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1 le hinge sequence (amino acids D43 to S49 in Rhodobacter capsulatus).
2 b3 -type cytochrome c oxidase (cbb3 -Cox) of Rhodobacter capsulatus.
3 RegB-RegA two-component regulatory system in Rhodobacter capsulatus.
4 ssham reductive pentose phosphate pathway in Rhodobacter capsulatus.
5 ar to those in species of Rhizobiaceae or in Rhodobacter capsulatus.
6 ranscription factors and RNA polymerase from Rhodobacter capsulatus.
7 tron transfer in photosynthetic membranes of Rhodobacter capsulatus.
8 lex of Rb. sphaeroides compared with that of Rhodobacter capsulatus.
9  Ccl2 proteins in the Gram-negative bacteria Rhodobacter capsulatus.
10 d-type and mutant reaction center strains of Rhodobacter capsulatus.
11 ella abortus, Agrobacterium tumefaciens, and Rhodobacter capsulatus.
12 ed for the assembly of c-type cytochromes in Rhodobacter capsulatus.
13 ORF176 in the photosynthesis gene cluster in Rhodobacter capsulatus.
14 s proteins of Synechocystis sp. PCC 6301 and Rhodobacter capsulatus.
15 ytochrome c oxidase (Cox) in species such as Rhodobacter capsulatus.
16 illum brasilense, Rhodospirillum rubrum, and Rhodobacter capsulatus.
17 iochlorophyll and carotenoid biosynthesis in Rhodobacter capsulatus.
18  the crystal structure of thioredoxin-2 from Rhodobacter capsulatus.
19 to the ornithine lipid biosynthesis genes of Rhodobacter capsulatus.
20 ]hydrogenase of the photosynthetic bacterium Rhodobacter capsulatus.
21 ther bacterial species, such as the GTA from Rhodobacter capsulatus.
22 genes in the purple photosynthetic bacterium Rhodobacter capsulatus.
23 (CBB) reductive pentose phosphate pathway in Rhodobacter capsulatus.
24  (AerR) of photosynthesis gene expression in Rhodobacter capsulatus.
25 rocesses that affect reducing equivalents in Rhodobacter capsulatus.
26 e molybdenum cofactor in DMSO reductase from Rhodobacter capsulatus.
27 he purple nonsulfur photosynthetic bacterium Rhodobacter capsulatus.
28 from a different strain of R.sphaeroides and Rhodobacter capsulatus, a close relative of R. sphaeroid
29 endent photosynthetic (Ps) growth pathway in Rhodobacter capsulatus, a Ps- mutant (FJM13) was isolate
30            A clone containing this gene from Rhodobacter capsulatus, a purple non-sulfur photosynthet
31              In gram-negative bacteria, like Rhodobacter capsulatus, about 10 membrane-bound componen
32               The importance of manganese in Rhodobacter capsulatus acetone carboxylase has been esta
33 oordinating the positioning of succinyl-CoA, Rhodobacter capsulatus ALAS Asn-85 has a proposed role i
34                  X-ray crystal structures of Rhodobacter capsulatus ALAS reveal that a conserved acti
35 n reported to encode C-8 vinyl reductases in Rhodobacter capsulatus and Arabidopsis thaliana, respect
36 tic basis of GTA production in the bacterium Rhodobacter capsulatus and characterization of novel pha
37 o highly divergent photosynthetic organisms, Rhodobacter capsulatus and Heliophilum fasciatum.
38 -acyl-chain homoserine lactone production by Rhodobacter capsulatus and Paracoccus denitrificans.
39                      Using mutant strains of Rhodobacter capsulatus and Rhodobacter sphaeroides in wh
40 wn to complement RubisCO deletion strains of Rhodobacter capsulatus and Rhodobacter sphaeroides under
41 ufX, the protein encoded by the pufX gene of Rhodobacter capsulatus and Rhodobacter sphaeroides, has
42 iously isolated from both R. sphaeroides and Rhodobacter capsulatus and shown to regulate the anaerob
43 n is greatly repressed in a B12 auxotroph of Rhodobacter capsulatus and that B12 regulation of gene e
44 d and reduced wild-type cytochrome c(2) from Rhodobacter capsulatus and the lysine 93 to proline muta
45 ics of wild-type xanthine dehydrogenase from Rhodobacter capsulatus and variants at Arg-310 in the ac
46 tobacter vinelandii, Haemophilus influenzae, Rhodobacter capsulatus, and Clostridium pasterianum.
