ライフサイエンスコーパス: Rhodobacter capsulatus

1 le hinge sequence (amino acids D43 to S49 in Rhodobacter capsulatus).

2 ar to those in species of Rhizobiaceae or in Rhodobacter capsulatus.

3 ranscription factors and RNA polymerase from Rhodobacter capsulatus.

4 tron transfer in photosynthetic membranes of Rhodobacter capsulatus.

5 lex of Rb. sphaeroides compared with that of Rhodobacter capsulatus.

6 Ccl2 proteins in the Gram-negative bacteria Rhodobacter capsulatus.

7 d-type and mutant reaction center strains of Rhodobacter capsulatus.

8 ella abortus, Agrobacterium tumefaciens, and Rhodobacter capsulatus.

9 illum brasilense, Rhodospirillum rubrum, and Rhodobacter capsulatus.

10 ed for the assembly of c-type cytochromes in Rhodobacter capsulatus.

11 ORF176 in the photosynthesis gene cluster in Rhodobacter capsulatus.

12 s proteins of Synechocystis sp. PCC 6301 and Rhodobacter capsulatus.

13 iochlorophyll and carotenoid biosynthesis in Rhodobacter capsulatus.

14 the crystal structure of thioredoxin-2 from Rhodobacter capsulatus.

15 to the ornithine lipid biosynthesis genes of Rhodobacter capsulatus.

16 ]hydrogenase of the photosynthetic bacterium Rhodobacter capsulatus.

17 ther bacterial species, such as the GTA from Rhodobacter capsulatus.

18 b3 -type cytochrome c oxidase (cbb3 -Cox) of Rhodobacter capsulatus.

19 genes in the purple photosynthetic bacterium Rhodobacter capsulatus.

20 (CBB) reductive pentose phosphate pathway in Rhodobacter capsulatus.

21 (AerR) of photosynthesis gene expression in Rhodobacter capsulatus.

22 rocesses that affect reducing equivalents in Rhodobacter capsulatus.

23 e molybdenum cofactor in DMSO reductase from Rhodobacter capsulatus.

24 he purple nonsulfur photosynthetic bacterium Rhodobacter capsulatus.

25 RegB-RegA two-component regulatory system in Rhodobacter capsulatus.

26 ssham reductive pentose phosphate pathway in Rhodobacter capsulatus.

27 from a different strain of R.sphaeroides and Rhodobacter capsulatus, a close relative of R. sphaeroid

28 endent photosynthetic (Ps) growth pathway in Rhodobacter capsulatus, a Ps- mutant (FJM13) was isolate

29 A clone containing this gene from Rhodobacter capsulatus, a purple non-sulfur photosynthet

30 In gram-negative bacteria, like Rhodobacter capsulatus, about 10 membrane-bound componen

31 The importance of manganese in Rhodobacter capsulatus acetone carboxylase has been esta

32 oordinating the positioning of succinyl-CoA, Rhodobacter capsulatus ALAS Asn-85 has a proposed role i

33 X-ray crystal structures of Rhodobacter capsulatus ALAS reveal that a conserved acti

34 n reported to encode C-8 vinyl reductases in Rhodobacter capsulatus and Arabidopsis thaliana, respect

35 tic basis of GTA production in the bacterium Rhodobacter capsulatus and characterization of novel pha

36 o highly divergent photosynthetic organisms, Rhodobacter capsulatus and Heliophilum fasciatum.

37 -acyl-chain homoserine lactone production by Rhodobacter capsulatus and Paracoccus denitrificans.

38 Using mutant strains of Rhodobacter capsulatus and Rhodobacter sphaeroides in wh

39 wn to complement RubisCO deletion strains of Rhodobacter capsulatus and Rhodobacter sphaeroides under

40 ufX, the protein encoded by the pufX gene of Rhodobacter capsulatus and Rhodobacter sphaeroides, has

41 iously isolated from both R. sphaeroides and Rhodobacter capsulatus and shown to regulate the anaerob

42 n is greatly repressed in a B12 auxotroph of Rhodobacter capsulatus and that B12 regulation of gene e

43 d and reduced wild-type cytochrome c(2) from Rhodobacter capsulatus and the lysine 93 to proline muta

44 ics of wild-type xanthine dehydrogenase from Rhodobacter capsulatus and variants at Arg-310 in the ac

45 tobacter vinelandii, Haemophilus influenzae, Rhodobacter capsulatus, and Clostridium pasterianum.

