Effect of irradiation and modified atmosphere packaging on the microbiological safety of minced pork stored under temperature abuse conditions

The safety of irradiated pork packed in 25% CO₂:75% N₂ and stored at abuse temperature (10 or 15°C) was assessed by inoculation studies involving Salmonella typhimurium, Listeria monocytogenes, Escherichia coli, Yersinia enterocolitica and Clostridium perfringens . Irradiation to a dose of 1.75 kGy reduced pathogen numbers to below the detection limit of 10² cells g^-1. When higher inoculum levels were used (10⁶ cells g^-1) irradiation at 1.75 kGy reduced pathogen numbers by 1 –>5 log₁₀ cycles depending on strain. Clostridium perfringens was the most resistant, and Y. enterocolitica the most sensitive of the pathogens studied.
In all cases when high numbers (10⁶ to 10⁷g^-1) of spoilage and/or pathogenic bacteria were present initially on the pork the meat appeared spoiled, and although irradiation reduced the number of microorganisms, the meat was still unacceptable from a sensory viewpoint after treatment.
It was concluded that the microbiological safety of irradiated, modified atmosphere packaged (MAP) pork is better than that of unirradiated MAP pork.     

Impact of nitrite on detection of Listeria monocytogenes in selected ready-to-eat (RTE) meat and seafood products

ABSTRACT:  The impact of sodium nitrite (NaNO₂) on detection and recovery of Listeria monocytogenes from select ready-to-eat (RTE) foods including smoked salmon, smoked ham, beef frankfurters, and beef bologna was assessed. Nitrite-containing (NC; 100 to 200 ppm NaNO₂) or nitrite-free (NF) foods were inoculated with a 5-strain cocktail of L. monocytogenes by immersion into Butterfield's buffer solution containing 5.4 to 7.4 × 10³ L. monocytogenes per milliliter. Inoculated products were vacuum-packaged and stored at 5 °C. A weekly comparative analysis was performed for presence of L. monocytogenes using 5 detection methods on products held at 5 °C for up to 8 wk. L. monocytogenes initially present at <100 CFU/g during the first 2 wk of storage increased throughout the study, attaining final populations of approximately 1 × 10⁴ to 1 × 10⁵ CFU/g. Lactic acid bacteria predominated throughout the study in all products. Exposure to NaNO₂ (100 to 200 ppm) resulted in 83% to 99% injury to the L. monocytogenes strains tested. The genetic-based BAX^® System (DuPont™ Qualicon, Wilmington, Del., U.S.A.) and modified USDA/FSIS methods detected 98% to 100% of Listeria -positive food samples and were consistently superior to and significantly different ( P < 0.05) from conventional cultural methods in recovering Listeria from NC samples. Data show that nitrite-induced injury adversely affects detection and recovery of L. monocytogenes from NC food, confirming earlier findings that nitrite-induced injury masks L. monocytogenes detection in NC RTE food products. Nitrite-injured Listeria can subsequently repair upon nitrite depletion and grow to high levels over extended refrigerated storage.     

Gelation mechanism of surimi studied by 1h NMR relaxation measurements

ABSTRACT:  In order to elucidate the gelation mechanism of surimi, the temperature dependence of water proton spin–spin relaxation time (¹H T ₂) has been described by a theoretical approach, in which the exposed protein surface is taken into account. Water ¹H T ₂ measured for horse mackerel surimi in the presence of 2.5% NaCl was analyzed on the basis of the consideration for the denaturation and the aggregation of protein in order to explain the macroscopic structural change during the heating and the cooling processes. The temperature dependence of water ¹H T ₂ and the fraction of rigid component gave a clear explanation for the gelation mechanism of surimi. Differential scanning calorimetry thermogram and dynamic viscoelastic measurements supported the results of nuclear magnetic resonance (NMR) measurements. It has been demonstrated that the measurement of NMR relaxation times is useful to describe the gelation mechanism of surimi.     

