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1 inct pathways for arginine breakdown in each halophile.
2  are considerably larger, on average, in the halophile.
3 spects of theories for understanding extreme halophiles.
4 e in the domain Archaea are obligate extreme halophiles.
5 than for the corresponding proteins from non-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                                 Most extreme halophiles are optimized for the use of one of these two
10 ne knockouts and replacements, indicate this halophile can serve as an excellent model system among t
11  acids do comprise a foldable set within the halophile environment.
12   This result indicates that the capacity of halophiles for aerobic respiration may have been acquire
13                              Archaebacterial halophiles (Haloarchaea) are oxygen-respiring heterotrop
14 the stability of 2Fe-2S ferredoxins from the halophile Haloarcula marismortui and the non-halophile a
15 mologs in the genomic sequences of two other halophiles, Haloarcula marismortui and Haloferax volcani
16  HpyA, the sole histone encoded in the model halophile Halobacterium salinarum, is not involved in DN
17                  In the CysRS of the extreme halophile Halobacterium species NRC-1, deletion of the p
18 m the chromosome of an archaeon, the extreme halophile Halobacterium strain NRC-1.
19 ross archaeal lineages: a photoheterotrophic halophile (Halobacterium salinarum NRC-1), a hydrogenotr
20 e report the complete sequence of an extreme halophile, Halobacterium sp. NRC-1, harboring a dynamic
21 V) prepared from the polar lipids of extreme halophiles, Halobacterium halobium and Halobacterium sal
22              Using the genetically tractable halophile Haloferax volcanii as a model system, we descr
23 nucleosome occupancy map, as observed in the halophile Haloferax volcanii.
24 ification enzymes in the mesophilic moderate halophile Haloferax volcanii.
25  acidophile, Sulfolobus sofataricus (Sso); a halophile, Haloferax volcanii (Hvo); and a hyperthermoph
26              In anaerobic batch culture, the halophile Halomonas halodenitrificans is shown to be abl
27 omal proteins from all organisms, especially halophiles, has distinct positive and negative regions a
28                   The archaeon TBP, from the halophile/hyperthermophile organism Pyrococcus woesei, i
29 ehaviors of Halobacterium NRC-1, an archaeal halophile, in sublethal levels of Mn(II), Fe(II), Co(II)
30 inding proteins, whereas underrepresented in halophiles, in which nonspecific nucleic acid binding is
31 ospira halophila, one of the most-xerophilic halophiles, inhabits biophysically stressful and energet
32 his, genomes that descend from methanogen-to-halophile intermediates are necessary.
33  focused on nonmethanogenic thermophiles and halophiles, leaving it unclear whether these represent t
34                                Some of these halophiles may have been preserved over geological times
35 anism of the cyclodipeptide oxidase from the halophile Nocardiopsis dassonvillei (NdasCDO), a compone
36 types: they were either methanogens, extreme halophiles, or ('sulphur-dependent') extreme thermophile
37 sly described Thermococcus kodakaraensis and halophile proteins.
38 oximately 15% of ribosomal proteins from non-halophiles share this property.
39 and the hvDHFRs by a common mechanism, not a halophile-specific mechanism, such as the binding of hyd
40                       The functions of these halophile-specific peptides are largely unknown.
41 c techniques are available--the methanogens, halophiles, Sulfolobales, and Thermococcales--with the a
42     Many archaeal sequences (methanogens and halophiles) tend to align best with the Gram-positive se
43 ends to be lower for ribosomal proteins from halophiles than for the corresponding proteins from non-
44                 Vibrio parahaemolyticus is a halophile that inhabits brackish waters and a wide range
45 orth: Haloarchaea) are predominantly aerobic halophiles that are thought to have evolved from anaerob
46 is may result from the specific lifestyle of halophiles that require high intracellular salt concentr
47 ns of gain and loss shaped the methanogen-to-halophile transition.
48 encing projects are under way, including two halophiles, two Thermoplasma, and a methanogen.
49                                              Halophiles utilize two distinct osmoprotection strategie
50 ns show the definite archaeal nature of this halophile with additional similarities to the Gram-posit