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Journal articles on the topic 'Chryseomonas luteola'

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Published: 4 June 2021

Last updated: 6 February 2022

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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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5

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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7

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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8

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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11

Hawkins, Richard E., Richard A. Moriarty, Drew E. Lewis, and Edward C. Oldfield. "Serious Infections Involving the CDC Group Ve Bacteria Chryseomonas luteola and Flavimonas oryzihabitans." Clinical Infectious Diseases 13, no. 2 (March 1, 1991): 257–60. http://dx.doi.org/10.1093/clinids/13.2.257.

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12

Smith-Grenier, L. L., and A. Adkins. "Isolation and characterization of soil microorganisms capable of utilizing the herbicide diclofop-methyl as a sole source of carbon and energy." Canadian Journal of Microbiology 42, no. 3 (March 1, 1996): 221–26. http://dx.doi.org/10.1139/m96-033.

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Six nonfermentative Gram-negative bacilli were isolated from Manitoban soils after enrichment with diclofopmethyl. Microscopic examination and physiological and biochemical tests have identified the organisms as Sphingomonas paucimobilis, Acinetobacter baumannii, Chryseomonas luteola, Pseudomonas aureofaciens, Pseudomonas cepacia, and Pseudomonas fluorescens. Growth curve studies showed that each of the isolates was able to grow in minimal medium with diclofop-methyl as the sole source of carbon and energy. Chemical analysis confirmed that all of the added diclofop-methyl (1.5 μg ∙ mL−1) had been utilized after 31 h of incubation at 25 °C Key words: diclofop-methyl, biodegradation, herbicide.

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13

Smith-Grenier, L. L., and A. Adkins. "Degradation of diclofop-methyl by pure cultures of bacteria isolated from Manitoban soils." Canadian Journal of Microbiology 42, no. 3 (March 1, 1996): 227–33. http://dx.doi.org/10.1139/m96-034.

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Pure cultures of Chryseomonas luteola and Sphingomonas paucimobilis isolated from Manitoban soils were able to utilize diclofop-methyl (methyl-2-[4-(2,4-dichlorophenoxy)phenoxy]propanoate) as the sole source of carbon and energy. An actively growing culture of C. luteola completely degraded 1.5 μg diclofop-methyl∙mL−1to diclofop acid and 4-(2,4-dichlorophenoxy)phenol within 71 h, as determined by gas chromatographic analysis. The accumulation of these metabolites in the growth medium resulted in the cessation of growth, indicating the organism's inability to degrade phenoxyphenol in the presence of diclofop acid. Sphingomonas paucimobilis mineralized 1.5 μg diclofop-methyl∙mL−1to diclofop acid within 54 h. A biphasic growth pattern indicated that this organism was capable of degrading diclofop acid to 4-(2,4-dichlorophenoxy)phenol and 2,4-dichlorophenol and (or) phenol. Neither of the organisms was able to utilize 2,4 -dichlorophenol as the sole source of carbon and energy.Key words: diclofop-methyl, biodegradation, herbicide.

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14

Chihab, W., A. S. Alaoui, and M. Amar. "Chryseomonas luteola Identified as the Source of Serious Infections in a Moroccan University Hospital." Journal of Clinical Microbiology 42, no. 4 (April 1, 2004): 1837–39. http://dx.doi.org/10.1128/jcm.42.4.1837-1839.2004.

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15

Doublet, Benoît, Frédéric Robin, Isabelle Casin, Laëtitia Fabre, Anne Le Fleche, Richard Bonnet, and François-Xavier Weill. "Molecular and Biochemical Characterization of the Natural Chromosome-Encoded Class A β-Lactamase from Pseudomonas luteola." Antimicrobial Agents and Chemotherapy 54, no. 1 (November 2, 2009): 45–51. http://dx.doi.org/10.1128/aac.00427-09.

