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putida</title> <meta name="description" content="Search results for: pseudomonas putida"> <meta name="keywords" content="pseudomonas putida"> <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 class="d-block d-lg-none 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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="pseudomonas putida"> <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> 323</div> </div> </div> </div> <h1 class="mt-3 mb-3 text-center" style="font-size:1.6rem;">Search results for: pseudomonas putida</h1> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">323</span> Optimization Studies on Biosorption of Ni(II) and Cd(II) from Wastewater Using Pseudomonas putida in a Packed Bed Bioreactor </h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=K.Narasimhulu">K.Narasimhulu</a>, <a href="https://publications.waset.org/abstracts/search?q=Y.%20Pydi%20Setty">Y. Pydi Setty</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The objective of this present study is the optimization of process parameters in biosorption of Ni(II) and Cd(II) ions by Pseudomonas putida using Response Surface Methodology in a Packed bed bioreactor. The experimental data were also tested with theoretical models to find the best fit model. The present paper elucidates RSM as an efficient approach for predictive model building and optimization of Ni(II) and Cd(II) ions using Pseudomonas putida. In packed bed biosorption studies, comparison of the breakthrough curves of Ni(II) and Cd(II) for Agar immobilized and PAA immobilized Pseudomonas putida at optimum conditions of flow rate of 300 mL/h, initial metal ion concentration of 100 mg/L and bed height of 20 cm with weight of biosorbent of 12 g, it was found that the Agar immobilized Pseudomonas putida showed maximum percent biosorption and bed saturation occurred at 20 minutes. Optimization results of Ni(II) and Cd(II) by Pseudomonas putida from the Design Expert software were obtained as bed height of 19.93 cm, initial metal ion concentration of 103.85 mg/L, and flow rate of 310.57 mL/h. The percent biosorption of Ni(II) and Cd(II) is 87.2% and 88.2% respectively. The predicted optimized parameters are in agreement with the experimental results. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=packed%20bed%20bioreactor" title="packed bed bioreactor">packed bed bioreactor</a>, <a href="https://publications.waset.org/abstracts/search?q=response%20surface%20mthodology" title=" response surface mthodology"> response surface mthodology</a>, <a href="https://publications.waset.org/abstracts/search?q=pseudomonas%20putida" title=" pseudomonas putida"> pseudomonas putida</a>, <a href="https://publications.waset.org/abstracts/search?q=biosorption" title=" biosorption"> biosorption</a>, <a href="https://publications.waset.org/abstracts/search?q=waste%20water" title=" waste water"> waste water</a> </p> <a href="https://publications.waset.org/abstracts/16551/optimization-studies-on-biosorption-of-niii-and-cdii-from-wastewater-using-pseudomonas-putida-in-a-packed-bed-bioreactor" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/16551.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">452</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">322</span> Decoloriation of Rhodamine-B Dye by Pseudomonas putida on Activated Carbon</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=U.%20K.%20Ghosh">U. K. Ghosh</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20Ullhyan"> A. Ullhyan</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Activated carbon prepared from mustard stalk was applied to decolorize Rhodamine-B dye bearing synthetic wastewater by simple adsorption and simultaneous adsorption and biodegradation (SAB) using Pseudomonas putida MTCC 1194. Results showed that percentage of Rhodamine-B dye removal was 82% for adsorption and 99.3% for SAB at pH 6.5, adsorbent dose 10 g/L and temperature 32ºC. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=activated%20carbon" title="activated carbon">activated carbon</a>, <a href="https://publications.waset.org/abstracts/search?q=mustard%20stalk" title=" mustard stalk"> mustard stalk</a>, <a href="https://publications.waset.org/abstracts/search?q=Rhodamine-B" title=" Rhodamine-B"> Rhodamine-B</a>, <a href="https://publications.waset.org/abstracts/search?q=adsorption" title=" adsorption"> adsorption</a>, <a href="https://publications.waset.org/abstracts/search?q=SAB" title=" SAB"> SAB</a>, <a href="https://publications.waset.org/abstracts/search?q=Pseudomonas%20putida" title=" Pseudomonas putida"> Pseudomonas putida</a> </p> <a href="https://publications.waset.org/abstracts/25637/decoloriation-of-rhodamine-b-dye-by-pseudomonas-putida-on-activated-carbon" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/25637.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">360</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">321</span> Assessing Storage of Stability and Mercury Reduction of Freeze-Dried Pseudomonas putida within Different Types of Lyoprotectant</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=A.%20A.%20M.%20Azoddein">A. A. M. Azoddein</a>, <a href="https://publications.waset.org/abstracts/search?q=Y.%20Nuratri"> Y. Nuratri</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20B.%20Bustary"> A. B. Bustary</a>, <a href="https://publications.waset.org/abstracts/search?q=F.%20A.%20M.%20Azli"> F. A. M. Azli</a>, <a href="https://publications.waset.org/abstracts/search?q=S.%20C.%20Sayuti"> S. C. Sayuti</a> </p> <p class="card-text"><strong>Abstract:</strong></p> <em>Pseudomonas putida</em> is a potential strain in biological treatment to remove mercury contained in the effluent of petrochemical industry due to its mercury reductase enzyme that able to reduce ionic mercury to elementary mercury. Freeze-dried <em>P. putida </em>allows easy, inexpensive shipping, handling and high stability of the product. This study was aimed to freeze dry <em>P. putida </em>cells with addition of lyoprotectant. Lyoprotectant was added into the cells suspension prior to freezing. Dried <em>P. putida </em>obtained was then mixed with synthetic mercury. Viability of recovery <em>P. putida</em> after freeze dry was significantly influenced by the type of lyoprotectant. Among the lyoprotectants, tween 80/ sucrose was found to be the best lyoprotectant. Sucrose able to recover more than 78% (6.2E+09 CFU/ml) of the original cells (7.90E+09CFU/ml) after freeze dry and able to retain 5.40E+05 viable cells after 4 weeks storage in 4oC without vacuum. Polyethylene glycol (PEG) pre-treated freeze dry cells and broth pre-treated freeze dry cells after freeze-dry recovered more than 64% (5.0 E+09CFU/ml) and >0.1% (5.60E+07CFU/ml). Freeze-dried <em>P. putida</em> cells in PEG and broth cannot survive after 4 weeks storage. Freeze dry also does not really change the pattern of growth <em>P. putida</em> but extension of lag time was found 1 hour after 3 weeks of storage. Additional time was required for freeze-dried <em>P. putida</em> cells to recover before introduce freeze-dried cells to more complicated condition such as mercury solution. The maximum mercury reduction of PEG pre-treated freeze-dried cells after freeze dry and after storage 3 weeks was 56.78% and 17.91%. The maximum of mercury reduction of tween 80/sucrose pre-treated freeze-dried cells after freeze dry and after storage 3 weeks were 26.35% and 25.03%. Freeze dried <em>P. putida</em> was found to have lower mercury reduction compare to the fresh <em>P. putida</em> that has been growth in agar. Result from this study may be beneficial and useful as initial reference before commercialize freeze-dried <em>P. putida</em>. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Pseudomonas%20putida" title="Pseudomonas putida">Pseudomonas putida</a>, <a href="https://publications.waset.org/abstracts/search?q=freeze-dry" title=" freeze-dry"> freeze-dry</a>, <a href="https://publications.waset.org/abstracts/search?q=PEG" title=" PEG"> PEG</a>, <a href="https://publications.waset.org/abstracts/search?q=tween80%2FSucrose" title=" tween80/Sucrose"> tween80/Sucrose</a>, <a href="https://publications.waset.org/abstracts/search?q=mercury" title=" mercury"> mercury</a>, <a href="https://publications.waset.org/abstracts/search?q=cell%20viability" title=" cell viability"> cell viability</a> </p> <a href="https://publications.waset.org/abstracts/38542/assessing-storage-of-stability-and-mercury-reduction-of-freeze-dried-pseudomonas-putida-within-different-types-of-lyoprotectant" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/38542.