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1 c bacteria Rhodobacter sphaeroides 2.4.1 and Rhodopseudomonas acidophila 10050.
2 in Rhodobacter sphaeroides), lamellar (as in Rhodopseudomonas acidophila and Phaeospirillum molischia
3 e B800-B850 complex and B800-B820 complex of Rhodopseudomonas acidophila are 7+/-0.5 ps and 6+/-0.5 p
4 rotein light harvesting complex 2 (LH2) from Rhodopseudomonas acidophila at the single-protein level.
5 tructures of LH-II from Rs. molischianum and Rhodopseudomonas acidophila furnish a complete model of
6 ht-harvesting complex of the purple bacteria Rhodopseudomonas acidophila strain 10050 at a maximal re
7 brane light-harvesting complex II (LH2) from Rhodopseudomonas acidophila strain 10050 has been refine
8 the peripheral light-harvesting complex from Rhodopseudomonas acidophila strain 10050 reveals a membr
9 the intact light-harvesting complex LH2 from Rhodopseudomonas acidophila were bound to mica surfaces
10  Single light-harvesting complexes LH-2 from Rhodopseudomonas acidophila were immobilized on various
11                              In the LH2 from Rhodopseudomonas acidophila, the equivalent part of the
12 ly obtained for the related LH2 complex from Rhodopseudomonas acidophila.
13 atility that is a defining characteristic of Rhodopseudomonas, different ecotypes have evolved to tak
14                          The bacterial genus Rhodopseudomonas is comprised of photosynthetic bacteria
15 re is considerable genotypic diversity among Rhodopseudomonas isolates.
16 acteria, including Rhodobacter, Methylibium, Rhodopseudomonas, Methyloversatilis, Caldilinea, Thiobac
17 he B800 and B850 rings in the LH2 complex of Rhodopseudomonas molischianum using fully quantum mechan
18 d a synthetic community of phototrophs using Rhodopseudomonas palustris (R. palustris) and an enginee
19                         The cbb(I) region of Rhodopseudomonas palustris (Rp. palustris) contains the
20 th of Rhodospirillum rubrum (Rs. rubrum) and Rhodopseudomonas palustris (Rp. palustris) RubisCO-defic
21 we identified a Ca(2+)-dependent enzyme from Rhodopseudomonas palustris (Rpa3624) and showed that it
22 electron transfer flavoprotein (Bf-ETF) from Rhodopseudomonas palustris (RpaETF).
23     The protein acetyltransferase (Pat) from Rhodopseudomonas palustris (RpPat) inactivates AMP-formi
24 croscopy structures of RC-LH1 complexes from Rhodopseudomonas palustris A 2.65-A resolution structure
25 ee of such genes from Ochrobactrum anthropi, Rhodopseudomonas palustris and Agrobacterium tumefaciens
26 lation efficiency over a range of genes from Rhodopseudomonas palustris and E. coli was achieved usin
27 ranscriptional activator, similar to AadR of Rhodopseudomonas palustris and FixK proteins of rhizobia
28 of p-coumarate by the phototrophic bacterium Rhodopseudomonas palustris and found that it also follow
29 wo related LuxI homologs, RpaI and BtaI from Rhodopseudomonas palustris and photosynthetic stem-nodul
30    We show that two other bacterial species, Rhodopseudomonas palustris and Shewanella putrefaciens,
31 BAC system from the photosynthetic bacterium Rhodopseudomonas palustris as the first member of the tr
32                                              Rhodopseudomonas palustris assimilates CO2 by the Calvin
33 ome BphP1 and its natural partner PpsR2 from Rhodopseudomonas palustris bacteria.
34 ucturally characterize enzymes of the GRM of Rhodopseudomonas palustris BisB18 and demonstrate their
35           Here, we exploit the advantages of Rhodopseudomonas palustris BphP1 bacterial phytochrome,
36 was purified from the phototrophic bacterium Rhodopseudomonas palustris by sequential Q-Sepharose, ph
37                            The flavodoxin of Rhodopseudomonas palustris CGA009 (Rp9Fld) supplies high
38                                              Rhodopseudomonas palustris CGA009 is a purple non-sulfur
39                       The genome sequence of Rhodopseudomonas palustris CGA009 revealed a surprising
40 nthesis in Rhodobacter sphaeroides 2.4.1 and Rhodopseudomonas palustris CGA009.
