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1 ns include the major cell surface protein in Halobacterium, a glycoprotein with a partially character
2                        The ease of culturing Halobacterium and the availability of methods for its ge
3  physical/functional interaction network for Halobacterium, and an interface to detailed stochastic/k
4 lable transcriptomics data in Archaeoglobus, Halobacterium, and Thermococcus spp.
5                  For example, Sulfolobus and Halobacterium are extremely divergent.
6  Fractionation experiments in Pyrococcus and Halobacterium cells revealed that, in vivo, the dimeric
7 ococcus morrhuae, Natronobacterium gregoryi, Halobacterium cutirubrum, Halobacteriurn trapanicum, Met
8            We have analyzed the phenotype of Halobacterium deletion mutants lacking mre11 and/or rad5
9 rotein SpoVJ, Mg2+, and Co2+ chelatases, the Halobacterium GvpN gas vesicle synthesis protein, dynein
10  the dimeric POR from a mesophilic archaeon, Halobacterium halobium (21% identity).
11 from the polar lipids of extreme halophiles, Halobacterium halobium and Halobacterium salinarum, reta
12 bacteriorhodopsin crystals generated in live Halobacterium halobium bacteria and confirmed by electro
13 obe for membrane protein unfolding, we chose Halobacterium halobium bacteriorhodopsin (bR) as a model
14         Spontaneous Evn-resistant mutants of Halobacterium halobium contained mutations in hairpins 8
15                      A mutant of an archaeon Halobacterium halobium has been isolated that exhibits r
16                    The bop gene of wild-type Halobacterium halobium NRC-1 is transcriptionally induce
17             Exposure of purple membrane from Halobacterium halobium to sublytic concentrations of Tri
18  Escherichia coli or the halophilic archaeum Halobacterium halobium were constructed.
19                       Mutants of an archaeon Halobacterium halobium, resistant to the universal inhib
20 -purple transition in the purple membrane of Halobacterium halobium.
21 bacteria and against the halophilic archaeon Halobacterium halobium.
22 remely halophilic archaeum (archaebacterium) Halobacterium halobium.
23                     HMG-CoA reductase of the halobacterium Haloferax volcanii was initially partially
24      Although the genomes of closely related Halobacterium, Haloquadratum, and Haloarcula (>90% avera
25  protein family, Archaerhodopsin-3 (Arch) of halobacterium Halorubrum sodomense, was recently shown t
26 e predicted exosome in the Methanococcus and Halobacterium lineages.
27 eening transformants of an orange (Pum- bop) Halobacterium mutant for purple (Pum+ bop+) colonies on
28                                           In Halobacterium NRC-1 and in Helicobacter pylori, our meth
29            The extremely halophilic archaeon Halobacterium NRC-1 can switch from aerobic energy produ
30    Deletion of the arsADRC gene cluster in a Halobacterium NRC-1 Deltaura3 strain resulted in increas
31                                          The Halobacterium NRC-1 genome codes for 2,630 predicted pro
32 replication system of the model haloarchaeon Halobacterium NRC-1 is encoded within a circular chromos
33 istance in the extremely halophilic archaeon Halobacterium NRC-1 withstanding up to 110 J/m2 with no
34 he exception of Thermoplasma acidophilum and Halobacterium NRC-1) and some bacteria, including the hy
35 ave reconstructed physiological behaviors of Halobacterium NRC-1, an archaeal halophile, in sublethal
36 on from the bop promoter in the haloarchaeon Halobacterium NRC-1, is highly induced under oxygen-limi
37 ibe the metabolic and regulatory networks of Halobacterium NRC-1.
38 ther there is redundancy of this function in Halobacterium or the gene was misannotated.
39 ere tested with an F1- ATPase, isolated from Halobacterium saccharovorum, by evaluating the rate of A
40 hat share similarity (36 to 56 percent) with Halobacterium salinarium Bat, Azotobacter vinelandii NIF
41 odopsin photocycle in the purple membrane of Halobacterium salinarium have been detected by time-reso
42                       The purple membrane of Halobacterium salinarium is a two-dimensional lattice of
43 rent organisms (Saccharomyces cerevisiae and Halobacterium salinarium NRC-1).
