < 0.05). Chitosan films with acetic and propionic acid solvents had low WVP and TSM and high TS, while films with lactic acid solvent had high E and TSM and the lowest TS. Fourier-transform infrared showed peak shifting in the spectra with different solvents and at different pH values. Chitosan films with lactic acid solvent showed a peak shift to a lower frequency range. The NH₃⁺ band was absent in the pH 5.0 chitosan film spectra.     

Functional, Nutritional, Mycological, and Akara-making Properties of Stored Cowpea Meal

ABSTRACT: Cowpea meal was packaged in high-density polyethylene bags, stored at -18 °C, 21 °C/55% RH, 37 °C/55% RH, and evaluated at 0, 4, 8, 12, 18, and 24 mo for functional, nutritional, mycological, and akara-making properties. Moisture content of meal varied no more than 0.5% and there were no marked changes in yeast and mold populations. Meal stored at -18 and 21 °C retained color, foam capacity, and akara-making quality for 24 mo. Overall, storage of cowpea meal at 37 °C was detrimental to its foaming characteristics, a key measure of performance in akara-making. A decline in protein solubility was also observed in the 37 °C samples.     

Mechanical and Barrier Properties of Edible Chitosan Films as affected by Composition and Storage

Oxygen permeability coefficients (OP), water vapor permeability coefficients (WVP), ethylene permeability coefficients (EP), tensile strength (TS) and percent elongation (%E) at break values were determined for chitosan films plasticized with glycerin at two concentrations (0.25 and 0.50 mL/g chitosan). Film samples were tested after 0, 2, 4, 8 and 12 wk of storage. After an initial drop in permeability during the first 2 wk of storage, mean OP (4.6 × 10^?5 cc/m-day-atm) and mean EP (2.3 × 10^?4 cc./m.day.atm) remained constant while mean WVP (2.2 × 10^?1 g/m-day-atm) decreased with respect to storage time. TS values (15–30 MPa) decreased and %E values (25%–45%) increased with respect to storage time. The stability of OP and EP values with storage was not expected, while the change in mechanical properties was as expected.     

Effect of the presence of glycerol and Tween 20 on the chemical and physical properties of films based on chitosan with different degree of deacetylation

Chitosans with two different deacetylation degree (DD) (60.9% and 96%) were used to elaborate edible films. The influence of the degree of deacetylation and the presence of glycerol and Tween 20 in the formulation on the surface tension of the film forming solutions as well as on the chemical structure, optical and mechanical properties and water vapor permeability (WVP) of the resulting films were studied.IR spectra showed no significant differences on the chemical structures of chitosan of the different films. However, X-ray diffraction analysis indicated that the use of chitosan with higher DD and the use of glycerol as additive resulted in higher crystallinity. Films made of chitosan with the lower DD (60.9%) were found to have higher tensile strength (TS) and elongation (E) in a tensile test. Degree of deacetylation did not have any effect on WVP. The presence of glycerol resulted in less resistant, more elastic and more permeable films.The presence of Tween 20 improved the wettability of film solutions and affected significatively mechanical, optical and barrier properties of the films. A positive interaction between glycerol and Tween 20 was observed for WVP.     

甘油与甲基纤维素对高直链玉米淀粉- 壳聚糖复合膜性能的影响

以高直链玉米淀粉(HACS)和壳聚糖(CS)为基本材料,甘油为增塑剂,甲基纤维素(MC)为增强剂制备可食性复合膜,研究高直链玉米淀粉与壳聚糖的质量比,甘油的添加量以及甲基纤维素的添加量对复合膜物理性能的影响,包括抗拉强度(TS)、断裂伸长率(E)、水蒸气透过系数(WVP)和色度。结果表明,壳聚糖添加量的增大与甘油添加量的增加都使高直链玉米淀粉- 壳聚糖复合膜的抗拉强度降低,断裂伸长率和WVP 显著增大,膜颜色变黄;甲基纤维素的添加改善了复合膜的机械性能和WVP,随着甲基纤维素添加量的增加,复合膜的抗拉强度和断裂伸长率都随之增大,WVP 逐渐降低,且对膜的颜色没有显著影响。     

