ライフサイエンスコーパス: Rhodobacter sphaeroides

1 edox activity of individual purple bacteria (Rhodobacter sphaeroides).

2 at high and low pH in nitrite reductase from Rhodobacter sphaeroides.

3 sfer in single reaction center crystals from Rhodobacter sphaeroides.

4 n multilayers of photoproteins isolated from Rhodobacter sphaeroides.

5 n-Bassham CO(2) fixation pathway) operons of Rhodobacter sphaeroides.

6 ion of AppA, an oxygen and light sensor from Rhodobacter sphaeroides.

7 olog, RpoH(II), in the alpha-proteobacterium Rhodobacter sphaeroides.

8 ase PrrB in response to low oxygen levels in Rhodobacter sphaeroides.

9 beta-apoprotein from the core LH complex of Rhodobacter sphaeroides.

10 photosynthesis in the alpha-proteobacterium Rhodobacter sphaeroides.

11 bb operons, responsible for CO2 fixation, in Rhodobacter sphaeroides.

12 gulator of photosynthesis gene expression in Rhodobacter sphaeroides.

13 rates photosynthetic growth in the bacterium Rhodobacter sphaeroides.

14 n a thriving culture of the purple bacteria, Rhodobacter sphaeroides.

15 ic membranes from PufX+ and PufX- strains of Rhodobacter sphaeroides.

16 like that found in the alpha-proteobacterium Rhodobacter sphaeroides.

17 ssion of adhI, the gene encoding GSH-FDH, in Rhodobacter sphaeroides.

18 esis gene expression in the purple bacterium Rhodobacter sphaeroides.

19 genes of the Calvin-Benson-Bassham cycle of Rhodobacter sphaeroides.

20 (35% identity, 54% similarity) to PmtA from Rhodobacter sphaeroides.

21 s encoded in the second chemotaxis operon of Rhodobacter sphaeroides.

22 odified photosynthetic reaction centers from Rhodobacter sphaeroides.

23 iochlorophyll dimer in reaction centers from Rhodobacter sphaeroides.

24 oleucine at position 265 of the M subunit in Rhodobacter sphaeroides.

25 t regulate photosynthesis gene expression in Rhodobacter sphaeroides.

26 was studied in the reaction center (RC) from Rhodobacter sphaeroides.

27 anoic acid) (19Fu-FA), in phospholipids from Rhodobacter sphaeroides.

28 fixation pathway (cbbI and cbbII) operons of Rhodobacter sphaeroides.

29 ntrast and fluorescence microscopy images of Rhodobacter sphaeroides.

30 ed from purified BcsA and BcsB proteins from Rhodobacter sphaeroides.

31 been performed on cytochrome c oxidase from Rhodobacter sphaeroides.

32 oteins making up the split kinase, is met in Rhodobacter sphaeroides.

33 response of the bacterial reaction center of Rhodobacter sphaeroides.

34 film formation in the monotrichous bacterium Rhodobacter sphaeroides.

35 in detergent-solubilized bc(1) complex from Rhodobacter sphaeroides.

36 of mitochondria and many bacteria, including Rhodobacter sphaeroides.

37 h surprising similarity to the fla2 locus of Rhodobacter sphaeroides.

38 of similarity to the original pucBA genes of Rhodobacter sphaeroides 2.4.1 (designated puc1) was iden

39 2 complexes from the photosynthetic bacteria Rhodobacter sphaeroides 2.4.1 and Rhodopseudomonas acido

40 catalyze 9M5-FuFA and 9D5-FuFA synthesis in Rhodobacter sphaeroides 2.4.1 and Rhodopseudomonas palus

41 ulation of photosynthesis gene expression in Rhodobacter sphaeroides 2.4.1 have been well studied ove

42 Rhodobacter sphaeroides 2.4.1 is a facultative photohete

43 Rhodobacter sphaeroides 2.4.1 is a facultative photosynt

44 The hemF gene of Rhodobacter sphaeroides 2.4.1 is predicted to code for a

45 Part of the oxygen responsiveness of Rhodobacter sphaeroides 2.4.1 tetrapyrrole production in

46 hemA gene codes for one of two synthases in Rhodobacter sphaeroides 2.4.1 which catalyze the formati

47 The complex genome of Rhodobacter sphaeroides 2.4.1, composed of chromosomes I

48 ing sequence for PrrA, a global regulator in Rhodobacter sphaeroides 2.4.1, is poorly defined.

