Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Wyszukujesz frazę "pseudomonas" wg kryterium: Temat


Tytuł:
Diversity of Pseudomonas species associated with soft rot of plants in Poland
Autorzy:
Zolobowska, L
Pospieszny, H.
Powiązania:
https://bibliotekanauki.pl/articles/65211.pdf
Data publikacji:
2001
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
Pseudomonas fluorescens
Polska
Pseudomonas
polymerase chain reaction
occurrence
Pseudomonas putida
heterogeneity
identification
plant
Opis:
A total of 94 pectolytic and 60 nonpectolytic Pseudomonas isolates were obtained from 250 samples of rotted vegetable specimens representing various economically important vegetables. The isolates were identified on the basis of standard biochemical tests. Pseudomonas fluorescens biovar V and II and Pseudomonas putida were the most abundant species among pectolytic isolates and Pseudomonas fluorescens biovar I among nonpectolytic ones. Only 3 Pseudomonas viridiflava isolates were identified and all of them were obtained from potato. Isolates of pectolytic phenotype were scattered among nonpectolytic ones irrespective of their taxonomical status. Isolates identified biochemically, as Pseudomonas marginalis were also present in nonpectolytic group. PCR method is unsuitable for identification and differentiation of bacteria belonging to pectolytic fluorescens Pseudomonas group due to great diversity of species. However, the results of PCR amplification of the genes encoding pectate lyase suggest that genes responsible for production of this enzyme may also be present in isolates of nonpectolytic phenotype.
Z 250 prób, z różnych gatunków roślin warzywnych z objawami mokrej zgnilizny wyodrębniono 94 izolaty pektynolitycznych i 60 izolatów nie pektynolitycznych bakterii z rodzaju Pseudomonas. Identyfikację i różnicowanie izolatów przeprowadzono przy zastosowaniu standardowych testów fizjologiczno-biochemicznych. Spośród izolatów z grupy pektolitycznych Pseudomonas najliczniej występował gatunek P. fluorescens, który był reprezentowany przez 4 biowary (oprócz czwartego), przy czym dominowały biowary II i V. Mniej licznie występował gatunek P. putida, a P. viridiflava był reprezentowany jedynie przez 3 izolaty, pochodzące z ziemniaka. Podobna była struktura populacji izolatów z grupy niepektolitycznych Pseudomonas. Metoda PCR okazała się być mało przydatna do wykrywania i różnicowania izolatów z grupy pektolitycznych Pseudomonas ze względu na duże ich zróżnicowanie. Amplifikacja DNA metodą PCR wykazała, że geny kodujące enzym liazy pektynowej występują także w izolatach niepektolitycznych rodzaju Pseudomonas.
Źródło:
Journal of Plant Protection Research; 2001, 41, 1
1427-4345
Pojawia się w:
Journal of Plant Protection Research
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Effect of Pseudomonas spp. on inoculation of young plants of Fraxinus excelsior stem with Diplodia mutila
Autorzy:
Przybyl, K
Powiązania:
https://bibliotekanauki.pl/articles/41535.pdf
Data publikacji:
2003
Wydawca:
Polska Akademia Nauk. Instytut Dendrologii PAN
Tematy:
young plant
Fraxinus excelsior
Pseudomonas cepacia
Pseudomonas fluorescens
Diplodia mutila
stem
Pseudomonas aureofaciens
fungi
in vitro
inoculation
Pseudomonas
European ash
bacteria
plant
Opis:
Bacteria Pseudomonas aureofaciens, P. cepacia and P. fluorescens biovar I was tested againts fungus Diplodia mutila on stems of 2-year-old plants of European ash in greenhouse experiments. The interaction of bacteria and fungus was assessed on the base of length of necrotic lesions, caused by D. mutila, extended from point of inoculation. The strongest antagonistic effect was noted in the case of P. aureofaciens
Źródło:
Dendrobiology; 2003, 50
1641-1307
Pojawia się w:
Dendrobiology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
A comparison between Pseudomonas aureofaciens (chlororaphis) and P. fluorescens in biological control of cotton seedling damping-off disease
Autorzy:
Samavat, S.
Heydari, A.
Zamanizadeh, H.R.
Rezaee, S.
Aliabadi, A.A.