Effect of surimi quality on properties of edible films based on Alaska pollack

Transparent and flexible edible/biodegradable films were successfully made from frozen Alaska pollack surimi. The effects of surimi quality on film formation, tensile strength (TS), elongation at break (EAB), water vapour permeability (WVP), light transmission, transparency, film solubility, protein solubility, and enzyme hydrolysis of surimi films were investigated. Thawed Alaska pollack surimi was incubated at 30 °C for 20 min (slight protein denaturation) and at 30 °C for 5 h (complete protein denaturation) in order to intentionally lower the surimi quality. Slight protein denaturation caused decreased EAB of the films and the complete denaturation gave rise to reduction of TS and EAB. The remaining of film properties were not markedly influenced by the loss of surimi quality. Hydrogen bonds, together with ionic bonds, played an important role in the formation of surimi films, but hydrophobic interactions were more involved when surimi with complete protein denaturation was used for the film preparation.     

Development and characterization of cassava starch and soy protein concentrate based edible films

The sensory attributes, mechanical, water vapour permeability (WVP) and solubility properties of cassava starch and soy protein concentrate (SPC)‐based edible films of varying levels of glycerol were studied. Addition of SPC and glycerol up to 30% and 20%, respectively, reduced stickiness and improved colour and appearance of the films. Tensile strength (TS), elastic modulus (EM) and elongation at break (EAB) of films increased, while film solubility (FS) and WVP decreased with SPC and glycerol up to 50% and 20% level, respectively, ranging from 20.33 to 26.94 MPa (TS), 41.33 to 72.76 MPa (EM), 7.90 to 12.28 MPa (EAB), 15.07 to 31.90% (FS) and 2.62 to 4.13 g H₂O mm m^?2 day kPa (WVP). The TS, EAB and WVP were higher for the biofilms than for low‐density polyethylene and cellophane films.     

Peanut Protein Film as Affected by Drying Temperature and pH of Film Forming Solution

Films were made from peanut protein concentrate solution of pH 6.0, 7.5 or 9.0, and dried at 70, 80 or 90°C. Both total solubility and protein solubility of film decreased with increasing temperature but increased with increasing pH. Film color was darker and more yellow when pH increased. Tensile strength (TS) and elongation (E) increased but water vapor permeability (WVP) and oxygen permeability (OP) decreased as temperature increased. At pH 9 and 90°C, film had the lowest WVP and OP, and the highest TS.     

冷藏、冻藏时间对玉米醇溶蛋白膜影响

不同冷藏、冻藏时间对玉米醇溶蛋白膜特性有一定影响,蛋白膜机械特性、平衡水分含量和水蒸汽透过率随冷藏、冻藏时间变化而变化。随着冷藏、冻藏时间不断增加,蛋白膜抗拉强度和延伸率都呈下降趋势；但冷藏条件下蛋白膜机械特性较冻藏条件下为好；蛋白膜平衡水分含量随时间增加而降低；蛋白膜水蒸汽透过率随冷藏、冻藏时间增加而上升。     

Physical and mechanical properties of water resistant sodium alginate films

Properties of sodium alginate films were modified using two different methods of CaCl₂ treatment, i.e. the direct addition of CaCl₂ into film making solution (mixing films) and the immersion of alginate films into CaCl₂ solutions (immersion films), and their treatment effects on tensile strength (TS), percentage elongation at break (E), water vapor permeability (WVP), and water solubility (WS) of the films were investigated. TS and E of the mixing films were not changed considerably, but those of the immersion films changed considerably with significant (P<0.05) increase in TS and decrease in E. WVP of the immersion films decreased significantly (P<0.05), but that of the mixing films did not decreased. Water resistance measured by WS was not improved with the mixing films, but the alginate films became water resistant when they treated by immersing in higher than 2 g/100 ml CaCl₂ solutions. Water adsorption by the films also decreased in the immersion films. Swelling ratio (SR) of the immersion film decreased with temperature without affecting WS of the films.     

Combined Effects of Proteins and Polysaccharides on Physical Properties of Whey Protein Concentrate-based Edible Films

ABSTRACT: The water-vapor permeability (WVP) and mechanical properties of edible films formed from dry blends or co-dried preparations of protein-polysaccharide powders prepared from whey protein concentrate (WPC)-45 and alginate, pectin, carrageenan, or konjac flour (WPC-45-to-polysaccharide ratio of 95:5 w/w) were investigated. Films were prepared from 8% WPC using WPC-45 (45% protein powder), consisting of 17.76 g of WPC-45 in 82.84 g of water per 100 g solution to give 8% protein w/w. Films formed from co-dried powders had lower WVP and higher tensile strength (TS), elastic modulus (EM) ( P < 0.05), and elongation (EL) than equivalent films formed from the dry blended powders. Films containing alginate had lower WVP and higher TS, EM, and EL than films containing pectin, carrageenan, or konjac flour. There is potential to alter the physical properties of hydrophilic films by combining whey protein and polysaccharide components.     

