The current spreading of nanomaterial applications supports the search for further possible functions of theses diminutive particles. The antibacterial potentiality of zinc oxide (ZnO) nanoparticles (NPs), compared with conventional ZnO powder, against nine bacterial strains, mostly foodborne including pathogens, was evaluated using qualitative and quantitative assays. ZnO NP was more efficient as antibacterial agent than powder. Gram‐positive bacteria were generally more sensitive to ZnO than Gram negatives. The exposure of Salmonella typhimurium and Staphylococcus aureus to their relevant minimal inhibitory concentrations from ZnO NP reduced the cell number to zero within 8 and 4 h, respectively. Scanning electron micrographs of the treated bacteria with NPs exhibited that the disruptive effect of ZnO on S. aureus was vigorous as all treated cells were completely exploded or lysed after only 4 h from exposure. Promising results of ZnO NP antibacterial activity suggest its usage in food systems as preservative agent after further required investigations and risk assessments.
PRACTICAL APPLICATIONS
Foodborne pathogen invasion is still a recurrent serious problem facing researchers and food industry overseers. The introduction of novel powerful antimicrobial agents is of great importance for the control of pathogenic bacteria, especially antibiotic‐resistant strains. Zinc oxide (ZnO) nanoparticle (NP) could be one of these potential alternatives. This study focused on ZnO NP because of its increasing presence in many marketable products and that supports its application in food industries as a reasonably safe agent. The demonstrated antibacterial activity of ZnO NP recommends its possible application in the food preservation field; otherwise it can be applied as a potent sanitizing agent for disinfecting and sterilizing food industry equipment and containers against the attack and contamination with foodborne pathogenic bacteria.
Lactobacilli belong to the group of lactic acid bacteria (LAB), that have several distinguished abilities such as production of lactic acid, enzymes such as β-Galactosidase and natural antimicrobial substances called bacteriocins. Bacteriocin is a biopreservative agent potential of suppressing growth of some contaminant bacteria in food industry but its commercial availability is limited and costly. The study aimed to select isolates of Lactobacillus spp. potential for producing bacteriocins to suppress the growth of Escherichia coli ATCC 25922 and Bacillus subtilis NCIB3610, and to optimize the process of bacteriocin production. Results obtained in this study showed that L. acidophilus isolate CH1 was selected as the best candidate for bacteriocin among the four isolates that tested. The largest amounts of the bacteriocins were synthesized only in MRS medium was supplemented with K 2 HPO 4 (1.0%), Tween 80 (1%), Beef extract (1%), glucose, cyctein and peptone extract (1%). The optimization of culture conditions for bacteriocin production areas showed that corn steep liquor medium was the best medium for all isolates against Bacillus subtilis while no effect was observed on Escherichia coli ATCC 25922 except when used MRS medium. The optimum conditions for bacteriocin production were pH 6.0, temperature 34˚C with 4% Phenyl acetamide showing the greatest growth inhibition areas.
Anaerobic fungi colonize the rumen and degrade cellulose and hemicellulose, which enable them to be key players in the lignocellulose fermentation. Consequently, an expansion of knowledge about rumen fungi could increase animal productivity, utilization of lignified forages like alfalfa hay, and enhance fibrolytic enzymes production. Here, we used an Internal Transcribed Spacer 1 (ITS1) clone library to investigate the anaerobic rumen fungi in camel and to investigate their ability to produce cellulase and xylanase in vitro. Rumen fluid was collected from camels fed Egyptian clover (n = 14), and wheat straw (n = 7) and fecal samples were collected from camels fed wheat straw and concentrates (n = 5), or natural grazing plants (n = 10). Neocallimastix and Cyllamyces were the most abundant anaerobic fungi in all camel groups. An anaerobic rumen fungi media containing alfalfa hay as a carbon source was inoculated by rumen and fecal samples to assess the ability of anaerobic rumen fungi in camel gut to produce cellulase and xylanase. The anaerobic gut fungi in the camel is diverse and has cellulolytic and xylanolytic activities, fungal culture from rumen samples of camel fed wheat straw (R2) exhibited highest cellulase production. In addition, many of the sequences in the current study have no equivalent cultured representative, indicating a novel diversity within the camel gut.
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