Control of the bacteriological condition of calf brain. I. Impact of improving hygiene

Sixty calves of the Dutch Friesian (FH) breed were stunned mechanically. Without previously having been stunned, another 30 calves were stuck according to the Jewish rite. Upon opening of the skulls (1–2 h post mortem) brains of mechanically stunned calves were collected either conventionally (n = 30) or ‘hygienically’ (n = 30), i.e. using a fresh pair of surgical gloves during each removal to avoid cross contamination. For ritually slaughtered animals only the hygienic procedure was followed. Samples of 10 g were excised from undamaged hemispheres and in the mechanically stunned treatment group also from the site of impact of the captive bolt. After storage in polystyrene trays at 3 ± 1°C for 7 days sampling was repeated. Bacteriological examination included the assessment of aerobic colony counts at 30°C for 3 days (ACC-30) and 4°C for 14 days (ACC-4) and Enterobacteriaceae colony counts at 37°C for 20 h (ECC). In conventionally collected samples the ACC-30 and ACC-4 were 3.8 and 3.0 log₁₀ cfu g^?1 at day 1 and 6.2 and 6.4 log₁₀ cfu g^?1 at day 8. With hygienic collection these counts were reduced by approximately 1 log unit. Whilst by conventional practice the ECCs, at day 1 and 8 were 2.6 and 4.8 log₁₀ cfu g^?1 these counts were 1.8 and 2.6 log₁₀ cfu g^?1 for hygienic practice. In samples excised from the site of impact of the captive bolt the hygienic procedure had similar, though less marked effects. On day 1 brains from ritually slaughtered animals had a bacteriological contamination similar to that found in the hemispheres of mechanically stunned calves. However, whilst at day 8 their mean ECCs were 3.4 and 3.5 log₁₀ cfu g^?1 the percentages of plates ‘positive’ for Enterobacteriaceae were only 10% in the ritually vs. 53% in the mechanically stunned group. The Enterobacteriaceae in this case were composed of psychrotrophic non-pathogenic genera of environmental origin. Salmonella was not isolated from any sample.     

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.     

Non-conventional fermentation at laboratory scale of cocoa beans: Using probiotic microorganisms and substitution of mucilage by fruit pulps

In a non-conventional lab-scale fermentation of cocoa beans using probiotic microorganisms and substituting the cocoa pulp for fruit pulp, physicochemical, microbiological and quality parameters were investigated. Two hundred grams of beans were fermented in a controlled environmental chamber (temperature ramp rate of 25°C for 48 h; 35°C for 48 h and 45°C for 48 h; and 65% HR). pH, titratable acid, citric, lactic and acetic acids, as well as sugars and ethanol were measured. A cut test was also performed on the cocoa beans fermented 5 and 6 days. As the fermentation time progressed, citric acid concentration decreased until 0.53 g kg⁻¹, whereas both lactic and acetic acids increased until 0.44 and 16.58 g kg⁻¹, respectively. Sucrose content decreased from 12.26 g kg⁻¹ (in fresh) to 6.54 g kg⁻¹ on the 6th day. Fructose and glucose contents increased in the cotyledons from day five, reaching a maximum concentration of 1.14 and 1.01 g kg⁻¹, respectively, on day six. Yeasts were the main microorganisms during the first 24–48 h (8.4 log CFU g⁻¹), while bacterial counts reached its highest number (7.8 log CFU g⁻¹) on day four. Beans fermented 5 and 6 days resulted in more fermented beans (>81%) and less violet ones (<18.4%) than the control.     

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.     

Microbiological quality of retail fresh fish fillets in The Netherlands

A total of 242 samples of ready-for-sale fish fillets of validated good sensory quality was examined for colony counts at 20, 30 and 37°C, Enterobacteriaceae at 37°C, Escherichia coli, Salmonella and Vibrio parahaemolyticus in 10 g aliquots. Staphylococcus aureus and yeast and mould propagules. Gram negative pathogens were not detected in any sample. The following reference values were found attainable: colony counts at 30°C, 10⁶ g^?1; E. coli 10 g^?1; S. aereus 10² g^?1; yeast and mould propagules 10⁴ g^?1. These reference values include, as customary, a tolerance of about 20% of samples exceeding the stated levels without, however, reaching the next log₁₀ level.     

