Total inactivation of lipoxygenase in whole soya bean by pulsed light and the effect of pulsed light on the chemical properties of soya milk produced from the treated soya beans

The inactivation of lipoxygenase (LOX) in the whole soya bean prevents lipid oxidation that produces an off‐flavour of soya food. The inactivation of lipoxygenase in the whole soya bean by pulsed light (PL) was examined with three distances (5, 7 and 9 cm) from the PL strobe and for different durations. Soya bean was treated with PL with and without ice surrounding the soya bean sample tray for limiting the rise in sample temperature. Results show that without ice surrounding the sample tray, the lowest LOX residual activity was 4.7%, 0.4% and 0.0% for 80‐s duration at 5 cm distance from the PL strobe, 110 s at 7 cm from the strobe and 150 s at 9 cm from the strobe, respectively; the soya bean temperature after treatment was 109.6, 116.3 and 114.8 °C, respectively. The instantaneous temperatures of the soya bean core measured during PL operating were above 100 °C. The lipoxygenase band was disappeared after longest PL treatments of each distance compared with the LOX band control as assessed by electrophoresis. The pulsed light had no negative effect on peroxide value of produced soya milk. However, PL reduced significantly the total solid amount and changed the colour of the produced soya milk. The residual activity with sample cooling by ice during treatment was 79.0%, 98.8% and 95.7%, with sample temperatures of 81.7, 91.2 and 66.9 °C, respectively. This study indicates that PL illumination could fully inactivate LOX in whole soya beans, with the photo‐thermal effect of PL as the main factor responsible for the inactivation of LOX.     

Inactivation of Escherichia coli O157:H7 on Inoculated Alfalfa Seeds with Pulsed Ultraviolet Light and Response Surface Modeling

: Escherichia coli O157:H7‐inoculated alfalfa seeds with seed layer thicknesses of 1.02 to 6.25 mm were subjected to pulsed UV light for up to 90 s at a 8‐cm distance from the UV strobe. Population reductions higher than 4 log₁₀ colony‐forming units (CFU)/g were achieved. For effect of distance from the UV strobe, seeds with 6.25‐mm layer thickness were treated 3 to 13 cm from the strobe. Reductions at shorter distances, such as 60 s at 5 cm (1.93 log₁₀ CFU/g) and 60 to 90 s at 8 cm (4.89 log₁₀ CFU/g), were significantly higher (P≤ 0.05). Data from the treatments were used to develop empirical models as a function of distance or layer thickness and treatment time for predicting the population of E. coli O157:H7 during pulsed UV‐light treatment. This study demonstrates that pulsed UV light holds promise for eliminating pathogens from alfalfa seeds, and the models developed can be useful predictive tools.     

高静压技术对豆浆中脂肪氧合酶的钝化效果及其动力学分析

研究了高静压技术(HHP)对豆浆中脂肪氧合酶(LOX)活性的钝化作用,并进行失活动力学分析。结果表明:HHP处理能显著钝化豆浆中LOX活性。用300～600MPa压力处理5～20min,对LOX活性有显著的钝化效果(P<0.05),并且随处理压力和处理时间的增加,酶的失活率提高。当压力500MPa,保压时间0min时也有一定的钝化LOX效果;当压力600MPa处理10min以上,豆浆LOX活性被完全抑制。用500MPa处理5min,可以达到与传统巴氏杀菌相同的钝酶效果(P>0.05)。HHP技术钝化豆浆LOX的过程可用一级动力学模型拟合(R2>0.900)。随着压力的升高和处理时间的延长,k值逐渐升高,D值逐渐减小;动力学参数ZP和Va分别为125.94MPa和-45.290cm3/mol。HHP技术在钝化豆浆中脂肪氧合酶活性方面比传统巴氏杀菌彻底,效果更好。其在改善豆浆品质方面具有良好的应用前景。     

Physicochemical and Functional Properties of Insoluble Dietary Fiber Isolated from Bambara Groundnut (Vigna subterranea [L.] Verdc.)

