Reducing Salmonella on cantaloupes and honeydew melons using wash practices applicable to postharvest handling, foodservice, and consumer preparation

Washing conditions that included a soak or brush scrub were evaluated for removal of Salmonella from the surface of smooth (honeydew) or complex (cantaloupe) melon rinds. Melon rinds were spot-inoculated onto a 2.5 cm2 area of rind (squares) with approximately 6.0 log(10) CFU/square of an avirulent nalidixic acid-resistant strain of Salmonella typhimurium. Melons were washed by immersion in 1500 ml of water or 200 ppm total chlorine and allowed to soak or were scrubbed over the entire melon surface with a sterile vegetable brush for 60 s. Inoculated sites, uninoculated sites ("next to" sites) that were adjacent to inoculated sites, and sites on the side of the melon opposite (remote sites) the inoculated site were excised and pummeled in a stomacher for 2 min prior to plating onto tryptic soy or bismuth sulfite agar supplemented with 50 microg/ml nalidixic acid. S. typhimurium was reduced on the rind of cantaloupe by 1.8 log CFU/melon after soaking for 60 s in 200 ppm total chlorine, which was significantly better than the 0.7 log CFU/melon achieved with soaking in water. For both water and 200 ppm total chlorine, scrubbing with a vegetable brush was shown to be significantly (0.9 log CFU/cantaloupe) more effective than soaking alone. When honeydew melons were soaked or scrubbed in water, reductions of 2.8 log CFU/melon or >4.6 log CFU/melon (four of five samples), respectively, were observed. However, when water treatments were used, the presence of Salmonella-positive "next to" and remote sites indicated that bacteria were spread from inoculated site on the rind to uninoculated sites either through the rinse water (40-70 CFU/ml of Salmonella) or scrub brush (400-500 CFU/brush). Transfer to other sites occurred more often with cantaloupe than honeydew melons. This transfer was eliminated when 200 ppm total chlorine was used. When 200 ppm total chlorine was used, Salmonella could not be detected in the water or on the scrub brush. For optimal microbial removal in food service and home settings, melons should be scrubbed with a clean brush under running water. However, to ensure the benefits of brushing, instructions for cleaning and sanitizing brushes must also be emphasized. For food service settings where concentration and pH can be adequately measured, the use of chlorinated water may provide additional benefit.     

ATP bioluminescence assay for estimation of microbial populations of fresh-cut melon

Estimation of microbial numbers in foods by conventional microbiological techniques takes days, so there is a need for faster methods that can give results in minutes. Research was undertaken to investigate the use of bioluminescent ATP determination and a firefly luciferase assay to estimate the initial population of aerobic mesophilic bacteria on fresh-cut melons immediately after preparation and during storage at 5 or 15 degrees C for up to 12 days. Populations of aerobic mesophilic bacteria on fresh-cut cantaloupe prepared immediately from unsanitized whole melons averaged 3.42 log CFU/g, corresponding to an ATP value of 5.40 log fg/g. Populations for fresh-cut honeydew prepared from unsanitized whole melon averaged 1.97 log CFU/g, corresponding an ATP value of 3.94 log fg/g. Fresh-cut pieces prepared from cantaloupe or honeydew melons sanitized with either chlorine (200 ppm free chlorine) or hydrogen peroxide (2.5%) had similar ATP values: 3.1 log fg/g (corresponding to bacterial counts 1.7 log CFU/g) for cantaloupes and 2.6 log fg/g (corresponding to bacterial counts of 0.48 CFU/g) for fresh-cut honeydew. Positive linear correlations for ATP concentrations and microbial populations were found for fresh-cut cantaloupe (R2 = 0.99) and honeydew R2 = 0.95) during storage at 5 degrees C for up to 12 days. ATP values in fresh-cut melons inoculated with either aerobic mesophilic bacteria or yeast and mold were significantly higher (P < 0.05) than control values and parallel total plate counts on plate count agar. Results of this study indicate that the bioluminescent ATP assay can be used to monitor total microbial populations on fresh-cut melon after preparation and during storage for quality control purposes to establish specific sell-by or consume-by dates.     