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">355</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">320</span> Mercury Removal Using Pseudomonas putida (ATTC 49128): Effect of Acclimatization Time, Speed, and Temperature of Incubator Shaker</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=A.%20A.%20M.%20Azoddein">A. A. M. Azoddein</a>, <a href="https://publications.waset.org/abstracts/search?q=R.%20M.%20Yunus"> R. M. Yunus</a>, <a href="https://publications.waset.org/abstracts/search?q=N.%20M.%20Sulaiman"> N. M. Sulaiman</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20B.%20Bustary"> A. B. Bustary</a>, <a href="https://publications.waset.org/abstracts/search?q=K.%20Sabar"> K. Sabar</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Microbes have been used to solve environmental problems for many years. The use microorganism to sequester, precipitate or alter the oxidation state of various heavy metals has been extensively studied. Processes by which microorganism interacts with toxic metal are very diverse. The purpose of this research is to remove the mercury using Pseudomonas putida, pure culture ATTC 49128 at optimum growth parameters such as techniques of culture, acclimatization time and speed of incubator shaker. Thus, in this study, the optimum growth parameters of P.putida were obtained to achieve the maximum of mercury removal. Based on the optimum parameters of Pseudomonas putida for specific growth rate, the removal of two different mercury concentration, 1 ppm and 4 ppm were studied. A mercury-resistant bacterial strain which is able to reduce ionic mercury to metallic mercury was used to reduce ionic mercury from mercury nitrate solution. The overall levels of mercury removal in this study were between 80% and 90%. The information obtained in this study is of fundamental for understanding of the survival of P.putida ATTC 49128 in mercury solution. Thus, microbial mercury environmental pollutants removal is a potential biological treatment for waste water treatment especially in petrochemical industries in Malaysia. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Pseudomonas%20putida" title="Pseudomonas putida">Pseudomonas putida</a>, <a href="https://publications.waset.org/abstracts/search?q=growth%20kinetic" title=" growth kinetic"> growth kinetic</a>, <a href="https://publications.waset.org/abstracts/search?q=biosorption" title=" biosorption"> biosorption</a>, <a href="https://publications.waset.org/abstracts/search?q=mercury" title=" mercury"> mercury</a>, <a href="https://publications.waset.org/abstracts/search?q=petrochemical%20waste%20water" title=" petrochemical waste water"> petrochemical waste water</a> </p> <a href="https://publications.waset.org/abstracts/19360/mercury-removal-using-pseudomonas-putida-attc-49128-effect-of-acclimatization-time-speed-and-temperature-of-incubator-shaker" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/19360.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">667</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">319</span> Antifungal Potential of the Plant Growth-Promoting Rhizobacteria Infecting Kidney Beans</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Zhazira%20Shemsheyeva">Zhazira Shemsheyeva</a>, <a href="https://publications.waset.org/abstracts/search?q=Zhanara%20Suleimenova"> Zhanara Suleimenova</a>, <a href="https://publications.waset.org/abstracts/search?q=Olga%20Shemshura"> Olga Shemshura</a>, <a href="https://publications.waset.org/abstracts/search?q=Gulnaz%20Mombekova"> Gulnaz Mombekova</a>, <a href="https://publications.waset.org/abstracts/search?q=Zhanar%20Rakhmetova"> Zhanar Rakhmetova</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Bacteria that colonize plant roots and promote plant growth are referred to as plant growth-promoting rhizobacteria (PGPR). They not only provide nutrients to the plants (direct plant growth promotion) and protect plants against the phytopathogens (indirect plant growth promotion) but also increase the soil fertility. Indirectly PGPRs improve the plant growth by becoming a biocontrol agent for a fungal pathogen. The antifungal activities of the PGPrhizobacteria were assayed against different species of phytopathogenic fungi such as Fusarium tricinctum, Fusarium oxysporum, Sclerotiniasclerotiorum, and Botrytis cinerea. Pseudomonas putidaSM-1, Azotobacter sp., and Bacillus thuringiensis AKS/16 strains have been used in experimental tests on growth inhibition of phytopathogenic fungi infecting Kidney beans. Agar well diffusion method was used in this study. Diameters of the zones of inhibition were measured in millimeters. It was found that Bacillus thuringiensis AKS/16 strain showed the lowest antifungal activity against all fungal pathogens tested. Zones of inhibition were 15-18 mm. In contrast, Pseudomonas putida SM-1 exhibited good antifungal activity against Fusarium oxysporum and Fusarium tricinctum by producing 29-30 mm clear zones of inhibition. The moderate inhibitory effect was shown by Azotobacter sp. against all fungal pathogens tested with zones of inhibition from24 to 26 mm. In summary, Pseudomonas putida SM-1 strain demonstrated the potential of controlling root rot diseases in kidney beans. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=PGPR" title="PGPR">PGPR</a>, <a href="https://publications.waset.org/abstracts/search?q=pseudomonas%20putida" title=" pseudomonas putida"> pseudomonas putida</a>, <a href="https://publications.waset.org/abstracts/search?q=kindey%20beans" title=" kindey beans"> kindey beans</a>, <a href="https://publications.waset.org/abstracts/search?q=antifungal%20activity" title=" antifungal activity "> antifungal activity </a> </p> <a href="https://publications.waset.org/abstracts/120943/antifungal-potential-of-the-plant-growth-promoting-rhizobacteria-infecting-kidney-beans" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/120943.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">154</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">318</span> Biological Treatment of Tannery Wastewater Using Pseudomonas Strains</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=A.%20Benhadji">A. Benhadji</a>, <a href="https://publications.waset.org/abstracts/search?q=R.%20Maachi"> R. Maachi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Environmental protection has become a major economic development issues. Indeed, the environment has become both market growth factor and element of competition. It is now an integral part of all industrial strategies. Ecosystem protection is based on the reduction of the pollution load in the treatment of liquid waste. The physicochemical techniques are commonly used which a transfer of pollution is generally found. Alternative to physicochemical methods is the use of microorganisms for cleaning up the waste waters. The objective of this research is the evaluation of the effects of exogenous added Pseudomonas strains on pollutants biodegradation. The influence of the critical parameters such as inoculums concentration and duration treatment are studied. The results show that Pseudomonas putida is found to give a maximum reduction in chemical organic demand (COD) in 4 days of incubation. However, toward to protect biological pollution of environment, the treatment is achieved by electro coagulation process using aluminium electrodes. The results indicate that this process allows disinfecting the water and improving the electro coagulated sludge quality. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=tannery" title="tannery">tannery</a>, <a href="https://publications.waset.org/abstracts/search?q=pseudomonas" title=" pseudomonas"> pseudomonas</a>, <a href="https://publications.waset.org/abstracts/search?q=biological%20treatment" title=" biological treatment"> biological treatment</a>, <a href="https://publications.waset.org/abstracts/search?q=electrocoagulation%20process" title=" electrocoagulation process"> electrocoagulation process</a>, <a href="https://publications.waset.org/abstracts/search?q=sludge%20quality" title=" sludge quality"> sludge quality</a> </p> <a href="https://publications.waset.org/abstracts/26978/biological-treatment-of-tannery-wastewater-using-pseudomonas-strains" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/26978.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">368</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">317</span> Bioremediation as a Treatment of Aromatic Hydrocarbons in Wastewater</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Hen%20Friman">Hen Friman</a>, <a href="https://publications.waset.org/abstracts/search?q=Alex%20Schechter"> Alex Schechter</a>, <a href="https://publications.waset.org/abstracts/search?q=Yeshayahu%20Nitzan"> Yeshayahu Nitzan</a>, <a href="https://publications.waset.org/abstracts/search?q=Rivka%20Cahan"> Rivka Cahan</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The treatment of aromatic hydrocarbons in wastewater resulting from oil spills and chemical manufactories is becoming a key concern in many modern countries. Benzene, ethylbenzene, toluene and xylene (BETX) contaminate groundwater as well as soil. These compounds have an acute effect on human health and are known to be carcinogenic. Conventional removal of these toxic materials involves separation and burning of the wastes, however, the cost of chemical treatment is very high and energy consuming. Bioremediation methods for removal of toxic organic compounds constitute an attractive alternative to the conventional chemical or physical techniques. Bioremediation methods use microorganisms to reduce the concentration and toxicity of various chemical pollutants Toluene is biodegradable both aerobically and anaerobically, it can be growth inhibitory to microorganisms at elevated concentrations, even to those species that can use it as a substrate. In this research culture of Pseudomonas putida was grown in bath bio-reactor (BBR) with toluene 100 mg/l as a single carbon source under constant voltage of 125 mV, 250 mV and 500 mV. The culture grown in BBR reached to 0.8 OD660nm while the control culture that grown without external voltage reached only to 0.6 OD660nm. The residual toluene concentration after 147 h, in the BBR operated under external voltage (125 mV) was 22 % on average, while in the control BBR it was 81 % on average. <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=aromatic%20hydrocarbons" title=" aromatic hydrocarbons"> aromatic hydrocarbons</a>, <a href="https://publications.waset.org/abstracts/search?q=BETX" title=" BETX"> BETX</a>, <a href="https://publications.waset.org/abstracts/search?q=toluene" title=" toluene"> toluene</a>, <a href="https://publications.waset.org/abstracts/search?q=pseudomonas%20putida" title=" pseudomonas putida"> pseudomonas putida</a> </p> <a href="https://publications.waset.org/abstracts/38419/bioremediation-as-a-treatment-of-aromatic-hydrocarbons-in-wastewater" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/38419.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">316</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">316</span> Removal of Heavy Metals Pb, Zn and Cu from Sludge Waste of Paper Industries Using Biosurfactant</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Nurul%20Hidayati">Nurul Hidayati</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Increasing public awareness of environmental pollution influences the search and development of technologies that help in clean up of organic and inorganic contaminants such as metals. Sludge waste of paper industries as toxic and hazardous material from specific source contains Pb, Zn, and Cu metal from waste soluble ink. An alternative and eco-friendly method of remediation technology is the use of biosurfactants and biosurfactant-producing microorganisms. Soil washing is among the methods available to remove heavy metal from sediments. The purpose of this research is to study effectiveness of biosurfactant with concentration = CMC for the removal of heavy metals, lead, zinc and copper in batch washing test under four different biosurfactant production by microbial origin. Pseudomonas putida T1(8), Bacillus subtilis 3K, Acinetobacter sp, and Actinobacillus sp was grown on mineral salt medium that had been already added with 2% concentration of molasses that it is a low cost application. The samples were kept in a shaker 120 rpm at room temperature for 3 days. Supernatants and sediments of sludge were separated by using a centrifuge and samples from supernatants were measured by atomic absorption spectrophotometer. The highest removal of Pb was up to 14,04% by Acinetobacter sp. Biosurfactant of Pseudomonas putida T1(8) have the highest removal for Zn and Cu up to 6,5% and 2,01% respectively. Biosurfactants have a role for removal process of the metals, including wetting, contact of biosurfactant to the surface of the sediments and detachment of the metals from the sediment. Biosurfactant has proven its ability as a washing agent in heavy metals removal from sediments, but more research is needed to optimize the process of removal heavy metals. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=biosurfactant" title="biosurfactant">biosurfactant</a>, <a href="https://publications.waset.org/abstracts/search?q=removal%20of%20heavy%20metals" title=" removal of heavy metals"> removal of heavy metals</a>, <a href="https://publications.waset.org/abstracts/search?q=sludge%20waste" title=" sludge waste"> sludge waste</a>, <a href="https://publications.waset.org/abstracts/search?q=paper%20industries" title=" paper industries"> paper industries</a> </p> <a href="https://publications.waset.org/abstracts/15107/removal-of-heavy-metals-pb-zn-and-cu-from-sludge-waste-of-paper-industries-using-biosurfactant" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/15107.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">331</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">315</span> Effect of Chemical Mutagen on Seeds Germination of Lima Bean</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=G.%20Ultanbekova">G. Ultanbekova</a>, <a href="https://publications.waset.org/abstracts/search?q=Zh.%20Suleimenova"> Zh. Suleimenova</a>, <a href="https://publications.waset.org/abstracts/search?q=Zh.%20Rakhmetova"> Zh. Rakhmetova</a>, <a href="https://publications.waset.org/abstracts/search?q=G.%20Mombekova"> G. Mombekova</a>, <a href="https://publications.waset.org/abstracts/search?q=S.%20Mantieva"> S. Mantieva</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Plant Growth Promoting Rhizobacteria (PGPR) are a group of free-living bacteria that colonize the rhizosphere, enhance plant growth of many cereals and other important agricultural crops and protect plants from disease and abiotic stresses through a wide variety of mechanisms. The use of PGPR has been proven to be an environmentally sound way of increasing crop yields by facilitating plant growth. In the present study, strain improvement of PGPR isolates were carried out by chemical mutagenesis for the improvement of growth and yield of lima bean. Induced mutagenesis is widely used for the selection of microorganisms producing biologically active substances and further improving their activities. Strain improvement is usually done by classical mutagenesis which involves exposing the microbes to chemical or physical mutagens. The strains of Pseudomonas putida 4/1, Azotobacter chroococcum Р-29 and Bacillus subtilis were subjected to mutation process for strain improvement by treatment with a chemical agent (sodium nitrite) to cause mutation and were observed for its consequent action on the seeds germination and plant growth of lima bean (Phaseolus lunatus). Bacterial mutant strains of Pseudomonas putida M-1, Azotobacter chroococcum M-1 and Bacillus subtilis M-1, treated with sodium nitrite in the concentration of 5 mg/ml for 120 min, were found effective to enhance the germination of lima bean seeds compared to parent strains. Moreover, treatment of the lima bean seeds with a mutant strain of Bacillus subtilis M-1 had a significant stimulation effect on plant growth. The length of the stems and roots of lima bean treated with Bacillus subtilis M-1 increased significantly in comparison with parent strain in 1.6 and 1.3 times, respectively. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=chemical%20mutagenesis" title="chemical mutagenesis">chemical mutagenesis</a>, <a href="https://publications.waset.org/abstracts/search?q=germination" title=" germination"> germination</a>, <a href="https://publications.waset.org/abstracts/search?q=kidney%20bean" title=" kidney bean"> kidney bean</a>, <a href="https://publications.waset.org/abstracts/search?q=plant%20growth%20promoting%20rhizobacteria%20%28PGPR%29" title=" plant growth promoting rhizobacteria (PGPR)"> plant growth promoting rhizobacteria (PGPR)</a> </p> <a href="https://publications.waset.org/abstracts/100013/effect-of-chemical-mutagen-on-seeds-germination-of-lima-bean" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/100013.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">198</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">314</span> Al₂O₃ Nano-Particles Impact on Pseudomonas Putida Gene Expression: Implications for Environmental Risk</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Nina%20Doskocz">Nina Doskocz</a>, <a href="https://publications.waset.org/abstracts/search?q=Katarzyna%20Affek"> Katarzyna Affek</a>, <a href="https://publications.waset.org/abstracts/search?q=Magdalena%20Matczuk"> Magdalena Matczuk</a>, <a href="https://publications.waset.org/abstracts/search?q=Monika%20Za%C5%82%C4%99ska-Radziwi%C5%82%C5%82"> Monika Załęska-Radziwiłł</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Wastewater treatment is a critical environmental issue, especially in the face of increasing urbanization and industrialization. One of the emerging issues related to wastewater is the presence of nanoparticles (NPs) - tiny particles with dimensions measured in nanometers. These nanoparticles are widely used in various industries, including medicine, electronics, and consumer products. With technological advances, NPs are increasingly finding their way into water and wastewater systems, posing new environmental challenges that require urgent research and regulation. Therefore, research on the impact of nanoparticles on wastewater treatment processes is critical to protect environmental health and ensure sustainable development in the face of advancing nanotechnology. Traditional ecotoxicological tests are often inadequate for routine analysis as they do not provide insight into the mechanisms of toxicity of these compounds. The development of (geno)toxicity biomarkers for nanoparticles will greatly aid in the rapid assessment and prediction of the effects of current and emerging nanomaterials on various organisms. However, despite growing interest in gene expression responses to nanoparticle-induced stress, the toxic mechanisms of action and defense responses against nanoparticle toxicity remain poorly understood. The aim of our research was to investigate the expression of several molecular biomarkers related to essential cellular functions - such as oxidative stress, xenobiotic detoxification, and mitochondrial electron transport - in Pseudomonas putida in response to Al₂O₃ nanoparticles found in wastewater, both before and after biological treatment, as well as in their native form. Real-time PCR (qPCR) was used to assess gene expression changes after 1 hour and 16 hours of exposure to Al₂O₃ NPs and wastewater containing these nanoparticles, both before and after biological treatment. In addition, gene expression measurements were performed on P. putida in the presence of bulk Al₂O₃ (pristine and in wastewater). The results showed increased expression of ahpC, katE and ctaD genes, indicating oxidative stress, increased detoxification capacity and impaired mitochondrial function. Both untreated and treated wastewater containing nanoparticles caused significant changes in gene expression, demonstrating the persistent bioactivity and potential toxicity of these nanoparticles. Nanoparticles exhibited greater reactivity and bioavailability compared to their bulk counterparts. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=nanoparticles" title="nanoparticles">nanoparticles</a>, <a href="https://publications.waset.org/abstracts/search?q=wastewater" title=" wastewater"> wastewater</a>, <a href="https://publications.waset.org/abstracts/search?q=gene%20expression" title=" gene expression"> gene expression</a>, <a href="https://publications.waset.org/abstracts/search?q=qPCR" title=" qPCR"> qPCR</a> </p> <a href="https://publications.waset.org/abstracts/191056/al2o3-nano-particles-impact-on-pseudomonas-putida-gene-expression-implications-for-environmental-risk" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/191056.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">17</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">313</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">312</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">311</span> Response of Canola Traits to Integrated Fertilization Systems</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Khosro%20Mohammadi">Khosro Mohammadi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In order to study the effect of different resources of farmyard manure, compost and biofertilizers on grain yield and quality of canola (Talaieh cultivar), an experiment was conducted at Kurdistan region. Experimental units were arranged in split-split plots design based on randomized complete blocks with three replications. Main plots consisted of two locations with difference in soil texture (L1): Agricultural Research Center of Sanandaj and (L2): Islamic Azad University of Sanandaj, as location levels. Also, five strategies for obtaining the base fertilizer requirement including (N1): farmyard manure; (N2): compost; (N3): chemical fertilizers; (N4): farm yard manure + compost and (N5): farm yard manure + compost + chemical fertilizers were considered in split plots. Four levels of biofertilizers were (B1): Bacillus lentus and Pseudomonas putida; (B2): Trichoderma harzianum; (B3): Bacillus lentus and Pseudomonas putida & Trichoderma harzianum; and (B4): control. Results showed that location, different resources of fertilizer and interactions of them have a significant effect on grain yield. The highest grain yield (4660 kg/ha) was obtained from treatment, that farmyard manure, compost and biofertilizers were co application in clay loam soil (Gerizeh station). Different methods of fertilization have a significant effect on leaf chlorophyll. Highest amount of chlorophyll (38 Spad) was obtained from co application of farmyard manure, chemical fertilizers and compost (N5 treatment). Location, basal fertilizers and biofertilizers have a significant effect on N, S and N/S of canola seed. Oil content was decreased in Gerizeh station, but oil yield had a significant increasing than Azad University station. Co application of compost and farmyard manure produced highest percent of oleic acid (61.5 %) and linoleic acid (22.9 %). Co application of compost and farmyard manure has a significant increase in oleic acid and linoleic acid. Finally, L1N5B3 treatment, that compost, farmyard manure and biofertilizers were co application in Gerizeh station in compare to other treatments, selected as a best treatment of experiment. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=soil%20texture" title="soil texture">soil texture</a>, <a href="https://publications.waset.org/abstracts/search?q=organic%20fertilizer" title=" organic fertilizer"> organic fertilizer</a>, <a href="https://publications.waset.org/abstracts/search?q=chemical%20fertilizer" title=" chemical fertilizer"> chemical fertilizer</a>, <a href="https://publications.waset.org/abstracts/search?q=oil" title=" oil"> oil</a>, <a href="https://publications.waset.org/abstracts/search?q=Canola" title=" Canola"> Canola</a> </p> <a href="https://publications.waset.org/abstracts/27156/response-of-canola-traits-to-integrated-fertilization-systems" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/27156.