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fluorescens (Pf)</title> <meta name="description" content="Search results for: pseudomonad fluorescens (Pf)"> <meta name="keywords" content="pseudomonad fluorescens (Pf)"> <meta name="viewport" content="width=device-width, initial-scale=1, minimum-scale=1, maximum-scale=1, user-scalable=no"> <meta charset="utf-8"> <link href="https://cdn.waset.org/favicon.ico" type="image/x-icon" rel="shortcut icon"> <link href="https://cdn.waset.org/static/plugins/bootstrap-4.2.1/css/bootstrap.min.css" rel="stylesheet"> <link href="https://cdn.waset.org/static/plugins/fontawesome/css/all.min.css" rel="stylesheet"> <link href="https://cdn.waset.org/static/css/site.css?v=150220211555" rel="stylesheet"> </head> <body> <header> <div class="container"> <nav class="navbar navbar-expand-lg navbar-light"> <a class="navbar-brand" href="https://waset.org"> <img src="https://cdn.waset.org/static/images/wasetc.png" alt="Open Science Research Excellence" title="Open Science Research Excellence" /> </a> <button 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action="https://publications.waset.org/abstracts/search"> <div id="custom-search-input"> <div class="input-group"> <i class="fas fa-search"></i> <input type="text" class="search-query" name="q" placeholder="Author, Title, Abstract, Keywords" value="pseudomonad fluorescens (Pf)"> <input type="submit" class="btn_search" value="Search"> </div> </div> </form> </div> </div> <div class="row mt-3"> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Commenced</strong> in January 2007</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Frequency:</strong> Monthly</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Edition:</strong> International</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Paper Count:</strong> 24</div> </div> </div> </div> <h1 class="mt-3 mb-3 text-center" style="font-size:1.6rem;">Search results for: pseudomonad fluorescens (Pf)</h1> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">24</span> Combined Aplication of Indigenous Pseudomonas fluorescens and the AM Fungi as the Potential Biocontrol Agents of Banana Fusarium wilt</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Eri%20Sulyanti">Eri Sulyanti</a>, <a href="https://publications.waset.org/abstracts/search?q=Trimurti%20Habazar"> Trimurti Habazar</a>, <a href="https://publications.waset.org/abstracts/search?q=Eti%20Farda%20Husen"> Eti Farda Husen</a>, <a href="https://publications.waset.org/abstracts/search?q=Abdi%20Dharma"> Abdi Dharma</a>, <a href="https://publications.waset.org/abstracts/search?q=Nasril%20Nasir"> Nasril Nasir</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this study, combination of some biocontrol agents with different mechanisms was an alternative to improve the effectiveness of the biological control agents. Single and combined applications of indigenous Pseudomonas fluorescens and Arbuscular Mychorrhizae Fungi (AM Fungi) isolates were tested to induce the resistance on susceptible Cavendish banana against F.oxysporum f. sp. cubense race 4 under greenhouse conditions. These isolates originally isolated from healthy banana rhizosphere at endemic Fusarium wilt areas in the centre of production banana in West Sumatra. These researches were conducted with Randomized Block Design with 16 treatments and 10 replications. The treatments were three indigenous isolates of Pseudomonas fluorescens (Par1-Cv, Par4-Rj1, Par2-Jt1) and 3 isolates of AM Fungi (Gl1BuA4, Gl2BuA6, and Gl1KeP3. The biocontrol agents were applied as single agents and combination two of them. This study demonstrated that the application of combination biocontrol organisms Pseudomonas fluorescens and AM Fungi provided were more effective than single application. The combination of Par1-Cv and Gl1BuA4 isolates was the most effective to control Fusarium wilt and followed by the combination of Par1-Cv and Gl2BuA6 and Par2-Jt1 and Gl1P3. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=pseudomonad%20fluorescens%20%28Pf%29" title="pseudomonad fluorescens (Pf)">pseudomonad fluorescens (Pf)</a>, <a href="https://publications.waset.org/abstracts/search?q=arbuscular%20mychorrhizae%20fungi%20%28AM%20Fungi%29%20indigenous%20isolates" title=" arbuscular mychorrhizae fungi (AM Fungi) indigenous isolates"> arbuscular mychorrhizae fungi (AM Fungi) indigenous isolates</a>, <a href="https://publications.waset.org/abstracts/search?q=fusarium%20oxysporum%20f.%20sp.%20cubense" title=" fusarium oxysporum f. sp. cubense"> fusarium oxysporum f. sp. cubense</a>, <a href="https://publications.waset.org/abstracts/search?q=soil%20rhizosphere" title=" soil rhizosphere"> soil rhizosphere</a> </p> <a href="https://publications.waset.org/abstracts/37182/combined-aplication-of-indigenous-pseudomonas-fluorescens-and-the-am-fungi-as-the-potential-biocontrol-agents-of-banana-fusarium-wilt" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/37182.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">307</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">23</span> Genome Analyses of Pseudomonas Fluorescens b29b from Coastal Kerala</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Wael%20Ali%20Mohammed%20Hadi">Wael Ali Mohammed Hadi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Pseudomonas fluorescens B29B, which has asparaginase enzymatic activity, was isolated from the surface coastal seawater of Trivandrum, India. We report the complete Pseudomonas fluorescens B29B genome sequenced, identified, and annotated from a marine source. We find the genome at most minuscule a 7,331,508 bp single circular chromosome with a GC content of 62.19% and 6883 protein-coding genes. Three hundred forty subsystems were identified, including two predicted asparaginases from the genome analysis of P. fluorescens B29B for further investigation. This genome data will help further industrial biotechnology applications of proteins in general and asparaginase as a target. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=pseudomonas" title="pseudomonas">pseudomonas</a>, <a href="https://publications.waset.org/abstracts/search?q=marine" title=" marine"> marine</a>, <a href="https://publications.waset.org/abstracts/search?q=asparaginases" title=" asparaginases"> asparaginases</a>, <a href="https://publications.waset.org/abstracts/search?q=Kerala" title=" Kerala"> Kerala</a>, <a href="https://publications.waset.org/abstracts/search?q=whole-genome" title=" whole-genome"> whole-genome</a> </p> <a href="https://publications.waset.org/abstracts/139283/genome-analyses-of-pseudomonas-fluorescens-b29b-from-coastal-kerala" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/139283.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">215</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">22</span> Chitin Degradation in Pseudomonas fluorescens</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Azhar%20Alhasawi">Azhar Alhasawi</a>, <a href="https://publications.waset.org/abstracts/search?q=Vasu%20D.%20Appanna"> Vasu D. Appanna</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Chitin, the second most abundant bio-polymer in nature after cellulose, composed of β (1→4) linked N-acetylglucosamine (GlcNAc), is a major structural component in the cell walls of fungi and the shells of crustaceans. Chitin and its derivatives are gaining importance of economic value due to its biological activity and its industrial and biomedical applications. There are several methods to hydrolyze chitin to NAG, but they are typically expensive and environmentally unfriendly. Chitinase which catalyzes the breakdown of chitin to NAG has received much attention owing to its various applications in biotechnology. The presented research examines the ability of the versatile soil microbe, Pseudomonas fluorescens grown in chitin medium to produce chitinase and a variety of value-added products under abiotic stress. We have found that with high pH, Pseudomonas fluorescens enable to metabolize chitin more than with neutral pH and the overexpression of chitinase was also increased. P-dimethylaminobenzaldehyde (DMAB) assay for NAG production will be monitored and a combination of sodium dodecyl polyacrylamide gels will be used to monitor the proteomic and metabolomic changes as a result of the abiotic stress. The bioreactor of chitinase will also be utilized. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Pseudomonas%20fluorescens" title="Pseudomonas fluorescens">Pseudomonas fluorescens</a>, <a href="https://publications.waset.org/abstracts/search?q=chitin" title=" chitin"> chitin</a>, <a href="https://publications.waset.org/abstracts/search?q=DMAB" title=" DMAB"> DMAB</a>, <a href="https://publications.waset.org/abstracts/search?q=chitinase" title=" chitinase"> chitinase</a> </p> <a href="https://publications.waset.org/abstracts/6211/chitin-degradation-in-pseudomonas-fluorescens" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/6211.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">354</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">21</span> Effects of Probiotic Pseudomonas fluorescens on the Growth Performance, Immune Modulation, and Histopathology of African Catfish (Clarias gariepinus)</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Nelson%20R.%20Osungbemiro">Nelson R. Osungbemiro</a>, <a href="https://publications.waset.org/abstracts/search?q=O.%20A.