Lipoxygenase activity in walnuts and almonds

The objective of this experiment was to investigate lipoxygenase (LOX) activity in walnut or almond homogenates. Walnut or almond kernels were heated with hot air at 55 °C for 2 or 10 min, or 60 °C for 2 or 10 min. The homogenates of untreated or heat treated walnut kernels exhibited greater LOX activity than the homogenates of untreated or heat treated almond kernels. Short-time heat treatments of 55 °C for 2 min or greater reduce LOX activity, retard the development of oxidative rancidity, and extend the shelf-life of walnuts and almonds during distribution and storage. Short-time heat treatments of walnut or almond kernels designed to control insect pests for international trade did not promote rancidity when compared to untreated walnuts or almonds.     

鲜食核桃仁抑制褐变与脱色方法及货架期保鲜效应

鲜核桃仁因易于褐变而难以作为成品生产与销售。本实验以‘香玲’核桃湿鲜坚果为试材,分别对新鲜核桃仁、已褐变核桃仁进行不同工艺参数下4 种方法抑制褐变以及2 种方法脱色处理,根据20 ℃货架期下色值变化和感官观测结果,选取两组实验的最佳处理条件分别为1.0%（质量分数,后同）抗坏血酸（ascorbic acid,AsA）＋0.05%柠檬酸（citric acid,CA）浸泡5 min（抑制褐变）以及1.0% AsA 20 ℃下浸泡1 h（脱色）。分别用两种方法单独处理或与1 kJ/m2短波紫外线（ultraviolet radiation C,UVC）复合处理,以同等条件下去离子水处理为对照组,统一用30 μm厚的聚乙烯袋包装,5 ℃货架保鲜。结果表明,两组实验中,单独处理和UVC复合处理均可持续抑制多酚氧化酶（polyphenol oxidase,PPO）、过氧化物酶（peroxidase,POD）活力升高,苯丙氨酸解氨酶（phenylalanine ammonia lyase,PAL）活力在货架14～21 d时较对照组显著提高（P＜0.05）,第56天时抑制褐变的单一和复合处理组及脱色的复合处理组酸价均显著低于对照组（P＜0.05）。两组实验中复合处理可同时延缓细菌和霉菌的滋生,部分提高总抗氧化活性（ferric reducing/antioxidant power,FRAP）;核桃仁过氧化值（peroxide value,POV）有所增加,含油率未受明显影响,1,1-二苯基-2-三硝基苯肼（1,1-diphenyl-2-picrylhydrazyl,DPPH）自由基清除能力与对照组差异不明显。核桃仁种衣和去皮核桃仁的PPO活力均受AsA的竞争性抑制。5 ℃货架56 d时,脱色组复合处理核桃仁的亮度（L*值）达到与抑制褐变处理同等效果,且核桃仁无可见霉变。本研究结果可为鲜核桃仁的商品化生产提供理论与技术依据。     

Effects of Dielectric and Steam Heating Treatments on the Storage Stability of Pecan Kernels

Pecan kernels, exposed to dielectric heating treatments for 1, 2, and 2.5 min at 43 MHz, and kernels from in-shell pecans subjected to atmospheric steam for 4 min were evaluated over 16 wk of accelerated storage for flavor quality, formation of hydroperoxides, and moisture equilibrium. All heat treatments were effective in stabilizing flavor quality during storage. Initial peroxide values were greater for higher intensity heat treatments; however, at the end of storage values for these treatments were lower. Moisture equilibrium of the kernels was affected by high heat treatments, which exhibited an initial drying effect and retardation of equilibration during storage. Lipoxygenase was identified in extracts from pecan kernels; however, substances extracted during isolation of the enzyme interfered with reliable replication of results and prevented quantitative analyses in relation to inactivation by heat treatment.     

