Bibliografías temáticas / Pseudomonas

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Literatura académica sobre el tema "Pseudomonas"

Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 25 de julio de 2025

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Artículos de revistas sobre el tema "Pseudomonas"

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Godfrey, S. A. C., S. A. Harrow, J. W. Marshall, and J. D. Klena. "Characterization by 16S rRNA Sequence Analysis of Pseudomonads Causing Blotch Disease of Cultivated Agaricus bisporus." Applied and Environmental Microbiology 67, no. 9 (2001): 4316–23. http://dx.doi.org/10.1128/aem.67.9.4316-4323.2001.

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ABSTRACT Bacterial blotch of Agaricus bisporus has typically been identified as being caused by either Pseudomonas tolaasii (brown blotch) or Pseudomonas gingeri(ginger blotch). To address the relatedness of pseudomonads able to induce blotch, a pilot study was initiated in which pseudomonads were selectively isolated from mushroom farms throughout New Zealand. Thirty-three pseudomonad isolates were identified as being capable of causing different degrees of discoloration (separable into nine categories) of A. bisporus tissue in a bioassay. These isolates were also identified as unique using r
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Freitas, J. Renato de, and James J. Germida. "Pseudomonas cepacia and Pseudomonas putida as winter wheat inoculants for biocontrol of Rhizoctonia solani." Canadian Journal of Microbiology 37, no. 10 (1991): 780–84. http://dx.doi.org/10.1139/m91-134.

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Pseudomonas cepacia R55 and R85 and Pseudomonas putida R104, antagonistic towards plant pathogenic fungi in vitro, were assessed as seed inoculants for winter wheat (cv. Norstar) grown in a growth chamber in soil infested with Fusarium solani or Rhizoctonia solani isolate AG-1, AG 2-1, or AG-3. Infestation of soil with R. solani AG-1 or AG 2-1 reduced root dry weight of uninoculated plants by 62 and 78%, respectively, whereas R. solani AG-3 or F. solani had no effect on plant biomass. Pseudomonad inoculants increased (relative to plants subjected to disease) the winter wheat root dry weight by
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FARRAG, SEHAM A., and ELMER H. MARTH. "Behavior of Listeria monocytogenes when Incubated Together with Pseudomonas Species in Tryptose Broth at 7 and 13°C." Journal of Food Protection 52, no. 8 (1989): 536–39. http://dx.doi.org/10.4315/0362-028x-52.8.536.

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Tryptose broth (TB) was inoculated with Listeria monocytogenes (strain Scott A or California), Pseudomonas aeruginosa, Pseudomonas flourescens, or a combination of L. monocytogenes plus Pseudomonas species, and incubated at 7 or 13°C for 8 weeks. McBride Listeria Agar was used to determine numbers of L. monocytogenes and Pseudomonas Isolation Agar to enumerate Pseudomonas species at 0, 7, 14, 28, 42, or 56 d. At 13°C, presence of P. fluorescens had a slight negative effect on growth of L. monocytogenes strain Scott A, and was somewhat detrimental to its survival during the extended incubation.
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Katsuwon, J., R. Zdor, and A. J. Anderson. "Superoxide dismutase activity in root-colonizing pseudomonads." Canadian Journal of Microbiology 39, no. 4 (1993): 420–29. http://dx.doi.org/10.1139/m93-061.

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Several saprophytic fluorescent pseudomonads that are aggressive root colonizers express similar specific activities of superoxide dismutase during growth in liquid culture. The pseudomonads have the potential to produce hydrogen peroxide sensitive and hydrogen peroxide insensitive isoforms of superoxide dismutase with distinct mobilities in nondenaturing polyacrylamide gel electrophoresis. Synthesis of the hydrogen peroxide insensitive form is enhanced by limited iron availability, by exposure to Mn2+, and to a lesser extent by external sources of superoxide anion. Unlike Pseudomonas aerugino
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McSpadden Gardener, Brian B. "Diversity and Ecology of Biocontrol Pseudomonas spp. in Agricultural Systems." Phytopathology® 97, no. 2 (2007): 221–26. http://dx.doi.org/10.1094/phyto-97-2-0221.

