ライフサイエンスコーパス: capsulatus

1 uence (amino acids D43 to S49 in Rhodobacter capsulatus).

2 purple photosynthetic bacterium Rhodobacter capsulatus.

3 mbly but also regulates Cu homeostasis in R. capsulatus.

4 ochrome c oxidase (cbb3 -Cox) of Rhodobacter capsulatus.

5 ive pentose phosphate pathway in Rhodobacter capsulatus.

6 hotosynthesis gene expression in Rhodobacter capsulatus.

7 not required for expression of acxABC in R. capsulatus.

8 ng signals to enhance genetic exchange in R. capsulatus.

9 phaeroides are more complex than those of R. capsulatus.

10 t affect reducing equivalents in Rhodobacter capsulatus.

11 cofactor in DMSO reductase from Rhodobacter capsulatus.

12 during anaerobic photosynthetic growth of R. capsulatus.

13 nsulfur photosynthetic bacterium Rhodobacter capsulatus.

14 o-component regulatory system in Rhodobacter capsulatus.

15 ive pentose phosphate pathway in Rhodobacter capsulatus.

16 in species of Rhizobiaceae or in Rhodobacter capsulatus.

17 reviously known cyt c biogenesis genes of R. capsulatus.

18 is in some gram-negative bacteria such as R. capsulatus.

19 d previously in a bc(1) complex mutant of R. capsulatus.

20 containing bacterium and a predecessor to R. capsulatus.

21 e to support the photosynthetic growth of R. capsulatus.

22 factors and RNA polymerase from Rhodobacter capsulatus.

23 r in photosynthetic membranes of Rhodobacter capsulatus.

24 the biogenesis of the cyt cbb3 oxidase of R. capsulatus.

25 active CcoN-CcoO subcomplex was found in R. capsulatus.

26 ense, Rhodospirillum rubrum, and Rhodobacter capsulatus.

27 Bacillus cereus ATCC 10987 and Methylococcus capsulatus.

28 heme-apocytochrome c ligation complex in R. capsulatus.

29 l and carotenoid biosynthesis in Rhodobacter capsulatus.

30 her plsC316 nor plsC3498 was essential in R. capsulatus.

31 structure of thioredoxin-2 from Rhodobacter capsulatus.

32 f this non-phosphorus membrane lipid from R. capsulatus.

33 hine lipid biosynthesis genes of Rhodobacter capsulatus.

34 of the photosynthetic bacterium Rhodobacter capsulatus.

35 al species, such as the GTA from Rhodobacter capsulatus.

36 taproteobacterium, 4 Mbp), and Methylococcus capsulatus (a gammaproteobacterium, 3.3 Mbp).

37 rent strain of R.sphaeroides and Rhodobacter capsulatus, a close relative of R. sphaeroides.

38 In gram-negative bacteria, like Rhodobacter capsulatus, about 10 membrane-bound components (CcmABCDE

39 The importance of manganese in Rhodobacter capsulatus acetone carboxylase has been established thro

40 the positioning of succinyl-CoA, Rhodobacter capsulatus ALAS Asn-85 has a proposed role in regulating

41 X-ray crystal structures of Rhodobacter capsulatus ALAS reveal that a conserved active site seri

42 M. capsulatus, along with other methanotrophs, has been the

43 These results suggest that the R. capsulatus alpha subunit is not important for RcNtrC int

44 hane monooxygenase (pMMO) from Methylococcus capsulatus and ammonia monooxygenase (AMO) of Nitrosomon

45 o encode C-8 vinyl reductases in Rhodobacter capsulatus and Arabidopsis thaliana, respectively.

46 GTA production in the bacterium Rhodobacter capsulatus and characterization of novel phages that pos

47 ergent photosynthetic organisms, Rhodobacter capsulatus and Heliophilum fasciatum.

48 flagellatus were more similar to those in M. capsulatus and M. extorquens than to the ones in the mor

49 A comparative analysis of R. capsulatus and other alpha-proteobacterial promoters wit

50 homoserine lactone production by Rhodobacter capsulatus and Paracoccus denitrificans.