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ABSTRACT Pseudomonas luteola (formerly classified as CDC group Ve-1 and named Chryseomonas luteola) is an unusual pathogen implicated in rare but serious infections in humans. A novel β-lactamase gene, bla LUT-1, was cloned from the whole-cell DNA of the P. luteola clinical isolate LAM, which had a weak narrow-spectrum β-lactam-resistant phenotype, and expressed in Escherichia coli. This gene encoded LUT-1, a 296-amino-acid Ambler class A β-lactamase with a pI of 6 and a theoretical molecular mass of 28.9 kDa. The catalytic efficiency of this enzyme was higher for cephalothin, cefuroxime, and cefotaxime than for penicillins. It was found to be 49% to 59% identical to other Ambler class A β-lactamases from Burkholderia sp. (PenA to PenL), Ralstonia eutropha (REUT), Citrobacter sedlakii (SED-1), Serratia fonticola (FONA and SFC-1), Klebsiella sp. (KPC and OXY), and CTX-M extended-spectrum β-lactamases. No gene homologous to the regulatory ampR genes of class A β-lactamases was found in the vicinity of the bla LUT-1 gene. The entire bla LUT-1 coding region was amplified by PCR and sequenced in five other genetically unrelated P. luteola strains (including the P. luteola type strain). A new variant of bla LUT-1 was found for each strain. These genes (named bla LUT-2 to bla LUT-6) had nucleotide sequences 98.1 to 99.5% identical to that of bla LUT-1 and differing from this gene by two to four nonsynonymous single nucleotide polymorphisms. The bla LUT gene was located on a 700- to 800-kb chromosomal I-CeuI fragment, the precise size of this fragment depending on the P. luteola strain.

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16

Ramana, KV, MA Kareem, C. H. V. Sarada, Sujeesh Sebastian, Rajasekharreddy Lebaka, MS Ratnamani, and Ratna Rao. "Chryseomonas luteola bacteremia in a patient with left pyocele testis with Fournier′s scrotal gangrene." Indian Journal of Pathology and Microbiology 53, no. 3 (2010): 574. http://dx.doi.org/10.4103/0377-4929.68280.

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17

Rahav, Galia, Albert Simhon, Yoav Mattan, Allon E. Moses, and Theodore Sacks. "Infections with Chryseomonas luteola (CDC Group Ve-1) and Flavimonas oryzihabitans (CDC Group Ve-2)." Medicine 74, no. 2 (March 1995): 83–88. http://dx.doi.org/10.1097/00005792-199503000-00003.

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18

Önal, Seçil, Şenay Hamarat Baysal, and Guven Ozdemir. "Studies on the applicability of alginate-entrapped Chryseomonas luteola TEM 05 for heavy metal biosorption." Journal of Hazardous Materials 146, no. 1-2 (July 2007): 417–20. http://dx.doi.org/10.1016/j.jhazmat.2007.03.005.

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19

Rodríguez, Cecilia, Hiram Medrano, Nuria Rocha, Alberto Gallegos, Martha Rosales, and Rubén González-Laredo. "Tratamiento biológico de madera para eliminar pitch en la producción de celulosa." Madera y Bosques 11, no. 1 (August 31, 2016): 19–27. http://dx.doi.org/10.21829/myb.2005.1111259.

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Se realizó un estudio biotecnológico para abatir el contenido resinoso de astilla de pino del estado de Durango y evitar los problemas asociados con la formación de pitch en la producción de pulpa mecánica. Se aislaron 49 cepas nativas que degradaron ácidos resínicos y precursores de pitch. Entre las mejores cepas se identificaron a Paecilomyces sp., Penicillum sp., Phialophora sp., Trichosporon sp., Rhodotorula sp., Cryptococcus sp. y Chryseomonas luteola. Esta última fue la más eficiente con un rendimiento de 87,3 % a nivel matraz, por lo que fue probada preliminarmente en fermentación sólida tipo heap leaching. La cepa Paecilomyces sp. rindió 86,6 % de efectividad a nivel matraz y fue probada en fermentación semisólida. Los resultados de las pruebas a nivel matraz fueron muy superiores a los obtenidos de manera preliminar en las fermentaciones sólidas.

