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1 rmentative Escherichia coli and phototrophic Rhodopseudomonas palustris.
2 pounds, using the purple nonsulfur bacterium Rhodopseudomonas palustris.
3  phototrophic growth by the purple bacterium Rhodopseudomonas palustris.
4 nd meta-hydroxybenzoate, was investigated in Rhodopseudomonas palustris.
5 rylation and other major metabolic traits in Rhodopseudomonas palustris.
6 ass II c-type cytochrome, cytochrome c' from Rhodopseudomonas palustris.
7 as part of an interactome mapping project in Rhodopseudomonas palustris.
8  in two strains of the anoxygenic phototroph Rhodopseudomonas palustris.
9 he nonsulfur purple photosynthetic bacterium Rhodopseudomonas palustris.
10 e nonsulfur anoxygenic phototropic bacterium Rhodopseudomonas palustris.
11 ters in Escherichia coli and nitrogenases in Rhodopseudomonas palustris.
12 he wild-type light harvesting 2 complexes of Rhodopseudomonas palustris.
13  on a complex ribosomal protein mixture from Rhodopseudomonas palustris.
14 om digested ribosomal proteins isolated from Rhodopseudomonas palustris.
15 radation by the photoheterotrophic bacterium Rhodopseudomonas palustris.
16 een described for the phototrophic bacterium Rhodopseudomonas palustris.
17 d compounds from the phototrophic bacterium, Rhodopseudomonas palustris.
18 nd sequenced from the phototrophic bacterium Rhodopseudomonas palustris.
19 lation efficiency over a range of genes from Rhodopseudomonas palustris and E. coli was achieved usin
20 ranscriptional activator, similar to AadR of Rhodopseudomonas palustris and FixK proteins of rhizobia
21 of p-coumarate by the phototrophic bacterium Rhodopseudomonas palustris and found that it also follow
22 wo related LuxI homologs, RpaI and BtaI from Rhodopseudomonas palustris and photosynthetic stem-nodul
23 trogenase, including Azotobacter vinelandii, Rhodopseudomonas palustris, and Methanosarcina barkeri.
24 totacticum, Novosphingobium aromaticivorans, Rhodopseudomonas palustris, and Thermus thermophilus.
25 ere, we developed the anoxygenic phototroph, Rhodopseudomonas palustris, as a biocatalyst capable of
26                            This enzyme, from Rhodopseudomonas palustris, assembles as a unique hexame
27                                              Rhodopseudomonas palustris assimilates CO2 by the Calvin
28       In the purple photosynthetic bacterium Rhodopseudomonas palustris, at least 10 AMP-forming acyl
29 ome BphP1 and its natural partner PpsR2 from Rhodopseudomonas palustris bacteria.
30  enzyme of anaerobic benzoate degradation by Rhodopseudomonas palustris, benzoyl coenzyme A (CoA) red
31 ucturally characterize enzymes of the GRM of Rhodopseudomonas palustris BisB18 and demonstrate their
32 was purified from the phototrophic bacterium Rhodopseudomonas palustris by sequential Q-Sepharose, ph
33                       The genome sequence of Rhodopseudomonas palustris CGA009 revealed a surprising
34                                           In Rhodopseudomonas palustris CGA010, the LysR type regulat
35 rowing cells of the photosynthetic bacterium Rhodopseudomonas palustris continue to metabolize acetat
36                             Reduced (Fe(II)) Rhodopseudomonas palustris cytochrome c' (Cyt c') is mor
37 gy transfer kinetics during the refolding of Rhodopseudomonas palustris cytochrome c' reveals dramati
38 me loop formation for iso-1-cytochrome c and Rhodopseudomonas palustris cytochrome c', shows that fol
39 s in the anoxygenic photosynthetic bacterium Rhodopseudomonas palustris, designated regulatory protei
40 plexes has been investigated in membranes of Rhodopseudomonas palustris grown under high- and low-lig
41 bolic fluxes in the photosynthetic bacterium Rhodopseudomonas palustris grown with (13)C-labeled acet
42                                              Rhodopseudomonas palustris grows photoheterotrophically
43  4-hydroxybenzoate (4-HBA) to benzoyl-CoA by Rhodopseudomonas palustris have been identified.
44 totrophic bacteria Rhodospirillum rubrum and Rhodopseudomonas palustris In vivo metabolite analysis o
45              Quorum sensing in the bacterium Rhodopseudomonas palustris involves the RpaI signal synt
46                                              Rhodopseudomonas palustris is a purple, facultatively ph
47                                              Rhodopseudomonas palustris is among the most metabolical
48                 The photosynthetic bacterium Rhodopseudomonas palustris is one of just a few prokaryo
49                                              Rhodopseudomonas palustris is unique among characterized
50                         The photoheterotroph Rhodopseudomonas palustris is unusual in that it produce
51                                              Rhodopseudomonas palustris metabolizes aromatic compound
52      CYP199A2, a cytochrome P450 enzyme from Rhodopseudomonas palustris, oxidatively demethylates 4-m
53 ssion of the cbb(I) CO(2) fixation operon of Rhodopseudomonas palustris, possibly in response to a re
54 nspect, based on benchmarking results from a Rhodopseudomonas palustris proteomics dataset.
55                         The cbb(I) region of Rhodopseudomonas palustris (Rp. palustris) contains the
56 th of Rhodospirillum rubrum (Rs. rubrum) and Rhodopseudomonas palustris (Rp. palustris) RubisCO-defic
57     The protein acetyltransferase (Pat) from Rhodopseudomonas palustris (RpPat) inactivates AMP-formi
58 ight harvesting 1 (RC-LH1) core complex from Rhodopseudomonas palustris shows the reaction center sur
59                                              Rhodopseudomonas palustris strain JSC-3b isolated from a
60                                              Rhodopseudomonas palustris strain RCB100 degrades 3-chlo
61  show that the iron-oxidizing photoautotroph Rhodopseudomonas palustris TIE-1 accepts electrons from
62 r the phototrophic Fe(II)-oxidizing bacteria Rhodopseudomonas palustris TIE-1 and the Fe(III)-reducin
63           Here we report the discovery, with Rhodopseudomonas palustris TIE-1 as a model organism, of
64                         The purple bacterium Rhodopseudomonas palustris TIE-1 expresses multiple smal
65                                              Rhodopseudomonas palustris TIE-1 is a gram-negative bact
66  the phototrophic Fe(II)-oxidizing bacterium Rhodopseudomonas palustris TIE-1 oxidizes magnetite (Fe3
67 eport the physiological study of a mutant in Rhodopseudomonas palustris TIE-1 that is unable to produ
68                                 Here, we use Rhodopseudomonas palustris TIE-1 to identify factors tha
69 trophic) growth by the alpha-proteobacterium Rhodopseudomonas palustris TIE-1.
70 es of the model hopanoid-producing bacterium Rhodopseudomonas palustris TIE-1.
71 denosylmethionine (SAM) methyltransfase from Rhodopseudomonas palustris to remove arsenic from contam
72                                          The Rhodopseudomonas palustris transcriptional regulator Rpa
73  purple photosynthetic alpha-proteobacterium Rhodopseudomonas palustris, two protein acetyltransferas
74 re we show that the photosynthetic bacterium Rhodopseudomonas palustris uses an acyl-HSL synthase to
75         Heterologous expression of arsM from Rhodopseudomonas palustris was shown to confer As(III) r
76 nd RpBphP3 from the photosynthetic bacterium Rhodopseudomonas palustris work in tandem to modulate sy

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