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Diverse Pseudomonas spp. may act as biological controls of plant pathogens, but the ecology of those natural populations is not well understood. And, while biocontrol potential has been identified in multiple pseudomonad strains, the linkages between genotype and phenotype have yet to be fully delineated. However, intensive studies of one class of biocontrol strains, i.e., those that can produce 2,4-diacetylphloroglucionl (DAPG), have provided new insights into the diversity, distribution, and interactions of biocontrol pseudomonads. Those studies also laid the foundation for future research a
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Rahman, Mizanur, Mohammad Jobayer, Nadira Akter, Farook Ahamed, SM Shamsuzzaman, and Kazi Zulfiquer Mamun. "Rapid detection of Pseudomonad at species level by multiplex PCR in surgical units and ICU of Dhaka Medical College Hospital." Bangladesh Journal of Medical Microbiology 10, no. 2 (2016): 22–26. http://dx.doi.org/10.3329/bjmm.v10i2.51928.

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Pseudomonads are the most important gram negative organisms involved in various types of infection. This cross sectional study was conducted from January to December 2010 to isolate and identify Pseudomonad at species level in different clinical samples by culture and multiplex polymerase chain reaction (PCR) and to evaluate the efficacy of PCR in rapid detection of the bacteria at species level. Wound swab and tips of endotracheal tube were collected from hospitalized patients from different surgical units and intensive care unit (ICU) of Dhaka Medical College Hospital, Dhaka. Pseudomonads we
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Campbell, James N., Kenneth Conn, Linnea Sorlie, and Fred D. Cook. "Inhibition of growth in canola seedlings caused by an opportunistic Pseudomonas sp. Under laboratory and field conditions." Canadian Journal of Microbiology 32, no. 3 (1986): 201–7. http://dx.doi.org/10.1139/m86-041.

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If Pseudomonas rp2, a field-isolated fluorescent pseudomonad, is present on canola (rape) seeds at the time of sprouting, it causes an inhibition of root growth leading to death or delayed maturation of the plant. Inhibitory strains of this type comprise less than 10% of the fluorescent pseudomonads isolated from local field samples, but they were found in widely dispersed sources. By present standards, these Pseudomonas strains would be considered soil saprophytes, since they survive in sterile soil at 4 and −20 °C in the absence of plant material, and since they do not match taxonomically wi
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Beaulieu, C., S. Gill, L. Miville, and P. Dion. "Genetic regions of Pseudomonas aureofaciens strain 211 involved in nopaline catabolism." Canadian Journal of Microbiology 34, no. 7 (1988): 843–49. http://dx.doi.org/10.1139/m88-145.

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A DNA fragment from the nopaline catabolism region of the Ti plasmid of Agrobacterium tumefaciens showed no detectable homology to the total DNA of several nopaline-utilizing strains of Pseudomonas spp. From one of these pseudomonads, Pseudomonas aureofaciens strain 211, mutants defective in the catabolism of nopaline but not arginine, have been obtained by mutagenesis with transposon Tn5, and also with TnV using a new suicide plasmid vector. The DNA fragment bearing the TnV insertion has been cloned and found to hybridize with DNA of every pseudomonad tested, independently of the capacity to
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Meyer, Jean-Marie, Valérie A. Geoffroy, Nader Baida, et al. "Siderophore Typing, a Powerful Tool for the Identification of Fluorescent and Nonfluorescent Pseudomonads." Applied and Environmental Microbiology 68, no. 6 (2002): 2745–53. http://dx.doi.org/10.1128/aem.68.6.2745-2753.2002.

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ABSTRACT A total of 301 strains of fluorescent pseudomonads previously characterized by conventional phenotypic and/or genomic taxonomic methods were analyzed through siderotyping, i.e., by the isoelectrophoretic characterization of their main siderophores and pyoverdines and determination of the pyoverdine-mediated iron uptake specificity of the strains. As a general rule, strains within a well-circumscribed taxonomic group, namely the species Pseudomonas brassicacearum, Pseudomonas fuscovaginae, Pseudomonas jessenii, Pseudomonas mandelii, Pseudomonas monteilii, “Pseudomonas mosselii,” “Pseud
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Tryfinopoulou, P., E. Tsakalidou, and G. J. E. Nychas. "Characterization of Pseudomonas spp. Associated with Spoilage of Gilt-Head Sea Bream Stored under Various Conditions." Applied and Environmental Microbiology 68, no. 1 (2002): 65–72. http://dx.doi.org/10.1128/aem.68.1.65-72.2002.

