Effects of Zataria multiflora Boiss. essential oil and nisin on Bacillus cereus ATCC 11778

The effects of different concentrations of Zataria multiflora Boiss. essential oil (EO, 0.0%, 0.005%, 0.015%, 0.03% and 0.045%) and nisin (N, 0.0, 0.25, 0.5, 1.5 and 2.5 μg ml⁻¹), pH values (7.4, 6.5 and 6.0), temperatures (Ts, 10, 20 and 30 °C) and storage times (Ds, up to 43 days) on log₁₀ probability percentage of growth initiation (log P%) of one vegetative cell of Bacillus cereus in brain heart infusion broth were evaluated in a factorial design study. The log P% of the organism was significantly affected (P < 0.01) by the values of EO, N, pH, T and D.The combinations of T ⩾ 20 °C, EO ⩽ 0.03% and pH values (7.4, 6.5 and 6.0) could not obviously affect the growth of the organism in this study. Whereas, the strong inhibitory action was observed by increasing EO concentration to 0.045 at T ⩾ 20 °C and selected pH values (7.4, 6.5 and 6.0) and by decreasing temperature to 10 °C at EO ⩾ 0.015% and pH values used in this study. The inhibitory effect of N also was enhanced by decreasing storage temperature to 10 °C at the selected pH values (7.4, 6.5 and 6.0) in this study.The growth of the organisms was strongly affected by increasing EO concentration to 0.03% in combination with N concentrations used at the selected temperatures in this study. The growth of the organism was completely inhibited at combinations EO ⩾ 0.015%, N ⩾ 1.5 μg ml⁻¹, T ⩽ 30 °C and pH ⩽ 7.4 during 43 days of storage in this study. This synergistic effect of EO and N was enhanced in lower pH values (6.5 and 6.0) in the present study. The growth of organism was completely inhibited at combinations of EO ⩾ 0.005 and N ⩾ 1.5 μg ml⁻¹ at pH = 6.0, and EO ⩾ 0.03 and N ⩾ 0.5 μg ml⁻¹ at pH ⩽ 6.5 during the study at the selected Ts (30, 20 and 10 °C).     

Antimicrobial resistance of Salmonella spp. and Escherichia coli isolated from table eggs

The antimicrobial sensitivity of Salmonella spp. and Escherichia coli isolated from the shells and contents of table eggs sampled from sale outlets in Trinidad was determined using the disc diffusion method. The phage types of S. Enteritidis isolates, the phenotypic characteristics of E. coli isolates and the presence of O157 strain were also investigated. Of a total of 74 isolates of Salmonella tested, 17 (22.9%) exhibited resistance to one or more of the seven antimicrobial agents used compared with 104 (88.1%) of 118 E. coli isolates. The difference was statistically significant (P < 0.05; X²). For both microorganisms, resistance was relatively high to streptomycin (54.2%) and tetracycline (35.9%) but low to gentamicin (11.5%) and sulphamethoxazole/trimethoprim (9.4%). Only 1 (1.4%) isolate of Salmonella was multi-resistant while 55 (46.6%) of E. coli isolates were resistant to three or more antimicrobial agents. The frequency of resistance to antimicrobial agents amongst both bacteria was not significantly (P > 0.05; X²) affected by the location of isolation on the egg (shell or content) or source of eggs (farms, shopping malls or other retailers). Eight (19.5%) of 41 S. Enteritidis isolates tested were resistant compared to 4 (26.7%) of 15 isolates of S. Ohio. All S. Enteritidis isolates belonged to phage type 1 (PT1) and all E. coli isolates were non-haemolytic, non-mucoid, sorbitol fermenters and non-O157 strains. It was concluded that the relatively high resistance amongst the bacteria tested could pose therapeutic problems in consumers, particularly in egg-borne salmonellosis or colibacillosis.     