46 purple bacteria Rhodobacter sphaeroides and Rhodobacter capsulatus, and is essential in controlling

47 the purple bacteria Rhodobacter sphaeroides, Rhodobacter capsulatus, and Rhodopseudomonas viridis has

48 sarcosine dehydrogenase-related protein from Rhodobacter capsulatus, and the regulatory subunit from

49 In this study, using Rhodobacter capsulatus apocytochrome c(2) as a Ccm subst

50 (CBB) reductive pentose phosphate pathway in Rhodobacter capsulatus are organized in at least two ope

51 A-null mutants of the facultative phototroph Rhodobacter capsulatus are unable to grow under photosyn

52 rg/Glu135Arg mutants of Escherichia coli and Rhodobacter capsulatus bacterioferritins are unable to a

53 To probe the role of the hinge region, Rhodobacter capsulatus bc(1) complex was used as a model

54 ught to be the C. aurantiacus homolog of the Rhodobacter capsulatus bchG gene is reported.

55 reaction center mutants were constructed in Rhodobacter capsulatus by replacing segments of the M su

56 e occupancy in photosynthetic membranes from Rhodobacter capsulatus by using inhibitor titrations and

57 yme dimethylsulfoxide reductase (DMSOR) from Rhodobacter capsulatus catalyzes the conversion of dimet

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

59 ed that the photosynthesis gene cluster from Rhodobacter capsulatus coded for the transcription facto

60 by the heme ligation core complex, which in Rhodobacter capsulatus contains at least the CcmF, CcmH,

61 The facultative phototrophic bacterium Rhodobacter capsulatus contains only one form of cytochr

62 n located at position L286 of the ef loop of Rhodobacter capsulatus cyt b could alleviate movement im

63 rein we studied Zn(2+)-induced inhibition of Rhodobacter capsulatus cyt bc(1) using enzyme kinetics,

64 The latter residue is M183 in Rhodobacter capsulatus cyt c1, and previous mutagenesis

65 ues were replaced with Lys and five modified Rhodobacter capsulatus Cyt c2 molecules in which positiv

66 Redox transitions in the Rhodobacter capsulatus cytochrome bc(1) complex were inv

67 dues in the cytochrome c(1) component of the Rhodobacter capsulatus cytochrome bc(1) complex, phenyla

68 erved from the Rieske protein in a sample of Rhodobacter capsulatus cytochrome bc1 complex uniformly

69 on chemistry and spectroscopic properties of Rhodobacter capsulatus cytochrome c' (RCCP) have been co

70 Gly 34 and the adjacent Pro 35 of Rhodobacter capsulatus cytochrome c(2) (or Gly 29 and Pr

71 ations at 9 positions in the hinge region of Rhodobacter capsulatus cytochrome c(2) and have determin

72 In the case of Rhodobacter capsulatus cytochrome c(2), the sixth heme l

73 he dissociation constants for the binding of Rhodobacter capsulatus cytochrome c2 and its K93P mutant

74 of binding of imidazole to eight mutants of Rhodobacter capsulatus cytochrome c2 that differ in over

75 In many Gram-negative bacteria, including Rhodobacter capsulatus, cytochrome c maturation (Ccm) is

76 RC) mutants created in the background of the Rhodobacter capsulatus D(LL) mutant, in which the D heli

77 Genetic analysis of ccoGHIS in Rhodobacter capsulatus demonstrated that ccoG, ccoH, cco

78 R. sphaeroides dimethyl sulfoxide reductase, Rhodobacter capsulatus dimethyl sulfoxide reductase, and

79 During the photosynthetic growth of Rhodobacter capsulatus, electrons are conveyed from the

80 nanosecond flash photolysis and RCs from the Rhodobacter capsulatus F(L181)Y/Y(M208)F/L(M212)H mutant

81 gB/RegA two-component regulatory system from Rhodobacter capsulatus functions as a global regulator o

82 The Rhodobacter capsulatus genome contains three genes (olsA

83 Among these species, Rhodobacter capsulatus has a periplasmic Cyt c2Rc and a

84 iogenesis in the purple non-sulfur bacterium Rhodobacter capsulatus have been carried out.