APPLICATION OF CHLORINE TO REDUCE POPULATIONS OF ESCHERICHIA COLI ON BEEF

The effects of chlorine against 2 strains of E. coli attached to the surface of beef carcass tissue (BCT) were examined using a model carcass washer. Lean and adipose BCT with approximately 5 log ₁₀ CFU/cm ² E. coli bacteria were spray-treated with water and sodium hypochlorite (NaOCl) to give chlorine concentrations of 50, 100, 250, 500, or 800ppm, incubated for 24 h, 4C, and E. coli populations enumerated. Spray treatments with water did significantly (P < 0.05) reduce the bacterial populations of either organism attached to lean or adipose BCT, as compared to populations of controls; however, reductions were less than 0.60 log ₁₀ CFU/cm ². Treatments with 500 and 800 ppm chlorine against E. coli ATCC 25922 attached to BCT resulted in the greatest reductions of 1.22 and 1.28 log ₁₀ CFU/cm ², respectively. At 800 ppm chlorine , E. coli O157:H7 ATCC 43895 attached to BCT was reduced by 1.04 log ₁₀ CFU/cm ², whereas spray treatments with 50, 100, 250, and 500 ppm chlorine resulted in reductions of < 1 log ₁₀ CFU/cm ². Spray treatments with chlorine from sodium hypochlorite solutions reduced populations of E. coli, however, these reductions were not sufficient to completely inactivate the bacteria attached to red meat .     

Elimination of Listeria monocytogenes in soft and red smear cheeses by irradiation with low energy electrons

Soft and red smear cheeses are frequently contaminated by Listeria monocytogenes , sometimes at relatively high concentration (< 10⁵ CFUg^-1). This bacterium is radiosensitive (D₁₀ value of approximately 0.45 kGy) but irradiation of the whole cheese by X-rays induced off-flavours when the dose exceeded 1.0 kGy. Irradiation could be effective in eliminating L. monocytogenes only from lightly contaminated cheeses (> 10²CFU g^-1).
L. monocytogenes appears only in the rind (where the pH is greater than 6.3) and never grows in the core of the cheese. Under these conditions, a specific irradiation of the rind after ripening, with a low-energy electron beam at relatively high doses (up to 3.0 kGy), allows the total elimination of L. monocytogenes in heavily contaminated samples (10⁵-10⁶ CFU g^-1) without noticeable modifications of the organoleptic properties of the cheese.     

The increase of CO2 permeability of paper packaging with increasing hydration

CO₂ transport through hydrated paper was studied using gas chromatography to measure CO₂ permeability (P) and diffusivity (D). With increasing water content from 0 to 0.8 g water/g paper, P and D increased from 3.47 to 9.03 × 10⁻⁶ m³ m⁻² s⁻¹ bar⁻¹ and from 1.35 to 3.51 × 10⁻⁵ m² s⁻¹, respectively. This resulted from structural changes in the cellulose network as reported in the literature; water sorption isotherms were used to explain these changes using BET theory.     

Re-examination of the interactions between starch and salts of metals from the non-transition groups

The interactions between potato starch and the salts of alkali–earth metals and lead were examined by using scanning electron microscopy/energy dispersive spectroscopy (SEM/EDS), differential scanning calorimetry (DSC), ¹⁷O and ³⁵Cl NMR. For the starch blended with saturated solutions of the salts, gel-like, shear-thinning or semi-solid appearances were observed in relation to the ion property of the salts. The volume of saturated salt solutions required for producing shear-thinning properties correlated significantly with the property of anions. SEM and EDS studies on the starches after soaking in 0.5  M salt solutions suggest that both divalent cations and accompanying anions of the salts penetrated into the granule during soaking treatments. Also, the cations (especially Mg²⁺ and Pb²⁺) and anions both displayed some influence on the onset ( T _o) and peak ( T _p) temperatures as well as the enthalpy change (Δ H ) during thermolysis of the starches. From these results and NMR data, the major ion species (anions or cations) interacting directly with starch could be elucidated partially with respect to the salt variety and concentration and preparation condition. The roles of free water content and water structure in the physical characteristics of the starch systems examined were negligible.     

