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1 Génétique Moléculaire, Génomique, Microbiologie, UMR 7156, CNRS and Université Louis-Pasteur, 28 rue Goethe, 67000 Strasbourg, France
2 Laboratoire de Physiopathologie des Infections Bactériennes Émergentes et Nosocomiales, Faculté de Médecine, Université Louis-Pasteur, 3 rue Koeberlé, 67000 Strasbourg, France
3 Génoscope Centre National de Séquençage, 2 rue Gaston Crémieux, CP5706, 91057 Evry cedex, France
Correspondence
Marie-Claire Lett
lett{at}gem.u-strasbg.fr
An arsenite-oxidizing bacterium, designated strain ULPAs1T, was isolated from industrial sludge heavily contaminated with arsenic. Cells of this isolate were Gram-negative, curved rods, motile by means of a polar flagellum. The strain was positive for oxidase and catalase activities, was able to reduce nitrate to nitrite, used acetate, lactate and peptone as organic carbon sources under aerobic conditions and was able to oxidize arsenite (As[III]) to arsenate (As[V]). 16S rRNA gene sequence analysis and the absence of dodecanoic fatty acids suggested that this strain represents a member of the genus Herminiimonas of the family Oxalobacteraceae, order Burkholderiales in the Betaproteobacteria. Genomic DNADNA hybridization between strain ULPAs1T and Herminiimonas fonticola S-94T and between strain ULPAs1T and Herminiimonas aquatilis CCUG 36956T revealed levels of relatedness of <10 %, well below the recommended 70 % species cut-off value. Thus, strain ULPAs1T (=CCM 7303T=DSM 17148T=LMG 22961T) is the type strain of a novel species of Herminiimonas, for which the name Herminiimonas arsenicoxydans sp. nov. is proposed.
Present address: Division of Bacterial Infection, Institute of Medical Science, University of Tokyo, 4-6-1, Shirokanedai, Minato-ku, Tokyo 108-8639, Japan.
Present address: Department of Biology, Laboratory of Ecology, Physiology and Biochemistry of Microorganisms, University of Konstanz, D-78457 Konstanz, Germany.
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