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ABSTRACT The population dynamics of pseudomonads in gilt-head sea bream Mediterranean fish (Sparus aurata) stored under different conditions were studied. Phenotypic analysis and sodium dodecyl sulfate-polyacrylamide gel electrophoresis of whole-cell proteins were performed to identify a total of 106 Pseudomonas strains isolated from S. aurata stored under different temperatures (at 0, 10, and 20°C) and packaging conditions (air and a modified atmosphere of 40% CO2-30% N2-30% O2). Pseudomonas lundensis was the predominant species, followed by Pseudomonas fluorescens, while Pseudomonas fragi an
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Tesis sobre el tema "Pseudomonas"

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Frenken, Leo G. "Pseudomonas glumae lipase : characterization, biogenese and protein engineering = Pseudomona glumae lipase /." [S.l. : s.n.], 1993. http://www.gbv.de/dms/bs/toc/131132261.pdf.

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Wilson, Neil Lewis. "Integrons in pseudomonads are associated with hotspots of genomic diversity." Phd thesis, Australia : Macquarie University, 2008. http://hdl.handle.net/1959.14/13295.

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Thesis (PhD)--Macquarie University, Division of Environmental & Life Sciences, Department of Biological Sciences, 2008.<br>Bibliography: p. 257-274.<br>Literature review -- General materials and methods -- Characterisation of strain collection -- Distribution of integrons and gene cassettes in pseudomonas -- Genomic context of pseudomonas integrons -- Evolutionary analysis of pseudomonas spp. integrons 199 -- Final discussion -- Appendix -- References.<br>Integrons associated with mobile genetic elements have played a central role in the emergence and spread of multiple antibiotic resistance i
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Bredenbruch, Florian. "Einfluss des Pseudomonas-Quinolon-Signals auf die interbakterielle Kommunikation von Pseudomonas aeruginosa." [S.l.] : [s.n.], 2006. http://deposit.ddb.de/cgi-bin/dokserv?idn=979194091.

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Manuel, Jerrylynn Laguras. "An Investigation of the Impact of the Stringent Response on the Growth Inhibition of Sclerotinia sclerotiorum by Biocontrol Pseudomonads Pseudomonas sp. DF41 and Pseudomonas chlororaphis PA23." American Society for Microbiology, 2011. http://hdl.handle.net/1993/4791.

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The stringent response (SR) is a global regulatory mechanism that allows bacteria to survive starvation. The plant surface is one environment where a fluctuation in nutrient availability is experienced. Because both Pseudomonas sp. DF41 and Pseudomonas chlororaphis PA23 are able to protect canola from the fungal pathogen Sclerotinia sclerotiorum when applied as a foliar spray, we sought to investigate the impact of this response on the antifungal activities of these two biocontrol strains. The SR exerts its effects on gene transcription through production of the alarmone(p)ppGpp. Metabol
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Turner, Keith Holte. "Bistability in Pseudomonas aeruginosa." Thesis, Harvard University, 2012. http://dissertations.umi.com/gsas.harvard:10159.

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The opportunistic pathogen P. aeruginosa is a leading cause of hospital-accquired infections, and is also the primary cause of morbidity and mortality in patients with cystic fibrosis (CF). In this thesis, I describe the identification and characterization of a novel LysR-type transcription regulator (LTTR) of P. aeruginosa named BexR. I show that BexR exhibits reversible ON/OFF bistable expression, which leads to the bistable expression of several genes including one encoding a virulence factor. I present results suggesting that this bistable expression depends on positive feedback of BexR. T
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Silistre, Hazel. "Riboregulation in Pseudomonas aeruginosa." Thesis, University of Nottingham, 2016. http://eprints.nottingham.ac.uk/32634/.