不同气调包装对核桃仁贮藏品质的影响

将生核桃仁原料分别采用低O2高CO2的聚乙烯(PE)及复合材料(KNY17//CPE80)材料包装密封后,置于(2±1)℃冷库贮藏;以普通聚乙烯(PE)包装为对照,通过定期检测相关品质指标,研究不同气调方法对核桃仁的影响。结果表明：纳米包装和低O2高CO2的PE包装保鲜效果最好,两者均能显著抑制核桃仁过氧化值、酸价升高,保持良好外观品质,而且两种方法贮藏的生核桃仁加工成琥珀核桃仁后,经高温加速贮藏试验,过氧化值、酸价、羰基价都显著低于对照组。     

Physicochemical properties and oxidative stabilities of mealworm (<Emphasis Type="Italic">Tenebrio molitor</Emphasis>) oils under different roasting conditions

Physicochemical properties and oxidative stabilities of mealworm (Tenebrio molitor) oils under different roasting conditions were investigated. Oils were extracted using n-hexane from mealworms roasted at 200°C for 0, 5, 10, and 15 min and physicochemical properties and oxidative stabilities of oils were analyzed. Roasting increased the color intensity and the oleic acid and δ-tocopherol contents, but decreased linoleic acid, and α- and γ-tocopherol contents. An improvement in oxidative stability was observed in roasted mealworm oils, demonstrated by induction time and peroxide values. Mealworm oil contained abundant essential fatty acids and exhibited a superior oxidative stability.     

Survival of Salmonella enteritidis phage type 30 on inoculated almonds stored at -20, 4, 23, and 35 degrees C

To evaluate the survival of Salmonella on raw almond surfaces, whole almond kernels were inoculated with Salmonella Enteritidis phage type (PT) 30 collected from a 24-h broth culture or by scraping cells from an agar lawn. Kernels inoculated with lawn-collected cells to 8, 5, 3, and 1 log CFU per almond after a 24-h drying period were stored for 161 days at 23 +/- 3 degrees C. Calculated rates of reduction were similar for the four inoculum levels (0.22, 0.28, 0.29, and 0.22 log CFU/month, respectively). Kernels inoculated to 7.1 or 8.0 log CFU per almond after drying were stored for 171 or 550 days, respectively, at selected temperatures, including -20 +/- 2 degrees C, 4 +/- 2 degrees C, 23 +/- 3 degrees C, and 35 +/- 2 degrees C. No significant reductions of Salmonella were observed during storage at -20 and 4 degrees C over 550 days. At 35 degrees C, a biphasic survival curve was observed, with calculated reductions of 1.1 log CFU/month from days 0 to 59 and no significant reduction from days 59 to 171. At 23 degrees C, reductions of 0.18 and 0.30 log CFU/month were calculated for 171 and 550 days of storage, respectively. When combined with data from the study of inoculum levels, an overall average calculated reduction at 23 degrees C was 0.25 +/- 0.05 log CFU/month. Significantly greater reductions were observed during the 24-h drying period when broth-collected cells were used as the inoculum, suggesting that cells collected from agar lawns were more resistant to drying. However, after initial drying, the rates of reduction at 23 degrees C did not differ significantly between the inoculum preparation methods. Salmonella Enteritidis PT 30 survives for long periods on almond kernels under a variety of commonstorage conditions.     

Effect of hot water and hydrogen peroxide treatments on survival of salmonella and microbial quality of whole and fresh-cut cantaloupe

Cantaloupe melon has been associated with outbreaks of salmonellosis. Contamination might be introduced into the flesh from the rind by cutting or by contact of cut pieces with contaminated rinds. Our objectives were to investigate the efficacy of hot water or hot 5% hydrogen peroxide treatments in reducing the population of native microflora and inoculated Salmonella on cantaloupe rind and transfer to fresh-cut tissue during cutting. Whole cantaloupes, inoculated with a cocktail of Salmonella serovars to give 4.6 log CFU/cm2 and stored at 5 or 20 degrees C for up to 5 days, were treated with hot water (70 or 97 degrees C) or 5% hydrogen peroxide (70 degrees C) for 1 min at 0, 1, 3, or 5 days postinoculation. Aerobic mesophilic bacteria and yeast and mold on treated whole melon and fresh-cut pieces were significantly (P < 0.05) reduced by all three treatments. Treatments with hot water (70 and 97 degrees C) caused a 2.0- and 3.4-log CFU/cm2 reduction of Salmonella on whole cantaloupe surfaces irrespective of days of postinoculation storage prior to treatment up to 5 days at 5 or 20 degrees C, respectively. Treatment with 5% hydrogen peroxide (70 degrees C) caused a 3.8-log CFU/cm2 reduction of Salmonella. Fresh-cut pieces prepared from untreated inoculated melons and those treated with 70 degrees C hot water were positive for Salmonella. However, fresh-cut pieces prepared from inoculated whole melon dipped in water (97 degrees C) or hydrogen peroxide (70 degrees C) for 60 s were negative for Salmonella, as determined by dilution plating onto agar medium, but were positive after enrichment at days 3 and 5 of storage at 5 degrees C. The ability to detect Salmonella in fresh-cut pieces was dependent on the initial level of inoculation. The results of this study indicate that the use of hot water (97 degrees C) or heated hydrogen peroxide to reduce the population of Salmonella on contaminated whole cantaloupes will enhance the microbial safety of the fresh-cut product.     