49 The rdxBHIS gene cluster of Rhodobacter sphaeroides 2.4.1, located downstream of the

50 vitro binding of PrrA, a global regulator in Rhodobacter sphaeroides 2.4.1, to the PrrA site 2, withi

51 he facultative phototrophic proteobacterium, Rhodobacter sphaeroides 2.4.1, was custom-designed and m

52 latory system is a major global regulator in Rhodobacter sphaeroides 2.4.1.

53 recent highlights taken from the studies of Rhodobacter sphaeroides 2.4.1.

54 induction of the photosynthetic apparatus in Rhodobacter sphaeroides 2.4.1.

55 photosynthetic reaction center isolated from Rhodobacter sphaeroides 2.4.1.

56 Analysis of the Rhodobacter sphaeroides 2.4.3 genome revealed four previ

57 The metabolically versatile purple bacterium Rhodobacter sphaeroides 2.4.3 is a denitrifier whose gen

58 The gene encoding this protein in Rhodobacter sphaeroides 2.4.3, designated cycP, was isol

59 was obtained from overexpressing variants of Rhodobacter sphaeroides 2.4.3.

60 Anoxygenic photosynthetic growth of Rhodobacter sphaeroides, a member of the alpha subclass

61 In Rhodobacter sphaeroides, a photosynthetic alpha-proteoba

62 The aa(3)-type cytochrome c oxidase of Rhodobacter sphaeroides, a proteobacterium of the alpha

63 In the photosynthetic bacterium Rhodobacter sphaeroides, a transcriptional response to t

64 In the photosynthetic bacterium Rhodobacter sphaeroides, a water soluble cytochrome c2 (

65 ce of F6P) to the recombinant wild-type (WT) Rhodobacter sphaeroides adenosine 5'-diphosphate-(ADP)-g

66 previously observed in another TRAP-PBP (the Rhodobacter sphaeroides alpha-keto acid-binding protein)

67 ed-type RbcL subunits in the proteobacterium Rhodobacter sphaeroides also fold with GroEL/ES.

68 4, and 2.5 angstrom resolution) of TSPO from Rhodobacter sphaeroides and a mutant that mimics the hum

69 uced secondary quinone acceptor (Q(B)(-)) in Rhodobacter sphaeroides and Blastochloris viridis RCs.

70 lity assemblies are available: the bacterium Rhodobacter sphaeroides and chromosome 16 of the mouse g

71 ltiple heme groups (diheme cytochrome c from Rhodobacter sphaeroides and Desulfovibrio vulgaris Hilde

72 o tracks obtained from the bacterial species Rhodobacter sphaeroides and Escherichia coli.

73 xidases and by the respiratory oxidases from Rhodobacter sphaeroides and Paracoccus denitrificans).

74 nt amino acid sequence similarity to PrrA of Rhodobacter sphaeroides and related proteins in other al

75 l transcription regulator in purple bacteria Rhodobacter sphaeroides and Rhodobacter capsulatus, and

76 Recently, Argonautes of the bacteria Rhodobacter sphaeroides and Thermus thermophilus were de

77 age the cytoplasmic chemoreceptor cluster in Rhodobacter sphaeroides and Vibrio cholerae.

78 several sources (bovine heart mitochondria, Rhodobacter sphaeroides, and Paracoccus denitrificans).

79 ribosomal RNAs from Rhodocyclus gelatinosa, Rhodobacter sphaeroides, and Pseudomonas cepacia were de

80 (Chromatium vinosum, Rhodospirillum rubrum, Rhodobacter sphaeroides, and Rhodocyclus gelatinosa), th

81 the B12-binding domain family present in the Rhodobacter sphaeroides AppA protein binds heme and sens

82 of detergent-solubilized bc(1) complex from Rhodobacter sphaeroides are described.

83 g the putative H-channel in the oxidase from Rhodobacter sphaeroides are examined by site-directed mu

84 n the photosynthetic reaction center (RC) of Rhodobacter sphaeroides are investigated by site-directe

85 he absorption spectrum of intact vesicles in Rhodobacter sphaeroides, as well as the well-established

86 window using the photosensory module of the Rhodobacter sphaeroides bacteriophytochrome BphG1 and th

87 The Rhodobacter sphaeroides bacteriophytochrome BphG1 is unc

88 Arg-94 in cytochrome b of the Rhodobacter sphaeroides bc(1) complex is fully conserved

89 on between the two identical active sites in Rhodobacter sphaeroides BchNB that drives sequential and

90 obacterium tuberculosis genomes as well as a Rhodobacter sphaeroides benchmark dataset.