玉米淀粉/壳聚糖/魔芋葡甘露聚糖复合膜的制备及物性研究

以玉米淀粉、壳聚糖、魔芋葡甘露聚糖(KGM)为成膜基材。通过研究成膜配方中壳聚糖与KGM质量比、玉米淀粉、甘油、吐温-80等材料的质量分数对复合抗拉强度(TS)、断裂伸长率(EAB)、水蒸气透过系数(WVP)和不透明度(Opacity)的影响,以主成分分析法计算复合膜综合分为评价指标,利用正交实验对复合膜成膜配方进行优化。结果表明:当壳聚糖与KGM质量比1.0∶0.6、玉米淀粉质量分数10%、甘油质量分数0.50%、吐温-80质量分数0.30%时,复合膜TS为(22.53±0.16)MPa,EAB为(20.07±1.18)%,WVP为(1.87±0.01)×10~(-12)g·cm~(-1)·s~(-1)·Pa~(-1),不透明度为(4.13±0.07)mm~(-1),复合膜性能最优。     

The antimicrobial,mechanical, physical and structural properties of chitosan–gallic acid films

Chitosan films incorporated with various concentrations of gallic acid were prepared and investigated for antimicrobial, mechanical, physical and structural properties. Four bacterial strains that commonly contaminate food products were chosen as target bacteria to evaluate the antimicrobial activity of the prepared gallic acid–chitosan films. The incorporation of gallic acid significantly increased the antimicrobial activities of the films against Escherichia coli, Salmonella typhimurium, Listeria innocua and Bacillus subtilis. Chitosan films incorporated with 1.5 g/100 g gallic acid showed the strongest antimicrobial activity. It was also found that tensile strength (TS) of chitosan film was significantly increased when incorporating 0.5 g/100 g gallic acid. Inclusion of 0.5 g/100 g gallic acid also significantly decreased water vapor permeability (WVP) and oxygen permeability (OP). Microstructure of the films was investigated by Fourier transform infrared spectroscopy (FT-IR) and scanning electron microscopy (SEM) and it was found that gallic acid was dispersed homogenously into the chitosan matrix.     

Effects of storage conditions and acid solvent types on structural,mechanical and physical properties of kudzu starch (Pueraria lobata)‐chitosan composite films

Effects of acid solvents (acetic, lactic and malic acid) on properties of kudzu starch‐chitosan composite films were evaluated at −20 or 25°C during storage of 60 days. The yellowness of films enhanced, whereas water content and water vapour permeability of films declined with increasing storage time. Tensile strength of films choosing acetic and lactic acid as solvents, and solubility of all the films increased within 30 days thereafter decreased. Storage temperature had no impact on X‐ray diffraction, water content and solubility. Under the same storage conditions, the film using acetic acid as solvent presented the strongest mechanical property, the smallest solubility and the lightest colour. The film made from lactic acid solution was the most flexible and the yellowiest. The film with malic acid solvent showed the highest ordering degree, the lowest water content and the best water barrier property.     

Physical properties of PVOH/chitosan-blended films cast from different solvents

Homopolymer films of chitosan and polyvinyl alcohol (PVOH) and blended films consisting of PVOH and chitosan were cast from different organic acid solvents: acetic acid (AA), citric acid (CA), lactic acid (LA) and malic acid (MA) and characterized for mechanical and barrier properties. Intermolecular interactions were investigated with FTIR. Cross-linking and interactions with the solvent system resulted in a wide range of properties. Also, the effect of blends and acid solvent on the mechanical properties [tensile strength (TS), % breaking elongation (%BE)] and barrier properties [water vapor permeability (WVP)] was investigated. The organic acid used as a solvent affected mechanical properties and the WVP of PVOH/chitosan films blends. TS and %BE of PVOH/chitosan films were 13.5–221.9 Mpa and 5.2–451.8%, respectively. The WVP ranged from 0.19 to 0.62 ng m/m² s Pa. The range of properties, both intermediate from the component polymers and extending beyond either individual component suggests molecular interactions and cross-linking within the blends. Elucidation of these interactions continues.     

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.