Chloroflexus aurantiacus J-10-fl

Names | Chloroflexus aurantiacus J-10-fl |
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Accession numbers | NC_010175 |
Background | The phylum Chloroflexi is an early branching anoxygenic phototroph lineage within the Bacteria. Often grouped as the green non-sulfur bacterial (GNSB) branch of the 16S rRNA tree of life, this name is misleading, as not all members are green and some use sulfide. Its members are apparently metabolically diverse and widely distributed in nature. Although these organisms generally stain Gram-negative, a lipopolysaccharide-containing outer membrane is not present and the peptidoglycan is a variant that usually contains L-ornithine as the diamino acid. Most members of the Chloroflexi exhibit gliding motility. Members of the Family Chloroflexaceae are gliding filamentous, anoxygenic phototrophs. The "green" members of this family (Chloroflexus spp., Chloronema spp., Oscillochloris spp., and Chlorothrix spp.) synthesize bacteriochlorophylls a and c and use chlorosomes as their light harvesting antennae, while the "red" members of this family (Heliothrix and Roseiflexus spp.) only synthesize bacteriochlorophyll a and thus lack chlorosomes. The phylum Chloroflexi is heterogeneous with regard to metabolic properties, exhibiting two different pathways for carbon fixation (reductive pentose phosphate (Calvin cycle) and 3-hydroxy-propionate pathways), and their photosynthetic apparatus is a hybrid between that of green sulfur bacteria and purple bacteria.C. aurantiacus has characteristics typical of both the green sulfur bacteria and the purple bacteria. Lateral gene transfer, however, has blurred the evolutionary history of photosynthetic prokaryotes. It is a thermophilic, filamentous gliding phototroph, forming massive accumulations as conspicuous mats in neutral to alkaline hot springs. It is found at higher temperatures than any other anoxygenic phototroph; its optimal growth temperature lies between 50 and 60 degrees C in laboratory cultures. It is typically found as the lower layer of a microbial mat with cyanobacteria growing in layers above it. In springs high in sulfide, however, Chloroflexus may be found alone.Chloroflexus grows primarily as a photoheterotroph and appears to consume the organic products of the autotrophic cyanobacteria in its native habitat. Some strains can grow autotrophically, however, using hydrogen or sulfide as an electron donor. The CO2 fixation mechanism, the 3-hydroxypropionate pathway, is unique among all phototrophs. Cells appear to lack ribulose bisphosphate carboxylase activity. The light-harvesting apparatus consists of chlorosomes appressed to the cell membrane. The chlorosomes are somewhat smaller that those of the green sulfur bacteria. The chlorosomes contain the accessory bacteriochlorophyll c. Light-harvesting complexes containing Bchl a similar to those of the purple bacteria are located in the cell membrane. The pheophytin-quinone type photochemical reaction centers are also similar to those of the purple bacteria. The cells, however, lack internal membranes typical of the purple bacteria (modified from http://genome.jgi-psf.org/finished_microbes/chlau/chlau.home.html). (HAMAP: CHLAA) |
Taxonomy | |
Kingdom: | Bacteria |
Phylum: | Chloroflexi |
Class: | Chloroflexi |
Order: | Chloroflexales |
Family: | Chloroflexaceae |
Genus: | Chloroflexus |
Species: | aurantiacus |
Strain | NA |
Complete | Yes |
Sequencing centre | (05-DEC-2007) US DOE Joint Genome Institute, 2800 Mitchell Drive B100, Walnut Creek, CA 94598-1698, USA (21-DEC-2007) National Center for Biotechnology Information, NIH, Bethesda, MD 20894, USA |
Sequencing quality | Level 6: Finished |
Sequencing depth | NA |
Sequencing method | Sanger |
Isolation site | Hakone hot spring area in Japan |
Isolation country | Japan |
Number of replicons | 1 |
Gram staining properties | Negative |
Shape | Filamentous |
Mobility | Yes |
Flagellar presence | No |
Number of membranes | 1 |
Oxygen requirements | Anaerobic |
Optimal temperature | 52.0 |
Temperature range | Thermophilic |
Habitat | Specialized |
Biotic relationship | Free living |
Host name | NA |
Cell arrangement | Filaments |
Sporulation | NA |
Metabolism | Carbon dioxide fixation |
Energy source | Photosynthetic, Phototroph |
Diseases | NA |
Pathogenicity | No |
Glycolysis / Gluconeogenesis
Citrate cycle (TCA cycle)
Pentose phosphate pathway
Fatty acid metabolism
Synthesis and degradation of ketone bodies
Ubiquinone and other terpenoid-quinone biosynthesis
Purine metabolism
Pyrimidine metabolism
Alanine, aspartate and glutamate metabolism
Glycine, serine and threonine metabolism
Cysteine and methionine metabolism
Valine, leucine and isoleucine degradation
Valine, leucine and isoleucine biosynthesis
Lysine biosynthesis
Arginine and proline metabolism
Histidine metabolism
Phenylalanine, tyrosine and tryptophan biosynthesis
Selenocompound metabolism
D-Glutamine and D-glutamate metabolism
D-Alanine metabolism
Streptomycin biosynthesis
Peptidoglycan biosynthesis
Pyruvate metabolism
Chloroalkane and chloroalkene degradation
Glyoxylate and dicarboxylate metabolism
Butanoate metabolism
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
Lipoic acid metabolism
Folate biosynthesis
Porphyrin and chlorophyll metabolism
Terpenoid backbone biosynthesis
Sulfur metabolism
Aminoacyl-tRNA biosynthesis
Citrate cycle (TCA cycle)
Pentose phosphate pathway
Fatty acid metabolism
Synthesis and degradation of ketone bodies
Ubiquinone and other terpenoid-quinone biosynthesis
Purine metabolism
Pyrimidine metabolism
Alanine, aspartate and glutamate metabolism
Glycine, serine and threonine metabolism
Cysteine and methionine metabolism
Valine, leucine and isoleucine degradation
Valine, leucine and isoleucine biosynthesis
Lysine biosynthesis
Arginine and proline metabolism
Histidine metabolism
Phenylalanine, tyrosine and tryptophan biosynthesis
Selenocompound metabolism
D-Glutamine and D-glutamate metabolism
D-Alanine metabolism
Streptomycin biosynthesis
Peptidoglycan biosynthesis
Pyruvate metabolism
Chloroalkane and chloroalkene degradation
Glyoxylate and dicarboxylate metabolism
Butanoate metabolism
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
Lipoic acid metabolism
Folate biosynthesis
Porphyrin and chlorophyll metabolism
Terpenoid backbone biosynthesis
Sulfur metabolism
Aminoacyl-tRNA biosynthesis