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">403</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">310</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">309</span> The Role of Ionic Strength and Mineral Size to Zeta Potential for the Adhesion of P. putida to Mineral Surfaces</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Fathiah%20Mohamed%20Zuki">Fathiah Mohamed Zuki</a>, <a href="https://publications.waset.org/abstracts/search?q=Robert%20George%20Edyvean"> Robert George Edyvean</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Electrostatic interaction energy (∆EEDL) is a part of the Extended Derjaguin-Landau-Verwey-Overbeek (XDLVO) theory, which, together with van der Waals (∆EVDW) and acid base (∆EAB) interaction energies, has been extensively used to investigate the initial adhesion of bacteria to surfaces. Electrostatic or electrical double layer interaction energy is considerably affected by surface potential, however it cannot be determined experimentally and is usually replaced by zeta (ζ) potential via electrophoretic mobility. This paper focuses on the effect of ionic concentration as a function of pH and the effect of mineral grain size on ζ potential. It was found that both ionic strength and mineral grain size play a major role in determining the value of ζ potential for the adhesion of P. putida to hematite and quartz surfaces. Higher ζ potential values lead to higher electrostatic interaction energies and eventually to higher total XDLVO interaction energy resulting in bacterial repulsion. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=XDLVO" title="XDLVO">XDLVO</a>, <a href="https://publications.waset.org/abstracts/search?q=electrostatic%20interaction%20energy" title=" electrostatic interaction energy"> electrostatic interaction energy</a>, <a href="https://publications.waset.org/abstracts/search?q=zeta%20potential" title=" zeta potential"> zeta potential</a>, <a href="https://publications.waset.org/abstracts/search?q=P.%20putida" title=" P. putida"> P. putida</a>, <a href="https://publications.waset.org/abstracts/search?q=mineral" title=" mineral "> mineral </a> </p> <a href="https://publications.waset.org/abstracts/24721/the-role-of-ionic-strength-and-mineral-size-to-zeta-potential-for-the-adhesion-of-p-putida-to-mineral-surfaces" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/24721.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">446</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">308</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">307</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">306</span> Effect of Different Salts on Pseudomonas taetrolens’ Ability to Lactobionic Acid Production</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=I.%20Sarenkova">I. Sarenkova</a>, <a href="https://publications.waset.org/abstracts/search?q=I.%20Ciprovica"> I. Ciprovica</a>, <a href="https://publications.waset.org/abstracts/search?q=I.%20Cinkmanis"> I. Cinkmanis</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Lactobionic acid is a disaccharide formed from gluconic acid and galactose, and produced by oxidation of lactose. Productivity of lactobionic acid by microbial synthesis can be affected by various factors, and one of them is a presence of potassium, magnesium and manganese ions. In order to extend lactobionic acid production efficiency, it is necessary to increase the yield of lactobionic acid by optimising the fermentation conditions and available substrates for <em>Pseudomonas taetrolens</em> growth. The object of the research was to determinate the application of K<sub>2</sub>HPO<sub>4</sub>, MnSO<sub>4</sub>, MgSO<sub>4</sub> × 7H<sub>2</sub>O salts in different concentration for effective lactose oxidation to lactobionic acid by <em>Pseudomonas taetrolens</em>. <em>Pseudomonas taetrolens</em> NCIB 9396 (NCTC, England) and <em>Pseudomonas taetrolens</em> DSM 21104 (DSMZ, Germany) were used for the study. The acid whey was used as the study object. The content of lactose in whey samples was determined using MilcoScan<sup>TM</sup> Mars (Foss, Denmark) and high performance liquid chromatography (Shimadzu LC 20 Prominence, Japan). The content of lactobionic acid in whey samples was determined using the high performance liquid chromatography. The impact of studied salts differs, Mn<sup>2+</sup> and Mg<sup>2+</sup> ions enhanced fermentation instead of K<sup>+</sup> ions. Results approved that Mn<sup>2+</sup> and Mg<sup>2+ </sup>ions are necessary for <em>Pseudomonas taetrolens</em> growth. The study results will help to improve the effectiveness of lactobionic acid production with <em>Pseudomonas taetrolens</em> NCIB 9396 and DSM 21104. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=lactobionic%20acid" title="lactobionic acid">lactobionic acid</a>, <a href="https://publications.waset.org/abstracts/search?q=lactose%20oxidation" title=" lactose oxidation"> lactose oxidation</a>, <a href="https://publications.waset.org/abstracts/search?q=Pseudomonas%20taetrolens" title=" Pseudomonas taetrolens"> Pseudomonas taetrolens</a>, <a href="https://publications.waset.org/abstracts/search?q=whey" title=" whey"> whey</a> </p> <a href="https://publications.waset.org/abstracts/103914/effect-of-different-salts-on-pseudomonas-taetrolens-ability-to-lactobionic-acid-production" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/103914.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">156</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">305</span> Antibiotic Susceptibility Profile and Horizontal Gene Transfer in Pseudomonas sp. Isolated from Clinical Specimens</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Sadaf%20Ilyas">Sadaf Ilyas</a>, <a href="https://publications.waset.org/abstracts/search?q=Saba%20Riaz"> Saba Riaz</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The extensive use of antibiotics has led to increases emergence of antibiotic-resistant organisms. Pseudomonas is a notorious opportunistic pathogen involoved in nosocomial infections and exhibit innate resistance to many antibiotics. The present study was conducted to assess the prevalence, levels of antimicrobial susceptibility and resistance mechanisms of Pseudomonas. A total of thirty clinical strains of Pseudomonas were isolated from different clinical sites of infection. All clinical specimens were collected from Chughtais Lahore Lab. Jail road, during 8-07-2010 to 11-01-2011. Biochemical characterization was done using routine biochemical tests. Antimicrobial susceptibility was determined by Kirby-Baeur method. The plasmids were isolated from all the strains and digested with restriction enzyme PstI and EcoRI. Transfer of Multi-resistance plasmid was checked via transformation and conjugation to confirm the plasmid mediated resistance to antibiotics. The prevalence of Pseudomonas in clinical specimens was found out to be 14% of all bacterial infections. IPM has shown to be the most effective drug against Pseudomonas followed by CES, PTB and meropenem, wheareas most of the Pseudomonas strains have developed significant resistance against Penicillins and some Cephalasporins. Antibiotic resistance determinants were carried by plasmids, as they conferred resistance to transformed K1 strains. The isolates readily undergo conjugation, transferring the resistant genes to other strains, illustrating the high rates of cross infection and nosocomial infection in the immunocompromised patients. <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=antibiotics" title=" antibiotics"> antibiotics</a>, <a href="https://publications.waset.org/abstracts/search?q=drug%20resistance" title=" drug resistance"> drug resistance</a>, <a href="https://publications.waset.org/abstracts/search?q=horizontal%20gene%20transfer" title=" horizontal gene transfer"> horizontal gene transfer</a> </p> <a href="https://publications.waset.org/abstracts/43006/antibiotic-susceptibility-profile-and-horizontal-gene-transfer-in-pseudomonas-sp-isolated-from-clinical-specimens" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/43006.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">345</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">304</span> Formaldehyde Degradation from Indoor Air by Encapsulated Microbial Cells</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=C.