Effects of temperatures and storage time on resting populations of Escherichia coli O157:H7 and Pseudomonas fluorescens in vitro

Assessment of microbial interactions is crucial for documenting bacterial growth in pure and mixed cultures and their potential for biological applications. Pseudomonas fluorescens (non-plant pathogenic and non-pectinolytic) has been used as a biocontrol microbe for plant pathogens and food-borne bacteria. We determined the growth of Escherichia coli O157:H7 (Ec) and P. fluorescens(Pf) in monocultures and co-cultures in sterile distilled water (SDW), buffered peptone water (BPW) and trypticase soy broth (TSB). The effects of temperatures (5, 10, 15, 20, 25, 35, and 37 °C) and storage time (0, 2, 4, 6, 24, and 48 h) on bacteria populations were assessed. Bacteria counts in monocultures in SDW ranged from 2.14 to 3.03 and 2.54 to 3.31 Log CFU/ml for Ec and Pf; respectively. In BPW, mean bacteria counts (monocultures) ranged from 3.15 to 6.14 and 2.54 to 6.41 Log CFU/ml for Ec and Pf, respectively. Ec populations in co-culture varied with storage temperatures and time. After 48 h, Ec 43894 monocultures in TSB ranged from 2.17 to 8.75 and 2.31 to 8.85 Log CFU/ml at 20 and 35 °C; respectively. In co-cultures with Pf 2-79, Ec 43894 counts ranged from 1.71 to 5.83 (20 °C) and 1.90 to 9.03 Log CFU/ml (35 °C) in TSB. The reductions of Ec by Pf 2-79 varied among strains and generally ranged from 0.20 to 0.90, 0.63 to 1.18, and 0 to 0.56 Log CFU/ml in BPW (10 °C). Substrate availability, storage temperatures, and time significantly (P < 0.05) impacted Ec populations in co-culture. The liquid substrate experiments indicated suppressive conditions of Ec by Pf, however; the reduction of produce contamination by E. coli O157:H7 during transitory temperature abuse conditions such as the transportation of produce from fields needs further investigation.     

Nitrite level of pickled vegetables in Northeast China

Nitrite is commonly present in pickled vegetables. Nitrite has been proven to have adverse effects on health, including changing the normal form of hemoglobin and the formation of carcinogenic nitrosamines. The aim of our study was to determine the levels of nitrite in pickled vegetable samples consumed in Harbin, China. In this study, 218 samples of pickled turnip (PT) (n = 42, packaged (PK) = 19; unpackaged (UPK) = 23), pickled tuber mustard (PTM) (n = 44, PK = 23; UPK = 21), pickled cucumber (PCC) (n = 48, PK = 25; UPK = 23), and pickled cabbage (PCB) (n = 84, PK = 39; UPK = 45) were analyzed between October 2011 and December 2011, using colorimetric nitrite assay based on the Griess reaction. A nitrite level of <5 mg/kg was normally predominant in 147 (67%) samples of the investigated pickled vegetables, ranging from 0.01 mg/kg to 42.03 mg/kg, while a nitrite level of >20 mg/kg was detected in 9 (4%) samples. The overall nitrite content was 4.02 ± 0.62 mg/kg for PT, 4.52 ± 1.07 mg/kg for PTM, 3.91 ± 0.69 mg/kg for PCC, and 4.86 ± 0.80 mg/kg for PCB. The content of nitrite in unpackaged pickled vegetables (PT, 5.47 ± 0.89; PTM, 6.84 ± 2.02; PCC, 5.32 ± 1.27; PCB, 6.41 ± 1.28; and total, 6.08 ± 0.71 mg/kg) was significantly higher than those in packaged products (PT, 2.68 ± 0.72; PTM, 2.30 ± 0.55; PCC, 2.62 ± 0.54; PCB, 3.08 ± 0.81; and total, 2.73 ± 0.36 mg/kg) (P < 0.05). The variance in the concentration of nitrite in the pickled vegetables probably resulted from differences in quality, processing technique, and storage condition of the pickled vegetables. Our results indicated that, in China, low level nitrite is widely present in pickled vegetables. It is therefore important to assess the content of nitrite in pickled vegetables in China.     