Bambara groundnut (BGN) is a widely cultivated legume with a rich nutritional profile, yet despite its many benefits it still remains underutilized. To highlight its potential value, 4 BGN varieties—brown, red, black eye, and brown eye were subjected to sequential enzymatic treatments followed by centrifugation to obtain the insoluble dietary fiber (IDF) fraction. The IDFs were vacuum‐dried and evaluated for color, hydration properties, fat absorption, polyphenolic compounds, neutral sugars, and uronic acids. An optimized white bread formulation was also determined using brown BGN‐IDF in an optimal (IV) mixture design. Three mixture components constrained at lower and upper limits (water: 57% to 60%, yeast: 2.3% to 5.3%, and BGN‐IDF: 7% to 10%) were evaluated for their effects on responses of specific loaf volume, gumminess, chewiness, and resilience of the loaves. All BGN‐IDFs differed significantly (P ≤ 0.05) across all color parameters. Polyphenols were significantly (P ≤ 0.05) highest in red and brown BGN‐IDFs. Arabinose/galactose (31.04% to 37.12%), xylose (16.53% to 27.30%), and mannose (14.48% to 22.24%) were the major sugars identified. Swelling capacity was significantly (P ≤ 0.05) highest for brown eye BGN‐IDF (7.72 ± 0.49 mL/g). Water retention capacity ranged from 1.63 to 2.01 g water/g dry weight. Fat absorption for red BGN‐IDF differed significantly (P ≤ 0.05). Furthermore, the best optimal white bread formulation enriched with brown BGN‐IDF was established with numerical optimization at 59.5% water, 4.3% yeast, and 8.5% BGN‐IDF. Overall positive physicochemical and functional properties were observed for BGN‐IDFs, and it was shown that an optimal white bread enriched with BGN‐IDF could be produced.     

Soybean variety and storage effects on soymilk flavour and quality

Soymilk prepared from five soybean cultivars, grown in Ontario, were analysed for protein, oil, mineral composition, viscosity, colour, lipoxygenase (LOX) activities and flavour profile. Among the five soybean cultivars, the Vinton 81 variety contained the highest protein and the lowest fat. The yield of soymilk from all five cultivars was similar. Major differences were observed in viscosity and in the composition of both the soymilk and the okara. Higher protein and fat extractability was found in soymilk made from S08‐80 and Vinton 81 varieties. Their okara protein contents were also among the highest. Minimum extractability was observed with S03W4 cultivar. Soymilk made from S 03W4 and Vinton 81 cultivars had the whitest colour (lowest ΔE values). Viscosity values were the highest for S08‐80, FG1 and S20‐20 varieties. Headspace solid‐phase microextraction gas chromatography was used to analyse volatile compounds in soymilk. A total of fourteen volatiles were identified, among which aldehydes and their corresponding alcohols were the major compounds. Similar volatile compounds were identified in all the samples analysed but at different concentrations. The highest LOX activity was observed in the Vinton 81 and S20‐20 soybean cultivars, which had the highest total volatile and hexanal contents. A positive correlation (correlation coefficient = 0.82) between enzymatic activity and the total volatiles was observed. Vinton 81 cultivar was subjected to storage (at 18 °C and 50% relative humidity) for a period of 10 months. Soymilk was prepared at different times during storage. The results showed that the soymilk colour, LOX and total volatiles were significantly (P < 0.05) affected by the storage of the soybeans over time.     

Hydrothermal treatments of two cowpea (Vigna unguiculata L. Walp) varieties: effect of micronisation on physicochemical and structural characteristics