44                                          The Halobacterium salinarium purple membrane is a two-dimens
45 c residues within the N-terminal half of the Halobacterium salinarium signal transducer HtrI [the hal
46 amily of transducer proteins in the Archaeon Halobacterium salinarium using a site-specific multiple
47 amily of transducer proteins in the Archaeon Halobacterium salinarium was identified.
48 dopsin (bR), the light-driven proton pump in Halobacterium salinarium, involves this kind of a change
49 mutant forms of bacteriorhodopsin (sbR) from Halobacterium salinarium, produced by Escherichia coli o
50 n functions as a light-driven proton pump in Halobacterium salinarium.
51 nd pumps protons across the cell membrane of Halobacterium salinarium.
52  proton pump found in the purple membrane of Halobacterium salinarium.
53 driven proton pump in the purple membrane of Halobacterium salinarium.
54 rom the extremely halophilic archaebacterium Halobacterium salinarium.
55  as described earlier for halorhodopsin from Halobacterium salinarium.
56 -terminal regions of HemAT from the archaeon Halobacterium salinarum (HemAT-Hs) and from the Gram-pos
57    The spectral tuning of halorhodopsin from Halobacterium salinarum (shR) during anion transport was
58                 Sensory rhodopsin I (SRI) in Halobacterium salinarum acts as a receptor for single-qu
59  and bR-containing purple membranes (PMs) of Halobacterium salinarum and demonstrated that this cell
60                  Halophilic archaea, such as Halobacterium salinarum and Natronobacterium pharaonis,
61 helix, visual pigment-like proteins found in Halobacterium salinarum and related halophilic Archaea.
62                 Using bacteriorhodopsin from Halobacterium salinarum and the translocon SecYEG from E
63 noparticles into the purple membrane (PM) of Halobacterium salinarum archaea, which can unidirectiona
64 otein A, a beta-barrel, eubacterial MP, (ii) Halobacterium salinarum bacteriorhodopsin, an alpha-heli
65 pic protein bacterioopsin, the apoprotein of Halobacterium salinarum bacteriorhodopsin.
66 d a homologous gene replacement strategy for Halobacterium salinarum based on ura3, which encodes the
67                                              Halobacterium salinarum displays four distinct kinetic f
68 ious research revealed that the haloarchaeon Halobacterium salinarum encodes four diphtheria toxin re
69 d oxidative stress responses of the archaeon Halobacterium salinarum exposed to ionizing radiation (I
70 ss conditions in the model archaeal organism Halobacterium salinarum For yeast, our method correctly
71 stribution of Z-DNA-forming sequences in the Halobacterium salinarum GRB chromosome was analyzed by d
72  (Chroococcidiopsis cubana cyanobacteria and Halobacterium salinarum halophilic archaea) to detect th
73 yptic peptides from bovine serum albumin and Halobacterium salinarum in a high throughput liquid chro
74                    Dodecin from the archaeal Halobacterium salinarum is a riboflavin storage device.
75          Signal transduction in the archaeon Halobacterium salinarum is mediated by three distinct su
76 I and the mutant D73E, both reconstituted in Halobacterium salinarum lipids, using FTIR difference sp
77 s a dimer when functionally expressed in the Halobacterium salinarum membrane.
78 y rhodopsin II (SRII) by flash photolysis of Halobacterium salinarum membranes genetically engineered
79               Sensory rhodopsin II (SRII) in Halobacterium salinarum membranes is a phototaxis recept
80 s carry out light-driven proton transport in Halobacterium salinarum membranes.
81 have constructed a model for this process in Halobacterium salinarum NRC-1 through the data-driven di
82 al lineages: a photoheterotrophic halophile (Halobacterium salinarum NRC-1), a hydrogenotrophic metha
83 rotein and in the extended C-terminus of the Halobacterium salinarum protein.
