Changes in appearance and natural microflora on iceberg lettuce treated in warm,chlorinated water and then stored at refrigeration temperature

The objective of this study was to determine the effect of warm, chlorinated water on the survival and subsequent growth of naturally occurring microorganisms and visual quality of fresh-cut iceberg lettuce. After dipping cut lettuce leaves in water containing 20 mg l⁻¹free chlorine for 90 s at 50°C, samples were stored at 5 or 15°C for up to 18 or 7 days, respectively. Populations of aerobic mesophiles, psychrotrophs, Enterobacteriaceae, lactic acid bacteria, and yeasts and molds were determined. The visual appearance and development of brown discoloration were monitored. Treatment of lettuce in warm (50°C) chlorinated water delayed browning of lettuce. Shelf life of lettuce stored at 5°C, as determined by subjective evaluation of color and general appearance, was about 5 days longer than that of lettuce stored at 15°C. Treatment in warm (50°) water, with or without 20 mg l⁻¹chlorine, and in chlorinated water at 20°C significantly (α= 0·05) reduced the initial population of mesophilic aerobic microflora by 1·73–1·96 log₁₀cfu g⁻¹. Populations increased, regardless of treatment, as storage time at 5°C and 15°C increased. The same trends were observed in populations of psychrotrophs and Enterobacteriaceae. Yeast populations increased slightly in lettuce stored at 5°C but were consistently about 3 logs lower than mesophilic aerobes. Populations of molds and lactic acid bacteria were less than 2 log₁₀cfu g⁻¹throughout storage at 5 or 15°C. Results suggest that heat (50°C) treatment may have delayed browning and reduced initial populations of some groups of micro-organisms naturally occurring on iceberg lettuce, but enhanced microbial growth during subsequent storage.     

Effect of temperature and chlorination of pre-washing water on shelf-life and physiological properties of ready-to-use iceberg lettuce

The effects of cold and warm, chlorinated water as well as warm water without chlorination for pre-washing trimmed, cored iceberg lettuce heads was assessed regarding the shelf-life and physiological properties of the resulting ready-to-use (RTU) produce. On a pilot-plant scale, lettuce heads were shredded with or without pre-washing (50 °C, no chlorine; 4 and 50 °C, 200 mg/l free chlorine; 60 s). After shredding, lettuce was washed for 90 s (tap water, 4 °C), spin-dried, packaged in 200 g consumer-sized bags, and stored at 4 °C for ≤ 9 days. Samples were analyzed for their headspace O₂ and CO₂ levels, sensory properties, microbiological status, and phenylalanine ammonia-lyase (PAL) activity at regular intervals throughout processing and storage. Parallelly, instrumental color and texture measurements were performed. All pre-washing procedures of lettuce heads lowered the initial counts of total aerobic bacteria, pseudomonades, and Enterobacteriaceae by ≥ 1.63, ≥ 1.55, and ≥ 1.85 log₁₀ cfu/g, respectively, while the single-wash of shredded lettuce in tap water without any pre-washing resulted in significantly smaller reduction rates (0.23, 0.11, and 0.71 log₁₀ cfu/g, respectively). During storage, all pre-washing procedures had a persistent effect on bacterial counts of the RTU lettuce. Furthermore, all pre-washing procedures delayed vascular tissue browning at cut edges and retarded the decline in the overall visual quality of the samples. Whereas wound-induced PAL synthesis was reduced by the use of warm water (± chlorine), O₂ depletion and CO₂ evolution in the corresponding bags were slightly enhanced, thus proving that processing kept the food as a living tissue.Industrial relevanceReady to use fresh like produce is getting increasing attention and industrial relevance. The aim of this study was to specifically overcome problems associated with product heterogeneity. Interestingly, the use of warm tap water without chlorination as a pre-washing step proved as effective alternative to the application of cold chlorinated water without substantially compromising vitality and freshness of the product.     

