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1

Palacio, Rosario, Cecilia Cornejo, and Verónica Seija. "Comamonas kerstersii." Revista chilena de infectología 37, no. 2 (2020): 147–48. http://dx.doi.org/10.4067/s0716-10182020000200147.

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2

Zhu, Daochen, Changxiao Xie, Ying Huang, Jianzhong Sun, and Weimin Zhang. "Description of Comamonas serinivorans sp. nov., isolated from wheat straw compost." International Journal of Systematic and Evolutionary Microbiology 64, Pt_12 (2014): 4141–46. http://dx.doi.org/10.1099/ijs.0.066688-0.

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A Gram-stain-negative bacterium, designated SP-35T, was isolated from compost and was subjected to a taxonomic study. This isolate was short-rod-shaped and non-spore-forming. Phylogenetic analysis based on 16S rRNA sequence comparison indicated the isolate was related to the genus Comamonas . 16S rRNA gene sequence analysis showed that its closest neighbours were the type strains Comamonas odontotermitis Dant 3-8T (96.8 % similarity), Comamonas testosteroni DSM 50244T (96.5 %), Comamonas guangdongensis CY01T (95.9 %) and Comamonas composti YY287T (95.6 %). Using phylogenetic analysis, DNA–DNA
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3

Chou, Jui-Hsing, Shih-Yi Sheu, Kuan-Yin Lin, Wen-Ming Chen, A. B. Arun, and Chiu-Chung Young. "Comamonas odontotermitis sp. nov., isolated from the gut of the termite Odontotermes formosanus." International Journal of Systematic and Evolutionary Microbiology 57, no. 4 (2007): 887–91. http://dx.doi.org/10.1099/ijs.0.64551-0.

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A bacterial strain, designated Dant 3-8T, isolated from the gut of the termite Odontotermes formosanus, was investigated by a polyphasic taxonomic approach. The cells were rod-shaped, Gram-negative, non-pigmented, non-spore-forming and non-fermentative. Phylogenetic analyses using the 16S rRNA gene sequence showed that the strain formed a monophyletic branch towards the periphery of the evolutionary radiation occupied by the genus Comamonas, its closest neighbours being Comamonas testosteroni DSM 50244T (96.4 % sequence similarity), Comamonas koreensis KCTC 12005T (96.0 %) and Comamonas terrig
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4

Sun, Li-Na, Jun Zhang, Qing Chen, Jian He, Qin-Fen Li, and Shun-Peng Li. "Comamonas jiangduensis sp. nov., a biosurfactant-producing bacterium isolated from agricultural soil." International Journal of Systematic and Evolutionary Microbiology 63, Pt_6 (2013): 2168–73. http://dx.doi.org/10.1099/ijs.0.045716-0.

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A novel biosurfactant-producing strain, designated YW1T, was isolated from agricultural soil. Its taxonomic position was investigated using a polyphasic approach. The cells were short rods, Gram-negative, non-sporulating and motile. Phylogenetic analysis based on 16S rRNA gene sequences revealed that strain YW1T was a member of the genus Comamonas , and showed highest sequence similarities to Comamonas aquatica LMG 2370T (98.5 %), Comamonas kerstersii LMG 3475T (97.7 %) and Comamonas terrigena LMG 1253T (97.7 %). Furthermore, DNA–DNA hybridization experiments against these three strains gave r
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5

Zhang, Jun, Yueqiang Wang, Shungui Zhou, Chunyuan Wu, Jian He, and Fangbai Li. "Comamonas guangdongensis sp. nov., isolated from subterranean forest sediment, and emended description of the genus Comamonas." International Journal of Systematic and Evolutionary Microbiology 63, Pt_3 (2013): 809–14. http://dx.doi.org/10.1099/ijs.0.040188-0.