Microbiological quality of mechanically recovered poultry meat treated with high hydrostatic pressure and nisin

The combined effect of high hydrostatic pressure processing, addition of nisin and acidification on aerobic mesophilic and psychrotrophic bacterial populations of mechanically recovered poultry meat (MRPM) kept under refrigeration (2°C) was evaluated 1, 15 and 30 days after pressurization. Nisin (0, 12.055, 100 and 200 ppm) and glucono-delta-lactone (GdL; 0 and 1%) were added to MRPM. Vacuum-packaged samples were treated at 350 or 450 MPa and 2°C for 15 min using both continuous pressurization and three-cycle oscillatory pressurization for 5 min per cycle. In some samples a reduction of mesophile counts between 3.0544 and 5.0538 log cfu g⁻¹was found. Psychrotrophes seemed to be more sensitive; in samples with 100 ppm of nisin and GdL treated at 450 MPa with cycles they were reduced to undetectable levels (a lethality of approximately 7.055 log units). Cycle pressurization showed slightly better results than continuous pressurization. The combination of 350 MPa, 100 ppm of nisin and 1% of GdL was enough to extend the shelf life of MRPM during the 30 day chilled storage.     

Effect of warm,chlorinated water on the microbial flora of shredded iceberg lettuce

An optimization technique was used to determine suitable times of exposure and temperatures for maximum destruction of microorganisms in shredded iceberg lettuce dipped in warm, chlorinated (100 μg/ml) water in a model system. Shredded lettuce washed for 3 min at 47°C and packaged in high oxygen transmission rate (6000–8000 cc m² 24 h) bags maintained an acceptable appearance after 7 days in storage at 1±1°C. Initial microbial loads were reduced by approximately 3 log cfu g⁻¹ in lettuce washed in chlorinated water at 47°C, and 1 log cfu g⁻¹ at 4°C. Pilot plant scale studies confirmed observations in the model system. The microbial flora of shredded lettuce packaged in the raw state and after a 3 min wash in 100 g ml⁻¹ chlorine at 4 or 47°C was dominated by psychrotrophic bacteria, particularly species of Pseudomonas, throughout the storage period. Numbers of these microorganisms were significantly lower than in raw lettuce or lettuce washed at 4°C until the 15th day in storage. Gas composition inside the bags was not affected by the washes.     

Steam treatment reduces the skin microflora population on deheaded and eviscerated whole catfish

This study tested the efficacy of steam exposures for 0, 30, 60, 90 and 120 s on reducing skin microflora of whole deheaded and eviscerated catfish. Microbiological analyses of skin were performed after treatment and on days 2, 4, 6, 8, 10 and 14 days of storage at 4°C. Catfish skin samples were examined for total (APC), coliform (CPC), and psychrotrophic (PPC) plate counts. Results indicated that as steam treatment duration increased greater reduction of catfish skin microflora was achieved. Mean bacterial counts determined on steam-treated catfish skins were significantly (P<0·05) lower than controls at all sample times. Steam treatment for 120 s was the most effective treatment modality, with APC, PPC and CPC lower than control by 2·3, 3·5 and 3·4 log cfu cm⁻²after 4 days of storage at 4°C. Skin APC and CPC were reduced below the limit of detection (1·8 log cfu cm⁻²) following a 30-s exposure, and remained at this level until day 4 of storage at 4°C. Skin PPC were reduced by 2 log cfu cm⁻²following 120-s steam exposure. Steam application to whole deheaded eviscerated catfish may prove useful to sanitize catfish skin prior to further processing into valuable consumer products.     

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.     

Effect of High Doses of High and Low Intensity UV Irradiation on Surface Microbiological Counts and Storage-Life of Fish

Ultraviolet (UV) irradiation at 254 run and doses of 300 mWs/cm² from a photochemical reactor (16.6 min at 300 μW/cm²) or 4.8 Ws/cm² from a high intensity UV-C lamp (40 sec at 120–180 mW/cm² reduced surface microbial count on mackerel by two to three log cycles. UV treated mackerel wrapped in 1 mil polyethylene and packed in -1°C ice had at least a 7 day longer shelf life than conventional ice-packed untreated controls. Spray washing with water containing 10 ppm chlorine by itself or in combination with UV irradiation was necessary to reduce surface counts on rough surfaced fish to the same extent as that on smooth surfaced fish. When UV irradiated and packed in 0°C ice, surface microbial counts on vacuum packaged mackerel lagged by 4 days those on mackerel wrapped in 1 mil polyethylene.     

Oscillatory High Pressure Processing Applied to Mechanically Recovered Poultry Meat for Bacterial Inactivation

The effect of oscillatory high pressure processing on mesophile and psychrotroph populations of mechanically recovered poultry meat (MRPM) was evaluated. Vacuum‐packaged samples were subjected to cycles by alternating moderate pressure (60 MPa) and high pressure (450 MPa) at 20 °C, once or several times so that the total time under high pressure was 15 min. A continuous treatment at 450 MPa for 15 min at 20 °C was also performed. Oscillatory treatments did not generate significantly higher decreases in counts of both populations than continuous pressurization. Reductions from 3.2 to 3.8 log CFU g^–1 were found for mesophiles. Psychrotrophs proved more sensitive: one of the cyclic treatments induced a lethality of 5.2 log CFU g ^–1. Pressurization improves the microbiological quality of MRPM.     