91 s study we show that the PpsR repressor from Rhodobacter sphaeroides binds to DNA in a redox-dependen

92 Rhodobacter sphaeroides biotin sulfoxide reductase (BSOR

93 Conditions for heterologous expression of Rhodobacter sphaeroides biotin sulfoxide reductase in Es

94 he mapping of the photosynthetic membrane of Rhodobacter sphaeroides by atomic force microscopy (AFM)

95 Facultative phototrophs such as Rhodobacter sphaeroides can switch between heterotrophic

96 The reaction center (RC) from Rhodobacter sphaeroides captures light energy by electro

97 logous expression experiments indicated that Rhodobacter sphaeroides CbbR responded to the same metab

98 Anomalous difference Fourier analyses of Rhodobacter sphaeroides CcO crystals, with cadmium added

99 chrome c oxidase (CcO) was studied using two Rhodobacter sphaeroides CcO mutants involving direct lig

100 Rhodobacter sphaeroides cells contain curved membrane in

101 Rhodobacter sphaeroides cells containing an in-frame del

102 onstrate that FLAG-tagged PpsR isolated from Rhodobacter sphaeroides cells contains bound heme.

103 In Rhodobacter sphaeroides chromatophores, cytochromes (cyt

104 However, we have observed in Rhodobacter sphaeroides chromatophores, that when a frac

105 The chemosensory pathway of Rhodobacter sphaeroides comprises multiple homologues of

106 analysis of G78S, A200T and Delta F94-F98 in Rhodobacter sphaeroides confirmed and extended these obs

107 The cbb(3) cytochrome c oxidase of Rhodobacter sphaeroides consists of four nonidentical su

108 structure of a complex of BcsA and BcsB from Rhodobacter sphaeroides containing a translocating polys

109 measured in reaction centers from mutants of Rhodobacter sphaeroides containing a tyrosine residue ne

110 e of chromatophores isolated from strains of Rhodobacter sphaeroides containing light harvesting comp

111 erized light-harvesting complex 2 (LH2) from Rhodobacter sphaeroides containing the N = 7 carotenoid

112 Reaction centers from the Y(L167) mutant of Rhodobacter sphaeroides, containing a highly oxidizing b

113 The reaction center (RC) from Rhodobacter sphaeroides converts light into chemical ene

114 Here, the solution structure of the Rhodobacter sphaeroides core light-harvesting complex be

115 ynthase (HOS) and heme A synthase (HAS) from Rhodobacter sphaeroides (Cox10 and Cox15, respectively)

116 on transfer were also studied in a series of Rhodobacter sphaeroides cyt bc(1) mutants involving resi

117 series of 21 mutants in the cyt b ef loop of Rhodobacter sphaeroides cyt bc1 were prepared to examine

118 For Rhodobacter sphaeroides CytcO (cytochrome aa3), it appea

119 protein to cytochrome c(1) (cyt c(1)) in the Rhodobacter sphaeroides cytochrome bc(1) complex was stu

120 bc(1) complex was studied using a series of Rhodobacter sphaeroides cytochrome bc(1) mutants in whic

121 ng methionine (M185) in cytochrome c1 of the Rhodobacter sphaeroides cytochrome bc1 complex with Lys

122 Binding of zinc to the outside surface of Rhodobacter sphaeroides cytochrome c oxidase inhibits th

123 as engineered onto the C-terminal end of the Rhodobacter sphaeroides cytochrome c oxidase subunit II.

124 ve mutant, E101A, in the K proton pathway of Rhodobacter sphaeroides cytochrome c oxidase.

125 ble residues around the BNC are evaluated in Rhodobacter sphaeroides cytochrome c oxidase.