47  purple bacteria Rhodobacter sphaeroides and Rhodobacter capsulatus, and is essential in controlling
48 the purple bacteria Rhodobacter sphaeroides, Rhodobacter capsulatus, and Rhodopseudomonas viridis has
49 sarcosine dehydrogenase-related protein from Rhodobacter capsulatus, and the regulatory subunit from
50                         In this study, using Rhodobacter capsulatus apocytochrome c(2) as a Ccm subst
51 (CBB) reductive pentose phosphate pathway in Rhodobacter capsulatus are organized in at least two ope
52 A-null mutants of the facultative phototroph Rhodobacter capsulatus are unable to grow under photosyn
53 rg/Glu135Arg mutants of Escherichia coli and Rhodobacter capsulatus bacterioferritins are unable to a
54       To probe the role of the hinge region, Rhodobacter capsulatus bc(1) complex was used as a model
55 ught to be the C. aurantiacus homolog of the Rhodobacter capsulatus bchG gene is reported.
56 ngs, primarily for the model GTA produced by Rhodobacter capsulatus but also for newly identified GTA
57  reaction center mutants were constructed in Rhodobacter capsulatus by replacing segments of the M su
58 e occupancy in photosynthetic membranes from Rhodobacter capsulatus by using inhibitor titrations and
59 yme dimethylsulfoxide reductase (DMSOR) from Rhodobacter capsulatus catalyzes the conversion of dimet
60                                          The Rhodobacter capsulatus cbb(3)-type cytochrome c oxidase
61 ed that the photosynthesis gene cluster from Rhodobacter capsulatus coded for the transcription facto
62  by the heme ligation core complex, which in Rhodobacter capsulatus contains at least the CcmF, CcmH,
63       The facultative phototrophic bacterium Rhodobacter capsulatus contains only one form of cytochr
64                                           In Rhodobacter capsulatus, Cu-detoxification and Cu deliver
65 n located at position L286 of the ef loop of Rhodobacter capsulatus cyt b could alleviate movement im
66 rein we studied Zn(2+)-induced inhibition of Rhodobacter capsulatus cyt bc(1) using enzyme kinetics,
67                The latter residue is M183 in Rhodobacter capsulatus cyt c1, and previous mutagenesis
68 ues were replaced with Lys and five modified Rhodobacter capsulatus Cyt c2 molecules in which positiv
69                     Redox transitions in the Rhodobacter capsulatus cytochrome bc(1) complex were inv
70 dues in the cytochrome c(1) component of the Rhodobacter capsulatus cytochrome bc(1) complex, phenyla
71 eme b(L) side of the QH(2) oxidation site in Rhodobacter capsulatus cytochrome bc(1).
72 erved from the Rieske protein in a sample of Rhodobacter capsulatus cytochrome bc1 complex uniformly
73 on chemistry and spectroscopic properties of Rhodobacter capsulatus cytochrome c' (RCCP) have been co
74            Gly 34 and the adjacent Pro 35 of Rhodobacter capsulatus cytochrome c(2) (or Gly 29 and Pr
75 ations at 9 positions in the hinge region of Rhodobacter capsulatus cytochrome c(2) and have determin
76                               In the case of Rhodobacter capsulatus cytochrome c(2), the sixth heme l
77 he dissociation constants for the binding of Rhodobacter capsulatus cytochrome c2 and its K93P mutant
78  of binding of imidazole to eight mutants of Rhodobacter capsulatus cytochrome c2 that differ in over
79    In many Gram-negative bacteria, including Rhodobacter capsulatus, cytochrome c maturation (Ccm) is
80 RC) mutants created in the background of the Rhodobacter capsulatus D(LL) mutant, in which the D heli
81 xpressed in Escherichia coli (DeltaribB) and Rhodobacter capsulatus (DeltaccoA) mutants.
