1-18 of 18
Keywords: hyperthermophile
Close
Follow your search
Access your saved searches in your account

Would you like to receive an alert when new items match your search?
Close Modal
Sort by
Articles
Articles
Articles
Biochem Soc Trans (2013) 41 (1): 443–450.
Published: 29 January 2013
...David Prangishvili; Eugene V. Koonin; Mart Krupovic Archaeal viruses, especially viruses that infect hyperthermophilic archaea of the phylum Crenarchaeota, constitute one of the least understood parts of the virosphere. However, owing to recent substantial research efforts by several groups...
Includes: Supplementary data
Articles
Biochem Soc Trans (2009) 37 (1): 92–96.
Published: 20 January 2009
...Qunxin She; Changyi Zhang; Ling Deng; Nan Peng; Zhengjun Chen; Yun Xiang Liang Sulfolobus belongs to the hyperthermophilic archaea and it serves as a model organism to study archaeal molecular biology and evolution. In the last few years, we have focused on developing genetic systems for Sulfolobus...
Articles
Biochem Soc Trans (2009) 37 (1): 123–126.
Published: 20 January 2009
... are microbial stress-response elements, although it was recently shown that knocking out all known chromosomally located TA loci in Escherichia coli did not have an impact on survival under certain types of stress. The hyperthermophilic crenarchaeon Sulfolobus solfataricus encodes at least 26 vapBC (where vap...
Articles
Biochem Soc Trans (2009) 37 (1): 69–73.
Published: 20 January 2009
...; although it is a type IA topoisomerase, its reaction is ATP-dependent; and it is the only hyperthermophile-specific protein. All these features have made reverse gyrase the subject of biochemical, structural and functional studies, although they have not shed complete light on the evolution, mechanism...
Articles
Biochem Soc Trans (2009) 37 (1): 36–41.
Published: 20 January 2009
... of investigations of the hyperthermophilic and acidophilic crenarchaeote Sulfolobus solfataricus have been performed in recent years. Mostly, the reactions to DNA damage caused by UV light have been analysed. Whole-genome transcriptomics have demonstrated that a UV-specific response in S. solfataricus does...
Articles
Articles
Biochem Soc Trans (2005) 33 (1): 22–24.
Published: 01 February 2005
...M. Guiral; C. Aubert; M.-T. Giudici-Orticoni Aquifex aeolicus is a microaerophilic, hydrogen-oxidizing, hyperthermophilic bacterium containing three [NiFe] hydrogenases. Two of these three enzymes (one membrane-bound and one soluble) have been purified and characterized. The Aquifex hydrogenases...
Articles
Biochem Soc Trans (2004) 32 (2): 188–192.
Published: 01 April 2004
...M.R. Johnson; C.I. Montero; S.B. Conners; K.R. Shockley; M.A. Pysz; R.M. Kelly Although much attention has been paid to the genetic, biochemical and physiological aspects of individual hyperthermophiles, how these unique micro-organisms relate to each other and to their natural habitats must...
Articles
Biochem Soc Trans (2004) 32 (2): 303–304.
Published: 01 April 2004
...H. Ahmed; B. Tjaden; R. Hensel; B. Siebers Genome data as well as biochemical studies have indicated that – as a peculiarity within hyperthermophilic Archaea – Thermoproteus tenax uses three different pathways for glucose metabolism, a variant of the reversible EMP (Embden–Meyerhof–Parnas) pathway...
Articles
Biochem Soc Trans (2004) 32 (2): 168–171.
Published: 01 April 2004
...D.W. Schwartzman; C.H. Lineweaver We revisit the case for the hyperthermophilic scenario for the origin of life and the last common ancestor. Evidence includes studies of phylogenetic trees, rRNA, G and C content, hyperthermophilic proteins, correlations between maximal temperature tolerances...
Articles
Biochem Soc Trans (2004) 32 (2): 305.
Published: 01 April 2004
...H. Walden; G. Taylor; H. Lilie; T. Knura; R. Hensel The triosephosphate isomerase of the hyperthermophilic crenarchaeum Thermoproteus tenax (TtxTIM) represents a homomeric tetramer. Unlike the triosephosphate isomerases of other hyperthermophiles, however, the association of the TtxTIM tetramers...
Articles
Articles
Biochem Soc Trans (2004) 32 (2): 172–174.
Published: 01 April 2004
... hyperthermophile sulphate reduction thermophile Abbreviations used: E a , activation energy; SRR, sulphate reduction rate; YSNP, Yellowstone National Park. 172 Biochemical Society Transactions (2004) Volume 32, part 2 Sulphate metabolism among thermophiles and hyperthermophiles in natural aquatic...
Articles
Biochem Soc Trans (2004) 32 (2): 204–208.
Published: 01 April 2004
...: Fuselloviridae , Lipothrixviridae and Rudiviridae . They all have double-stranded DNA genomes and infect hyperthermophilic crenarchaea of the orders Sulfolobales and Thermoproteales. Representatives of the different viral families share a few homologous ORFs (open reading frames). However, about 90% of all ORFs...
Articles
Biochem Soc Trans (2004) 32 (2): 298–302.
Published: 01 April 2004
...’ that is not addressed by traditional screening. 1 To whom correspondence should be addressed (e-mail dcowan@uwc.ac.za ). Thermophiles 2003, a held at University of Exeter, 15–19 September 2003 19 September 2003 © 2004 Biochemical Society 2004 biocatalyst gene discovery hyperthermophile...
Articles
Biochem Soc Trans (2004) 32 (2): 231–235.
Published: 01 April 2004
...D. Leduc; S. Graziani; L. Meslet-Cladiere; A. Sodolescu; U. Liebl; H. Myllykallio The hyperthermophilic anaerobic archaeon Pyrococcus abyssi , which lacks thymidine kinase, incorporates label from extracellular uracil, but not from thymidine, into its DNA. This implies that P. abyssi must...