Discovery of a novel antimicrobial peptide using membrane binding-based approach

Most known antimicrobial peptides (AMPs) can bind to bacterial cells as the first step to exert their antimicrobial activity. Based on this membrane-binding activity, a novel antimicrobial peptide MDpep9 with the sequence Lys-Ser-Ser-Ser-Pro-Pro-Met-Asn-His was purified from housefly larvae. MDpep9 effectively inhibited the growth of the test bacteria (Escherichia coli, Salmonella typhimurium, Staphylococcus aureus, Shigella dysenteria, Pseudomonas aeruginosa, Bacillus subtilis, and Streptococcus pneumoniae), with MIC (minimal inhibitory concentration) values ranged from 9 to 72 μg/ml. Among these bacteria, the Gram-positive bacterium, B. subtilis 9372 was the most sensitive. Furthermore, the antimicrobial mode study showed that cytoplasmic cell membrane is the target for MDpep9 which can exert its antimicrobial action by disrupting and disintegrating bacterial cell membranes, leading ultimately to loss of cytoplasmic membrane integrity. Moreover, the acidic environment around bacterial cell membrane induced molecular unfolding and increased surface hydrophobicity of MDpep9, promoting the interaction of peptide with bacterial lipid membrane. Our results indicate membrane-binding strategy opens the road to simple and cheap large-scale production of a safe antimicrobial peptide from housefly.     

Comparative efficacies of various chemical sanitizers for warewashing operations in restaurants

This study compared the efficacies of two traditional with two experimental sanitizers for use in tableware cleaning operations in restaurants and foodservice operations. This was done by investigating the maximum number of cleaning cycles that a single recommended quantity of each sanitizer could treat and still produce a 5-log bacterial reduction on test tableware items. Cream cheese and whole milk were inoculated with Escherichia coli K12 and Listeria innocua and subsequently used for contamination of the tableware items. These items were washed with automatic (49 °C) and manual (43 °C) dishwashers then treated with electrolyzed-oxidizing water (EO), quaternary ammonium compound, sodium hypochlorite and an acidic sanitizer. For the lowest efficacies, after six and eight manual washing cycles in the same solution, ≥5 log reductions were achieved on both E. coli K12 contaminated trays and plates, respectively, exposed to the chlorine and quaternary ammonium sanitizers. For automatic washing with chlorine sanitizer, the minimum wash cycles for the bacteria were seven and nine for the trays and plates, respectively. For drinking glasses contaminated with bacteria, 14 and 17 washing cycles produced ≥5 log reductions for manual and automatic washings, respectively.     

Inhibitory effects of selected plant essential oils on the growth of four pathogenic bacteria: E. coli O157:H7, Salmonella Typhimurium,Staphylococcus aureus and Listeria monocytogenes

Twenty eight essential oils were evaluated for their antibacterial properties, against four pathogenic bacteria (Escherichia coli O157:H7, Listeria monocytogenes 2812 1/2a, Salmonella Typhimurium SL 1344 and Staphylococcus aureus). Essential oils were introduced into Brain Heart Infusion agar (BHI) (15 ml) at a concentration of 0.003%, 0.006%, 0.013%, 0.025%, 0.05%, 0.1%, 0.2%, 0.4% and 0.8% (vol/vol) to determine the minimum inhibitory concentration (MIC) and the maximal tolerated concentration (MTC) for each pathogen evaluated. Results showed that the most active essential oils against bacteria tested were Corydothymus capitatus, Cinnamomum cassia, Origanum heracleoticum, Satureja montana, and Cinnamomum verum (bark). These showed a MIC ⩽ 0.05% (vol/vol) for all bacteria tested. For the MTC, with the exception of S. Typhimurium and L. monocytogenes where a MTC of 0.025% (vol/vol) was observed in presence of Cinnamomum verum and Cinnamomum cassia, respectively, a MTC ⩽ 0.013% (vol/vol) was observed for all other bacteria and the three other most active essential oils. Three oils (Satureja hortensis, Thymus vulgaris carvacroliferum, Origanum compactum) showed a MIC ⩽ 0.1% (vol/vol) for all bacteria tested. Seven oils (Thymus vulgaris thymoliferum, Thymus serpyllum, Thymus satureioides, Cymbopogon martinii, Pimenta dioica, Cinnamomum verum (leaf), Eugenia caryophyllus) showed a lower antimicrobial activity showing a MIC ⩽ 0.4% (vol/vol) against the four bacteria tested. Finally, 13 essential oils were less active showing a MIC value ⩾ 0.8% (vol/vol) against at least one bacterium.     