41                                           In Rhodopseudomonas palustris CGA010, the LysR type regulat
42 rowing cells of the photosynthetic bacterium Rhodopseudomonas palustris continue to metabolize acetat
43                             Reduced (Fe(II)) Rhodopseudomonas palustris cytochrome c' (Cyt c') is mor
44 gy transfer kinetics during the refolding of Rhodopseudomonas palustris cytochrome c' reveals dramati
45 me loop formation for iso-1-cytochrome c and Rhodopseudomonas palustris cytochrome c', shows that fol
46 plexes has been investigated in membranes of Rhodopseudomonas palustris grown under high- and low-lig
47 bolic fluxes in the photosynthetic bacterium Rhodopseudomonas palustris grown with (13)C-labeled acet
48                                              Rhodopseudomonas palustris grows photoheterotrophically
49                    The alpha-proteobacterium Rhodopseudomonas palustris has three annotated PIMT gene
50  4-hydroxybenzoate (4-HBA) to benzoyl-CoA by Rhodopseudomonas palustris have been identified.
51 totrophic bacteria Rhodospirillum rubrum and Rhodopseudomonas palustris In vivo metabolite analysis o
52              Quorum sensing in the bacterium Rhodopseudomonas palustris involves the RpaI signal synt
53                                              Rhodopseudomonas palustris is a purple, facultatively ph
54                                              Rhodopseudomonas palustris is among the most metabolical
55                 The photosynthetic bacterium Rhodopseudomonas palustris is one of just a few prokaryo
56              The purple non-sulfur bacterium Rhodopseudomonas palustris is recognized as a critical m
57                                              Rhodopseudomonas palustris is unique among characterized
58                         The photoheterotroph Rhodopseudomonas palustris is unusual in that it produce
59                                              Rhodopseudomonas palustris metabolizes aromatic compound
60 nspect, based on benchmarking results from a Rhodopseudomonas palustris proteomics dataset.
61 ight harvesting 1 (RC-LH1) core complex from Rhodopseudomonas palustris shows the reaction center sur
62                                              Rhodopseudomonas palustris strain JSC-3b isolated from a
63                                              Rhodopseudomonas palustris strain RCB100 degrades 3-chlo
64  show that the iron-oxidizing photoautotroph Rhodopseudomonas palustris TIE-1 accepts electrons from
65 r the phototrophic Fe(II)-oxidizing bacteria Rhodopseudomonas palustris TIE-1 and the Fe(III)-reducin
66           Here we report the discovery, with Rhodopseudomonas palustris TIE-1 as a model organism, of
67                         The purple bacterium Rhodopseudomonas palustris TIE-1 expresses multiple smal
68                                              Rhodopseudomonas palustris TIE-1 grows photoautotrophica
69                                              Rhodopseudomonas palustris TIE-1 is a gram-negative bact
70  the phototrophic Fe(II)-oxidizing bacterium Rhodopseudomonas palustris TIE-1 oxidizes magnetite (Fe3
71 eport the physiological study of a mutant in Rhodopseudomonas palustris TIE-1 that is unable to produ
72                                 Here, we use Rhodopseudomonas palustris TIE-1 to identify factors tha
73 es of the model hopanoid-producing bacterium Rhodopseudomonas palustris TIE-1.
74 ain during EEU in the phototrophic bacterium Rhodopseudomonas palustris TIE-1.
75 trophic) growth by the alpha-proteobacterium Rhodopseudomonas palustris TIE-1.
76 denosylmethionine (SAM) methyltransfase from Rhodopseudomonas palustris to remove arsenic from contam
77 volved the anoxygenic phototrophic bacterium Rhodopseudomonas palustris to use formate as the sole ca
78                                          The Rhodopseudomonas palustris transcriptional regulator Rpa
79 re we show that the photosynthetic bacterium Rhodopseudomonas palustris uses an acyl-HSL synthase to
80         Heterologous expression of arsM from Rhodopseudomonas palustris was shown to confer As(III) r
81 nd RpBphP3 from the photosynthetic bacterium Rhodopseudomonas palustris work in tandem to modulate sy
82 idated a genome-scale model of metabolism in Rhodopseudomonas palustris, a metabolically versatile gr
83 trogenase, including Azotobacter vinelandii, Rhodopseudomonas palustris, and Methanosarcina barkeri.