126 d characterization of a series of mutants in Rhodobacter sphaeroides designed to reduce Q(B) via the

127 center (RC) of the photosynthetic bacterium Rhodobacter sphaeroides determines the rate and free ene

128 guanine dinucleotide)molybdenum cofactor in Rhodobacter sphaeroides dimethyl sulfoxide reductase (DM

129 rate the Tyr-114 --> Ala and Phe variants of Rhodobacter sphaeroides DMSOR and insert a Tyr residue i

130 clarification of the active site of oxidized Rhodobacter sphaeroides DMSOR, we have adopted the minim

131 e (ICM) development process was performed in Rhodobacter sphaeroides during adaptation from high-inte

132 ivo and in vitro evidence that the genome of Rhodobacter sphaeroides encodes functional enzymes for C

133 The genome of Rhodobacter sphaeroides encodes the components of two di

134 Here, proton translocation by the Rhodobacter sphaeroides enzyme was studied using purifie

135 In the oxidized state both mutants of the Rhodobacter sphaeroides enzyme, D132A and K362M, show ov

136 onia eutropha (epsilon = 19.0 per mille) and Rhodobacter sphaeroides (epsilon = 22.4 per mille).

137 The analogous site in Rhodobacter sphaeroides ETF-QO is asparagine 338.

138 n the vicinity of the iron-sulfur cluster of Rhodobacter sphaeroides ETF-QO.

139 the photosynthetic reaction center (RC) from Rhodobacter sphaeroides exhibits a cation-pi complex for

140 The Rhodobacter sphaeroides extra cytoplasmic function sigma

141 Rhodobacter sphaeroides f. sp. denitrificans biotin sulf

142 s found in a subset of FNR homologs, such as Rhodobacter sphaeroides FnrL, resulted in a mutant strai

143 Rhodobacter sphaeroides, for example, has multiple homol

144 The LH1 and LH2 complexes of Rhodobacter sphaeroides form ring structures of 16 and 9

145 e facultatively phototrophic proteobacterium Rhodobacter sphaeroides, formation of the photosynthetic

146 bilized at the Qi-site of the bc1 complex of Rhodobacter sphaeroides forms a hydrogen bond with a nit

147 ight harvesting 1 antenna (LH1) complex from Rhodobacter sphaeroides funnels excitation energy to the

148 de variants in a training set from a GC-rich Rhodobacter sphaeroides genome.

149 Rhodobacter sphaeroides grown in a Mn(II)-rich medium re

150 Rhodobacter sphaeroides has a complex chemosensory pathw

151 Rhodobacter sphaeroides has a complex chemosensory syste

152 Rhodobacter sphaeroides has a more complex chemotaxis sy

153 hyde oxidation in the facultative phototroph Rhodobacter sphaeroides has allowed the identification o

154 osynthetic membrane of the purple phototroph Rhodobacter sphaeroides has been characterised to a leve

155 cture of the light-harvesting I complex from Rhodobacter sphaeroides has been examined by site-direct

156 R from the anoxygenic phototrophic bacterium Rhodobacter sphaeroides has been known as an oxygen- and

157 ic reaction center from the purple bacterium Rhodobacter sphaeroides has been modified such that the

158 ve protochlorophyllide reductase (DPOR) from Rhodobacter sphaeroides has been purified from an Azotob

159 The TspO outer membrane protein of Rhodobacter sphaeroides has been shown to be involved in

160 The structure of the reaction center from Rhodobacter sphaeroides has been solved by using x-ray d

161 the transcriptional antirepressor AppA from Rhodobacter sphaeroides has been studied in the light an

162 n of the photosynthetic reaction center from Rhodobacter sphaeroides has been studied through the cha

163 Rhodobacter sphaeroides has both membrane-associated and

164 -electron tomography to the purple bacterium Rhodobacter sphaeroides has demonstrated a heretofore un

165 Rhodobacter sphaeroides has multiple copies of chemotaxi

166 Rhodobacter sphaeroides has multiple homologues of most

167 The purple photosynthetic bacterium Rhodobacter sphaeroides has three loci encoding multiple

168 ome c(2) to photosynthetic reaction centers (Rhodobacter sphaeroides) has been measured to high preci

169 the pufX gene of Rhodobacter capsulatus and Rhodobacter sphaeroides, has been further characterized.