The efficacy of grape seed extract,citric acid and lactic acid on the inactivation of Vibrio parahaemolyticus in shucked oysters

The efficacy of grape seed extract (GE), citric acid (CA) or lactic acid (LA) on the inactivation of Vibrio parahaemolyticus in shucked oysters was studied. The minimum inhibitory concentration (MIC) of GE, CA or LA against V. parahaemolyticus in TSB-1% NaCl was also determined. The shucked oysters were artificially inoculated with V. parahaemolyticus, the inoculated shucked oysters (25 g) were then dipped in solution of GE (0.0, 10.0, 20.0, 50.0, 100, 200, 300 and 500 mg mL⁻¹), CA (0.0, 5.0, 10.0, 15.0, 20.0, 50.0, 100, 200 and 300 mg mL⁻¹) or LA (0.0, 1.0, 5.0, 10.0, 15.0, 20.0, 50.0, 100 and 150 mg mL⁻¹) for 10 min. The population of V. parahaemolyticus in shucked oysters was determined. The MICs of GE, CA or LA against V. parahaemolyticus were 10.0, 5.0 or 1.0 mg mL⁻¹, respectively. A 500, 300 or 150 mg mL⁻¹ GE, CA or LA solutions were needed to reduce the population of V. parahaemolyticus to below the detection level (1.0 log g⁻¹) in shucked oysters.     

Inactivation of Staphylococcus saprophyticus in chicken meat and purge using thermal processing,high pressure processing,gamma radiation,and ultraviolet light (254 nm)

Staphylococcus saprophyticus is a common contaminant in meat and poultry, and causes urinary tract infections after colonization of the gastrointestinal tract, followed by accidental transfer of contaminated feces to the urethra. There is limited information regarding the inactivation kinetics of S. saprophyticus in meat and poultry. When S. saprophyticus was suspended in ground chicken meat (GCM) the thermal processing D₁₀ was 6.26, 0.60 and 0.09 min at 55, 60 and 65 °C, respectively. When S. saprophyticus was inoculated into GCM and subjected to high pressure processing (5 °C, 0–25 min) at 200, 300 or 400 MPa the HPP D₁₀ was 15.5, 9.43, and 3.54 min, respectively. When the S. saprophyticus cocktail was inoculated into GCM and irradiated (5 and −20 °C) the gamma radiation D₁₀ were 0.64 and 0.77 kGy, respectively. When S. saprophyticus was inoculated into chicken purge which was then placed on food contact surfaces including stainless steel, and high density polyethylene and polypropylene and treated with UV-C (0–60 mJ/cm²) the UV-C D₁₀ ranged from 14.9 to 18.5 mJ/cm². These results indicate the inactivation kinetics for S. saprophyticus are consistent with those for other foodborne pathogens and could be controlled in poultry meat and purge without difficulty.     

Inhibition of Listeria monocytogenes in vitro and in goat milk by liposomal nanovesicles containing bacteriocins produced by Lactobacillus sakei subsp. sakei 2a