A new process for preparing transparent alkalised duck egg and its quality

When fresh duck (Anas plotyrhyncus) eggs (pH 8·0–8·5) are heated, their albumen develops a turbid gel. Through appropriate alkalisation (pH 11·5–12·8), the gel's transparency can be increased. The transparency of the heated duck egg-white is affected by pH value, heating temperature, heating rate and salt concentration. This research deals with the process for preparing the transparent alkalised duck egg and the change in its quality when stored. If fresh duck eggs are pickled in a solution of 42 g NaOH+50 g NaCl litre^?1 (25·3°C) for 8 days, removed, put in a water bath and heated at 70°C for 10 min they become transparent, their hardness and penetration increasing with storage. Total bacterial count and volatile basic nitrogen also increase with storage. The total bacterial count and the volatile basic nitrogen were 4·6 × 10⁶ cfu g^?1, 0·32 mg g^?1 when stored at a temperature of under 25°C for 4 weeks, respectively.     

The behaviour of log phase Escherichia coli at temperatures below the minimum for sustained growth

The behaviour of cold-adapted, log phase Escherichia coli broth cultures during incubation at 2°C or 6°C for upto 8 days, and during subsequent incubation at 12°C, was determined by measurement of absorbance values at 600 nm (A₆₀₀), enumeration of colony forming units (cfu) on plate count agar (PCA) and violet red bile agar (VRBA), and measurement of the length of cells viewed under phase contrast illumination. The A₆₀₀ values and the mean length of cells remained constant for cultures incubated at 2°C; however, numbers of cfu recovered on PCA declined by about 1 log cfu over 8 days, while the numbers of cfu recovered on VRBA declined by about 1 log cfu during the first day, and by about a further log cfu by day 8. For cultures incubated at 6°C, A₆₀₀ values increased about 0·6 log A₆₀₀ units during the first 4 days and declined by less than 0·1 log A₆₀₀ unit during the next 4 days. The numbers of cfu recovered on PCA increased by about 0·5 log cfu unit during the first day at 6°C and declined by about 1 log cfu during the subsequent 7 days. The numbers of cfu recovered on VRBA did not increase during the first day at 6°C, and at that and subsequent times were between 0·3 and 0·8 log cfu less than the log numbers recovered on PCA. The mean lengths of cells declined from 5 to less than 4 μ m during the first day at 6°C, but increased to 8 μ m between the fourth and eighth days, with the mean length of the longest 10% of cells increasing from 6 to 18 μ m. For cultures incubated at 12°C after incubation at 2°C or 6°C for 4 and 8 days, both A₆₀₀ values and enumeration of colonies on PCA indicated the initiation of growth after about 15 h. However, cultures that had been incubated at 2°C proceeded to sustained exponential growth, while cells in cultures that had been incubated at 6°C elongated during incubation at 12°C between 10 and 30 h. The division of elongated cells to cells of normal size resulted in numbers of cfu increasing at rates greater than the exponential growth rate at 12°C. The observations may have implications for the control of mesophilic pathogen proliferation in raw meats and other chilled foods.     

Microbiological hazards involved in fresh‐cut lettuce processing

BACKGROUND: The increasing consumption of produce all over the world has resulted in increasing concern by the regulatory agencies with respect to the level of safety performed by the processors. The objective of the present study was to investigate the hazards involved in the various steps of fresh‐cut lettuce processing (reception/selection of raw material, washing, rinsing, sanitisation and final product) by means of microbiological analyses of microbial groups used as indicators of hygienic conditions and of pathogens. RESULTS: High microbial loads of mesophilic and psychrotrophic bacteria and Pseudomonas spp. were found in the ram reception (～6 log colony‐forming units (CFU) g^?1), which were reduced by a single logarithmic cycle for the last two microbial groups after the sanitisation step (P < 0.05), the latter being ineffective against the first microbial group (P > 0.05). Lower counts of yeasts and moulds, total coliforms (35 °C) and faecal coliforms (44 °C) were observed in the initial step (3.49–4.53 log CFU g^?1, 0.65–1.55 log most probable number (MPN) g^?1 and 0.50–0.90 log MPN g^?1 respectively), these values increasing significantly after the sanitisation step for yeasts and moulds (～5 log CFU g^?1) but remaining unaltered for coliforms (P > 0.05). Salmonella spp. were not found in any of the experiments carried out, while the presence of Escherichia coli was observed in the final product. CONCLUSIONS : Practices compromising the hygienic quality of the final product during commercial storage were observed and corrective measures suggested. To the best of the authors' knowledge, these are the first data on microbiological safety in Brazilian fresh‐cut processing plants. Copyright © 2008 Society of Chemical Industry     

