Effects of Lactobacillus rhamnosus GG addition in ice cream

A 2⁴ full factorial experimental design was applied to verify the effects of Lactobacillus rhamnosus GG (LGG) addition in retail-manufactured ice cream stored at two different freezing temperatures (−16°C and −28°C) and containing two different levels of sugar (15–22%) and fat (5–10%). In addition to microbial counts, the pH, acidity, viscosity of the mixes and functional properties of the ice creams were evaluated. Both fresh and frozen-thawed LGG cells underwent preliminary resistance tests to bile, antibiotics and acidity. The LGG strain proved to be highly resistant to most of the stress factors. When the micro-organism was added to ice cream mixes in a quantity of 10⁸ cfu/g, it did not change the overrun, firmness or melting behaviour of the finished product. Regardless of formulation, no count decay of LGG cells was observed in ice cream stored for up to 1 year.     

Viability of probiotic micro-organisms (Lactobacillus acidophilus La-5 and Bifidobacterium animalis subsp. lactis Bb-12) in ice cream

The purpose of this research was to determine the survival of two probiotic micro-organisms in ice creams (4% fat). The micro-organisms were Lactobacillus acidophilus La-5 and Bifidobacterium animalis subsp . lactis Bb-12 . To meet this objective, an ice cream mixture was formulated and subjected to three treatments. Treatment 1 was inoculated with L. acidophilus , treatment 2 with B. lactis and the third treatment was inoculated with a mixture of both bacteria inoculated in 1 : 1 proportions. The inoculation was with 4% culture for each treatment. The final products were stored at −25°C for 60 days. The ice cream inoculated with L. acidophilus had a final concentration of 2 × 10 ⁶ cfu/g and the survival rate was 87%. The treatment inoculated with B. lactis had a final concentration of 9 × 10 ⁶ cfu/g, with a logarithmic decrease of 10%. When both micro-organisms were inoculated together, the survival rate was 86%.     

MICROBIOLOGICAL QUALITY OF THE DAIRY PRODUCT PEDHA AND ITS IMPROVEMENT USING GAMMA RADIATION

Eighteen pedha samples procured from A and B grade retail shops were examined for their overall microbiological quality and for the presence of foodborne pathogens viz. Staphylococcus aureus, Salmonella sp., Coliforms , Listeria monocytogenes, Yersinia enterocolitica and Bacillus cereus. The microbiological quality of pedha samples from B grade shops was very poor as compared to pedha from A grade shop as evidenced by the very high total bacterial counts (6 × 10⁷ cfu/g), high counts of S. aureus (as high as 7 × 10⁶ cfu/g) and presence of coliforms and Listeria and Yersinia sp. in 33% of the samples. All the samples from A grade shops were also positive for S. aureus though negative for coliforms , Yersinia, Salmonella, Listeria and B. cereus. Gamma irradiation of pedha at a dose of 3kGy at 0C reduced overall bacterial load by five log cycles and S. aureus and coliforms could be totally eliminated. However, 5 kGy dose was necessary to eliminate S. aureus if the initial number exceed 1 × 10⁵ cfu/g. Inoculated pack studies confirmed that 3 kGy dose was sufficient for the complete elimination of up to 1 × 10⁵ cfu/g of S. aureus. A dose of 3 kGy had minimal effect on the sensory quality of pedha and even pedha samples irradiated at 5 kGy dose were acceptable. Treatment with 3 kGy dose of gamma radiation totally eliminated S. aureus and coliforms in pedha, thereby ensuring their microbial safety.     

The effects of different incubation temperatures on the acetaldehyde content and viable bacteria counts of bio-yogurt made from ewe's milk

Yogurt and bio-yogurt were manufactured from ewe's milk using a starter culture and a probiotic culture. Incubation was carried out at 37°C and 42°C until pH 4.6 was reached and the yogurts were stored at 4 +1°C for 14 days. Analysis after 1, 7 and 14 days showed that incubation temperature and storage time significantly influenced overall properties of the samples. During the storage, whey separation and pH decreased, but titratable acidity, lactic acid and volatile fatty acid contents increased. Viable bacterial counts in all bio-yogurts were above 10⁷ cfu g⁻¹ at the end of storage.     

