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The genome of deep-sea vent chemolithoautotroph Thiomicrospira crunogena XCL-2
Authors:Scott Kathleen M  Sievert Stefan M  Abril Fereniki N  Ball Lois A  Barrett Chantell J  Blake Rodrigo A  Boller Amanda J  Chain Patrick S G  Clark Justine A  Davis Carisa R  Detter Chris  Do Kimberly F  Dobrinski Kimberly P  Faza Brandon I  Fitzpatrick Kelly A  Freyermuth Sharyn K  Harmer Tara L  Hauser Loren J  Hügler Michael  Kerfeld Cheryl A  Klotz Martin G  Kong William W  Land Miriam  Lapidus Alla  Larimer Frank W  Longo Dana L  Lucas Susan  Malfatti Stephanie A  Massey Steven E  Martin Darlene D  McCuddin Zoe  Meyer Folker  Moore Jessica L  Ocampo Luis H  Paul John H  Paulsen Ian T  Reep Douglas K  Ren Qinghu  Ross Rachel L
Institution:Biology Department, University of South Florida, Tampa, Florida, United States of America. kscott@cas.usf.edu
Abstract:Presented here is the complete genome sequence of Thiomicrospira crunogena XCL-2, representative of ubiquitous chemolithoautotrophic sulfur-oxidizing bacteria isolated from deep-sea hydrothermal vents. This gammaproteobacterium has a single chromosome (2,427,734 base pairs), and its genome illustrates many of the adaptations that have enabled it to thrive at vents globally. It has 14 methyl-accepting chemotaxis protein genes, including four that may assist in positioning it in the redoxcline. A relative abundance of coding sequences (CDSs) encoding regulatory proteins likely control the expression of genes encoding carboxysomes, multiple dissolved inorganic nitrogen and phosphate transporters, as well as a phosphonate operon, which provide this species with a variety of options for acquiring these substrates from the environment. Thiom. crunogena XCL-2 is unusual among obligate sulfur-oxidizing bacteria in relying on the Sox system for the oxidation of reduced sulfur compounds. The genome has characteristics consistent with an obligately chemolithoautotrophic lifestyle, including few transporters predicted to have organic allocrits, and Calvin-Benson-Bassham cycle CDSs scattered throughout the genome.
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