Green tea extract as a natural antioxidant to extend the shelf-life of fresh-cut lettuce

Green tea extract (GT) was evaluated as a preservative treatment for fresh-cut lettuce. Different quality markers, e.g. respiration, browning, ascorbic acid and carotenoid content were evaluated. GT concentration (0.25, 0.5 and 1 g 100 mL^− 1) and temperature (20 °C and 50 °C) were tested. Optimal GT treatment (0.25 g 100 mL^− 1 at 20 °C) was compared with chlorine (120 ppm at 20 °C). High GT concentrations (0.5 g 100 mL^− 1 and 1.0 g 100 mL^− 1) maintained better prevent ascorbic acid and carotenoid loss than 0.25 g 100 mL^− 1 GT and chlorine. GT increased browning of samples, probably due to the content of polyphenols of the treatment; the use of heat-shock reduced this negative effect. GT and heat-shock combined also showed negative effects, reducing the antioxidant content (ascorbic acid and carotenoids). No significant differences were observed between chlorine and optimal GT (0.25 g 100 mL^− 1 at 20 °C) in browning appearance and sensory properties. GT better kept the antioxidant activity of the samples than chlorine.

Industrial relevance

An alternative treatment for minimally processed Iceberg lettuce is tested, based on its antioxidant capacity. Minimally processed industry is constantly looking for new treatments to avoid the use of chlorine which is a standard at the moment.     

Combined effects of thymol, carvacrol and temperature on the quality of non conventional poultry patties

The combined effect of thymol (0–300 ppm), carvacrol (0–300 ppm), and temperature (0–18 °C) on the quality of non conventional poultry patties packaged in air and modified atmosphere (MAP: 40% CO_2; 30%O₂; 30% N₂) was investigated using a simplex centroid mixture design. The patties were monitored for microbiological (total viable count, Enterobacteriaceae, lactic acid bacteria, Pseudomonas spp.) physico-chemical (pH, colour) and sensory attributes. For the patties mixed with the antimicrobials and stored at low temperature (0–3 °C) a reduction of the cell load of about 1–1.5 log cfu/g was observed. The log reduction was lower at the end of storage time and decreased with the increase of the temperature. For the poultry patties packaged in MAP the higher log reduction for Pseudomonas spp. during all the storage time was observed. In both packaging atmospheres the combination of the essential oils and low temperature determined no modification for off-odour during the first 4 days of storage.     

Texture changes in dry-cured ham pieces by mild thermal treatments at the end of the drying process

The present study evaluated the effects of mild thermal treatments at the end of the drying process on physicochemical characteristics and instrumental and sensory texture in dry-cured ham. Experiment 1: effect of thermal treatments (4–46 °C) for 4 h and 24 h. Experiment 2: time effect (4–168 h) of thermal treatments at 30 °C and 36 °C. Both experiments were done on small dry-cured ham dices. Experiment 3: time effect (4–168 h) of thermal treatment at 30 °C on both instrumental and sensory texture of 4-cm-thick sections of dry-cured ham. The thermal treatment at 30 °C for 168 h on both dry-cured ham muscle dices (20 mm × 20 mm × 15 mm) and dry-cured ham sections (4 cm thick) decreased softness, adhesiveness and pastiness in BF muscle, without increasing hardness in SM muscle or affecting moisture, a_w and proteolysis index.     

Sensory shelf life determination of a processed meat product ‘rullepølse’ and microbial metabolites as potential indicators