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The opportunistic human pathogen Pseudomonas aeruginosa controls virulence, production of secondary metabolites, motility, biofilm formation, growth in anaerobic conditions, intracellular and intercellular signalling and the switch from an acute to a chronic mode of infection at the transcriptional and post-transcriptional levels by modulation of the Gac/Rsm system. Cell density-dependent signal accumulation and environmental stimulators such as pH changes and ion limitation activate the GacS/GacA two-component system which in turn triggers transcription of the small regulatory RNAs RsmY and R
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Daly, Philip J. "Permeability of pseudomonas aeruginosa." Thesis, Aston University, 1986. http://publications.aston.ac.uk/12458/.

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Ullstrom, Catherine Ann MacDonald. "Comparison of protein OprF from Pseudomonas syringae with protein OprF from Pseudomonas aeruginosa." Thesis, University of British Columbia, 1990. http://hdl.handle.net/2429/29200.

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The major outer membrane protein OprF from Pseudomonas aeruginosa was compared with OprF from the fluorescent phytopathogen Pseudomonas syringae. The P. syringae oprF gene was subcloned and sequenced and found to code for a sequence of 344 amino acids containing a 24 amino acid leader sequence. The mature protein, with a deduced molecular weight of 34,225, contained four cysteine residues and an alanine-proline rich area. Comparison of the P. syringae OprF amino acid sequence with the P. aeruginosa OprF and the E. coli OmpA sequences showed that the sequences were most similar at the carboxy-t
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Shafik, Hussain latif. "Taxonomie des pseudomonas phytopathogènes du groupe de pseudomonas syringae : études phénotypique et génotypique." Angers, 1994. http://www.theses.fr/1994ANGE0012.

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La taxonomie des pseudomonas fluorescents phytopathogènes oxydase négative bien qu'ayant évolué dans le temps est actuellement floue et insatisfaisante. Ce groupe comprend 52 pathovars de p. Syringae et 5 espèces proches (p. Cichorii et p. Viridiflava, p. Amygdali, p. Ficuserectae, p. Meliae). Les caractères phénotypiques (20 caractères biochimiques et l'assimilation de 147 substrats hydrocarbones) de 655 souches des pathovars de p. Syringae et des 5 espèces proches ont été étudiés. Les données ont été interprétées par l'utilisation d'une méthode de taxonomie numérique et du coefficient de cap
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Linscott, Andrea J. (Andrea Jane). "Regulatory Divergence of Aspartate Transcarbamoylase from the Pseudomonads." Thesis, University of North Texas, 1996. https://digital.library.unt.edu/ark:/67531/metadc277625/.

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Aspartate transcarbamoylase (ATCase) was purified from 16 selected bacterial species including existing Pseudomonas species and former species reassigned to new genera. An enormous diversity was seen among the 16 enzymes with each class of ATCase being represented. The smallest class, class C, with a catalytically active homotrimer, at 100 kDa, was found in Bacillus and other Gram positive bacteria. In this report, the ATCases from the Gram negatives, Shewanella putrefaciens and Stenotrophomonas maltophilia were added to class C membership. The enteric bacteria typify class B ATCases at 310 kD
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Libros sobre el tema "Pseudomonas"

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Ramos, Juan-Luis, ed. Pseudomonas. Springer US, 2004. http://dx.doi.org/10.1007/978-1-4419-9088-4.

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Ramos, Juan-Luis, Johanna B. Goldberg, and Alain Filloux, eds. Pseudomonas. Springer Netherlands, 2015. http://dx.doi.org/10.1007/978-94-017-9555-5.

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Ramos, Juan L., and Alain Filloux, eds. Pseudomonas. Springer Netherlands, 2010. http://dx.doi.org/10.1007/978-90-481-3909-5.

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Ramos, Juan-Luis, ed. Pseudomonas. Springer US, 2004. http://dx.doi.org/10.1007/978-1-4419-9084-6.

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Ramos, Juan-Luis, ed. Pseudomonas. Springer US, 2004. http://dx.doi.org/10.1007/978-1-4419-9086-0.

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Montie, Thomas C., ed. Pseudomonas. Springer US, 1998. http://dx.doi.org/10.1007/978-1-4899-0120-0.

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Ramos, Juan-Luis, and Alain Filloux, eds. Pseudomonas. Springer Netherlands, 2007. http://dx.doi.org/10.1007/978-1-4020-6097-7.

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Ramos, Juan-Luis, and Roger C. Levesque, eds. Pseudomonas. Springer US, 2006. http://dx.doi.org/10.1007/0-387-28881-3.

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C, Montie Thomas, ed. Pseudomonas. Plenum Press, 1998.

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1956-, Ramos Juan-Luis, ed. Pseudomonas. Kluwer Academic/Plenum, 2004.

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Capítulos de libros sobre el tema "Pseudomonas"

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Cohen, Taylor S., Dane Parker, and Alice Prince. "Pseudomonas aeruginosa Host Immune Evasion." In Pseudomonas. Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-9555-5_1.

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Pizarro-Tobías, Paloma, Zulema Udaondo, Amalia Roca, and Juan L. Ramos. "Events in Root Colonization by Pseudomonas putida." In Pseudomonas. Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-9555-5_10.

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Holloway, Bruce. "My Memories of Pseudomonas in the Twentieth Century." In Pseudomonas. Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-9555-5_11.

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Dieppois, Guennaelle, Onya Opota, Jorge Lalucat, and Bruno Lemaitre. "Pseudomonas entomophila: A Versatile Bacterium with Entomopathogenic Properties." In Pseudomonas. Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-9555-5_2.

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Hughes, Ami Joy, and Alan R. Hauser. "Pseudomonas Activation of the Inflammasome." In Pseudomonas. Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-9555-5_3.

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Casabona, María-Guillermina, Sylvie Elsen, Valentina Cogoni, and Ina Attrée. "P. aeruginosa Type VI Secretion Machinery: Another Deadly Syringe." In Pseudomonas. Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-9555-5_4.

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Toyofuku, Masanori, George A. O’Toole, and Nobuhiko Nomura. "Anaerobic Life Style of Pseudomonas aeruginosa." In Pseudomonas. Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-9555-5_5.

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Mercado-Blanco, Jesús. "Pseudomonas Strains that Exert Biocontrol of Plant Pathogens." In Pseudomonas. Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-9555-5_6.

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Morita, Yuji, Junko Tomida, and Yoshiaki Kawamura. "Resistance and Response to Anti-Pseudomonas Agents and Biocides." In Pseudomonas. Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-9555-5_7.

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Wysoczynski, Christina L., and Mair E. A. Churchill. "Lessons from the QSCR Structure for Quorum Sensing." In Pseudomonas. Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-9555-5_8.

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Actas de conferencias sobre el tema "Pseudomonas"

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Videla, H. A., S. G. Gómez. de Saravia, M. F. L. de Mele, and P. S. Guiamet. "Bioelectrochemical Assessment of Biofilm Effects on MIC of Two Different Steels of Industrial Interest." In CORROSION 1990. NACE International, 1990. https://doi.org/10.5006/c1990-90123.

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Abstract SAE 1020 and X-60 steel samples were assayed in laboratory experiments against two different microbial strains isolated from cutting-oil emulsions: Pseudomonas fluorescens and Desulfovibrio vulgaris to evaluate their resistance to microbial attack. Several electrodes were immersed during different periods of time either in a Pseudomonas fluorescens or in a Desulfovibrio vulgaris pure culture and in a mixed culture of Pseudomonas fluorescens + Desulfovibrio vulgaris. The relationship between the corrosive attack and bacterial biofilms was assessed in each case by using electrochemical
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Evseev, Peter, Nikolay Tkachenko, and Konstantin Miroshnikov. "Diversity of Tailed Bacteriophages Infecting Pseudomonas Aeruginosa." In 2024 IEEE International Multi-Conference on Engineering, Computer and Information Sciences (SIBIRCON). IEEE, 2024. http://dx.doi.org/10.1109/sibircon63777.2024.10758485.

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Luo, J. S., X. Campaignolle, J. Bullen, M. W. Mittelman, D. C. White, and J. F. Zibrida. "Influence of Molybdate on Microbiologically Influenced Corrosion of Mild Steel." In CORROSION 1992. NACE International, 1992. https://doi.org/10.5006/c1992-92186.