Spore-forming bacteria in commercial cooked,pasteurised and chilled vegetable purées

In commercial purées of broccoli, carrot, courgette, leek, potato and split pea, pasteurized in their final packaging and analysed at two periods, Bacillus spp. were the dominant aerobic mesophilic bacteria (AMB). Initial numbers were generally lower than 2 log cfu g⁻¹. They increased up to 6–8 log cfu g⁻¹after about 20 days of storage at 10°C. At 4°C, numbers of AMB after 20 days were lower than 3 log cfu g⁻¹in potato purée, lower than 4 log cfu g⁻¹in leek purée, and between 3 and 6 log cfu g⁻¹in other products. Strict anaerobes were in markedly lower numbers than AMB. At all storage temperatures tested courgette purée usually showed the most rapid bacterial growth and spoilage. On this product, an increase in storage temperature from 4°C to 10°C resulted in a threefold reduction in time to 5 log cfu g⁻¹, and time to spoilage. Growth kinetics of AMB in courgette purée at 20°C, 15°C, 10°C, 6·5°C and 4°C were determined using a mathematical model. Three hundred and forty eight isolates were identified using the API system. Bacillus circulans, B. macerans and B. polymyxa were among the main species isolated from products stored at 4°C and 10°C, while B. subtilis and B. licheniformis were the dominant species in product stored at abuse temperature. Bacillus cereus was isolated from all storage conditions, but mostly from products stored at abuse temperature.     

Acidified sodium chlorite as an alternative to chlorine to control microbial growth on shredded carrots while maintaining quality

Shredded carrots are particularly susceptible to microbial growth and quality deterioration as a result of a large cut surface area to mass ratio. Acidified sodium chlorite (ASC) in the concentration range 500–1200 µL L^?1 has been shown to have stronger efficacy against pathogens and spoilage bacteria than chlorine and does not form carcinogenic products. However, ASC in this concentration range aggravates tissue damage. The objective of this study was to optimize ASC treatment parameters to balance antimicrobial activity with quality retention of shredded carrots. Shredded carrots were immersed for either 1 min in 100, 250 or 500 µL L^?1 ASC solutions or 2 min in 200 µL L^?1 chlorine or water (control). Treated samples were spin‐dried and packaged in polypropylene bags and stored at 5 °C for up to 21 days. Carrots were evaluated at 7‐day intervals for visual appearance, package atmosphere composition (O₂ and CO₂), product firmness, tissue electrolyte leakage and pH. The microbial growth, including total aerobic bacterial counts, total coliforms/Escherichia coli, yeast and mold counts and lactic acid bacterial counts on the products was also determined. Treatments with all concentrations of ASC reduced the aerobic bacterial counts, coliform/E. coli counts, yeast mold and counts and lactic acid bacterial populations by 1.2–2.0 log cfu g^?1 when compared with the water‐washed and unwashed samples. During storage, unwashed samples had a sharp increase in lactic acid bacterial populations accompanied by a sharp decline in pH readings and rapid loss in firmness and tissue integrity; samples washed with 100 µL L^?1 ASC maintained the best overall visual quality, accompanied by the retention of tissue integrity and firmness. Therefore, 100 µL L^?1 was determined as the optimum concentration of ASC for maintaining overall quality and firmness, inhibiting microbial growth and prolonging the shelf‐life of shredded carrots. Copyright © 2006 Society of Chemical Industry     

Chitosan inhibits growth of spoilage micro-organisms in chilled pork products

The aim of this study was to develop novel preservation systems for chilled, comminuted pork products that are sold raw using the natural compound chitosan (polymeric ß -1,4- N -acetylglucosamine). In vitro testing showed that viable numbers of Saccharomycodes ludwigii were reduced by up to 4 log cfu ml⁻¹ on exposure to 0·05% chitosan in 0·9% saline at pH 6·2. Higher concentrations of chitosan (0·25 and 0·5%) were required to achieve similar levels of inactivation withLactobacillus viridescens, Lac. sake and Listeria innocua. Torulaspora delbrueckii and Salmonella enteritidis PT4 were resistant to chitosan at the concentrations tested in this study (up to 0·5%). Trials in real foods showed that dipping of standard and skinless pork sausages in chitosan solutions (1·0%) reduced the native microflora (total viable counts, yeasts and moulds, and lactic acid bacteria) by approximately 1–3 log cfu g⁻¹ for 18 days at 7°C. Chitosan treatment increased the shelf-life of chilled skinless sausages from 7 to 15 days. Addition of 0·3 and 0·6% chitosan to an unseasoned minced pork mixture reduced total viable counts, yeasts and moulds, and lactic acid bacteria by up to 3 log cfu g⁻¹ for 18 days at 4°C compared with the untreated control. The results indicated that chitosan was an effective inhibitor of microbial growth in chilled comminuted pork products.     

