ライフサイエンスコーパス: hyperthermophilic archaea

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1 d response mechanism that is present even in hyperthermophilic archaea.

2 enzymes in sugar and peptide fermentation of hyperthermophilic archaea.

3 ting experiments for bacteria and 90-99% for hyperthermophilic archaea.

4 like CPSase such as those present in several hyperthermophilic archaea.

5 ases are involved in peptide fermentation by hyperthermophilic archaea.

6 communities dominated by several species of hyperthermophilic Archaea.

7 f structures and complete genomes of several hyperthermophilic archaea and bacteria revealed that org

8 bilizes tRNAs from thermophilic bacteria and hyperthermophilic archaea and is required for growth at

9 interaction with uracil is not restricted to hyperthermophilic archaea and that the polymerase from m

10 quences (ISs) are abundant and widespread in hyperthermophilic archaea, but few experimental studies

11 So far, little is known about how hyperthermophilic Archaea cope with such pyrimidine dama

12 ) accumulates as a compatible solute in many hyperthermophilic archaea (e.g., Archaeoglobus fulgidus)

13 Here we describe a consortium of three hyperthermophilic archaea enriched from a continental ge

14 e that the intracellular proteins of certain hyperthermophilic archaea, especially the crenarchaea Py

15 Several enzymes of DNA metabolism from hyperthermophilic archaea exhibit unusual biochemical fe

16 Hyperthermophilic archaea grow at temperatures that dest

17 In particular, the approaches employed by hyperthermophilic archaea have been a general source of

18 f the DNA replication-associated proteins of hyperthermophilic archaea have yielded considerable insi

19 In hyperthermophilic archaea, however, TIM exists as a tetr

20 Inositol monophosphatase (EC 3.1.3.25) in hyperthermophilic archaea is thought to play a role in t

21 esults suggest that many DNA repair genes of hyperthermophilic archaea may not be recognized because

22 Hsp16.5, isolated from the hyperthermophilic Archaea Methanococcus jannaschii, is a

23 o establish the key cell-cycle parameters of hyperthermophilic archaea of the genus Sulfolobus.

24 perties when compared even to Fds from other hyperthermophilic archaea or bacteria.

25 the TATA-box binding protein (TBP) from the hyperthermophilic archaea Pyrococcus woesei.

26 riginated in an extreme environment, such as hyperthermophilic archaea (Pyrococcus furiosus), are sig

27 Divergence of the hyperthermophilic Archaea, Pyrococcus furiosus and Pyroc

28 d over a contiguous 16 kb region between two hyperthermophilic Archaea, Pyrococcus furiosus and Therm

29 esponses have been of particular interest in hyperthermophilic archaea, since these microbes live und

30 RNA-encoding DNA analysis places many of the hyperthermophilic Archaea (species with an optimum growt

31 ficity and binding mechanism of MCM from the hyperthermophilic Archaea Sulfolobus solfataricus on var

32 However, in hyperthermophilic archaea that live optimally at tempera

33 Cell extracts of the proteolytic and hyperthermophilic archaea Thermococcus litoralis, Thermo

34 Viruses infecting hyperthermophilic archaea typically do not encode DNA po

35 s of recombination involving short ssDNAs in hyperthermophilic archaea, we evaluated oligonucleotide-

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