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Abstract The effect of molybdate ion on the corrosion of mild steel in an aerobic medium containing a Pseudomonas biofilm and sulfate reducing bacteria has been investigated. Changes in specimen open circuit potentials correlated with changes in microbial activities. Formation of a microbial film by Pseudomonas on the metal surface could be characterized by changes of phase angle at the lowest frequency; and molybdate functioned as a corrosion inhibitor in the presence of sulfate reducing bacteria.
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Das, Dipankar, Subhasish Kamilya, Vertika Rai, et al. "Antibiotic susceptibility profiling of Pseudomonas aeruginosa in nosocomial infection." In 2024 15th International Conference on Computing Communication and Networking Technologies (ICCCNT). IEEE, 2024. http://dx.doi.org/10.1109/icccnt61001.2024.10723982.

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Agrawal, Akshat, Piyush Shrivastava, Shweta Mittal, Ankur Saharia, Ghanshyam Singh, and Manish Tiwari. "A Photonic Crystal Fiber Based Pseudomonas Aeruginosa Bacteria Sensor." In 2024 4th International Conference on Technological Advancements in Computational Sciences (ICTACS). IEEE, 2024. https://doi.org/10.1109/ictacs62700.2024.10841150.

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Нейдорф, А. Р., М. А. Морозова, and М. М. Оганисян. "THE PROBLEM OF ASSESSING WATER QUALITY IN THE CULTIVATION OF STURGEON IN THE USV." In DEVELOPMENT AND MODERN PROBLEMS OF AQUACULTURE. ООО "ДГТУ-Принт" Адресс полиграфического предприятия 344003 пл Гагарина, зд. 1, 2023. http://dx.doi.org/10.23947/aquaculture.2023.79-81.

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The article discusses the results of the analysis of microbiological indicators of water quality in the basins of the UZV. The analysis of pool water was carried out according to 8 indicators (HPV, E. coli, generalized coliform bacteria, spores of sulfite-reducing clostridium, enterococci, Pseudomonas aeromonas, Pseudomonas). Pathogenicity and antibiotic resistance factors of isolated strains of pathogenic aeromonads and pseudomonads were determined
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Vlasova, A. I., and O. M. Minaeva. "Efficiency of Pseudomonas aureofaciens colonization in wheat rhizosphere under model condition." In 2nd International Scientific Conference "Plants and Microbes: the Future of Biotechnology". PLAMIC2020 Organizing committee, 2020. http://dx.doi.org/10.28983/plamic2020.274.

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The survival of Pseudomonas aureofaciens in the wheat rhizosphere was studied. A significant increase in the number of pseudomonads and tetracycline resistant bacteria was shown when introduced into the model system of strains.
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Gerasimchuk, A. L., D. V. Antsiferov, P. A. Bukhtiyarova, and D. A. Ivasenko. "OBTAINING A LIPOPHILIC BACTERIAL CONSORTIUM FOR FAT DEPOSITS UTILIZATION." In STATE AND DEVELOPMENT PROSPECTS OF AGRIBUSINESS. DSTU-PRINT, 2020. http://dx.doi.org/10.23947/interagro.2020.1.81-84.

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Bacterial strains with lipolytic activities Pseudomonas citronellolis A13, Pseudomonas extremaustralis Б11, Pseudomonas nitroreducens Д14, Pseudomonas sp. B21, Microvirgula curvata B37, Brevibacillus sp. 28Д, Bacillus subtilis spp. B10, B34 were isolated from fat-containing industrial wastewater of food industry and were used for obtaining a lipophilic bacterial consortium that perspective for fat deposits utilization.
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Kokoulin, M. S., E. V. Sokolova, L. A. Romanenko, Yu N. Elkin та N. A. Komandrova. "Липополисахариды морских бактерий рода Pseudomonas". У XVI Всероссийская молодежная школа-конференция памяти В. Е. Васьковского "Актуальные проблемы химии и биологии". Дальневосточное отделение Российской академии наук, 2017. http://dx.doi.org/10.47471/16_2017_09_04_09_09.