170 ochrome c oxidoreductase (EC 1.10.2.2)) from Rhodobacter sphaeroides have been characterized using el

171 Photosynthetic reaction centers from Rhodobacter sphaeroides have identical ubiquinone-10 mol

172 Previous studies of the oxidase from Rhodobacter sphaeroides have shown that all of the pumpe

173 Photosynthetic reaction centers from Rhodobacter sphaeroides have three ubiquinone-binding si

174 containing dimethyl sulfoxide reductase from Rhodobacter sphaeroides have yielded new insight into it

175 ction center in chromatophore membranes from Rhodobacter sphaeroides, have allowed us to demonstrate

176 ons of this extra fragment were generated in Rhodobacter sphaeroides in an effort to investigate its

177 cyt bc (1) from the photosynthetic bacterium Rhodobacter sphaeroides in complex with the fungicide az

178 n of the cytochrome c2-docked bc1 complex in Rhodobacter sphaeroides in terms of an ensemble of favor

179 cture for a translocator protein (TSPO) from Rhodobacter sphaeroides in which some of the electron de

180 The Rhodobacter sphaeroides intracytoplasmic membrane (ICM)

181 Rhodobacter sphaeroides is a metabolically diverse photo

182 center from the purple non-sulfur bacterium Rhodobacter sphaeroides is a quasi-symmetric heterodimer

183 BlrB in Rhodobacter sphaeroides is a single domain, flavin-based

184 The diheme cytochrome c (DHC) from Rhodobacter sphaeroides is a soluble protein with a mass

185 ranscriptional response to singlet oxygen in Rhodobacter sphaeroides is controlled by the group IV si

186 itch between aerobic and anaerobic growth in Rhodobacter sphaeroides is controlled by the RegA/RegB t

187 genes involved in photosystem development in Rhodobacter sphaeroides is dependent upon three major re

188 Z) of the facultative phototrophic bacterium Rhodobacter sphaeroides is induced upon a drop of oxygen

189 experiments have shown that ICM assembly in Rhodobacter sphaeroides is initiated at indentations of

190 Flagellar motility in Rhodobacter sphaeroides is notably different from that i

191 Rhodobacter sphaeroides is specifically related to Parac

192 roles is 5-aminolevulinic acid (ALA), and in Rhodobacter sphaeroides its formation occurs via the She

193 for whole cells of photosynthetic bacterium Rhodobacter sphaeroides lacking cytochrome c(2) as natur

194 these chromatophores can be spherical (as in Rhodobacter sphaeroides), lamellar (as in Rhodopseudomon

195 that the facultative phototrophic bacterium Rhodobacter sphaeroides, like the closely related Rhodob

196 Rhodobacter sphaeroides lipid A (RsDPLA) could not induc

197 The lipid A analogues lipid IVa and Rhodobacter sphaeroides lipid A (RSLA) exhibit an uncomm

198 PS(EC)), Salmonella minnesota (LPS(SM)), and Rhodobacter sphaeroides (LPS(RS)) and examined their act

199 saccharide from the photosynthetic bacterium Rhodobacter sphaeroides (LPS-RS), a TLR4 inhibitor, prev

200 mide gel electrophoresis at 4 degrees C from Rhodobacter sphaeroides M21, which lacks the peripheral

201 In the purple phototrophic bacterium Rhodobacter sphaeroides, many protein complexes congrega

202 1O2, we show that the phototrophic bacterium Rhodobacter sphaeroides mounts a transcriptional respons

203 n proton translocation of the bc(1) complex, Rhodobacter sphaeroides mutants expressing His-tagged cy

204 gment in bacterial cytochrome bc(1) complex, Rhodobacter sphaeroides mutants expressing His-tagged cy

205 ragment in bacterial cytochrome bc1 complex, Rhodobacter sphaeroides mutants expressing His-tagged cy

206 ieske iron-sulfur proteins in solution, four Rhodobacter sphaeroides mutants expressing His-tagged cy

207 ion of quinol in the cytochrome bc1 complex, Rhodobacter sphaeroides mutants, H198N and H111N, lackin

208 structure of the axial mutant (Met182Thr) of Rhodobacter sphaeroides nitrite reductase in which the a

209 lectron transfer in heterologously expressed Rhodobacter sphaeroides nitrite reductase.

210 idic residue near the protein surface (D132, Rhodobacter sphaeroides numbering) and leads to another

211 An arginine (R481) (Rhodobacter sphaeroides numbering), positioned between t

212 ater and a pair of arginines, R481 and R482 (Rhodobacter sphaeroides numbering), that interact direct

213 annel is well-defined as D132(I) (subunit I; Rhodobacter sphaeroides numbering), the entrance of the

214 Three strains of Rhodobacter sphaeroides of diverse origin have been unde

215 ns by transferring a nif cluster from either Rhodobacter sphaeroides or Klebsiella oxytoca.