Sensory profiling was performed for a Danish lightly fermented heat-processed cold cut pork product termed ‘rullepølse’. Product samples were stored under modified atmosphere (MAP, 30% CO₂/70% N₂) for 0, 28 and 34 days and with subsequent aerobic storage for 4 days (MAP–OPEN) at temperatures of 4 °C and 8 °C. Microbial growth and metabolism was also measured with a focus on lactic acid bacteria (LAB) and their organic acid metabolites including lactic acid, acetic acid and α-ketoisocaproic acid. These acids were examined for sensory shelf life indexing potential for the ‘rullepølse’. Storage temperature exerted distinct impacts on the sensory characterised shelf life of ‘rullepølse’ stored under MAP and MAP–OPEN conditions. The MAP stored ‘rullepølse’ with subsequent 4 days storage in air (MAP–OPEN) could be stored for at least 28 days at 4 °C without a decrease in the sensory quality when opened. Whilst MAP stored ‘rullepølse’ at 8 °C with subsequent open storage (MAP–OPEN), compared to the lower temperature displayed a reduced shelf life of less than 28 days if sensory quality of the ‘rullepølse’ was to be maintained. The stage of sensory deterioration was correlated with high bacterial counts exceeding 10⁶ CFU g⁻¹. With respect to indexing ability of the examined organic acids none were found to have clear potential for prediction of the sensory deterioration.     

Microbial, physical-chemical and sensory spoilage during the refrigerated storage of cooked pork loin processed by the sous vide method

The aim was to study spoilage during the refrigerated storage of cooked pork loin processed by the sous vide method. Samples were packaged under vacuum into polyamide-polypropylene pouches, cooked at an oven temperature/time of 70 °C/12 h, chilled at 3 °C and stored at 2 °C for 0, 5 or 10 weeks. Microbial (psychrotrophs, lactic acid bacteria, Enterobacteriaceae, moulds and yeasts), physical–chemical (pH, water activity, TBARS, acidity, L^*a^*b^* colour, texture profile analysis and shear force) and sensory (appearance, odour, flavour, texture and acceptance) parameters were determined. The results showed that sensory spoilage preceded microbiological spoilage of sous vide pork loin. Counts bellow 1 log cfu/g of psychrotrophs, anaerobic psychrotrophs, Enterobacteriaceae and lactic acid bacteria were detected in any control week, while moderate counts (2–3 log cfu/g) of moulds and yeasts were found. Minor changes in water activity, lipid oxidation, CIELab colour, hardness, cohesiveness or gumminess were associated with spoilage of pork loin, only decreases of lactic acid, springiness and shear force were observed. The pork loin was unacceptable after 10 weeks. This loss of acceptance was mainly due to the deterioration of meaty flavour and odour, although the loss of appearance, juiciness and firmness also contributed. Moderate warmed-over and rancidity were detected. The sensory analysis was the most effective method for determining the shelf life of the sous vide pork-based dishes.     

Flavour formation in pork semimembranosus: Combination of pan-temperature and raw meat quality

Flavour development and overall eating quality of pork semimembranosus were investigated with regard to different raw meat qualities (feeding/fasting strategy; control/low glycogen level, gender; castrate/female, slaughter live-weight; 84 kg/110 kg) combined with frying temperature (150 °C/240 °C). It was further investigated whether the precursor levels of glycogen, IMP, inosine, and hypoxanthine in the raw meat were correlated to the raw meat quality and fried/grilled attributes. Pork schnitzels were fried on a pan (155 °C) or grill–pan (240–250 °C) to a core temperature of 70 °C. Frying temperature was the one factor with greatest influence on the sensory attributes, and pan-grilled schnitzels had significantly higher scores in fried/grilled attributes regardless of meat quality compared to pan-fried schnitzels. Texture was not appreciably influenced by any treatment. There was no correlation between precursor levels and raw meat qualities or fried sensory attributes. Gender and slaughter live-weight had no pronounced influence on flavour and overall eating quality.     