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A facultatively anaerobic bacterium, strain CY01T, isolated from subterranean forest sediment collected from Guangdong Province, China, was investigated using a polyphasic taxonomic approach. The cells were short rods, Gram-negative, non-sporulating and motile. Phylogenetic analysis based on 16S rRNA gene sequences showed that strain CY01T showed highest sequence similarities to Comamonas thiooxydans S23T (98.0 %), Comamonas testosteroni JCM 5832T (97.9 %), Comamonas koreensis KCTC 12005T (97.7 %) and Comamonas odontotermitis LMG 23579T (97.0 %). The major respiratory quinone was ubiquinone-8.
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6

Wauters, Georges, Thierry De Baere, Anne Willems, Enevold Falsen, and Mario Vaneechoutte. "Description of Comamonas aquatica comb. nov. and Comamonas kerstersii sp. nov. for two subgroups of Comamonas terrigena and emended description of Comamonas terrigena." International Journal of Systematic and Evolutionary Microbiology 53, no. 3 (2003): 859–62. http://dx.doi.org/10.1099/ijs.0.02450-0.

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7

M, Dimova. "Potentially Beneficial Comamonas Testosteroni Bacteria for Plants Growing in HCB-Polluted Soil." Open Access Journal of Microbiology & Biotechnology 6, no. 4 (2021): 1–7. http://dx.doi.org/10.23880/oajmb-16000208.

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The bioaugmantation effect of bacterial strains on plant development in organochlorine pesticides (OCP) polluted soil has been in the focus of attention, however there is little information about Comamonas testosteroni strains influence. The investigation was performed by classic methods. The results of the research showed that Comamonas testosteroni UCM B-400 and B-401has a high destroying potential to xenobiotics in the soil, and also has a positive effect on plant development. The tomato plants ability to develop under conditions with Comamonas testosteroni UCM B-400 and B-401 bioaugmentati
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8

Abraham, JoEllyn M., and Gary L. Simon. "Comamonas testosteroni Bacteremia." Infectious Diseases in Clinical Practice 15, no. 4 (2007): 272–73. http://dx.doi.org/10.1097/ipc.0b013e31802ce475.

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9

Liu, Xue-jiao, Xi-wen Qiao, Tian-min Huang, Lu Li, and Sai-ping Jiang. "Comamonas kerstersii bacteremia." Médecine et Maladies Infectieuses 50, no. 3 (2020): 288–90. http://dx.doi.org/10.1016/j.medmal.2019.12.005.

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10

Narayan, Kunwar Digvijay, Shachindra K. Pandey, and Subrata K. Das. "Characterization of Comamonas thiooxidans sp. nov., and Comparison of Thiosulfate Oxidation with Comamonas testosteroni and Comamonas composti." Current Microbiology 61, no. 4 (2010): 248–53. http://dx.doi.org/10.1007/s00284-010-9602-9.

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11

Yu, Xin-Yan, Yong-Feng Li, Jin-Wei Zheng, et al. "Comamonas zonglianii sp. nov., isolated from phenol-contaminated soil." International Journal of Systematic and Evolutionary Microbiology 61, no. 2 (2011): 255–58. http://dx.doi.org/10.1099/ijs.0.019612-0.

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A bacterial strain, designated BF-3T, was isolated from phenol-contaminated soil and investigated using a polyphasic taxonomic approach. Cells were Gram-reaction-negative, non-sporulating, non-motile, short rods. Phylogenetic analysis based on 16S rRNA gene sequences showed that strain BF-3T formed a monophyletic branch at the periphery of the evolutionary radiation occupied by the genus Comamonas; it showed highest sequence similarities to Comamonas aquatica LMG 2370T (96.8 %), C. nitrativorans DSM 13191T (96.4 %), C. odontotermitis LMG 23579T (96.4 %), C. kerstersii LMG 3475T (96.3 %), C. ko
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12

Hatayama, Kouta. "Comamonas humi sp. nov., isolated from soil." International Journal of Systematic and Evolutionary Microbiology 64, Pt_12 (2014): 3976–82. http://dx.doi.org/10.1099/ijs.0.067439-0.