216 bout 25 A from an aspartic acid (D132 in the Rhodobacter sphaeroides oxidase) near the cytoplasmic ("

217 Calculations with structures of Rhodobacter sphaeroides, Paracoccus denitrificans, and b

218 agged membrane protein, Reaction Center from Rhodobacter sphaeroides, performed 2400 crystallization

219 eled ubiquinones in the Q(A) binding site in Rhodobacter sphaeroides photosynthetic reaction centers.

220 directed evolution to change the product of Rhodobacter sphaeroides phytoene desaturase (crtI gene p

221 The PrrBA two-component activation system of Rhodobacter sphaeroides plays a major role in the induct

222 In Rhodobacter sphaeroides PRK, four alcohol side chains, c

223 vesting 1 (LH1) integral membrane complex of Rhodobacter sphaeroides provides a convenient model syst

224 f SgTAM to the l-tyrosine ammonia lyase from Rhodobacter sphaeroides provides insight into the struct

225 eaction centers from photosynthetic bacteria Rhodobacter sphaeroides R-26 was measured.

226 RC) from the photosynthetic purple bacterium Rhodobacter sphaeroides R-26 were determined by fitting

227 ion center from the photosynthetic bacterium Rhodobacter sphaeroides R-26.

228 Starting from a platform Rhodobacter sphaeroides RC bearing several amino acid ch

229 es of electron transfer between six modified Rhodobacter sphaeroides RCs in which negatively charged

230 visible and near-infrared spectral region to Rhodobacter sphaeroides RCs to accurately track the timi

231 otein complexes, and used it to reconstitute Rhodobacter sphaeroides reaction center complexes, demon

232 ectrochemical midpoint potentials as Q(A) in Rhodobacter sphaeroides reaction centers (RCs) and in RC

233 s during photosynthesis have been studied in Rhodobacter sphaeroides reaction centers from wild type

234 f the primary electron-transfer processes in Rhodobacter sphaeroides reaction centers have been exami

235 namics relationship was also demonstrated in Rhodobacter sphaeroides reaction centers having inhibite

236 The Rhodobacter sphaeroides reaction centre is a relatively

237 ctron conduction across the highly tractable Rhodobacter sphaeroides reaction centre is characterized

238 nding processes in cytochrome c oxidase from Rhodobacter sphaeroides reduced to different degrees wer

239 210 in the photosynthetic reaction center of Rhodobacter sphaeroides results in the generation of a f

240 spectra of the aa3 cytochrome c oxidase from Rhodobacter sphaeroides reveal pH-dependent structural c

241 zed photosynthetic reaction center (RC) from Rhodobacter sphaeroides, revealed an RC concentration-de

242 ction centers (RCs) from the purple bacteria Rhodobacter sphaeroides, Rhodobacter capsulatus, and Rho

243 In a Rhodobacter sphaeroides ribulose 1,5-bisphosphate carbox

244 We found that the Argonaute of Rhodobacter sphaeroides (RsAgo) associates with 15-19 nt

245 xes from the photosynthetic purple bacterium Rhodobacter sphaeroides (Rsbc(1)), stabilized with the q

246 Raman spectra of CcO from bovine (bCcO) and Rhodobacter sphaeroides (RsCcO).

247 ryl lipid A derived from the nontoxic LPS of Rhodobacter sphaeroides (RsDPLA) has been shown to be a

248 res of a full-length LOV domain protein from Rhodobacter sphaeroides (RsLOV).

249 s impediment does not extend to Rubisco from Rhodobacter sphaeroides (RsRubisco)-a red-type Rubisco a

250 action centers (RCs) of the purple bacterium Rhodobacter sphaeroides runs selectively over one of the

251 39T mutant of translocator protein TSPO from Rhodobacter sphaeroides should be used to 1.65 instead o

252 Structures of the ISP from Rhodobacter sphaeroides show that serine 154 and tyrosin

253 the photosynthetic reaction center (RC) from Rhodobacter sphaeroides shows contacts between hydrophob

254 This work summarizes knowledge of the Rhodobacter sphaeroides sigma(E) -ChrR pair, a member of

255 Rhodobacter sphaeroides sigma(E) is a member of the extr

256 In reaction centers of Rhodobacter sphaeroides, site-directed mutagenesis has i

257 The DNA sequences of chromosomes I and II of Rhodobacter sphaeroides strain 2.4.1 have been revised,

258 Rhodobacter sphaeroides strain 2.4.3 is capable of diver

259 The denitrification phenotypes of Rhodobacter sphaeroides strains with and without norEF g

260 Rhodobacter sphaeroides synthesizes spheroidene as the m

261 cale TRN model for the alpha-Proteobacterium Rhodobacter sphaeroides that comprises 120 gene clusters