Powiązania:
https://bibliotekanauki.pl/articles/66475.pdf
Data publikacji:
2014
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
Pseudomonas aureofaciens
Pseudomonas fluorescens
biological control
cotton
seedling
damping off disease
plant disease
Opis:
Due to the importance of the biological control of plant diseases, testing and introducing new biocontrol-active microorganisms is a major concern among plant pathologists. The causal agent of cotton seedling damping-off disease is Rhizoctonia solani. In this regard, we tried to investigate the antagonistic activities of Pseudomonas aureofaciens (chlororaphis) 30–84 (phenazine producing wild type and non-phenazine producing mutant) strains on R. solani, in comparison with some isolates of P. fluorescent under both in vitro (laboratory) and in vivo (greenhouse) conditions. In the laboratory experiment, the inhibitory effects of all the bacteria, on the growth of R. solani, were evaluated using the dual culture procedure. Results showed that five isolates of P. fluorescent along with both strains of P. aureofaciens significantly inhibited the growth of R. solani. Effective bacterial antagonists were then evaluated in a greenhouse experiment where cotton seeds were coated with their suspensions and were sown in pasteurised field-soil. The soil had been pre-inoculated with a virulent isolate of R. solani. The efficacy of the bacterial antagonists was evaluated by counting the number of surviving seedlings in different treatments, at 15 and 60 days after sowing, for determining pre- and post-emergence damping-off incidence. According to the results of the greenhouse experiment, at both intervals, two isolates of P. fluorescens along with both strains of P. aureofaciens caused significant increases in the number of healthy seedlings, in comparison with the untreated control, and a commonly used fungicide (carboxin-thiram). The efficacy of phenazine producing a wild type strain of P. aureofaciens was higher than its non-phenazine producing mutant, indicating that phenazine plays an important role in the antagonistic activity of P. aureofaciens. Effective bacterial antagonists were then studied for their antagonistic mechanisms. The results showed that all four bacteria employed different mechanisms. The bacteria produced siderophore, and volatile metabolites and non-volatile metabolites, in their antagonistic activities. The results of this study suggest that P. auerofaciens may be a new biocontrol agent for controlling cotton seedling mortality disease.
Źródło:
Journal of Plant Protection Research; 2014, 54, 2
1427-4345
Pojawia się w:
Journal of Plant Protection Research
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Media optimization for depolymerization of alginate by Pseudomonas aeruginosa AG LSL-11
Autorzy:
Koti, B.A.
Manohar, S.
Lalitha, J.
Powiązania:
https://bibliotekanauki.pl/articles/11457.pdf
Data publikacji:
2014
Wydawca:
Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Tematy:
depolymerization
alginate
Pseudomonas aeruginosa
bacteria
Opis:
An agar degrading bacterium Pseudomonas aeruginosa AG LSL-11 was acclimatized to alginate for the production of alginase. Production parameters such as pH, temperature, influence of simple carbohydrates and nitrogen sources, and effect of NaCl on growth and alginase production were carried out. Maximum growth was observed at pH 9.0 and 35 °C, while alginase was produced optimally at pH 9.0 and 30 °C. The alginase produced by Pseudomonas aeruginosa AG LSL-11 was inducible by alginate, and repressed by other simple sugar when supplemented along with alginate in the medium. The bacterium did not require NaCl for growth and production of alginase. The activity staining of partially purified culture supernatant after native PAGE revealed the presence of a single alginase.
Źródło:
International Letters of Natural Sciences; 2014, 14
2300-9675
Pojawia się w:
International Letters of Natural Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Methods for eradication of the biofilms formed by opportunistic pathogens using novel techniques – A review
Autorzy:
Zabielska, Julia
Tyfa, Agnieszka
Kunicka-Styczyńska, Alina
Powiązania:
https://bibliotekanauki.pl/articles/764814.pdf
Data publikacji:
2016
Wydawca:
Uniwersytet Łódzki. Wydawnictwo Uniwersytetu Łódzkiego
Tematy:
biofilm eradication
Pseudomonas aeruginosa
microbial colonization
Opis:
W niekorzystnych warunkach środowiska, mikroorganizmy zasiedlają zarówno powierzchnie abiotyczne, jak i biotyczne takie jak tkanki zwierzęce czy roślinne, tworząc struktury biofilmu charakteryzujące się wysoką opornością. Adhezja mikroorganizmów, szczególnie patogenów oportunistycznych, niesie niebezpieczeństwo zasiedlania materiałów medycznych, co może doprowadzić do infekcji u osób z obniżoną odpornością. Chociaż dotychczasowe badania wskazują różne metody zapobiegania tworzeniu biofilmu, jego całkowita eliminacja ze środowiska jest nadal niemożliwa. Przedstawione opracowanie stanowi przegląd nowoczesnych metod usuwania dojrzałego biofilmu tworzonego przez patogeny oportunistyczne. Spośród wielu metod opisano m.in. zastosowanie: zimnej plazmy, ultradźwięków, pola elektrycznego, ozonowania wody, terapii fagowej, enzymów działających bezpośrednio na macierz biofilmu, bakteriocyn, środków chemicznych syntetycznych oraz pochodzenia naturalnego.