85 molybdenum-containing Me(2)SO reductase from Rhodobacter capsulatus have been examined spectroscopica

86 Q variant of the xanthine dehydrogenase from Rhodobacter capsulatus have been examined to ascertain w

87 f bc1 complexes and isolated c1 subunit from Rhodobacter capsulatus have been obtained using a variet

88 A Rhodobacter capsulatus hemC mutant has been isolated and

89 or selection in a Rubisco deletion strain of Rhodobacter capsulatus identified a residue in the amino

90 CrtJ from Rhodobacter capsulatus is a regulator of genes involved

91 ductase (or the cytochrome bc1 complex) from Rhodobacter capsulatus is composed of the Fe-S protein,

92 In this study, we show that SenC from Rhodobacter capsulatus is involved in the assembly of a

93 oid, and light harvesting gene expression in Rhodobacter capsulatus is repressed under aerobic growth

94 rophyll and carotenoid biosynthesis genes in Rhodobacter capsulatus is repressed under aerobic growth

95 The HelA protein of Rhodobacter capsulatus is the ATP-binding-cassette subun

96 onstrate that the expression of hem genes in Rhodobacter capsulatus is transcriptionally repressed in

97 The purple bacterium Rhodobacter capsulatus is unique among Rhodobacteriacae

98 g protein from the photosynthetic bacterium, Rhodobacter capsulatus, is shown in vitro to activate th

99 the facultative phototrophic (Ps) bacterium Rhodobacter capsulatus, it is constituted by the cyt b,

100 bsence of serum, while a synthetic analog of Rhodobacter capsulatus lipid A (B 975) requires both rsC

101 estingly, while relatively nontoxic in mice, Rhodobacter capsulatus LPS stimulated RAW cell NF-kappaB

102 The bacterium Rhodobacter capsulatus mediates this process by repressi

103 -c1 subcomplex in chromatophore membranes of Rhodobacter capsulatus mutants lacking the Rieske iron-s

104 Herein, using Rhodobacter capsulatus mutants that have modifications i

105 n center has been trapped in two D(LL)-based Rhodobacter capsulatus mutants that have Tyr at position

106 It was previously shown that the Rhodobacter capsulatus NtrC enhancer-binding protein act

107 Rhodobacter capsulatus NtrC is an enhancer-binding prote

108 The Rhodobacter capsulatus NtrC protein is a bacterial enhan

109 ight-harvesting 2 (LH2, B800-850) mutants of Rhodobacter capsulatus obtained by combinatorial mutagen

110 Rhodobacter capsulatus produces various c-type cytochrom

111 with the phytoene desaturase gene (crtI) of Rhodobacter capsulatus, producing carotenoids with short

112 7, staphylococcal phage straight phiPVL, two Rhodobacter capsulatus prophages and two Mycobacterium t

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

114 Expression of the Rhodobacter capsulatus puc operon, which codes for struc

115 e P(+)Q(B)(-) is created in this manner in a Rhodobacter capsulatus RC containing the F(L181)Y-Y(M208

116 ion of the formate dehydrogenase enzyme from Rhodobacter capsulatus (RcFDH) by means of hydrophobic i

117 A large scale mutation of the Rhodobacter capsulatus reaction center M-subunit gene, s

118 an (RR) studies are reported for a series of Rhodobacter capsulatus reaction centers (RCs) containing

119 The primary photochemistry in Rhodobacter capsulatus reaction centers (RCs) containing

120 f the primary electron transfer reactions in Rhodobacter capsulatus reaction centers (RCs) having fou

