Chromosomal Arsenic Resistance Genes from Sulfobacillus Thermosulfidooxidans and a Demonstration that the Genetic Diversity of arsB among the Sulfobacilli is Similar to that of their 16S rRNA Genes

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Arsenic resistance genes were isolated from the moderately thermophilic, Gram-positive iron and sulfur-oxidizing bacterium, Sulfobacillus thermosulfidooxidans. Only arsR and arsB genes were present and attempts to identify an arsC using degenerate PCR primers or dependent arsC genes as probes in Southern hybridization experiments were unsuccessful. Although enhanced resistance to arsenite was not detected when the ars genes were cloned in Escherichia coli, the kumamolisin-As and arsRB genes were induced by arsenite. RT-PCR experiments suggested that transcription of the cloned kumamolisin-As-like and arsRB genes is linked in Escherichia coli, but not in Sb. thermosulfidooxidans. The gene order kumamolisin-As precursor, arsR and arsB was maintained among three strains of Sb. thermosulfidooxidans isolated from three continents. Southern hybridization using a Sb. thermosulfidooxidans arsB gene fragment as a probe gave a positive hybridization signal using S. acidophilus but not with S. thermotolerans genomic DNA. Comparison of partial sequence data of the arsB and 16S rRNA genes suggested that the two types of genes have undergone a similar evolutionary history and therefore that the arsB genes were present in the ancestral Sulfobacillus before its divergence into species.

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Advanced Materials Research (Volumes 71-73)

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171-174

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May 2009

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© 2009 Trans Tech Publications Ltd. All Rights Reserved

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[1] R. S Golovacheva and G.I. Karavaiko: Microbiology Vol 5 (1979), p.658 (Russian).

Google Scholar

[2] M. Dopson and E.B. Lindstrom: Microbial Ecol. Vol 48 (2004), p.19.

Google Scholar

[3] N. Okibe, M. Gericke, K.B. Hallberg and D.B. Johnson: (2003). Appl. Environ. Microbiol. Vol 69 (2003), p. (1936).

Google Scholar

[4] P.R. Norris, D.A. Clark, J. Owen and S. Waterhouse: Microbiology Vol 142 (1996), p.775.

Google Scholar

[5] V.S. Melamud, T.A. Pivovarova, T.P. Tourova, T.V. Kalganova, G.A. Osipov, A.M. Lysenko, T.F. Kondrat'eva and G. I Karavaiko: Microbiology Vol 72 (2002), p.605 (Russian).

DOI: 10.1023/a:1026007620113

Google Scholar

[6] T.I. Bogdanova, I.A. Tsapilna, T.F. Kondrat'eva, V.I. Duda, N.E. Suzina, V.S. Melamud, T.P. Tourova and G.I. Karavaiko: Intl. J. Sys. Evol. Microbiol. Vol 56 (2006), p.1039.

Google Scholar

[7] M. Tuffin, P. de Groot, S.M. Deane and D.E. Rawlings: Microbiology Vol 151 (2005), p.3027.

Google Scholar

[8] A.A. Kotzé, M. Tuffin, S.M. Deane and D.E. Rawlings: Microbiology Vol 152 (2006), p.3551.

Google Scholar

[9] M. Tuffin, S.B. Hector, S.M. Deane and D.E. Rawlings: Appl. Environ. Microbiol. Vol 72 (2006), p.2247.

Google Scholar

[10] L.S. Tisa and B.P. Rosen: J. Biol. Chem. Vol 265 (1989), p.190.

Google Scholar

[11] G. Ji and S. Silver: Proc. Natl. Acad. Sci. USA Vol 89 (1992), p.9474.

Google Scholar

[12] R. Mukhopadhyay, B.P. Rosen, L.T. Phung and S. Silver: FEMS Microbiol. Rev. Vol 26 (2002), p.311.

Google Scholar

[13] B.P. Rosen: Trends Microbiol. Vol 7 (1999), p.207.

Google Scholar

[14] T.M. Gihring, P.L. Bond, S. Peters and J.F. Banfield: Extremophiles Vol 7 (2003), p.123.

Google Scholar