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Smirnova, S. V., and А. A. Zhdanova. "VIRULENCE FACTORS OF PSEUDOMONAS AERUGINOSA." In Инновационное развитие агропромышленного, химического, лесного комплексов и рациональное природопользование. НовГУ им. Ярослава Мудрого, 2023. http://dx.doi.org/10.34680/978-5-89896-873-1/2023.innovation.38.

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Informes sobre el tema "Pseudomonas"

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ศิวรังสรรค์, นภา. การทำให้บริสุทธิ์บางส่วนและการตรวจสอบลักษณะเฉพาะของไลเปสจาก Pseudomonas aeruginosa : รายงานผลการวิจัย. จุฬาลงกรณ์มหาวิทยาลัย, 1997. https://doi.org/10.58837/chula.res.1997.22.

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Pseudomonas aeruginosa เป็นแบคทีเรียที่แยกได้จากตะกอนในบ่อเลี้ยงกุ้งในประเทศไทย สามารถถูกชักนำให้ผลิตเอนไซม์ไลเปสสูงขึ้นได้โดยเลี้ยงที่อุณหภูมิ 37 องศาเซลเซียส pH 7.0 ในอาหารสูตรปรับต่ำที่มี 0.13 % (NH[subscript4])[subscript2SO[subscript4] เป็นแหล่งไนโตรเจนและมี 2% ฟรุกโตสเป็นแหล่งคาร์บอน และพบว่าการผลิตไลเปสถูกกดดันในสภาวะที่มีกลูโคสด้วยกระบวนการคาตาบอไลต์รีเพรสชั่น เมื่อทำให้ crude เอนไซม์เข้ม้นขึ้นโดยอุลตราฟิลเตรชั่นและแยกโดย Sephadex G-100 คอลัมน์โครมาโตกราฟีเอนไซม์ไลเปสที่ความบริสุทธิ์ขึ้น 10.92 เท่า จากการศึกษาสมบัติของไลเปสที่มีความบริสุทธิ์บางส่วนนี้ พบว่าเอนไซม์ประกอบด้วยหน่วยย่อยที่ม
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ธนียวัน, จิราภรณ์, กอบชัย ภัทรกุลวณิชย์ та ขนิษฐา วงษ์นิกร. การโคลนและลักษณะสมบัติของยีนกลุ่ม rhl ที่เกี่ยวข้องกับการสังเคราะห์โมโนแรมโนลิพิดทางชีวภาพของ Pseudomonas aeruginosa A41 : รายงานผลการวิจัย. จุฬาลงกรณ์มหาวิทยาลัย, 2006. https://doi.org/10.58837/chula.res.2006.41.

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Pseudomonas sp. A41 ที่แยกจากน้ำทะเลอ่าวไทย มีความสามารถในการผลิตแรมโนลิพิดจากลักษณะทางสัณฐานวิทยาและสมบัติทางชีวเคมีร่วมกับข้อมูลลำดับนิวคลีโอไทด์ของ 16S rDNA สามารถจำแนกสายพันธุ์ A41 เป็น Pseudomonas aeruginosa แยกยีนที่เกี่ยวข้องกับการสังเคราะห์แรมโนลิพิดจาก Pseudomonas aeruginosa A41 โดยเทคนิคเซาท์เธอร์นไฮบริไดเซชันจีโนมิกดีเอ็นเอกับดีเอ็นเอติดตาม rhlR หรือ rhlA โคลนชิ้นดีเอ็นเอที่ให้ผลบวกเข้าในพลาสมิดเวกเตอร์และหาลำดับนิวคลีโอไทด์ของชิ้นดีเอ็นเอแทรกสอด จากลำดับนิวคลีโอไทด์ทั้งสิ้น 4,965 bp พบกรอบอ่านรหัสเปิด (ORF) ที่สมบูรณ์จำนวน 4 แห่ง และไม่สมบูรณ์ 1 แห่ง กรอบอ่านรหัสเปิดทั้งหมดมีทิศทาง
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Ornston, L. N. Negative Control of Biodegradation in Pseudomonas. Defense Technical Information Center, 1988. http://dx.doi.org/10.21236/ada193875.