%20Bello-Olusoji"> O. A. Bello-Olusoji</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20Oladipupo"> M. Oladipupo</a> </p> <p class="card-text"><strong>Abstract:</strong></p> This study was carried out to determine the effects of probiotics Pseudomonas fluorescens on the growth performance, histology examination and immune modulation of African Catfish, (Clarias gariepinus) challenged with Clostridium botulinum. P. fluorescens, and C. botulinum isolates were removed from the gut, gill and skin organs of procured adult samples of Clarias gariepinus from commercial fish farms in Akure, Ondo State, Nigeria. The physical and biochemical tests were performed on the bacterial isolates using standard microbiological techniques for their identification. Antibacterial activity tests on P. fluorescens showed inhibition zone with mean value of 3.7 mm which indicates high level of antagonism. The experimental diets were prepared at different probiotics bacterial concentration comprises of five treatments of different bacterial suspension, including the control (T1), T2 (10³), T3 (10⁵), T4 (10⁷) and T5 (10⁹). Three replicates for each treatment type were prepared. Growth performance and nutrients utilization indices were calculated. The proximate analysis of fish carcass and experimental diet was carried out using standard methods. After feeding for 70 days, haematological values and histological test were done following standard methods; also a subgroup from each experimental treatment was challenged by inoculating Intraperitonieally (I/P) with different concentration of pathogenic C. botulinum. Statistically, there were significant differences (P < 0.05) in the growth performance and nutrient utilization of C. gariepinus. Best weight gain and feed conversion ratio were recorded in fish fed T4 (10⁷) and poorest value obtained in the control. Haematological analyses of C. gariepinus fed the experimental diets indicated that all the fish fed diets with P. fluorescens had marked significantly (p < 0.05) higher White Blood Cell than the control diet. The results of the challenge test showed that fish fed the control diet had the highest mortality rate. Histological examination of the gill, intestine, and liver of fish in this study showed several histopathological alterations in fish fed the control diets compared with those fed the P. fluorescens diets. The study indicated that the optimum level of P. fluorescens required for C. gariepinus growth and white blood cells formation is 10⁷ CFU g⁻¹, while carcass protein deposition required 10⁵ CFU g⁻¹ of P. fluorescens concentration. The study also confirmed P. fluorescens as efficient probiotics that is capable of improving the immune response of C. gariepinus against the attack of a virulent fish pathogen, C. botulinum. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Clarias%20gariepinus" title="Clarias gariepinus">Clarias gariepinus</a>, <a href="https://publications.waset.org/abstracts/search?q=Clostridium%20botulinum" title=" Clostridium botulinum"> Clostridium botulinum</a>, <a href="https://publications.waset.org/abstracts/search?q=probiotics" title=" probiotics"> probiotics</a>, <a href="https://publications.waset.org/abstracts/search?q=Pseudomonas%20fluorescens" title=" Pseudomonas fluorescens"> Pseudomonas fluorescens</a> </p> <a href="https://publications.waset.org/abstracts/90399/effects-of-probiotic-pseudomonas-fluorescens-on-the-growth-performance-immune-modulation-and-histopathology-of-african-catfish-clarias-gariepinus" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/90399.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">163</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">20</span> Biological Control of Karnal Bunt by Pseudomonas fluorescens </h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Geetika%20Vajpayee">Geetika Vajpayee</a>, <a href="https://publications.waset.org/abstracts/search?q=Sugandha%20Asthana"> Sugandha Asthana</a>, <a href="https://publications.waset.org/abstracts/search?q=Pratibha%20Kumari"> Pratibha Kumari</a>, <a href="https://publications.waset.org/abstracts/search?q=Shanthy%20Sundaram">Shanthy Sundaram</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Pseudomonas species possess a variety of promising properties of antifungal and growth promoting activities in the wheat plant. In the present study, Pseudomonas fluorescens MTCC-9768 is tested against plant pathogenic fungus Tilletia indica, causing Karnal bunt, a quarantine disease of wheat (Triticum aestivum) affecting kernels of wheat. It is one of the 1/A1 harmful diseases of wheat worldwide under EU legislation. This disease develops in the growth phase by the spreading of microscopically small spores of the fungus (teliospores) being dispersed by the wind. The present chemical fungicidal treatments were reported to reduce teliospores germination, but its effect is questionable since T. indica can survive up to four years in the soil. The fungal growth inhibition tests were performed using Dual Culture Technique, and the results showed inhibition by 82.5%. The interaction of antagonist bacteria-fungus causes changes in the morphology of hyphae, which was observed using Lactophenol cotton blue staining and Scanning Electron Microscopy (SEM). The rounded and swollen ends, called ‘theca’ were observed in interacted fungus as compared to control fungus (without bacterial interaction). This bacterium was tested for its antagonistic activity like protease, cellulose, HCN production, Chitinase, etc. The growth promoting activities showed increase production of IAA in bacteria. The bacterial secondary metabolites were extracted in different solvents for testing its growth inhibiting properties. The characterization and purification of the antifungal compound were done by Thin Layer Chromatography, and Rf value was calculated (Rf value = 0.54) and compared to the standard antifungal compound, 2, 4 DAPG (Rf value = 0.54). Further, the in vivo experiments showed a significant decrease in the severity of disease in the wheat plant due to direct injection method and seed treatment. Our results indicate that the extracted and purified compound from the antagonist bacteria, P. fluorescens MTCC-9768 may be used as a potential biocontrol agent against T. indica. This also concludes that the PGPR properties of the bacteria may be utilized by incorporating it into bio-fertilizers. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=antagonism" title="antagonism">antagonism</a>, <a href="https://publications.waset.org/abstracts/search?q=Karnal%20bunt" title=" Karnal bunt"> Karnal bunt</a>, <a href="https://publications.waset.org/abstracts/search?q=PGPR" title=" PGPR"> PGPR</a>, <a href="https://publications.waset.org/abstracts/search?q=Pseudomonas%20fluorescens" title=" Pseudomonas fluorescens"> Pseudomonas fluorescens</a> </p> <a href="https://publications.waset.org/abstracts/67517/biological-control-of-karnal-bunt-by-pseudomonas-fluorescens" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/67517.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">405</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">19</span> Mechanisms Involved in Biological Control of Fusarium Wilt</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Bensaid%20Fatiha">Bensaid Fatiha</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The objective of our present work is the description of the antagonistic capacities of one strain of Pseudomonas fluorescens and the nonpathogenic fungic isolate Fusarium oxysporum against phytopathogenic agent Fusarium oxysporum F. Sp. lycopersici. This work has been achieved in two main parts: the first is interested on the in vitro antagonistic activities; the second was interested to study the soil receptiveness of fusarium wilt tomato. The use of strain of fluorescent Pseudomonas and a non-pathogenic strain of F. oxysporum in the different antagonism tests, has allowed assuring a certain bio-protection from the plants of tomatoes opposite to F. oxysporum F. Sp. lycopersici, agent of a wilt of tomato. These antagonistic have shown a substantial in vitro antagonistic activity on the three mediums (KB, PDA, KB+PDA) against F. oxysporum F. Sp. lycopersici, by inhibiting its growth mycelium with rate of inhibition going until 80 % with non-pathogen of Fusarium oxysporum and 60 % with strain of fluorescens Pseudomonas. Soil microbial balance, between the antagonistic population and that of pathogenic, can be modulated through microbiological variations or abiotic additives influencing directly or indirectly the metabolic behavior microbial. In this experiment, addition of glucose or EDTA, could increase or decrease the resistance of soil by activation of pathogenic or antagonists, as a result of modification and modulation in their metabolic activities. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=fluorescents" title="fluorescents">fluorescents</a>, <a href="https://publications.waset.org/abstracts/search?q=nonpathogenic" title=" nonpathogenic"> nonpathogenic</a>, <a href="https://publications.waset.org/abstracts/search?q=fusarium%20oxysporum" title=" fusarium oxysporum"> fusarium oxysporum</a>, <a href="https://publications.waset.org/abstracts/search?q=fusarium%20wilt" title=" fusarium wilt"> fusarium wilt</a>, <a href="https://publications.waset.org/abstracts/search?q=antagonism" title=" antagonism"> antagonism</a>, <a href="https://publications.waset.org/abstracts/search?q=biological%20control" title=" biological control"> biological control</a>, <a href="https://publications.waset.org/abstracts/search?q=soil%20receptivity" title=" soil receptivity"> soil receptivity</a> </p> <a href="https://publications.waset.org/abstracts/23547/mechanisms-involved-in-biological-control-of-fusarium-wilt" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/23547.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">461</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">18</span> Microbial Bioagent Triggered Biochemical Response in Tea (Camellia sinensis) Inducing Resistance against Grey Blight Disease and Yield Enhancement</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Popy%20Bora">Popy Bora</a>, <a href="https://publications.waset.org/abstracts/search?q=L.%20C.%20Bora"> L. C. Bora</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20Bhattacharya"> A. Bhattacharya</a>, <a href="https://publications.waset.org/abstracts/search?q=Sehnaz%20S.%20Ahmed"> Sehnaz S. Ahmed</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Microbial bioagents, viz., Pseudomonas fluorescens, Bacillus subtilis, and Trichoderma viride were assessed for their ability to suppress grey blight caused by Pestalotiopsis theae, a major disease of tea crop in Assam. The expression of defense-related phytochemicals due to the application of these bioagents was also evaluated. The individual bioagents, as well as their combinations, were screened for their bioefficacy against P. theae in vitro using nutrient agar (NA) as basal medium. The treatment comprising a combination of the three bioagents, P. fluorescens, B. subtilis, and T. viride showed significantly the highest inhibition against the pathogen. Bioformulation of effective bioagent combinations was further evaluated under field condition, where significantly highest reduction of grey blight (90.30%), as well as the highest increase in the green leaf yield (10.52q/ha), was recorded due to application of the bioformulation containing the three bioagents. The application of the three bioformulation also recorded an enhanced level of caffeine (4.15%) and polyphenols (22.87%). A significant increase in the enzymatic activity of phenylalanine ammonia-lyase, peroxidase and polyphenol oxidase were recorded in the plants treated with the microbial bioformulation of the three bioagents. The present investigation indicates the role of microbial agents in suppressing disease, inducing plant defense response, as well as improving the quality of tea. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=enzymatic%20activity" title="enzymatic activity">enzymatic activity</a>, <a href="https://publications.waset.org/abstracts/search?q=grey%20blight" title=" grey blight"> grey blight</a>, <a href="https://publications.waset.org/abstracts/search?q=microbial%20bioagents" title=" microbial bioagents"> microbial bioagents</a>, <a href="https://publications.waset.org/abstracts/search?q=Pestalotiopsis%20theae" title=" Pestalotiopsis theae"> Pestalotiopsis theae</a>, <a href="https://publications.waset.org/abstracts/search?q=phytochemicals" title=" phytochemicals"> phytochemicals</a>, <a href="https://publications.waset.org/abstracts/search?q=plant%20defense" title=" plant defense"> plant defense</a>, <a href="https://publications.waset.org/abstracts/search?q=tea" title=" tea "> tea </a> </p> <a href="https://publications.waset.org/abstracts/113669/microbial-bioagent-triggered-biochemical-response-in-tea-camellia-sinensis-inducing-resistance-against-grey-blight-disease-and-yield-enhancement" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/113669.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">142</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">17</span> Effect of Biopesticide to Control Infestation of Whitefly Bemisia tabaci (Gennadius) on the Culantro Eryngium foetidum L.</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Udomporn%20Pangnakorn">Udomporn Pangnakorn</a>, <a href="https://publications.waset.org/abstracts/search?q=Sombat%20Chuenchooklin"> Sombat Chuenchooklin</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Effect of the biopesticide from entomopathogenic nematode (Steinernema thailandensis n. sp.), bacteria ISR (Pseudomonas fluorescens), wood vinegar and fermented organic substances from plants: (neem Azadirachta indica + citronella grass Cymbopogon nardus Rendle + bitter bush Chromolaena odorata L.) were tested on culantro (Eryngium foetidum L.). The biopesticide was carried out for reduction infestation of the major insects pest (whitefly Bemisia tabaci (Gennadius)). The experimental plots were located at farmers’ farm in Tumbol Takhian Luean, Nakhon Sawan Province, Thailand. This study was undertaken during the drought season (lately November to May). The populations of whitefly were observed and recorded every hour up to 3 hours with insect net and yellow sticky traps after the treatments were applied. The results showed that bacteria ISR was the highest effectiveness for control whitefly infestation on culantro, the whitefly numbers on insect net were 12.5, 10.0, and 7.5 after spraying in 1hr, 2hr, and 3hr, respectively. While the whitefly on yellow sticky traps showed 15.0, 10.0, and 10.0 after spraying in 1hr, 2hr, and 3hr, respectively. Furthermore, overall the experiments showed that treatment of bacteria ISR found the average whitefly numbers only 8.06 and 11.0 on insect net and sticky tap respectively, followed by treatment of nematode found the average whitefly with 9.87 and 11.43 on the insect net and sticky tap, respectively. Therefore, the application of biopesticide from entomopathogenic nematodes, bacteria ISR, organic substances from plants and wood vinegar combined with natural enemies is the alternative method of Integrated Pest Management (IPM) for against infestation of whitefly. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=whitefly%20%28Bemisia%20tabaci%20Gennadius%29" title="whitefly (Bemisia tabaci Gennadius)">whitefly (Bemisia tabaci Gennadius)</a>, <a href="https://publications.waset.org/abstracts/search?q=culantro%20%28Eryngium%20foetidum%20L.%29" title=" culantro (Eryngium foetidum L.)"> culantro (Eryngium foetidum L.)</a>, <a href="https://publications.waset.org/abstracts/search?q=entomopathogenic%20nematode%20%28Steinernema%20thailandensis%20n.%20sp.%29" title=" entomopathogenic nematode (Steinernema thailandensis n. sp.)"> entomopathogenic nematode (Steinernema thailandensis n. sp.)</a>, <a href="https://publications.waset.org/abstracts/search?q=bacteria%20ISR%20%28Pseudomonas%20fluorescens%29" title=" bacteria ISR (Pseudomonas fluorescens)"> bacteria ISR (Pseudomonas fluorescens)</a>, <a href="https://publications.waset.org/abstracts/search?q=wood%20vinegar" title=" wood vinegar"> wood vinegar</a>, <a href="https://publications.waset.org/abstracts/search?q=fermented%20organic%20substances" title=" fermented organic substances"> fermented organic substances</a> </p> <a href="https://publications.waset.org/abstracts/36589/effect-of-biopesticide-to-control-infestation-of-whitefly-bemisia-tabaci-gennadius-on-the-culantro-eryngium-foetidum-l" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/36589.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">374</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">16</span> Enzyme Producing Psyhrophilic Pseudomonas app. Isolated from Poultry Meats</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Ali%20Aydin">Ali Aydin</a>, <a href="https://publications.waset.org/abstracts/search?q=Mert%20Sudagidan"> Mert Sudagidan</a>, <a href="https://publications.waset.org/abstracts/search?q=Aysen%20Coban"> Aysen Coban</a>, <a href="https://publications.waset.org/abstracts/search?q=Alparslan%20Kadir%20Devrim"> Alparslan Kadir Devrim </a> </p> <p class="card-text"><strong>Abstract:</strong></p> Pseudomonas spp. (specifically, P. fluorescens and P. fragi) are considered the principal spoilage microorganisms of refrigerated poultry meats. The higher the level psychrophilic spoilage Pseudomonas spp. on carcasses at the end of processing lead to decrease the shelf life of the refrigerated product. The aim of the study was the identification of psychrophilic Pseudomonas spp. having proteolytic and lipolytic activities from poultry meats by 16S rRNA and rpoB gene sequencing, investigation of protease and lipase related genes and determination of proteolytic activity of Pseudomonas spp. In the of isolation procedure, collected chicken meat samples from local markets and slaughterhouses were homogenized and the lysates were incubated on Standard method agar and Skim Milk agar for selection of proteolytic bacteria and tributyrin agar for selection of lipolytic bacteria at +4 °C for 7 days. After detection of proteolytic and lipolytic colonies, the isolates were firstly analyzed by biochemical tests such as Gram staining, catalase and oxidase tests. DNA gene sequencing analysis and comparison with GenBank revealed that 126 strong enzyme Pseudomonas spp. were identified as predominantly P. fluorescens (n=55), P. fragi (n=42), Pseudomonas spp. (n=24), P. cedrina (n=2), P. poae (n=1), P. koreensis (n=1), and P. gessardi (n=1). Additionally, protease related aprX gene was screened in the strains and it was detected in 69/126 strains, whereas, lipase related lipA gene was found in 9 Pseudomonas strains. Protease activity was determined using commercially available protease assay kit and 5 strains showed high protease activity. The results showed that psychrophilic Pseudomonas strains were present in chicken meat samples and they can produce important levels of proteases and lipases for food spoilage to decrease food quality and safety. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Pseudomonas" title="Pseudomonas">Pseudomonas</a>, <a href="https://publications.waset.org/abstracts/search?q=chicken%20meat" title=" chicken meat"> chicken meat</a>, <a href="https://publications.waset.org/abstracts/search?q=protease" title=" protease"> protease</a>, <a href="https://publications.waset.org/abstracts/search?q=lipase" title=" lipase"> lipase</a> </p> <a href="https://publications.waset.org/abstracts/31581/enzyme-producing-psyhrophilic-pseudomonas-app-isolated-from-poultry-meats" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/31581.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">387</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">15</span> Acute and Chronic Effect of Biopesticide on Infestation of Whitefly Bemisia tabaci (Gennadius) on the Culantro Cultivation</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=U.%20Pangnakorn">U. Pangnakorn</a>, <a href="https://publications.waset.org/abstracts/search?q=S.%20Chuenchooklin"> S. Chuenchooklin</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Acute and chronic effects of biopesticide from entomopathogenic nematode (<em>Steinernema thailandensis</em> n. sp.), bacteria ISR (<em>Pseudomonas fluorescens</em>), wood vinegar and fermented organic substances from plants: (neem <em>Azadirachta indica</em> + citronella grass <em>Cymbopogon nardus </em>Rendle + bitter bush <em>Chromolaena odorata </em>L<em>.</em>) were tested on culantro (<em>Eryngium foetidum</em> L.). The biopesticide was investigated for infestation reduction of the major insect pest whitefly (<em>Bemisia tabaci</em> (Gennadius)). The experimental plots were located at a farm in Nakhon Sawan Province, Thailand. This study was undertaken during the drought season (late November to May). Effectiveness of the treatment was evaluated in terms of acute and chronic effect. The populations of whitefly were observed and recorded every hour up to 3 hours with insect nets and yellow sticky traps after the treatments were applied for the acute effect. The results showed that bacteria ISR had the highest effectiveness for controlling whitefly infestation on culantro; the whitefly numbers on insect nets were 12.5, 10.0 and 7.5 after 1 hr, 2 hr, and 3 hr, respectively while the whitefly on yellow sticky traps showed 15.0, 10.0 and 10.0 after 1 hr, 2 hr, and 3 hr, respectively. For chronic effect, the whitefly was continuously collected and recorded at weekly intervals; the result showed that treatment of bacteria ISR found the average whitefly numbers only 8.06 and 11.0 on insect nets and sticky traps respectively, followed by treatment of nematode where the average whitefly was 9.87 and 11.43 on the insect nets and sticky traps, respectively. In addition, the minor insect pests were also observed and collected. The biopesticide influenced the reduction number of minor insect pests (red spider mites, beet armyworm, short-horned grasshopper, pygmy locusts, etc.) with only a few found on the culantro cultivation. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=whitefly%20%28Bemisia%20tabaci%20Gennadius%29" title="whitefly (Bemisia tabaci Gennadius)">whitefly (Bemisia tabaci Gennadius)</a>, <a href="https://publications.waset.org/abstracts/search?q=culantro%20%28Eryngium%20foetidum%20L.%29" title=" culantro (Eryngium foetidum L.)"> culantro (Eryngium foetidum L.)</a>, <a href="https://publications.waset.org/abstracts/search?q=acute%20and%20chronic%20effect" title=" acute and chronic effect"> acute and chronic effect</a>, <a href="https://publications.waset.org/abstracts/search?q=entomopathogenic%20nematode%20%28Steinernema%20thailandensis%20n.%20sp.%29" title=" entomopathogenic nematode (Steinernema thailandensis n. sp.)"> entomopathogenic nematode (Steinernema thailandensis n. sp.)</a>, <a href="https://publications.waset.org/abstracts/search?q=bacteria%20ISR%20%28Pseudomonas%20fluorescens%29" title=" bacteria ISR (Pseudomonas fluorescens)"> bacteria ISR (Pseudomonas fluorescens)</a> </p> <a href="https://publications.waset.org/abstracts/43237/acute-and-chronic-effect-of-biopesticide-on-infestation-of-whitefly-bemisia-tabaci-gennadius-on-the-culantro-cultivation" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/43237.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">281</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">14</span> Effect of Fertilization and Combined Inoculation with Azospirillum brasilense and Pseudomonas fluorescens on Rhizosphere Microbial Communities of Avena sativa (Oats) and Secale Cereale (Rye) Grown as Cover Crops</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Jhovana%20Silvia%20Escobar%20Ortega">Jhovana Silvia Escobar Ortega</a>, <a href="https://publications.waset.org/abstracts/search?q=Ines%20Eugenia%20Garcia%20De%20Salamone"> Ines Eugenia Garcia De Salamone</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Cover crops are an agri-technological alternative to improve all properties of soils. Cover crops such as oats and rye could be used to reduce erosion and favor system sustainability when they are grown in the same agricultural cycle of the soybean crop. This crop is very profitable but its low contribution of easily decomposable residues, due to its low C/N ratio, leaves the soil exposed to erosive action and raises the need to reduce its monoculture. Furthermore, inoculation with the plant growth promoting rhizobacteria contributes to the implementation, development and production of several cereal crops. However, there is little information on its effects on forage crops which are often used as cover crops to improve soil quality. In order to evaluate the effect of combined inoculation with Azospirillum brasilense and Pseudomonas fluorescens on rhizosphere microbial communities, field experiments were conducted in the west of Buenos Aires province, Argentina, with a split-split plot randomized complete block factorial design with three replicates. The factors were: type of cover crop, inoculation and fertilization. In the main plot two levels of fertilization 0 and 7 40-0-5 (NPKS) were established at sowing. Rye (Secale cereale cultivar Quehué) and oats (Avena sativa var Aurora.) were sown in the subplots. In the sub-subplots two inoculation treatments are applied without and with application of a combined inoculant with A. brasilense and P. fluorescens. Due to the growth of cover crops has to be stopped usually with the herbicide glyphosate, rhizosphere soil of 0-20 and 20-40 cm layers was sampled at three sampling times which were: before glyphosate application (BG), a month after glyphosate application (AG) and at soybean harvest (SH). Community level of physiological profiles (CLPP) and Shannon index of microbial diversity (H) were obtained by multivariate analysis of Principal Components. Also, the most probable number (MPN) of nitrifiers and cellulolytics were determined using selective liquid media for each functional group. The CLPP of rhizosphere microbial communities showed significant differences between sampling times. There was not interaction between sampling times and both, types of cover crops and inoculation. Rhizosphere microbial communities of samples obtained BG had different CLPP with respect to the samples obtained in the sampling times AG and SH. Fertilizer and depth of sampling also caused changes in the CLPP. The H diversity index of rhizosphere microbial communities of rye in the sampling time BG were higher than those associated with oats. The MPN of both microbial functional types was lower in the deeper layer since these microorganisms are mostly aerobic. The MPN of nitrifiers decreased in rhizosphere of both cover crops only AG. At the sampling time BG, the NMP of both microbial types were larger than those obtained for AG and SH. This may mean that the glyphosate application could cause fairly permanent changes in these microbial communities which can be considered bio-indicators of soil quality. Inoculation and fertilizer inputs could be included to improve management of these cover crops because they can have a significant positive effect on the sustainability of the agro-ecosystem. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=community%20level%20of%20physiological%20profiles" title="community level of physiological profiles">community level of physiological profiles</a>, <a href="https://publications.waset.org/abstracts/search?q=microbial%20diversity" title=" microbial diversity"> microbial diversity</a>, <a href="https://publications.waset.org/abstracts/search?q=plant%20growth%20promoting%20rhizobacteria" title=" plant growth promoting rhizobacteria"> plant growth promoting rhizobacteria</a>, <a href="https://publications.waset.org/abstracts/search?q=rhizosphere%20microbial%20communities" title=" rhizosphere microbial communities"> rhizosphere microbial communities</a>, <a href="https://publications.waset.org/abstracts/search?q=soil%20quality" title=" soil quality"> soil quality</a>, <a href="https://publications.waset.org/abstracts/search?q=system%20sustainability" title=" system sustainability"> system sustainability</a> </p> <a href="https://publications.waset.org/abstracts/68602/effect-of-fertilization-and-combined-inoculation-with-azospirillum-brasilense-and-pseudomonas-fluorescens-on-rhizosphere-microbial-communities-of-avena-sativa-oats-and-secale-cereale-rye-grown-as-cover-crops" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/68602.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">404</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13</span> Effectiveness of the Flavonoids Isolated from Thymus inodorus by Different Solvents against Some Pathogenis Microorganisms</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=N.%20Behidj">N. Behidj</a>, <a href="https://publications.waset.org/abstracts/search?q=K.%20Benyounes"> K. Benyounes</a>, <a href="https://publications.waset.org/abstracts/search?q=T.%20Dahmane"> T. Dahmane</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20Allem"> A. Allem</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The aim of this study was to investigate the antimicrobial activity of flavonoids isolated from the aerial part of a medicinal plant which is <em>Thymus inodorus</em>by the middle agar diffusion method on following microorganisms. We have <em>Staphylococcus aureus, Escherichia coli, Pseudomonas fluorescens, AspergillusNiger, Aspergillus fumigatus and Candida albicans.</em> During this study, flavonoids extracted by stripping with steam are performed. The yields of flavonoids is 7.242% for the aqueous extract and 28.86% for butanol extract, 29.875% for the extract of ethyl acetate and 22.9% for the extract of di - ethyl. The evaluation of the antibacterial effect shows that the diameter of the zone of inhibition varies from one microorganism to another. The operation values obtained show that the bacterial strain P fluoresces, and 3 yeasts and molds; <em>A. Niger</em>, <em>A. fumigatus</em> and <em>C. albicans</em>are the most resistant. But it is noted that, <em>S. aureus</em> is shown more sensitive to crude extracts, the stock solution and the various dilutions. Finally for the minimum inhibitory concentration is estimated only with the crude extract of <em>Thymus inodorus</em> flavonoid.Indeed, these extracts inhibit the growth of Gram + bacteria at a concentration varying between 0.5% and 1%. While for bacteria to Gram -, it is limited to a concentration of 0.5%. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=antimicrobial%20activity" title="antimicrobial activity">antimicrobial activity</a>, <a href="https://publications.waset.org/abstracts/search?q=organic%20extracts" title=" organic extracts"> organic extracts</a>, <a href="https://publications.waset.org/abstracts/search?q=aqueous%20extracts" title=" aqueous extracts"> aqueous extracts</a>, <a href="https://publications.waset.org/abstracts/search?q=Thymus%20numidicus" title=" Thymus numidicus"> Thymus numidicus</a> </p> <a href="https://publications.waset.org/abstracts/53887/effectiveness-of-the-flavonoids-isolated-from-thymus-inodorus-by-different-solvents-against-some-pathogenis-microorganisms" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/53887.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">185</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">12</span> Bacteriological Characterization of Drinking Water Distribution Network Biofilms by Gene Sequencing Using Different Pipe Materials</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=M.%20Zafar">M. Zafar</a>, <a href="https://publications.waset.org/abstracts/search?q=S.