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 .     

EFFECT OF NITRITE AND STORAGE TEMPERATURE ON THE ORGANOLEPTIC QUALITY AND TOXINOGENESIS BY Clostridium botulinum IN VACUUM-PACKAGED SIDE BACON

The effect of nitrite and storage temperature and toxinogenesis by Clostridium botulinum in vacuum-packed side bacon was investigated. In two series of experiments (A & B) bacon packs were prepared with levels of 0, 50, 100, 150 and 200 ppm nitrite and inoculated with C botulinum at 10² spores/g and 10⁴ spores/g. Packs A were incubated at 20 and 30° C and packs B at 30°C only. Both were held for a maximum of 32 days and analyzed for toxin at intervals of 2, 4, 8, 16 and 32 days. At 20°C none of the controls without nitrite was found to be toxic after 32 days. At 30°C inhibition of toxin formation at the higher nitrite levels was observed at 32 days. Organoleptic evaluation of the bacon packs stored at 30° C showed about one-third of the toxic samples examined were acceptable to the panel.     

Microbiological quality of ice creams commercialized in some cities in the state of Rio de Janeiro, Brazil

The microbiological quality of 60 ice cream samples of three commercial brands (A, B and C) of various flavours, commercialized in some towns in the State of Rio de Janeiro, Brazil, was evaluated. Total bacteria count (TCB), coliforms at 35°C (CT), coliforms at 44°C (CF) and presence of Staphylococcus aureus were performed on all samples. TCB ranged from 2.0 × 10 ² to 6.9 × 10 ⁵ cfu/mL, CT from < 3–≥ 2400 MPN/mL, CF from < 3–1100 MPN/mL and S. aureus from < 10–1.4 × 10 ⁶ cfu/mL. The level of bacterial contamination found in this study reflects the unhygienic conditions prevalent in manufacturing and storage of ice creams. Actions are thus necessary by the Brazilian regulatory agencies to require the ice cream processing plants to adopt quality guarantee systems, such as good manufacturing practices and hazard analysis and critical control points system.     

SURVIVAL OF THREE SALMONELLA SEROTYPES ON BEEF TRIMMINGS DURING SIMULATED COMMERCIAL FREEZING AND FROZEN STORAGE

This study investigated the survival of three Salmonella serotypes (S. Brandenberg, S. Dublin and S. Typhimurium) on beef trimmings during simulated commercial freezing, frozen storage for 9 months and subsequent abusive slow thawing and refreezing conditions. This was achieved by plating samples monthly and after thawing and refreezing on nonselective Tryptic Soy Agar (TSA) and selective Xylose Lysine Desoxycholate Agar (XLD) and incubating both at 37C for 24 h to determine Salmonella counts, aerobic counts and the presence, if any, of sublethal injury of this pathogen. Two freezing temperatures (−18C or −35C) to simulate slow or rapid freezing respectively, and two inoculation levels (10³ cfu g⁻¹ or 10⁵ cfu g⁻¹) were used. Aerobic counts and counts of all the Salmonella serotypes did not change significantly (p > 0.05) during frozen storage or for any of the other treatments applied in this study. This finding was attributed to the insulating nature of the subcutaneous fat layer in this manufacturing cut. These results are important with respect to food safety associated with ground beef processing.     

Sensory Acceptability and Stability of Probiotic Microorganisms and Vitamin C in Fermented Acerola (Malpighia emarginata DC.) Ice Cream

ABSTRACT:  Six fermented acerola ice creams were produced, containing different starter cultures ( Bifidobacterium longum , Bi.lactis , and traditional yogurt starter culture— Streptococcus thermophilus and Lactobacillus delbrueckii spp. bulgaricus ) and final pH (5 and 4.5). The ice creams were evaluated for probiotic culture viability, vitamin C stability, and sensory acceptance. Mix fermentations were stopped when pH 5.0 and 5.5 were attained. However, after the addition of acerola pulp the determined pH were 4.5 and 5, respectively. Mixes were frozen and stored for 15 wk at −18 °C. The viable counts for probiotic cultures remained above the recommended minimum limit of 10⁶ cfu/g during 15 wk storage even in products with pH 4.5. Vitamin C concentration remained around 140 mg/100 g of product. The attributes of aroma, taste, texture, and overall acceptance obtained scores in the range of 5.15 to 7.22. The fermented acerola ice cream was a suitable food for the delivery of vitamin C and Bifidobacterium strains with excellent viability and acceptable sensory characteristics.     