Effects of added phenolics on the storage stability of avocado and coconut oils

This study investigated the effects of added phenolics on the storage stability of avocado and coconut oils. Avocado and coconut oils in the absence (control oil) and presence (treated oil) of caffeic acid (CA) or p‐coumaric acid (pCA) were stored at 20 and 60 °C for 50 days. The total phenolic content, peroxide value, p‐anisidine value (p‐AV), free fatty acids (FFAs) and FA composition of the obtained oils were examined on days 0, 7, 15, 23, 35 and 50. Results showed that storage at 60 °C accelerated oil oxidation, and the CA or pCA helped preserve avocado and coconut oils to different extents. CA and pCA protected some desirable unsaturated fatty acids at 60 °C, but facilitated the hydrolysis of triglycerides. Substantially extractable phenolics were still detected in the treated oils after either storage. Incorporation of phenolics into oil products is feasible and beneficial for increasing oil stability and nutritional value.     

Rancidity in hazelnuts due to volatile aliphatic aldehydes

Hazelnut kernels became rancid on storage under ambient conditions in the presence of air. The kernels have a high oil content. The oil contains approximately 75 g per 100 g oleic acid (18:1) and 9 g per 100 g linoleic acid (18:2). Rancidity was detected organoleptically, by gas chromatography/mass spectrometry of the volatile off-flavour compounds and by reduction in both the total fatty acid content (g per 100 g oil) and the iodine value (g per 100 g oil). There was an accumulation of volatile alkanals, 2-alkenals and alkanoic acids on storage of the kernels at ambient temperature in the presence of oxygen. Hexanal (derived from oxidation of linoleic acid) and octanal (derived from oxidation of oleic acid) increased over tenfold on storage, whilst there was concomitant decrease in fatty acid content (83 g per 100 g oil) and iodine value (79) during the same period. It is suggested that analysis of volatile aldehydes such as hexanal and octanal could be used to assess rancidity in foods or oils rather than relatively nonspecific tests such as iodine or peroxide value. There was no evidence in this work that the rancidity was due to microbial spoilage.     

Volatile compounds and changes in flavour‐related enzymes during cold storage of high‐intensity pulsed electric field‐ and heat‐processed tomato juices

BACKGROUND: The effects of high‐intensity pulsed electric field (HIPEF) processing (35 kV cm^?1 for 1500 µs, using 4 µs bipolar pulses at 100 Hz) on the production of volatile compounds and flavour‐related enzymes in tomato juice were investigated and compared with those of thermal processing (90 °C for 30 or 60 s). RESULTS: Tomato juice treated by HIPEF showed lower residual lipoxygenase (LOX) activity (70.2%) than juice heated at 90 °C for 60 s (80.1%) or 30 s (93.2%). In contrast, hydroperoxide lyase (HPL) was almost completely inactivated when the juice was subjected to 90 °C for 60 s, whereas roughly 50% of the control tomato juice was depleted after HIPEF treatment or thermal processing at 90 °C for 30 s. A slight decrease was observed in the initial LOX activity of treated and untreated samples during storage, whereas initial HPL activity was strongly affected over time. CONCLUSION: HIPEF‐treated juice exhibited higher levels of compounds contributing to tomato aroma than untreated and heat‐treated juices throughout storage. Thus HIPEF processing can preserve flavour quality and stability of tomato juice compared with conventional thermal treatments. Copyright © 2010 Society of Chemical Industry     