82               Genetic analysis of ccoGHIS in Rhodobacter capsulatus demonstrated that ccoG, ccoH, cco
83 R. sphaeroides dimethyl sulfoxide reductase, Rhodobacter capsulatus dimethyl sulfoxide reductase, and
84          During the photosynthetic growth of Rhodobacter capsulatus, electrons are conveyed from the
85 nanosecond flash photolysis and RCs from the Rhodobacter capsulatus F(L181)Y/Y(M208)F/L(M212)H mutant
86 gB/RegA two-component regulatory system from Rhodobacter capsulatus functions as a global regulator o
87                                           In Rhodobacter capsulatus, gene rcc01865 encodes a putative
88                                          The Rhodobacter capsulatus genome contains three genes (olsA
89 dentified the small terminase from the model Rhodobacter capsulatus GTA, which then allowed predictio
90                         Among these species, Rhodobacter capsulatus has a periplasmic Cyt c2Rc and a
91 iogenesis in the purple non-sulfur bacterium Rhodobacter capsulatus have been carried out.
92 molybdenum-containing Me(2)SO reductase from Rhodobacter capsulatus have been examined spectroscopica
93 Q variant of the xanthine dehydrogenase from Rhodobacter capsulatus have been examined to ascertain w
94 f bc1 complexes and isolated c1 subunit from Rhodobacter capsulatus have been obtained using a variet
95                                            A Rhodobacter capsulatus hemC mutant has been isolated and
96 or selection in a Rubisco deletion strain of Rhodobacter capsulatus identified a residue in the amino
97                                    CrtJ from Rhodobacter capsulatus is a regulator of genes involved
98 ductase (or the cytochrome bc1 complex) from Rhodobacter capsulatus is composed of the Fe-S protein,
99            The Anf3 protein in the bacterium Rhodobacter capsulatus is essential for diazotrophic (i.
100        In this study, we show that SenC from Rhodobacter capsulatus is involved in the assembly of a
101 oid, and light harvesting gene expression in Rhodobacter capsulatus is repressed under aerobic growth
102 rophyll and carotenoid biosynthesis genes in Rhodobacter capsulatus is repressed under aerobic growth
103                          The HelA protein of Rhodobacter capsulatus is the ATP-binding-cassette subun
104 onstrate that the expression of hem genes in Rhodobacter capsulatus is transcriptionally repressed in
105                         The purple bacterium Rhodobacter capsulatus is unique among Rhodobacteriacae
106 g protein from the photosynthetic bacterium, Rhodobacter capsulatus, is shown in vitro to activate th
107  the facultative phototrophic (Ps) bacterium Rhodobacter capsulatus, it is constituted by the cyt b,
108 bsence of serum, while a synthetic analog of Rhodobacter capsulatus lipid A (B 975) requires both rsC
109 estingly, while relatively nontoxic in mice, Rhodobacter capsulatus LPS stimulated RAW cell NF-kappaB
110                                The bacterium Rhodobacter capsulatus mediates this process by repressi
111 -c1 subcomplex in chromatophore membranes of Rhodobacter capsulatus mutants lacking the Rieske iron-s
112                                Herein, using Rhodobacter capsulatus mutants that have modifications i
113 n center has been trapped in two D(LL)-based Rhodobacter capsulatus mutants that have Tyr at position
114             It was previously shown that the Rhodobacter capsulatus NtrC enhancer-binding protein act
115                                              Rhodobacter capsulatus NtrC is an enhancer-binding prote
116                                          The Rhodobacter capsulatus NtrC protein is a bacterial enhan
117 ight-harvesting 2 (LH2, B800-850) mutants of Rhodobacter capsulatus obtained by combinatorial mutagen
118  dinucleotide (bis-MGD) cofactor in FDH from Rhodobacter capsulatus of this study also completely rea
119                                              Rhodobacter capsulatus produces various c-type cytochrom
120  with the phytoene desaturase gene (crtI) of Rhodobacter capsulatus, producing carotenoids with short
121 7, staphylococcal phage straight phiPVL, two Rhodobacter capsulatus prophages and two Mycobacterium t
122                         A mutant form of the Rhodobacter capsulatus PrrA homologue, whose activity is
123                            Expression of the Rhodobacter capsulatus puc operon, which codes for struc
124 e P(+)Q(B)(-) is created in this manner in a Rhodobacter capsulatus RC containing the F(L181)Y-Y(M208
125 ion of the formate dehydrogenase enzyme from Rhodobacter capsulatus (RcFDH) by means of hydrophobic i
126                A large scale mutation of the Rhodobacter capsulatus reaction center M-subunit gene, s
127 an (RR) studies are reported for a series of Rhodobacter capsulatus reaction centers (RCs) containing
128                The primary photochemistry in Rhodobacter capsulatus reaction centers (RCs) containing
129 f the primary electron transfer reactions in Rhodobacter capsulatus reaction centers (RCs) having fou
130 mary charge separation events in a series of Rhodobacter capsulatus reaction centers (RCs) that have
131           In the purple non-sulfur bacterium Rhodobacter capsulatus, RegA and RegB comprise a two-com
132                                              Rhodobacter capsulatus regulates many metabolic processe
133 , V, F, H, K, and Q in purple photosynthetic Rhodobacter capsulatus results in hydroquinone oxidation
134                                           In Rhodobacter capsulatus, ribulose 1,5-bisphosphate carbox
135 tion systems in photosynthetic bacteria, the Rhodobacter capsulatus RNA polymerase (RNAP) that contai
136                                              Rhodobacter capsulatus SB 1003 belongs to the group of p
137        Furthermore, the non-As(III) oxidizer Rhodobacter capsulatus SB1003 heterologously expressing
138 ressed in its genetically tractable relative Rhodobacter capsulatus SB1003.
