Hydrogenobacter thermophilus TK-6

Names | Hydrogenobacter thermophilus TK-6 |
---|---|
Accession numbers | NC_013799, CP002221 |
Background | Hydrogenobacter thermophilus (strain DSM 6534 / IAM 12695 / TK-6) is a strictly thermophilic, obligate chemoautotrophic and hydrogen-oxidizing Gram-negative bacterium isolated from a hot spring located in Mine, Izu, Japan. Phylogenetic analysis based on the 16S ribosomal DNA sequence show that the strain is the deepest branching point among the Bacteria. In accordance with this, distinctive characteristics, such as unusual composition of cellular fatty acids (C18:0 and C20:1 as major fatty acids), a novel sulfur-containing quinone called methionaquinone and a characteristic carbon anabolism (via the reductive tricarboxylic acid cycle), have been reported. Moreover, it is able to assimilate ammonium using glutamine synthetase (GS). Its optimal growth temperature is around 70 to 75 degrees Celsius. (Adapted from: http://ijs.sgmjournals.org/cgi/reprint/34/1/5.pdf). (EBI Integr8) |
Taxonomy | |
Kingdom: | Bacteria |
Phylum: | Aquificae |
Class: | Aquificae |
Order: | Aquificales |
Family: | Aquificaceae |
Genus: | Hydrogenobacter |
Species: | thermophilus |
Strain | TK-6 |
Complete | Yes |
Sequencing centre | (11-FEB-2010) National Center for Biotechnology Information, NIH, Bethesda, MD 20894, USA (25-MAR-2009) Contact:Hiroyuki Arai The University of Tokyo, Department of Biotechnology Yayoi 1-1-1, Bunkyo-ku, Tokyo |
Sequencing quality | Level 6: Finished |
Sequencing depth | NA |
Sequencing method | Sanger |
Isolation site | Soil near hot-spring in Izu Peninsula, Japan |
Isolation country | Japan |
Number of replicons | 2 |
Gram staining properties | Negative |
Shape | NA |
Mobility | No |
Flagellar presence | No |
Number of membranes | 2 |
Oxygen requirements | Aerobic |
Optimal temperature | NA |
Temperature range | Thermophilic |
Habitat | NA |
Biotic relationship | Free living |
Host name | NA |
Cell arrangement | NA |
Sporulation | NA |
Metabolism | Hydrogen oxidizer |
Energy source | Chemolithoautotroph |
Diseases | NA |
Pathogenicity | No |
Glycolysis / Gluconeogenesis
Citrate cycle (TCA cycle)
Pentose phosphate pathway
Purine metabolism
Pyrimidine metabolism
Alanine, aspartate and glutamate metabolism
Valine, leucine and isoleucine biosynthesis
Lysine biosynthesis
Histidine metabolism
Phenylalanine, tyrosine and tryptophan biosynthesis
Selenocompound metabolism
D-Glutamine and D-glutamate metabolism
D-Alanine metabolism
Lipopolysaccharide biosynthesis
Peptidoglycan biosynthesis
Nitrotoluene degradation
C5-Branched dibasic acid metabolism
One carbon pool by folate
Carbon fixation pathways in prokaryotes
Thiamine metabolism
Riboflavin metabolism
Nicotinate and nicotinamide metabolism
Pantothenate and CoA biosynthesis
Biotin metabolism
Lipoic acid metabolism
Folate biosynthesis
Terpenoid backbone biosynthesis
Aminoacyl-tRNA biosynthesis
Citrate cycle (TCA cycle)
Pentose phosphate pathway
Purine metabolism
Pyrimidine metabolism
Alanine, aspartate and glutamate metabolism
Valine, leucine and isoleucine biosynthesis
Lysine biosynthesis
Histidine metabolism
Phenylalanine, tyrosine and tryptophan biosynthesis
Selenocompound metabolism
D-Glutamine and D-glutamate metabolism
D-Alanine metabolism
Lipopolysaccharide biosynthesis
Peptidoglycan biosynthesis
Nitrotoluene degradation
C5-Branched dibasic acid metabolism
One carbon pool by folate
Carbon fixation pathways in prokaryotes
Thiamine metabolism
Riboflavin metabolism
Nicotinate and nicotinamide metabolism
Pantothenate and CoA biosynthesis
Biotin metabolism
Lipoic acid metabolism
Folate biosynthesis
Terpenoid backbone biosynthesis
Aminoacyl-tRNA biosynthesis