On-farm and postharvest processing sources of bacterial contamination to melon rinds

Multistate and international foodborne illness outbreaks, particularly involving cantaloupe and often involving rare Salmonella spp., have increased dramatically over the past 13 years. This study assessed the sources and extent of melon rind contamination in production fields and at processing and packing facilities. In the spring of 1999, cantaloupe (Cucumis melo L. [reticulatus group] cv. Cruiser) sampled from two sites in the Rio Grande River Valley showed that postharvest-processed melon rinds often had greater plate counts of bacterial contaminants than field-fresh melons. Cantaloupe in the field had 2.5 to 3.5 log CFU g(-1) rind total coliforms by aerobic plate counts, whereas washed melons had 4.0 to 5.0 log CFU g(-1). In the fall of 1999, coliforms on honeydew melons (C. melo [inodorous group] cv. Honey Brew) ranged from 2.6 to 3.7 log CFU g(-1) after processing, and total and fecal coliforms and enterococci never fell below 2.5 log CFU g(-1). A hydrocooler at another site contaminated cantaloupe rinds with up to 3.4 log CFU g(-1) total and fecal enterococci; a secondary rinse with chlorinated water incompletely removed these bacteria. Sources of coliforms and enterococci were at high levels in melon production soils, especially in furrows that were flood irrigated, in standing water at one field, and in irrigation water at both sites. At one processing facility, wash water pumped from the Rio Grande River may not have been sufficiently disinfected prior to use. Because soil, irrigation water, and process water were potential sources of bacterial contamination, monitoring and management on-farm and at processing and packing facilities should focus on water quality as an important control point for growers and packers to reduce bacterial contamination on melon rinds.     

Effectiveness of potassium lactate and sodium diacetate in combination with irradiation to control Listeria monocytogenes on frankfurters

ABSTRACT:  The use of antimicrobial ingredients in combination with irradiation is an effective antilisterial intervention strategy for ready-to-eat meat products. Microbial safety was evaluated for frankfurters formulated with 0% or 3% added potassium lactate/sodium diacetate solution and inoculated with Listeria monocytogenes before or after treatment with irradiation (0, 1.8, or 2.6 kGy). Frankfurters were stored aerobically or vacuum packaged and L. mo nocytogenes counts and APCs were determined while refrigerated. The incorporation of lactate/diacetate with or without irradiation had a strong listeriostatic effect for aerobically stored frankfurters. Outgrowth was suppressed and counts were not different from initial counts (5.2 log CFU/frank compared with 5.0 log CFU/frank); however, those without the additive increased steadily (5.4 to 9.3 log CFU/frank). Irradiation treatments alone had higher L. monocytogenes counts after 3 wk. For vacuum-packaged frankfurters, both the addition of lactate/diacetate and irradiation were effective at controlling growth after 8 wk. Large and incremental reductions in total counts were seen for irradiation treatments. Initial counts were reduced by 3 log CFU with the application of 1.8 kGy while 2.6 kGy decreased counts over 5 log CFU. These reductions were maintained throughout storage for lactate/diacetate-treated frankfurters. By 8 wk, L. monocytogenes counts on 1.8 and 2.6 kGy irradiated frankfurters without lactate/diacetate increased to 7.43 and 6.13 log CFU, respectively. Overall, lactate/diacetate retarded the outgrowth of L. monocytogenes on frankfurters throughout aerobic storage and the combination of irradiation and 3% lactate/diacetate reduced and retarded growth of L. monocytogenes , especially during the last 2 wk of vacuum-packaged storage.     

MICROBIAL QUALITY OF FRESH‐CUT ICEBERG LETTUCE WASHED IN WARM OR COLD WATER AND IRRADIATED IN A MODIFIED ATMOSPHERE PACKAGE*

ABSTRACT

The microbial keeping quality of fresh‐cut iceberg lettuce was determined after being washed in either cold water (5C) for 3 min or warm water (47C) for 2 min followed by a cold water rinse (5C) and packaged in a modified atmosphere film bag. The lettuce samples were treated with gamma radiation to 0, 1 or 2 kGy while maintaining a refrigerated temperature (4C). The samples were analyzed for total aerobic, total coliform and Enterobacteriaceae counts after refrigerated storage up to 12 days. No difference in aerobic counts was observed between the hot‐ and cold‐washed samples immediately after washing. The coliform and Enterobacteriaceae counts were reduced by 2 log after the warm water wash and no difference for the cold water‐washed sample. The irradiation treatment at 1 kGy reduced the aerobic, coliform and Enterobacteriaceae counts by 2 log for the warm‐washed samples. At the 2‐kGy treatment level, the aerobic and coliform counts were reduced by 3 log for the cold‐washed lettuce, whereas the Enterobacteriaceae counts were reduced by only 2 log. The observed log reductions in bacterial counts after irradiation were maintained for 12 days when stored at 4C. The combination of a cold water wash and irradiation to 2 kGy had the best microbial keeping quality.