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A bacterial strain, designated GAU11T, was isolated from soil in Japan. Cells of the strain were Gram-stain-negative, aerobic, non-motile rods. The 16S rRNA gene sequence of strain GAU11T showed high similarity to those of Comamonas zonglianii BF-3T (98.8 %), Pseudacidovorax intermedius CC21T (96.4 %), Acidovorax caeni R-24608T (96.2 %), Alicycliphilus denitrificans K601T (96.2 %), Pseudorhodoferax soli TBEA3T (95.9 %) and Comamonas terrigena LMG 1253T (95.9 %). Strain GAU11T contained ubiquinone 8 as the sole ubiquinone and diphosphatidylglycerol, phosphatidylethanolamine and phosphatidylglyc
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13

M, V. Dharsandia1, Khanpara1 Charmi, K. Sadikot2 A, H. Kansagra2 C, and K. Rawal2 K. "Comamonas Testosteroni Emerging Gastrointestinal Pathogen." People's Journal of Scientific Research 16, no. 1 (2023): 1–3. https://doi.org/10.5281/zenodo.8077219.

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Comamonas testosteroni newly emerging microorganism previously known as Pseudomonas testosteroni is common environmental bacterium that is not known to be a part of the human commensal organism. Since its identification as a human pathogen in 1987, numerous reports have drizzled in, implicating this organism for various infections. Comamonas testosteroni are rare isolates in microbiology laboratories and have been infrequently reported as an infectious agent in routine clinical practice. Comamonas testosteroni has been rarely observed as an infectious agent in clinical practice. Comamonas test
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14

Opota, Onya, Barbara Ney, Giorgio Zanetti, Katia Jaton, Gilbert Greub, and Guy Prod'hom. "Bacteremia caused by Comamonas kerstersii in a patient with diverticulosis." Journal of Clinical Microbiology 52, no. 3 (2013): 1009–12. https://doi.org/10.1128/JCM.02942-13.

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We report for the first time a case of bacteremia caused by Comamonas kerstersii in a 65-year-old patient with sign of diverticulosis. In addition, we review the isolation of Comamonas sp. and related organisms in our hospital over 25 years.
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15

Khalki, H., H. Deham, A. Taghouti, G. Yahyaoui, and M. Mahmoud. "Appendicite à Comamonas testosteroni." Médecine et Maladies Infectieuses 46, no. 3 (2016): 168–70. http://dx.doi.org/10.1016/j.medmal.2015.12.009.

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16

Cooper, Gary R., Edward D. Staples, Kenneth A. Iczkowski, and Cornelius J. Clancy. "Comamonas (Pseudomonas) testosteroni endocarditis." Cardiovascular Pathology 14, no. 3 (2005): 145–49. http://dx.doi.org/10.1016/j.carpath.2005.01.008.

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17

Carolo, G., M. Ganau, E. De Micheli, M. Gerosa, and M. Solbiati. "P1466 Comamonas testosteroni spondylodiscitis." International Journal of Antimicrobial Agents 29 (March 2007): S410. http://dx.doi.org/10.1016/s0924-8579(07)71305-5.

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18

Ryan, Michael P., Ludmila Sevjahova, Rachel Gorman, and Sandra White. "The Emergence of the Genus Comamonas as Important Opportunistic Pathogens." Pathogens 11, no. 9 (2022): 1032. http://dx.doi.org/10.3390/pathogens11091032.

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Comamonas spp. are non-fermenting Gram-negative bacilli. They were first discovered in 1894, and since then, twenty-four species have been characterized. The natural habitat of these bacteria is soil, wastewater/sludge, fresh water such as ponds and rivers, and the animal intestinal microbiome. They were also isolated from industrial settings, such as activated sludge and polluted soil, and from the hospital environment and clinical samples, such as urine, pus, blood, feces, and kidney. Comamonas spp. are associated with environmental bioremediation and are considered an important environmenta
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19

Dimova, Mariia, Liudmyla Dankevych, Nadiya Yamborko та Galyna Iutynska. "POLYPHASIC TAXONOMY ANALYSE OF COMAMONAS TESTOSTERONІ RESISTANT ТО HEXACHLOROBENZENE". Journal of microbiology, biotechnology and food sciences 11, № 5 (2022): e4711. http://dx.doi.org/10.55251/jmbfs.4711.