The effects of a hydrothermal treatment consisting of tempering (to 41% moisture) and heating to 153 °C (micronisation) on the structural and physicochemical characteristics of two cowpea varieties were studied. The untreated varieties had similar cooking times, although cooked Bechuana white cowpeas were significantly (P ≤ 0.05) softer and had a higher incidence of splitting than Var. 462 cowpeas. This may be due in part to differences in cotyledon structure affecting water uptake during cooking. The hydrothermal treatment changed the physical structure and chemical properties of the cowpea seeds. This led to significant (P ≤ 0.05) reductions in the cooking time of micronised Bechuana white and Var. 462 cowpeas, by 47 and 36% respectively, as compared with control samples. Micronisation caused physical fissuring of the seed coat and cotyledon and significantly (P ≤ 0.05) reduced the bulk density of treated seeds. These changes in the physical structure significantly (P ≤ 0.05) improved the initial water uptake during soaking and cooking, increased the enzyme‐susceptible starch and reduced the protein solubility and hydration capacity of the cowpea seeds. Cooked (60 min) micronised cowpeas also had significantly (P ≤ 0.05) more splits and a significantly (P ≤ 0.05) softer texture than control samples. Copyright © 2005 Society of Chemical Industry     

Mitigation of Major Peanut Allergens by Pulsed Ultraviolet Light

Peanut allergy represents one of the most severe IgE-mediated reactions with food, but to date, the only effective way to prevent peanut allergy is total avoidance. If allergens could be mitigated during food processing before a product reaches the consumer, this would substantially lessen the food allergy problem. The efficacy of pulsed ultraviolet light (PUV), a novel food processing technology, on reducing peanut allergens, was examined. This study revealed for the first time that PUV was also capable of deactivating Ara h 2, the most potent allergenic protein of peanut. Protein extracts from raw and roasted peanuts were treated for 2, 4, and 6?min and peanut butter slurry was treated for 1, 2, and 3?min in a Xenon Steripulse XL 3000? PUV system. The distance from the central axis of the lamp was varied at 10.8, 14.6, and 18.2?cm. The SDS?CPAGE showed a reduction in the protein band intensity for Ara h 1, Ara h 2, and Ara h 3 at the energy levels ranging from 111.6 to 223.2?J/cm². Reduction of the protein band intensity for peanut allergens increased with treatment time but decreased with increased distance from the PUV lamp. The ELISA for peanut extracts and peanut butter slurry showed a reduction in IgE binding of up to 12.9- and 6.7-folds, respectively, compared to control.     

The influence of LOX‐less barley malt on the flavour stability of wort and beer

The aim of this study was to investigate the influence of lipoxygenase‐less (LOX‐less) barley malt on the quality of wort and beer, with the main focus on beer flavour stability. In the current study, pilot‐scale (1000 L) brewing trials were conducted with a control barley malt AC Metcalfe and a LOX‐less barley malt, PolarStar. The results clearly indicated that the LOX‐less barley malt showed less nonenal potential than the control, although LOX activities in both barley malts were relatively low. The beer brewed from the LOX‐less barley malt contained much lower concentrations of trans‐2‐nonenal (T2N) and gamma‐nonalactone, especially after the (forced or natural) aging of the beer, compared with the beer brewed under the same conditions using the control malt. The sensory panel evaluation indicated similar results in the general flavour profile. The freshness scores of beer brewed from the LOX‐less malt were higher than those from the control malt, and this was more pronounced after forced aging. In addition, the beer brewed from LOX‐less malt had a much better foam stability, almost 30 s (NIBEM test). These results confirm that the use of the LOX‐less barley malt was beneficial to beer flavour stability and foam stability. Copyright © 2014 The Institute of Brewing & Distilling     

Relationship between growth of food‐spoilage yeast in high‐sugar environments and sensitivity to high‐intensity pulsed UV light irradiation