Inhibition of Bacillus cereus and Bacillus weihenstephanensis in raw vegetables by application of washing solutions containing enterocin AS-48 alone and in combination with other antimicrobials

Enterocin AS-48 is a broad-spectrum cyclic antimicrobial peptide produced by Enterococcus faecalis. In the present study, the bacteriocin was tested alone and in combination with other antimicrobials for decontamination of Bacillus inoculated on alfalfa, soybean sprouts and green asparagus. Washing with enterocin AS-48 solutions reduced viable cell counts of Bacillus cereus and Bacillus weihenstephanensis by 1.0–1.5 and by 1.5–2.38 log units right after application of treatment, respectively. In both cases, the bacteriocin was effective in reducing the remaining viable population below detection levels during further storage of the samples at 6 °C, but failed to prevent regrowth in samples stored at 15 or 22 °C. Application of washing treatments containing enterocin AS-48 in combination with several other antimicrobials and sanitizers (cinnamic and hydrocinnamic acids, carvacrol, polyphosphoric acid, peracetic acid, hexadecylpyridinium chloride and sodium hypochlorite) greatly enhanced the bactericidal effects. The combinations of AS-48 and sodium hypochlorite, peracetic acid or hexadecylpyridinium chloride provided the best results. After application of the combined treatments on alfalfa sprouts contaminated with B. cereus or with B. weihenstephanensis, viable bacilli were not detected or remained at very low concentrations in the treated samples during a 1-week storage period at 15 °C. Inhibition of B. cereus by in situ produced bacteriocin was tested by cocultivation with the AS-48 producer strain E. faecalis A-48-32 inoculated on soybean sprouts. Strain A-48-32 was able to grow and produce bacteriocin on sprouts both at 15 and 22 °C. At 15 °C, growth of B. cereus was completely inhibited in the cocultures, while a much more limited effect was observed at 22 °C. The results obtained for washing treatments are very encouraging for the application of enterocin AS-48 in the decontamination of sprouts. Application of washing treatments containing AS-48 alone can serve to reduce viable cell counts of bacilli in samples stored under refrigeration, while application of combined treatments should be recommended to avoid proliferation of the surviving bacilli under temperature-abuse conditions.     

Inactivation of Escherichia coli in orange juice using ozone

This research investigated the efficacy of gaseous ozone for the inactivation of Escherichia coli ATCC 25922 and NCTC 12900 strains in orange juice. Orange juice inoculated with E. coli (10⁶ CFU mL^− 1) as a challenge microorganism was treated with ozone at 75–78 µg mL^− 1 for different time periods (0–18 min). The efficacy of ozone for inactivation of both strains of E. coli was evaluated as a function of different juice types: model orange juice, fresh unfiltered juice, juice without pulp, and juice filtered through 500 µm or 1 mm sieves. Fast inactivation rates for total reduction of E. coli were achieved in model orange juice (60 s) and in juice with low pulp content (6 min). However, in unfiltered juice inactivation was achieved after 15–18 min. This indicated that juice organic matter interferes with antibacterial activity of gaseous ozone. The effect of prior acid (pH 5.0) exposure of E. coli strains on the inactivation efficacy of ozone treatment was also investigated. There was a strain effect observed, where prior acid exposure resulted in higher inactivation times in some cases by comparison with the control cells. However, the overarching influence on inactivation efficacy of ozone was related to the pulp content. Generally, the applied gaseous ozone treatment of orange juice resulted in a population reduction of 5 log cycles.

Industrial relevance

To facilitate the preservation of unstable nutrients many juice processors have investigated alternatives to thermal pasteurisation, including un-pasteurised short shelf life juices with high retail value. This trend has continued within the European Union. However within the US recent regulations by the FDA have required processors to achieve a 5-log reduction in the numbers of the most resistant pathogens in their finished products. Pathogenic E. coli may survive in acid environments such as fruit juices for long periods. This study demonstrates that the use of ozone as a non-thermal technology is effective for inactivation of E. coli and acid exposed E. coli in orange juice. Information on the design of the ozone treatment for inactivation of E. coli which results into safe juice products is also among the main outputs of this work. Ozone auto-decomposition makes this technology safe for fruit juice processing.     