QUALITY LOSS of DOUBLE CONCENTRATED TOMATO PASTE: EVOLUTION of the MICROBIAL FLORA and MAIN ANALYTICAL PARAMETERS DURING STORAGE AT DIFFERENT TEMPERATURES

This study deals with nonsterile canning of double concentrate tomatoes (30° Brix) stored for 210 days at three different temperatures (4, 10 and 25C) in 200 kg drums. the evolving analytical composition (soluble solids, total solids, glucose, fructose, pH, total acidity, volatile acidity, citric acid, malic acid, succinic acid, hydroxymethylfurfural (HMF) and color parameters) that the product underwent during storage was dependent both on storage temperature and on different aerobic levels within the drum (top and bottom sections). the microbial profile (yeast, lactic acid bacilli and molds) was correlated with many important metabolites (D- and L-lactic acids, ethanol, acetic acid and diacetyl). the results indicate that the increase of these substances is dependent both on storage temperature as well as the oxygen tension within the drums.
Taken all together, the analytical findings offer a great help in evaluating the quality of semifinished tomatoes. We also found that lactic bacteria grow rapidly at 25C and after 15 days their number from both sampling areas in the drums (i.e., 10 cm below the sample surface and 15 cm above the bottom of each drum) is already greater than 10⁵ cfu/ml. At 10C, 30 days were needed to reach such a cell concentration, and after 45 days the level reaches 10⁷-10⁸ cfu/ml. By contrast, at 4C there were differences between top and bottom sampling areas. In the top area, 10⁵ cfu/ml was reached after 60 days, while for the bottom area this was reached after 120 days. Regarding yeast at 25C.     

Super Chilling Enhances Preservation of the Freshness of Salted Egg Yolk During Long-Term Storage

ABSTRACT:  Pasteurized egg yolk with 10% (w/w) salt was stored at 5, –5, –15, –20, and –30 °C for 1 to 6 mo, respectively. Changes in generation of volatiles of the stored samples (5 and −5 °C for 6 mo) were analyzed by SPME-GC-MS. Emulsifying properties of egg yolk stored at −5, −15, −20, and −30 °C for 1 mo, respectively, were also evaluated by measurement of emulsion particle diameters in model emulsions prepared with the yolk samples. In addition, structural changes in low-density lipoprotein (LDL) in the egg yolks dependent on storage conditions for 6 mo were evaluated by ³¹P–NMR. Volatile compounds such as hexanal, 2-methylbutanal, and 3-methylbutanal increased in egg yolk during storage at 5 °C; however, volatile compounds hardly increased in any samples stored at −5 °C (super chilling). The mean emulsion particle diameter in super chilled egg yolk was significantly smaller than that in egg yolk stored at the other lower temperatures. In addition, the results of ³¹P–NMR evaluation suggested that prevention of structural changes of LDL resulted in maintenance of emulsifying properties of egg yolk. Thus, these results indicate that super chilling is an effective means of preserving salted egg yolk during long-term storage.     

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.     

Enterobacter sakazakii survives spray drying

Four strains of Enterobacter sakazakii were inoculated into 35% reconstituted skim milk at 10⁷ and 10² cfu/g dry wt. After spray-drying in a Buchi mini spray drier (inlet 160°C and outlet 90°C), the resulting powders were analysed for E. sakazakii by enrichment and enumeration. In all cases, E. sakazakii survived the spray drying process and were detected in the powders with a low inoculum and enumerated in all the powders with the high inoculum for at least 12 weeks. The results emphasize that the controls in place to prevent E. sakazakii from getting to the spray drier are essential.     