PRACTICAL APPLICATIONS

Fresh‐cut lettuce, when washed in either cold or warm water, shows neither an appreciable removal of the microbial load nor a significant increase in the keeping quality when compared with unwashed fresh‐cut controls. Placing the washed lettuce into modified atmosphere packaging (MAP) did not lessen the overall bacteriologic load, and after 12 days of storage at 4C, the microbial counts increased. However, gamma irradiation of the washed, MAP‐stored lettuce to a dose of 2 kGy significantly reduces the overall microbe count, thereby increasing both the shelf life and the safety of the produce. A 2‐kGy dose of gamma irradiation provides a pathogen‐free, long shelf life, fresh‐cut lettuce that is bacteriologically safer and sensorially indistinguishable from bagged, nonirradiated, fresh‐cut lettuce.     

Gamma Irradiation Effects on Shelf Life and Gel Forming Properties of Washed Red Hake (Urophycis chuss) Fish Mince

Fresh washed red hake (Urophycis chuss) mince without cryoprotectants was irradiated at 0 (control), 0.66 and 1.31 kGy and stored aerobically at 3.3°C. The total aerobic plate counts of the control and the low and high levels irradiated samples remained less than 10⁶ CFU/ g for 4, 10, and 17 days, respectively. Gel strength decreased after irradiation of mince, and such decreases were dose-dependent. Irradiation extended sensory shelf life of unfrozen fish mince 12–18 days and microbiologically (<10⁶ CFU/g) 6–13 days longer than the unirradiated control.     

Shelf Life and Sensory Characteristics of Baby Spinach Subjected to Electron Beam Irradiation

Abstract: The use of ionizing radiation for the control of foodborne pathogens and extending the shelf life of fresh iceberg lettuce and fresh spinach has recently been approved by the U.S. Food and Drug Administration. The efficacy of electron beam irradiation for controlling foodborne pathogens has been reported. For this experiment, the effectiveness of electron beam irradiation on the microbiological and sensory characteristics of fresh spinach was studied. Total aerobic plate counts were reduced by 2.6 and 3.2 log CFU/g at 0.7 and 1.4 kGy, respectively. Lactic acid bacteria were reduced at both doses of e-beam but grew slowly over the 35 d of the experiment. Yeasts and molds were not reduced in samples exposed to 0.7 kGy whereas 1.4 kGy significantly reduced microbial counts. Gas compositions (O₂ and CO₂) were significantly different than controls. Oxygen levels inside the spinach sample bags decreased over time; however, O₂ levels did not drop below 1% that can induce anaerobic fermentation. CO₂ levels for all treatments increased through day 4; yet 7 d after irradiation, CO₂ level differences were not significant in both control and irradiated samples. Irradiation dose did not affect the basic tastes, aromatics, or mouth feels of fresh spinach, however; hardness attributes decreased as irradiated dose increased and slimy attributes of fresh spinach were higher in control samples compared to irradiated samples.     

Effect of electron beam irradiation on color and microbial bioburden of red paprika

The effect of irradiation with electron beams on the microbiological quality and color properties of red paprika was examined. The irradiation doses ranged from 0 to 12.5 kGy. The counts performed were total mesophilic aerobic microorganisms, Enterobacteriaceae, coliforms, sulfite-reducing clostridia, molds, and yeasts. It was concluded that molds, yeasts, and sulfite-reducing clostridia were the most resistant species, although a 10-kGy dose of irradiation leads to optimum sanitation. Extractable color and apparent color were analyzed to appraise the incidence of the irradiation treatments in the color properties of red paprika. Extractable color was determined according to the American Spice Trade Association method, and apparent color was analyzed by reflectance using the CIELab color space. Data showed no significant differences between the color properties of irradiated and nonirradiated samples. Irradiation was a suitable procedure to minimize the bioburden of red paprika with small modifications of its color properties.     