The inconvenient environmental conditions force microorganisms to colonize either abiotic surfaces or animal and plant tissues and, therefore, form more resistant structures – biofilms. The phenomenon of microbial adherence, opportunistic pathogens in particular, is of a great concern. Colonization of medical devices and biofilm formation on their surface, may lead to severe infections mainly in humans with impaired immune system. Although, current research consider various methods for prevention of microbial biofilms formation, still, once a biofilm is formed, its elimination is almost impossible. This study focuses on the overview of novel methods applied for eradication of mature opportunistic pathogens' biofilms. Among various techniques the following: cold plasma, electric field, ultrasounds, ozonated water treatment, phagotherapy, matrix targeting enzymes, bacteriocins, synthetic chemicals and natural origin compounds used for biofilm matrix disruption were briefly described.
Źródło:
Acta Universitatis Lodziensis. Folia Biologica et Oecologica; 2016, 12; 26-37
1730-2366
2083-8484
Pojawia się w:
Acta Universitatis Lodziensis. Folia Biologica et Oecologica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Increased production of carrageenase by Pseudomonas aeruginosa ZSL-2 using Taguchi experimental design
Autorzy:
Ziayoddin, M.
Lalitha, J.
Shinde, M.
Powiązania:
https://bibliotekanauki.pl/articles/11042.pdf
Data publikacji:
2014
Wydawca:
Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Tematy:
production
carrageenase
Pseudomonas aeruginosa
Taguchi method
Opis:
The culture conditions for the production of carrageenase were optimized using one-factor-at-a-time method combined with orthogonal array design. With the one-factor-at-a-time method revealed optimal conditions for carrageenase production were 24 h of fermentation period, 28 °C incubation temperature at pH 8.0 with NaNO3 as nitrogen source and carrageenan as carbon source in MMS media. Further optimization of carrgeenase production by using orthogonal experimental design L9 (34) with four factors, temperature, pH, NH4NO3 and carrageenan with their relevant levels revealed optimised conditions for carrageenase production were temperature of 28 °C, pH 8.0, 2 g L-1 NaNO3 and 2 g L-1 carrageenan. The order of the factors affecting the fermentation process was found to be temperature > pH > NaNO3 > carrageenan. The temperature played a significant role on the carrageenase production. Higher carrageenase yield with activity of 0.542 ±0.045 U ml-1 was obtained in the optimised medium when compared to those of basal medium. Carrageenase hydrolysed products of carrageenan were identified by LC-ESI-MS as neocarrabiose, neocarrabiose-4 sulfate, neocarratetraose, neocarratetraose-4 sulfate, anhydrogalactose, galactose, galactose-4 sulphate and sulphate.
Źródło:
International Letters of Natural Sciences; 2014, 12, 2
2300-9675
Pojawia się w:
International Letters of Natural Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
A Bioremediation Study of Raw and Treated Crude Petroleum Oil Polluted Soil with Aspergillus niger and Pseudomonas aeruginosa
Autorzy:
Ojewumi, M. E.
Anenih, E. V.
Taiwo, O. S.
Adekeye, B. T.
Awolu, O. O.
Ojewumi, E. O.