The relationship between prior growth of food‐spoilage yeast in high‐sugar environments and their subsequent survival postpulsed UV (PUV) irradiation was investigated. Test yeast were separately grown to early stationary phase in YPD broth containing increasing concentrations of glucose (1–50% w/v) and were flashed with ≤40 pulses of broad‐spectrum light at lamp discharge energy settings of 3.2, 7.2 and 12.8 J (equivalent to UV doses of 0.53, 1.09 and 3.36 μJ cm^?2, respectively) and their inactivation measured. Findings showed that prior growth in high‐sugar conditions (≥30% glucose w/v) enhanced the sensitivity of all nine representative strains of Zygosaccharomyces bailii, Z. rouxii and Saccharomyces cerevisiae yeast to PUV irradiation. Significant differences in inactivation amongst different yeast types also occurred depending on amount of UV dose applied, where the order of increasing sensitivity of osmotically stressed yeast to PUV irradiation was shown to be Z. rouxii, Z. bailii and >S. cerevisiae. For example, a 1.2‐log order difference in CFU mL^?1 reduction occurred between Z. bailii 11 486 and S. cerevisiae 834 when grown in 50% w/v sugar samples and treated with the uppermost test UV dosage of 3.36 μJ cm^?2, where these two yeast strains were reduced by 3.8 and 5.0 log orders, respectively, after this PUV treatment regime compared to untreated controls. The higher the UV dose applied the greater the reduction in yeast numbers. For example, a 1.0‐, 1.4‐ and 4.0‐log order differences in CFU mL^?1 numbers occurred for S. cerevisiae 834 grown in 15% w/v sugar samples and then treated with PUV dose of 0.53, 1.09 and 3.36 μJ cm^?2, respectively. These findings support the development of PUV for the treatment of high‐sugar foods that are prone to spoilage by osmotolerant yeast.     

Ultraviolet and Pulsed Electric Field Treatments Have Additive Effect on Inactivation of E. coli in Apple Juice

ABSTRACT: Apple juice inoculated with Escherichia coli ATCC 23472 was processed continuously using either ultraviolet (UV), high‐voltage pulsed electric field (PEF), or a combination of the PEF and UV treatment systems. Apple juice was pumped through either of the systems at 3 flow rates (8, 14, and 20 mL/min). E. coli was reduced by 3.46 log CFU/mL when exposed in a 50 cm length of UV treatment chamber at 8 mL/min (2.94 s treatment time with a product temperature increase of 13 °C). E. coli inactivation of 4.87 log CFU/mL was achieved with a peak electric field strength of 60 kV/cm and 11.3 pulses (average pulse width of 3.5 μs, product temperature increased to 52 °C). E. coli reductions resulting from a combination treatment of UV and PEF applied sequentially were evaluated. A maximum E. coli reduction of 5.35 log CFU/mL was achieved using PEF (electrical field strength of 60 kV/cm, specific energy of 162 J/mL, and 11.3 pulses) and UV treatments (length of 50 cm, treatment time of 2.94 s, and flow rate of 8 mL/min). An additive effect was observed for the combination treatments (PEF and UV), regardless of the order of treatment (P > 0.05). E. coli reductions of 5.35 and 5.30 log CFU/mL with PEF treatment (electrical field strength of 60 kV/cm, specific energy of 162 J/mL, and 11.3 pulses) followed by UV (length of 30 cm, treatment time of 1.8 s, and flow rate of 8 mL/min) and UV treatment followed by PEF (same treatment conditions), respectively. No synergistic effect was observed.     

Pulsed UV light as a postprocessing intervention for decontamination of hard‐cooked peeled eggs

The efficiency of pulsed UV light (PL) for inactivation of E. coli K12 on hard‐cooked eggs was investigated. Temperature, colour and texture were recorded to determine adverse effects on quality. Distance from the quartz window (5.5, 9.5 cm) and time (1–30 s) was set as the experimental variables. Results indicated that E. coli K12 viability decreased at closer distances and increased time (P < 0.05). Bacterial populations were reduced to 3.54 log CFU per egg and 3.23 log CFU per egg after 15 and 20 s at 5.5 cm and 9.5 cm, respectively. Scanning electron micrographs revealed the existence of photophysical mechanisms, bacterial overlapping and internalisation interfering inactivation. Treated samples experienced slight thermal increases (6–9 °C) contributing to the preservation of colour and texture, not significantly different from untreated samples (P > 0.05). Our findings support the use of PL to enhance the safety of hard‐cooked eggs although bacterial shadowing may have significant implications on treatment efficiency.     