Effect of hydrogen peroxide treatment on microbial quality and appearance of whole and fresh-cut melons contaminated with Salmonella spp

The efficacy of hydrogen peroxide treatment on the inactivation of Salmonella spp. inoculated on the external surface of cantaloupe and honeydew melon was investigated. Salmonella was inoculated onto whole cantaloupe and honeydew melon to a final concentration of 4.65 log(10) CFU/cm(2) and 3.13 log(10) CFU/g, respectively. Inoculated whole melons stored at 5 degrees C for up to 7 days were washed with water, 2.5% and 5% hydrogen peroxide at day 0 and 5. Hydrogen peroxide (2.5% and 5%) treatments of whole melon for 5 min caused a 3 log(10) CFU/cm(2) reduction of the indigenous surface microflora and a 3.0 log(10) CFU/cm(2) reduction in Salmonella spp. on all melon surfaces. The efficacy of the hydrogen peroxide treatments was less when the interval between inoculation and treatment of cantaloupe exceeded 24 h. Unlike cantaloupe fresh-cut pieces, Salmonella was not recovered from fresh-cut pieces prepared from treated whole honeydew melon. Growth of Salmonella occurred in cantaloupe fresh-cut pieces stored at 10 or 20 degrees C, and by 2 weeks, levels reached approximately 1 log CFU/g. A rapid decline in appearance and overall acceptability was observed in fresh-cut pieces prepared from untreated whole cantaloupe. While Salmonella was recovered from fresh-cut pieces from and whole treated cantaloupe, sanitizing the surface of contaminated whole melons with hydrogen peroxide before and after cutting and storage of the fresh-cut pieces at 5 degrees C can enhance the microbial safety and acceptability rating for about 2 weeks after processing.     

Effect of sanitizer treatments on Salmonella Stanley attached to the surface of cantaloupe and cell transfer to fresh-cut tissues during cutting practices

The ability of Salmonella Stanley to attach and survive on cantaloupe surfaces, its in vivo response to chlorine or hydrogen peroxide treatments, and subsequent transfer to the interior tissue during cutting was investigated. Cantaloupes were immersed in an inoculum containing Salmonella Stanley (10(8) CFU/ml) for 10 min and then stored at 4 or 20 degrees C for up to 5 days. Periodically, the inoculated melons were washed with chlorine (1,000 ppm) or hydrogen peroxide (5%), and fresh-cut tissues were prepared. The incidence of Salmonella Stanley transfer from the rinds to the fresh-cut tissues during cutting practices was determined. A population of 3.8 log10 CFU/cm2 of Salmonella Stanley was recovered from the inoculated rinds. No significant (P < 0.05) reduction of the attached Salmonella population was observed on cantaloupe surfaces stored at 4 or 20 degrees C for up to 5 days, and the population was not reduced after washing with water. Salmonella Stanley was recovered in fresh-cut pieces prepared from inoculated whole cantaloupes with no sanitizer treatment. Washing with chlorine or hydrogen peroxide solutions was most effective immediately after inoculation, resulting in an approximate 3.0-log10 CFU/cm2 reduction, and the level of recovered Salmonella population transferred to fresh-cut samples was reduced to below detection. The effectiveness of both treatments diminished when inoculated cantaloupes stored at 4 or 20 degrees C for more than 3 days were analyzed, and the fresh-cut pieces prepared from such melons were Salmonella positive. Salmonella outgrowth occurred on inoculated fresh-cut cubes stored above 4 degrees C.     

Validation of individual and multiple-sequential interventions for reduction of microbial populations during processing of poultry carcasses and parts