51 e with large and small subunit genes from R. capsulatus and R. sphaeroides, also supported the unrela

52 Using mutant strains of Rhodobacter capsulatus and Rhodobacter sphaeroides in which the pufX

53 ment RubisCO deletion strains of Rhodobacter capsulatus and Rhodobacter sphaeroides under both photoh

54 tein encoded by the pufX gene of Rhodobacter capsulatus and Rhodobacter sphaeroides, has been further

55 e localized proton entry into the RCs of Rb. capsulatus and Rps. viridis as well as locate a site of

56 tence of a second metal site in RCs from Rb. capsulatus and Rps. viridis.

57 repressed in a B12 auxotroph of Rhodobacter capsulatus and that B12 regulation of gene expression is

58 d wild-type cytochrome c(2) from Rhodobacter capsulatus and the lysine 93 to proline mutant of cytoch

59 type xanthine dehydrogenase from Rhodobacter capsulatus and variants at Arg-310 in the active site ha

60 eria Rhodobacter sphaeroides and Rhodobacter capsulatus, and is essential in controlling the metaboli

61 acteria Rhodobacter sphaeroides, Rhodobacter capsulatus, and Rhodopseudomonas viridis has been invest

62 Thus, RCs from Rb. sphaeroides, Rb. capsulatus, and Rps. viridis each have a structurally an

63 hydrogenase-related protein from Rhodobacter capsulatus, and the regulatory subunit from bovine pyruv

64 In this study, using Rhodobacter capsulatus apocytochrome c(2) as a Ccm substrate, we dem

65 peptide designed to serve as a model for R. capsulatus apocytochrome c(2) have also been carried out

66 Thus, no additional factors from R. capsulatus are necessary for the recognition of high-GC

67 ive pentose phosphate pathway in Rhodobacter capsulatus are organized in at least two operons, each p

68 DsbA-null and DsbB-null single mutants of R. capsulatus are Ps(+) and produce c-type cytochromes, unl

69 ts of the facultative phototroph Rhodobacter capsulatus are unable to grow under photosynthetic condi

70 hat some OlsA enzymes, like the enzyme of R. capsulatus, are bifunctional and involved in both membra

71 R. sphaeroides cyt cy can act at least in R. capsulatus as an electron carrier between the cyt bc1 co

72 ubunits (Bchl and BchN) were expressed in R. capsulatus as S tag fusion proteins that facilitated aff

73 mutants of Escherichia coli and Rhodobacter capsulatus bacterioferritins are unable to associate int

74 h antibodies against cytochrome P460 from M. capsulatus Bath indicated that the expression level of c

75 tion of the genome sequence of Methylococcus capsulatus Bath is an important event in molecular micro

76 at a cytochrome P460 similar to that from M. capsulatus Bath may be present in the type II methanotro

77 and used to identify a DNA fragment from M. capsulatus Bath that contains cyp, the gene encoding cyt

78 was used to identify a DNA fragment from M. capsulatus Bath that contains occ, the gene encoding cyt

79 ethane monooxygenase (pMMO) in Methylococcus capsulatus Bath was assessed by analysis of transcripts

80 e complex (NADH dehydrogenase [NDH]) from M. capsulatus Bath, along with NADH and duroquinol, to enzy

81 from the obligate methylotroph Methylococcus capsulatus Bath.

82 isolated from the methanotroph Methylococcus capsulatus Bath.

83 he methane-oxidizing bacterium Methylococcus capsulatus Bath.

84 We have purified pMMO from Methylococcus capsulatus (Bath) and detected activity.

85 encoding MMOR was cloned from Methylococcus capsulatus (Bath) and expressed in Escherichia coli in h

86 indings extend previous work on pMMO from M. capsulatus (Bath) and provide new insight into the funct

87 thane mono-oxygenase (sMMO) of Methylococcus capsulatus (Bath) catalyses the O2-dependent and NAD(P)H

88 hane monooxygenase system from Methylococcus capsulatus (Bath) catalyzes the oxidation of methane to

89 hane monooxygenase (sMMO) from Methylococcus capsulatus (Bath) catalyzes the selective oxidation of m

90 X-ray structures of MMOH from Methylococcus capsulatus (Bath) cocrystallized with dibromomethane or

91 bstrate, catalyzed by MMO from Methylococcus capsulatus (Bath) gave only cubylmethanol as the product

92 have been identified, and the Methylococcus capsulatus (Bath) genome has been sequenced.