The fate of Clostridium perfringens spores exposed to ozone and/or mild heat pretreatment on beef surfaces followed by modified atmosphere packaging

Clostridium perfringens is a natural contaminant of raw beef products that can proliferate to dangerous cell levels under conditions of temperature abuse. Spores of the bacterium were inoculated onto irradiated London broil beef at levels of 3 log₁₀ spores/g beef. Samples of beef (7.5×10.0×1.0 cm) were treated with aqueous ozone (5 ppm O₃ for 5 min), or heat (60°C for 30 min), or both and then vacuum-packaged to 2 kPa for up to 10 d storage at 37°C, 25°C, or 4°C. Storage at 37°C resulted in increases in viable counts after 1 d to over 7 log₁₀ cfu/g beef, whereas storage at 4°C prevented spore germination and growth for all treatments. At 25°C, heat-treated beef samples reached 6 log₁₀ cfu/g viable counts in 2 d and spores/vegetative cells on control or ozone-treated samples did not germinate or grow through the first day of vacuum-packaged storage. Modified atmospheres with increasing CO₂ concentration were also compared with regard to bacterial survival during beef storage at 25°C. C. perfringens spores remained dormant in control and ozone-treated beef during a 10-d storage at 25°C. Pretreatment with heat increased germination and outgrowth during storage of beef, whereas ozone treatment and no treatment controls were effective in inhibiting spore germination and outgrowth in combination with increasing CO₂ concentrations above 30% or refrigeration. These data support the avoidance of heat in the pretreatment of raw beef.     

Indigenous microorganisms from iceberg lettuce with adherence and antagonistic potential for use as protective culture

The antagonistic effect of the indigenous microflora on pathogens was investigated by using Salmonella Typhimurium, Staphylococcus aureus and Listeria innocua as challenge microorganisms. 18 strains strongly adherent to the leaves of iceberg lettuce were selected and their taxonomic status was determined with the aid of API NE20, BBL CRYSTAL™ E/NF systems and 16 S rDNA sequencing. In the majority of cases (15/19), the identification by biochemical testing did not agree with that of 16 S rDNA sequencing. Six strains exerted antagonistic effects on S. Typhimurium and L. innocua, when overnight cultures or cell free culture supernatants were investigated in the agar diffusion test. In vivo experiments showed that the inoculation of lettuce with P. putida LTH 5878 by dipping and pre-incubation decreased the numbers of S. Typhimurium, L. innocua and S. aureus below the level of detection (< 100 cfu/g) after storage for 7–8 d at 4 °C. The dependency of the antagonistic efficacy on the numbers of P. putida LTH 5878 was determined using point inoculation. The study of the effect of the pseudomonades/pathogen ratio on the reduction of pathogens showed that the antagonistic activity of Pseudomonas is stronger against S. Typhimurium than against L. innocua. A major reduction was achieved for the counts of L. innocua at ratios of greater than 100:1 whereas for S. Typhimurium a ratio of 0.1:1 was already effective. The sensory properties of the inoculated and stored lettuce were in general better than those of the untreated control.

Industrial relevance

The increasing importance of minimally processed ready-to-eat (RTE) vegetables has initiated many studies using surface treatments for microbial decontamination. However, most treatments such as the use of chlorine or ozone have not proven highly effective or desirable. This study is of high relevance because it evaluates the potential of endogenous microbial populations with high surface adherence properties as a competitive tool against pathogenic microorganisms. This is an intriguing concept which deserves further development because of its potential as an new biological food preservation process.     

Susceptibility of stored product insects to high concentrations of ozone at different exposure intervals