Application of slightly acidic electrolyzed water as a potential non-thermal food sanitizer for decontamination of fresh ready-to-eat vegetables and sprouts

The sanitization efficacy of slightly acidic electrolyzed water (SAEW) against food pathogens on selected fresh ready-to-eat (RTE) vegetables and sprouts was evaluated and compared to sodium hypochlorite (NaOCl) solution. RTE vegetables and sprouts were dip-inoculated with Escherichia coli (E. coli) and Salmonella spp. and dip-treated with SAEW, NaOCl solution for 5 min. SAEW treatment significantly (p < 0.05) reduced the total aerobic mesophilic bacteria from Chinese celery, lettuce and daikon sprouts by 2.7, 2.5 and 2.45 log₁₀CFU/g, respectively relative to un-treated. Pathogens were significantly (p < 0.05) reduced from Chinese celery, lettuce and daikon sprouts by 2.7, 2.8 and 2.8 log₁₀CFU/g (E. coli) and 2.87, 2.91 and 2.91 log₁₀CFU/g (Salmonella spp.), respectively following a SAEW treatment. SAEW and NaOCl solution showed no significant sanitization difference (p > 0.05). Results demonstrate that SAEW at low chlorine concentration and a near neutral pH is a potential non-thermal food sanitizer that could represent an alternative to NaOCl solution and would reduce the amount of free chlorine used in fresh-cut vegetables industry, since the same microbial reduction as NaOCl solution is obtained.     

Antibacterial activity and mechanism of cinnamon essential oil against Escherichia coli and Staphylococcus aureus

Cinnamon essential oil (EO) exhibited effective antibacterial activity against foodborne spoilage and pathogenic bacteria in model systems using Escherichia coli and Staphylococcus. The minimum inhibition concentration (MIC) of cinnamon EO was similar for both bacteria (1.0 mg/ml) while the minimum bactericide concentration (MBC) were 4.0 mg/ml and 2.0 mg/ml for E. coli and Staphylococcus aureus. GC–MS analysis confirmed that cinnamaldehyde was the major constituent in cinnamon EO (92.40%). Much effort was focused on elucidating the mechanism of antibacterial action of cinnamon EO against E. coli and S. aureus by observing the changes of cell microstructure using scanning electron microscope, determination of cell permeability, membrane integrity and membrane potential. After adding cinnamon EO at MIC level, there were obvious changes in the morphology of bacteria cells indicating cell damage. When cinnamon EO were added at MBC levels, the cells were destroyed. Cinnamon EO led to leakage of small electrolytes, causing rapid increase in the electric conductivity of samples at the first few hours. The values for E. coli and S. aureus reached 60% and 79.4% respectively at 7 h. Moreover, the concentration of proteins and nucleic acids in cell suspension also rose with increased cinnamon EO. Bacterial metabolic activity was decreased 3–5 folds as reflected by the results of membrane potential. Overall, S. aureus was more susceptible to cinnamon EO than E. coli.     

Pre-processed bovine milk quality in Trinidad: Prevalence and characteristics of bacterial pathogens and occurrence of antimicrobial residues in milk from collection centres