Lactobacillus sakei subsp. sakei 2a is a bacteriocinogenic lactic acid bacteria isolated from a Brazilian meat product, capable to inhibit Listeria monocytogenes in vitro and in foods. In this study, bacteriocin produced by this strain were encapsulated in phosphatidylcholine (FC) and 1,2-dioleoyloxy-3-trimethylammonium-propane (DOTAP) liposomes, separately and in combination, were characterized and evaluated for activity against L. monocytogenes in vitro and in experimentally contaminated UHT goat milk, during storage at 7 °C for 14 days and 30 °C for 24 h. The FC and DOTAP/FC (3:1) nanovesicles containing bacteriocins (12.800 AU mL⁻¹) presented zeta potential of −1.54 and + 38.13 mV, Entrapment Efficiency of 80.0% and 94.1%, and diameter of 91.19 and 81.49 nm, respectively. DOTAP/FC nanovesicle presented excellent stability, and maintained the same physicochemical characteristics over 28 days. Both free and encapsulated bacteriocins controlled L. monocytogenes growth in BHI medium and goat milk stored at 30 °C for at least 8 h, in a similar pattern. After 24 h in BHI medium, bacteriocins encapsulated in FC nanovesicles were more effective (p < 0.05) than free bacteriocins. However, in goat milk, no significant differences (p ≥ 0.05) were observed for the two types of nanovesicles. At 7 °C, both free and encapsulated bacteriocins retarded the L. monocytogenes growth, and after 5 days, counts were 5 log lower than in the controls, both in BHI and in goat milk. Encapsulation of bacteriocin in FC and DOTAP/FC nanovesicles did not affect the antimicrobial activity, but the advantages of their application for control of L. monocytogenes in goat milk based dairy products, when compared to free bacteriocins, remain unclear and more studies are needed.     

Decimal reduction times of acid-adapted and non-adapted Escherichia coli O157:H7, Salmonella spp., and Listeria monocytogenes in young Cocos nucifera Linn. liquid endosperm

The study established the decimal reduction times at 55 °C (D_55 °C values) of acid-adapted and non-adapted Escherichia coli O157:H7, Salmonella enterica, and Listeria monocytogenes in young coconut liquid endosperm. Acid adaptation of the test pathogens was conducted by cultivating cells in a gradually acidifying nutrient broth supplemented with 1% glucose. Results showed that acid adaptation had varying influence on the subsequent thermal resistances of the pathogens. The non-adapted E. coli O157:H7 exhibited the greatest resistance among the tested pathogens with a D_55 °C of 23.20 min. Prior adaptation to acidity decreased the D_55 °C to 16.16 min. On the other hand, acid adaptation increased the D_55 °C values of S. enterica and L. monocytogenes from 8.76 to 10.55 min, and from 7.47 to 18.09 min, respectively. The D_55 °C of the non-adapted E. coli O157:H7 was used to establish a pasteurization process schedule with an order of lethality equal to 5-logarithmic (99.999%) reduction. Sensory evaluation revealed that the overall acceptability, color, aroma, coconut flavor, and freshness characteristics of non-pasteurized and pasteurized liquid endosperms were not significantly different (p > 0.05). Moreover, the sensory quality attributes of coconut beverages (80:20 vol/vol endosperm-to-water ratio, soluble solids adjusted to 10 °Brix with sucrose) prepared from both non-pasteurized and pasteurized liquid endosperm samples did not significantly vary. The results obtained from the study may be used in the establishment and validation of thermal process schedules for young coconut liquid endosperm beverages.     

Survival and inhibition of Staphylococcus aureus in commercial and hydrated tahini using acetic and citric acids

Tahini (sesame paste) is a low-moisture ready-to-eat food that has been linked to foodborne outbreaks and recalls. The objectives of this study were to investigate the behavior of Staphylococcus aureus in commercial and hydrated tahini at 10, 21 and 37 °C and to inhibit S. aureus in these products by 0.1, 0.3 and 0.5% acetic or citric acid. S. aureus was able to survive in commercial tahini with reductions of 3.3, 1.6 and 0.7 log₁₀ CFU/g at 37, 21 and 10 °C, respectively; while it grew in hydrated tahini with an increase of 3.9, 3.0 and 1.8 log₁₀ CFU/ml at 37, 21 and 10 °C, respectively, by 28d. Citric or acetic acid at ≤ 0.5% reduced S. aureus in commercial tahini by ≤ 2.3 log₁₀ CFU/ml by 28d compared to control at all of the tested temperatures. However, acetic and citric acid were more inhibitory at 37 and 10 °C, respectively. In hydrated tahini, viable S. aureus cells were not detected in the presence of 0.5 or 0.3% acetic acid after 7 and 14d, respectively, at both 21 and 37 °C; and after 14 and 28d, respectively at 10 °C. Acetic acid at 0.1% also reduced S. aureus numbers to undetectable levels after 14 and 28d at 21 and 37 °C, respectively. S. aureus cells were also not detected in the presence of 0.5% citric acid by 21d at all of the tested temperatures, or 0.1 and 0.3% citric acid by 28 and 21d, respectively at 21 °C. Acetic and citric acids could be used in tahini or tahini-based products to reduce the potential risk associated with S. aureus.     

