ライフサイエンスコーパス: halophile

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1 inct pathways for arginine breakdown in each halophile.

2 are considerably larger, on average, in the halophile.

3 than for the corresponding proteins from non-halophiles.

4 e in the domain Archaea are obligate extreme halophiles.

5 spects of theories for understanding extreme halophiles.

6 halophile Haloarcula marismortui and the non-halophile anabaena.

7 an unusual peptide that is unique to several halophile archaeal cysteinyl-tRNA synthetases (CysRS), w

8 at approximately 67% ribosomal proteins from halophiles are negatively charged, whereas only up to ap

9 ne knockouts and replacements, indicate this halophile can serve as an excellent model system among t

10 acids do comprise a foldable set within the halophile environment.

11 This result indicates that the capacity of halophiles for aerobic respiration may have been acquire

12 Archaebacterial halophiles (Haloarchaea) are oxygen-respiring heterotrop

13 the stability of 2Fe-2S ferredoxins from the halophile Haloarcula marismortui and the non-halophile a

14 mologs in the genomic sequences of two other halophiles, Haloarcula marismortui and Haloferax volcani

15 In the CysRS of the extreme halophile Halobacterium species NRC-1, deletion of the p

16 m the chromosome of an archaeon, the extreme halophile Halobacterium strain NRC-1.

17 ross archaeal lineages: a photoheterotrophic halophile (Halobacterium salinarum NRC-1), a hydrogenotr

18 e report the complete sequence of an extreme halophile, Halobacterium sp. NRC-1, harboring a dynamic

19 V) prepared from the polar lipids of extreme halophiles, Halobacterium halobium and Halobacterium sal

20 Using the genetically tractable halophile Haloferax volcanii as a model system, we descr

21 nucleosome occupancy map, as observed in the halophile Haloferax volcanii.

22 ification enzymes in the mesophilic moderate halophile Haloferax volcanii.

23 acidophile, Sulfolobus sofataricus (Sso); a halophile, Haloferax volcanii (Hvo); and a hyperthermoph

24 In anaerobic batch culture, the halophile Halomonas halodenitrificans is shown to be abl

25 omal proteins from all organisms, especially halophiles, has distinct positive and negative regions a

26 The archaeon TBP, from the halophile/hyperthermophile organism Pyrococcus woesei, i

27 ehaviors of Halobacterium NRC-1, an archaeal halophile, in sublethal levels of Mn(II), Fe(II), Co(II)

28 types: they were either methanogens, extreme halophiles, or ('sulphur-dependent') extreme thermophile

29 sly described Thermococcus kodakaraensis and halophile proteins.

30 oximately 15% of ribosomal proteins from non-halophiles share this property.

31 and the hvDHFRs by a common mechanism, not a halophile-specific mechanism, such as the binding of hyd

32 The functions of these halophile-specific peptides are largely unknown.

33 c techniques are available--the methanogens, halophiles, Sulfolobales, and Thermococcales--with the a

34 Many archaeal sequences (methanogens and halophiles) tend to align best with the Gram-positive se

35 ends to be lower for ribosomal proteins from halophiles than for the corresponding proteins from non-

36 Vibrio parahaemolyticus is a halophile that inhabits brackish waters and a wide range

37 is may result from the specific lifestyle of halophiles that require high intracellular salt concentr

38 encing projects are under way, including two halophiles, two Thermoplasma, and a methanogen.

39 ns show the definite archaeal nature of this halophile with additional similarities to the Gram-posit

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