The study was conducted to assess the impact of the changes in the milk collection system in Trinidad (from twice daily collection to once, introduction of chilling facilities to the collection centres and transportation of milk to the processing plant in insulated truck instead of in metal churns at ambient temperature) on the microbial load and antimicrobial residue quality of the milk as well as the temperature and pH of milk, using standard methods. The presence of antimicrobial residues was detected using the Delvo test kit. Of a total of 266 milk samples from churns, the mean ± sd temperature and log₁₀ ± sd TAPC per ml was 20.36 ± 7.91 °C and 6.3 ± 1.09 respectively. For 20 milk samples from the chillers, the mean temperature and log₁₀ ± sd TAPC per ml was 15.10 ± 2.73 °C and 7.04 ± 0.33 respectively compared with corresponding values for 36 samples collected from the truck, 11.64 ± 4.22 °C and 7.11 ± 0.62 respectively (P < 0.05; X²). The mean TAPC, staphylococcal and E. coli counts per ml of milk from churns were significantly (P < 0.05; X²) higher for milk at low temperature (0–20 °C) compared with milk at high temperature (>30 °C). Eight (4.2%) of 192 milk samples tested contained antimicrobial residues. Of 168 S. aureus isolates tested, 24 (14.3%) were enterotoxigenic while 53 (45.3%) of 117 isolates tested exhibited resistance to various antimicrobial agents while of 386 isolates of E. coli tested, 3 (0.8%) were O157 strain and 129 (64.5%) of 200 isolates exhibited resistance to antimicrobial agents. It was concluded that despite the changes, the microbial load of milk was still high suggesting poor sanitary practices at the farm level. The detection of antimicrobial residues agents coupled with toxigenic S. aureus and E. coli isolates could pose health hazards to consumers.     

Sanitization potency of slightly acidic electrolyzed water against pure cultures of Escherichia coli and Staphylococcus aureus,in comparison with that of other food sanitizers

The sanitization potency of slightly acidic electrolyzed water (SAEW) on pure cultures of Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) was evaluated. The potency was compared with that of strong acidic electrolyzed water (StAEW) and sodium hypochlorite (NaOCl) solution. SAEW (ca. pH 5.8 and 21 mg/l available chlorine concentration; ACC) resulted into >5 log₁₀CFU/ml reduction of E. coli and S. aureus after 90 s of exposure. The relative bacterial reduction potency at each exposure time was in the order StAEW > NaOCl > SAEW and increased with exposure time, with relative effect being 90 s > 60 s > 30 s. The results indicate that SAEW with low ACC and near neutral pH can potentially sanitize E. coli and S. aureus within a short period of exposure presenting a potential replacement to NaOCl solution commonly used in the food industry.     

Studies on antibacterial activity and antibacterial mechanism of a novel polysaccharide from Streptomyces virginia H03

A novel polysaccharide isolated from the broth of Streptomyces virginia H03 exhibited strong antibacterial activities on food spoilage and food poisoning microorganisms such as Staphylococcus aureus, Bacillus subtilis, Listeria monocytogenes, Escherichia coli, Zygosaccharomyces bailii and Candida utilis. The minimal inhibitory concentrations of the polysaccharide determined by the double broth dilution method were 15.6, 31.3, 31.3, 31.3, 125 and 125 (μg/ml) against the microorganisms mentioned above, respectively. The possible targets of the polysaccharide in bacteria might be cell wall, cytoplasmic membrane and DNA as indicated by electron microscopy, leakage of protein, cytoplasmic membrane permeability and DNA binding, respectively. Moreover, the antibacterial activity remained unchanged after being treated at 100 °C for 10 min, which indicated that the polysaccharide had a good heat-stability. In addition, it was safe according to mouse toxicity. All of these suggested that the polysaccharide might be used as a potential antimicrobial in food.     

Antimicrobial activity of malic acid against Listeria monocytogenes,Salmonella Enteritidis and Escherichia coli O157:H7 in apple,pear and melon juices