93 MmoS from M. capsulatus (Bath) has been cloned, expressed, and purifi

94 losinus trichosporium OB3b and Methylococcus capsulatus (Bath) have a similar secondary structure top

95 soluble methane monooxygenase (sMMO) from M. capsulatus (Bath) have clarified discrepancies that exis

96 genase hydroxylase (MMOH) from Methylococcus capsulatus (Bath) in frozen 4:1 buffer/glycerol solution

97 rystal structures of MMOH from Methylococcus capsulatus (Bath) in the diiron(II), diiron(III), and mi

98 ethane monooxygenase system of Methylococcus capsulatus (Bath) includes three protein components: a 2

99 hane monooxygenase (sMMO) from Methylococcus capsulatus (Bath) is a multicomponent enzyme system requ

100 hane monooxygenase (sMMO) from Methylococcus capsulatus (Bath) is a three-component enzyme system tha

101 25) from the pseudothermophile Methylococcus capsulatus (Bath) is a three-component enzyme system tha

102 MmoS from Methylococcus capsulatus (Bath) is the multidomain sensor protein of a

103 ld very similar to the one found here for M. capsulatus (Bath) MMOR-Fd.

104 A mononuclear copper center present in M. capsulatus (Bath) pMMO is absent in M. trichosporium OB3

105 as a metal center occupied by zinc in the M. capsulatus (Bath) pMMO structure is occupied by copper i

106 ed previously in the crystal structure of M. capsulatus (Bath) pMMO.

107 ys on membrane-bound pMMO from Methylococcus capsulatus (Bath) reveal that zinc inhibits pMMO at two

108 DNA sequencing of the Methylococcus capsulatus (Bath) sMMO genes confirmed previously identi

109 By mapping these residues on to the M. capsulatus (Bath) sMMO hydroxylase crystal structure, fu

110 Western blot analysis of Methylococcus capsulatus (Bath) soluble cell extracts showed that MMOD

111 thane monooxygenase effector protein from M. capsulatus (Bath) than that from M. trichosporium OB3b.

112 of pMMO from the methanotroph Methylococcus capsulatus (Bath) to a resolution of 2.8 A.

113 By cultivating Methylococcus capsulatus (Bath) under methane stress conditions and hi

114 oxygenase (sMMO) isolated from Methylococcus capsulatus (Bath) utilizes a carboxylate-bridged diiron

115 ns of methanotrophs, including Methylococcus capsulatus (Bath), express a membrane-bound or particula

116 Using MMOH from Methylococccus capsulatus (Bath), the effects of MMOB and MMOD on metal

117 hane monooxygenase (sMMO) from Methylococcus capsulatus (Bath), toluene monooxygenase (ToMO) from Pse

118 hane monooxygenase (sMMO) from Methylococcus capsulatus (Bath), toluene monooxygenase (ToMO) from Pse

119 hane monooxygenase (sMMO) from Methylococcus capsulatus (Bath).

120 hane monooxygenase (sMMO) from Methylococcus capsulatus (Bath).

121 dies have focused on pMMO from Methylococcus capsulatus (Bath).

122 O-C was purified recently from Methylococcus capsulatus (Bath).

123 MOR-FAD) of the reductase from Methylococcus capsulatus (Bath).

124 be the role of the hinge region, Rhodobacter capsulatus bc(1) complex was used as a model, and variou

125 etergent dispersed chromatophore-embedded R. capsulatus bc(1) complex, we demonstrated that while sti

126 was identified 127 bp upstream of acxA in R. capsulatus, but this activator lacked key features of si

127 in photosynthetic membranes from Rhodobacter capsulatus by using inhibitor titrations and ubiquinone

128 sulfoxide reductase (DMSOR) from Rhodobacter capsulatus catalyzes the conversion of dimethyl sulfoxid

129 of the CBB pathway and regulation of the R. capsulatus cbb genes were studied by using a combination

130 of the heme-Cu-containing subunit CcoN of R. capsulatus cbb(3)-Cox proceeds independently of that of

131 The Rhodobacter capsulatus cbb(3)-type cytochrome c oxidase (cbb(3)-Cox)

132 In contrast, the R. capsulatus ccdA was homologous to the cyt c biogenesis g

133 lecular genetic studies, we inferred that R. capsulatus CcmF, CcmH, and CcmI interact with each other