%20Rasheed"> S. Rasheed</a>, <a href="https://publications.waset.org/abstracts/search?q=Imran%20Hashmi"> Imran Hashmi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Very little is concerned about the bacterial contamination in drinking water biofilm which provide a potential source for bacteria to grow and increase rapidly. So as to understand the microbial density in DWDs, a three-month study was carried out. The aim of this study was to examine biofilm in three different pipe materials including PVC, PPR and GI. A set of all these pipe materials was installed in DWDs at nine different locations and assessed on monthly basis. Drinking water quality was evaluated by different parameters and characterization of biofilm. Among various parameters are Temperature, pH, turbidity, TDS, electrical conductivity, BOD, COD, total phosphates, total nitrates, total organic carbon (TOC) free chlorine and total chlorine, coliforms and spread plate counts (SPC) according to standard methods. Predominant species were Bacillus thuringiensis, Pseudomonas fluorescens , Staphylococcus haemolyticus, Bacillus safensis and significant increase in bacterial population was observed in PVC pipes while least in cement pipes. The quantity of DWDs bacteria was directly depended on biofilm bacteria and its increase was correlated with growth and detachment of bacteria from biofilms. Pipe material also affected the microbial community in drinking water distribution network biofilm while Similarity in bacterial species was observed between systems due to same disinfectant dose, time period and plumbing pipes. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=biofilm" title="biofilm">biofilm</a>, <a href="https://publications.waset.org/abstracts/search?q=DWDs" title=" DWDs"> DWDs</a>, <a href="https://publications.waset.org/abstracts/search?q=pipe%20material" title=" pipe material"> pipe material</a>, <a href="https://publications.waset.org/abstracts/search?q=bacterial%20population" title=" bacterial population"> bacterial population</a> </p> <a href="https://publications.waset.org/abstracts/43105/bacteriological-characterization-of-drinking-water-distribution-network-biofilms-by-gene-sequencing-using-different-pipe-materials" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/43105.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">347</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">11</span> Retrospective Study of Bronchial Secretions Cultures Carried out in the Microbiology Department of General Hospital of Ioannina in 2017</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=S.%20Mantzoukis">S. Mantzoukis</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20Gerasimou"> M. Gerasimou</a>, <a href="https://publications.waset.org/abstracts/search?q=P.%20Christodoulou"> P. Christodoulou</a>, <a href="https://publications.waset.org/abstracts/search?q=N.%20Varsamis"> N. Varsamis</a>, <a href="https://publications.waset.org/abstracts/search?q=G.%20Kolliopoulou"> G. Kolliopoulou</a>, <a href="https://publications.waset.org/abstracts/search?q=N.%20Zotos"> N. Zotos</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Purpose: Patients in Intensive Care Units (ICU) are exposed to a different spectrum of microorganisms relative to the hospital. Due to the fact that the majority of these patients are intubated, bronchial secretions should be examined. Material and Method: Bronchial secretions should be taken with care so as not to be mixed with sputum or saliva. The bronchial secretions are placed in a sterile container and then inoculated into blood, Mac Conkey No2, Chocolate, Mueller Hinton, Chapman and Saboureaud agar. After this period, if any number of microbial colonies are detected, gram staining is performed and then the isolated organisms are identified by biochemical techniques in the automated Microscan system (Siemens) followed by a sensitivity test in the same system using the minimum inhibitory concentration MIC technique. The sensitivity test is verified by a Kirby Bauer test. Results: In 2017 the Laboratory of Microbiology received 365 samples of bronchial secretions from the Intensive Care Unit. 237 were found positive. S. epidermidis was identified in 1 specimen, A. baumannii in 60, K. pneumoniae in 42, P. aeruginosa in 50, C. albicans in 40, P. mirabilis in 4, E. coli in 4, S. maltophilia in 6, S. marcescens in 6, S. aureus in 12, S. pneumoniae in 1, S. haemolyticus in 4, P. fluorescens in 1, E. aerogenes in 1, E. cloacae in 5. Conclusions: The majority of ICU patients appear to be a fertile ground for the development of infections. The nature of the findings suggests that a significant part of the bacteria found comes from the unit (nosocomial infection). <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=bronchial%20secretions" title="bronchial secretions">bronchial secretions</a>, <a href="https://publications.waset.org/abstracts/search?q=cultures" title=" cultures"> cultures</a>, <a href="https://publications.waset.org/abstracts/search?q=infections" title=" infections"> infections</a>, <a href="https://publications.waset.org/abstracts/search?q=intensive%20care%20units" title=" intensive care units"> intensive care units</a> </p> <a href="https://publications.waset.org/abstracts/103223/retrospective-study-of-bronchial-secretions-cultures-carried-out-in-the-microbiology-department-of-general-hospital-of-ioannina-in-2017" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/103223.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">185</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">10</span> Reduction of Terpene Emissions from Oriented Strand Boards (OSB) by Bacterial Pre-Treatment</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Bernhard%20Widhalm">Bernhard Widhalm</a>, <a href="https://publications.waset.org/abstracts/search?q=Cornelia%20Rieder-Gradinger"> Cornelia Rieder-Gradinger</a>, <a href="https://publications.waset.org/abstracts/search?q=Ewald%20Srebotnik"> Ewald Srebotnik</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Pine wood (Pinus sylvestris L.) is the basic raw material for the production of Oriented Strand Boards (OSB) and the major source of volatile organic compounds, especially terpenes (like α- and β-pinene). To lower the total emission level of OSB, terpene metabolising microorganisms were therefore applied onto pine wood strands for the production of emission-reduced boards. Suitable microorganisms were identified during preliminary tests under laboratory conditions. At first, their terpene degrading potential was investigated in liquid culture, followed by laboratory tests using unsterile pine wood particles and strands. The main focus was laid on an adoptable terpene reduction in a short incubation time. An optimised bacterial mixture of Pseudomonas putida and Pseudomonas fluorescens showed the best results and was therefore used for further experiments on a larger scale. In an industry-compatible testing procedure, pine wood strands were incubated with the bacterial mixture for a period of 2 to 4 days. Incubation time was stopped by drying the strands. OSB were then manufactured from the pre-treated strands and emissions were measured by means of SPME/GC-MS analysis. Bacterial pre-treatment of strands resulted in a reduction of α-pinene- and β-pinene-emissions from OSB by 40% and 70%, respectively, even after only 2 days of incubation. The results of the investigation provide a basis for the application of microbial treatment within the industrial OSB production line, where shortest possible incubation times are required. For this purpose, the performance of the bacterial mixture will have to be further optimised. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=GC-MS" title="GC-MS">GC-MS</a>, <a href="https://publications.waset.org/abstracts/search?q=OSB" title=" OSB"> OSB</a>, <a href="https://publications.waset.org/abstracts/search?q=Pseudomonas%20sp." title=" Pseudomonas sp."> Pseudomonas sp.</a>, <a href="https://publications.waset.org/abstracts/search?q=terpene%20degradation" title=" terpene degradation"> terpene degradation</a> </p> <a href="https://publications.waset.org/abstracts/56194/reduction-of-terpene-emissions-from-oriented-strand-boards-osb-by-bacterial-pre-treatment" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/56194.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">268</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">9</span> Characterization of Bacteriophage for Biocontrol of Pseudomonas syringae, Causative Agent of Canker in Prunus spp.</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Mojgan%20Rabiey">Mojgan Rabiey</a>, <a href="https://publications.waset.org/abstracts/search?q=Shyamali%20Roy"> Shyamali Roy</a>, <a href="https://publications.waset.org/abstracts/search?q=Billy%20Quilty"> Billy Quilty</a>, <a href="https://publications.waset.org/abstracts/search?q=Ryan%20Creeth"> Ryan Creeth</a>, <a href="https://publications.waset.org/abstracts/search?q=George%20Sundin"> George Sundin</a>, <a href="https://publications.waset.org/abstracts/search?q=Robert%20W.%20Jackson"> Robert W. Jackson</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Bacterial canker is a major disease of Prunus species such as cherry (Prunus avium). It is caused by Pseudomonas syringae species including P. syringae pv. syringae (Pss) and P. syringae pv. morsprunorum race 1 (Psm1) and race 2 (Psm2). Concerns over the environmental impact of, and developing resistance to, copper controls call for alternative approaches to disease management. One method of control could be achieved using naturally occurring bacteriophage (phage) infective to the bacterial pathogens. Phages were isolated from soil, leaf, and bark of cherry trees in five locations in the South East of England. The phages were assessed for their host range against strains of Pss, Psm1, and Psm2. The phages exhibited a differential ability to infect and lyse different Pss and Psm isolates as well as some other P. syringae pathovars. However, the phages were unable to infect beneficial bacteria such as Pseudomonas fluorescens. A subset of 18 of these phages were further characterised genetically (Random Amplification of Polymorphic DNA-PCR fingerprinting and sequencing) and using electron microscopy. The phages are tentatively identified as belonging to the order Caudovirales and the families Myoviridae, Podoviridae, and Siphoviridae, with genetic material being dsDNA. Future research will fully sequence the phage genomes. The efficacy of the phage, both individually and in cocktails, to reduce disease progression in vivo will be investigated to understand the potential for practical use of these phages as biocontrol agents. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=bacteriophage" title="bacteriophage">bacteriophage</a>, <a href="https://publications.waset.org/abstracts/search?q=pseudomonas" title=" pseudomonas"> pseudomonas</a>, <a href="https://publications.waset.org/abstracts/search?q=bacterial%20cancker" title=" bacterial cancker"> bacterial cancker</a>, <a href="https://publications.waset.org/abstracts/search?q=biological%20control" title=" biological control"> biological control</a> </p> <a href="https://publications.waset.org/abstracts/108768/characterization-of-bacteriophage-for-biocontrol-of-pseudomonas-syringae-causative-agent-of-canker-in-prunus-spp" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/108768.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">151</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">8</span> Microbial Reduction of Terpenes from Pine Wood Material</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Bernhard%20Widhalm">Bernhard Widhalm</a>, <a href="https://publications.waset.org/abstracts/search?q=Cornelia%20Rieder-Gradinger"> Cornelia Rieder-Gradinger</a>, <a href="https://publications.waset.org/abstracts/search?q=Thomas%20Ters"> Thomas Ters</a>, <a href="https://publications.waset.org/abstracts/search?q=Ewald%20Srebotnik"> Ewald Srebotnik</a>, <a href="https://publications.waset.org/abstracts/search?q=Thomas%20Kuncinger"> Thomas Kuncinger</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Terpenes are natural components in softwoods and rank among the most frequently emitted volatile organic compounds (VOC) in the wood-processing industry. In this study, the main focus was on α- and β-pinene as well as Δ3-carene, which are the major terpenes in softwoods. To lower the total emission level of wood composites, defined terpene degrading microorganisms were applied to basic raw materials (e.g. pine wood particles and strands) in an optimised and industry-compatible testing procedure. In preliminary laboratory tests, bacterial species suitable for the utilisation of α-pinene as single carbon source in liquid culture were selected and then subjected to wood material inoculation. The two species Pseudomonas putida and Pseudomonas fluorescens were inoculated onto wood particles and strands and incubated at room temperature. Applying specific pre-cultivation and daily ventilation of the samples enabled a reduction of incubation time from six days to one day. SPME measurements and subsequent GC-MS analysis indicated a complete absence of α- and β-pinene emissions after 24 hours from pine wood particles. When using pine wood strands rather than particles, bacterial treatment resulted in a reduction of α- and β-pinene by 50%, while Δ3-carene emissions were reduced by 30% in comparison to untreated strands. Other terpenes were also reduced in the course of the microbial treatment. The method developed here appears to be feasible for industrial application. However, growth parameters such as time and temperature as well as the technical implementation of the inoculation step will have to be adapted for the production process. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=GC-MS" title="GC-MS">GC-MS</a>, <a href="https://publications.waset.org/abstracts/search?q=pseudomonas" title=" pseudomonas"> pseudomonas</a>, <a href="https://publications.waset.org/abstracts/search?q=SPME" title=" SPME"> SPME</a>, <a href="https://publications.waset.org/abstracts/search?q=terpenes" title=" terpenes"> terpenes</a> </p> <a href="https://publications.waset.org/abstracts/48124/microbial-reduction-of-terpenes-from-pine-wood-material" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/48124.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">347</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">7</span> Characterization and Pcr Detection of Selected Strains of Psychrotrophic Bacteria Isolated From Raw Milk</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Kidane%20workelul">Kidane workelul</a>, <a href="https://publications.waset.org/abstracts/search?q=Li%20xu"> Li xu</a>, <a href="https://publications.waset.org/abstracts/search?q=Xiaoyang%20Pang"> Xiaoyang Pang</a>, <a href="https://publications.waset.org/abstracts/search?q=Jiaping%20Lv"> Jiaping Lv</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Dairy products are exceptionally ideal media for the growth of microorganisms because of their high nutritional content. There are several ways that milk might get contaminated throughout the milking process, including how the raw milk is transported and stored, as well as how long it is kept before being processed. Psychrotrophic bacteria are among the one which can deteriorate the quality of milk mainly their heat resistance proteas and lipase enzyme. For this research purpose 8 selected strains of Psychrotrophic bacteria (Entrococcus hirae, Pseudomonas fluorescens, Pseudomonas azotoformans, Pseudomonas putida, Exiguobacterium indicum, Pseudomonas paralactice, Acinetobacter indicum, Serratia liquefacients)are chosen and try to determine their characteristics based on the research methodology protocol. Thus, the 8 selected strains are cultured, plated incubate, extracted their genomic DNA and genome DNA was amplified, the purpose of the study was to identify their Psychrotrophic properties, lipase hydrolysis positive test, their optimal incubation temperature, designed primer using the noble strain P,flourescens conserved region area in target with lipA gene, optimized primer specificity as well as sensitivity and PCR detection for lipase positive strains using the design primers. Based on the findings both the selected 8 strains isolated from stored raw milk are Psychrotrophic bacteria, 6 of the selected strains except the 2 strains are positive for lipase hydrolysis, their optimal temperature is 20 to 30 OC, the designed primer specificity is very accurate and amplifies for those strains only with lipase positive but could not amplify for the others. Thus, the result is promising and could help in detecting the Psychrotrophic bacteria producing heat resistance enzymes (lipase) at early stage before the milk is processed and this will safe production loss for the dairy industry. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=dairy%20industry" title="dairy industry">dairy industry</a>, <a href="https://publications.waset.org/abstracts/search?q=heat-resistant" title=" heat-resistant"> heat-resistant</a>, <a href="https://publications.waset.org/abstracts/search?q=lipA" title=" lipA"> lipA</a>, <a href="https://publications.waset.org/abstracts/search?q=milk" title=" milk"> milk</a>, <a href="https://publications.waset.org/abstracts/search?q=primer%20and%20psychrotrophic" title=" primer and psychrotrophic"> primer and psychrotrophic</a> </p> <a href="https://publications.waset.org/abstracts/183519/characterization-and-pcr-detection-of-selected-strains-of-psychrotrophic-bacteria-isolated-from-raw-milk" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/183519.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">64</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">6</span> Use of Metallic and Bimetallic Nanostructures as Constituents of Active Bio-Based Films</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Lina%20F.%20Ballesteros">Lina F. Ballesteros</a>, <a href="https://publications.waset.org/abstracts/search?q=Hafsae%20Lamsaf"> Hafsae Lamsaf</a>, <a href="https://publications.waset.org/abstracts/search?q=Miguel%20A.%20Cerqueira"> Miguel A. Cerqueira</a>, <a href="https://publications.waset.org/abstracts/search?q=Lorenzo%20M.%20Pastrana"> Lorenzo M. Pastrana</a>, <a href="https://publications.waset.org/abstracts/search?q=Sandra%20Carvalho"> Sandra Carvalho</a>, <a href="https://publications.waset.org/abstracts/search?q=Jose%20A.%20Teixeira"> Jose A. Teixeira</a>, <a href="https://publications.waset.org/abstracts/search?q=S.%20Calderon%20V."> S. Calderon V.</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The use of bio-based packaging materials containing metallic and bimetallic nanostructures is relatively modern technology. In this sense, the food packaging industry has been investigating biological and renewable resources that can replace petroleum-based materials to reduce the environmental impact and, at the same time, including new functionalities using nanotechnology. Therefore, the main objective of the present work consisted of developing bio-based poly-lactic acid (PLA) films with Zinc (Zn) and Zinc-Iron (Zn-Fe) nanostructures deposited by magnetron sputtering. The structural, antimicrobial, and optical properties of the films were evaluated when exposed at 60% and 96% relative humidity (RH). The morphology and elemental analysis of the samples were determined by scanning (transmission) electron microscopy (SEM and STEM), and inductively coupled plasma optical emission spectroscopy (ICP-OES). The structure of the PLA was monitored before and after deposition by Fourier transform infrared spectroscopy (FTIR) analysis, and the antimicrobial and color assays were performed by using the zone of inhibition (ZOI) test and a Minolta colorimeter, respectively. Finally, the films were correlated in terms of the deposit conditions, Zn or Zn-Fe concentrations, and thickness. The results revealed PLA films with different morphologies, compositions, and thicknesses of Zn or Zn-Fe nanostructures. The samples showed a significant antibacterial and antifungal activity against E. coli, P. aeruginosa, P. fluorescens, S. aureus, and A. niger, and considerable changes of color and opacity at 96% RH, especially for the thinner nanostructures (150-250 nm). On the other hand, when the Fe fraction was increased, the lightness of samples increased, as well as their antimicrobial activity when compared to the films with pure Zn. Hence, these findings are relevant to the food packaging field since intelligent and active films with multiple properties can be developed. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=biopolymers" title="biopolymers">biopolymers</a>, <a href="https://publications.waset.org/abstracts/search?q=functional%20properties" title=" functional properties"> functional properties</a>, <a href="https://publications.waset.org/abstracts/search?q=magnetron%20sputtering" title=" magnetron sputtering"> magnetron sputtering</a>, <a href="https://publications.waset.org/abstracts/search?q=Zn%20and%20Zn-Fe%20nanostructures" title=" Zn and Zn-Fe nanostructures"> Zn and Zn-Fe nanostructures</a> </p> <a href="https://publications.waset.org/abstracts/135084/use-of-metallic-and-bimetallic-nanostructures-as-constituents-of-active-bio-based-films" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/135084.