Minimal inhibitory (MIC) and minimal bactericidal (MBC) concentrations of malic acid against Listeria monocytogenes, Salmonella Enteritidis and Escherichia coli O157:H7 inoculated in apple, pear and melon juices stored at 5, 20 and 35 °C were evaluated. MICs and MBCs against L. monocytogenes, S. Enteritidis and E. coli O157:H7 were significantly affected by storage temperature, juice characteristics and type of microorganism. Malic acid was more effective at 35 and 20 °C than at 5 °C in all studied fruit juices. E. coli O157:H7 was more resistant to malic acid than S. Enteritidis and L. monocytogenes. Apple, pear and melon juices without malic acid were inhibitory to E. coli O157:H7, S. Enteritidis and L. monocytogenes at 5 °C, whereas, MBCs of 1.5% (v/v) of malic acid in apple and pear juices, and 2% (v/v) in melon juice at 5 °C were needed to reduce E. coli O157:H7, those concentrations being higher than those required to reduce S. Enteritidis and L. monocytogenes in those fruit juices. In addition, concentrations of 2%, 2.5% and 2.5% (v/v) of malic acid added to apple, pear and melon juices, respectively, were required to inactivate the three pathogens by more than 5 log cycles after 24 h of storage at 5 °C. Transmission electron microscopy showed that malic acid produced damage in the cell cytoplasm of pathogens without apparent changes in the cell membrane.     

Effect of combined ozone and organic acid treatment for control of Escherichia coli O157:H7 and Listeria monocytogenes on enoki mushroom

This study evaluated the effects of ozonated water (1, 3, and 5 ppm) alone with different exposure times (0.5, 1, 3, or 5 min), and combinations of 3 ppm ozone with 1% organic acids (acetic, citric, or lactic acids) during 5-min exposure for control of Escherichia coli O157:H7 and Listeria monocytogenes on enoki mushroom and to observe the regrowth of these pathogenic bacteria on treated enoki mushroom during storage for 10 days at 15 °C. Results showed that ozone treatment gave less than 1.0- and 0.5-log count reductions on E. coli O157:H7 and L. monocytogenes, respectively. Efficacy was improved with combined 3 ppm ozone and 1% citric acid treatment, resulting in 2.26- and 1.32-log count reductions, respectively. During storage at 15 °C (10 days) after combined treatment and packaging, populations of E. coli O157:H7 and L. monocytogenes increased to more than 8.0 log cfu/g, indicating that the combined treatment did not have a residual antimicrobial effect during storage. Although the storage study did not show control of these pathogens, the combined ozone–organic acid treatment was more effective than individual treatments in reducing initial population levels of these pathogens on enoki mushroom.     

Screening of Turkish endemic Teucrium montbretii subsp. pamphylicum extracts for antioxidant and antibacterial activities

The antioxidant and antimicrobial activities of Teucrium montbretii Bentham subsp. pamphylicum P.H. Davis (Lamiaceae) methanolic extracts were investigated. Total contents of phenolic compounds, flavonols and flavanols were determined by Folin–Ciocalteu colorimetric, Neu’s reagent solution and vanillin colorimetric methods, respectively. Total phenolics were 99.4 mg gallic acid equivalents (GAE)/g. Total flavanols and flavonols were 43.8 mg catechin equivalents (CE)/g and 0.5 mg rutin equivalents (RE)/g, respectively. At 100 ppm, the free radical scavenging activity was 58.6%. Antioxidant activity measured by the phosphomolybdenum method was 191.5 mg/g. Antibacterial activity was assessed (1%, 2.5%, 5%, 7.5% and 10% w/v) by the agar diffusion method against 10 species. Concentrations of 1% and 2.5% were not effective against any of the bacteria. The most resistant bacterium was Salmonella typhi while Listeria monocytogenes showed the highest sensitivity.     

Partial characterization of a class IIa pediocin produced by Pediococcus parvulus 133 strain isolated from meat (Mexican “chorizo”)

Pediocin-like bacteriocins are antimicrobial substances produced by some bacteria with high antilisterial activity. Several isolates of Pediococcus acidilactici and two Pediococcus parvulus strains of vegetable origin have been reported to produce this kind of peptide. This work presents the partial characterization of the bacteriocin produced by P. parvulus 133 found in meat and confirms its identity as a heat resistant, antilisterial bacteriocin. This peptide has a relatively narrow inhibitory spectrum but a high antilisterial activity. Pediocin remained active after heating to 121 °C, but its thermoresistance varied with pH. The pH selective adsorption method resulted in a 150-fold concentration of antimicrobial activity. The final extract was obtained by ultrafiltration and resulted in an additional 10-fold concentration of activity. Molecular weight was estimated as 5 kDa and isoelectric point was 8.65. The sequence of the first 17 aminoacids at the N-terminal end of the bacteriocin showed complete coincidence with that previously reported for pediocin A1 (AcH) and with an antilisterial peptide produced by Bacillus coagulans. High sequence similarity was also found with two other antilisterial bacteriocins.     