Low‐protein amino acid‐supplemented diets in broiler chickens: effects on performance,carcass characteristics,whole‐body composition and efficiencies of nutrient utilisation

Two concurrent trials were conducted to investigate the influence of low‐protein amino acid‐supplemented diets on the performance, carcass characteristics, whole‐body composition and efficiencies of nutrient utilisation by the male broiler chicken from age 3 to 6 weeks. The first trial comprised five isoenergetic (13.0 MJ kg⁻¹) diets containing 225 (control), 210, 190, 172 or 153 g kg⁻¹ crude protein (CP) supplemented with essential amino acids (EAAs) to meet the minimum National Research Council recommendations. In the second trial a composite mixture of non‐essential amino acids (NEAAs) was added to the lower‐CP diets (ie 210–153 g kg⁻¹) such that they became isoproteinous (N × 6.25) with the 225 g kg⁻¹ control. Neither the lowering of dietary CP nor NEAA supplementation had any significant influence on weight gain or the relative weights of the various carcass cuts. However, chicks fed the lowest‐CP diets consumed more feed (P ≤ 0.05) and had poorer (P ≤ 0.05) feed conversion efficiency (FCE). NEAA supplementation enhanced FCE to the control levels. Whole‐body compositional analysis showed that lowering dietary CP increased (P ≤ 0.01) total body fat in a linear fashion (P ≤ 0.001; r = −0.72). Equalising dietary CP with the control (ie maintaining identical energy/protein ratio) by NEAA supplementation did not correct for the fat deposition. Total body protein (g kg⁻¹) was identical with the control with or without NEAA supplementation. Dietary energy, protein retention efficiency (PRE) and protein efficiency ratio (PER) were more efficient (P ≤ 0.01) in the lower‐protein diets, while NEAA supplementation significantly (P ≤ 0.01) decreased the efficiency of N utilisation. Reducing dietary CP from 225 to 153 g kg⁻¹ decreased N excretion in a highly significant linear fashion (P ≤ 0.001; r = 0.73). The nutritional and environmental implications of the increased body fat deposition on the one hand and the decreased N excretion on the other in the low‐protein‐fed chickens are discussed and the need to harmonise these apparently conflicting interests is emphasised. © 2000 Society of Chemical Industry     

Effect of Pulsed Ultraviolet Light and High Hydrostatic Pressure on the Antigenicity of Almond Protein Extracts

The efficacy of pulsed ultraviolet light (PUV) and high hydrostatic pressure (HHP) on the IgE binding to the almond extracts was studied using sodium dodecyl sulfate polyacrylamide-gel electrophoresis, Western blot, and enzyme-linked immunosorbent assay (ELISA) probed with human plasma containing IgE antibodies to almond allergens and a polyclonal antibody against almond major protein. Crude almond protein extracts were treated with PUV (3 pulses/s, 10 cm from lamp) for 0.5, 1, 2, 3, 4, 6, 7, and 10 min. In comparison, boiling treatments were also carried out. The HHP treatments were conducted at 600 MPa for 5, 15, and 30 min at three temperatures of 4 °C, 21 °C, and 70 °C. Western blots and indirect ELISA demonstrated a reduction in the levels of allergens and IgE binding in PUV-treated extracts at 7 min, which was found to be the optimal time for PUV exposure. Boiling was not as effective as PUV in reducing the overall IgE-binding of the almond extracts. Unlike PUV, HHP did not affect the allergen levels and IgE binding under the conditions tested.     

Inactivation of Escherichia coli O157:H7 and Listeria monocytogenes inoculated on raw salmon fillets by pulsed UV-light treatment

The efficacy of pulsed UV‐light to inactivate of Escherichia coli O157:H7 and Listeria monocytogenes Scott A on salmon fillets was investigated in this study by evaluating the effects of treatment times and distance from the UV strobe. The sterilization system generated 5.6 J cm^?2 per pulse at the lamp surface for an input voltage of 3800 V and three pulses per second. Skin or muscle side inoculated salmon fillet (8 cm × 1.5 cm) in a Petri dish was placed on shelf at three different distances from the UV strobe; 3, 5, and 8 cm. At each distance, the pulsed UV‐light treatment was performed for 15, 30, 45, and 60 s. For E. coli O157:H7, maximum log₁₀ reduction was 1.09 log₁₀ CFU g^?1 on muscle side at 8 cm for 60‐s treatment, whereas 0.86 log₁₀ CFU g^?1 reduction on skin at 5 cm for 30‐s treatment. For L. monocytogenes Scott A, maximum reduction was 1.02 log₁₀ CFU g^?1 at 8 cm for 60‐s treatment on skin side, whereas 0.74 log₁₀ CFU g^?1 reduction on muscle at 8 cm for 60‐s treatment. The fillet's surface temperature increased up to 100degrC within 60‐s treatment time. Therefore, some fish samples were overheated after 30 and 45 s at 3‐ and 5‐cm distances from light source, respectively, which resulted in visual colour and quality changes. Overall, this study demonstrated that about one log reduction (c. 90%) of E. coli O157:H7 or L. monocytogenes could be achieved at 60‐s treatment at 8 cm distance without affecting the quality.     