Modified Atmosphere Packaging of Fresh Beansprouts

Freshly harvested beansprouts displayed a respiration rate of about 1 mmol O₂ kg⁻¹ h⁻¹ at 10°C which was strongly dependent on temperature, a 10-fold increase being observed every 16·5°C (z=16·5°C, ie Q₁₀=4·4). This commodity is also characterised by a high initial microbial load (about 10⁷ cells g⁻¹). During storage at various temperatures from 1 to 20°C, oxygen uptake rates dramatically increased with time and this phenomenon was well correlated with the development of aerobic microorganisms which reached 10⁹ cells g⁻¹ after 2 days at 20°C or 9 days at 1°C. Beansprouts were packaged in films, with permeabilities ranging from 950 to 200000 ml O₂ m⁻² day⁻¹ atm⁻¹, and stored at 8°C. Due to plant and microbial metabolism, oxygen concentrations decreased steadily within all packs until the onset of plant tissue decay. The latter occurred after 5–6 days with the least permeable films but did not occur within when the film permeability was over 100000 ml O₂ m⁻² day⁻¹ atm⁻¹. However, such films favoured brown discolouration, exudation texture and breakdown. The orientated polypropylene film (OPP) induced anoxic condition within 2 days and favoured anaerobic metabolism and necrosis of the sprouts. In all packages there was a rapid development of aerobic microorganisms and lactic acid bacteria that resulted in the accumulation of acetate and lactate and a decrease in pH. Thus, it clearly appeared that tissue decay was enhanced by microbial activity. At 8°C, 0·24 m² of film per kg of sprouts provided the optimal atmosphere composition (ie 5% oxygen and 15% carbon dioxide) when a film permeability of 50000 ml O₂ m⁻² day⁻¹ atm⁻¹ was used. These conditions allowed a shelf-life of 4–5 days.     

Ultrasonication and Fresh Produce (Cos lettuce) Preservation

Washing Cos lettuce in various sanitizers at different concentrations with and without ultrasonication (40 KHz) reduced the microbiological counts by 1 to 2.5 log colony‐forming units (CFU)/g immediately after washing. Ultrasonication of Cos lettuce in water, chlorinated water, peracetic acid, hydrogen peroxide, and their combinations at various temperatures (4 °C, 20 °C, 35 °C, 47 °C, and 50 °C) had no significant effects (P > 0.05) on the total or the psychrophilic counts during storage at 10 °C. The total count in Cos lettuce reached 9.74 ± 0.035 log CFU/g after ultrasonication (2 min at 50 °C) in chlorinated water (100 mg/L) and storage for 6 d at 10 °C. Extending the ultrasonication (40 kHz) of Cos lettuce for up to 20 min did not improve the bactericidal effect of ultrasonication. However, long‐time ultrasonication (20 min) caused significant (P < 0.05) damage to the quality of Cos lettuce tissues.     

Quality of minimally processed carrots as affected by warm water washing and chlorination

Different applications of cold and warm tap water (4 °C and 50 °C) with and without chlorination, respectively, in the washing of uncut peeled carrots (Daucus carota L.) were conducted, and their effects on sensory and microbiological properties during storage for 9 days at 4 °C were assessed. To minimise cross-contamination of almost sterile inner root parts with the highly contaminated outer cortex during processing the peeled carrots were washed prior to cutting. The washing treatments were carried out using a commercial processing line, thus facilitating the scale-up to industrial production. Populations of aerobic mesophilic bacteria, lactic acid bacteria and enterobacteria on these minimally processed carrots were determined, and the sensorial quality of shredded carrots was evaluated by a sensory panel throughout storage. Additionally, colour, texture, sugars, and trichloromethanes were analysed. Washing uncut carrots with cold chlorinated water (200 mg/l, 4 °C) and warm tap water (50 °C) ensured sugar retention and reduced aerobic mesophilic bacteria by 1.7 and 2.0 log₁₀ colony forming units per gram (cfu/g), respectively, while washing with warm chlorinated water (200 mg/l) resulted in a 2.3 log₁₀ cfu/g reduction. By-product formation due to chlorination was negligible. Sensorial properties of the latter samples were slightly affected. It was shown that both washing uncut knife-peeled carrots with cold chlorinated water (4 °C) and warm tap water (50 °C), respectively, provided good microbiological safety paired with improved sensorial properties. Moreover, fresh-like character of the products was retained, as indicated by the persisting respiration of the living tissues.Industrial relevanceMinimally processed vegetables are an increasing market. Shelf-life extension and consumer safety are of immense relevance for the fresh-cut industry; therefore, the application of antimicrobial agents such as chlorine is widespread. However, various consumer groups object to the use of chlorinated water. The present study aimed at comparing the efficacy of cold and warm tap water with and without chlorination, respectively, in washing uncut carrots during the production of shredded, packaged carrots while operating on pilot-plant scale under conditions of industrial practice. In view of microbial reduction and maintenance of sensory properties, the use of cold chlorinated water and warm tap water, respectively, proved to be effective for washing peeled carrots. By-product formation due to chlorination was negligible.     