Effect of UV-C irradiation on the inactivation of inoculated pathogens and quality of chicken breasts during storage

In this study, we evaluated the inactivation of foodborne pathogens inoculated on chicken breasts by UV-C treatment. Chicken breasts were inoculated with Campylobacter jejuni, Listeria monocytogenes, and Salmonella enterica serovar Typhimurium at 6–7 log CFU/g. The inoculated chicken breasts were then irradiated with UV-C light of dose 0, 0.5, 1, 3, and 5 kJ/m². Microbiological data indicated that the populations of the foodborne pathogens decreased significantly (p < 0.05) with increasing UV-C irradiation. In particular, UV-C irradiation at 5 kJ/m² reduced the initial populations of C. jejuni, L. monocytogenes, and S. typhimurium by 1.26, 1.29, and 1.19 log CFU/g, respectively. After UV-C irradiation, the samples were individually packed using polyethylene terephthalate containers and stored at 4 ± 1 °C for 6 d. The pH of the control increased more than the samples irradiated at 0.5, 1, 3, and 5 kJ/m², while TBARS values increased during storage regardless of UV-C irradiation. UV-C irradiation caused negligible changes in Hunter L, a, and b values. These results suggest that UV-C irradiation can be useful in improving the microbial safety of chicken breasts during storage, without impairing quality.     

Histamine content and histamine-forming bacteria in mahi-mahi (Coryphaena hippurus) fillets and dried products

Forty-two mahi-mahi fillets and 17 dried products sold in retail markets in Taiwan were tested for histamine and histamine-forming bacteria. The levels of pH, salt content, water content, Aw, TVBN, APC, TC and Escherichia coli in mahi-mahi fillet samples ranged from 5.6 to 6.5, 0.05 to 2.44%, 70.9 to 82.8%, 0.95 to 0.99, 5.9 to 23.5 mg/100 g, 3.1 to 7.0 log CFU/g, <3 to 1650 MPN/g and <3 to 45 MPN/g, respectively. The levels of pH, salt content, water content, Aw, TVBN, APC, TC and E. coli in dried mahi-mahi samples ranged from 5.7 to 6.4, 0.63 to 20.13%, 7.1 to 42.9%, 0.51 to 0.85, 21.4 to 133.9 mg/100 g, 3.6 to 8.7 log CFU/g, <3 to 5900 MPN/g and <3 to 2500 MPN/g, respectively. The average content of various biogenic amines in fillets samples was less than 0.3 mg/100 g. Four of the 17 dried samples (23.4%) had histamine levels greater than the FDA guideline of 5 mg/100 g for scombroid fish and/or product with one of them containing 68.15 mg/100 g of histamine, which is greater than the 50 mg/100 g hazard action level. Eight histamine-producing bacterial isolates, capable of producing 12.6 ppm–562 ppm of histamine in trypticase soy broth supplemented with 1.0% l-histidine (TSBH), were identified as Raoultella ornithinolytica (three isolates), Pantoea agglomerans (two isolates), Proteus vulgaris (two isolates) and Enterobacter amnigenus (one isolate), by 16S rDNA sequencing with PCR amplification.     