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     

Effects of Lactic and Acetic Acid on Survival of Salmonella enteritidis During Refrigerated and Frozen Storage of Chicken Meats

Chicken leg and breast meat samples inoculated with Salmonella enteritidis [4–5 log most probable number (MPN)/cm²] were dipped into lactic acid (LA; 1% and 3%) and acetic acid (AA; 1% and 2%) solutions for 10 min. After packaging, samples were stored at 4 °C (10 days) or −18 °C (6 months). Immediately after dipping into 1% LA, 3% LA, 1% AA, and 2% AA solutions, S. enteritidis counts on leg meat samples were reduced by 0.75, 1.21, 0.85, and 0.95 log MPN/cm², while the reductions were 0.97, 1.72, 0.92, and 1.58 log MPN/cm² on breast meat samples, respectively. The differences between the water-washed control and the acid-treated groups for Salmonella counts were statistically significant (P < 0.05). Salmonella counts on leg meat samples treated with 1% LA, 1% AA, and 2% AA were reduced by 0.54–1.52 log MPN/cm² (P < 0.05) during storage at 4 °C. However, for the breast meat samples, only Salmonella counts of water-washed controls were significantly reduced during refrigerated storage (P < 0.05). S. enteritidis counts on organic acid-treated samples were reduced by 0.13–0.55 log MPN/cm² during storage at −18 °C for 6 months, while the reduction on the water-washed controls was 0.64 log MPN/cm². It can be concluded that lactic or acetic acid treatment could be useful especially for reducing the initial Salmonella contamination. On the other hand, this pathogen could survive on poultry meats during refrigerated and frozen storage even following lactic or acetic acid decontamination.     

Use of nanoliposome loaded with chitosan-epigallocatechin gallate conjugate for shelf-life extension of refrigerated Asian sea bass (Lates calcarifer) slices

Treatments of chitosan-epigallocatechin gallate (CE) conjugate nanoliposome (CELP) and unencapsulated CE conjugate (UNCE) at different concentrations (0.025  and 0.05 g 100 g⁻¹) on quality and shelf-life of Asian sea bass slices (ASB-S) kept at 4 °C were studied. Total viable count of ASB-S treated with 0.05 g 100 g⁻¹ CELP (SB-CELP-0.05) was less than permissible limit (6 log CFUg⁻¹ sample) within 15 days. Moreover, SB-CELP-0.05 sample had the lowest pathogenic and spoilage bacterial count than remaining samples during the storage (P < 0.05). Lower thiobarbituric acid reactive substances and peroxide values were obtained for SB-CELP-0.05 sample than those treated with 0.05 g 100 g⁻¹ UNCE (SB-UNCE-0.05) at the end of storage (P < 0.05). The result was also advocated by higher polyunsaturated fatty acid content of SB-CELP-0.05 than SB-UNCE-0.05 (P < 0.05). Therefore, CELP efficiently extended ASB-S shelf-life with high consumer acceptability at 4 °C for minimum 12 days, whereas control had the shelf-life less than 6 days.     

Short communication: Effect of freezer storage time and thawing method on the recovery of Mycoplasma bovis from bovine colostrum

Mycoplasma bovis is an important cause of mastitis in dairy cattle, and pneumonia, arthritis, and otitis in calves. Milk and colostrum are considered important sources of infection for calves. knowledge on the effect of on-farm freezing (?18°C) and thawing methods on the recovery of M. bovis from colostrum samples is missing. In this study, 2 separate experiments were performed. The first experiment consisted of a longitudinal study examining the survival [as measured by log(10) reduction] of 2 M. bovis strains in frozen colostrum over 14 wk. The second experiment examined the effect of different thawing temperatures (45 and 20°C), thawing frequencies (once or twice), and initial colostrum titer (10⁴ or 10⁶ cfu/mL) on M. bovis survival. A single freeze-thaw cycle led to an approximate 1 log reduction of M. bovis titer, independent of the thawing temperature. Freezing for 14 wk did not significantly further reduce the titer of bacteria compared with freezing for 2 wk. A second freeze-thaw cycle further reduced the M. bovis count by approximately 0.5 log compared with a single freeze-thaw cycle. Thawing temperature and initial bacterial concentration did not significantly affect M. bovis reduction. In conclusion, storage of colostrum samples in the freezer at ?18°C during epidemiological studies, herd monitoring, or test and cull programs will probably have little influence on qualitative bacteriological test results for M. bovis. The epidemiological or clinical relevance of an approximate 1 log reduction of M. bovis in colostrum is currently unclear.     

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.     

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.