Behaviour of Listeria monocytogenes and Staphylococcus aureus in sliced,vacuum-packaged raw milk cheese stored at two different temperatures and time periods

The behaviour of Listeria monocytogenes and Staphylococcus aureus in raw milk cheese slices packaged under vacuum was evaluated. Artificially contaminated 80-day ripened cheese was portioned, vacuum packaged, and then stored for 28 days at 4 °C and for 56 days at 10 °C. Bacterial counts were obtained before vacuum packaging and then weekly during storage. At the end of ripening, the initial L. monocytogenes count was 4.46 ± 0.89 log cfu g⁻¹; weekly bacterial counts remained substantially unchanged in the samples stored at 4 °C but decreased to 3.54 ± 1.54 log cfu g⁻¹ in those stored at 10 °C. The initial S. aureus count before vacuum packaging was 3.60 ± 0.78 log cfu g⁻¹; it then gradually decreased to 2.60 ± 1.32 log cfu g⁻¹ in the samples stored at 4 °C and to about 1.9 log cfu g⁻¹ in those stored at 10 °C.     

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.     

Physicochemical and microbiological changes in postmortem crayfish (Procambarus clarkii) stored at 4 °C and 25 °C

The physicochemical and microbiological parameters of postmortem crayfish stored at 4 °C and 25 °C were evaluated in order to reduce safety risks of crayfish from temperature abuse during transportation and storage. Results showed that hepatopancreas of postmortem crayfish had significantly higher contents of total volatile basic nitrogen, biogenic amines (BAs) and higher microbial loads than tail meat, regardless of storage temperature. Enterobacteriaceae and Pseudomonas counts reached log 6.41 log₁₀ CFU g⁻¹ and 6.31 log₁₀ CFU g⁻¹ in hepatopancreas of crayfish at 25 ℃ for 6 h. Putrescine and cadaverine were the main BAs in tail meat with levels of 28.18 ± 0.73 mg kg⁻¹ and 187.32 ± 3.57 mg kg⁻¹, respectively, whilst cadaverine, spermidine and spermine were the major BAs in hepatopancreas, reaching 283.45 ± 3.95 mg kg⁻¹, 62.87 ± 9.02 mg kg⁻¹ and 155.31 ± 4.55 mg kg⁻¹, respectively, after postmortem storage at 25 °C for 12 h. With time increasing, Acinetobacter, Flavobacterium, Aeromonas and Chryseobacterium at 25 °C and Acinetobacter, Flavobacterium, Psychrobacter at 4 °C in tail meat as well as Bacteroides and Muribaculaceae at 25 °C, and Acinetobacter, Psychrobacter at 4 °C in hepatopancreas, gradually became the major genus at the end of storage. Based on the results of spoilage microorganisms and biogenic amines, crayfish stored at 4 °C and 25 °C could be edible within 24 h and 6 h, respectively.     

Effects of storage conditions,microencapsulation and inclusion in chocolate particles on the stability of probiotic bacteria in ice cream

Three technological approaches to enhance viable counts of probiotic bacteria in ice cream were examined: post-freezing inoculation, use of a microencapsulated culture (spray-coating technology) and inclusion of cultures in chocolate or tablet particles. When a free-cell powder (FCP) of Bifidobacterium longum R0175 was added to the soft ice cream before hardening, a drop of almost 3 log cfu g⁻¹ occurred during production and storage, while it was of only 0.43 log cfu g⁻¹ for Lactobacillus rhamnosus R0011. However, inoculation with a powder of microencapsulated cells (MEP) improved stability of B. longum. The viability of probiotics was further improved when the MEP was incorporated into chocolate particles, which were subsequently blended into the ice cream. Viability losses of the FCP culture during storage at −16 °C in a household freezer having periodic defrost cycles were 10 times higher than when constantly maintained at −20 °C.     

