The prevalence and some metabolic traits of Brochothrix thermosphacta in meat and meat products packaged in different ways

BACKGROUND: The effect of Brochothrix thermosphacta on the quality of meat and meat products is of vital importance in connection with Regulation EC/178/2002 extending the definition of unsafe foodstuffs to encompass all those which are unfit for human consumption. This study aimed to determine the prevalence of B. thermosphacta in meat and meat products packaged under different conditions and to estimate the effect of B. thermosphacta strains on product quality based on their protein and lipid degradation activity. RESULTS: B. thermosphacta was absent in only two of 132 samples. All other samples were contaminated with this bacterium (10¹ to 10⁹cfu g^?1 meat and 10² to 10⁸cfu g^?1meat product). In products stored under high‐oxygen atmosphere Brochothrix cells accounted for almost 100% total mesophilic count (TMC) and below 50% TMC in oxygen‐free atmosphere. While the tested B. thermosphacta strains did not show any proteolytic activity, most of them displayed lipolytic activity at 25 °C and some even at 4 °C. CONCLUSION: B. thermosphacta is commonly present in meat and meat products packaged in different ways. This bacterium can display lipolytic activity also at refrigeration temperature. Its over‐proliferation can be inhibited through vacuum packaging or packaging under a modified atmosphere with reduced oxygen content. Copyright © 2011 Society of Chemical Industry     

Shelf‐life extension of vacuum‐packaged sea bream (Sparus aurata) fillets by combined γ‐irradiation and refrigeration: microbiological,chemical and sensory changes

The combined effect of γ‐irradiation and refrigeration on the shelf‐life of vacuum‐packaged sea bream (Sparus aurata) fillets was studied by monitoring the microbiological, chemical and sensory changes of non‐irradiated and irradiated fish samples using low‐dose irradiation doses of 1 and 3 kGy. Fish species such as sea bream and sea bass are very popular in the Mediterranean countries due to their high quality characteristics, and their preservation is a constant challenge given their extreme perishability. Irradiation (3 kGy) dramatically reduced populations of bacteria, namely, total viable counts (3 vs 7 log cfu g^?1) for the non‐irradiated samples, Pseudomonas spp (<2 vs 7.6 log cfu g^?1), H₂S‐producing bacteria typical of Shewanella putrefaciens (<2 vs 5.9 log cfu g^?1), Enterobacteriaceae (<2 vs 6.0 log cfu g^?1) and lactic acid bacteria (<2 vs 3.5 log cfu g^?1) after 10 days of storage. The effect was more pronounced at the higher dose (3 kGy). Lactic acid bacteria, Enterobacteriaceae and H₂S‐producing bacteria typical of Shewanella putrefaciens showed higher sensitivity to γ‐radiation than did the rest of the microbial species. Of the chemical indicators of spoilage, Trimethylamine (TMA) values of non‐irradiated sea bream increased very slowly, whereas for irradiated samples significantly lower values were obtained reaching a final value of 7.9 and 6.3 mg N per 100 g muscle at 1 and 3 kGy respectively (day 42). Total volatile basic nitrogen (TVB‐N) values increased slowly attaining a value of 67.3 mg N per 100 g for non‐irradiated sea bream during refrigerated storage, whereas for irradiated fish, lower values of 52.8 and 43.1 mg N per 100 g muscle were recorded (day 42). Thiobarbituric acid (TBA) values for irradiated sea bream samples were higher than respective non‐irradiated fish and increased slowly until day 21 of storage, reaching final values of 1.1 (non‐irradiated), 2.0 (1 kGy) and 2.2 mg malonaldehyde kg^?1 muscle (3 kGy), respectively (day 42). Sensory evaluation showed a good correlation with bacterial populations. On the basis of overall acceptability scores (sensory evaluation) a shelf‐life of 28 days (3 kGy) was obtained for vacuum‐packaged sea bream, compared with a shelf‐life of 9–10 days for the non‐irradiated sample. Copyright © 2004 Society of Chemical Industry     

Spoilage-related microbiota associated with chilled beef stored in air or vacuum pack