121 mary charge separation events in a series of Rhodobacter capsulatus reaction centers (RCs) that have

122 In the purple non-sulfur bacterium Rhodobacter capsulatus, RegA and RegB comprise a two-com

123 Rhodobacter capsulatus regulates many metabolic processe

124 , V, F, H, K, and Q in purple photosynthetic Rhodobacter capsulatus results in hydroquinone oxidation

125 In Rhodobacter capsulatus, ribulose 1,5-bisphosphate carbox

126 tion systems in photosynthetic bacteria, the Rhodobacter capsulatus RNA polymerase (RNAP) that contai

127 Rhodobacter capsulatus SB 1003 belongs to the group of p

128 ressed in its genetically tractable relative Rhodobacter capsulatus SB1003.

129 etion mutant of the photosynthetic bacterium Rhodobacter capsulatus served as a host.

130 We have purified the Rhodobacter capsulatus sigma N protein, which is distinc

131 bacter sphaeroides, like the closely related Rhodobacter capsulatus species, contains both the previo

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

133 The photosynthetic bacterium Rhodobacter capsulatus synthesizes c-type cytochromes un

134 e previously reported that mutant strains of Rhodobacter capsulatus that have alanine insertions (+nA

135 Here, we show in Rhodobacter capsulatus that in the absence of DsbA cytoc

136 r-diameter gene transfer agents of bacterium Rhodobacter capsulatus that transfer random 4.5-kbp (1.5

137 In Gram-negative bacteria, including Rhodobacter capsulatus, the membrane protein CycH acts a

138 In the photosynthetic bacterium Rhodobacter capsulatus, the NtrB and NtrC proteins (RcNt

139 In the purple, photosynthetic bacterium, Rhodobacter capsulatus, the RegB/RegA two-component syst

140 In Rhodobacter capsulatus, the soluble cytochrome (cyt) c2

141 Earlier work indicated that in Rhodobacter capsulatus these atoms are provided by two c

142 For DMSOR from Rhodobacter capsulatus, thiolate dissociation has theref

143 In this study, the ability of Rhodobacter capsulatus to maintain a balanced intracellu

144 us complementation assays between E.coli and Rhodobacter capsulatus to show that, despite their diffe

145 to form cytochrome c, leading in the case of Rhodobacter capsulatus to the loss of photosynthetic pro

146 In Rhodobacter capsulatus, two open reading frames (ORFs) c

147 Gram-negative bacteria like Rhodobacter capsulatus use intertwined pathways to carry

148 eps at the Qi-site of the cyt bc1 complex of Rhodobacter capsulatus using atomistic molecular dynamic

149 Rhodobacter capsulatus utilizes two terminal oxidases fo

150 In this study, the fnrL locus from Rhodobacter capsulatus was cloned and sequenced.

151 utant of the purple photosynthetic bacterium Rhodobacter capsulatus was functionally complemented wit

152 A mutant of Rhodobacter capsulatus was identified in which an operon

153 bacterial xanthine dehydrogenase (XDH) from Rhodobacter capsulatus was immobilized on an edge-plane

154 he purple nonsulfur photosynthetic bacterium Rhodobacter capsulatus was purified to homogeneity and c

155 ubisco) employing the phototrophic bacterium Rhodobacter capsulatus was used to select a catalyticall

156 etic analysis in the Gram-negative bacterium Rhodobacter capsulatus was used to show that the helABC

157 DMSO reductase (DMSOR) from Rhodobacter capsulatus, well-characterised as a molybdoe

158 These genes from Rhodobacter capsulatus were cloned separately into expre

159 rome (cyt)-deficient mutants, 771 and K2, of Rhodobacter capsulatus were isolated.

160 ing/unfolding reaction of cytochrome c2 from Rhodobacter capsulatus were performed as a function of g

161 regulator from the photosynthetic bacterium Rhodobacter capsulatus, were obtained by specific intera

162 he closest known homolog is the bluB gene of Rhodobacter capsulatus, which is implicated in the biosy

163 The ISP of Rhodobacter capsulatus within the intact cytochrome bc(1