139 etion mutant of the photosynthetic bacterium Rhodobacter capsulatus served as a host.
140                         We have purified the Rhodobacter capsulatus sigma N protein, which is distinc
141 bacter sphaeroides, like the closely related Rhodobacter capsulatus species, contains both the previo
142                       A transposon mutant of Rhodobacter capsulatus, strain Mal7, that was incapable
143                 The photosynthetic bacterium Rhodobacter capsulatus synthesizes c-type cytochromes un
144 e previously reported that mutant strains of Rhodobacter capsulatus that have alanine insertions (+nA
145                             Here, we show in Rhodobacter capsulatus that in the absence of DsbA cytoc
146 r-diameter gene transfer agents of bacterium Rhodobacter capsulatus that transfer random 4.5-kbp (1.5
147         In Gram-negative bacteria, including Rhodobacter capsulatus, the membrane protein CycH acts a
148              In the photosynthetic bacterium Rhodobacter capsulatus, the NtrB and NtrC proteins (RcNt
149     In the purple, photosynthetic bacterium, Rhodobacter capsulatus, the RegB/RegA two-component syst
150                                           In Rhodobacter capsulatus, the soluble cytochrome (cyt) c2
151               Earlier work indicated that in Rhodobacter capsulatus these atoms are provided by two c
152                               For DMSOR from Rhodobacter capsulatus, thiolate dissociation has theref
153                In this study, the ability of Rhodobacter capsulatus to maintain a balanced intracellu
154 us complementation assays between E.coli and Rhodobacter capsulatus to show that, despite their diffe
155 to form cytochrome c, leading in the case of Rhodobacter capsulatus to the loss of photosynthetic pro
156                                           In Rhodobacter capsulatus, two open reading frames (ORFs) c
157                  Gram-negative bacteria like Rhodobacter capsulatus use intertwined pathways to carry
158 eps at the Qi-site of the cyt bc1 complex of Rhodobacter capsulatus using atomistic molecular dynamic
159                                              Rhodobacter capsulatus utilizes two terminal oxidases fo
160           In this study, the fnrL locus from Rhodobacter capsulatus was cloned and sequenced.
161 utant of the purple photosynthetic bacterium Rhodobacter capsulatus was functionally complemented wit
162                                  A mutant of Rhodobacter capsulatus was identified in which an operon
163  bacterial xanthine dehydrogenase (XDH) from Rhodobacter capsulatus was immobilized on an edge-plane
164 he purple nonsulfur photosynthetic bacterium Rhodobacter capsulatus was purified to homogeneity and c
165 ubisco) employing the phototrophic bacterium Rhodobacter capsulatus was used to select a catalyticall
166 etic analysis in the Gram-negative bacterium Rhodobacter capsulatus was used to show that the helABC
167                  DMSO reductase (DMSOR) from Rhodobacter capsulatus, well-characterised as a molybdoe
168                             These genes from Rhodobacter capsulatus were cloned separately into expre
169 rome (cyt)-deficient mutants, 771 and K2, of Rhodobacter capsulatus were isolated.
170 ing/unfolding reaction of cytochrome c2 from Rhodobacter capsulatus were performed as a function of g
171  regulator from the photosynthetic bacterium Rhodobacter capsulatus, were obtained by specific intera
172 he closest known homolog is the bluB gene of Rhodobacter capsulatus, which is implicated in the biosy
173                                   The ISP of Rhodobacter capsulatus within the intact cytochrome bc(1

 
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