%20C.%20Castro">C. C. Castro</a>, <a href="https://publications.waset.org/abstracts/search?q=T.%20Senechal"> T. Senechal</a>, <a href="https://publications.waset.org/abstracts/search?q=D.%20Lahem"> D. Lahem</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20L.%20Hantson"> A. L. Hantson</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Formaldehyde is one of the most representative volatile organic compounds present in the indoor air of residential units and workplaces. Increased attention has been given to this toxic compound because of its carcinogenic effect in health. Biological or enzymatic transformation is being explored to degrade this pollutant. Pseudomonas putida is a bacteria able to synthesize formaldehyde dehydrogenase, an enzyme known to use formaldehyde as a substrate and transform it into less toxic compounds. The immobilization of bacterial cells in the surface of different supports through spraying or dip-coating is herein proposed. The determination of the enzymatic activity on the coated surfaces was performed as well as the study of its effect on formaldehyde degradation in an isolated chamber. Results show that the incorporation of microbial cells able to synthesize depolluting enzymes can be an innovative, low-cost, effective and environmentally friendly solution for indoor air depollution. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=cells%20encapsulation" title="cells encapsulation">cells encapsulation</a>, <a href="https://publications.waset.org/abstracts/search?q=formaldehyde" title=" formaldehyde"> formaldehyde</a>, <a href="https://publications.waset.org/abstracts/search?q=formaldehyde%20dehydrogenase" title=" formaldehyde dehydrogenase"> formaldehyde dehydrogenase</a>, <a href="https://publications.waset.org/abstracts/search?q=indoor%20air%20depollution" title=" indoor air depollution"> indoor air depollution</a> </p> <a href="https://publications.waset.org/abstracts/98563/formaldehyde-degradation-from-indoor-air-by-encapsulated-microbial-cells" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/98563.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">177</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">303</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">302</span> Production of Biosurfactant by Pseudomonas luteola on a Reject from the Production of Anti-scorpion Serum</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Radia%20Chemlal">Radia Chemlal</a>, <a href="https://publications.waset.org/abstracts/search?q=Youcef%20Hamidi"> Youcef Hamidi</a>, <a href="https://publications.waset.org/abstracts/search?q=Nabil%20Mameri"> Nabil Mameri</a> </p> <p class="card-text"><strong>Abstract:</strong></p> This study deals with the production of biosurfactant by the Pseudomonas luteola strain on three different culture media (semi-synthetic medium M1, whey, and pharmaceutical reject) in the presence of gasoil. The monitoring of bacterial growth by measuring the optical density at 600 nm by spectrophotometer and the surface tension clearly showed the ability of Pseudomonas luteola to produce biosurfactants at various conditions of the culture medium. The biosurfactant produced in the pharmaceutical reject medium generated a decrease in the surface tension with a percentage of 19.4% greater than the percentage obtained when using whey which is 7.0%. The pharmaceutical rejection is diluted at various percentages ranging from 5% to 100% in order to study the effect of the concentration on the biosurfactant production. The best result inducing the great reduction of the surface tension value is obtained at the dilution of 30% with the pharmaceutical reject. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=biosurfactant" title="biosurfactant">biosurfactant</a>, <a href="https://publications.waset.org/abstracts/search?q=pseudomonas%20luteola" title=" pseudomonas luteola"> pseudomonas luteola</a>, <a href="https://publications.waset.org/abstracts/search?q=whey" title=" whey"> whey</a>, <a href="https://publications.waset.org/abstracts/search?q=antiscorpionic%20serum" title=" antiscorpionic serum"> antiscorpionic serum</a>, <a href="https://publications.waset.org/abstracts/search?q=gas%20oil" title=" gas oil"> gas oil</a> </p> <a href="https://publications.waset.org/abstracts/159333/production-of-biosurfactant-by-pseudomonas-luteola-on-a-reject-from-the-production-of-anti-scorpion-serum" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/159333.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">102</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">301</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">353</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">300</span> Functional Diversity of Pseudomonas: Role in Stimulation of Bean Germination and Common Blight Biocontrol</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Slimane%20Mokrani">Slimane Mokrani</a>, <a href="https://publications.waset.org/abstracts/search?q=Nabti%20El%20hafid"> Nabti El hafid</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Description of the subject: Currently, several efforts focus on the study of biodiversity, microbial biotechnology, and the use of ecological strategies. Objectives: The aim of this present work is to determine the functional diversity of bacteria in rhizospheric and non-rhizospheric soils of different plants. Methods: Bacteria were isolated from soil and identified based on physiological and biochemical characters and genotypic taxonomy performed by 16S rDNA and BOX-PCR. As well as the characterization of various PGPR traits. Then, they are tested for their effects on the stimulation of seed germination and the growth of Phaseolus vulgaris L. As well as their biological control activities with regard to the phytopathogenic bacterial isolate Xapf. Results and Discussion: The biochemical and physiological identification of 75 bacterial isolates made it possible to associate them with the two groups of fluorescent Pseudomonas (74.67%) and non-fluorescent Pseudomonas (25.33%). The identification by 16S rDNA of 27 strains made it possible to attribute the majority of the strains to the genus Pseudomonas (81.48%), Serratia (7.41%) and Bacillus (11.11%). The bacterial strains showed a high capacity to produce IAA, siderophores, HCN and to solubilize phosphate. A significant stimulation of germination and growth was observed by applying the Pseudomonas strains. Furthermore, significant reductions in the severity and intensity of the disease caused caused by Xapf were observed. Conclusion: The bacteria described in this present study endowed with different PGPR activities seem to be very promising for their uses as biological control agents and bio-fertilization. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=biofertilization" title="biofertilization">biofertilization</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=phaseolus%20vulgaris%20L" title=" phaseolus vulgaris L"> phaseolus vulgaris L</a>, <a href="https://publications.waset.org/abstracts/search?q=pseudomonas" title=" pseudomonas"> pseudomonas</a>, <a href="https://publications.waset.org/abstracts/search?q=Xanthomonas%20axonopodis%20pv.%20phaseoli%20var.%20fuscans%20and%20common%20blight" title=" Xanthomonas axonopodis pv. phaseoli var. fuscans and common blight"> Xanthomonas axonopodis pv. phaseoli var. fuscans and common blight</a> </p> <a href="https://publications.waset.org/abstracts/159039/functional-diversity-of-pseudomonas-role-in-stimulation-of-bean-germination-and-common-blight-biocontrol" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/159039.