In order to study the spoilage-related microbiota of beef at species level, a combination of culture-independent and culture-dependent methods was used to analyse nine different beef samples stored at 4 °C in air or in vacuum pack. Plate counts on selective agars after 0, 7 and 20 days of storage showed that vacuum packaging reduced the viable counts of Brochothrix thermosphacta, Pseudomonas spp. and Enterobacteriaceae, whereas the growth of lactic acid bacteria (LAB) was unaffected. Storage in vacuum pack mainly affected viable counts and not necessarily the species diversity of microbial populations on meat. Such populations were studied by PCR-DGGE of DNA directly extracted from meat and from bulk cells from culture media, followed by sequencing of DGGE fragments. Pseudomonas spp., Carnobacterium divergens, B. thermosphacta, Rahnella spp. and Serratia grimesii, or close relatives were detected in the meat at time zero. The use of the culture-independent method highlighted the occurrence of species that were not detected by plating. Photobacterium spp. occurred in most meat samples stored in air or in vacuum pack, which indicates this organism probably has a role in spoilage. In contrast, culture-dependent analysis allowed detection of bacterial species that were not found in DNA extracted directly from meat. This was the case for several species of Serratia or Rhanella among the enterobacteria, and Leuconostoc spp. among the LAB. Besides advancing our knowledge of the species involved in the spoilage of vacuum-packaged meat, this study shows the benefits of combining culture-based and direct approaches to enhance understanding of populations of spoilage bacteria.     

Bacteriological quality of sheep meat in Mhow town of India

The purpose of this study was to investigate bacterial load in ready‐to‐sale sheep meat with special reference to Salmonella. Samples were collected from 100 sheep carcasses from retail meat shops in domestic markets. On carcasses, where bacterial counts were obtained, the mean of the log₁₀ aerobic plate count was 7.26 cfu g^?1, and that of total coliform count and total Escherichia coli count was 4.11 log₁₀ cfu g^?1 and 3.03 log₁₀ cfu g^?1, respectively. All the samples (100) were found positive for coliforms, 49.0% were positive for E. coli and 3.0% were positive for Salmonella. The isolates were serotyped as Salmonella infantis having antigenic structure 6, 7: r: 1, 5. Antibiogram revealed highest (100.0%) sensitivity towards amikacin, ceftriaxone, ciprofloxacin, chloramphenicol, colistin sulphate, gentamicin and nalidixic acid followed by cefuroxime and tetracycline (66.67% each) and cotrimoxazole (33.33%). All the strains were resistant to ampicillin.     

Effect of dietary supplementation with vitamin E on characteristics of vacuum‐packed lamb

The effect of dietary vitamin E supplementation on lamb during vacuum‐packed storage was studied. Thirty‐six weaned male Manchego breed lambs were offered four dietary treatments (20, 270, 520 and 1020 mg vitamin E kg^?1 feed). Lambs were fed the vitamin E‐supplemented diet from 13 until 26 kg live weight. Pieces of M. longissimus dorsi were stored under vacuum at 2 ± 1 °C in the dark and meat quality was assessed after 5, 14 and 28 days of storage. Dietary supplementation significantly increased the α‐tocopherol concentration in the muscle (P < 0.001). Initially, lipid oxidation, meat colour and bacterial load were similar in all groups. In meat of non‐supplemented lambs the thiobarbituric acid reactive substance value increased throughout storage, whereas in meat of supplemented lambs it did not increase. Meat pigments and discolouration proportion were significantly affected by storage time (P < 0.001). The bacterial load was low initially, but after 28 days of storage it was close to 7 log₁₀ colony‐forming units (cfu) cm^?2 and Enterobacteriaceae surpassed the limit of acceptability of 2.5 log₁₀ cfu cm^?2, making the lamb unsuitable for human consumption. Meat of supplemented lambs displayed less lipid oxidation than that of their non‐supplemented counterparts, while meat colour and bacterial load were not affected by supplementation. Copyright © 2007 Society of Chemical Industry     

Control of microbial growth and rancidity in rabbit carcasses by modified atmosphere packaging