Ozone is a highly reactive gas with insecticidal activity. Past studies have indicated that ozone technology has potential as a management tool to control insect pests in bulk grain storage facilities. The objective of this study was to determine the efficacy of short periods of exposure to high ozone concentrations to kill all life stages of red flour beetle (Tribolium castaneum (Herbst)) (Coleoptera: Tenebrionidae), and Indianmeal moth (Plodia interpunctella (Hübner)) (Lepidoptera: Pyralidae), adult maize weevil (Sitophilus zeamais (Motsch.)) (Coleoptera: Curculionidae) and adult rice weevil (S. oryzae (L)) (Coleoptera: Curculionidae). Insects were treated with six ozone concentrations between 50 and 1800 ppm. The specific objective was to determine minimal time needed to attain 100% mortality. The most ozone-tolerant stages of T. castaneum were pupae and eggs, which required a treatment of 180 min at 1800 ppm ozone to reach 100% mortality. Eggs of P. interpunctella also required 180 min at 1800 ppm ozone to reach 100% mortality. Ozone treatments of 1800 ppm for 120 min and 1800 ppm for 60 min were required to kill all adult S. zeamais and adult S. oryzae, respectively. The results indicate that high ozone concentrations reduce the treatment times significantly over previously described results. Our results also provide new baseline information about insect tolerance to ozone treatment.     

Production and stability of chlorine dioxide in organic acid solutions as affected by pH, type of acid, and concentration of sodium chlorite, and its effectiveness in inactivating Bacillus cereus spores

We studied the production and stability of chlorine dioxide (ClO₂) in organic acid solutions and its effectiveness in killing Bacillus cereus spores. Sodium chlorite (5000, 10,000, or 50,000 μg/ml) was added to 5% acetic, citric, or lactic acid solution, adjusted to pH 3.0, 4.0, 5.0, or 6.0, and held at 21 °C for up to 14 days. The amount of ClO₂ produced was higher as the concentration of sodium chlorite was increased and as the pH of the acid solutions was decreased. However, the stability in production of ClO₂ was enhanced by increasing the pH of the organic acid solutions. To evaluate the lethal activity of ClO₂ produced in various acid solutions as affected by acidulant and pH, suspensions of B. cereus spores were treated at 21 °C for 1, 3, 5, or 10 min in hydrochloric acid or organic acid solutions (pH 3.0, 4.0, 5.0, or 6.0) containing ClO₂ at concentrations of 100, 50, or 25 μg/ml. Populations of viable spores treated with ClO₂ at concentrations of 100 or 50 μg/ml in organic acid solutions decreased more rapidly than populations treated with the same concentrations of ClO₂ in HCl. Rates of inactivation tended to increase with higher pH of ClO₂ solutions. Results show that ClO₂ formed in organic acid solutions has higher stability and is more lethal to B. cereus spores than ClO₂ formed at the same concentration in HCl solution. This finding emphasizes the benefits of using organic acid solutions to prepare ClO₂ intended for use as an antimicrobial.     

Effects of soaking, germination and fermentation on phytic acid, total and in vitro soluble zinc in brown rice

Rice is an important staple food in Asian countries. In rural areas it is also a major source of micronutrients. Unfortunately, the bioavailability of minerals, e.g. zinc from rice, is low because it is present as an insoluble complex with food components such as phytic acid. We investigated the effects of soaking, germination and fermentation with an aim to reduce the content of phytic acid, while maintaining sufficient levels of zinc, in the expectation of increasing its bioavailability. Fermentation treatments were most effective in decreasing phytic acid (56–96% removal), followed by soaking at 10 °C after preheating (42–59%). Steeping of intact kernels for 24 h at 25 °C had the least effect on phytic acid removal (<20%). With increased germination periods at 30 °C, phytic acid removal progressed from 4% to 60%. Most wet processing procedures, except soaking after wet preheating, caused a loss of dry mass and zinc (1–20%). In vitro solubility, as a percentage of total zinc in soaked rice, was significantly higher than in untreated brown rice while, in steeped brown rice, it was lower (p < 0.05). Fermentation and germination did not have significant effects on the solubility of zinc. The expected improvement due to lower phytic acid levels was not confirmed by increasing levels of in vitro soluble zinc. This may result from zinc complexation to other food components.     