Changes in aerobic plate counts (APC), total coliform counts (TCC), Escherichia coli counts (ECC), and Salmonella incidence on poultry carcasses and parts and in poultry processing water were evaluated. Bacterial counts were estimated before and after individual interventions and after poultry carcasses were exposed to multiple-sequential interventions at various stages during the slaughter process. Individual and multiple-sequential interventions were evaluated at three processing plants: (i) plant A (New York wash, postevisceration wash, inside-outside bird washes 1 and 2, chlorine dioxide wash, chlorine dioxide wash plus chlorine chiller, chiller exit spray, and postchiller wash), (ii) plant B (New York wash, inside-outside bird washes 1 and 2, trisodium phosphate wash, and chlorine chiller), and (iii) plant C (trisodium phosphate wash and chlorine chiller). The majority of individual interventions effectively or significantly (P < 0.05) reduced microbial populations on or in carcasses, carcass parts, and processing water. Reductions in APC, TCC, and ECC due to individual interventions ranged from 0 to 1.2, 0 to 1.2, and 0 to 0.8 log CFU/ml, respectively. Individual interventions reduced Salmonella incidence by 0 to 100% depending on the type of process and product. Multiple-sequential interventions resulted in significant reductions (P < 0.05) in APC, TCC, ECC, and Salmonella incidence of 2.4, 2.8, and 2.9 log CFU/ml and 79%, respectively, at plant A; 1.8, 1.7, and 1.6 log CFU/ml and 91%, respectively, at plant B; and 0.8, 1.1, and 0.9 log CFU/ml and 40%, respectively, at plant C. These results enabled validation of in-plant poultry processing interventions and provide a source of information to help the industry in its selection of antimicrobial strategies.     

Bioluminescence ATP assay for estimating total plate counts of surface microflora of whole cantaloupe and determining efficacy of washing treatments

The surface microflora of cantaloupes were estimated using a bioluminescence ATP assay, and results were compared to plate count data. Cantaloupes were treated as follows: (i) water washed, or (ii) washed in solutions of sodium hypochlorite (1,000 mg/liter) or hydrogen peroxide (5%) for 5 min. Bioluminescence ATP assay results showed differences in ATP level/cm2 of cantaloupes dipped in chlorine or hydrogen peroxide solution; ATP levels in these washed samples were lower than in controls due to antimicrobial action of the treatments on the cantaloupe surface. Linear correlations were found between the bioluminescence ATP assay and aerobic plate counts of unwashed cantaloupe (r2 = 0.995) and those washed with water (r2 = 0.990) determined before storage. Lower correlations between the bioluminescence ATP assay and the aerobic plate counts were observed on cantaloupes stored for 120 h at 20 degrees C (r2 = 0.751) than at 4 degrees C (r2 = 0.980) without washing treatment. Lower correlation at 20 degrees C may be the result of clusters or growth that occurred in chains. ATP levels of washed cantaloupes correlated well with bacterial plate counts (r2 = 0.999). A reliable minimum detectable threshold using the bioluminescence ATP assay was established at 3 log10 fg/cm2 corresponding to 4 log10 CFU/cm2. Bioluminescence ATP assay is not recommended for washed samples where the microbial load is near or below the threshold. Therefore, the bioluminescence ATP assay will be recommended for quick estimation of total microbial load on cantaloupe surfaces where the population is expected to exceed this threshold. The assay can save the industry time by eliminating the required incubation required by the conventional methods.     

Use of irradiation to control foodborne pathogens and extend the refrigerated market life of rabbit meat

This study set out to evaluate the microbiological status of rabbit meat and the possibility of using irradiation to control foodborne pathogenic bacteria and extend the refrigerated storage life of meat. Rabbit meat samples were γ irradiated at doses of 0, 1.5 and 3 kGy. The samples were stored at refrigeration temperature, then the effects of irradiation and storage on their microbiological, chemical and sensory properties were studied. Irradiation at 1.5 kGy significantly reduced the counts of Staphylococcus aureus, Listeria monocytogenes, Enterococcus faecalis and enterobacteriaceae but was not enough for complete elimination of Salmonella. However, 3 kGy dose reduced the counts of S. aureus, L. monocytogenes, E. faecalis and enterobacteriaceae by more than 3, 3, 1.4 and 4 log units, respectively, while Salmonella was not detected. On the other hand, irradiation at 1.5 and 3 kGy significantly reduced the counts of aerobic mesophilic bacteria, psychrophilic bacteria and molds and yeasts and prolonged the refrigerated shelf-life of samples to 12 and 21 days, respectively, compared to 6 days for non-irradiated controls. Irradiation of samples significantly increased their amounts of thiobarbituric acid reactive substances (TBARS) but had no significant effects on their total volatile nitrogen (TVN) contents, while storage significantly increased the TBARS and TVN for irradiated and non-irradiated samples. γ irradiation showed no significant effects on the sensory properties of raw meat. Moreover, fried burgers prepared from irradiated rabbit meat showed high sensory acceptability similar to those prepared from non-irradiated meat.     