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">81</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">299</span> The Biofertilizer Effect of Pseudomonas of Salt Soils of the North-West Algerian, Study of Comportment of Bean (Vicia Faba)</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Djoudi%20Abdelhak">Djoudi Abdelhak</a>, <a href="https://publications.waset.org/abstracts/search?q=Djibaoui%20Rachid"> Djibaoui Rachid</a>, <a href="https://publications.waset.org/abstracts/search?q=Reguieg%20Yassaad%20Houcine"> Reguieg Yassaad Houcine</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Our study focuses on the identification of some species of Pseudomonas (P4, P5, P7 and P8) isolated from saline soils in northwestern Algeria and the effect of their metabolites on the growth of Alternaria alternata the causative agent of the blight of the bean disease (Vicia faba). We are also interested in stimulating the growth of this plant species in saline conditions (60 mM/l NaCl) and the absence of salts. The analysis focuses on rates of inhibition of mycelial growth of Alternaria alternata strain and the rate of growth of plants inoculated with strains of Pseudomonas expressed by biometrics. According to the results of the in-vitro test, P5 and P8 species and their metabolites showed a significant effect on mycelia growth and production of spores of Alternaria alternata. The in-vivo test shows that the species P8 and P5 were significantly and positively influencing the growth in biometric parameters of the bean in saline and salt-free condition. Inoculation with strain P5 has promoted the growth of the bean in stem height, stem fresh weight and dry weight of stems of 108.59%, 115.28%, 104.33%, respectively, in the presence of salt Inoculation with strain P5 has fostered the growth of the bean stem fresh weight of 112.47% in the presence of salt The effect of Pseudomonas species on the development of Vicia faba and the growth of Alternaria alternata is considering new techniques and methods of biological production and crop protection. <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=vicia%20faba" title=" vicia faba"> vicia faba</a>, <a href="https://publications.waset.org/abstracts/search?q=alternaria%20alternata" title=" alternaria alternata"> alternaria alternata</a>, <a href="https://publications.waset.org/abstracts/search?q=promoting%20of%20plant%20growth" title=" promoting of plant growth"> promoting of plant growth</a> </p> <a href="https://publications.waset.org/abstracts/30608/the-biofertilizer-effect-of-pseudomonas-of-salt-soils-of-the-north-west-algerian-study-of-comportment-of-bean-vicia-faba" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/30608.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">392</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">298</span> Role of Interleukin-36 in Response to Pseudomonas aeruginosa Infection</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Muslim%20Idan%20Mohsin">Muslim Idan Mohsin</a>, <a href="https://publications.waset.org/abstracts/search?q=Mohammed%20Jasim%20Al-Shamarti"> Mohammed Jasim Al-Shamarti</a>, <a href="https://publications.waset.org/abstracts/search?q=Rusul%20Idan%20Mohsin"> Rusul Idan Mohsin</a>, <a href="https://publications.waset.org/abstracts/search?q=Ali%20A.%20Majeed"> Ali A. Majeed</a> </p> <p class="card-text"><strong>Abstract:</strong></p> One of the causative agents of the lower respiratory tract (LRT) is Pseudomonas aeruginosa, which can lead to severe infection associated with a lung infection. There are many cytokines that are secreted in response to bacterial infection, in particular interleukin IL-36 cytokine in response to P. aeruginosa infection. The involvement of IL-36 in the P. aeruginosa infection could be a clue to find a specific way for treatments of different inflammatory and degenerative lung diseases. IL36 promotes primary immune response via binding to the IL-36 receptor (IL-36R). Indeed, an overactivity of IL-36 might be an initiating factor for many immunopathologic sceneries in pneumonia. Here we demonstrate if the IL-36 cytokine increases in response P. aeruginosa infection that is isolated from lower respiratory tract infection (LRT). We demonstrated that IL-36 expression significantly unregulated in human lung epithelial (A549) cells after infected by P. aeruginosa at mRNA level. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=IL36" title="IL36">IL36</a>, <a href="https://publications.waset.org/abstracts/search?q=Pseudomonas%20aeruginosa" title=" Pseudomonas aeruginosa"> Pseudomonas aeruginosa</a>, <a href="https://publications.waset.org/abstracts/search?q=LRT%20infection" title=" LRT infection"> LRT infection</a>, <a href="https://publications.waset.org/abstracts/search?q=A549%20cells" title=" A549 cells"> A549 cells</a> </p> <a href="https://publications.waset.org/abstracts/119670/role-of-interleukin-36-in-response-to-pseudomonas-aeruginosa-infection" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/119670.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">232</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">297</span> Bioremediation of Phenanthrene by Monocultures and Mixed Culture Bacteria Isolated from Contaminated Soil</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=A.%20Fazilah">A. Fazilah</a>, <a href="https://publications.waset.org/abstracts/search?q=I.%20Darah"> I. Darah</a>, <a href="https://publications.waset.org/abstracts/search?q=I.%20Noraznawati"> I. Noraznawati</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Three different bacteria capable of degrading phenanthrene were isolated from hydrocarbon contaminated site. In this study, the phenanthrene-degrading activity by defined monoculture was determined and mixed culture was identified as <em>Acinetobacter</em> sp. P3d, <em>Bacillus </em>sp. P4a and <em>Pseudomonas</em> sp. P6. All bacteria were able to grow in a minimal salt medium saturated with phenanthrene as the sole source of carbon and energy. Phenanthrene degradation efficiencies by different combinations (consortia) of these bacteria were investigated and their phenanthrene degradation was evaluated by gas chromatography. Among the monocultures,<em> Pseudomonas</em> sp. P6 exhibited 58.71% activity compared to <em>Acinetobacter</em> sp. P3d and <em>Bacillus</em> sp. P4a which were 56.97% and 53.05%, respectively after 28 days of cultivation. All consortia showed high phenanthrene elimination which were 95.64, 79.37, 87.19, 79.21% for Consortia A, B, C and D, respectively. The results indicate that all of the bacteria isolated may effectively degrade target chemical and have a promising application in bioremediation of hydrocarbon contaminated soil purposes. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=phenanthrene" title="phenanthrene">phenanthrene</a>, <a href="https://publications.waset.org/abstracts/search?q=consortia" title=" consortia"> consortia</a>, <a href="https://publications.waset.org/abstracts/search?q=acinetobacter%20sp.%20P3d" title=" acinetobacter sp. P3d"> acinetobacter sp. P3d</a>, <a href="https://publications.waset.org/abstracts/search?q=bacillus%20sp.%20P4a" title=" bacillus sp. P4a"> bacillus sp. P4a</a>, <a href="https://publications.waset.org/abstracts/search?q=pseudomonas%20sp.%20P6" title=" pseudomonas sp. P6"> pseudomonas sp. P6</a> </p> <a href="https://publications.waset.org/abstracts/47580/bioremediation-of-phenanthrene-by-monocultures-and-mixed-culture-bacteria-isolated-from-contaminated-soil" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/47580.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">296</span> Biofouling Control during the Wastewater Treatment in Self-Support Carbon Nanotubes Membrane: Role of Low Voltage Electric Potential</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Chidambaram%20Thamaraiselvan">Chidambaram Thamaraiselvan</a>, <a href="https://publications.waset.org/abstracts/search?q=Carlos%20Dosoretz"> Carlos Dosoretz</a> </p> <p class="card-text"><strong>Abstract:</strong></p> This work will explore the influence of low voltage electric field, both alternating (AC) and direct (DC) currents, on biofouling control to highly electrically conductive self-supporting carbon nanotubes (CNT) membranes at conditions which encourage bacterial growth. A mutant strain of Pseudomonas putida S12 was used a model bacterium. The antibiofouling studies were performed with flow-through mode connecting an electric circuit in resistive mode. Major emphasis was placed on AC due to its ability of repulsing and inactivating bacteria. The observations indicate that an AC potential >1500 mV, 1 kHz frequency, 100 Ω external resistance on ground side and pulse wave above the offset (+0.45) almost completely prevented attachment of bacteria (>98.5%) and bacterial inactivation (95.3±2.5%). Findings suggest that at the conditions applied, direct electron transfer might be dominant in a decrease of cell viability. AC resulted more effective than DC, both in terms of biofouling reduction compared to cathodic DC and in terms of cell inactivation compared to anodic DC. This electrically polarized CNT membranes offer a viable antibiofouling strategy to hinder biofouling and simplify membrane care during filtration. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=bacterial%20attachment" title="bacterial attachment">bacterial attachment</a>, <a href="https://publications.waset.org/abstracts/search?q=biofouling%20control" title=" biofouling control"> biofouling control</a>, <a href="https://publications.waset.org/abstracts/search?q=low%20electric%20potential" title=" low electric potential"> low electric potential</a>, <a href="https://publications.waset.org/abstracts/search?q=water%20treatment" title=" water treatment"> water treatment</a> </p> <a href="https://publications.waset.org/abstracts/68570/biofouling-control-during-the-wastewater-treatment-in-self-support-carbon-nanotubes-membrane-role-of-low-voltage-electric-potential" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/68570.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">270</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">295</span> Application of Box-Behnken Response Surface Design for Optimization of Essential Oil Based Disinfectant on Mixed Species Biofilm</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Anita%20Vidacs">Anita Vidacs</a>, <a href="https://publications.waset.org/abstracts/search?q=Robert%20Rajko"> Robert Rajko</a>, <a href="https://publications.waset.org/abstracts/search?q=Csaba%20Vagvolgyi"> Csaba Vagvolgyi</a>, <a href="https://publications.waset.org/abstracts/search?q=Judit%20Krisch"> Judit Krisch</a> </p> <p class="card-text"><strong>Abstract:</strong></p> With the optimization of a new disinfectant the number of tests could be decreased and the cost of processing too. Good sanitizers are eco-friendly and allow no resistance evolvement of bacteria. The essential oils (EOs) are natural antimicrobials, and most of them have the Generally Recognized As Safe (GRAS) status. In our study, the effect of the EOs cinnamon, marjoram, and thyme was investigated against mixed species bacterial biofilms of Escherichia coli, Listeria monocytogenes, Pseudomonas putida, and Staphylococcus aureus. The optimal concentration of EOs, disinfection time and level of pH were evaluated with the aid of Response Surface Box-Behnken Design (RSD) on 1 day and 7 days old biofilms on metal, plastic, and wood surfaces. The variable factors were in the range of 1-3 times of minimum bactericide concentration (MBC); 10-110 minutes acting time and 4.5- 7.5 pH. The optimized EO disinfectant was compared to industrial used chemicals (HC-DPE, Hypo). The natural based disinfectants were applicable; the acting time was below 30 minutes. EOs were able to eliminate the biofilm from the used surfaces except from wood. The disinfection effect of the EO based natural solutions was in most cases equivalent or better compared to chemical sanitizers used in food industry. <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=Box-Behnken%20design" title=" Box-Behnken design"> Box-Behnken design</a>, <a href="https://publications.waset.org/abstracts/search?q=disinfectant" title=" disinfectant"> disinfectant</a>, <a href="https://publications.waset.org/abstracts/search?q=essential%20oil" title=" essential oil"> essential oil</a> </p> <a href="https://publications.waset.org/abstracts/83407/application-of-box-behnken-response-surface-design-for-optimization-of-essential-oil-based-disinfectant-on-mixed-species-biofilm" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/83407.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">220</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">294</span> Contribution to the Production of Phenazine Antibiotics Effect Type Compounds by Some Strains of Pseudomonas spp.fluorescent</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Nac%C3%A9ra%20Benoussaid">Nacéra Benoussaid</a>, <a href="https://publications.waset.org/abstracts/search?q=Lehalali%20Meriem"> Lehalali Meriem</a>, <a href="https://publications.waset.org/abstracts/search?q=Benchabane%20Messaoud"> Benchabane Messaoud</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Our work focuses on the production of compound antibiotic effect of volatile nature namely hydrogen cyanide and the production and identification of molecules phénazinique by some strains of fluorescent Pseudomonas spp isolated from the rhizosphere of some trees for a possible use as bio pesticides antifungal effect and/or antibiotic. We tested the production of hydrogen cyanide of 21 strains of Pseudomonas spp. fluorescent among them 19 strains (90, 47%) showed a positive cyanogenesis.The antagonism test executed in vitro showed that Pseudomonas strains have a higher anti fungal effect relative to their antibacterial effect with diameters of inhibition zones up to 3, 9 cm recorded by the strain F48 against Coleosporiumsp compared with recorded results against bacteria with a maximum inhibition of 1, 26 cm among this antagonistic strain.Three strains were selected by testing for producing phénazines namely PI9, BB9 and F20. The effect of the antimicrobial activity was performed on different culture media (GN, King B, ISP2 and PDA). The results of our study allowed us to retain the King B medium as ideal medium for the production of secondary metabolite. The produced phenazinique compounds was extracted from various organic solvents, and after the results of antibiographie against germs - targets, the extracts of ethyl acetate gave the best results compared to dichloromethane and hexane.The Analysis of these compounds of antibiotic phenazinique effect within layer chromatography (CCM) and high performance liquid chromatography( HPLC) indicate that both strains PI9 and F20 are productive of phenazine-1-carboxylic acid (PCA). The BB9 strain is suspected to be productive of another phenazinique compound. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Pseudomonas%20ssp.%20fluorescents" title="Pseudomonas ssp. fluorescents">Pseudomonas ssp. fluorescents</a>, <a href="https://publications.waset.org/abstracts/search?q=antagonism%20in%20vitro" title=" antagonism in vitro"> antagonism in vitro</a>, <a href="https://publications.waset.org/abstracts/search?q=secondary%20metabolite" title=" secondary metabolite"> secondary metabolite</a>, <a href="https://publications.waset.org/abstracts/search?q=phenazines" title=" phenazines"> phenazines</a>, <a href="https://publications.waset.org/abstracts/search?q=biopesticide." title=" biopesticide."> biopesticide.</a> </p> <a href="https://publications.waset.org/abstracts/21842/contribution-to-the-production-of-phenazine-antibiotics-effect-type-compounds-by-some-strains-of-pseudomonas-sppfluorescent" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/21842.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">511</span> </span> </div> </div> <ul class="pagination"> <li class="page-item disabled"><span class="page-link">&lsaquo;</span></li> <li class="page-item active"><span class="page-link">1</span></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=pseudomonas%20putida&page=2">2</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=pseudomonas%20putida&page=3">3</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=pseudomonas%20putida&page=4">4</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=pseudomonas%20putida&page=5">5</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=pseudomonas%20putida&page=6">6</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=pseudomonas%20putida&page=7">7</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=pseudomonas%20putida&page=8">8</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=pseudomonas%20putida&page=9">9</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=pseudomonas%20putida&page=10">10</a></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=pseudomonas%20putida&page=11">11</a></li> <li class="page-item"><a class="page-link" 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