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MeSH Review

Betaproteobacteria

 
 
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Disease relevance of Betaproteobacteria

 

High impact information on Betaproteobacteria

  • Nitrate-reducing beta-Proteobacteria were isolated on monoterpenes as sole carbon source and electron donor [6].
  • When we compared genera within the most dominant group, the beta-proteobacteria, differences between unamended and cadmium-amended libraries were much larger [7].
  • Instead, it appears that urease in beta-proteobacterial autotrophic ammonia oxidizers is the product of divergent evolution in the common ancestor of gamma- and beta-proteobacteria that was initiated before their divergence during speciation [8].
  • On the other hand, the beta-rhizobia were grouped with free-living nitrogen-fixing beta-proteobacteria on the basis of the nifH phylogenetic tree [9].
  • The intron shows a higher sequence affiliation with introns in tRNA(Ile)(CAU) and tRNA(Arg)(CCU) genes in alpha- and beta-proteobacteria, respectively, than with other cyanobacterial tRNA(Leu)(UAA) group I introns [10].
 

Chemical compound and disease context of Betaproteobacteria

  • Recent research on microbial degradation of aromatic and other refractory compounds in anoxic waters and soils has revealed that nitrate-reducing bacteria belonging to the Betaproteobacteria contribute substantially to this process [11].
  • The extremely low content of 2-hydroxyputrescine is remarkable, since this unique diamine is a common marker for beta-proteobacteria [12].
  • Sterolibacterium denitrificans gen. nov., sp. nov., a novel cholesterol-oxidizing, denitrifying member of the beta-Proteobacteria [13].
  • Methylibium petroleiphilum gen. nov., sp. nov., a novel methyl tert-butyl ether-degrading methylotroph of the Betaproteobacteria [14].
  • The quantity of three members belonging to beta-proteobacteria accounted for 34% of total 16S rDNA copies measured from the "heavier" fraction of DNA that was contributed from the DNA of microorganisms capable of incorporating 13C-labeled naphthalene into their genetic biomarkers [15].
 

Gene context of Betaproteobacteria

 

Analytical, diagnostic and therapeutic context of Betaproteobacteria

References

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  2. Diversity of alpha-halocarboxylic acid dehalogenases in bacteria isolated from a pristine soil after enrichment and selection on the herbicide 2,2-dichloropropionic acid (Dalapon). Marchesi, J.R., Weightman, A.J. Environ. Microbiol. (2003) [Pubmed]
  3. Assimilation of polysaccharides and glucose by major bacterial groups in the Delaware Estuary. Elifantz, H., Malmstrom, R.R., Cottrell, M.T., Kirchman, D.L. Appl. Environ. Microbiol. (2005) [Pubmed]
  4. Benzoate-coenzyme A ligase from Thauera aromatica: an enzyme acting in anaerobic and aerobic pathways. Schühle, K., Gescher, J., Feil, U., Paul, M., Jahn, M., Schägger, H., Fuchs, G. J. Bacteriol. (2003) [Pubmed]
  5. Microbial community in acidic hydrothermal waters of volcanically active White Island, New Zealand. Donachie, S.P., Christenson, B.W., Kunkel, D.D., Malahoff, A., Alam, M. Extremophiles (2002) [Pubmed]
  6. Biotransformation of monoterpenes, bile acids, and other isoprenoids in anaerobic ecosystems. Hylemon, P.B., Harder, J. FEMS Microbiol. Rev. (1998) [Pubmed]
  7. Shifts in rhizoplane communities of aquatic plants after cadmium exposure. Stout, L.M., Nüsslein, K. Appl. Environ. Microbiol. (2005) [Pubmed]
  8. Urease-encoding genes in ammonia-oxidizing bacteria. Koper, T.E., El-Sheikh, A.F., Norton, J.M., Klotz, M.G. Appl. Environ. Microbiol. (2004) [Pubmed]
  9. Legume symbiotic nitrogen fixation by beta-proteobacteria is widespread in nature. Chen, W.M., Moulin, L., Bontemps, C., Vandamme, P., Béna, G., Boivin-Masson, C. J. Bacteriol. (2003) [Pubmed]
  10. Nested evolution of a tRNA(Leu)(UAA) group I intron by both horizontal intron transfer and recombination of the entire tRNA locus. Rudi, K., Fossheim, T., Jakobsen, K.S. J. Bacteriol. (2002) [Pubmed]
  11. The genome sequence of an anaerobic aromatic-degrading denitrifying bacterium, strain EbN1. Rabus, R., Kube, M., Heider, J., Beck, A., Heitmann, K., Widdel, F., Reinhardt, R. Arch. Microbiol. (2005) [Pubmed]
  12. Alcaligenes faecalis subsp. parafaecalis subsp. nov., a bacterium accumulating poly-beta-hydroxybutyrate from acetone-butanol bioprocess residues. Schroll, G., Busse, H.J., Parrer, G., Rölleke, S., Lubitz, W., Denner, E.B. Syst. Appl. Microbiol. (2001) [Pubmed]
  13. Sterolibacterium denitrificans gen. nov., sp. nov., a novel cholesterol-oxidizing, denitrifying member of the beta-Proteobacteria. Tarlera, S., Denner, E.B. Int. J. Syst. Evol. Microbiol. (2003) [Pubmed]
  14. Methylibium petroleiphilum gen. nov., sp. nov., a novel methyl tert-butyl ether-degrading methylotroph of the Betaproteobacteria. Nakatsu, C.H., Hristova, K., Hanada, S., Meng, X.Y., Hanson, J.R., Scow, K.M., Kamagata, Y. Int. J. Syst. Evol. Microbiol. (2006) [Pubmed]
  15. A quantitative assay for linking microbial community function and structure of a naphthalene-degrading microbial consortium. Yu, C.P., Chu, K.H. Environ. Sci. Technol. (2005) [Pubmed]
  16. In-situ enumeration and probing of pyrene-degrading soil bacteria. Jjemba, P.K., Kinkle, B.K., Shann, J.R. FEMS Microbiol. Ecol. (2006) [Pubmed]
  17. The amo operon in marine, ammonia-oxidizing gamma-proteobacteria. Alzerreca, J.J., Norton, J.M., Klotz, M.G. FEMS Microbiol. Lett. (1999) [Pubmed]
  18. A third lineage with two-piece tmRNA. Sharkady, S.M., Williams, K.P. Nucleic Acids Res. (2004) [Pubmed]
  19. Functional and structural analyses of trichloroethylene-degrading bacterial communities under different phenol-feeding conditions: laboratory experiments. Futamata, H., Harayama, S., Hiraishi, A., Watanabe, K. Appl. Microbiol. Biotechnol. (2003) [Pubmed]
 
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