Half‐carcasses of rabbit packed under four different modified atmospheres (MA; A: 30% CO₂ + 70% O₂; B: 30% CO₂ + 30% O₂ + 40% N₂; C: 40% CO₂ + 60% N₂; D: 80% CO₂ + 20% O₂) and stored at 1 °C over 20 days, were assessed in relation to bacteria (total viable counts (TVC), lactic acid bacteria (LAB), Enterobacteriaceae and Pseudomonas) and rancidity development as 2‐thiobarbituric acid reactive substances (TBARS). None of the MA tested produced mean counts greater than 5 log CFU cm^?2 for TVC and LAB, or greater 2 log CFU cm^?2 for Pseudomonas and Enterobacteriaceae. All MA showed an inhibitory effect on microbial growth, especially on growth of the spoilage bacteria Pseudomonas and Enterobacteriaceae. This inhibition was more relevant in atmospheres with higher CO₂ concentrations (types C and D). Significant differences in rancidity levels between MA types (p < 0.01) were observed 10 days post‐packing. In general these values were higher in MA type A, which showed a significant increase in TBARS values (p < 0.05) over time. Copyright © 2005 Society of Chemical Industry     

Evaluation of the Spoilage of Raw Chicken Breast Fillets Using Fourier Transform Infrared Spectroscopy in Tandem with Chemometrics

The aim of this work was to evaluate the potential of Fourier transform infrared (FTIR) spectroscopy as a rapid and accurate technique to detect and predict the onset of spoilage in fresh chicken breast fillets stored at 3, 8, and 30 °C. Chicken breasts were excised from carcasses at 6 h post-mortem; cut in fillets; packed in air; stored at 3, 8, and 30?ºC; and periodically examined for FTIR, pH, microbiological analysis, and sensory assessment of freshness. Partial least squares regression allowed estimations of total viable counts (TVC), lactic acid bacteria (LAB), Pseudomonas spp., Brochothrix thermosphacta, Enterobacteriaceae counts and pH, based on FTIR spectral data. Analysis of an external set of samples allowed the evaluation of the predictability of the method. The correlation coefficients (R²) for prediction were 0.798, 0.832, 0.789, 0.810, 0.857, and 0.880, and the room mean square error of prediction were 0.789, 0.658, 0.715, 0.701, 0.756 log cfu g^?1 and 0.479 for TVC, LAB, Pseudomonas spp., B. thermosphacta, Enterobacteriaceae, and pH, respectively. The spectroscopic variables that can be linked and used by the models to predict the spoilage/freshness of the samples, pH, and microbial counts were the absorbency values of 375 wave numbers from 1,700 to 950 cm^?1. A principal component analysis led to the conclusion that the wave numbers that ranges from 1,408 to 1,370 cm^?1 and from 1,320 to 1,305 cm^?1 are strongly connected to changes during spoilage. These wave numbers are linked to amides and amines and may be considered potential wave numbers associated with the biochemical changes during spoilage. Discriminant analysis of spectral data was successfully applied to support sensory data and to accurately bound samples freshness. According to the results presented, it is possible to conclude that FTIR spectroscopy can be used as a reliable, accurate, and fast method for real time freshness evaluation of chicken breast fillets during storage.     

Use of Lysozyme,Nisin, and EDTA Combined Treatments for Maintaining Quality of Packed Ostrich Patties

ABSTRACT: The antimicrobial effectiveness of lysozyme, nisin, and ethylene diamine tetraacetic acid (EDTA) combination treatments (Mix₁: 250 ppm lysozyme, 250 ppm nisin, 5 mM EDTA; Mix₂: 500 ppm lysozyme, 500 ppm nisin, 5 mM EDTA) on bacterial growth of ostrich patties packaged in air, vacuum, and 2 different modified atmospheres (MAP₁: 80% O₂, 20% CO₂; MAP₂: 5% O₂, 30% CO₂, 65% N₂) was evaluated. Moreover, the lipid oxidation was evaluated as well as color and sensory characteristics. The growth of total viable counts and lactic acid bacteria were strongly inhibited by the antimicrobial treatments in all the running time (Inhibition Index >97%) whereas for Enterobacteriaceae and Pseudomonas spp. lower inhibition indices from 12% to about 28% were observed. The lipid oxidation was more pronounced in the control respect to the treated meat patties. Moreover, the mixture at low concentration of lysozyme and nisin showed the best antioxidative effect. High concentrations of lysozyme and nisin showed the greatest color loss. Also, off-odors for the untreated patties developed faster than the treated samples. Practical Application: Great interest is developing in food bio-preservation, because of the ever-increasing needs to protect consumers' health and to valorize the naturalness and safety of food products.     