Production of Enterotoxin-B in Cured Meats

SUMMARY— A variety of laboratory cured hams were inoculated with 10³−10⁶ cells of S. aureus strain S-6 and incubated at 10, 22 and 30°C anaerobically for up to 16 weeks. Enterotoxin-B was detected by gel-diffusion in hams with original pH over 5.30, up to 9.2% NaCl (brine) and 0.54 ppm undissociated nitrous acid. There was better toxin production at 30° than at 22° or 10°C. Toxin was detected at 10°C after at least 2 weeks incubation and in most samples after 8 weeks when pH was greater than 5.6. Toxic hams had more than 4 × 10⁶ cells/g. Contaminants were always less than 10⁵/g. Tween 80 inhibited toxin production at 30° but not at 10°C. Toxic hams looked normal even after 2 months incubation at 10°C.     

Quality changes of European catfish (Silurus glanis) from warm-water aquaculture during storage on ice

Gutted European catfish (Silurus glanis) from warm-water aquaculture was stored in ice for 30 days. The limit of saleability was reached after approximately 20 days, and cooked fillets became inedible after about 27 days. Quality changes were investigated using established analytical methods; pH, total volatile bases (TVB), thiobarbituric acid number and texture measurements by Instron were not usefully predictive of shelf-life or possible storage time. The Fish Tester and Torrymeter values decreased from 848 to 376 and 111 to 61, respectively. On day 27 the total aerobic bacterial counts had reached some 10⁸/cm² skin surface but only 10⁵/g muscle. Hypoxanthine concentrations increased steadily to 17.2 mg/100 g, and ammonia levels increased from 11.5 to 18.7 mg/100 g muscle. There were no differences in the patterns obtained by isoelectric focusing of sarcoplasmic proteins from fresh and spoiled European catfish.     

Effect of technological parameters on the characteristics of kasseri cheese made from raw or pasteurized ewes' milk

Two groups of kasseri cheese (pasta filata type) were manufactured from raw or pasteurized ewes' milk, without starter cultures. Cheeses of each group were divided into two subgroups: the first was ripened and stored at 4°C and packaged in plastic film; the second ripened and stored at 15°C and coated with paraffin wax. Milk pasteurization and technological parameters had a significant effect on the pH ( P  < 0.05), while only technological parameters had an effect on the total solids content. At day 120, the range of mean cfu/g counts for the mesophilic aerobic flora was 9.5 × 10⁷−1.4 × 10⁸; for the thermophilic streptococci, the range was 2.6 × 10⁷−7.6 × 10⁷; and for the thermophilic bacilli, 9.8 × 10⁶−1.7 × 10⁷. Changes in the N fractions became significant after 30 days of ripening. For mature 120-day-old cheeses, the percentage of total N soluble at pH 4.6 was 22.7%–22.9% in raw milk cheeses and 19.0%–21.7% in pasteurized milk cheeses. The percentage of total N soluble at 12% TCA was 10.1%–12.2% in raw milk cheeses and 7.3%–11.5% in pasteurized milk cheeses; the percentages of total N soluble at 5% PTA were 3.1%–4.0% and 2.6%–3.6%, respectively. The residual α_s-casein percentages at day 120 ranged between 63% and 78% of the respective area at day 1; the residual β-casein ranged between 67% and 75%. There were some characteristic differences in the reverse phase-HPLC peptide profiles of the four cheeses. In general, the effect of the different ripening conditions was more pronounced in cheeses made from pasteurized milk.     

SURVIVAL OF ESCHERICHIA COLI, STAPHYLOCOCCUS AUREUS AND SALMONELLA ENTERITIDIS IN FROZEN CHICKEN HAMBURGER

The survival of food pathogens during frozen storage of chicken hamburgers was evaluated. Hamburgers were contaminated with Escherichia coli (ECHC), Staphylococcus aureus (SAFH) and Salmonella Enteritidis (SE86), separately, and stored at −18C for 28 days. Results demonstrated reductions of 0.63 log₁₀ cfu/g, 0.73 log₁₀ cfu/g and 0.27 log₁₀ most probable number/g in the populations of ECHC, SAFH and SE86, respectively. These microorganisms were also stored at −18C in 0.1% peptone water and presented significantly different reductions ( P <  0.05) when compared with frozen hamburgers, suggesting that components of chicken hamburger may exert a cryoprotective effect on microbial cells.