One-Pot Synthesis,Crystal Structure,and Thermal Decomposition Behavior of 1,1ʹ-Diamino-4,4ʹ,5,5ʹ-Tetranitro-2,2ʹ-Biimidazole

1,1?-Diamino-4,4?,5,5?-tetranitro-2,2?-biimidazole (DATNBI) was synthesized, by employing one-pot facile method, from 4,4?,5,5?-tetranitro-2,2?-biimidazole. The crystal structure was determined by X-ray diffraction for the first time. DATNBI crystallized in monoclinic system P2₁/c, with a crystal density of 1.934 g cm^?3 at 293(2) K and 2.019 g cm^?3 at 130(2) K, respectively. Its crystal parameters at 293 K are a = 4.8833(15) Å, b = 6.960(2) Å, c = 6.928(4) Å, α = γ = 90°, β = 93.418(6)°, V = 591.1(3) ?³, Z = 2, μ = 0.178 mm^?1, and F(000) = 348. The thermal stability and non-isothermal kinetics of DATNBI were studied by differential scanning calorimeter (DSC) with heating rates of 5, 10, 15, and 20 K min^?1. The apparent activation energy (E_a) at the first decomposition peak calculated by Kissinger, Ozawa, and Starink equations were 85.50, 89.67, and 86.10 kJ mol^?1, respectively. For the second peak, these were 116.49, 119.82, and 117.45 kJ mol^?1, respectively, with individual pre-exponential factors lnA = 18.40 s^?1 and lnA = 25.11 s^?1. The thermogravimetry-Fourier transform infrared spectroscopy (TG-FTIR) analysis of thermal decomposition products reveals that the main decomposition gas products are H₂O, N₂O, CO₂, and NO₂. Based on the new crystalline densities, the detonation velocity and pressure predicted by EXPLO5 are 9062 m s^?1 and 36.4 GPa, respectively.     

Antimicrobial efficacy of cinnamon oil against Salmonella in almond based matrices

Reduced moisture enhances resistance of Salmonella and subsequently reduces the antimicrobial efficacy of thermal treatment. Alternative and supplementary non-thermal intervention methods are urgently needed. In this study, Cinnamonum cassia oil was tested for its antimicrobial effect against outbreak strains Salmonella Enteritidis PT30 and S. Tennessee K4643. Minimal inhibitory concentration and minimal bactericidal concentration for both strains were 0.05% (v/v) and 0.1% (v/v), respectively. Death curves showed that including 0.1% and 0.15% (v/v) C. cassia oil resulted in ∼7 Log reduction of bacteria within 2 h and 1 h, respectively. However, the antimicrobial efficacy of C. cassia oil was reduced when S. Enteritidis PT30 existed in low moisture condition. When S. Enteritidis PT30 was established on almonds/paper discs, 0.4% C. cassia oil resulted in ∼1.7 Log₁₀ CFU/almond or 3.2 Log₁₀ CFU/disc reduction within 2 h at room temperature, respectively. S. Enteritidis PT30 established on both almonds and paper discs were very stable, there was only a 0.80 Log₁₀ CFU/almond and 1.20 Log₁₀ CFU/disc reduction during 9-week and 7-week storage at room temperature, respectively. C. cassia oil intervention increased S. Enteritidis PT30 reduction on both almonds and paper discs during storage with more reduction on paper discs. 0.4% C. cassia oil treatment reduced S. Enteritidis PT30 on paper disc to undetectable level within 4 weeks, but only led to 2 Log₁₀ CFU reduction on almonds, indicating a protection effect from the almond matrix or almond surface components. Additionally, S. Enteritidis PT30 established on paper disc coated with almond surface components exhibited higher resistance to desiccation and C. cassia oil treatment, further demonstrating the protection role of food matrix. In conclusion, C. cassia oil is effective against S. Enteritidis PT30 and S. Tennessee K4643, but its antimicrobial efficacy against the tested Salmonella was compromised by low moisture environment and food matrix.     