Gamma irradiation as a means to eliminate Listeria monocytogenes from frozen chicken meat

Cells of Listeria monocytogenes ATCC 35152 were sensitive to gamma irradiation in phosphate buffer, pH 7.00 (D₁₀, dose required for 10% survival—0.15 kGy) at 0–5°C. The cells showed higher radiation survival when irradiated under frozen condition, with a D₁₀ of 0.3 kGy. The protection offered by shrimp/chicken/kheema homogenates (100 g litre^?1) was evidenced by even higher D₁₀ values (0.5 kGy) at both 0–5°C and cryogenic temperature. Boneless chicken meat samples were artificially inoculated with L monocytogenes ATCC 35152 cells at low (5 × 10³) colony-forming unit (cfu) g^?1 and high (5 × 10⁶ cfu g^?1) concentrations and irradiated at 1, 3, 4, 6 kGy doses under cryogenic conditions. The efficacy of the radiation process was evaluated by detecting L monocytogenes during storage at 2–4°C in the irradiated samples. These studies, when repeated with three other serotypes of L monocytogenes, clearly suggested the need for a dose of 3 kGy for elimination of 10³ cfu cells of L monocytogenes g^?1 from air-packed frozen chicken meat.     

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

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

Effect of Nanoemulsified and Microencapsulated Mexican Oregano (Lippia graveolens Kunth) Essential Oil Coatings on Quality of Fresh Pork Meat

Fresh meat is a highly perishable food. This work aimed to evaluate the influence of Mexican oregano (Lippia graveolens Kunth) incorporated into active coatings (ACs) spread on fresh pork meat as free (FEO), nanoemulsified (NEO), and microencapsulated (MEO) essential oil (EO), on its microbiological, physicochemical and sensory properties during 15 d at 4 ± 1 °C. Thymol and γ‐terpinene were identified in the EO. In vitro effect of 2.85 mg EO/cm² was tested against Brochothrix thermosphacta, Micrococcus luteus, Lactobacillus plantarum, Pseudomonas fragi, and Salmonella Infantis. FEO antioxidant capacity (DPPH assay) was significantly higher than that of thymol, NEO and MEO (93.53%, 89.92%, 77.79%, and 78.50% inhibition, respectively), and similar to BHA (96.03%) and gallic acid (95.57%). FEO, NEO, and MEO ACs on meat caused growth inhibition of lactic acid bacteria (5 log population reduction) and Pseudomonas spp. (4 log reduction), whereas ≤1.5 log population reduction was observed for B. thermosphacta and Salmonella Infantis. Meat microbiota was more efficiently controlled by MEO than by FEO or NEO. ACs delayed lipid and oxymyoglobin oxidation of fresh pork meat. After 15 d of cold storage meat added with EO coatings was desirable for panelists, whereas untreated (UT) samples were undesirable. Active coatings are a significant alternative method for fresh meat preservation.     

Technology-induced selection towards the spoilage microbiota of artisan-type cooked ham packed under modified atmosphere

