Candidatus ruthia magnifica: Difference between revisions
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==Cell structure and metabolism== | ==Cell structure and metabolism== | ||
R. Magnifica gains energy by sulfur oxidation through ''sox''(sulfur oxidation) and ''dsr'' (dissimilatory sulfite reductase) genes. When there is no environmental sulfur available, it may oxidize its sulfur granules through the use of ''dsr'' homologs. | R. Magnifica gains energy by sulfur oxidation through ''sox''(sulfur oxidation) and ''dsr'' (dissimilatory sulfite reductase) genes. When there is no environmental sulfur available, it may oxidize its sulfur granules through the use of ''dsr'' homologs. | ||
==Ecology== | ==Ecology== |
Revision as of 08:48, 3 May 2007
A Microbial Biorealm page on the genus Candidatus ruthia magnifica
Classification
Higher order taxa
Bacteria(Kindgdom); Proteobacteria(Phylum); Gammaproteobacteria(Class); sulfur-oxidizing symbionts(order)[NCBI, [1]]
Species
NCBI: Taxonomy |
Candidatus Ruthia magnifica
Description and significance
R. magnifica is a chemoautotrophic bacteria that lives symbiotically with a giant clam, a Metazoan with a genus and species of Calyptogena magnifica. It lives in an environment that may be characterized as a hydrothermal vent. It uses the chemical energy of reduced sulfur emanating from vents to provide their hosts with carbon and a large array of additional necessary nutrients such as essential amino acids and vitamins.[3] In return, the hosts provide the bacteria with inorganic substrates necessary for chemoautotrophic activity. R. magnifica itself lives in the gut and ciliary food groove of C. magnifica.[3] The sequencing of the R. magnifica genome is important in determining its metabolism and the compounds it is able to produce. Which, in turn, will give insight into the metabolism and biology of the host. R. magnifica is the first intracellular, sulfur-oxidizing endosymbiont to have its genome sequenced. It also has the largest genome of any intracellular symbiont sequenced to date and may represent an early intermediate in the evolution toward a plastid-like chemoautotrophic organelle.[3]
Genome structure
R. magnifica has 1,119 genes that encode 1,953 proteins. A single circular chromosome contains genes which are predicted to encode all the proteins necessary for all the metabolic pathways typical of free-living chemoautotrophs, including carbon fixation, sulfur oxidation, nitrogen assimilation, amino acid and cofactor/vitamin biosynthesis.[3]
Cell structure and metabolism
R. Magnifica gains energy by sulfur oxidation through sox(sulfur oxidation) and dsr (dissimilatory sulfite reductase) genes. When there is no environmental sulfur available, it may oxidize its sulfur granules through the use of dsr homologs.
Ecology
Describe any interactions with other organisms (included eukaryotes), contributions to the environment, effect on environment, etc.
Pathology
Due to its need for sulfer and its niche of hydrothermic vents, it is not likely to find R. magnifica in the same environment as humans. Therefore, it is not considered a pathogen and is not currently thought to cause any disease.
Application to Biotechnology
no known compounds that are useful in the Biotechnology are produced by R. magnifica
Current Research
Enter summaries of the most recent research here--at least three required
References
[2]] NCBI Taxonomy
[3] LG Newton, T. Woyke, "The Calyptogena magnifica Chemoautotrophic Symbiont Genome". Science. 2007. Volume 315. p. 998.
Edited by Albert Noniyev, student of Rachel Larsen and Kit Pogliano