Viability of multi-strain mixtures of Listeria monocytogenes, Salmonella typhimurium, or Escherichia coli O157:H7 inoculated into the batter or onto the surface of a soudjouk-style fermented semi-dry sausage

The fate of Listeria monocytogenes, Salmonella typhimurium, or Escherichia coli O157:H7 were separately monitored both in and on soudjouk. Fermentation and drying alone reduced numbers of L. monocytogenes by 0.07 and 0.74 log₁₀ CFU/g for sausages fermented to pH 5.3 and 4.8, respectively, whereas numbers of S. typhimurium and E. coli O157:H7 were reduced by 1.52 and 3.51 log₁₀ CFU/g and 0.03 and 1.11 log₁₀ CFU/g, respectively. When sausages fermented to pH 5.3 or 4.8 were stored at 4, 10, or 21 °C, numbers of L. monocytogenes, S. typhimurium, and E. coli O157:H7 decreased by an additional 0.08–1.80, 0.88–3.74, and 0.68–3.17 log₁₀ CFU/g, respectively, within 30 days. Storage for 90 days of commercially manufactured soudjouk that was sliced and then surface inoculated with L. monocytogenes, S. typhimurium, and E. coli O157:H7 generated average D-values of ca. 10.1, 7.6, and 5.9 days at 4 °C; 6.4, 4.3, and 2.9 days at 10 °C; 1.4, 0.9, and 1.6 days at 21 °C; and 0.9, 1.4, and 0.25 days at 30 °C. Overall, fermentation to pH 4.8 and storage at 21 °C was the most effective treatment for reducing numbers of L. monocytogenes (2.54 log₁₀ CFU/g reduction), S. typhimurium (5.23 log₁₀ CFU/g reduction), and E. coli O157:H7 (3.48 log₁₀ CFU/g reduction). In summary, soudjouk-style sausage does not provide a favorable environment for outgrowth/survival of these three pathogens.     

Effects of rapid chilling of carcasses and time of deboning on weight loss and technological quality of pork semimembranosus muscle

The effect of rapid air chilling of carcasses in the first 3 h of chilling at −31 °C (then at 2–4 °C, till 24 h post-mortem) and the possibility of earlier deboning (8 h post-mortem) after rapid air chilling, compared to conventional air chilling (at 2–4 °C, till 24 h post-mortem) on weight loss and technological quality (pH value, tenderness, drip loss, cooking loss and colour - L^*a^*b^* values) of pork M. semimembranosus was investigated. Under the rapid chilling conditions, weight loss was 0.8% at 8 h post-mortem and increased to 1.4% at 24 h post-mortem when weight loss was 2.0% under conventional chilling. Carcasses that were rapid chilled had significantly lower (P < 0.001) internal temperature in the deep leg at 4 (25.7 °C), 6 (13.0 °C), 8 (6.2 °C) and 24 h (3.8 °C) post-mortem compared to conventional chill treatment (32.7, 24.2, 19.1 and 5.1 °C, respectively). Rapid chilling reduced significantly (P < 0.05) the rate of pH value decline at 8 h (6.02) post-mortem in M. semimembranosus compared to conventional chill treatment (5.88). Compared to conventional chilling, in M. semimembranosus deboned in different time post-mortem, rapid chilling had a positive significant effect on drip loss (P < 0.05, muscles deboned 8 h post-mortem), cooking loss (P < 0.001) and incidence of pale colour (L^* value). Rapid chilling i.e. rapid chilling and earlier deboning had neither positive nor negative significant effects (P > 0.05) on other investigated technological quality parameters of M. semimembranosus (tenderness, a^* value and b^* value) compared to conventional chilling.     