HYGIENIZATION OF INDIAN CHICKEN MEAT BY IONIZING RADIATION

Both fresh and frozen chicken meat were evaluated for microbiological status by screening for total bacterial counts and for the presence of pathogens like Enterobacteria , Bacillus cereus, coagulase positive Staphylococci and Salmonella spp. Most of the samples exhibited heavy bacterial contamination (1.2 × 10⁵ - 2.6 × 10⁶/g), mainly with Staphylococcus spp. (1.5 × 10⁴ - 2.8 × 10⁵/g). All the chicken samples also showed the presence of Salmonellae (3 × 10¹ - 2.1 × 10²/g). Among the different serotypes observed in chickens . S. typhimurium was common in fresh as well as frozen chicken. Radicidation at 2 kGy at cryogenic conditions (−40°C) was efficient in eliminating the natural pathogenic contamination of the poultry . Salmonella spp. viz. S. seftenberg and S. typhimurium differed in radiation sensitivity, the D₁₀ values in phosphate buffer (pH 7.2) being 0.25 kGy and 0.12 kGy, respectively. Chicken homogenate (10%) offered approximately 2-fold protection to these cells. Chicken samples artificially inoculated with a heavy inoculum (10⁸ cells/g) of these 2 serotypes required higher gamma radiation doses of 4–5 kGy. The findings suggested that a dose of 2 kGy is adequate for normally contaminated chicken samples, but for the heavily contaminated chicken a dose of 4–5 kGy, depending upon the predominating Salmonella serotype present, is required .     

EFFECTS OF LOW CONCENTRATIONS OF H2O2 ON LIPID OXIDATION AND OF STORAGE AND pH ON NONHEME IRON CONTENT OF RAW BEEF MUSCLE

Ground beef samples were prepared from semimembranosus muscles, and beef muscle residue devoid of heme pigments was prepared by repeated washing of the ground muscle with distilled-deionized water. When ground muscle, or muscle residue samples treated with metmyoglobin-H₂O₂ (4 mg metmyoglobin/g muscle residue; 1:0.1 to 1:1 for molar ratio of metmyoglobin to H₂O²) were stored at 4°C for 0 or 6 days, no changes in nonheme iron content were observed. Similarly, nonheme iron content of stored samples was not affected by pH (5.5, 6.0 or 6.5). While metmyoglobin-H₂O² added to water-extracted beef muscle residue catalyzed the oxidation of the indigenous lipids, treatment of the residue with H₂O² alone had no effect on the oxidation.     

1H NMR Studies of Water in Chicken Breast Marinated with Different Phosphates

ABSTRACT: Samples of boneless, skinless chicken breasts were vacuum tumbled in 7% salt and 1.2% of either disodium pyrophosphate, tetrasodium pyrophosphate, tetrapotassium pyrophosphate, sodium tripolyphosphate, or glass phosphate, and studied using ¹H NMR. Spin-lattice (T₁) values ranged from 568 to 642 ms, with highest values seen for phosphate-treated samples. Increases with treatment were attributed to changes in moisture. Cooking reduced T₁ values due to loss of moisture and setting of the protein gel. Compression produced further reductions in T₁ values. Little dispersion in R₂ with pulse spacing (τ) was observed for uncooked samples.     