THERMAL DEATH PARAMETERS of ORANGE JUICE and EFFECT of MINIMAL HEAT TREATMENT and CARBON DIOXIDE ON SHELF-LIFE

Freshly squeezed, refrigerated orange juice has a relatively short shelf-life, which could be extended by minimal processing. D and z values of orange juice microflora were obtained using the capillary method, as well as a plate heat exchanger. the effect of low levels of CO₂ on the shelf-life of the juice was also evaluated. the D₆₀ value of typical orange juice flora was about 5 s and the z was 4–5C. A combination of minimal heat treatment (15 s at 60C) and 6 mM CO₂ extended the storage life of orange juice to 35 days at 4C.
Carbon dioxide flushed into a 10% headspace of 350 ml jars resulted in 6 mM dissolved CO₂ in the juice at 4C. This level of CO₂ extended the shelf-life of unpasteurized juice to 25 days at 4C and 10 days at 10C, as compared to 17 and 5 days without CO₂, respectively. No significant difference in organoleptic evaluations was found between minimally heat treated juices with or without CO₂ and fresh untreated juices without CO₂ during the first week of storage.     

Reduction of Salmonella enteritidis population sizes on almond kernels with infrared heat

Catalytic infrared (IR) heating was investigated to determine its effect on Salmonella enterica serovar Enteritidis population sizes on raw almond kernels. Using a double-sided catalytic IR heating system, a radiation intensity of 5,458 W/m2 caused a fast temperature increase at the kernel surface and minimal temperature differences between the top and bottom kernel surfaces. Exposure of dry kernels to IR heat for 30, 35 and 45 s resulted in maximum kernel surface temperatures of 90, 102, and 113 degrees C, and when followed by immediate cooling at room temperature, yielded a 0.63-, 1.03-, and 1.51-log reduction in S. enterica population sizes, respectively. The most efficacious decontamination treatment consisted of IR exposure, followed by holding of the kernels at warm temperature for 60 min, which effected a greater than 7.5-log reduction in S. enterica on the kernels. During that treatment, the kernel surface temperature rose to 109 degrees C and gradually decreased to 80 degrees C. Similar IR and holding treatments with lower maximum kernel surface temperatures of 104 and 100 degrees C yielded reductions of 5.3 and 4.2 log CFU/g kernel, respectively. During these treatments, moisture loss from the kernels was minimal and did not exceed 1.06%. Macroscopic observations suggested that kernel quality was not compromised by the IR-holding combination treatment, as skin morphology, meat texture, and kernel color were indistinguishable from those of untreated kernels. Our studies indicate that IR heating technology is an effective dry pasteurization for raw almonds.     

A dry-inoculation method for nut kernels

A dry-inoculation method for almonds and walnuts was developed to eliminate the need for the postinoculation drying required for wet-inoculation methods. The survival of Salmonella enterica Enteritidis PT 30 on wet- and dry-inoculated almond and walnut kernels stored under ambient conditions (average: 23 °C; 41 or 47% RH) was then compared over 14 weeks. For wet inoculation, an aqueous Salmonella preparation was added directly to almond or walnut kernels, which were then dried under ambient conditions (3 or 7 days, respectively) to initial nut moisture levels. For the dry inoculation, liquid inoculum was mixed with sterilized sand and dried for 24 h at 40 °C. The dried inoculated sand was mixed with kernels, and the sand was removed by shaking the mixture in a sterile sieve. Mixing procedures to optimize the bacterial transfer from sand to kernel were evaluated; in general, similar levels were achieved on walnuts (4.8–5.2 log CFU/g) and almonds (4.2–5.1 log CFU/g). The decline of Salmonella Enteritidis populations was similar during ambient storage (98 days) for both wet-and dry-inoculation methods for both almonds and walnuts. The dry-inoculation method mimics some of the suspected routes of contamination for tree nuts and may be appropriate for some postharvest challenge studies.     