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Based on the analysing phenotypic and genotypic properties, the taxonomic position of isolates # 46 and # 47 was established and assigned to the species Comamonas testosteronі UCM B-400 and UCM B-401. Isolates were selected from the soil with organochlorine wastes landfill of chemical enterprises in Kalush, Ivano-Frankivsk region, Ukraine. The strains are resistant to high hexachlorobenzene concentrations. According to morphological, cultural and biochemical properties, the studied strains are related to typical members of the Comamonadaceae family, they are motile gram-negative rods, aerobic,
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20

Horowitz, H., S. Gilroy, S. Feinstein, and G. Gilardi. "Endocarditis associated with Comamonas acidovorans." Journal of Clinical Microbiology 28, no. 1 (1990): 143–45. http://dx.doi.org/10.1128/jcm.28.1.143-145.1990.

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21

Horinouchi, Masae, Toshiaki Hayashi, and Toshiaki Kudo. "Steroid degradation in Comamonas testosteroni." Journal of Steroid Biochemistry and Molecular Biology 129, no. 1-2 (2012): 4–14. http://dx.doi.org/10.1016/j.jsbmb.2010.10.008.

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22

Zhao, Jian-Shen, and Owen P. Ward. "Microbial degradation of nitrobenzene and mono-nitrophenol by bacteria enriched from municipal activated sludge." Canadian Journal of Microbiology 45, no. 5 (1999): 427–32. http://dx.doi.org/10.1139/w99-026.

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Using a mixture of three mono nitrophenols as sole carbon, nitrogen and energy sources, mixed cultures were enriched from municipal activated sludge to degrade both nitrophenols and nitrobenzene. Bacterial growth and degradation rate could be increased by supplementing the medium with 0.1% YE. Microorganisms were isolated from the nitrophenols enrichment, and they were identified as strains of Comamonas testosteroni and Acidovorax delafieldii. These strains showed broad degradation ability toward nitrophenols and nitrobenzene.Key words: biodegradation, nitrobenzene, nitrophenol, Comamonas test
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23

Rong, Kassie, Johan Delport, and Fatimah AlMutawa. "Comamonas kerstersii Bacteremia of Unknown Origin." Case Reports in Infectious Diseases 2022 (March 27, 2022): 1–3. http://dx.doi.org/10.1155/2022/1129832.

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Comamonas kerstersii (C. kerstersii) is a Gram-negative bacillus abundant in the environment and rarely implicated in human disease. Previously considered nonpathogenic, its scarcity in literature may be partly due to the unreliability of past phenotypic tests used for its identification. In recent years, the development of matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) mass spectrometry (MS) has enabled fast and accurate laboratory identification of C. kerstersii. Since the first report of human infection in 2013, several others have emerged, with most cases involving
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24

Stonecipher, Karl G., Harold G. Jensen, Peter R. Kastl, Alan Faulkner, and J. James Rowsey. "Ocular Infections Associated With Comamonas acidovorans." American Journal of Ophthalmology 112, no. 1 (1991): 46–49. http://dx.doi.org/10.1016/s0002-9394(14)76211-7.

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25

Almuzara, M., C. Barberis, F. Veiga, et al. "Unusual presentations of Comamonas kerstersii infection." New Microbes and New Infections 19 (September 2017): 91–95. http://dx.doi.org/10.1016/j.nmni.2017.07.003.

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26

Qu, Yuanyuan, Xuwang Zhang, Qiao Ma, et al. "Indigo biosynthesis by Comamonas sp. MQ." Biotechnology Letters 34, no. 2 (2011): 353–57. http://dx.doi.org/10.1007/s10529-011-0778-2.

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27

Biswas, J. S., J. Fitchett, and G. O'Hara. "Comamonas kerstersii and the Perforated Appendix." Journal of Clinical Microbiology 52, no. 8 (2014): 3134. http://dx.doi.org/10.1128/jcm.00909-14.

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28

Jin, Long, Joshua A. Perper, and Stephen J. Cina. "Comamonas TestosteroniMeningitis in a Homeless Man." Journal of Forensic Sciences 53, no. 5 (2008): 1198–99. http://dx.doi.org/10.1111/j.1556-4029.2008.00810.x.

