Archaeal phylogeny based on proteins of the transcription and translation machineries:tackling the Methanopyrus kandleri paradox
Brochier C, Forterre P, Gribaldo S (2004) Archaeal phylogeny based on proteins of the transcription and translation machineries:tackling the Methanopyrus kandleri paradox. Genome Biol 5(3):R17
Kates M, Kushner DJ, Matheson AT (eds). Elsevier, Amsterdam
Dalgaard JZ, Garrett RA (1993) Archaeal hyperthermophile genes. In: Kates M, Kushner DJ, Matheson AT (eds) The biochemistry of Archaea (Archaebacteria). Elsevier, Amsterdam, p 535
The genome of M. acetivorans reveals extensive metabolic and physiological diversity
Galagan JE, Nusbaum C, Roy A, et al. (2002) The genome of M. acetivorans reveals extensive metabolic and physiological diversity. Genome Res 12:532-542
Relationships between genomic GC content, RNA secondary structures and optimal growth temperature in prokaryotes
Galtier N, Lobry JR (1997) Relationships between genomic GC content, RNA secondary structures and optimal growth temperature in prokaryotes. J Mol Evol 44:632-636
High guanine-cytosine content is not an adaptation to high temperature: A comparative analysis amongst prokaryotes
Hurst LD, Merchant AR (2001) High guanine-cytosine content is not an adaptation to high temperature: a comparative analysis amongst prokaryotes. Proc R Soc Lond B 268:493-497
Compositional changes in RNA, DNA and proteins for bacterial adaptation to higher and lower temperatures
Nakashima H, Fukuchi S, Nishikawa K (2003) Compositional changes in RNA, DNA and proteins for bacterial adaptation to higher and lower temperatures. J Biochem 133:507-513
Evidence for strong selective constraint acting on the nucleotide composition of 16S ribosomal RNA genes
Wang H-C, Hickey DA (2002) Evidence for strong selective constraint acting on the nucleotide composition of 16S ribosomal RNA genes. Nucleic Acids Res 30:2501-2507