Temporal Check‐All‐That‐Apply Characterization of Syrah Wine

Temporal Check‐All‐That‐Apply (TCATA) is a new dynamic sensory method for which analysis techniques are still being developed and optimized. In this study, TCATA methodology was applied for the evaluation of wine finish by trained panelists (n = 13) on Syrah wines with different ethanol concentrations (10.5% v/v and 15.5% v/v). Raw data were time standardized to create a percentage of finish duration, subsequently segmented into thirds (beginning, middle, and end) to capture panel perception. Results indicated the finish of the high ethanol treatments lasted longer (approximately 12 s longer) than the low ethanol treatment (P ≤ 0.05). Within each finish segment, Cochran's Q was conducted on each attribute and differences were detected amongst treatments (P ≤ 0.05). Pairwise tests showed the high ethanol treatments were more described by astringency, heat/ethanol burn, bitterness, dark fruit, and spices, whereas the low ethanol treatment was more characterized by sourness, red fruit, and green flavors (P ≤ 0.05). This study demonstrated techniques for dealing with the data generated by TCATA. Furthermore, this study further characterized the influence of ethanol on wine finish, and by extension wine quality, with implications to winemakers responsible for wine processing decisions involving alcohol management.     

Comparative evaluation of weaning foods from Glyricidia and Leucaena leaf protein concentrates and some commercial brands in Nigeria

Three studies were conducted to evaluate the nutritive potential of Glyricidia leaf protein concentrate (GLPC) and Leucaena leaf protein concentrate (LLPC) in infant weaning foods. The first two trials evaluated 10 laboratory‐formulated weaning foods, in which soybean meal (SBM) was replaced at levels of 0, 25, 50, 75 and 100% with either GLPC or LLPC, and subsequently compared them nutritionally with three commercial weaning foods (coded CFB, CFC and CFN) currently on sale in Nigeria in a 28 day feeding trial using weanling albino rats. Thereafter the best GLPC‐ and LLPC‐based weaning foods, in terms of animal performance consistent with low cost of the foods (designated GL50 and LL25 respectively), were compared with the best commercial weaning food (CFB) in a 14 day rehabilitative potential trial using rats that had previously been protein depleted. In the first trial the final weight was highest in rats fed the 50% GLPC‐based food (159.8 ± 9.5 g) and lowest in rats fed CFN (114.7 ± 9.7 g), while the feed efficiency was best in rats fed the 50% GLPC‐based food and CFC and worst in rats fed the 100% GLPC‐based food and CFN. The nitrogen retention (NR) did not differ significantly (P ≥ 0.05), while the apparent nitrogen digestibility (AND) and ‘operative’ protein efficiency ratio (PER) decreased with increasing level of replacement of SBM with GLPC (R² = 0.61, P ≤ 0.05 and R² = 0.67, P ≤ 0.05 respectively). In the second trial the highest weight gain was observed in rats fed the 25% LLPC‐based food (3.4 ± 0.5 g day^?1). Feed consumption was not significantly (P ≥ 0.05) influenced by dietary treatment, but rats fed the laboratory‐formulated diets containing 0 and 25% LLPC utilised their food more efficiently (3.0 ± 0.4/0.2 respectively) than rats fed the other diets, including the commercial foods. While NR did not differ significantly (P ≥ 0.05), there was a decrease in AND and PER with increasing level of SBM replacement with LLPC (R² = 0.96, P ≤ 0.01 and R² = 0.89, P ≤ 0.05 respectively). Among all the organs weighed in the first two trials, only the relative weight of the lungs was significantly (P ≤ 0.05) affected. Neither the haematological variables nor the serum metabolites were significantly influenced by dietary treatment, except for the packed cell volume of rats fed the LLPC‐based foods. The economics of food production showed that all the laboratory‐formulated foods were cheaper than the commercial foods, with the 50% SBM + 50% GLPC (GL50) and 75% SBM + 25% LLPC (LL25) formulae proving to be the most nutritious. On rehabilitation, rats fed LL25 recovered lost weight faster than those fed GL50, followed by rats fed the best commercial diet (CFB), while the whole‐body and liver protein contents were identical. The incorporation of LPC/SBM mixtures into local food formulae is suggested as a valid intervention strategy for tackling the endemic protein under‐nutrition, especially among vulnerable groups, in sub‐Saharan Africa. Copyright © 2003 Society of Chemical Industry     