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29

Jong, Govardus A. H., Arie Geerlof, Joke Stoorvogel, Jaap A. Jongejan, Simon Vries, and Johannis A. Duine. "Quinohaemoprotein Ethanol Dehydrogenase from Comamonas testosteroni." European Journal of Biochemistry 230, no. 3 (2008): 899–905. http://dx.doi.org/10.1111/j.1432-1033.1995.0899g.x.

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30

Bofill, Lina, Mireya Wessolossky, Enrique Vicent, et al. "Septic Shock Due to Comamonas acidovorans." Infectious Diseases in Clinical Practice 5, no. 1 (1996): 73. http://dx.doi.org/10.1097/00019048-199601000-00018.

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31

Stampi, S., F. Zanetti, A. Bergamaschi, and G. De Luca. "Comamonas acidovoranscontamination of dental unit waters." Letters in Applied Microbiology 29, no. 1 (1999): 52–55. http://dx.doi.org/10.1046/j.1365-2672.1999.00575.x.

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32

Zhang, Jun, Yueqiang Wang, Shungui Zhou, Chunyuan Wu, Jian He, and Fangbai Li. "Comamonas guangdongensis sp. nov., isolated from subterranean forest sediment, and emended description of the genus Comamonas." International Journal of Systematic and Evolutionary Microbiology 63, Pt_5 (2013): 1936. http://dx.doi.org/10.1099/ijs.0.x00006-0.

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33

DİMOVA, Mariia, Galyna IUTYNSKA, Iryna LEVCHUK, and Nadiya YAMBORKO. "Bioremediation of HCB-contaminated soil using Comamonas testosteroni and Zea mays L." EURASIAN JOURNAL OF SOIL SCIENCE (EJSS) 11, no. 4 (2022): 316–21. http://dx.doi.org/10.18393/ejss.1125125.

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Bioremediation measures to restore soil ecosystems are environmentally safe, promising and relevant. Soil ecosystems contaminated with hexachlorobenzene require remediation measures. Studying the effectiveness of applying the microbial remediator Comamonas testosteroni UCM B-400, phytoremediator Zea mays L. cultivar Olena and microbial and phytoremediation complex to remove hexachlorobenzene contamination was carried out. The HCB content was determined by chromatographic method, the microbial groups reactions to application of various remediators in the soil were studied by classical microbiol
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34

Falih, Aysar Ihsan, and Naresh K. Y. "Isolation Identification and Charecterization of Pencillinase Producing Bacteria from Soil." SAR Journal of Pathology and Microbiology 6, no. 04 (2025): 123–45. https://doi.org/10.36346/sarjpm.2025.v06i04.001.

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Aim: To identify the penicillin resistance organisms in soil sample collected from the hospital area. Methods: Bacteria were grown on nutrient agar medium and sub cultured in nutrient broth with different concentrations of Penicillin. The resistance organisms were characterized by 16s rRNA gene sequencing and blast analysis. Results: A total of 21 cultural were identified as penicillin resistance organisms. Out of 21 cultures we have characterized four cultures and identified as Pseudomonas putida, Pseudomonas fluorescens, Comamonas sp. KBB4, Bacterium SM2-6. Conclusion: Pseudomonas putida, Ps
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35

Cheng, Zhongyi, Wenjing Cui, Zhongmei Liu та ін. "A switch in a substrate tunnel for directing regioselectivity of nitrile hydratases towards α,ω-dinitriles". Catalysis Science & Technology 6, № 5 (2016): 1292–96. http://dx.doi.org/10.1039/c5cy01997d.

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36

Wang, Yun-Hao, Zhou Huang, and Shuang-Jiang Liu. "Chemotaxis Towards Aromatic Compounds: Insights from Comamonas testosteroni." International Journal of Molecular Sciences 20, no. 11 (2019): 2701. http://dx.doi.org/10.3390/ijms20112701.

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Chemotaxis is an important physiological adaptation that allows many motile bacteria to orientate themselves for better niche adaptation. Chemotaxis is best understood in Escherichia coli. Other representative bacteria, such as Rhodobacter sphaeroides, Pseudomonas species, Helicobacter pylori, and Bacillus subtilis, also have been deeply studied and systemically summarized. These bacteria belong to α-, γ-, ε-Proteobacteria, or Firmicutes. However, β-Proteobacteria, of which many members have been identified as holding chemotactic pathways, lack a summary of chemotaxis. Comamonas testosteroni,
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37

Li, Yapeng, Huixin Fan, Boqiao Li, and Xiaobo Liu. "Environmental Impact of Xenobiotic Aromatic Compounds and Their Biodegradation Potential in Comamonas testosteroni." International Journal of Molecular Sciences 25, no. 24 (2024): 13317. https://doi.org/10.3390/ijms252413317.