84 roton pump bacteriorhodopsin in the archaeon Halobacterium salinarum requires coordinate synthesis of
85  A fusion protein in which the C-terminus of Halobacterium salinarum sensory rhodopsin I (SRI) is con
86                                              Halobacterium salinarum sensory rhodopsin II (HsSRII) is
87 low for the archaea using the model organism Halobacterium salinarum sp. NRC-1 and demonstrate its ap
88 dation, we discovered an RNase (VNG2099C) in Halobacterium salinarum that is transcriptionally co-reg
89 eless HtrI, a phototaxis transducer found in Halobacterium salinarum that transmits signals from the
90                              Chimeras of the Halobacterium salinarum transducers HtrI and HtrII were
91  As a test case, bacteriorhodopsin (bR) from Halobacterium salinarum was crystallized from a bicellar
92                                              Halobacterium salinarum was used as the model organism a
93  dried purple membrane patches purified from Halobacterium salinarum with infrared vibrational scatte
94 membranes (formed from lipids extracted from Halobacterium salinarum), yet systematic analyses based
95      Using this method, we demonstrated that Halobacterium salinarum, a hypersaline-adapted archaeal
96 conditions of limited iron, the extremophile Halobacterium salinarum, a salt-loving archaeon, mounts
97  transcriptional response is identifiable in Halobacterium salinarum, an archaeal model organism.
98 e Bacteria (termed HemAT-Hs for the archaeon Halobacterium salinarum, and HemAT-Bs for Bacillus subti
99 iorhodopsin, the light-driven proton pump of Halobacterium salinarum, consists of the membrane apopro
100 the first sensory rhodopsins in the archaeon Halobacterium salinarum, genome projects have revealed a
101 I), a repellent phototaxis receptor found in Halobacterium salinarum, has several homologous residues
102 ers in the phototaxis system of the archaeon Halobacterium salinarum, HtrI and HtrII, are methyl-acce
103  sole histone encoded in the model halophile Halobacterium salinarum, is not involved in DNA packagin
104 treme halophiles, Halobacterium halobium and Halobacterium salinarum, retain entrapped carboxyfluores
105 epellent phototaxis receptor in the archaeon Halobacterium salinarum, similar to visual pigments in i
106                        In the model archaeon Halobacterium salinarum, the transcription factor TrmB r
107     The deletion of halA in the haloarchaeon Halobacterium salinarum, whose cells are consistently ro
108 the cell membrane of the halophilic organism Halobacterium salinarum.
109 e inserted into the membrane of the archaeon Halobacterium salinarum.
110 gh its bound transducer HtrI in the archaeon Halobacterium salinarum.
111 ervation with the rhodopsins of the archaeon Halobacterium salinarum.
112 nsitive phototaxis responses in the archaeon Halobacterium salinarum.
113 aturally expressed in the purple membrane of Halobacterium salinarum.
114 the TrmB metabolic GRN in the model archaeon Halobacterium salinarum.
115 ystems analysis of the Cu stress response of Halobacterium salinarum.
116 cts of iron homeostasis in the model species Halobacterium salinarum.
117 duced proton pump in the halophilic archaeon Halobacterium salinarum.
118 found in the purple membrane of the archaeon Halobacterium salinarum.
119 entifying how this differs from the archaeon Halobacterium salinarum.
120 acterium Anabaena flos-aquae and the archaea Halobacterium salinarum.
121 h functions as a light-driven proton pump in Halobacterium salinarum.
122 e purple membrane of the salt marsh archaeon Halobacterium salinarum.
123 alorhodopsin, Jaws, derived from Haloarcula (Halobacterium) salinarum (strain Shark) and engineered t
124 oteins, as well as complex H. influenzae and Halobacterium samples, the model is shown to produce pro
125 lts from genetic and nutritional analyses of Halobacterium showed that mutants with lesions in open r
126 r in the genetically tractable Haloarchaeon, Halobacterium sp.