Postharvest Microbiology of Farm-reared, Tropical Freshwater Prawn (Macrobrachium Rosenbergii)

ABSTRACT: The microbiological quality of farm-reared, tropical freshwater prawn ( Macrobrachium rosenbergii ) stored at 2 different temperatures was studied. The prawn muscle was found to have the initial bacterial load of 10⁴ cfu/g. The lactics and vibrios were in the range of 10² cfu/g, while the E. coli , aeromonads, staphylococci, anaerobes, and molds were in the level of 10¹ cfu/g. Salmonella and Vibrio cholerae were present in the prawn muscle. The prawn muscle held at room temperature (28 ± 2 °C) was organoleptically acceptable up to 8 h, when the bacterial load was more than 10⁶ cfu/g. However, the prawn muscle stored at freezer temperatures (−10 to −15 °C) was found to be in acceptable condition even after 30 d of storage and the bacterial load was fluctuating in the range of 10³ to 10⁴ cfu/g.     

PURIFICATION AND CHARACTERIZATION OF TWO TOMATO POLYGALACTURONASEISOENZYMES

The properties of tomato polygalacturonases at two ripening stages were investigated. Two isoenzymes, PG I and II, were isolated from underripe fruits with an orange skin color. Fully ripe fruits contained only polygalacturonase II. PG I and II were purified by chromatography on DEAE-Sephadex A-50, Sephacryl S-200 and CM-agarose chromatography. PG I had a M_r of 199,500 as determined by Sephacryl S-300 gel filtration and was 50% inactivated at 66.5°C and pH 4.5 after incubation for 5 min. It had an activation energy (E_a) of 16.8 Kcallmol (70.3 times 10³ Jlmol), V_max of 27.7 units/mg protein and K_m value of 7.5 times 10⁻² mM polygalacturonic acid. PG II had a M_r of 45,700 and was 50% inactivated at 58°C under the same conditions. Both isozymes had a pH optimum of 4.6. PG II had an E_a value of 14.8 Kcallmol (61.9 times 10³ Jlmol), V_max value of 58.8 units/mg protein and K_m value of 3.8 times 10⁻² mM polygalacturonic acid. PGI gave rise to only one band during electrophoresis in polyacrylamide gels, whereas PG II showed one major and one minor band both with PG activity. Gel electrophoresis in the presence of sodium dodecyl sulfate resulted in two major bands (M_r= 47,500 and 41,000) for PG I and only one major band (M_r= 47,500) for PG II. PG I is composed of several subunits, all of which are glycoproteins.     

CHALLENGE STUDIES WITH PROTEOLYTIC CLOSTRIDIUM BOTULINUM IN YEAST AND CHEMICALLY LEAVENED CRUMPETS PACKAGED UNDER MODIFIED ATMOSPHERES

Challenge studies were done with proteolytic Clostridium botulinum (10³ spores/g) in yeast-and chemical-leavened crumpets (50-g) packaged in air with an ethanol vapor (2-G Ethicap®) generator or in 100% CO₂ and stored at ambient temperature (25C) for 30 days. Neurotoxin was detected in all gas- (CO₂) packaged crumpets after 5 days regardless of the method of leavening. While neurotoxin was delayed for 10 days in chemical-leavened Ethicap®-packaged crumpets, it was not detected in any similarly packaged yeast-leavened crumpets throughout storage. This inhibition of growth and neurotoxin production by C. botulinum was attributed to the production of ethanol by Saccharomyces cerevisiae in the yeast leavened crumpets, in conjunction with the ethanol vapor generated by the Ethicap® sachets (2-G), to levels to inhibitory to the growth of C. botulinum (>2.8% v/v). Subsequent challenge studies in sterile crumpets inoculated with either C. botulinum (10³ spores/g) or a co-inoculum of C. botulinum (10³ spores/g) and S. cerevisiae (10⁵ CFU/g) confirmed the significant role (p<0.001) of S. cerevisiae in enhancing the antibotulinal efficacy of ethanol vapor. These studies showed that the method of crumpet leavening could have a profound effect on the growth of and neurotoxin production by C. botulinum in crumpets packaged under modified atmospheres.     