134 henotypes upon overproduction of the CcmF-R. capsulatus CcmH (CcmF-CcmH(Rc)) couple in a growth mediu

135 In R. capsulatus, CcmI-null mutants are unable to produce c-ty

136 rains were compared with those expressing R. capsulatus CcoA and Rhizobium leguminosarum RibN as bona

137 sin, or an endogenous activity present in R. capsulatus, cleaves the hinge region of the Fe-S subunit

138 460 and cytochromes c' in N. europaea and M. capsulatus, confirm the importance of a heme-crosslink t

139 ligation core complex, which in Rhodobacter capsulatus contains at least the CcmF, CcmH, and CcmI co

140 cultative phototrophic bacterium Rhodobacter capsulatus contains only one form of cytochrome (cyt) c

141 respiratory electron transfer, unlike its R. capsulatus counterpart, Cyt cyRc.

142 In Rhodobacter capsulatus, Cu-detoxification and Cu delivery for cytoch

143 All R. capsulatus cycJ mutants studied so far excrete copious a

144 position L286 of the ef loop of Rhodobacter capsulatus cyt b could alleviate movement impairment res

145 ied Zn(2+)-induced inhibition of Rhodobacter capsulatus cyt bc(1) using enzyme kinetics, isothermal t

146 The latter residue is M183 in Rhodobacter capsulatus cyt c1, and previous mutagenesis studies reve

147 laced with Lys and five modified Rhodobacter capsulatus Cyt c2 molecules in which positively charged

148 Redox transitions in the Rhodobacter capsulatus cytochrome bc(1) complex were investigated by

149 cytochrome c(1) component of the Rhodobacter capsulatus cytochrome bc(1) complex, phenylalanine 138 a

150 and spectroscopic properties of Rhodobacter capsulatus cytochrome c' (RCCP) have been compared to da

151 n a conserved acidic patch (region 2) on Rb. capsulatus cytochrome c(1) suggests that these negativel

152 ly 34 and the adjacent Pro 35 of Rhodobacter capsulatus cytochrome c(2) (or Gly 29 and Pro 30 in vert

153 positions in the hinge region of Rhodobacter capsulatus cytochrome c(2) and have determined the struc

154 The mutation of Gly 34 to Ser in Rb. capsulatus cytochrome c(2) has been characterized in ter

155 In the case of Rhodobacter capsulatus cytochrome c(2), the sixth heme ligand Met96

156 ion constants for the binding of Rhodobacter capsulatus cytochrome c2 and its K93P mutant to the cyto

157 These results are consistent with R. capsulatus cytochrome c2 stabilizing the complex through

158 ram-negative bacteria, including Rhodobacter capsulatus, cytochrome c maturation (Ccm) is carried out

159 photosynthetic bacterium Rhodobacter (Rba.) capsulatus, cytochrome c(1) contains two additional cyst

160 created in the background of the Rhodobacter capsulatus D(LL) mutant, in which the D helix of the M s

161 d anaerobic photoautotrophic growth of the R.capsulatus deletion strain with 5% CO(2), but not with 1

162 Escherichia coli (DeltaribB) and Rhodobacter capsulatus (DeltaccoA) mutants.

163 Genetic analysis of ccoGHIS in Rhodobacter capsulatus demonstrated that ccoG, ccoH, ccoI and ccoS a

164 re we identified a CopZ-like chaperone in R. capsulatus, determined its cellular concentration and it

165 es dimethyl sulfoxide reductase, Rhodobacter capsulatus dimethyl sulfoxide reductase, and Shewanella

166 d to act as an apocytochrome c chaperone, R. capsulatus does not have the ability to produce holocyto

167 We utilized R. capsulatus:E. coli hybrid RNA polymerases assembled in v

168 A kinetic isotope study of the wild-type R. capsulatus enzyme indicates that, as previously determin

169 In specific mutant strains of R. capsulatus, expression of both the Calvin-Benson-Bassham

170 lash photolysis and RCs from the Rhodobacter capsulatus F(L181)Y/Y(M208)F/L(M212)H mutant (designated

171 in the hinge region (positions 43-49) of R. capsulatus Fe-S subunit was not essential per se for the

172 the main chain and side chain dynamics in R. capsulatus ferrocytochrome c(2) derived from (2)H NMR re

173 s confirm earlier results indicating that R. capsulatus ferrocytochrome c(2) exhibits minor rotationa

174 ile genetic manipulation, we purified the R. capsulatus form I enzyme and determined its basic kineti

175 The R. capsulatus form I enzyme was found to be subject to a ti

176 cently proposed phylogenetic placement of R. capsulatus form I RubisCO.