Powiązania:
https://bibliotekanauki.pl/articles/124955.pdf
Data publikacji:
2018
Wydawca:
Polskie Towarzystwo Inżynierii Ekologicznej
Tematy:
bioremediation
Aspergillus niger
Pseudomonas aeruginosa
pollution
Opis:
This study was conducted to investigate the degree of bioremediation that would occur in the samples of soil polluted with raw and treated crude petroleum (oil) with the aid of Aspergillus niger (fungi) and Pseudomonas aeruginosa (bacteria). This was achieved by monitoring the Organic carbon content in the soil over 45 days and pH over 25 days. Four systems of 500 g soil were polluted with 40 g treated crude petroleum, while four systems were contaminated with 40 g raw crude petroleum. The eight systems were labeled accordingly. Two systems for raw crude control and treated crude control (RCC and TCC) were left as control, two systems for raw crude Aspergillus niger and treated crude Aspergillus niger (RCA and TCA) were treated with Aspergillus niger only, two systems for raw crude Pseudomonas aeruginosa and treated crude Pseudomonas aeruginosa (RCP and TCP) were treated with Pseudomonas aeruginosa only and the last two systems for raw crude Aspergillus niger and Pseudomonas aeruginosa (RCAP and TCAP) were treated with both Pseudomonas aeruginosa and Aspergillus niger. At the end of the bioremediation period, the results obtained showed that the pH was not particularly a solid parameter to estimate the degree of bioremediation. This is because a proper trend in the results obtained could not be determined. Additionally, it was observed that Aspergillus niger (fungi) and Pseudomonas aeruginosa (bacteria) alone and separate remediate raw crude polluted soil better than treated crude polluted soil. This was determined by the TOC (Total Organic Carbon) values on the 45th day of the experiment.
Źródło:
Journal of Ecological Engineering; 2018, 19, 2; 226-235
2299-8993
Pojawia się w:
Journal of Ecological Engineering
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Opportunistic Gram-negative rods capability of creating biofilm structures on polivynyl chloride and styrene-acronitrile copolymer surfaces
Autorzy:
Zabielska, Julia
Kunicka-Styczyńska, Alina
Rajkowska, Katarzyna
Tyfa, Agnieszka
Powiązania:
https://bibliotekanauki.pl/articles/1038901.pdf
Data publikacji:
2015
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
Pseudomonas aeruginosa
biofilm
environmental strains
polymer surfaces
Opis:
Biofilms are highly organized microbial communities displaying high resistance to disinfectants and other external environmental factors. Medical equipment, such as stents and catheters, can be colonized by a variety of bacteria including opportunistic pathogens circulating in the environment and dangerous to immunocompromised patients. Application of materials resistant to biofilm formation will minimize the risk of patients' infection. Hence, the aim of this research was to determine the biofilm growth of environmental bacteria isolates on polyvinyl chloride and styrene-acronitrile copolymer surfaces. Nine strains (Pseudomonas aeruginosa, Burkholderia cepacia and Serratia liquefacies) isolated from cosmetics, and a reference P. aeruginosa strain ATCC 15442, were tested. The ability and dynamics of biofilm formation on intubation catheters (30°C, up to 24 h) in bacterial growth cultures (107-108 CFU/ml) was investigated, with subsequent sonication and quantification by agar plate count method. The results indicated that all the tested bacteria expressed a strong ability for the polymer surface adhesion, reaching 4.6 to 6.7 log CFU/cm2 after 30 minutes. Moreover, for the majority of strains, the level of 24-hour biofilm production was from 6.67-7.61 log CFU/cm2. This research indicates that the environmental strains circulating between the cosmetics and patients may pose a threat of biofilm formation on medical equipment surfaces, and presumably in the clinical surroundings as well.
Źródło:
Acta Biochimica Polonica; 2015, 62, 4; 733-737
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Screening of cellulase and pectinase by using Pseudomonas fluorescens and Bacillus subtilis
Autorzy:
Reetha, S.
Selvakumar, G.
Bhuvaneswari, G.
Thamizhiniyan, P.
Ravimycin, T.
Powiązania:
https://bibliotekanauki.pl/articles/11688.pdf
Data publikacji:
2014
Wydawca:
Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Tematy:
screening
cellulase
pectinase
Pseudomonas fluorescens
Bacillus subtilis
Opis:
A study was conducted to determine the Production of cellulase and pectinase enzyme by using Plant growth promoting rhizobacteria like Pseudomonas fluorescence and Bacillus subtilis. These to micro organism are isolated by serial dilution method. One gram of soil sample was diluted in to 10 ml of sterile distilled water and 1 ml of sample solution was serially diluted in 9ml of sterile water up to 10 dilution. Each sample from dilution 10-5 and 10-6 were taken and streaked in to KB and NA medium and incubate at 24 hrs. After 24 hrs Pseudomonas fluorescence and Bacillus subtilis was observed in the medium of KB and NA medium. Both the culture was sub cultured and maintain in the same for the further work. CMCase medium was prepared and sterilized by autoclave for 121 ºC for 15 minutes after sterilization these medium contain petriplate was streaked by bacteria and incubates for 48h after incubation period a clear halo zone was produced by these bacteria among these bacteria Pseudomonas fluorescence are able to produce high amount of cellulose compare to Bacillus subtilis. Pectin agar medium was prepared and sterilized by autoclave for 121 ºC for 15 minutes after sterilization these medium contain petriplate was streaked by bacteria incubates for 48h after incubation period a clear halo zone was produced by these bacteria, among these bacteria Pseudomonas fluorescence are able to produce high amount of Pectinase compare to Bacillus subtilis. Plant growth promoting rhizobacteria (PGPR) are beneficial bacteria that colonize plant roots and enhance plant growth by a wide variety of mechanisms.