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20

Membré, Jeanne-Marie, and Martine Kubaczka. "Degradation of pectic compounds during pasteurised vegetable juice spoilage by Chryseomonas luteola: a predictive microbiology approach." International Journal of Food Microbiology 42, no. 3 (July 1998): 159–66. http://dx.doi.org/10.1016/s0168-1605(98)00087-7.

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21

Wen, A. Y., I. K. Weiss, and R. B. Kelly. "Chryseomonas luteola bloodstream infection in a pediatric patient with pulmonary arterial hypertension receiving intravenous treprostinil therapy." Infection 41, no. 3 (January 18, 2013): 719–22. http://dx.doi.org/10.1007/s15010-012-0399-2.

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22

Van Der Merwe-Botha, M., and T. J. Britz. "Combined pre-degradation and anaerobic digestion for the treatment of a baker's yeast factory effluent." Water Science and Technology 36, no. 6-7 (September 1, 1997): 295–301. http://dx.doi.org/10.2166/wst.1997.0603.

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A Chryseomonas luteola strain was isolated from raw baker's yeast factory effluent as the dominant part of the microbial community and evaluated for its biodegradative activity, using the raw effluent as substrate. The strain was able to utilise the raw effluent and produce higher concentrations of energetically favourable metabolites and thereby, could contribute to the first degradation step in an anaerobic biological treatment process. A 3×4×3 factorial design indicated optimal degradation conditions in a specific environmental framework of 48 h incubation time, COD concentration of 30 g/l, pH of 6.0 and temperature of 35°C. The C. luteola strain was thereafter used in a pre-degradation step followed by an anaerobic digestion step in a 5 1 laboratory-scale hybrid digester. With the use of the pre-degraded effluent, significant improvements were found in the overall anaerobic digestion performance. These included increased COD (>15%) and TVFA (>50%) removals, especially propionic acid (88%) removal, as well as higher biogas yields (18%). The results also showed a prominent improvement in fatty acid utilisation and methanogenesis. The pre-degradation step resulted in better process control and increased stability of the system, even at relatively high organic loading rates (10 kg COD/m3.d). When the raw effluent was not pre-treated (control bioreactor), no improvement in bioreactor efficiency was observed.

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23

Laurent, P., L. Buchon, J. F. Guespin-Michel, and N. Orange. "Production of Pectate Lyases and Cellulases by Chryseomonas luteola Strain MFCL0 Depends on the Growth Temperature and the Nature of the Culture Medium: Evidence for Two Critical Temperatures." Applied and Environmental Microbiology 66, no. 4 (April 1, 2000): 1538–43. http://dx.doi.org/10.1128/aem.66.4.1538-1543.2000.

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ABSTRACT Several extracellular enzymes that are responsible for plant tissue maceration were detected in culture supernatant of the psychrotrophic bacterium Chryseomonas luteola MFCL0. Isoelectrofocusing experiments showed that pectate lyase (PL) activity resulted from the cumulative action of three major isoenzymes, designated PLI, PLII, and PLIII. Cellulolytic activity was also detected in culture supernatants. These enzymes exhibited different behaviors with respect to growth temperature. PLII was not regulated by temperature, whereas PLI and PLIII were regulated similarly by growth temperature. Maximal levels of PLI and PLIII were produced at 14°C when cells were grown in polygalacturonate-containing synthetic medium and at around 20 to 24°C in nutrient broth. In contrast, thermoregulation of cellulolytic activity production differed from thermoregulation of PL. The level of cellulolytic activity was low in all media at temperatures up to 20°C, and then it increased dramatically until the temperature was 28°C, which is the optimal temperature for growth of C. luteola. Previously, we defined the critical temperature by using the modified Arrhenius equation to characterize bacterial behavior. This approach consists of monitoring changes in the maximal specific growth rate as a function of temperature. Our most striking result was the finding that the temperature at which maximum levels of PLI and PLIII were produced in two different media was the same as the critical temperature for growth observed in these two media.