177 component regulatory system from Rhodobacter capsulatus functions as a global regulator of metabolic

178 An R. capsulatus gene responsible for long-chain acyl-homoseri

179 , resulted in decreased production of the R. capsulatus gene transfer agent, and gene transfer agent

180 In Rhodobacter capsulatus, gene rcc01865 encodes a putative regulatory

181 Using a R. capsulatus genetic system, the cyt c1 mutants M183K and

182 utotrophicus and sequence analysis of the R. capsulatus genome and were found to be clustered in simi

183 The Rhodobacter capsulatus genome contains three genes (olsA [plsC138],

184 Depletion of manganese from the R. capsulatus growth medium resulted in inhibition of aceto

185 ndings therefore demonstrate that, during R. capsulatus growth on minimal medium, the requirement for

186 f either olsA or plsC316 was required for R. capsulatus growth under the conditions tested.

187 e small terminase from the model Rhodobacter capsulatus GTA, which then allowed prediction of analogu

188 Among these species, Rhodobacter capsulatus has a periplasmic Cyt c2Rc and a membrane-bou

189 the purple non-sulfur bacterium Rhodobacter capsulatus have been carried out.

190 ontaining Me(2)SO reductase from Rhodobacter capsulatus have been examined spectroscopically and kine

191 the xanthine dehydrogenase from Rhodobacter capsulatus have been examined to ascertain whether Glu(2

192 The R. capsulatus HelX and Ccl2 proteins are predicted to funct

193 A Rhodobacter capsulatus hemC mutant has been isolated and used to sho

194 Phenotypic differences between the R.capsulatus host strain complemented with the wild-type r

195 rC enhancer-binding protein activates the R. capsulatus housekeeping RNA polymerase but not the Esche

196 Phenotypic analysis of the M. capsulatus hpnR deletion mutant demonstrated a potential

197 in a Rubisco deletion strain of Rhodobacter capsulatus identified a residue in the amino terminus of

198 orts efficiently photosynthetic growth of R. capsulatus in the absence of cyt c2 because it can media

199 y were in the proteobacterium, Methylococcus capsulatus, in which sterol biosynthesis is known, and i

200 cter sphaeroides, the form I RubisCO from R. capsulatus is a member of the green-like group and close

201 CrtJ from Rhodobacter capsulatus is a regulator of genes involved in the biosy

202 the cytochrome bc1 complex) from Rhodobacter capsulatus is composed of the Fe-S protein, cytochrome b

203 he Anf3 protein in the bacterium Rhodobacter capsulatus is essential for diazotrophic (i.e. nitrogen-

204 is study, we show that SenC from Rhodobacter capsulatus is involved in the assembly of a fully functi

205 mplementing them revealed that ccoNOQP in R. capsulatus is not flanked by the oxygen response regulat

206 ht harvesting gene expression in Rhodobacter capsulatus is repressed under aerobic growth conditions

207 t the expression of hem genes in Rhodobacter capsulatus is transcriptionally repressed in response to

208 The purple bacterium Rhodobacter capsulatus is unique among Rhodobacteriacae as it contai

209 om the photosynthetic bacterium, Rhodobacter capsulatus, is shown in vitro to activate the housekeepi

210 er, R. sphaeroides cyt cy, unlike that of R. capsulatus, is unable to function as an efficient electr

211 tive phototrophic (Ps) bacterium Rhodobacter capsulatus, it is constituted by the cyt b, cyt c1, and

212 operon essential for cyt c biogenesis, in R. capsulatus, it is located immediately downstream from ar

213 nts affected in cyt c oxidase activity in R. capsulatus led to the isolation of at least five classes

214 iator ADP had no effect on the ability of R. capsulatus LPS to stimulate NO production but significan

215 ms that govern the diverse means by which R. capsulatus maintains redox poise during photoheterotroph

216 The bacterium Rhodobacter capsulatus mediates this process by repressing expressio

217 membranes and cross-reacted with Rhodobactor capsulatus membranes.