Źródło:
International Letters of Natural Sciences; 2014, 08, 2
2300-9675
Pojawia się w:
International Letters of Natural Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Impedance Sensors Made in PCB and LTCC Technologies for Monitoring Growth and Degradation of Pseudomonal Biofilm
Autorzy:
Chabowski, K.
Junka, A. F.
Piasecki, T.
Nowak, D.
Nitsch, K.
Smutnicka, D.
Bartoszewicz, M.
Moczała, M.
Szymczyk, P.
Powiązania:
https://bibliotekanauki.pl/articles/221326.pdf
Data publikacji:
2017
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
Pseudomonas aeruginosa
biofilm
interdigitated sensor
impedance spectroscopy
Opis:
The suitability of low-cost impedance sensors for microbiological purposes and biofilm growth monitoring was evaluated. The sensors with interdigitated electrodes were fabricated in PCB and LTCC technologies. The electrodes were golden (LTCC) or gold-plated (PCB) to provide surface stability. The sensors were used for monitoring growth and degradation of the reference ATCC 15442 Pseudomonas aeruginosa strain biofilm in invitro setting. During the experiment, the impedance spectra of the sensors were measured and analysed using electrical equivalent circuit (EEC) modelling. Additionally, the process of adhesion and growth of bacteria on a sensor’s surface was assessed by means of the optical and SEM microscopy. EEC and SEM microscopic analysis revealed that the gold layer on copper electrodes was not tight, making the PCB sensors susceptible to corrosion while the LTCC sensors had good surface stability. It turned out that the LTCC sensors are suitable for monitoring pseudomonal biofilm and the PCB sensors are good detectors of ongoing stages of biofilm formation.
Źródło:
Metrology and Measurement Systems; 2017, 24, 2; 369-380
0860-8229
Pojawia się w:
Metrology and Measurement Systems
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Bioaktywne metabolity ryzosferowych bakterii PseudomonasJankiewicz
Bioactive metabolites of the rhizosphere Pseudomonas bacteria
Autorzy:
Jankiewicz, U.
Powiązania:
https://bibliotekanauki.pl/articles/339299.pdf
Data publikacji:
2010
Wydawca:
Instytut Technologiczno-Przyrodniczy
Tematy:
antagonizm
fitopatogen
Pseudomonas
antagonism
plant pathogen
Opis:
Celem badań było określenie, jakie metabolity, bioaktywne względem wybranych fitopatogenów zbóż, są syntetyzowane przez wyizolowane z ryzosfery pszenicy bakterie Pseudomonas. Do doświadczeń wybrano dwa różne szczepy bakterii Pseudomonas fluorescens, które charakteryzowały się w warunkach in vitro silnym antagonizmem w stosunku do fitopategenów zbóż z rodzaju Pyrenophora Alteria i Fusarium. Jak wykazały badania obydwa szczepy bakterii w warunkach doświadczeń intensywnie wydzielały cyjanowodór oraz siderofory, w tym piowerdynę. Kwas salicylowy lub jego pochodną wykryto w hodowli tylko jednego z badanych izolatów. Obydwa zastosowane w doświadczeniu szczepy P. fluorescens charakteryzowały się zdolnością do syntezy zewnątrzkomórkowych peptydaz o różnym poziomie aktywności. W hodowlach bekterii nie wykryto enzymów litycznych zdolnych do rozkładu wiązań glikozydowych - chitynazy i ß-1,3 glukanazy.