The microbiota associated with a highly-perishable Belgian artisan-type cooked ham was analyzed through plating and (GTG)₅-fingerprinting of isolates throughout its processing chain. The raw tumbled meat was characterized by the presence of a versatile microbiota around 4.8 log(cfu g⁻¹), consisting of lactic acid bacteria, staphylococci, Brochothrix thermosphacta, Gram-negative bacteria, and yeasts. Pasteurisation of the ham logs reduced bacterial counts below 2 log(cfu g⁻¹) and subsequent manipulations selected for leuconostocs and carnobacteria. Also, B. thermosphacta and several Enterobacteriaceae were found at this stage. During storage in an intermediate high-care area for 2 days, a selection towards certain Enterobacteriaceae (Hafnia alvei, Enterobacter spp., and Pantoea agglomerans) and lactic acid bacteria (mainly vagococci and Streptococcus parauberis) was observed. B. thermosphacta, Leuconostoc carnosum and carnobacteria were also detected, but only after allowing bacterial outgrowth by incubating the meat logs at 7 °C for four weeks. After a mild post-pasteurisation process and subsequent handling, incubation of the meat logs at 7 °C for four weeks led to outgrowth of Enterobacteriaceae (mainly Enterobacter spp. and Serratia spp.). B. thermosphacta, and lactic acid bacteria (Enterococcus faecalis, Leuc. carnosum, and Carnobacterium maltaromaticum) were also found. After slicing and packaging under modified atmosphere, the microbiota of the refrigerated end-product consisted of leuconostocs, carnobacteria, and B. thermosphacta.     

Shelf life extension of ground meat stored at 4 °C using chitosan and an oxygen absorber

The combined effect of chitosan (1%) and an oxygen absorber on shelf life extension of fresh ground meat stored at 4 °C was investigated. Parameters monitored over a 10‐day storage period were Total Viable Count (TVC), Pseudomonas spp., Brochothrix thermosphacta, lactic acid bacteria, Enterobacteriaceae, pH, thiobarbituric acid (TBA), colour, odour and taste. Microbial populations were reduced by 0.4–2.0 log CFU g^?1 for a given sampling day using either chitosan or the oxygen absorber, with the more pronounced effect being achieved by the combination of two. Thiobarbituric acid values for all samples increased during storage with the exception of samples treated with both chitosan and the oxygen absorber in which Thiobarbituric acid values decreased. Changes in pH values with time/different treatments were statistically insignificant. Colour parameters were affected by most treatments. On the basis of microbiological and sensory evaluation, a shelf life extension of 5–6 days was obtained for samples treated with the chitosan and the oxygen absorber combination.     

Combined effect of irradiation and modified atmosphere packaging on shelf-life extension of chicken breast meat: microbiological, chemical and sensory changes

In the present study the combined effect of gamma irradiation (2 and 4 kGy) and modified atmosphere packaging (MAP) (30% CO₂/70% N₂ and 70% CO₂/30% N₂) on shelf life extension of fresh chicken meat stored under refrigeration was investigated. The study was based on microbiological (TVC, Pseudomonas spp., Lactic Acid Bacteria, Yeasts, Brochothrix thermosphacta, Enterobacteriaceae), physicochemical (pH, TBA, color) and sensory (odor, taste) changes occurring in chicken samples. Microbial populations were reduced by 1–5 log cfu/g for a given sampling day depending on the specific treatment. The effect was more pronounced in the case of the combination of MAP (70% CO₂/30% N₂) and the higher irradiation dose of 4 kGy. Of the chemical indicators of spoilage, TBA values for all treatments remained lower than 1 mg malondialdehyde (MDA)/kg meat throughout the 25 day storage period. pH values varied between 6.4 (day 0) and 5.9 (day 25). The values of the color parameters L*, a* and b* were not considerably affected by MAP. Irradiation resulted in a small increase of the parameter a*. Irradiation had a greater effect in extending the shelf life of chicken as compared to MAP. Sensory evaluation showed that the combination of irradiation at 4 kGy and MAP (70% CO₂/30% N₂) resulted in the highest shelf-life extension by 12 days compared to the air packaged samples.     