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Krawiec, S. Cloning and expression of the sulfoxide/sulfone/sulfonate/sulfate genes in Pseudomonads and Thiobacillae. [Pseudomonas, Thiobacillus, Rhodococcus]. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/5653703.

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Lewis, Kim. Genetics of Persister Formation in Pseudomonas aeruginosa. Defense Technical Information Center, 2012. http://dx.doi.org/10.21236/ada580295.

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ธนียวัน, จิราภรณ์, ณัฐชนัญ ลีพิพัฒน์ไพบูลย์ та นพรัตน์ วานิชสุขสมบัติ. การติดตามการเจริญและการผลิตสารลดแรงตึงผิวชีวภาพที่ผลิตโดย Pseudomonas sp. สายพันธุ์ A41 ในอาหารที่มีน้ำมันและกรดไขมันเป็นแหล่งคาร์บอน : รายงานผลการวิจัย. จุฬาลงกรณ์มหาวิทยาลัย, 2004. https://doi.org/10.58837/chula.res.2004.38.

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Pseudomonas sp. สายพันธุ A41 คัดแยกได้จากน้ำทะเลในอ่าวไทย มีความสามารถผลิตสารลดแรงตึงผิวชีวภาพสูงสุดในภาวะที่ใช้น้ำมันปาล์มเป็นแหล่งคาร์บอน และใช้ NH4N03 เป็นแหล่งไนโตรเจน ในอาหารเลี้ยงเชื้อเหลวกำหนดสูตรโดยมีอัตราส่วนระหว่างคาร์บอนต่อไนโตรเจนเท่ากับ 10.29 ค่าความเป็นกรดเป็นด่างเท่ากับ 7.0 บ่มที่อุณหภูมิห้อง (30±℃), เขย่าที่ 200 รอบต่อนาที เป็นเวลา 72 ชั่วโมง มีค่า production yield (YP/S) 0.125 กรัมต่อกรัม ซึ่งมีค่ามากกว่าผลิตโดยใช้น้ำตาลกลูโคสเป็นแหล่งคาร์บอนซึ่งมีค่า production yield (YP/S) 0.113 กรัมต่อกรัม เมื่อนำสารลดแรงตึงผิวชีวภาพที่ผลิตได้ทำให้บริสุทธิ์ด้วยการสกัดโดยตัวทำละลายอินทรีย์พบ
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ชวนชื่น, รุ่งทิพย์, та ชาญวิทย์ ตรีพุทธรัตน์. การศึกษาอินทริกรอนส์ใน Pseudomonas aeruginosa และ Acinetobacter baumannii : รายงานวิจัย. จุฬาลงกรณ์มหาวิทยาลัย, 2011. https://doi.org/10.58837/chula.res.2011.105.

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ศึกษา class 1 integrons ในเชื้อ Pseudomonas aeruginosa (n=101) และ Acinetobacter baumannii (n=176) ที่แยกได้จากผู้ป่วยในโรงพยาบาล พบว่า เชื้อทุกตัวดื้อต่อยาปฏิชีวนะหลายชนิดพร้อมกัน เชื้อ P. aeruginosa จำนวน 96 isolates (95%) ให้ผลบวกต่อยีน intl1 โดยในเชื้อเหล่านี้เชื้อจำนวน 70 isolates (73%) มี gene cassette จัดรูปแบบ integron profile ได้ 12 รูปแบบ ซึ่งที่พบมากที่สุดคือ aadB-cmlA-aadA1 และมีเชื้อเพียง 1 isolate ที่สามารถถ่ายทอด class 1 integrons แบบขวางได้ ส่วน A. baumannii จำนวน 69 isolates (39%) ที่พบว่ามียีน intl1 โดยเชื้อจำนวน 42 isolates (61%) มี gene cassette จัดรูปแบบ integron profile ไ
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Schnider, Shirley. The biological properties of Pseudomonas aeruginosa bacteriophage 7V. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.771.

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Lessie, T. G. Genomic plasticity and catabolic potential of Pseudomonas cepacia. Office of Scientific and Technical Information (OSTI), 1996. http://dx.doi.org/10.2172/224251.

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Blake, Robert, and III. Transformation and Precipitation of Toxic Metals by 'Pseudomonas maltophilia'. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada238232.

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