262 enter (RC) from the photosynthetic bacterium Rhodobacter sphaeroides, that function in intermolecular

263 In RCs from Rhodobacter sphaeroides the protons involved in this pro

264 In the purple bacterium Rhodobacter sphaeroides the PSU forms spherical invagina

265 In the photosynthetic reaction center from Rhodobacter sphaeroides, the primary (Q(A)) and secondar

266 In Rhodobacter sphaeroides, the two cbb operons encoding du

267 This work uses the model bacterium Rhodobacter sphaeroides to begin to elucidate how 3-hydr

268 by the photosynthetic alpha-proteobacterium Rhodobacter sphaeroides to procure the cobamide it needs

269 otein, the light-harvesting LH2 complex from Rhodobacter sphaeroides, to patterned self-assembled mon

270 ); Mycobacterium tuberculosis (type II); and Rhodobacter sphaeroides (type III)] were tested for the

271 Cytochrome c(1) of Rhodobacter sphaeroides ubiquinol-cytochrome c oxidoredu

272 In the Q(A) site of RCs from Rhodobacter sphaeroides, ubiquinone-10 is reduced, by a

273 letion strains of Rhodobacter capsulatus and Rhodobacter sphaeroides under both photoheterotrophic an

274 The anoxygenic phototroph Rhodobacter sphaeroides uses 3-hydroxypropionate as a so

275 The reaction center (RC) from Rhodobacter sphaeroides uses light energy to reduce and

276 The aa(3)-type cytochrome c oxidase from Rhodobacter sphaeroides utilizes two proton-input channe

277 n photosynthetic reaction centers (RCs) from Rhodobacter sphaeroides was achieved by polarization sel

278 c(2) (cyt) and the reaction center (RC) from Rhodobacter sphaeroides was studied by mutation (to Ala)

279 The photosynthetic bacterium Rhodobacter sphaeroides was used as a model system to ex

280 ying the carotenoidless mutant strain R26 of Rhodobacter sphaeroides, we demonstrate by experiment an

281 the photoheterotrophic alpha-proteobacterium Rhodobacter sphaeroides, we identified a surprising feat

282 low-light-adapted chromatophore vesicle from Rhodobacter sphaeroides, we investigate the cooperation

283 oxidized forms of cytochrome c oxidase from Rhodobacter sphaeroides, we observe a displacement of he

284 from a magnesium chelatase (bchD) mutant of Rhodobacter sphaeroides were characterized.

285 ter from the purple photosynthetic bacterium Rhodobacter sphaeroides were covalently conjugated to ea

286 subtilis (expressed in Escherichia coli) and Rhodobacter sphaeroides were examined by analysis of cel

287 (P) in the photosynthetic reaction center of Rhodobacter sphaeroides were investigated by introducing

288 n kinetics of reaction centers isolated from Rhodobacter sphaeroides were shown to be inherently biph

289 atase H subunits from both Synechocystis and Rhodobacter sphaeroides were studied because of the diff

290 center (RC) from the photosynthetic bacteria Rhodobacter sphaeroides were studied by using site-direc

291 me c maturation proteins, CcmF and CcmH from Rhodobacter sphaeroides, were analyzed.

292 l1 and Mcl2, two malyl-CoA lyase homologs in Rhodobacter sphaeroides, were investigated by gene inact

293 vered in the photosynthetic purple bacterium Rhodobacter sphaeroides where it seems to replace phosph

294 heme protein from a denitrifying variant of Rhodobacter sphaeroides which may serve to store and tra

295 d by the genome of the alpha-proteobacterium Rhodobacter sphaeroides, which synthesizes a mitochondri

296 d reaction centers from the purple bacterium Rhodobacter sphaeroides with different primary electron

297 reaction of cytochrome c oxidase (COX) from Rhodobacter sphaeroides with hydrogen peroxide has been

298 ated Rieske fragment from the bc1 complex of Rhodobacter sphaeroides with nitrogens (14N and 15N) fro

299 crystals of cytochrome c oxidase (CcO) from Rhodobacter sphaeroides yield a previously unreported st

300 copper-containing nitrite reductase (NiR) of Rhodobacter sphaeroides yielded endogenous NO and the Cu