The fate of Escherichia coli O157 : H7 in Myzithra,Anthotyros, and Manouri whey cheeses during storage at 2 and 12°C

Myzithra, Anthotyros and Manouri whey cheeses were inoculated the day after production withEscherichia coli O157 : H7 at concentrations of approx. 1·8×10⁶cfu g⁻¹, and stored at 2 and 12°C for 30 and 20 days, respectively. The pH of the whey cheeses decreased from an initial value of approx. 6·20 to 5·83 or 5·60 (Myzithra) 5·75 or 5·20 (Anthotyros) and 5·80 or 5·30 (Manouri) by the end of the corresponding storage periods at 2 and 12°C, respectively. Escherichia coli O157 : H7 populations in the whey cheeses at the end of the 12°C storage period, had grown with an increase of approx. 1·3 log₁₀cfu g⁻¹. E. coli O157 : H7 populations in whey cheeses at the end of the 2°C storage period did not grow and decreased, with an approx. 2·5 log₁₀cfu g⁻¹reduction. Results showed that E. coli O157 : H7 can grow at 12°C and survive at 2°C storage in Myzithra, Anthotyros and Manouri whey cheeses, and therefore post-manufacturing contamination with this pathogen must be avoided by employing hygienic control programmes such as HACCP.     

Survival of Campylobacter coli in porcine liver

Enteropathogenic Campylobacter jejuni, Campylobacter coli and Campylobacter lari are currently the most common causes of acute infectious diarrhoeal illness in the UK and in most developed countries. Many domestic animals, including pigs, act as natural reservoirs of these organisms and infection may occur through the ingestion of contaminated foodstuffs. Therefore, the safety of porcine liver produced in Northern Ireland was assessed in relation toCampylobacter spp. Storage trials showed that Campylobacter spp. were not able to proliferate in liver at 37°C, but could persist at 4°C and 15°C. Survival was better, however, during storage at 4°C than at 15°C.Campylobacter were rapidly killed in raw liver homogenates and distilled water at 37°C, but not at 4°C. An initial inoculum of 8 log₁₀cfu g⁻¹C. coli was undetectable in liver homogenates after 24h storage at 37°C. Campylobacter coli were sensitive to freezing on liver slices at −18°C and were reduced by 5 log₁₀cycles after 7 days storage. Cells survived better on chilled liver slices and in autoclaved liver homogenates than in raw liver homogenates at all temperatures, which indicates the presence of a heat-labile antagonistic agent in raw liver homogenates. Growth and survival of C. coli was not affected by Lactobacillus plantarum, as C. coli was able to reach 8·5 log₁₀cfu ml⁻¹in 7 days and maintain its viability in the presence of 8·0 log₁₀cfu ml⁻¹L. plantarum. Thus, storage of C. coli on porcine liver at 4°C selected for the survival of this pathogen compared to similar storage at 37°C.Such information may be useful in identifying conditions and treatments that could be integrated in HACCP strategies, or be used to design processes that prevent proliferation and/or destroy Campylobacter spp. that may be present in liver.     

Strategies for raw sheep milk storage in smallholdings: Effect of freezing or long-term refrigerated storage on microbial growth

We assessed the effects of freezing and refrigeration over long periods on the microbiological quality of sheep milk. The raw milk was frozen in 1-L plastic bags or 5-L milk buckets and, after 1 mo, thawed at 7 or 25°C. We evaluated these samples immediately after thawing (d 0) and after 1 d of storage at 7°C. Furthermore, we stored fresh raw milk at 7°C for 10 d in the same packages and in a bulk milk cooler at 4°C (adding 10% of fresh raw milk daily). The total bacterial, total psychrotolerant, and proteolytic psychrotolerant counts were evaluated before and after thawing (for previously frozen milk) and daily (for refrigerated milk). The frozen-thawed milks showed no significant increase in bacterial counts immediately after thawing for all samples (<0.7 log cfu/mL), but only the samples packaged in 1-L bags and thawed at 7°C remained microbiologically adequate after 1 d of storage. Findings of the refrigerated samples were modeled using a modified Gompertz equation, obtaining a lag phase of around 0.5 (5-L bucket), 2.6 (1-L bag), and 7.0 (bulk milk cooler) d for total bacterial and total psychrotolerant counts. Maximum growth rates (µ_max) were 1.0 and 1.0 (5-L bucket), 1.2 and 1.3 (1-L bag) and 3.0 and 1.5 (bulk milk cooler) ln(cfu/mL) per day for total bacteria and total psychrotolerant counts, respectively. Compared with total bacteria and total psychrotolerant bacteria, psychrotolerant proteolytic bacteria grew slowly, reaching unacceptable counts only after 9 to 10 d of storage. The studied methods are interesting alternatives for preserving raw sheep milk on smallholdings.     