Impact of γ‐irradiation and thermal processing on the antigenicity of almond,cashew nut and walnut proteins

Whole unprocessed almonds, cashew nuts and walnuts were each subjected to γ‐irradiation (1, 5, 10 and 25 kGy) followed by heat processing including autoclaving (121 °C, 15 psi for 15 and 30 min), dry roasting (138 and 160 °C for 30 min each, 168 and 177 °C for 12 min each), blanching (100 °C for 5 and 10 min), oil roasting (191 °C, 1 min) and microwave heating (500 W for 1 and 3 min). Rabbit polyclonal antibodies were raised against each major protein isolated from defatted, but not subjected to γ‐irradiation and/or any thermal processing, almond, cashew nut and walnut flours. Immunoreactivity of almond, cashew nut and walnut proteins soluble in borate saline buffer, normalised to 1 mg protein ml^?1 for all samples, was determined by inhibition enzyme‐linked immunosorbent assay (ELISA) and Western blotting. ELISAs and Western blotting experiments indicated that almond, cashew nut and walnut proteins exposed to γ‐irradiation alone or followed by various thermal treatments remained antigenically stable. Copyright © 2004 Society of Chemical Industry     

Effect of various processing techniques and different levels of antioxidant on stability of rice bran during storage

Rice bran is a major cereal by‐product available for animal feeding in many parts of the world. It has a good balance of protein, fat, carbohydrates, fiber, vitamins and minerals. The greatest restriction to the use of rice bran is its instability during storage, leading to rancidity and the presence of heat‐labile antinutritional factors. Rice bran was treated to stabilize it by extrusion cooking, roasting, pelleting and adding antioxidant (125, 250 and 375 ppm). The rice bran so treated was stored for 345 days and analyzed every 15 days for free fatty acid, peroxide and iodine values. Heat treatments were effective in stabilizing rice bran by reducing the rancidity and increasing the storage life. Roasting was effective in stabilizing rice bran for only 180 days of storage. Raw and pelleted rice bran behaved similarly with regard to stability during storage for 345 days. Addition of antioxidant in rice bran was not effective for stabilizing FFA, peroxide and iodine values. There was no difference in dose rates of antioxidant of 125, 250 and 375 ppm. Extrusion cooking proved to be the most effective process for stabilizing rice bran for prolonged storage, and roasting would be the next choice. Addition of antioxidant in rice bran was not effective for stabilizing rice bran during storage. Copyright © 2004 Society of Chemical Industry     

Behavior of Listeria monocytogenes inoculated on cantaloupe surfaces and efficacy of washing treatments to reduce transfer from rind to fresh-cut pieces

Attachment and survival of Listeria monocytogenes on external surfaces (rind) of inoculated cantaloupe, resistance of the surviving bacteria to chlorine or hydrogen peroxide treatments, transfer of the pathogen from unsanitized and sanitized rinds to fresh-cut tissues during cutting and growth, and survival of L. monocytogenes on fresh-cut pieces of cantaloupe were investigated. Surface treatment with 70% ethanol to reduce the native microflora on treated melon, followed by immersion in a four-strain cocktail of L monocytogenes (10(8) CFU/ml) for 10 min, deposited 4.2 log10 CFU/cm2 and 3.5 log10 CFU/cm2 of L monocytogenes on treated and untreated cantaloupe rinds, respectively. L. monocytogenes survived on the treated or untreated cantaloupe rinds for up to 15 days during storage at 4 and 20 degrees C, but populations declined by approximately 1 to 2 log10 CFU/cm2. Fresh-cut pieces prepared from inoculated whole cantaloupes stored at 4 degrees C for 24 h after inoculation were positive for L. monocytogenes. Washing inoculated whole cantaloupes in solutions containing 1,000 ppm of chlorine or 5% hydrogen peroxide for 2 min at 1 to 15 days of storage at 4 degrees C after inoculation resulted in a 2.0- to 3.5-log reduction in L. monocytogenes on the melon surface. Fresh-cut pieces prepared from the sanitized melons were negative for L. monocytogenes. After direct inoculation onto fresh-cut pieces, L. monocytogenes survived, but did not grow, during 15 days of storage at 4 degrees C. Growth was evident by 4 h of storage at 8 and 20 degrees C. It is concluded that sanitizing with chlorine or hydrogen peroxide has the potential to reduce or eliminate the transfer of L. monocytogenes on melon surfaces to fresh-cut pieces during cutting.     

