Relevant bibliographies by topics / Chryseomonas luteola

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Chryseomonas luteola'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 February 2022

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Journal articles on the topic "Chryseomonas luteola"

1

Adolphs, M., K. Taraz, and H. Budzikiewicz. "Catecholate Siderophores from Chryseomonas luteola." Zeitschrift für Naturforschung C 51, no. 5-6 (June 1, 1996): 281–85. http://dx.doi.org/10.1515/znc-1996-5-603.

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Abstract Two catecholate siderophores (chrysobactin and chryseomonin) were isolated from an iron-deficient culture medium of Chryseomonas luteola. Their structures were elucidated by chemical degradation studies and spectroscopic methods, especially 2D-NMR techniques, and confirmed by synthesis. Chryseomonin constitutes a novel type of catecholate siderophore.
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2

Urbano, Baldari, Antonio Ascari Raccagni, and Giuseppe Montini. "Onycholysis caused by chryseomonas luteola." Journal of the European Academy of Dermatology and Venereology 4, no. 1 (July 28, 2006): 112–13. http://dx.doi.org/10.1111/j.1468-3083.1995.tb00301.x.

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3

URBANO, B. "Onycholysis caused by chryseomonas luteola." Journal of the European Academy of Dermatology and Venereology 4, no. 1 (February 1995): 112–13. http://dx.doi.org/10.1016/0926-9959(94)00092-e.

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4

Jayagopal, S., M. G. Berry, G. Ross, and A. J. Howcroft. "Hand infection caused by Chryseomonas luteola." British Journal of Plastic Surgery 57, no. 7 (October 2004): 694–95. http://dx.doi.org/10.1016/j.bjps.2004.05.028.

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Ghosh, S. K. "A Rare Infection Caused by Chryseomonas luteola." Journal of Infection 41, no. 1 (July 2000): 109–10. http://dx.doi.org/10.1053/jinf.2000.0660.

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6

Ozdemir, G., and S. H. Baysal. "Chromium and aluminum biosorption on Chryseomonas luteola TEM05." Applied Microbiology and Biotechnology 64, no. 4 (May 1, 2004): 599–603. http://dx.doi.org/10.1007/s00253-003-1479-0.

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De, Anuradha S., Parul P. Salunke, Harshal R. Parikh, and Sujata M. Baveja. "Chryseomonas luteola from Bile Culture in an Adult Male with Severe Jaundice." Journal of Laboratory Physicians 2, no. 01 (January 2010): 040–41. http://dx.doi.org/10.4103/0974-2727.66708.

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ABSTRACTA 60-year-old male was admitted in this hospital with severe jaundice, who had open cholecystectomy done 2 months ago. ERCP was performed and bile was sent for culture. It grew Chryseomonas luteola in pure culture. He underwent hepaticojejunostomy after 1 month. Total bilirubin improved gradually. His condition was stable on discharge. Prompt diagnosis of non-fermenters is required, as some of them are resistant to multiple antibiotics. Clinicians have to be made aware of the pathogenic role of C. luteola and its resistance to ampicillin and cephalosporins.
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Patil, KavitaG, ShankarG Karadesai, and ParagV Hawaldar. "Cutaneous abscess due to Chryseomonas luteola in a previously healthy adult." Annals of Tropical Medicine and Public Health 5, no. 4 (2012): 360. http://dx.doi.org/10.4103/1755-6783.102058.

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9

Buitrón, Germán, and Ariel González. "Characterization of the microorganisms from an acclimated activated sludge degrading phenolic compounds." Water Science and Technology 34, no. 5-6 (September 1, 1996): 289–94. http://dx.doi.org/10.2166/wst.1996.0562.

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The microorganisms responsible for the degradation of a mixture of phenol, 4-chlorophenol (4CP), 2,4-dichlorophenol (24DCP) and 2,4,6-trichlorophenol (246TCP) were isolated and characterized in terms of its degradation rate. Activated sludge was acclimated for 70 days to 40 mg phenols/l. After this period the microorganisms responsible for the chlorinated phenol degradation were isolated and identified. Four types of Gram negative bacteria (Aeromonas sp., Pseudomonas sp. Flavimonas oryzihabitans, and Chryseomonas luteola) and Mycobacterium sp. were identified. The degradation kinetics of each phenol by Aeromonas sp.,Pseudomonas sp. Flavimonas oryzihabitans, Chryseomonas luteola and activated sludge were determined. The degradation of phenolic compounds was sequential: phenol and 4CP were first degraded, following by 24DCP and then by 246TCP. The acclimated activated sludge was from one to two orders of magnitude faster than the pure strains, when uptake rates were calculated in terms of the viable biomass (CFU). The qx for acclimated activated sludge varied between 8.2 and 15.8 × 10−7 mg/CFU-d (407–784 mg/gVSS-d). Aeromonas sp. presented the highest qx of the pure strains, based on a VSS basis (33–57 mg/gVSS-d) but, in terms of viable biomass (5.0–15.6 × 10−8 mg/CFU-d) Pseudomonas sp. did. Specific substrate uptake rate was 1.8 mg chlorinated phenols/g VSS-d for non-acclimated activated sludge.
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10

Buitrón, Germán, Ariel González, and Luz M. López-Marín. "Biodegradation of phenolic compounds by an acclimated activated sludge and isolated bacteria." Water Science and Technology 37, no. 4-5 (February 1, 1998): 371–78. http://dx.doi.org/10.2166/wst.1998.0670.