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Xenobiotic aromatic compounds are the raw materials of necessities in modern life, such as plastics, pesticides, and antibiotics. To meet the global requirements, their production and consumption have continually increased, and thus, the vast amount of waste generated results in prominent environmental pollution. Fortunately, some microorganisms (e.g., Comamonas spp.) can specially use these pollutants as substrates for growth, allowing for the development of bioremediation technology to achieve sustainable development goals. Here, we describe common xenobiotic aromatic compounds used in our d
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38

Ojeda-Vargas, María del Mar, Andrés Suárez-Alonso, María de los Angeles Pérez-Cervantes, Esther Suárez-Gil, and Carmelo Monzón-Moreno. "Urinary tract infection associated with Comamonas acidovorans." Clinical Microbiology and Infection 5, no. 7 (1999): 443–44. http://dx.doi.org/10.1111/j.1469-0691.1999.tb00170.x.

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39

Linares, Mauricio, José Luis Pruneda-Paz, Luciana Reyna, and Susana Genti-Raimondi. "Regulation of testosterone degradation in Comamonas testosteroni." Journal of Steroid Biochemistry and Molecular Biology 112, no. 1-3 (2008): 145–50. http://dx.doi.org/10.1016/j.jsbmb.2008.09.011.

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40

Almuzara, M. N., R. Cittadini, C. Vera Ocampo, et al. "Intra-Abdominal Infections Due to Comamonas kerstersii." Journal of Clinical Microbiology 51, no. 6 (2013): 1998–2000. http://dx.doi.org/10.1128/jcm.00659-13.

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41

Cui, Mingchao, Fanzhong Chen, Jiamo Fu, Guoying Sheng, and Guoping Sun. "Microbial Metabolism of Quinoline by Comamonas sp." World Journal of Microbiology and Biotechnology 20, no. 6 (2004): 539–43. http://dx.doi.org/10.1023/b:wibi.0000043149.61562.3f.

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42

Duc, Ha Danh. "Degradation of chlorotoluenes by Comamonas testosterone KT5." Applied Biological Chemistry 60, no. 4 (2017): 457–65. http://dx.doi.org/10.1007/s13765-017-0299-3.

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43

Reina, Jordi, Isabel Llompart, and Pedro Alomar. "Acute suppurative otitis caused by Comamonas acidovorans." Clinical Microbiology Newsletter 13, no. 5 (1991): 38–39. http://dx.doi.org/10.1016/0196-4399(91)90006-h.

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44

DE VOS, P., K. KERSTERS, E. FALSEN, et al. "Comamonas Davis and Park 1962 gen. nov., nom. rev. emend., and Comamonas terrigena Hugh 1962 sp. nov., nom. rev." International Journal of Systematic Bacteriology 35, no. 4 (1985): 443–53. http://dx.doi.org/10.1099/00207713-35-4-443.

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45

Haçariz, Orçun, Charles Viau, Xue Gu, and Jianguo Xia. "Native Microbiome Members of C. elegans Act Synergistically in Biosynthesis of Pyridoxal 5′-Phosphate." Metabolites 12, no. 2 (2022): 172. http://dx.doi.org/10.3390/metabo12020172.

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The roles of the healthy microbiome on the host and the relationships between members of the microbiome remain to be fully characterized. Due to the complexity of the interactions between the mammalian microbiome and its host, the use of model organisms such as the nematode worm Caenorhabditis elegans is a promising strategy to study host-microbiome interactions in vivo, as well as bacterial crosstalk within the host. Previously it was found that native bacterial isolates of the worm, Chryseobacterium sp. CHNTR56 MYb120 and Comamonas sp. 12022 MYb131, possess genomic diversity in the biosynthe
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46

Tiwari, Shreekant, and Monalisah Nanda. "Bacteremia caused by Comamonas testosteroni an unusual pathogen." Journal of Laboratory Physicians 11, no. 01 (2019): 087–90. http://dx.doi.org/10.4103/jlp.jlp_116_18.