Effect of Aspergillus carbonarius amounts on winemaking and ochratoxin A contamination

Aspergillus carbonarius is the major ochratoxin A (OTA)-producing fungus that contaminates wine grapes. To investigate the effect of the initial amount of A. carbonarius on winemaking and ochratoxin A contamination, different conidial concentrations of A. carbonarius were manually added to the grape musts before fermentation. Sampling was carried out at different stages in alcoholic fermentation, including crushing, maceration, pressing and alcoholic fermentation. The levels of alcohols, soluble solids, and reducing sugars in the musts were analyzed before and during the whole procedure of alcoholic fermentation. Aspergillus spp. and other fungal contaminants increased rapidly after crushing, however most died at 48 h. OTA levels in the musts increased during the first 8–48 h and then decreased sharply in A. carbonarius inoculants (1 × 10⁴ to 1 × 10⁶ spores/g) in a spore concentration-dependent manner. Most OTA was retained in the pomaces fraction after the pressing operation. High amounts of A. carbonarius did not significantly affect yeast growth, sugar use, and alcoholic production during fermentation. In conclusion, high levels of contamination with A. carbonarius in the grape musts did not inhibit alcoholic fermentation, but caused high OTA residues in the wine produced.     

Tenacity of Bacillus cereus and Staphylococcus aureus in dried spices and herbs

Numerous studies examined the antimicrobial effects of spice and herb extracts, whereas little is known about the effects of dry condiments on the survival of microorganisms. This study investigated the impact of dried condiments on the survival of Bacillus cereus and B. thuringiensis spores as well as Staphylococcus aureus cells. In addition, the survival variability between different strains was evaluated. Condiments (allspice, basil, cinnamon, nutmeg, oregano, paprika, parsley and pepper) were artificially contaminated by a dry spiking method using sand as carrier matrix and as control. The results show that counts of B. cereus and B. thuringiensis spores (initial spore count 5.6 ± 0.2 log₁₀ cfu/g and 6.7 ± 0.1 log₁₀ cfu/g, respectively) did not decline significantly in all condiments over a period of 50 weeks. In contrast, in some of the spiked test materials, cell counts of S. aureus (initial cell count 8.1 ± 0.5 log₁₀ cfu/g) were reduced below the detection limit of 10 cfu/g within 10 weeks of storage. D values for S. aureus ranged between 5 and 31 days depending on the strain, condiment and initial contamination level. In conclusion, dried condiments may not affect the survival of spores but can significantly affect the survival of non-spore forming bacteria. As strain variability can occur, tenacity studies should be conducted including a variety of strains.     

Salmonella enterica serovar Choleraesuis on fresh-cut cucumber slices after reduction treatments

Cucumber is a popular fruit around the world and has been implicated in Salmonella food poisonings. S. Choleraesuis is a serovar that can cause pig and human infections but was rarely examined in food safety context. To investigate S. Choleraesuis behavior on cucumber slices, it was inoculated, at 10⁴ colony forming units (CFU)/mL, onto fresh-cut cucumber slices and subjected to reduction with either high hydrostatic pressurization (HHP), hydrogen peroxide (H₂O₂), or Peredibacter sp. BD2GS treatment, its reduction and survival during 48 h storage at 4 °C and 25 °C were compared.Reduction tests revealed that 5% H₂O₂ was most effective in killing S. Choleraesuis, with 97.5% reduction after 15 min action, compared to 90.7%, 87.7%, 29.2% and 60.2% reduction rates with HHP, 2.5% H₂O₂, high- and low-dose BD2GS treatments, respectively.At the end of storage, contrast to no changes at 4 °C, S. Choleraesuis counts rose significantly (p < 0.05) at 25 °C. Compared to control that reached 7.1 ± 0.1 log CFU/g, HHP, 5% and 2.5% H₂O₂ attained 6.3 ± 0.1, 6.7 ± 0.1 and 6.4 ± 0.2 log CFU/g correspondingly, whereas high- and low-dose BD2GS attained 4.9 ± 0.1 and 5.9 ± 0.1 log CFU/g respectively. A shared growth peak of between 9 h and 12 h was noted in all treatments except high-dose BD2GS where it occurred in the first 3 h. Results of this study revealed the effectiveness of 5% H₂O₂ in the reduction of S. Choleraesuis, and demonstrated that if not stored properly, contaminated cucumber slices, though treated, can still have potentials to cause S. Choleraesuis outbreaks.     