Effects of Low-dose Gamma Irradiation on the Shelf Life and Quality Characteristics of Cut Romaine Lettuce Packaged under Modified Atmosphere

Cut romaine lettuce, packaged under modified atmosphere, was subjected to 0.15 and 0.35 kGy gamma irradiation. Irradiation at 0.35 kGy decreased aerobic plate counts by 1.5 logs and yeast and mold counts by 1 log; these differences were maintained through the 22-d storage. Irradiation at 0.15 kGy caused smaller reductions in microbial counts. A decrease in headspace CO₂ was observed in the 0.35-kGy-treated lettuce, although CO₂ concentrations increased in all samples with storage. O₂ concentration was not affected by irradiation. Ten percent loss in firmness was observed at 0.35 kGy, while other sensory attributes such as color, generation of off-flavor, and appearance of visual defects were not affected.     

Use of mild irradiation doses to control pathogenic bacteria on meat trimmings for production of patties aiming at provoking minimal changes in quality attributes

The objectives of the present work were to assess the use of moderate doses of gamma irradiation (2 to 5 kGy) and to reduce the risk of pathogen presence without altering the quality attributes of bovine trimmings and of patties made of irradiated trimmings. Microbiological indicators (coliforms, Pseudomonas spp and mesophilic aerobic counts), physicochemical indicators (pH, color and tiobarbituric acid) and sensory changes were evaluated during storage. 5 kGy irradiation doses slightly increased off flavors in patties. Two pathogenic markers (Listeria monocytogenes and Escherichia coli O157:H7) were inoculated at high or low loads to trimming samples which were subsequently irradiated and lethality curves were obtained. Provided that using irradiation doses ≤ 2.5 kGy are used, reductions of 2 log CFU/g of L. monocytogenes and 5 log CFU/g of E. coli O157:H7 are expected. It seems reasonable to suppose that irradiation can be successfully employed to improve the safety of frozen trimmings when initial pathogenic bacteria burdens are not extremely high.     

Sensorial,nutritional and microbiological quality of fresh cilantro leaves as influenced by ionizing radiation and storage

The impact of gamma irradiation on aroma, appearance, nutritional, textural, and microbiological quality attributes of fresh cilantro (Coriandrum sativum L.) was investigated. Irradiation at doses up to 2 kGy did not significantly influence aroma, amount of total volatile compounds, color or overall visual quality. Although firmness of cilantro was reduced by irradiation at day 0, there was no significant difference among treatments after 3, 7 and 14 days of storage at 3 °C. Irradiation did not have a consistent effect on antioxidant power or phenolic content during the 14-day storage. In contrast, vitamin C content was lower at day 14 in samples irradiated at 2 and 3 kGy. Cilantro irradiated at 3 kGy had higher decay rate and off-odor scores than other samples after 14 days of storage. The total aerobic plate count of irradiated cilantro was significantly lower than that of nonirradiated controls immediately after irradiation and during the entire storage period. Our results suggest that fresh cilantro irradiated at 2 kGy retained its sensorial quality and shelf life.     

THE SHELF-LIFE OF MINIMALLY PROCESSED FRESH CUT MELONS

Honeydew and cantaloupe melons were surface sterilized by scrubbing with a hypochlorite solution at low level (200 ppm total available chlorine) and high level (2000 ppm total available chlorine), peeled and cut into “chunks”. Fruit pieces were dipped in a dilute hypochlorite solution (pH 6) of 50 ppm total available chlorine prior to packaging under an atmosphere of 95% N₂ and 5% O₂ and storage at 2.2C. Unwashed and water-washed samples were also prepared as controls. Microbial counts and sensory analyses were monitored during a 20 day storage period. Microbial counts of unwashed and water-washed samples were found to be significantly (p≤0.05) different from the fruits which were chlorine washed initially, and during the storage time. However, increasing the free available chlorine concentration tenfold did not result in any further significant increase in the shelf-life. Rapid decline was observed in all measured microbial and sensory quality factors of unwashed samples during storage. Proper sanitation and production practices along with raw material selection can ensure a shelf-life of 15 days for cantaloupe and honeydew pieces.     

