The Pelagibacterales are an order in the Alphaproteobacteria composed of free-living marine bacteria that make up roughly one in three cells at the ocean's surface.[2][3][4] Overall, members of the Pelagibacterales are estimated to make up between a quarter and a half of all prokaryotic cells in the ocean.[5]
Initially, this taxon was known solely by metagenomic data and was known as the SAR11 clade. It was first placed in the Rickettsiales, but was later raised to the rank of order, and then placed as sister order to the Rickettsiales in the subclass Rickettsidae.[4] It includes the highly abundant marine species Pelagibacter ubique.
Bacteria in this order are unusually small.[6] Due to their small genome size and limited metabolic function, Pelagibacterales have become a model organism for 'streamlining theory'.[5]
P. ubique and related species are oligotrophs (scavengers) and feed on dissolved organic carbon and nitrogen.[3] They are unable to fix carbon or nitrogen, but can perform the TCA cycle with glyoxylate bypass and are able to synthesise all amino acids except glycine,[7] as well as some cofactors.[8] They also have an unusual and unexpected requirement for reduced sulfur.[9]
P. ubique and members of the oceanic subgroup I possess gluconeogenesis, but not a typical glycolysis pathway, whereas other subgroups are capable of typical glycolysis.[10]
Unlike Acaryochloris marina, P. ubique is not photosynthetic — specifically, it does not use light to increase the bond energy of an electron pair — but it does possess proteorhodopsin (including retinol biosynthesis) for ATP production from light.[11]
SAR11 bacteria are responsible for much of the dissolved methane in the ocean surface. They extract phosphate from methylphosphonic acid.[12]
Although the taxon derives its name from the type species P. ubique (status Candidatus species), this species has not yet been validly published, and therefore neither the order name nor the species name has official taxonomic standing.[13]
^Giovannoni, S. J.; Tripp, H. J.; Givan, S.; Podar, M.; Vergin, K. L.; Baptista, D.; Bibbs, L.; Eads, J.; Richardson, T. H.; Noordewier, M.; Rappé, M. S.; Short, J. M.; Carrington, J. C.; Mathur, E. J. (2005). "Genome Streamlining in a Cosmopolitan Oceanic Bacterium". Science. 309 (5738): 1242–1245. Bibcode:2005Sci...309.1242G. doi:10.1126/science.1114057. PMID16109880. S2CID16221415.
^H. James Tripp; Joshua B. Kitner; Michael S. Schwalbach; John W. H. Dacey; Larry J. Wilhelm & Stephen J. Giovannoni (April 2008). "SAR11 marine bacteria require exogenous reduced sulfur for growth". Nature. 452 (7188): 741–4. Bibcode:2008Natur.452..741T. doi:10.1038/nature06776. PMID18337719. S2CID205212536.
^Schwalbach, M. S.; Tripp, H. J.; Steindler, L.; Smith, D. P.; Giovannoni, S. J. (2010). "The presence of the glycolysis operon in SAR11 genomes is positively correlated with ocean productivity". Environmental Microbiology. 12 (2): 490–500. doi:10.1111/j.1462-2920.2009.02092.x. PMID19889000.
^Giovannoni, S. J.; Bibbs, L.; Cho, J. C.; Stapels, M. D.; Desiderio, R.; Vergin, K. L.; Rappé, M. S.; Laney, S.; Wilhelm, L. J.; Tripp, H. J.; Mathur, E. J.; Barofsky, D. F. (2005). "Proteorhodopsin in the ubiquitous marine bacterium SAR11". Nature. 438 (7064): 82–85. Bibcode:2005Natur.438...82G. doi:10.1038/nature04032. PMID16267553. S2CID4414677.
^Don J. Brenner; Noel R. Krieg; James T. Staley (July 26, 2005) [1984(Williams & Wilkins)]. George M. Garrity (ed.). The Proteobacteria. Bergey's Manual of Systematic Bacteriology. Vol. 2C (2nd ed.). New York: Springer. pp. 1388. ISBN978-0-387-24145-6. British Library no. GBA561951.