Saturated hydrocarbons of Ulyanovsk oblast crude oils and waxes isolated from these oils

The composition and distribution of saturated hydrocarbons (alkanes, steranes, and terpanes) of oils from the Ulyanovsk oblast of the Volga-Urals oil-and-gas basin were studied. Wax fractions were isolated from crude oils, and C₄₈-C₅₂ high-molecular-mass n-alkanes, C₃₅-C₅₂ alkylcyclopentanes, and C₂₄-C₄₂ 2- and 3-monomethylalkanes were identified in these fractions. Based on the data on the composition of C₁₀-C₃₆ n-alkanes, C₁₉-C₃₅ terpanes, C₂₁-C₃₀ steranes, and C₄₀₊ alkanes, it was shown that the oils in question were generated by marine organic matter in carbonate sediments. Oil from the Novolabitovskoe field (1981–1992 m) substantially differs for the other oils in terpane and sterane compositions. These differences are supposedly due to another source of organic matter.     

负载型氮化物催化剂的性质及加氢精制性能

 采用N₂/H₂程序升温还原法制备了非负载型氮化钼(Mo₂N)和氮化镍钼(Ni₂Mo₃N)催化剂，并以Al₂O₃为载体制备了负载型氮化钼(Mo₂N/Al₂O₃)和氮化镍钼(Ni₂Mo₃N/Al₂O₃)催化剂。采用XRD、BET、H₂-TPR和NH₃-TPD等方法对制备的氮化物催化剂的性质进行了研究，并分别以含2%（质量分数，下同）噻吩和10%四氢萘的环己烷溶液为含硫、含芳烃的柴油模型化合物，考察了制备的负载型氮化物的加氢脱硫（HDS）及加氢脱芳烃（HAD）性能。结果表明，以金属氧化物为前驱物，采用N₂/H₂程序升温还原法制得的氮化钼为Mo₂N(γ型)、氮化镍钼为Ni₂Mo₃N；经钝化处理后，氮化物表面形成了金属氧化物保护层，其中Mo₂N/Al₂O₃和Ni₂Mo₃N/Al₂O₃表面氧化层的还原温度分别为350和300℃。Mo₂N/Al₂O₃和Ni₂Mo₃N/Al₂O₃催化剂的表面酸性以弱酸为主；二者均表现出较好的HDS性能，但Mo₂N/Al₂O₃的HDA性能很差，而Ni₂Mo₃N/Al₂O₃的HDA性能较Mo₂N/Al₂O₃有一定程度的提高，说明镍钼共存有利于提高金属组分的分散性及催化剂的加氢饱和性能。     

Inactivation behaviors of foodborne microorganisms in multi-frequency power ultrasound-treated orange juice

This study established the inactivation kinetic parameters of some pathogenic bacteria including Escherichia coli O157:H7, Salmonella enterica serotypes, and Listeria monocytogenes; and spoilage yeasts namely, Debaryomyces hansenii, Clavispora lusitaniae, Torulaspora delbrueckii, Pichia fermentans, and Saccharomyces cerevisiae in orange juice subjected to multi-frequency Dynashock power ultrasound treatment. All test organisms exhibited a biphasic inactivation behavior with a sigmoidal inactivation curve consisted of an initial inactivation lag, followed by logarithmic linear inactivation. Injury accumulation in the inactivation lag phase was established in acid-adapted bacteria. The time necessary to reduce initial inoculated populations by 5 log cycles (99.999%), T_5D values, significantly increased with acid adaptation. The T_5D of E. coli, S. enterica, and L. monocytogenes increased from 37.64, 36.87, and 34.59 respectively; to 54.72, 40.38, and 37.83 min respectively after acid exposure. Temperature increase due to sensible heat propagation during ultrasound treatment decreased the resistance of the test bacteria. The cocktail of E. coli O157:H7 had significantly greater resistance towards ultrasound treatment (T_5D = 54.72 min) than any of the individual strain (T_5D = 41.48–47.48 min) in the mix. Similar results were found in the composited (T_5D = 60.02 min) and individual species (T_5D = 20.31–59.04 min). The results established in this work provide baseline information on microbial behavior in multi-frequency ultrasound-treated orange juice for establishment of pasteurization process schedules.     