The study was aimed at estimating which metabolites (bioactive towards selected cereal plant phatogens) are synthesized by Pseudomonas isolated from wheat rhizosphere. Two different strains of Pseudomonas fluorescens characterised by the strong in vitro antagonism in relation to cereal plant phatogens of the genera Pyrenophora , Alterial and Fusarium were selected for experiments. Both bacterial strains under experimental conditions intensively released hydrogen cyanide and siderophores including pyoverdine. Salicylic acid and its derivative were found in the culture of only one of analysed isolates. Both strains of P. fluoroscens were able to synthesize extracellular peptidases of different activity. No hydrolysing enzymes able to decompose glycoside bonds (chitinase and ß-1.3 gluconase) were found bacterial cultures.
Źródło:
Woda-Środowisko-Obszary Wiejskie; 2010, 10, 2; 83-92
1642-8145
Pojawia się w:
Woda-Środowisko-Obszary Wiejskie
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Comparison of in vitro activity of doripenem, imipenem and meropenem against clinical isolates of Enterobacteriaceae, Pseudomonas and Acinetobacter in Southern Poland
Autorzy:
Drzewiecki, Artur
Bulanda, Małgorzata
Talaga, Katarzyna
Sodo, Anna
Adamski, Paweł
Powiązania:
https://bibliotekanauki.pl/articles/1396809.pdf
Data publikacji:
2012-10-01
Wydawca:
Index Copernicus International
Tematy:
doripenem
imipenem
meropenem
Enterobacteriaceae
Pseudomonas
Acinetobacter
Opis:
In the study we tested drug sensitivity to 3 carbapenems (doripenem, imipenem and meropenem) of Gram-negative clinical isolates from Southern Poland. Material and methods. 89 strains were examined: 42 from Pseudomonas genus, 16 Acinetobacter baumannii strains and 31 Enterobacteriaceae strains. Etests were used according to the producers instructions, MIC values were interpreted using EUCAST criteria. Results. Highest in vitro activity against Pseudomonas spp. was shown for doripenem, then meropenem and the lowest for imipenem (MIC values were definitely lower for doripenem; differences were statistically significant); A. baumannii strains showed similar sensitivity to doripenem, meropenem and imipenem (differences non-significant); all Enterobacteriaceae strains showed sensitivity to the tested antimicrobials. Conclusions. As a conclusion-doripenem, which has high in vitro activity (almost the same as imipenem and meropenem) as well as beneficial pharmacologic properties, may be an alternative solution in the treatment of multiresistant Gram-negative bacteria, especially in patients in severe status who require restrictive antibiotic regimens.
Źródło:
Polish Journal of Surgery; 2012, 84, 9; 449-453
0032-373X
2299-2847
Pojawia się w:
Polish Journal of Surgery
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The effects of nickel(II) complexes with imidazole derivatives on pyocyanin and pyoverdine production by Pseudomonas aeruginosa strains isolated from cystic fibrosis
Autorzy:
Gałczyńska, Katarzyna
Kurdziel, Krystyna
Adamus-Białek, Wioletta
Wąsik, Sławomir
Szary, Karol
Drabik, Marcin
Węgierek-Ciuk, Aneta
Lankoff, Anna
Arabski, Michał
Powiązania:
https://bibliotekanauki.pl/articles/1038905.pdf
Data publikacji:
2015
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
Pseudomonas sp.
cystic fibrosis
nickel complexes
pyocyanin
pyoverdine
Opis:
Pseudomonas aeruginosa infection is problematic in patients with cystic fibrosis (CF). P. aeruginosa secretes a diversity of pigments, such as pyocyanin and pyoverdine. The aim of this study was to evaluate the effects of complexes of nickel(II) ([Ni(iaa)2(H2O)2]·H2O (iaa = imidazole-4-acetate anion), [Ni(1-allim)6](NO3)2 (1-allim = 1-allylimidazole) and NiCl2 on pyocyanin and pyoverdine production by 23 strains of P. aeruginosa isolated from cystic fibrosis under growth conditions specific for the CF respiratory system. The antibacterial effects and biophysical properties of the tested substances were measured by spectrofluorometric techniques, as well as by laser interferometry, confocal and atomic force microscopy. The cytotoxic properties of all compounds were measured by Annexin/IP assay against A549 cells. All tested compounds have no effect on pyocyanin production and decrease the pyoverdine secretion in about 40% of tested P. aeruginosa strains at non-cytotoxic range of concentrations. Imidazole-4-acetate anion and 1-allylimidazole have good diffusion properties in the mature P. aeruginosa PAO1 biofilm. In conclusion, the tested nickel(II) complexes do not have clinical implications in P. aeruginosa eradication in cystic fibrosis. The diffusion properties of 1-allylimidazole and imidazole-4-acetate and their lack of effect on A549 cells suggest that they might be considered for chemical synthesis with other transition metals.