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Abstract Comamonas species are rare isolates in microbiology laboratories and have been infrequently reported as an infectious agent in routine clinical practice. They have a wide range of natural habitats including water, soil, and plants as well as from some hospital devices, such as intravenous lines and the reservoir water in the humidifiers of respiratory therapy equipment. Comamonas testosteroni is rarely recognized as a human pathogen. In spite of its uncommon human pathogenesis, there are few reports where it was reported as an aggressive opportunistic pathogen, and that was mostly rel
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47

Nwokeh, U. J., I. G. Okoro, and C. U. Orodeji. "ISOLATION, IDENTIFICATION AND PHYLOGENETIC CHARACTERIZATION OF POTASSIUM-SOLUBILIZING RHIZOBACTERIA ISOLATED FROM THE ROOTS OF Mimosa indica WEED." FUDMA JOURNAL OF SCIENCES 7, no. 1 (2023): 280–85. http://dx.doi.org/10.33003/fjs-2023-0701-1309.

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Most microorganisms residing within plant rhizosphere are of great importance to soil fertility. The either release plant nutrient into soil solution and make it available for plant absorption directly or indirectly, excrete enzymes or organic acids that facilitate the solubilization of insoluble minerals, such as potassium (K). A laboratory analysis was carried out at the Soil Science Laboratory in Michael Okpara University of Agriculture, Umudike, to isolate potassium-solubilizing rhizobacteria from Mimosa indica a weed that have invaded most agricultural land in the southeastern Nigeria. It
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48

Blöthe, Marco, and Eric E. Roden. "Microbial Iron Redox Cycling in a Circumneutral-pH Groundwater Seep." Applied and Environmental Microbiology 75, no. 2 (2008): 468–73. http://dx.doi.org/10.1128/aem.01817-08.

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ABSTRACT The potential for microbially mediated redox cycling of iron (Fe) in a circumneutral-pH groundwater seep in north central Alabama was studied. Incubation of freshly collected seep material under anoxic conditions with acetate-lactate or H2 as an electron donor revealed the potential for rapid Fe(III) oxide reduction (ca. 700 to 2,000 μmol liter−1 day−1). Fe(III) reduction at lower but significant rates took place in unamended controls (ca. 300 μmol liter−1 day−1). Culture-based enumerations (most probable numbers [MPNs]) revealed significant numbers (102 to 106 cells ml−1) of organic
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49

Reddy, Ashok Kumar, Somasheila I. Murthy, Subhadra Jalali, and Usha Gopinathan. "Post-operative endophthalmitis due to an unusual pathogen, Comamonas testosteroni." Journal of Medical Microbiology 58, no. 3 (2009): 374–75. http://dx.doi.org/10.1099/jmm.0.006072-0.

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Here, we describe the first report of post-operative endophthalmitis due to Comamonas testosteroni in an elderly diabetic patient after complicated cataract surgery. The isolate was identified by using Mini API strips. The patient was successfully treated with intravitreal ceftazidime and oral ciprofloxacin.
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50

Dimova, M. I., and G. O. Iutynska. "Fatty Acid Composition of Comamonas testosteroni under Hexachlorobenzene Loading Conditions." Mikrobiolohichnyi Zhurnal 84, no. 2 (2022): 24–32. http://dx.doi.org/10.15407/microbiolj84.02.024.

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Changes in the lipid composition in bacterial membranes are considered to be the most important adaptation mechanisms to adverse chemical factors. The aim of the study was to compare the hexachlorobenzene effects on the fatty acid composition of total lipids Comamonas testosteroni. Methods. The study was performed with C. testosteroni UCM B-400 and B-401, B-213 strains. Bacteria were grown in the Luria-Bertrani (LB) liquid medium containing 10 and 20 mg/L of hexachlorobenzene (HCB). After cultivation, the biomass was separated by centrifugation and the fatty acid composition of total lipids wa
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