Detection and characterization of Leucocin OZ,a new anti-listerial bacteriocin produced by Leuconostoc carnosum with a broad spectrum of activity

Leucocin OZ is a novel, anti-listerial, and plasmid-encoded small bacteriocin produced by Leuconostoc carnosum OZ, a lactic acid bacterium isolated from vacuum-packaged sucuk. The bacterium was found to be associated with the spoilage of this product. Leucocin OZ is sensitive to proteolytic enzymes, resistant to heat up to 121 °C for 15 min, and active over a wide range of pH (2–12). Leucocin OZ activity against L. plantarum cells was bactericidal in nature since exposure of cell suspensions of L. plantarum to leucocin produced cell viability loss, as determined from the reduction in cfu after treatment. SDS gel stained with Coomassie Brilliant Blue showed several polypeptide bands. Among these bands, the band responsible for antimicrobial activity shown against a wide range of Gram-positive bacteria many of which are associated with food spoilage and food borne diseases including Listeria monocytogenes was shown tentatively linked to 3.5 kDa protein, as understood from the formation of inhibition zone on a lawn of Lactobacillus plantarum NCDO955 corresponding to this band. Proteins in other bands exhibited no antimicrobial activity. Since Leuconostoc carnosum OZ-D2 is associated with spoilage, it cannot be used for in situ bacteriocin production. However, the antimicrobial peptide it produces can be alternatively used as biopreservative in foods to control the growth of spoilage bacteria and food borne pathogens such as L. monocytogenes.     

In vitro antibacterial activity of Australian native herb extracts against food-related bacteria

The antibacterial activities of water, ethanol and hexane extracts of five Australian herbs (Backhousia citriodora, Anetholea anisata, Eucalyptus staigerana, Eu. olida and Prostanthera incisa) against seven food-related bacteria (Enterococcus faecalis, Escherichia coli, Listeria monocytogenes, Pseudomonas aeruginosa, Salmonella Enteritidis, Sal. Typhimurium and Staphylococcus aureus) were determined by the microtitre broth microdilution assay. The water extracts of all the herbs displayed no or low antimicrobial activity against all of the bacteria tested with the exception of S. aureus. Relatively high levels of activity (minimum inhibitory concentrations of 125–15.6 μg ml⁻¹) against this pathogen were present in water extracts from all herbs except P. incisa. The ethanol and hexane extracts of all herbs displayed some activity against a number of the bacteria tested, with no one particular herb displaying an obviously higher level or range of activity. Staphylococcus aureus proved to be the most sensitive of the bacteria tested against the solvent extracts with all extracts displaying activity ranging from 125 to 7.8 μg ml⁻¹, while E. coli and L. monocytogenes, on the other hand, proved the least sensitive with only five of 15 herb/extract combinations displaying any activity against these pathogens. The extracts of the Australian native herbs examined in this study have potential for application in foods to increase shelf-life or promote safety.     

A Turkey survey of hygiene indicator bacteria and Yersinia enterocolitica in raw milk and cheese samples