84 totacticum, Novosphingobium aromaticivorans, Rhodopseudomonas palustris, and Thermus thermophilus.
85 ere, we developed the anoxygenic phototroph, Rhodopseudomonas palustris, as a biocatalyst capable of
86                            This enzyme, from Rhodopseudomonas palustris, assembles as a unique hexame
87       In the purple photosynthetic bacterium Rhodopseudomonas palustris, at least 10 AMP-forming acyl
88  enzyme of anaerobic benzoate degradation by Rhodopseudomonas palustris, benzoyl coenzyme A (CoA) red
89 s in the anoxygenic photosynthetic bacterium Rhodopseudomonas palustris, designated regulatory protei
90 nerated four sets of puc deletion mutants in Rhodopseudomonas palustris, each encoding a single type
91 ilis and diguanylate cyclase rpHK1S-Z16 from Rhodopseudomonas palustris, enhancing their enzymatic ac
92      CYP199A2, a cytochrome P450 enzyme from Rhodopseudomonas palustris, oxidatively demethylates 4-m
93 ssion of the cbb(I) CO(2) fixation operon of Rhodopseudomonas palustris, possibly in response to a re
94 f the closely related alpha-proteobacterium, Rhodopseudomonas palustris, revealed a small set of five
95 the metabolically versatile photoheterotroph Rhodopseudomonas palustris, the type of carbon substrate
96  purple photosynthetic alpha-proteobacterium Rhodopseudomonas palustris, two protein acetyltransferas
97 h reduces CO(2) to acetate, and diazotrophic Rhodopseudomonas palustris, which uses the acetate both
98 rmentative Escherichia coli and phototrophic Rhodopseudomonas palustris.
99 d compounds from the phototrophic bacterium, Rhodopseudomonas palustris.
100 nd sequenced from the phototrophic bacterium Rhodopseudomonas palustris.
101 action between Geobacter metallireducens and Rhodopseudomonas palustris.
102 aproteobacteria, Rhodobacter sphaeroides and Rhodopseudomonas palustris.
103  A and B domains, represented by RpArsM from Rhodopseudomonas palustris.
104  phototrophic growth by the purple bacterium Rhodopseudomonas palustris.
105 he wild-type light harvesting 2 complexes of Rhodopseudomonas palustris.
106 pounds, using the purple nonsulfur bacterium Rhodopseudomonas palustris.
107 nd meta-hydroxybenzoate, was investigated in Rhodopseudomonas palustris.
108 rylation and other major metabolic traits in Rhodopseudomonas palustris.
109 ass II c-type cytochrome, cytochrome c' from Rhodopseudomonas palustris.
110 as part of an interactome mapping project in Rhodopseudomonas palustris.
111  in two strains of the anoxygenic phototroph Rhodopseudomonas palustris.
112 he nonsulfur purple photosynthetic bacterium Rhodopseudomonas palustris.
113 e nonsulfur anoxygenic phototropic bacterium Rhodopseudomonas palustris.
114 ters in Escherichia coli and nitrogenases in Rhodopseudomonas palustris.
115  on a complex ribosomal protein mixture from Rhodopseudomonas palustris.
116 om digested ribosomal proteins isolated from Rhodopseudomonas palustris.
117 radation by the photoheterotrophic bacterium Rhodopseudomonas palustris.
118 een described for the phototrophic bacterium Rhodopseudomonas palustris.
119 nt-protein complex, from the purple bacteria Rhodopseudomonas (Rps.) acidophila strain 7050 has been
120 stal structure is very similar to the LH2 of Rhodopseudomonas (Rps.) acidophila.
121 ssion spectra from single LH2 complexes from Rhodopseudomonas (Rps.) acidophila.
122 plasmic (ICM) vesicles (chromatophores) from Rhodopseudomonas sphaeroides using an air-driven ultrace
123 ed from bacterial cells (chromatophores from Rhodopseudomonas sphaeroides) and mammalian cells (mu-op
124 eaction centers, Rhodobacter sphaeroides and Rhodopseudomonas viridis [containing ubiquinone (UQ) or
125 s in the photosynthetic reaction center from Rhodopseudomonas viridis and the ruthenated heme protein
126 ter sphaeroides, Rhodobacter capsulatus, and Rhodopseudomonas viridis has been investigated with tran
127 protein from Blastochloris viridis (formerly Rhodopseudomonas viridis) were reconstituted with ubiqui

 
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