OXIDATIVE DETERIORATION OF BORAGE AND EVENING PRIMROSE OILS AS ASSESSED BY NMR SPECTROSCOPY

A facile¹H NMR spectroscopic method was employed to monitor oxidation of borage (BO) and evening primrose (EPO) oils under Schaal oven conditions over a 96 h period at 60C. Relative changes of aliphatic to olefinic (R_ao) and aliphatic to diallylmethylene (R_ad) proton ratios during oxidation of these oils were calculated. An increase in R_ao and R_ad values was observed over the entire storage period. A highly significant correlation (r=0.950–0.995) existed between the conjugated diene values and changes in R_ao and R_ad during oxidation of both oils. The correlation coefficient between 2-thiobarbituric acid reactive substances (TBARS) and changes in R_ao and R_ad values was in the range of 0.972–0.982. Therefore, ¹H NMR methodology may be used as an effective means to simultaneously estimate both primary and secondary oxidation changes in borage and evening primrose oils.     

RADIATION STERILIZATION OF SPICES FOR HOSPITAL FOOD SERVICES AND PATIENT CARE

A survey of the commercial spices used by food services in a typical hospital environment revealed high contamination with microorganisms, i.e., 10⁴ to 10⁷ counts per gram. The predominant microorganisms were as followed (in colony counts/gram): (1) heat-resistant bacterial spores in black pepper, 1 × 10⁷; thyme, 2 × 10⁶; anise, 7 × 10⁴; curry powder, 4 × 10⁵; poultry seasoning, 8 × 10⁴; pickling spice, cardamom, and cumin, 1.5–3 × 10⁴; (2) mixed populations of vegetative cells and bacterial spores in cumin, 1 × 10⁶; (3) molds in cream of tartar, 2 × 10⁴. Sterility of food may be important in a hospital setting, especially in the care of immunocompromised patients. To eliminate the organisms, we recommend radiation treatment, accompanied by appropriate microbiological quality control. On the basis of radiation survival data, the composite natural flora would be reduced to the level of "commercial sterility" (defined as less than 10 organisms per gram((Kiss 1982) by the following minimum radiation doses (in kGy): black pepper, 13; thyme, 13; cumin, 12; anise, 10; curry, 7.3; pickling spice, 7; poultry seasoning, 6; cardamom, 9.4; cream of tartar, 4. For practical purposes, two dose levels can be recommended for treatment of spices in the hospital environment, low = 6–10 kGy and high = 10–15 kGy.     

The yeast flora of stored ready-to-use carrots and their role in spoilage

Spoilage of ready-to-use grated raw carrots packaged in polymeric films and stored at 10°C was investigated for involvement of yeasts. Cryptococcus albidus was only isolated during the first 3 days of storage, increasing to levels of 10⁵–10⁶g^-1. Candida lambica was more commonly isolated after 3–7 days of storage, and reached 10⁷–10⁸g^-1 after 12 days. Candida sake was present throughout storage, increasing from 10⁵–10⁶ after 3 days to 10⁷–10⁸ after 12 days. In some samples, Candida parapsilosis and Candida tropicalis were also isolated at levels similars to C. sake . All the yeasts isolated at the end of storage were fermentative species and their metabolism was characterized with a Warburg apparatus. Neither the number of yeasts nor the composition of the yeast flora were related to the deterioration of the product. Although Candida lambica inoculated on grated carrots caused spoilage after 12 days at 10°C, the high O₂ permeable film was most effective in reducing exudate.     