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The degradation of a mixture of phenol, 4-chlorophenol (4CP), 2,4-dichlorophenol (24DCP) and 2,4,6-trichlorophenol (246TCP) by acclimated activated sludge and by isolated bacteria was studied. Activated sludge was acclimated for 70 days to 40 mg phenols/l then the microorganisms responsible for the CP degradation were isolated and identified. Four types of Gram-negative bacteria (Aeromonas sp., Pseudomonas sp. Flavomonas oryzihabitans, and Chryseomonas luteola) were identified. Also, two acid-fast bacilli with distinct glycolipid patterns were isolated. From their chemical composition and their growth characteristics, both isolates appeared to be mycobacteria closely related to Mycobacterium peregrinum. The degradation kinetics of each phenol by Aeromonas sp., Pseudomonas sp. Flavomonas oryzihabitans, Chryseomonas luteola and activated sludge were determined. The acclimated activated sludge degradation rates were from one to two orders of magnitude higher than those of pure strains when uptake rates were calculated in terms of the viable biomass (CFU). The specific substrate uptake rate for acclimated activated sludge varied between 8.2 and 15.8 × 10−7 mg/CFU·d (407-784 mg/gVSS·d). Aeromonas sp. had the highest specific substrate uptake rate of the pure strains, based on a VSS basis (33-57 mg/gVSS·d) but, in terms of viable biomass (5.0-15.6 × 10−8 mg/CFU·d), the Pseudomonas sp. rate was the highest. Specific substrate uptake rates were 1.8 mg chlorinated phenols/g VSS·d for unacclimated activated sludge.
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Dissertations / Theses on the topic "Chryseomonas luteola"

1

El, Hamel Chahrazed. "Etude structurale de la porine OprF de Pseudomonas fluorescens et rôle de la région C-terminale dans la modulation de son activité ionophore en fonction de la température de croissance. Extension à la bactérie psychrotrophe Chryseomonas luteola." Rouen, 1999. http://www.theses.fr/1999ROUES084.

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La bactérie psychrotrophe P. Fluorescens MF0 est plus sensible aux antibiotiques de type β-lactamines à une température de croissance de 8°C qu'à une température de 28°C. Cette différence est parfaitement corrélée avec les valeurs de conductance obtenues pour les porines majoritaires de la membrane externe OprF à 8°C et 28°C puisqu'elles sont respectivement de 80 pS et 250 pS dans du NaCl 1M. Pour expliquer ce phénomène, les OprFs 8°C et 28°C ont été purifiées et les études de spectrométrie de masse et de dichroïsme circulaire ne montrent pas de différence dans leur structure primaire. Des mesures de cinétiques de digestion à la pronase ont conduit à une différence des valeurs de constantes de vitesse de dégradation impliquant ainsi une modification de la conformation protéique en fonction de la température de croissance. Les fragments protéolytiques de 18 kDa, résistant à l'action de la pronase, ont été purifiés et identifiés comme la partie N-terminale de la protéine native (177 acides aminés). Les deux fragments forment des canaux ioniques avec des valeurs de conductances similaires (65 et 75 pS dans NaCl 1M) impliquant que la région C-terminale est seule responsable de la modulation des canaux formes par l'OprF en fonction de la température de culture. La caractérisation du LPS associé aux OprFs met en évidence une différence de phosphorylation des LPS obtenus à partir de culture à 28°C et 8°C. Ainsi, l'association LPS-porine serait différente selon les températures de culture. Nous avons ensuite voulu rechercher une éventuelle généralisation de ce phénomène et nous avons choisi la bactérie psychrotrophe Chryseomonas luteola MCF10. La protéine majoritaire de la membrane externe (31 kDa) a été purifiée à 8°C et 28°C et son étude fonctionnelle montre des valeurs de conductances unitaires similaires quelle que soit la température de croissance. Cependant, la détermination de la séquence N-terminale ainsi que la séquence déduite du gène la caractérise comme une OmpA. L'utilisation des anticorps montre que C. Luteola est plus proche des entérobactéries que des pseudomonas. Ce résultat montre que le mécanisme de résistance décrit chez P. Fluorescens n'est pas systématiquement applicable à toute bactérie psychrotrophe.
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