Behaviour of Listeria monocytogenes in the presence of Listeria innocua during storage of minced beef under vacuum or in air at 0°C and 10°C

Minced beef was inoculated with low levels (1·2–1·7 log₁₀cfu g⁻¹) of Listeria monocytogenes or Listeria innocua, or a combination of the two strains. Inoculated samples were stored at 0 or 10°C under two packaging atmospheres (aerobic and vacuum) for up to 28 days and surviving organisms recovered on Palcam Agar. The only significant increases in numbers of Listeria spp. occurred in samples held at 10°C under aerobic conditions. In vacuum packs, growth of both strains was inhibited. Under aerobic conditions meat pH increased from an initial value of pH 5·85 to c. 8·85 within 28 days. The pH of vacuum packaged meat declined to c. 4·95 during the same period. These differences in pH may be related to differences in the nature and effects of different background microflora that were observed to develop under each of these packaging conditions.Pseudomonas spp. predominated in aerobically stored beef, whereas in vacuum packed beef lactic acid bacteria predominated. No significant differences were observed between the growth rates of Listeria spp. inoculated into beef mince in pure and mixed culture. This suggests that the more frequent prevalence of Listeria innocua than Listeria monocytogenes in meat and meat products is not due to overgrowth or inhibition of the pathogen (Listeria monocytogenes) by the non-pathogen(Listeria innocua) during low-temperature storage.     

Microbiological quality and potential public health risks of export meat from springbok (Antidorcas marsupialis) in Namibia

To assess the microbiological quality and safety of export game meat; i) a total of 80 pooled meat samples for aerobic plate count (APC) and Enterobacteriaceae ii) water used in harvesting and processing for microbiological quality and iii) meat and rectal contents for Salmonella spp. and Shiga toxin Escherichia coli (STEC) were evaluated in 2009 and 2010. No differences (p > 0.05) in the APCs were observed between the years, but the mean Enterobacteriaceae count for 2009 was 1.33 ± 0.69 log₁₀ cfu/cm² compared to 2.93 ± 1.50 log₁₀ cfu/cm² for 2010. Insignificant Heterotrophic Plate Count (HPC) levels were detected in 9/23 field water samples, while fecal bacterial (coliforms, Clostridium perfringens and enterococci) were absent in all samples. No Salmonella spp. was isolated and all E. coli isolates from meat were negative for STEC virulence genes (stx1, stx2, eae and hlyA), suggesting a negligible role by springbok in the epidemiology of STEC and Salmonella.     

Potential of a simple HPLC-based approach for the identification of the spoilage status of minced beef stored at various temperatures and packaging systems

The shelf life of minced beef stored (i) aerobically, (ii) under modified atmosphere packaging (MAP), and (iii) under MAP with oregano essential oil (MAP/OEO) at 0, 5, 10, and 15 °C was investigated. The microbial association of meat and the temporal biochemical changes were monitored. Microbiological analyses, including total viable counts (TVC), Pseudomonas spp., Brochothrix thermosphacta, lactic acid bacteria, Enterobacteriaceae, and yeasts/moulds, were undertaken, in parallel with sensory assessment, pH measurement and HPLC analysis of the organic acid profiles. Spectral data collected by HPLC were subjected to statistical analysis, including principal component analysis (PCA) and factorial discriminant analysis (FDA). This revealed qualitative discrimination of the samples based on their spoilage status. Partial least squares regression (PLS-R) was used to evaluate quantitative predictions of TVC, Pseudomonas spp., Br. thermosphacta, lactic acid bacteria, Enterobacteriaceae, and yeasts/moulds. Overall, the HPLC analysis of organic acids, was found to be a potential method to evaluate the spoilage and microbial status of a meat sample regardless of the storage conditions. This could be a very useful tool for monitoring the quality of meat batches during transportation and storage in the meat food chain.     

Effect of reduced oxygen atmosphere and sodium acetate treatment on the microbial quality changes of seer fish (Scomberomorus commerson) steaks stored in ice