Źródło:
Acta Biochimica Polonica; 2015, 62, 4; 739-745
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Growth Kinetics and Toxicity of Pseudomonas fredriksbergsis Grown on Phenol as Sole Carbon Source
Autorzy:
Aljbour, Salah H.
Khleifat, Khaled M.
Al Tarawneh, Amjad
Asasfeh, Batool
Qaralleh, Haitham
El-Hasan, Tayel
Magharbeh, Mousa K.
Al-Limoun, Muhamad O.
Powiązania:
https://bibliotekanauki.pl/articles/2027891.pdf
Data publikacji:
2021
Wydawca:
Polskie Towarzystwo Inżynierii Ekologicznej
Tematy:
phenol
biodegradation
Pseudomonas fredriksbergsis
Haldane model
GC-MS
Opis:
Phenol is one of the main pollutants that have a serious impact on the environment and can even be very critical to human health. The biodegradation of phenol can be considered an increasingly important pollution control process. In this study, the degradation of phenol by Pseudomonas fredriksbergsis was investigated for the first time under different growth conditions. Six different initial concentrations of phenol were used as the primary substrate. Culture conditions had an important effect on these cells' ability to biodegrade phenol. The best growth of this organism and its highest biodegradation level of phenol were noticed at pH 7, temperature 28 °C, and periods of 36 and 96 h, respectively. The highest biodegradation rate was perceived at 700 mg/L initial phenol concentration. Approximately 90% of the phenol (700 mg/L) was removed in less than 96 hours of incubation time. It was found that the Haldane model best fitted the relationship between the specific growth rate and the initial phenol concentration, whereas the phenol biodegradation profiles time could be adequately described by the modified Gompertz model. The parameters of the Haldane equation are: $0.062 h^{−1}$, 11 ppm, and 121 ppm for Haldane’s maximum specific growth rate, the half-saturation coefficient, and the Haldane’s growth kinetics inhibition coefficient, respectively. The Haldane equation fitted the experimental data by minimizing the sum of squared error (SSR) to $1.36×10^{-3}$.
Źródło:
Journal of Ecological Engineering; 2021, 22, 10; 251-263
2299-8993
Pojawia się w:
Journal of Ecological Engineering
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Biosorption of Chromium by Living Cells of Azotobacter s8, Bacillus subtilis and Pseudomonas aeruginosa using Batch System Reactor
Autorzy:
Kurniawan, Setyo Budi
Imron, Muhammad Fauzul
Purwanti, Ipung Fitri
Powiązania:
https://bibliotekanauki.pl/articles/123932.pdf
Data publikacji:
2019
Wydawca:
Polskie Towarzystwo Inżynierii Ekologicznej
Tematy:
Azotobacter
Bacillus subtilis
bacteria
biosorption
Cr
Pseudomonas Putida
Opis:
Chromium in wastewater is classified as one of the dangerous contaminants that require further treatment before being discharged to water body. The concentration of chromium in water body, especially river, has increased as many industries utilize chromium as raw material and then discharge their wastewater without any treatment. Biosorption is one of methods that are widely used to treat heavy metal containing wastewater. Bacteria are the most common microorganisms to be used as heavy metal treatment agent. Azotobacter s8, Bacillus subtilis and Pseudomonas putida had been proven to have a heavy metal resistant capability. The screening test showed that Minimum Inhibitory Concentration (MIC) value of chromium for all bacteria ranged from 100 to 250 mg/L of CrCl3. The chromium biosorption test by bacteria showed that Azotobacter s8 was able to remove 10.53%, and Bacillus subtilis was able to remove 5.68% chromium from 50 mg/L initial concentration, while Pseudomonas putida showed no chromium removal. The chromium biosorption capacity by Azotobacter s8 was 580.08 mg/g and 349.30 mg/g for Bacillus subtilis.
Źródło:
Journal of Ecological Engineering; 2019, 20, 6; 184-189
2299-8993
Pojawia się w:
Journal of Ecological Engineering
Dostawca treści:
Biblioteka Nauki
Artykuł

Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies