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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
MeSH Review

Chloroflexi

 
 
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Disease relevance of Chloroflexi

 

High impact information on Chloroflexi

  • These results challenge previous conclusions based on 16S ribosomal RNA and Hsp60/Hsp70 analyses that green nonsulfur bacteria or heliobacteria are the earliest phototrophs [3].
  • Bacterial communities in the methane hydrate-bearing sediments were dominated by members of the JS1 group, Planctomycetes, and Chloroflexi [4].
  • Stepwise cloning and molecular characterization of the HgiDI restriction-modification system from Herpetosiphon giganteus Hpa2 [2].
  • As sulfate was still available as an electron acceptor in these layers, the abundance of Chloroflexi might be promoted by the electron donor or the quality of the carbon source [5].
  • In particular, the members of the Chloroflexi were strongly MAR positive in the culture without NH4+ addition, in which nitrifying bacteria tended to decay [6].
 

Chemical compound and disease context of Chloroflexi

  • Sequential reductive dechlorination of meta-chlorinated polychlorinated biphenyl congeners in sediment microcosms by two different Chloroflexi phylotypes [7].
  • Carotenoid glucosides and menaquinones from the gliding bacterium Herpetosiphon giganteus Hp a2 [8].
  • The gliding bacterium Herpetosiphon giganteus Hp a2 was shown to contain gamma-carotene, one monoglucosyloxy and two new diglucosyloxy carotenoids with a x-O-acyldiglucosyloxy carotenoid as main component [8].
 

Biological context of Chloroflexi

 

Gene context of Chloroflexi

References

  1. Different lipid A types in lipopolysaccharides of phototrophic and related non-phototrophic bacteria. Weckesser, J., Mayer, H. FEMS Microbiol. Rev. (1988) [Pubmed]
  2. Stepwise cloning and molecular characterization of the HgiDI restriction-modification system from Herpetosiphon giganteus Hpa2. Düsterhöft, A., Erdmann, D., Kröger, M. Nucleic Acids Res. (1991) [Pubmed]
  3. Molecular evidence for the early evolution of photosynthesis. Xiong, J., Fischer, W.M., Inoue, K., Nakahara, M., Bauer, C.E. Science (2000) [Pubmed]
  4. Biogeographical distribution and diversity of microbes in methane hydrate-bearing deep marine sediments on the Pacific Ocean Margin. Inagaki, F., Nunoura, T., Nakagawa, S., Teske, A., Lever, M., Lauer, A., Suzuki, M., Takai, K., Delwiche, M., Colwell, F.S., Nealson, K.H., Horikoshi, K., D'Hondt, S., Jørgensen, B.B. Proc. Natl. Acad. Sci. U.S.A. (2006) [Pubmed]
  5. Deep biosphere-related bacteria within the subsurface of tidal flat sediments. Wilms, R., Köpke, B., Sass, H., Chang, T.S., Cypionka, H., Engelen, B. Environ. Microbiol. (2006) [Pubmed]
  6. Fate of 14C-labeled microbial products derived from nitrifying bacteria in autotrophic nitrifying biofilms. Okabe, S., Kindaichi, T., Ito, T. Appl. Environ. Microbiol. (2005) [Pubmed]
  7. Sequential reductive dechlorination of meta-chlorinated polychlorinated biphenyl congeners in sediment microcosms by two different Chloroflexi phylotypes. Fagervold, S.K., Watts, J.E., May, H.D., Sowers, K.R. Appl. Environ. Microbiol. (2005) [Pubmed]
  8. Carotenoid glucosides and menaquinones from the gliding bacterium Herpetosiphon giganteus Hp a2. Kleinig, H., Reichenbach, H. Arch. Microbiol. (1977) [Pubmed]
  9. Molecular characterization of novel red green nonsulfur bacteria from five distinct hot spring communities in Yellowstone National Park. Boomer, S.M., Lodge, D.P., Dutton, B.E., Pierson, B. Appl. Environ. Microbiol. (2002) [Pubmed]
  10. Channel-forming (Porin) activity in Herpetosiphon aurantiacus Hp a2. Harwardt, R., Maier, E., Reichenbach, H., Weckesser, J., Benz, R. J. Bacteriol. (2004) [Pubmed]
  11. Thermobaculum terrenum gen. nov., sp. nov.: a non-phototrophic gram-positive thermophile representing an environmental clone group related to the Chloroflexi (green non-sulfur bacteria) and Thermomicrobia. Botero, L.M., Brown, K.B., Brumefield, S., Burr, M., Castenholz, R.W., Young, M., McDermott, T.R. Arch. Microbiol. (2004) [Pubmed]
 
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