Effect of Combined Ozone and Organic Acid Treatment for Control of Escherichia coli O157:H7 and Listeria monocytogenes on Lettuce

ABSTRACT: This study was conducted to determine the effects of ozonated water (1, 3, and 5 ppm) alone with different exposure times (0.5,1,3, or5min), and combinations of 3 ppm ozone with 1% organic acids (acetic, citric, or lactic acids) during 1-min exposure for inactivating Escherichia coli O157:H7 and Listeria monocytogenes on lettuce and to observe the regrowth of these pathogenic bacteria on treated lettuce during storage for 10 d at 15°C. Results showed that 5 ppm ozone treatment for 5 min gave 1.09-log and 0.94-log reductions of E. coli O157:H7 and L. monocytogenes , respectively, indicating insignificant reductions compared with 3 ppm ozone treatment for 5 min. Treatment with 3 ppm ozone combined with 1 % citric acid for 1 min immersing resulted in 2.31 - and 1.84-log reductions ( P < 0.05), respectively. During storage at 15°C for 10 d after combined treatment and packaging, populations of E. coli O157:H7 and L. monocytogenes increased to approximately 9.0-log colony forming unit (CFU) /g, indicating that this treatment did not have a residual antimicrobial effect during storage. Although the storage study did not show control of these pathogens, the combined ozone-organic acid treatment was more effective in reducing population levels of these pathogens on lettuce than individual treatments.     

Inactivation of Listeria monocytogenes during drying and storage of peach slices treated with acidic or sodium metabisulfite solutions

This study evaluated whether treating inoculated peach slices with metabisulfite or acidic solutions enhanced inactivation of Listeria monocytogenes during dehydration and storage. Inoculated (five strain mixture of L. monocytogenes, 7.9 log cfu/g) peach slices were treated, dried for 6 h at 60°C and stored aerobically at 25°C for 14 d. Predrying treatments of inoculated peach slices included: (1) no treatment (control); or 10 min immersion in: (2) sterile water, (3) 4.18% sodium metabisulfite, (4) 3.40% ascorbic acid, or (5) 0.21% citric acid solutions. Samples were plated on tryptic soy agar with 0.1% pyruvate (TSAP) and PALCAM agar for enumeration of surviving bacteria. Immersion in sterile water reduced bacterial populations on peach slices by 0.7 log cfu/g (TSAP and PALCAM). Immersion in the sodium metabisulfite solution reduced populations by 1.5–2.0 log cfu/g, while acidic pretreatments reduced populations by 0.5–0.8 log cfu/g. After 6 h of dehydration, populations on control or water immersed slices were reduced by 3.2–3.4 log cfu/g, whereas populations on slices treated with sodium metabisulfite or acidic solutions were reduced by 4.3–5.1 log cfu/g (TSAP) and 5.3–6.2 log cfu/g (PALCAM), respectively. Bacteria were detectable by direct plating at 14 d of storage, except on acid treated slices. Immersion in acidic or metabisulfite solutions, before dehydration, should enhance inactivation of L. monocytogenes contamination on peach slices during dehydration and storage.     

Effect of ozonated water treatment on microbial control and on browning of iceberg lettuce (Lactuca sativa L.)

We examined the effect of ozonated water treatment on microbial control and quality of cut iceberg lettuce (Lactuca sativa L.). Fresh-cut lettuce was washed in ozonated water (3, 5, and 10 ppm) for 5 min at ambient temperature. The native bacterial population on the lettuce declined in response to a rise in ozone concentration. However, there was no further bacterial reduction (1.4 log CFU/g) above 5 ppm ozone. Although ozonated water treatment increased the phenylalanine ammonia lyase (PAL) activity of the lettuce stored at 10 degrees C compared with the water wash treatment after 1 day of storage, the concentration of ozone did not affect PAL activity. The a* value of the residue of the lettuce methanol extracts, which reflects the extent of browning, increased dramatically in lettuce treated with 10 ppm ozonated water compared with other treatments. Treatment with 3 or 5 ppm ozonated water resulted in more rapid changes in the a* value than after the water treatment. The combined treatment of hot water (50 degrees C, 2.5 min) followed by ozonated water (5 ppm, 2.5 min) had the same bactericidal effect as treatment with ozonated water (5 ppm, 5 min) or sodium hypochlorite (NaOCl, 200 ppm, 5 min), giving a reduction in bacteria numbers of 1.2 to 1.4 log CFU/g. The ascorbic acid content of the lettuce was not affected by these treatments. The combined treatment of hot water followed by ozonated water greatly inhibited PAL activity for up to 3 days of storage at 10 degrees C. Treatment with this combination greatly suppressed increases in the a* value, thus retarding the progress of browning compared with other treatments throughout the 6-day storage. NaOCl treatment also inhibited browning for up to 3 days of storage. Bacterial populations on the lettuce treated with sanitizers were initially reduced but then showed rapid growth compared with that of the water wash treatment, which did not reduce bacterial counts initially.     