218 0 kDa CcoI-CopZ protein complex in native R. capsulatus membranes.

219 ugh expressed and membrane-localized in a R. capsulatus mutant lacking CcoA, these transporters were

220 ex in chromatophore membranes of Rhodobacter capsulatus mutants lacking the Rieske iron-sulfur (Fe-S)

221 Herein, using Rhodobacter capsulatus mutants that have modifications in the hinge

222 been trapped in two D(LL)-based Rhodobacter capsulatus mutants that have Tyr at position M208 and la

223 f -10 promoter mutants did not facilitate R. capsulatus NtrC activation of the nifA1 promoter by the

224 It was previously shown that the Rhodobacter capsulatus NtrC enhancer-binding protein activates the R

225 s, an additional barrier to activation by R. capsulatus NtrC exists, probably a lack of the proper R.

226 Rhodobacter capsulatus NtrC is an enhancer-binding protein that acti

227 The Rhodobacter capsulatus NtrC protein is a bacterial enhancer-binding

228 trC exists, probably a lack of the proper R. capsulatus NtrC-E. coli RNA polymerase (protein-protein)

229 of high-GC promoters or for activation by R. capsulatus NtrC.

230 peptides of Rs. rubrum, Rb. sphaeroides, Rb. capsulatus, or Rps. viridis.

231 n carrying the G488A mutation produced in R. capsulatus over 30-fold higher beta-galactosidase activi

232 n in an E. coli plsC(Ts) mutant of either R. capsulatus plsC316 or olsA gene products supported growt

233 Rhodobacter capsulatus produces various c-type cytochromes using the

234 ytoene desaturase gene (crtI) of Rhodobacter capsulatus, producing carotenoids with shorter conjugate

235 occal phage straight phiPVL, two Rhodobacter capsulatus prophages and two Mycobacterium tuberculosis

236 Ccl2 (a soluble, truncated form of Ccl2) R. capsulatus proteins, respectively.

237 A mutant form of the Rhodobacter capsulatus PrrA homologue, whose activity is independent

238 Expression of the Rhodobacter capsulatus puc operon, which codes for structural polype

239 ore segment containing 43 amino acids of Rb. capsulatus PufX exhibited 59 and 55% alpha-helix in trif

240 o inhibited by low concentrations of the Rb. capsulatus PufX protein (approximately 50% inhibition at

241 f the C-terminus) of Rb. sphaeroides and Rb. capsulatus PufX were chemically synthesized.

242 M polypeptide, M43(44) and M231(233) in Rb. capsulatus (Rb. sphaeroides).

243 ) is created in this manner in a Rhodobacter capsulatus RC containing the F(L181)Y-Y(M208)F-L(M212)H-

244 ormate dehydrogenase enzyme from Rhodobacter capsulatus (RcFDH) by means of hydrophobic interactions.

245 A large scale mutation of the Rhodobacter capsulatus reaction center M-subunit gene, sym2-1, has b

246 e primary charge separation processes in Rb. capsulatus reaction centers (RCs) bearing the mutations

247 ies are reported for a series of Rhodobacter capsulatus reaction centers (RCs) containing mutations a

248 y electron transfer reactions in Rhodobacter capsulatus reaction centers (RCs) having four mutations:

249 separation events in a series of Rhodobacter capsulatus reaction centers (RCs) that have been genetic

250 A cosmid carrying the R. capsulatus reg locus was capable of complementing an R.

251 DNase I footprint analyses, using R. capsulatus RegA*, a constitutively active mutant version

252 the purple non-sulfur bacterium Rhodobacter capsulatus, RegA and RegB comprise a two-component regul

253 Rhodobacter capsulatus regulates many metabolic processes in respons

254 , and Q in purple photosynthetic Rhodobacter capsulatus results in hydroquinone oxidation rates that

255 In Rhodobacter capsulatus, ribulose 1,5-bisphosphate carboxylase-oxygen

256 d in vitro to form an active, recombinant R. capsulatus RNA polymerase with properties mimicking thos

257 straints on how RcNtrC interacts with the R. capsulatus RNA polymerase.