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24

Kostman, Jay R., Flora Solomon, and Thomas Fekete. "Infections with Chryseomonas luteola (CDC Group Ve-1) and Flavimonas oryzihabitans (CDC Group Ve-2) in Neurosurgical Patients." Clinical Infectious Diseases 13, no. 2 (March 1, 1991): 233–36. http://dx.doi.org/10.1093/clinids/13.2.233.

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25

Ozdemir, Guven, Nur Ceyhan, and Ebru Manav. "Utilization of an exopolysaccharide produced by Chryseomonas luteola TEM05 in alginate beads for adsorption of cadmium and cobalt ions." Bioresource Technology 96, no. 15 (October 2005): 1677–82. http://dx.doi.org/10.1016/j.biortech.2004.12.031.

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26

Ozdemir, Guven, N. Ceyhan, and E. Manav. "Utilization in alginate beads for Cu(II) and Ni(II) adsorption of an exopolysaccharide produced by Chryseomonas luteola TEM05." World Journal of Microbiology and Biotechnology 21, no. 2 (March 2005): 163–67. http://dx.doi.org/10.1007/s11274-004-1563-3.

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27

Van Der Merwe, M., and T. J. Britz. "The individual and combined influence of temperature, time, pH and COD concentration on the biodegradation activities of selected bacterial strains grown on raw Baker's yeast effluent." Water Science and Technology 30, no. 12 (December 1, 1994): 97–106. http://dx.doi.org/10.2166/wst.1994.0590.

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Five bacterial strains (Chryseomonas luteola, Fusobacterium mortiferum, Enterobacter agglomerans,Klebsiella oxytoca and an unidentified Gram-negative rod) were grown on raw baker's yeast effluent to assess the influence of environmental factors on biodegradation processes. A 3×4×3 factorial design was used to determine the effects of time, pH and COD concentration, at four different temperatures. Total volatile fatty acid production was chosen as the most representative indicator of biodegradation. Results showed that the strains differed greatly in their ability to produce anaerobic digester intermediary metabolites, under defined environmental conditions. The study showed that the degradation of the complex compounds in baker's yeast effluent could be enhanced by changing environmental factors. The most positive responses were obtained at the higher COD concentrations (30 g l−1), the higher pH values (6.0), after 24 to 48h incubation time and at the higher temperatures (35°C). The most positive effect (+355.00) was found forChryseomonas luteola at a 48h incubation time, COD concentration of 30 g l−1, pH of 6.0 and temperature of 35°C. The volatile fatty acid yields obtained by the strains differ from the statistical indications, but provide a valuable reference of the actual concentrations obtained during the experimental study. The factorial design represented the effects of environmental changes, while the quantitative TVFA data set gave experimental data. This study showed that the manipulation of various environmental factors in biologically controlled systems, such as anaerobic digesters, could further enhance the biodegradation efficiency of the microbial population in the raw effluent.

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28

Oehrle, Nathan W., Dale B. Karr, Robert J. Kremer, and David W. Emerich. "Enhanced attachment of Bradyrhizobium japonicum to soybean through reduced root colonization of internally seedborne microorganisms." Canadian Journal of Microbiology 46, no. 7 (July 1, 2000): 600–606. http://dx.doi.org/10.1139/w00-030.

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Internally seedborne microorganisms are those surviving common surface sterilization procedures. Such microbes often colonize the radicle surface of a germinating soybean (Glycine max) seed, introducing an undefined parameter into studies on attachment and infection by Bradyrhizobium japonicum. Bacterial isolates from surface-sterilized soybean seed, cv. Williams 82 and cv. Maverick, used in our studies, were identified as Agrobacterium radiobacter, Aeromonas sp., Bacillus spp., Chryseomonas luteola, Flavimonas oryzihabitans, and Sphingomonas paucimobilis. Growth of these microbes during seed germination was reduced by treating germinating seeds with 500 µg/mL penicillin G. The effects of this antibiotic on seedling development and on B. japonicum 2143 attachment, nodulation, and nitrogen fixation are reported here. Penicillin G treatment of seeds did not reduce seed germination or root tip growth, or affect seedling development. No differences in nodulation kinetics, nitrogen fixation onset or rates were observed. However, the number of B. japonicum attached to treated intact seedlings was enhanced 200-325%, demonstrating that other root-colonizing bacteria can interfere with rhizobial attachment. Penicillin G treatment of soybean seedlings can be used to reduce the root colonizing microbes, which introduce an undefined parameter into studies of attachment of B. japonicum to the soybean root, without affecting plant development.Key words: internally seedborne microorganisms, penicillin G, Bradyrhizobium japonicum, microbial attachment, soybean (Glycine max).