In this research, a total of 200 dairy (raw milk, cheese) samples obtained from Ankara, were examined for the presence of Yersinia spp., total coliform and Escherichia coli. As expected, raw milk 55% (55/100) were significantly contaminated with Yersinia spp., than cheese samples 14% (14/100). Y. enterocolitica was the most commonly isolated species, and was recovered from 47.3% in raw milk 35.7% in cheese samples. The other Yersinia spp. were identified as Y. frederiksenii (31.0%, 21.4%), Y. kristensenii (12.7%), Y. intermedia (7.2%, 7.1%) and atypical Yersinia spp. (1.8%, 35.7%) in raw milk and cheese samples, respectively. All the samples of cheese examined were negative for Y. kristensenii. All Y. enterocolitica strains tested gave negative results in the autoagglutination tests and crystal violet binding test.Furthermore total coliform bacteria and E. coli were investigated in these samples. According to the analysis results, most of the samples containing Yersinia spp.were found high number of viable count cell total coliform than E. coli. Total coliform bacteria and E. coli, were detected (3.0 × 10⁴ cfu/ml and 1.5 × 10⁴ cfu/ml) in four milk samples containing Y. enterocolitica while, they were detected (2.5 × 10⁴ cfu/ml and 1.0 × 10⁴ cfu/ml) in eight milk samples containing Y. enterocolitica. In the present study, total coliform bacteria and E. coli were detected >1.1 × 10⁵ cfu/g in six cheese samples containing Y. enterocolitica and atypical Yersinia spp. The results indicate that Yersinia spp. is more likely to be isolated from foods with a high level of coliforms than from foods with low coliform counts.     

Inhibition of foodborne pathogens by Hf-1, a novel antibacterial peptide from the larvae of the housefly (Musca domestica) in medium and orange juice

Antibacterial molecules from edible insects may serve as a potentially significant group of food preservatives. Hf-1, a novel peptide from larvae of housefly (Musca domestica) with molecular weight approximately 8.0 KD, inhibited food pathogens Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27553, Salmonella typhimurium 50013, Shigella dysenteriae 51302, Staphylococcus aureus 6538 and Bacillus subtilis 9372 with MIC ranging from 18 to 72 μg/ml. The presence of EDTA can enhance Hf-1 activity against Gram-negative bacteria. Hf-1 was bactericidal in orange juice, showing an antibacterial activity approximately equivalent to sodium benzoate. The mode of action of Hf-1 involved decreasing the cell surface hydrophobicity and damaging the cell membrane. The results suggested Hf-1 has the potential to be used as the food preservative.     

Antibacterial mechanism of bifidocin A,a novel broad-spectrum bacteriocin produced by Bifidobacterium animalis BB04

Bifidocin A, a novel broad-spectrum bacteriocin produced by Bifidobacterium animalis BB04, was isolated from the feces of a healthy centenarian. To understand the mechanism of the antibacterial action of bifidocin A against gram-negative bacteria, its effects at a minimum inhibitory concentration on cell morphology, intracellular organization, membrane permeability, membrane integrity, and membrane proton motive force (PMF) of Escherichia coli 1.90 were investigated. Scanning and transmission electron microscopy analyses showed that bifidocin A induced alterations in the morphology and intracellular organization of E. coli cells. The intracellular organization was more susceptible to changes induced by bifidocin A than the morphology. Bifidocin A treatment caused the leakage of K⁺ and inorganic phosphate, the release of ATP and UV-absorbing materials, and a collapse of the transmembrane electrical potential and pH gradient in E. coli cells. Confocal laser scanning microscopy images showed that E. coli cells treated with bifidocin A took up propidium iodide. These results suggested that the mechanism of action bifidocin A against E. coli involved dissipation of the PMF of the cytoplasmic membrane, an increase in membrane permeability, pore formation in the cell membrane, a change in membrane integrity, and complete cell disintegration.     

Effect of starter cultures on microbial ecosystem and biogenic amines in fermented sausage

The microbial ecology of fermented sausages inoculated with different starter cultures (Pediococcus pentosaceus + Staphylococcus xylosus, batch A; Lactobacillus farciminis + Staphylococcus saprophyticus, batch B) was studied by culture-dependent and independent methods. The concentration of biogenic amines, pH and a_w (water activity) were followed. The starter B can inhibit indigenous bacteria effectively judged by traditional microbiological method and PCR-DGGE fingerprint. There was no statistical difference in pH between batches A and B at 2 days when substantial amounts of BAs were produced, while the amounts of histamine, putrescine, cadaverine and tyramine in batch B was lower than in batch A significantly (P < 0.001). As a result, the starter cultures which can complete, grow well and inhibit amine-positive bacteria play an important role in reducing the production of BAs during ripening of fermented sausage.