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1 rmentative Escherichia coli and phototrophic Rhodopseudomonas palustris.
2 phototrophic growth by the purple bacterium Rhodopseudomonas palustris.
3 he wild-type light harvesting 2 complexes of Rhodopseudomonas palustris.
4 pounds, using the purple nonsulfur bacterium Rhodopseudomonas palustris.
5 nd meta-hydroxybenzoate, was investigated in Rhodopseudomonas palustris.
6 rylation and other major metabolic traits in Rhodopseudomonas palustris.
7 ass II c-type cytochrome, cytochrome c' from Rhodopseudomonas palustris.
8 as part of an interactome mapping project in Rhodopseudomonas palustris.
9 in two strains of the anoxygenic phototroph Rhodopseudomonas palustris.
10 he nonsulfur purple photosynthetic bacterium Rhodopseudomonas palustris.
11 e nonsulfur anoxygenic phototropic bacterium Rhodopseudomonas palustris.
12 ters in Escherichia coli and nitrogenases in 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 action between Geobacter metallireducens and Rhodopseudomonas palustris.
20 aproteobacteria, Rhodobacter sphaeroides and Rhodopseudomonas palustris.
21 A and B domains, represented by RpArsM from Rhodopseudomonas palustris.
22 croscopy structures of RC-LH1 complexes from Rhodopseudomonas palustris A 2.65-A resolution structure
23 idated a genome-scale model of metabolism in Rhodopseudomonas palustris, a metabolically versatile gr
24 ee of such genes from Ochrobactrum anthropi, Rhodopseudomonas palustris and Agrobacterium tumefaciens
25 lation efficiency over a range of genes from Rhodopseudomonas palustris and E. coli was achieved usin
26 ranscriptional activator, similar to AadR of Rhodopseudomonas palustris and FixK proteins of rhizobia
27 of p-coumarate by the phototrophic bacterium Rhodopseudomonas palustris and found that it also follow
28 wo related LuxI homologs, RpaI and BtaI from Rhodopseudomonas palustris and photosynthetic stem-nodul
29 We show that two other bacterial species, Rhodopseudomonas palustris and Shewanella putrefaciens,
30 trogenase, including Azotobacter vinelandii, Rhodopseudomonas palustris, and Methanosarcina barkeri.
31 totacticum, Novosphingobium aromaticivorans, Rhodopseudomonas palustris, and Thermus thermophilus.
32 BAC system from the photosynthetic bacterium Rhodopseudomonas palustris as the first member of the tr
33 ere, we developed the anoxygenic phototroph, Rhodopseudomonas palustris, as a biocatalyst capable of
38 enzyme of anaerobic benzoate degradation by Rhodopseudomonas palustris, benzoyl coenzyme A (CoA) red
39 ucturally characterize enzymes of the GRM of Rhodopseudomonas palustris BisB18 and demonstrate their
41 was purified from the phototrophic bacterium Rhodopseudomonas palustris by sequential Q-Sepharose, ph
47 rowing cells of the photosynthetic bacterium Rhodopseudomonas palustris continue to metabolize acetat
49 gy transfer kinetics during the refolding of Rhodopseudomonas palustris cytochrome c' reveals dramati
50 me loop formation for iso-1-cytochrome c and Rhodopseudomonas palustris cytochrome c', shows that fol
51 s in the anoxygenic photosynthetic bacterium Rhodopseudomonas palustris, designated regulatory protei
52 nerated four sets of puc deletion mutants in Rhodopseudomonas palustris, each encoding a single type
53 ilis and diguanylate cyclase rpHK1S-Z16 from Rhodopseudomonas palustris, enhancing their enzymatic ac
54 plexes has been investigated in membranes of Rhodopseudomonas palustris grown under high- and low-lig
55 bolic fluxes in the photosynthetic bacterium Rhodopseudomonas palustris grown with (13)C-labeled acet
59 totrophic bacteria Rhodospirillum rubrum and Rhodopseudomonas palustris In vivo metabolite analysis o
69 ssion of the cbb(I) CO(2) fixation operon of Rhodopseudomonas palustris, possibly in response to a re
71 d a synthetic community of phototrophs using Rhodopseudomonas palustris (R. palustris) and an enginee
72 f the closely related alpha-proteobacterium, Rhodopseudomonas palustris, revealed a small set of five
74 th of Rhodospirillum rubrum (Rs. rubrum) and Rhodopseudomonas palustris (Rp. palustris) RubisCO-defic
75 we identified a Ca(2+)-dependent enzyme from Rhodopseudomonas palustris (Rpa3624) and showed that it
77 The protein acetyltransferase (Pat) from Rhodopseudomonas palustris (RpPat) inactivates AMP-formi
78 ight harvesting 1 (RC-LH1) core complex from Rhodopseudomonas palustris shows the reaction center sur
81 the metabolically versatile photoheterotroph Rhodopseudomonas palustris, the type of carbon substrate
82 show that the iron-oxidizing photoautotroph Rhodopseudomonas palustris TIE-1 accepts electrons from
83 r the phototrophic Fe(II)-oxidizing bacteria Rhodopseudomonas palustris TIE-1 and the Fe(III)-reducin
88 the phototrophic Fe(II)-oxidizing bacterium Rhodopseudomonas palustris TIE-1 oxidizes magnetite (Fe3
89 eport the physiological study of a mutant in Rhodopseudomonas palustris TIE-1 that is unable to produ
94 denosylmethionine (SAM) methyltransfase from Rhodopseudomonas palustris to remove arsenic from contam
95 volved the anoxygenic phototrophic bacterium Rhodopseudomonas palustris to use formate as the sole ca
97 purple photosynthetic alpha-proteobacterium Rhodopseudomonas palustris, two protein acetyltransferas
98 re we show that the photosynthetic bacterium Rhodopseudomonas palustris uses an acyl-HSL synthase to
100 h reduces CO(2) to acetate, and diazotrophic Rhodopseudomonas palustris, which uses the acetate both
101 nd RpBphP3 from the photosynthetic bacterium Rhodopseudomonas palustris work in tandem to modulate sy