Electron-beam Irradiation Preserves the Quality of White Button Mushroom (Agaricus bisporus) Slices

ABSTRACT: The effect of electron-beam irradiation on microbial counts, color, texture, and enzyme activity of mushroom slices was evaluated at dose levels of 0.5, 1, 3.1, and 5.2-kGy. Irradiation levels above 0.5 kGy reduced total plate counts, yeast and mold, and psychrotrophic counts to below detectable levels and prevented micro-bial-induced browning. Firmness of all samples was similar during storage except for the 5.2-kGy sample. Color was preserved by irradiation as evidenced by the higher L values. Electron-beam irradiation at these levels did not affect the polyphenol oxidase activity. Irradiation at 1 kGy was most effective in extending shelf-life of mushroom slices.     

Effects of X-ray treatments on pathogenic bacteria, inherent microflora, color, and firmness on whole cantaloupe

Inactivation of inoculated Escherichia coli O157:H7, Listeria monocytogenes, Salmonella enterica and Shigella flexneri on whole cantaloupes using X-ray at different doses (0.1, 0.5, 1.0, 1.5, and 2.0 kGy) was studied. The effect of X-ray on quality parameters (color and texture) of untreated and treated whole cantaloupes was instrumentally determined. The effect of X-ray on microflora counts (mesophilic counts, psychrotrophic counts and yeast and mold counts) of untreated and treated whole cantaloupes was also determined during storage at 22°C for 20 days. A mixture of three strains of each tested organism was spot inoculated (100 μl), separately, onto the surface (5 cm(2)) of cantaloupe rinds (approximately 8-9 log CFU ml(-1)) separately, air dried (60 min), and then treated with X-ray at 22°C and 55% relative humidity. Surviving bacterial populations on cantaloupe surfaces were evaluated using a nonselective medium (tryptic soy agar) with a selective medium overlay for each bacterium; E. coli O157:H7 (CT-SMAC agar), L. monocytogenes (MOA), and S. enterica and S. flexneri (XLD). More than a 5 log CFU reduction was achieved after treatment with 2.0 kGy X-ray, for all tested pathogens. No significant effect of X-ray treatment on cantaloupe color or firmness was detected. Furthermore, treatment with X-ray significantly reduced the initial inherent microflora on whole cantaloupes and inherent levels were significantly (p<0.05) lower than the control sample throughout storage for 20 days.     

EFFECTIVENESS OF CHLORINE AND NISIN‐EDTA TREATMENTS OF WHOLE MELONS AND FRESH‐CUT PIECES FOR REDUCING NATIVE MICROFLORA AND EXTENDING SHELF‐LIFE1

Efficacy of nisin‐EDTA treatments as a sanitizing treatment for reducing native microflora of whole melons and extending shelf‐life of fresh‐cut pieces was compared to chlorine treatments. Whole cantaloupe and honeydew melons were washed with water, nisin (10 μg/mL)‐EDTA (0.02 M), or 200 ppm chlorine for 5 min at ～ 20C before fresh‐cut preparation and storage at 5C for 15 days with periodic microbiological sampling. In addition, some fresh‐cut pieces were washed with 10 μg/mL nisin‐EDTA or 50 ppm chlorine for 1 min before storage. Changes in appearance, odor, overall acceptability and the shelf‐life of the minimally processed fresh‐cut melons were investigated. Preliminary studies indicated that water washes, EDTA (0.002 to 0.2 M) or nisin (5 to 10 μg/mL) were not effective in reducing the microflora of whole melon when used individually. Nisin‐EDTA and chlorine treatments were significantly (P < 0.05) more effective in reducing native microflora than water washes. Nisin‐EDTA treatments were significantly (P < 0.05) more effective than chlorine in reducing populations of yeast and mold and Pseudomonas spp. on whole melon surfaces but were not as effective as chlorine treatments for reducing aerobic mesophilic bacteria, lactic acid bacteria and total gram‐negative bacteria. Microbial contaminants on fresh‐cut pieces washed with 50 ppm chlorine or nisin‐EDTA were further reduced. However, microbial populations increased throughout refrigerated storage irrespective of treatments. Odor, appearance, and overall acceptability ratings for cantaloupe and honeydew fresh‐cut pieces treated with nisin‐EDTA or chlorine were not significantly (P > 0.05) different from each other throughout the storage period (15 to 21 days). However, both treatments led to significantly (P < 0.05) improved ratings compared to the controls for the fresh‐cut pieces at 9 to 12 days of storage and thereafter. The results of this study suggest that treatments with nisin‐EDTA before and after fresh‐cut processing would improve the quality and extend the shelf‐life of fresh‐cut melon.