258 Rhodobacter capsulatus SB 1003 belongs to the group of purple nonsul

259 s genetically tractable relative Rhodobacter capsulatus SB1003.

260 responded to the same metabolic signal in R. capsulatus SBI/II and mutant strain backgrounds.

261 of the photosynthetic bacterium Rhodobacter capsulatus served as a host.

262 otein that activates transcription of the R. capsulatus sigma 70 RNA polymerase, but does not activat

263 It is proposed that RcNtrC recruits R. capsulatus sigma 70-RNA polymerase to the promoter throu

264 The addition of R. capsulatus sigma(70) to the E. coli core RNA polymerase

265 roides, like the closely related Rhodobacter capsulatus species, contains both the previously charact

266 n in the obligate methanotroph Methylococcus capsulatus strain Bath.

267 A transposon mutant of Rhodobacter capsulatus, strain Mal7, that was incapable of photoauto

268 reported that mutant strains of Rhodobacter capsulatus that have alanine insertions (+nAla mutants)

269 Here, we show in Rhodobacter capsulatus that in the absence of DsbA cytochrome c leve

270 ene transfer agents of bacterium Rhodobacter capsulatus that transfer random 4.5-kbp (1.5 mum) DNA se

271 This finding demonstrates that in R. capsulatus the dithiol:disulfide oxidoreductases DsbA an

272 to be Ps(+) Nadi(+), establishing that in R. capsulatus the inactivation of dsbA suppresses the c-typ

273 ram-negative bacteria, including Rhodobacter capsulatus, the membrane protein CycH acts as a putative

274 urple, photosynthetic bacterium, Rhodobacter capsulatus, the RegB/RegA two-component system is requir

275 In Rhodobacter capsulatus, the soluble cytochrome (cyt) c2 and membrane

276 For DMSOR from Rhodobacter capsulatus, thiolate dissociation has therefore been inv

277 In this study, the ability of Rhodobacter capsulatus to maintain a balanced intracellular oxidatio

278 n which mutants incapable of complementing R.capsulatus to photoautotrophic growth with 5% CO(2) were

279 tation assays between E.coli and Rhodobacter capsulatus to show that, despite their differences in si

280 ins either greatly reduced the ability of R. capsulatus to support growth or had little effect, respe

281 chrome c, leading in the case of Rhodobacter capsulatus to the loss of photosynthetic proficiency and

282 To facilitate studies of R. capsulatus transcription, we cloned and overexpressed al

283 In Rhodobacter capsulatus, two open reading frames (ORFs) carry the gen

284 Gram-negative bacteria like Rhodobacter capsulatus use intertwined pathways to carry out the pos

285 i-site of the cyt bc1 complex of Rhodobacter capsulatus using atomistic molecular dynamics simulation

286 brane topology of CcdA was established in R. capsulatus using ccdA:phoA and ccdA :lacZ gene fusions.

287 Rhodobacter capsulatus utilizes two terminal oxidases for aerobic re

288 e alpha- and beta-polypeptides of LH1 of Rb. capsulatus was also inhibited by low concentrations of t

289 ino acid sequencing, the PufX protein of Rb. capsulatus was identified, and from positive interaction

290 anthine dehydrogenase (XDH) from Rhodobacter capsulatus was immobilized on an edge-plane pyrolytic gr

291 nsulfur photosynthetic bacterium Rhodobacter capsulatus was purified to homogeneity and compared to t

292 oying the phototrophic bacterium Rhodobacter capsulatus was used to select a catalytically altered fo

293 DMSO reductase (DMSOR) from Rhodobacter capsulatus, well-characterised as a molybdoenzyme, will

294 s from Rhodobacter (Rb.) sphaeroides and Rb. capsulatus were carried out from pH 5 to 11.

295 These genes from Rhodobacter capsulatus were cloned separately into expression plasmi

296 eficient mutants, 771 and K2, of Rhodobacter capsulatus were isolated.

297 rom the photosynthetic bacterium Rhodobacter capsulatus, were obtained by specific interaction with a

298 nown homolog is the bluB gene of Rhodobacter capsulatus, which is implicated in the biosynthesis of B

299 ired for glycerophospholipid synthesis in R. capsulatus, while olsA acts as an alternative AGPAT that

300 The ISP of Rhodobacter capsulatus within the intact cytochrome bc(1) complex wa