Correlation of viscoelastic behavior with water state and ultrastructure in hot air-dried carrots

This study evaluated and correlated the viscoelastic behavior, water state and ultrastructure of hot air-dried carrots. The results revealed that with increasing time, hot air-drying increased loss tangent (Tan δ) and reduced storage (G′) and loss (G″) moduli, cell wall components including total pectin (Tp), hemicellulose (He), and cellulose (Ce), free water (reflected by relaxation time T₂₃ and relative area M₂₃) in vacuoles, and immobilized water (T₂₂ and M₂₂) in cytoplasm and extracellular space in carrots. Pearson's correlation analysis showed that G′ and G″ were positively correlated (p < 0.01) with T₂₂, T₂₃, M₂₃, Tp, He, and Ce in dried carrots, whereas Tan δ was negatively with these indicators (p < 0.01). Principal component regression analysis revealed that the contribution rate of principal factor 1 and 2 (F1 and F2) was 72.7 and 21.9%, respectively. The Tp, He, Ce, T₂₃, and M₂₃ (42.3, 42.7, 42.5, 43.8 and 44.2% of the explained variance, respectively) were well explained by F1. The G′, G″, and Tan δ could be predicted by the following regression equation, G′ = 0.696 × F1, G″ = 0.680 × F1, and Tan δ = 0.341 − 0.652 × F1. These relationships were consistent with the more pronounced changes (plasmolysis of cytoplasm, disruption of plasmalemma and tonoplast, and degradation of cell walls and middle lamella) in the ultrastructure of dried carrots.     

Thermal death of bacterial pathogens in linguiça smoking

Linguiça, a smoked sausage originally from Portugal, is often made in small quantities in California, without inspection. Campylobacter jejuni, Escherichia coli O157:H7, Listeria monocytogenes, Salmonella enterica serotype Newport, and Yersinia enterocolitica were added individually to batter representing California linguiça. Batter (≤1 mm thick), heated at 50, 55, and 60 °C, showed decimal reduction times ranging from >10 min for most trials at 50 °C to <2 min at 60 °C. Pork casings, stuffed with the batters to a diameter ≤3 cm, length 10 cm, and weight 75–80 g, were hot smoked; sausage centers were at ≥60 °C for ≥90 min. Contaminant levels in the batters (three experiments/pathogen) ranged from 2.3 × 10⁶ to 3.0 × 10¹⁰ CFU/g in various runs; reductions were ≥5 log₁₀ in all cases. These experiments indicate a reasonable margin of safety for products processed in this way.     

The Preparation of Wax Emulsions Stabilized by C5 Petroleum Resin

Wax emulsions were prepared by using paraffin wax and oxidized wax as raw materials, compound Wb-L as emulsifier, and C₅ petroleum resin as stabilizer. Its performance was studied. The results showed that when M _{C5 petroleum resin r}/M _{wax and oxidized wax} = 0.20, M _emulsifier/M _{wax and oxidized wax} = 0.50, M _water/M _{wax and oxidized wax} = 2.50, emulsifying time was 30 min, emulsifying temperature was 90–95°C, and stirring speed was 1,100 r/min, wax emulsions with good stability, dispersibility, and monodisperse particle size were obtained, giving a preservative solution in pencil board production.