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">121</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">5</span> Identification and Characterization of Oil-Degrading Bacteria from Crude Oil-Contaminated Desert Soil in Northeastern Jordan</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Mohammad%20Aladwan">Mohammad Aladwan</a>, <a href="https://publications.waset.org/abstracts/search?q=Adelia%20Skripova"> Adelia Skripova</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Bioremediation aspects of crude oil-polluted fields can be achieved by isolation and identification of bacterial species from oil-contaminated soil in order to choose the most active isolates and increase the strength of others. In this study, oil-degrading bacteria were isolated and identified from oil-contaminated soil samples in northeastern Jordan. The bacterial growth count (CFU/g) was between 1.06×10⁵ and 0.75×10⁹. Eighty-two bacterial isolates were characterized by their morphology and biochemical tests. The identified bacterial genera included: Klebsiella, Staphylococcus, Citrobacter, Lactobacillus, Alcaligenes, Pseudomonas, Hafnia, Micrococcus, Rhodococcus, Serratia, Enterobacter, Bacillus, Salmonella, Mycobacterium, Corynebacterium, and Acetobacter. Molecular identification of a universal primer 16S rDNA gene was used to identify four bacterial isolates: Microbacterium esteraromaticum strain L20, Pseudomonas stutzeri strain 13636M, Klebsilla pneumoniae, and uncultured Klebsilla sp., known as new strains. Our results indicate that their specific oil-degrading bacteria isolates might have a high strength of oil degradation from oil-contaminated sites. Staphylococcus intermedius (75%), Corynebacterium xerosis (75%), and Pseudomonas fluorescens (50%) showed a high growth rate on different types of hydrocarbons, such as crude oil, toluene, naphthalene, and hexane. In addition, monooxygenase and catechol 2,3-dioxygenase were detected in 17 bacterial isolates, indicating their superior hydrocarbon degradation potential. Total petroleum hydrocarbons were analyzed using gas chromatography for soil samples. Soil samples M5, M7, and M8 showed the highest levels (43,645, 47,805, and 45,991 ppm, respectively), and M4 had the lowest level (7,514 ppm). All soil samples were analyzed for heavy metal contamination (Cu, Cd, Mn, Zn, and Pb). Site M7 contains the highest levels of Cu, Mn, and Pb, while Site M8 contains the highest levels of Mn and Zn. In the future, these isolates of bacteria can be used for the cleanup of oil-contaminated soil. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=bioremediation" title="bioremediation">bioremediation</a>, <a href="https://publications.waset.org/abstracts/search?q=16S%20rDNA%20gene" title=" 16S rDNA gene"> 16S rDNA gene</a>, <a href="https://publications.waset.org/abstracts/search?q=oil-degrading%20bacteria" title=" oil-degrading bacteria"> oil-degrading bacteria</a>, <a href="https://publications.waset.org/abstracts/search?q=hydrocarbons" title=" hydrocarbons"> hydrocarbons</a> </p> <a href="https://publications.waset.org/abstracts/155484/identification-and-characterization-of-oil-degrading-bacteria-from-crude-oil-contaminated-desert-soil-in-northeastern-jordan" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/155484.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">126</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">4</span> Green Synthesis of Silver Nanoparticles Mediated by Plant by-Product Extracts</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Cristian%20Moisa">Cristian Moisa</a>, <a href="https://publications.waset.org/abstracts/search?q=Andreea%20Lupitu"> Andreea Lupitu</a>, <a href="https://publications.waset.org/abstracts/search?q=Adriana%20Csakvari"> Adriana Csakvari</a>, <a href="https://publications.waset.org/abstracts/search?q=Dana%20G.%20Radu"> Dana G. Radu</a>, <a href="https://publications.waset.org/abstracts/search?q=Leonard%20Marian%20Olariu"> Leonard Marian Olariu</a>, <a href="https://publications.waset.org/abstracts/search?q=Georgeta%20Pop"> Georgeta Pop</a>, <a href="https://publications.waset.org/abstracts/search?q=Dorina%20Chambre"> Dorina Chambre</a>, <a href="https://publications.waset.org/abstracts/search?q=Lucian%20Copolovici"> Lucian Copolovici</a>, <a href="https://publications.waset.org/abstracts/search?q=Dana%20Copolovici"> Dana Copolovici</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Green synthesis of nanoparticles (NPs) represents a promising, accessible, eco-friendly, and safe process with significant applications in biotechnology, pharmaceutical sciences, and farming. The aim of our study was to obtain silver nanoparticles, using plant wastes extracts resulted in the essential oils extraction process: Thymus vulgaris L., Origanum vulgare L., Lavandula angustifolia L., and in hemp processing for seed and fibre, Cannabis sativa. Firstly, we obtained aqueous extracts of thyme, oregano, lavender, and hemp (two monoicous and one dioicous varieties), all harvested in western part of Romania. Then, we determined the chemical composition of the extracts by liquid-chromatography coupled with diode array and mass spectrometer detectors. The compounds identified in the extracts were in agreement with earlier published data, and the determination of the antioxidant activity of the obtained extracts by DPPH (2,2-diphenyl-1-picrylhydrazyl) and ABTS (2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid)) assays confirmed their antioxidant activity due to their total polyphenolic content evaluated by Folin-Ciocalteu assay. Then, the silver nanoparticles (AgNPs) were successfully biosynthesised, as was demonstrated by UV-VIS, FT-IR spectroscopies, and SEM, by reacting AgNO₃ solution and plant extracts. AgNPs were spherical in shape, with less than 30 nm in diameter, and had a good bactericidal activity against Gram-positive (Staphylococcus aureus) and Gram-negative bacteria (Escherichia coli, Klebsiella pneumoniae, Pseudomonas fluorescens). <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=plant%20wastes%20extracts" title="plant wastes extracts">plant wastes extracts</a>, <a href="https://publications.waset.org/abstracts/search?q=chemical%20composition" title=" chemical composition"> chemical composition</a>, <a href="https://publications.waset.org/abstracts/search?q=high%20performance%20liquid%20chromatography%20mass%20spectrometer" title=" high performance liquid chromatography mass spectrometer"> high performance liquid chromatography mass spectrometer</a>, <a href="https://publications.waset.org/abstracts/search?q=HPLC-MS" title=" HPLC-MS"> HPLC-MS</a>, <a href="https://publications.waset.org/abstracts/search?q=scanning%20electron%20microscopy" title=" scanning electron microscopy"> scanning electron microscopy</a>, <a href="https://publications.waset.org/abstracts/search?q=SEM" title=" SEM"> SEM</a>, <a href="https://publications.waset.org/abstracts/search?q=silver%20nanoparticles" title=" silver nanoparticles"> silver nanoparticles</a> </p> <a href="https://publications.waset.org/abstracts/129078/green-synthesis-of-silver-nanoparticles-mediated-by-plant-by-product-extracts" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/129078.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">180</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">3</span> Response of Planktonic and Aggregated Bacterial Cells to Water Disinfection with Photodynamic Inactivation</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Thayse%20Marques%20Passos">Thayse Marques Passos</a>, <a href="https://publications.waset.org/abstracts/search?q=Brid%20Quilty"> Brid Quilty</a>, <a href="https://publications.waset.org/abstracts/search?q=Mary%20Pryce"> Mary Pryce</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The interest in developing alternative techniques to obtain safe water, free from pathogens and hazardous substances, is growing in recent times. The photodynamic inactivation of microorganisms (PDI) is a promising ecologically-friendly and multi-target approach for water disinfection. It uses visible light as an energy source combined with a photosensitiser (PS) to transfer energy/electrons to a substrate or molecular oxygen generating reactive oxygen species, which cause cidal effects towards cells. PDI has mainly been used in clinical studies and investigations on its application to disinfect water is relatively recent. The majority of studies use planktonic cells. However, in their natural environments, bacteria quite often do not occur as freely suspended cells (planktonic) but in cell aggregates that are either freely floating or attached to surfaces as biofilms. Microbes can form aggregates and biofilms as a strategy to protect them from environmental stress. As aggregates, bacteria have a better metabolic function, they communicate more efficiently, and they are more resistant to biocide compounds than their planktonic forms. Among the bacteria that are able to form aggregates are members of the genus Pseudomonas, they are a very diverse group widely distributed in the environment. Pseudomonas species can form aggregates/biofilms in water and can cause particular problems in water distribution systems. The aim of this study was to evaluate the effectiveness of photodynamic inactivation in killing a range of planktonic cells including Escherichia coli DSM 1103, Staphylococcus aureus DSM 799, Shigella sonnei DSM 5570, Salmonella enterica and Pseudomonas putida DSM 6125, and aggregating cells of Pseudomonas fluorescens DSM 50090, Pseudomonas aeruginosa PAO1. The experiments were performed in glass Petri dishes, containing the bacterial suspension and the photosensitiser, irradiated with a multi-LED (wavelengths 430nm and 660nm) for different time intervals. The responses of the cells were monitored using the pour plate technique and confocal microscopy. The study showed that bacteria belonging to Pseudomonads group tend to be more tolerant to PDI. While E. coli, S. aureus, S. sonnei and S. enterica required a dosage ranging from 39.47 J/cm2 to 59.21 J/cm2 for a 5 log reduction, Pseudomonads needed a dosage ranging from 78.94 to 118.42 J/cm2, a higher dose being required when the cells aggregated. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=bacterial%20aggregation" title="bacterial aggregation">bacterial aggregation</a>, <a href="https://publications.waset.org/abstracts/search?q=photoinactivation" title=" photoinactivation"> photoinactivation</a>, <a href="https://publications.waset.org/abstracts/search?q=Pseudomonads" title=" Pseudomonads"> Pseudomonads</a>, <a href="https://publications.waset.org/abstracts/search?q=water%20disinfection" title=" water disinfection"> water disinfection</a> </p> <a href="https://publications.waset.org/abstracts/68848/response-of-planktonic-and-aggregated-bacterial-cells-to-water-disinfection-with-photodynamic-inactivation" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/68848.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">296</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">2</span> Studies on the Bioactivity of Different Solvents Extracts of Selected Marine Macroalgae against Fish Pathogens</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Mary%20Ghobrial">Mary Ghobrial</a>, <a href="https://publications.waset.org/abstracts/search?q=Sahar%20Wefky"> Sahar Wefky</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Marine macroalgae have proven to be rich source of bioactive compounds with biomedical potential, not only for human but also for veterinary medicine. Emergence of microbial disease in aquaculture industries implies serious loses. Usage of commercial antibiotics for fish disease treatment produces undesirable side effects. Marine organisms are a rich source of structurally novel biologically active metabolites. Competition for space and nutrients led to the evolution of antimicrobial defense strategies in the aquatic environment. The interest in marine organisms as a potential and promising source of pharmaceutical agents has increased in the last years. Many bioactive and pharmacologically active substances have been isolated from microalgae. Compounds with antibacterial, antifungal and antiviral activities have been also detected in green, brown and red algae. Selected species of marine benthic algae belonging to the Phaeophyta and Rhodophyta, collected from different coastal areas of Alexandria (Egypt), were investigated for their antibacterial and antifungal, activities. Macroalgae samples were collected during low tide from the Alexandria Mediterranean coast. Samples were air dried under shade at room temperature. The dry algae were ground, using electric mixer grinder. They were soaked in 10 ml of each of the solvents acetone, ethanol, methanol and hexane. Antimicrobial activity was evaluated using well-cut diffusion technique In vitro screening of organic solvent extracts from the marine macroalgae Laurencia pinnatifida, Pterocladia capillaceae, Stepopodium zonale, Halopteris scoparia and Sargassum hystrix, showed specific activity in inhibiting the growth of five virulent strains of bacteria pathogenic to fish Pseudomonas fluorescens, Aeromonas hydrophila, Vibrio anguillarum, V. tandara, Escherichia coli and two fungi Aspergillus flavus and A. niger. Results showed that, acetone and ethanol extracts of all test macroalgae exhibited antibacterial activity, while acetone extract of the brown Sargassum hystrix displayed the highest antifungal activity. The extracts of seaweeds inhibited bacteria more strongly than fungi and species of the Rhodophyta showed the greatest activity against the bacteria rather than fungi tested. The gas liquid chromatography coupled with mass spectrometry detection technique allows good qualitative and quantitative analysis of the fractionated extracts with high sensitivity to the smaller amounts of components. Results indicated that, the main common component in the acetone extracts of L. pinnatifida and P. capillacea is 4-hydroxy-4-methyl2-pentanone representing 64.38 and 58.60%. Thus, the extracts derived from the red macroalgae were more efficient than those obtained from the brown macroalgae in combating bacterial pathogens rather than pathogenic fungi. The most preferred species over all was the red Laurencia pinnatifida. In conclusion, the present study provides the potential of red and brown macroalgae extracts for development of anti-pathogenic agents for use in fish aquaculture. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=bacteria" title="bacteria">bacteria</a>, <a href="https://publications.waset.org/abstracts/search?q=fungi" title=" fungi"> fungi</a>, <a href="https://publications.waset.org/abstracts/search?q=extracts" title=" extracts"> extracts</a>, <a href="https://publications.waset.org/abstracts/search?q=solvents" title=" solvents"> solvents</a> </p> <a href="https://publications.waset.org/abstracts/41755/studies-on-the-bioactivity-of-different-solvents-extracts-of-selected-marine-macroalgae-against-fish-pathogens" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/41755.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">437</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">1</span> Edible Active Antimicrobial Coatings onto Plastic-Based Laminates and Its Performance Assessment on the Shelf Life of Vacuum Packaged Beef Steaks</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Andrey%20A.%20Tyuftin">Andrey A. Tyuftin</a>, <a href="https://publications.waset.org/abstracts/search?q=David%20Clarke"> David Clarke</a>, <a href="https://publications.waset.org/abstracts/search?q=Malco%20C.%20Cruz-Romero"> Malco C. Cruz-Romero</a>, <a href="https://publications.waset.org/abstracts/search?q=Declan%20Bolton"> Declan Bolton</a>, <a href="https://publications.waset.org/abstracts/search?q=Seamus%20Fanning"> Seamus Fanning</a>, <a href="https://publications.waset.org/abstracts/search?q=Shashi%20K.%20Pankaj"> Shashi K. Pankaj</a>, <a href="https://publications.waset.org/abstracts/search?q=Carmen%20Bueno-Ferrer"> Carmen Bueno-Ferrer</a>, <a href="https://publications.waset.org/abstracts/search?q=Patrick%20J.%20Cullen"> Patrick J. Cullen</a>, <a href="https://publications.waset.org/abstracts/search?q=Joe%20P.%20Kerry"> Joe P. Kerry</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Prolonging of shelf-life is essential in order to address issues such as; supplier demands across continents, economical profit, customer satisfaction, and reduction of food wastage. Smart packaging solutions presented in the form of naturally occurred antimicrobially-active packaging may be a solution to these and other issues. Gelatin film forming solution with adding of natural sourced antimicrobials is a promising tool for the active smart packaging. The objective of this study was to coat conventional plastic hydrophobic packaging material with hydrophilic antimicrobial active beef gelatin coating and conduct shelf life trials on beef sub-primal cuts. Minimal inhibition concentration (MIC) of Caprylic acid sodium salt (SO) and commercially available Auranta FV (AFV) (bitter oranges extract with mixture of nutritive organic acids) were found of 1 and 1.5 % respectively against bacterial strains Bacillus cereus, Pseudomonas fluorescens, Escherichia coli, Staphylococcus aureus and aerobic and anaerobic beef microflora. Therefore SO or AFV were incorporated in beef gelatin film forming solution in concentration of two times of MIC which was coated on a conventional plastic LDPE/PA film on the inner cold plasma treated polyethylene surface. Beef samples were vacuum packed in this material and stored under chilling conditions, sampled at weekly intervals during 42 days shelf life study. No significant differences (p < 0.05) in the cook loss was observed among the different treatments compared to control samples until the day 29. Only for AFV coated beef sample it was 3% higher (37.3%) than the control (34.4 %) on the day 36. It was found antimicrobial films did not protect beef against discoloration. SO containing packages significantly (p < 0.05) reduced Total viable bacterial counts (TVC) compared to the control and AFV samples until the day 35. No significant reduction in TVC was observed between SO and AFV films on the day 42 but a significant difference was observed compared to control samples with a 1.40 log of bacteria reduction on the day 42. AFV films significantly (p < 0.05) reduced TVC compared to control samples from the day 14 until the day 42. Control samples reached the set value of 7 log CFU/g on day 27 of testing, AFV films did not reach this set limit until day 35 and SO films until day 42 of testing. The antimicrobial AFV and SO coated films significantly prolonged the shelf-life of beef steaks by 33 or 55% (on 7 and 14 days respectively) compared to control film samples. It is concluded antimicrobial coated films were successfully developed by coating the inner polyethylene layer of conventional LDPE/PA laminated films after plasma surface treatment. The results indicated that the use of antimicrobial active packaging coated with SO or AFV increased significantly (p < 0.05) the shelf life of the beef sub-primal. Overall, AFV or SO containing gelatin coatings have the potential of being used as effective antimicrobials for active packaging applications for muscle-based food products. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=active%20packaging" title="active packaging">active packaging</a>, <a href="https://publications.waset.org/abstracts/search?q=antimicrobials" title=" antimicrobials"> antimicrobials</a>, <a href="https://publications.waset.org/abstracts/search?q=edible%20coatings" title=" edible coatings"> edible coatings</a>, <a href="https://publications.waset.org/abstracts/search?q=food%20packaging" title=" food packaging"> food packaging</a>, <a href="https://publications.waset.org/abstracts/search?q=gelatin%20films" title=" gelatin films"> gelatin films</a>, <a href="https://publications.waset.org/abstracts/search?q=meat%20science" title=" meat science"> meat science</a> </p> <a href="https://publications.waset.org/abstracts/51243/edible-active-antimicrobial-coatings-onto-plastic-based-laminates-and-its-performance-assessment-on-the-shelf-life-of-vacuum-packaged-beef-steaks" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/51243.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">303</span> </span> </div> </div> </div> </main> <footer> <div id="infolinks" class="pt-3 pb-2"> <div class="container"> <div style="background-color:#f5f5f5;" class="p-3"> <div class="row"> <div class="col-md-2"> <ul class="list-unstyled"> About <li><a href="https://waset.org/page/support">About Us</a></li> <li><a href="https://waset.org/page/support#legal-information">Legal</a></li> <li><a target="_blank" rel="nofollow" href="https://publications.waset.org/static/files/WASET-16th-foundational-anniversary.pdf">WASET celebrates 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