Mathematical modelling of O2 consumption and CO2 production rates of whole mushrooms accounting for the effect of temperature and gas composition

Investigation of respiration rate of fresh produce, under different gas composition and temperatures, and respective mathematical modelling is central for the modified atmosphere packaging design. This work investigates the effect of temperature (4, 8, 12, 16, 20 °C) and gas composition (O₂ between 3 to 21% and CO₂ between 0 to 15%) on respiration rate of whole mushrooms. Oxygen and carbon dioxide respiration rates increased significantly (3–4 fold) as the temperature elevated from 4 to 20 °C and were in the range of 13.23 ± 3.12 to 102.41 ± 2.132 mL kg⁻¹ h⁻¹) and 14.33 ± 1.56 to 97.02 ± 2.51 mL kg⁻¹ h⁻¹) respectively. Low O₂ and high CO₂ levels reduced O₂ consumption and CO₂ production rates of whole mushrooms on average by a circa 47–60% at all temperatures as compared to the respiration rate at ambient air. Mathematical models were developed for RO₂ and RCO₂, by combining the Arrhenius and Michaelis–Menten uncompetitive equations. These models predicted well, O₂ consumption and CO₂ production rates of whole mushrooms as a function of both temperature and gas composition.     

OXIDATIVE STABILITY OF FRESH AND HEAT-PROCESSED DARK AND LIGHT MUSCLES OF MACKEREL (Scomber scombrus)

Oxidative stability of light and dark comminuted muscle of raw and thermally processed mackerel stored at 4C was studied over a 21 day period by monitoring changes in conjugated dienes (CD) and 2-thiobarbituric acid (TBA) values. The quantity of headspace (HS) volatiles, propanal, and hexanal as well as the ratio of aliphatic to olefinic (R_ao) or diallylmethylene (R_ad) protons in the proton nuclear magnetic resonance (¹ NMR) spectra of oils were determined. The content of CD of light and dark ground mackerel muscle samples exhibited a consistent increase over the entire storage period. Furthermore, secondary oxidation products as reflected in the TBA values and content of propanal, hexanal and HS gases, generally, showed a gradual increase in their level. The concentration of propanal, the dominant volatile of the HS gases, increased markedly up to day 6 of storage, but afterwards began to decline continuously. A similar trend was noted for hexanal, but at a lesser extent. The R_ao and R_ad values in the ¹H NMR spectra of lipids from all stored samples increased constantly during storage. In all samples, the dark ground muscle exhibited a higher degree of oxidation than its light counterpart. Furthermore, heat-processed dark comminuted muscle oxidized faster than its raw counterpart while generally an opposite trend was observed for the light ground muscle.     

Interactive packaging as protection against photodegradation of the colour of pasteurized, sliced ham.

Interactive packaging using oxygen absorbers with concomitant development of carbon dioxide and packaging material with low oxygen transmission rate (OTR: 2cm³m² 24 h atm^-3) has been found to completely eliminate discoloration of pasteurized, sliced ham normally encountered as a result of photo-oxidation of nitric oxide pigments during the first 24 h of display in illuminated chill cabinets. Further this packaging procedure has been found to be superior to conventional vacuum-packaging (90% initial vacuum) with regard to overall sensory evaluation, and equal to vacuum-packaging with 99% initial vacuum and interactive packaging using oxygen absorber, respectively, with regard to both overall sensory evaluation, and microbial load at the end of a storage period of 26 d.     

Texture Changes During the Ripening of Port Salut Argentino Cheese in 2 Sampling Zones

ABSTRACT: Texture changes during ripening of Port Salut Argentino cheese for different sampling zones were studied. Compression relaxation tests were performed and results were analyzed using both Maxwellian and Peleg's models. Elastic equilibrium modulus obtained from the Maxwellian model decreased from 1.22 to 0.11 10⁴Pa during ripening. The constants derived from Peleg's model, k₁ and k₂, diminished with ripening time from 1.18 to 0.71 min and from 1.27 to 1.12, respectively. Asymptotic equilibrium modulus from Peleg's model decreased from 0.95 to 0.07 10⁴Pa during ripening. Rate parameters derived from a 1st order kinetics applied to both equilibrium moduli showed that the decrease was faster in the external zone (0.0846 d⁻¹) than in the central zone (0.0368 d⁻¹). The correlation between equilibrium moduli, salt concentration, moisture content, and maturation indexes was obtained with a determination coefficient of 0.76.