The effect of reduced oxygen atmosphere and sodium acetate treatment on the microbial quality of seer fish (Scomberomorus commerson) steaks was determined during chilled storage (1–2 °C). The O₂ absorber reduced the oxygen content in the pack to less than 0.01% corresponding to 99.96% reduction within 24 h. The use of O₂ absorber with sodium acetate dip treatment (2% w/v) extended the sensory shelf life up to 25 days compared to only 12 days for control air packs and 20 days for untreated samples with O₂ absorber. A prominent lag phase was observed for many bacterium studied, particularly for the sodium acetate treated samples with O₂ absorber. On the day of sensory rejection, both the total mesophilic and psychrotrophic counts reached 7.7–8.1 and 7.1–7.9 log cfu/g, respectively. The sodium acetate treatment and reduced O₂ atmosphere affected the type of major spoilers. In air packed samples, H₂S-producers predominated followed by Brochothrix thermosphacta, Pseudomonas spp., where as in the untreated samples with O₂ absorber, H₂S-producers predominated the microbial flora followed by Lactobacillus spp. For treated samples with O₂ absorber, B. thermosphacta formed the major micro-flora followed by Lactobacillus spp. The use of O₂ absorber inhibited the growth of Pseudomonas spp., and total Enterobacteriaceae.     

Relation of biogenic amines to microbial and sensory changes of precooked chicken meat stored aerobically and under modified atmosphere packaging at 4 °C

The formation of biogenic amines and their correlation to microflora and sensory characteristics of a precooked chicken meat product stored aerobically and under modified atmosphere packaging (MAP) (30% CO₂, 70% N₂) was studied. Putrescine was the main amine formed both in aerobically and MA-packaged chicken samples. For the rest of the biogenic amines, including tyramine, histamine, and cadaverine, a stepwise increase was recorded throughout the 23-day storage period under the above packaging conditions. Spermidine was found in higher amounts, as compared to spermine in both aerobically and MA-packaged chicken samples at 4 °C. Formation of these amines in precooked chicken stored either aerobically or under a 30% CO₂, 70% N₂ atmosphere followed an inconsistent trend during the entire storage period at 4 °C. Agmatine, β-phenyl-ethylamine, and tryptamine were not detected in precooked chicken. Of the bacterial groups monitored, lactic acid bacteria (LAB) became the dominant bacteria after day 8 of storage under MAP while LAB were the dominant population of natural microflora of precooked chicken stored both aerobically or under MAP, reaching 7.5 and 8.0 log cfu/g, respectively, on day 23 of refrigerated storage. Enterobacteriaceae populations in chicken meat were below the detection limit (<1 log cfu/g) by pour plating throughout the 23-day storage period, irrespective of packaging conditions. Based on sensory data, after ca. 8 days for the precooked chicken meat stored aerobically and after 12 days under MAP (time to reach initial decomposition stage, score of 2) the putrescine and tyramine content of chicken samples were ca. 14–19 and 1.4 mg/kg, values that may be proposed as the limit for spoilage initiation of precooked chicken meat (respective TVC for both aerobically and MA-packaged chicken meat were ca. 6.5 log cfu/g).     

Inhibition of Brochothrix thermosphacta in broths and pork by myristoyl-L-methionine

The antibacterial properties of myristoyl-L-methionine (Myr-Met) were examined in commercial broths (APT, cooked meat medium), aqueous extracts of pork muscle, pork muscle slurries and at the surface of pork muscle discs inoculated with Brochothrix thermosphacta. Broths and muscle substrates were inoculated with B. thermosphacta to give an initial concentration of about 4 log cfu ml⁻¹or cm²and bacterial growth in the presence or absence of Myr-Met was determined by plate counts during 9 days of aerobic incubation at 4°C. In an aqueous muscle extract and APT broth Myr-Met was bactericidal at concentrations of 5 and 50 μg ml⁻¹, respectively, reducing B. thermosphacta to below recoverable levels (<1 log cfu ml⁻¹). Efficacy was diminished in substrates containing muscle or meat particles and 500 μg ml⁻¹Myr-Met only produced a transient bacteriostatic effect in pork muscle slurries. A concentration of 500 μg ml⁻¹Myr-Met was without effect upon the growth of B. thermosphacta in a commercial cooked meat medium or on the surface of inoculated pork muscle discs. To produce a significant inhibition of B. thermosphacta growth on pork muscle tissue it was necessary to increase the concentration of Myr-Met to 5000 μg ml⁻¹, using the sodium salt of Myr-Met to permit solublization. A mechanism to prevent Myr-Met inactivation in meat is necessary if Myr-Met is to be of practical value as a preservative.