127                    Our results show that the Halobacterium sp. has evolved a carefully orchestrated s
128    Comparison of the genome architectures of Halobacterium sp. NRC-1 and H. marismortui suggests a co
129                         We purified GCR from Halobacterium sp. NRC-1 and identified the sequence of 2
130        The genome of the halophilic archaeon Halobacterium sp. NRC-1 and predicted proteome have been
131 used for systematic whole-genome analysis of Halobacterium sp. NRC-1 and several other prokaryotes to
132 moautotrophicum and leucyl tRNA derived from Halobacterium sp. NRC-1 as an orthogonal tRNA-synthetase
133            The extremely halophilic archaeon Halobacterium sp. NRC-1 can grow phototrophically by mea
134                     Analysis of the complete Halobacterium sp. NRC-1 genome sequence showed that the
135  a brp paralog identified by analysis of the Halobacterium sp. NRC-1 genome, reduced bacteriorhodopsi
136 protein predicted to be encoded by a gene in Halobacterium sp. NRC-1 that is annotated as mercuric re
137 ty of ThrRS from Sulfolobus solfataricus and Halobacterium sp. NRC-1 was inhibited by borrelidin, whe
138 e complete sequence of an extreme halophile, Halobacterium sp. NRC-1, harboring a dynamic 2,571,010-b
139 l binding sites of the Cse4p protein; and in Halobacterium sp. NRC-1, we discoverd subtle differences
140 early five times as many as those encoded in Halobacterium sp. NRC-1--suggesting H. marismortui is si
141 ritional requirements for survival than does Halobacterium sp. NRC-1.
142                                              Halobacterium sp. NRC-1was used to express the N-termina
143 iZ gene in the extremely halophilic archaeon Halobacterium sp. strain NRC-1 blocked the ability of th
144 c respiration of the archaeal model organism Halobacterium sp. strain NRC-1 by using phenotypic and g
145                                  A strain of Halobacterium sp. strain NRC-1 carrying a null allele of
146                                The genome of Halobacterium sp. strain NRC-1 contains a large gene clu
147                  These results indicate that Halobacterium sp. strain NRC-1 contains an arsenite and
148                       The genome sequence of Halobacterium sp. strain NRC-1 encodes genes homologous
149        The genome of the halophilic archaeon Halobacterium sp. strain NRC-1 encodes homologs of the e
150                     Computer analysis of the Halobacterium sp. strain NRC-1 ORF Vng1581C gene and the
151                      The data also show that Halobacterium sp. strain NRC-1 possesses a high-affinity
152 mutants of the extremely halophilic archaeon Halobacterium sp. strain NRC-1 showed that open reading
153         A cbiP mutant strain of the archaeon Halobacterium sp. strain NRC-1 was auxotrophic for adeno
154 s was performed on cell lysates of wild-type Halobacterium sp. strain NRC-1, gas vesicle-deficient mu
155 e analysis of one such replicon, pNRC100, in Halobacterium sp. strain NRC-1, showed that it undergoes
156 tgenomic investigation of the model archaeon Halobacterium sp. strain NRC-1, we used whole-genome DNA
157  enzyme in the extremely halophilic archaeon Halobacterium sp. strain NRC-1.
158 ization in the extremely halophilic archaeon Halobacterium sp. strain NRC-1.
159 le of replication in the halophilic archaeon Halobacterium sp. strain S9.
160 that two major energy production pathways in Halobacterium sp., phototrophy and arginine fermentation
161 acks the three core exosome subunits, and in Halobacterium sp., the superoperon is divided into two p
162 mRNA and protein analyses of four strains of Halobacterium sp.: the wild-type, NRC-1; and three genet
163        In the CysRS of the extreme halophile Halobacterium species NRC-1, deletion of the peptide red
164 mosome of an archaeon, the extreme halophile Halobacterium strain NRC-1.
165                                              Halobacterium synthesized cobalamin in a chemically defi
166 ed method for gene knockouts/replacements in Halobacterium that relies on both selection and counters
167 plementary to that seen in Methanococcus and Halobacterium, Thermoplasma acidophilum lacks the RNase
168                      A cbiB mutant strain of Halobacterium was auxotrophic for adenosylcobinamide-GDP
169 or the repair of DNA double-strand breaks in Halobacterium, whereas Rad50 is dispensable.

 
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