Lysyl oxidase from jumbo squid (Dosidicus gigas) muscle: detection and partial purification

Lysyl oxidase (LOX) was detected and partially purified from jumbo squid (Dosidicus gigas) muscle, for the first time. A procedure for the purification of LOX from jumbo squid muscle which consisted of urea extraction, Sephadex G‐75 and anion exchange chromatography was developed. Activity of partially purified LOX was 390‐fold higher than the original extract. Two protein fractions with 32 and 24 kDa were detected by SDS‐PAGE. The enzyme was strongly inhibited by β‐aminopropionitrile fumarate, a specific LOX inhibitor. LOX was purified with 3.8% yield, showing a specific activity of 0.078 IU mg^?1 protein. This knowledge will help understand the behaviour of jumbo squid protein during cool storage or manufacture.     

The Interaction Between Lipoxygenase‐Catalyzed Oxidation and Autoxidation in Dry‐Cured Bacon and a Model System

A model system was conducted to characterize the interaction between lipid autoxidation and enzyme‐catalyzed oxidation in dry‐cured bacon. This involved the use of a hydroxyl radical (HO?) generating system and the extraction and purification of lipoxygenases (LOX) from pork belly. The results showed that LOX activity rapidly (P < 0.05) increased during the curing of dry‐cured bacon. This may be because of the hydroxyl‐radical‐mediated oxidation from LOX‐Fe²⁺ to LOX‐Fe³⁺, which activates LOX. In addition, experiments of the model system also showed that LOX activity could be inhibited by increasing the substrate concentration, although substrate type and concentration had no effect on autoxidation. Moreover, LOX enzyme‐catalyzed oxidation and autoxidation could act synergistically to promote lipid oxidation irrespective of the substrate (linoleic or arachidonic acid). These results provide useful information for regulating lipid oxidation during the production of dry‐cured pork products.     

Proximate compositions, pasting and rheological properties of mumu– a roasted maize meal

Genetically improved maize variety (TZRS‐W) grains were used to produce mumu– a roasted maize meal. The grains were divided into six treatment groups namely: non‐soaked, non‐cooked (NSNC); non‐soaked, cooked (NSC); soaked, non‐cooked (SNC); soaked, cooked (SC); germinated non‐cooked (GNC); and germinated, cooked (GC). Each group was roasted in the oven at 150 °C for 1 h to produce mumu. No significant differences (P ≤ 0.05) were found in the protein, fat, ash, fibre and carbohydrate contents of the different products. Soaking and germination without cooking resulted in lower breakdown viscosities of the products. The peak viscosity (20.17 Rapid Visco Unit (RVU)) and final viscosity (28 RVU) of the GNC samples were significantly higher (P ≤ 0.05) than the corresponding values (5.17–7.25 RVU) of the NSNC, NSC, SNC, SC and GC products. No significant differences (P ≤ 0.05) were found in the pasting temperatures (63.40–64.85 °C) between all the six groups. Germination for 24 h without cooking may yield poor quality products with low nutrient density.