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29

Dougnon, Victorien, Vincentia Marie Camille Houssou, Eugénie Anago, Chimène Nanoukon, Jibril Mohammed, Jerrold Agbankpe, Hornel Koudokpon, et al. "Assessment of the Presence of Resistance Genes Detected from the Environment and Selected Food Products in Benin." Journal of Environmental and Public Health 2021 (February 4, 2021): 1–10. http://dx.doi.org/10.1155/2021/8420590.

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Gram-negative bacilli can spread from the environment and through food products. This study aimed to characterize ESBL production and virulence genes from multidrug-resistant Gram-negative bacilli isolated from specimen collected from the environment, kitchen, and food products. A total of 130 samples were collected at local markets in seven different communities in Benin (Abomey-Calavi, Ouidah, Bohicon, Abomey, Parakou, Djougou, and Grand-Popo). Samples were cultured on McConkey and ChromID™ ESBL agar plates. The isolates were identified by the API 20E gallery. An antibiotic susceptibility test was carried out, and the detection of ESBL production and virulence-associated genes was carried out by Polymerase Chain Reaction (PCR). The data collected was coded and analyzed using GraphPad prism 7 software and Excel. The software R was used to calculate the correlation coefficient between the results of the detection of ESBL+ on agar and by the effect of the double synergy. The results showed that sixty-three (63) bacterial strains were isolated from the 130 samples, of which the dominant species was Chryseomonas luteola (10/63). The kitchen samples were the most contaminated with 36.50%. More than 40% of the isolates were resistant to at least three different classes of antibiotics. Also, blaSHV gene was detected in 33.33% (21/63) of the isolates and in all isolates of Pseudomonas aeruginosa (5/5%). 11.11% (7/63) of isolates were virulent with dominance of the fimH gene, especially with Escherichia coli (83.33%). The kitchen samples showed a high prevalence of ESBL-producing strains with fimH gene. This raises the problem of non-compliance with hygiene rules in community cooking and food handling.

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30

Holmes, B., A. G. Steigerwalt, R. E. Weaver, and D. J. Brenner. "Chryseomonas luteola comb. nov. and Flavimonas oryzihabitans gen. nov., comb. nov., Pseudomonas-Like Species from Human Clinical Specimens and Formerly Known, Respectively, as Groups Ve-1 and Ve-2." International Journal of Systematic Bacteriology 37, no. 3 (July 1, 1987): 245–50. http://dx.doi.org/10.1099/00207713-37-3-245.

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31

Fazii, P., A. Pelatti, C. Civitarese, C. Russi, F. Pistola, M. Stella, C. Crescenzi, et al. "DESCRIZIONE DI UN CASO DI ASCESSO CUTANEO CAUSATO DA CHRYSEOMONAS LUTEOLA." Microbiologia Medica 20, no. 3 (September 30, 2005). http://dx.doi.org/10.4081/mm.2005.3504.

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32

Goteri, Gaia. "Chryseomonas luteola: an unusual clinical infection mimicking a mediastinal malignant lymphoma." Pathology and Laboratory Medicine International, December 2010, 137. http://dx.doi.org/10.2147/plmi.s13645.

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33

S., Syafalni, Ismail Abustan, Norli Ismail, and Tan Soke Kwan. "Production of Bioflocculant by Chryseomonas Luteola and Its Application in Dye Wastewater Treatment." Modern Applied Science 6, no. 5 (April 25, 2012). http://dx.doi.org/10.5539/mas.v6n5p13.

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