PRACTICAL APPLICATIONS

Even though Brazilian poultry meat industries present high levels of quality control, the presence of bacterial pathogens in hamburgers may occur. In Brazil, chicken hamburgers are frequently commercialized frozen, and it is well established that frozen temperatures are able to avoid microbial growth. However, frozen temperatures can also be able to inactivate part of the bacterial population, and the magnitude of its effect will vary according to the type of food and the process that it was submitted. This study evaluated the survival of Escherichia coli , Staphylococcus aureus , and Salmonella Enteritidis in frozen hamburgers, aiming to verify if this process could provide an additional margin of safety to this product.     

THE EFFECT OF AEROBIC MESOPHILIC MICROFLORAL LEVELS ON THE ISOLATION OF INOCULATED LISTERIA MONOCYTOGENES STRAIN LM82 FROM SELECTED FOODS

The effect of aerobic mesophilic microfloral concentration on the isolation of Listeria monocytogenes LM82 was studied in 31 (18 cheeses and 7 noncheese) retail foods having standard plate counts of 10¹ to 10⁸ colony forming units (CFU)/g. Foods were spiked with L. monocytogenes and enriched at 30°C for 24 h in a selective enrichment broth used in a U.S. Food and Drug Administration method. Inoculum levels for isolation on modified McBride agar ranged from 0.1 to > 5 × 10³ with a geometric mean value of 5 inoculated CFU/g or 1.4 CFU/g. Pure Enterococcus (Streptococcus) faecalis ( 0 to 6 × 10⁶ inoculated CFU/mL ) in the absence of food matrix had no effect on the enrichment of L. monocytogenes. Ease of isolation of LM82 was independent of the food microflora concentration both generally and in the specific food type of 9 Brie cheeses. Competition, when it occurs, therefore, may be due to specific bacterial competitors rather than bacterial numbers .     

Development of a simple model based on chemical kinetics parameters for predicting respiration rate of carambola fruit

The respiration model was parameterised with experimental data obtained at temperatures 10, 15, 20, 25 and 30 °C by the closed system. Reaction orders of O₂ and CO₂ determined for respiration rate are 0.912 and −0.24, respectively. Estimates of A and E _a for rate coefficient are 5.219 _× 10¹⁰ h⁻¹ and 61.397 kJ mol⁻¹, respectively. The reliability of the model was verified against new data generated from 18 °C. An enzyme kinetics based model was likewise built and verified as a contrast. Verification results indicate that the chemical kinetics model performs very well and has superiority over the enzyme kinetics one. This study demonstrates that chemical kinetics can be used to underpin the development of simple respiration model and should facilitate the prediction of respiration rate for the carambola fruit in practice.     

Rapid dye reduction tests for the determination of microbiological quality of meat

Rapid dye reduction tests have been developed to determine the quality of meat. Three chemical indicators, resazurin and two tetrazolium compounds, were used to correlate the microbial numbers and reduction times in meat samples. Twenty-five surface samples from sheep carcasses were subjected to each reduction test. Total viable counts given were obtained at 37°C. Resazurin reduction time was 90–120 min when the bacterial counts ranged from 1.5×10⁶ to 7.7×10⁶/cm². Samples showing bacterial counts between 1.5×10⁶ and 6.0×10⁶/cm² reduced tetrazolium (NBT) in 360–390 min whereas samples containing bacterial counts of 2.1×10⁶/cm² took 420–450 min to reduce iodophenyl nitrophenyl tetrazolium (INT) dye. Regression equations relating the number of organisms per cm² and reduction time were applied to predict the microbiological quality of meat samples from reduction time data. Among the three dyes, resazurin gave the lowest reduction time.