Use of 1‐methylcyclopropene to extend the postharvest life of lettuce

This study examined the effect of fumigation of iceberg lettuce with 1‐methylcyclopropene (1‐MCP) at 0.1–1 µl l^?1 for 1–5 h on the storage life at 5 °C in air containing 0.1 µl l^?1 ethylene. 1‐MCP extended the storage life of shredded lettuce at all concentrations, with the optimal treatment being fumigation with 0.1 µl l^?1 1‐MCP for 1 h at 5 °C, which resulted in an extension in storage life of about 50% over untreated lettuce. Application of this treatment to whole lettuce heads resulted in a 100% increase in storage life. 1‐MCP thus appears to be of considerable commercial potential for the lettuce industry. © 2002 Society of Chemical Industry     

Evaluation of a pre-cut heat treatment as an alternative to chlorine in minimally processed shredded carrot

The effect of a pre-cut heat treatment (100 °C/45 s) as an alternative decontamination treatment to chlorinated-water (200 ppm active chlorine/1 min, 5 °C) was evaluated in minimally processed carrot (shredded). The quality of shredded carrots was studied just after minimal processing and during storage at 5 °C (10 days) by evaluating microbial (total mesophilic aerobic, yeast and moulds and lactic acid bacteria counts), physical–chemical (soluble solids content, pH, titratable acidity, whiteness index), physiological (peroxidase activity and headspace analysis) and sensorial attributes (colour, fresh-like appearance, aroma and general acceptance). The relationships between sensory perception of undesired changes, microbial contamination threshold, physico-chemical and physiological indices were investigated and compared between heat-treated and control samples. The use of heat in pre-cut carrot proved to be more efficient than chlorinated-water concerning microbial control (threshold concentration of 7 Log₁₀ cfu g^? 1), providing an acceptable fresh-like quality product during 10 days of storage (5 °C), which corresponds to a 3-day shelf-life extension compared to control samples. Heat-treated shredded carrot showed lower respiratory and POD activities than chlorinated samples suggesting that the use of heat provides a metabolic activity lowering effect besides the microbial effect which could be important to shelf-life extension of the fresh-cut product.Industrial relevanceIn minimally processed vegetables, namely in shredded carrot, chlorine solutions have been widely used by the industry for sanitization purposes. However, reduced microbiological efficiency allied to sensorial changes and eventual formation of carcinogenic chlorinated compounds pointed out the need for alternative decontamination methodologies. Also, the evermore conscious consumers are demanding minimization of the potentially negative impact of food processing on human health and the environment. From the practical experience of a fresh-cut industry directly involved in the R&D research project which supported this study, the marketability of minimally processed shredded carrot is limited due to rapid microbial growth and colour loss (decrease of orange intensity and/or whitening of the shreds). As a result, a pilot-plant scale study was performed, evaluating quality attributes of shredded carrot processed according to a clean pre-cut alternative decontamination process.     

Comparative Growth ofEscherichia coli0157:H7, Spoilage Organisms and Shelf-Life of Shredded Iceberg Lettuce Stored under Modified Atmospheres

The objective of this work was to compare organoleptic and microbiological spoilage with the survival of Escherichia coli 0157:H7 in modified atmosphere (MA) stored shredded lettuce. The rates of growth of E coli 0157:H7, increase in aerobic plate counts (APC g⁻¹), and rates of visual spoilage of shredded lettuce held under air or MA at 13 and 22°C were compared. Samples were inoculated with nalidixic acid-resistant E coli 0157:H7 (ATCC 35150) and placed in a chamber which was continuously flushed with gas mixtures of 0/10/90, 3/0/97, 5/30/65, 20/0/80 (O₂/CO₂/N₂, v/v) and held at 13 or 22°C. APC growth was inhibited in 5/30/65 (O₂/CO₂/N₂) at 13°C compared to all other atmospheres which were not significantly different from each other. The growth rates for both E coli 0157:H7 and APC were greatest in air at 22°C. Carbon dioxide concentration had no significant effect on the growth of E coli 0157:H7 at either temperature. The shelf-life of shredded lettuce, as judged by appearance, was extended in atmospheres containing 30% CO₂ by approximately 300% compared to air. The APC were similar at the time when the shredded lettuce samples were judged unacceptable regardless of shelf-life. However, the extended shelf-life provided by the MA allowed E coli 0157:H7 to grow to higher numbers compared to air-held shredded lettuce.     