SHELF-LIFE EVALUATIONS OF LIQUID FOODS TREATED BY PILOT PLANT PULSED ELECTRIC FIELD SYSTEM

There is a pressing need to validate the shelf-life extension of Pulsed Electric Field (PEF) treated foods. This study was designed to evaluate the shelf-lives of cranberry juice and chocolate milk as a function of PEF and the interaction of PEF+heat treatments. Cranberry juice was exposed to PEF and PEF+heat (60C), and chocolate milk to PEF+heat (105 and 112C). Microbial analysis and color measurement were performed on untreated and treated cranberry juice and chocolate milk aseptically packaged and stored at 4, 22, and 37 C for 197 and 119 days, respectively. Microbial analysis of cranberry juices demonstrated that the shelf-life of PEF and PEF+heat treated juices stored at 22 and 37 C increased significantly during 197 days (p<0.05). The shelf-life of chocolate milk treated by PEF+105C and PEF+112C increased significantly at all storage temperatures (p<0.05). The PEF nor PEF+heat treatments did not result in any significant differences in color retention of either cranberry juice or chocolate milk (p>0.05). This study presented that PEF and PEF+heat treatments were very effective to increase shelf-lives of cranberry juice and chocolate milk.     

Effect of previous chilled storage on rancidity development in frozen horse mackerel (Trachurus trachurus)

Rancidity development during frozen storage (?20 °C) of an underutilised medium‐fat‐content fish species, horse mackerel (Trachurus trachurus), was studied. Special attention was given to the effect of previous chilled storage (0, 1, 3 and 5 days) on the quality of the frozen fish. For this, chemical (free fatty acid and conjugated diene contents; peroxide value, PV; thiobarbituric acid index, TBA‐i; fluorescent compound formation) and sensory (rancid odour and taste) analyses were carried out. Hydrolytic rancidity showed an increase with frozen storage time; however, no effect of previous chilling time was observed on the frozen product. Oxidative rancidity measured by chemical (PV, TBA‐i and fluorescence) and sensory (odour and taste) indices increased with frozen storage time and also with previous chilling time. Satisfactory quality was maintained up to 7 months of frozen storage of horse mackerel provided that a short chilling time (not longer than 3 days) was employed. © 2002 Society of Chemical Industry     

Effects of brine concentration on shelf-life of hot-smoked tilapia (Oreochromis niloticus) stored at 4 °C

This work evaluated the effect of brine concentration on the shelf-life of hot-smoked tilapia (Oreochromis niloticus) stored at 4 °C. The fish were brined in solutions of 5%, 10%, and 15% NaCl and unsalted fish were used as controls. The fish were then smoked, cooled and stored at 4 °C. Oxidative rancidity measured by the peroxide value (PV), and thiobarbituric acid number (TBA) showed increases with the storage time and also as a result of the increasing salt content in fish muscle. Hot smoked tilapia can be stored safely under refrigerated conditions for over 35 days, and 5% brine was found to be optimal for storage.     

Disinfestation of red flour beetle (Tribolium castaneum) present in almonds (Prunus dulcis) using microwave heating and evaluation of quality and shelf life of almonds

Almonds (Prunus dulcis) are one of the high-value nuts facing insect pest infestation predicaments during post-harvest operations and subsequent storage. The red flour beetle (Tribolium castaneum) (Coleoptera: Tenebrionidae) is an economically important and notorious insect pest that globally infest almonds thereby resulting in high storage losses. Currently, the fumigants (hydrogen phosphide and propylene oxide) commonly used during almond storage pose a health hazard to the applicator and consumer as well as the environment. Other disadvantages of chemical methods include chemical residue, high exposure time (2–4 days), pest resistance, the demise of beneficial insects and incomplete disinfestation of the egg stage of the target pest. Among other physical disinfestation methods, the use of microwave as a disinfestation technique offer advantages of less processing time, lower energy consumption, clean technology, and no residues. Therefore to test the efficacy of microwave in pest control of stored almonds, we exposed life stages of T. castaneum to microwave irradiation at different power levels (120–600 W) and durations (30–90 s). Hundred percent mortality of all selected life stages was achieved at 480 and 600 W when infested almonds exposed for 90 and 60 s respectively. The quality attributes of treated almonds such as color difference, water activity, hardness, peroxide value, free fatty acid, and iodine value were measured and found to be acceptable. The fatty acid composition and sensory analysis demonstrated no significant difference (p > 0.05) in control and microwave treated almonds. The storage studies revealed that microwave treated almonds were free from infestation and rancidity for up to 12 months, whereas untreated almonds were spoiled within 3 months.