Effect of surface-active stabilizers on the surface properties of coconut milk emulsions

Previously we have demonstrated improved stability of coconut milk emulsions homogenized with various surface-active stabilizers, i.e., 1 wt% sodium caseinate, whey protein isolate (WPI), sodium dodecyl sulfate (SDS), or polyoxyethylene sorbitan monolaurate (Tween 20) [Tangsuphoom, N., & Coupland, J. N. (2008). Effect of surface-active stabilizers on the microstructure and stability of coconut milk emulsions. Food Hydrocolloids, 22(7), 1233–1242]. This study examines the changes in bulk and microstructural properties of those emulsions following thermal treatments normally used to preserve coconut milk products (i.e., −20 °C, −10 °C, 5 °C, 70 °C, 90 °C, and 120 °C). Calorimetric methods were used to determine the destabilization of emulsions and the denaturation of coconut and surface-active proteins. Homogenized coconut milk prepared without additives was destabilized by freeze–thaw, (−20 °C and −10 °C) but not by chilling (5 °C). Samples homogenized with proteins were not affected by low temperature treatments while those prepared with surfactants were stable to chilling but partially or fully coalesced following freeze–thaw. Homogenized coconut milk prepared without additives coalesced and flocculated after being heated at 90 °C or 120 °C for 1 h in due to the denaturation and subsequent aggregation of coconut proteins. Samples emulsified with caseinate were not affected by heat treatments while those prepared with WPI showed extensive coalescence and phase separation after being treated at 90 °C or 120 °C. Samples prepared with SDS were stable to heating but those prepared with Tween 20 completely destabilized by heating at 120 °C.     

Efficacy of adding detergents to sanitizer solutions for inactivation of Escherichia coli O157:H7 on Romaine lettuce

Numerous Escherichia coli O157:H7 outbreaks have been linked to consumption of fresh lettuce. The development of effective and easily implemented wash treatment could reduce such incidents. The purpose of this study was to evaluate the addition of food-grade detergents to sanitizer solutions for inactivation of E. coli O157:H7 on Romaine lettuce. Freshly-cut leaves of Romaine lettuce were dip-inoculated to achieve a final cell concentration of 7.8 ± 0.2 log CFU/g, air-dried for 2 h, and stored overnight at 4 °C. Leaves were then washed for 2 min in an experimental short chain fatty acid formulation (SCFA) or in one of the following solutions with or without 0.2% dodecylbenzenesulfonic acid or 0.2% sodium 2-ethyl hexyl sulfate: 1) deionized water; 2) 100 ppm chlorine dioxide; 3) 100 ppm chlorine; and 4) 200 ppm chlorine. Following wash treatment, samples were blended in neutralizing buffer (1:3) and surface plated on the selective media CT-SMAC. The efficacy of wash treatments, with or without the detergents, in inactivating E. coli O157:H7 cells on lettuce leaves were not significantly different. The most effective wash solution was SCFA, which was capable of reducing E. coli O157:H7 populations by more than 5 log CFU/g. The rest of the wash treatments resulted in a population reduction of less than 1 log CFU/g. The effectiveness of SCFA surpasses that of other sanitizer treatments tested in this study and requires further research to optimize treatments to preserve lettuce quality. Conventional detergents did not enhance the efficacy of any of the wash treatments tested during this study.