Recovery of heat-stressed E. coli O157:H7 from ground beef and survival of E. coli O157:H7 in refrigerated and frozen ground beef and in fermented sausage kept at 7°C and 22°C

A study was undertaken to obtain information on survival of Escherichia coli O157:H7 in ground beef subjected to heat treatment, refrigeration and freezing and on survival of E. coli O157:H7 in fermented sausage kept at 7°C and 22°C. For the challenge test, a mixture of E. coli O157:H7 strains (EH 321, EH 385, EH 302) was used and enumeration was performed on an isolation medium suitable for recovery of stressed organisms: modified Levine's eosin methylene blue agar (mEMB). Heat resistance of E. coli O157:H7 decreased after pre-incubation at a reduced temperature.Escherichia coli O157:H7 was more susceptible to heat inactivation after storage at 7°C and die-off was even more enhanced if cultures were frozen prior to heat inactivation. The enhanced reduction of the pathogen at 56°C after prior storage under refrigeration was confirmed in a test with inoculated ground beef.Escherichia coli O157:H7 was able to survive in ground beef at 7°C for 11 days and at −18°C for 35 days showing maximal one log reduction during the storage period. Thus, ground beef contaminated with E. coli O157:H7 will remain a hazard even if the ground beef is held at low or freezing temperatures. At both 7°C and 22°C, a gradual reduction of E. coli O157:H7 was noticed in fermented sausage over the 35 days storage period resulting in a 2 log decrease of the high inoculum (10⁶cfu 25 g⁻¹). For the low inoculum (10³cfu 25 g⁻¹) a 2·5 log reduction was obtained in 7 and 28 days storage at respectively 22 and 7°C. Application of good hygienic practices and implementation of HACCP in the beef industry are important tools in the control of E. coli O157:H7.     

Microflora of two varieties of sweet cherries: Burlat and Sweetheart

The epiphytic microflora of two widely cultivated sweet cherries ‘Burlat’ and ‘Sweetheart’ from Aragón (Spain), were characterized immediately after harvesting. Microbial analyses of total mesophilic aerobic, Enterobacteriaceae family and mould and yeast counts were carried out. Total mesophilic aerobic counts averaged 4·00 and 2·00 log cfu g⁻¹ for Burlat and Sweetheart cherries, respectively. The Enterobacteriaceae family was the microbial group with the lowest counts averaging 1·56 and 0·07 log cfu g⁻¹. Yeasts were the most prevalent micro-organisms in both varieties, with a mean of 4·10 and 2·30 log cfu g⁻¹ for Burlat and Sweetheart cherries. However, average mould counts slightly exceeded 2·00 log cfu g⁻¹. Statistical differences in microbial counts between the two varieties were detected. These results confirmed the lower susceptibility of Sweetheart cherries to microbial colonization and spoilage. Six hundred and seventy-nine strains, 103 belonging to the Enterobacteriaceae family, 100 mold strains and 442 yeast strains were isolated for the identification. Identification of Enterobacteriaceae species revealed that Pantoea agglomerans was the prevalent species in both varieties. Enterobacter cloacae and Serratia liquefaciens were also present on the Burlat cherry. Investigation of the external mycota led to three genera: Cladosporium, Alternaria and Penicillium. Yeasts were identified using the Deák and Beuchat simplified scheme (SIM) as belonging to five species included in three genera. Trichosporon pullulans was the dominant species, while Rhodotorula glutinis, Rhodotorula rubra, Cryptococcus albidus andCryptococcus neoformans were present at low numbers. Results of the yeast identification were compared with two commercially available kits, Api 20C AUX and PROLEAL. The PROLEAL values agreed with the SIM results; whereas the Api 20C AUX kit led to misidentifications in all strains tested.