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1 om Escherichia coli, Pseudomonas putida, and Ralstonia eutropha.
2 now rigorously tested for the phasin PhaP of Ralstonia eutropha.
3 -dependent FdsABG formate dehydrogenase from Ralstonia eutropha.
4        Wautersia eutropha, formerly known as Ralstonia eutropha, a gram-negative bacterium, accumulat
5 ng frame (ORF) encoding a homolog of NosX of Ralstonia eutropha, a putative maturation factor of nitr
6 -pathogenic, facultative chemolithoautotroph Ralstonia eutropha (Alcaligenes eutrophus) that fully co
7 rive photoelectrosynthetic CO(2) fixation by Ralstonia eutropha (also known as Cupriavidus necator) H
8 III polyhydroxybutyrate (PHB) synthases from Ralstonia eutropha and Chromatium vinosum, respectively,
9 lysis that the purified HypCD complexes from Ralstonia eutropha and Escherichia coli carry in additio
10 y recently reported for similar enzymes from Ralstonia eutropha and Hydrogenovibrio marinus, two supe
11 he highest 16S rRNA gene similarity was with Ralstonia eutropha and Ralstonia solanacearum.
12 identity with the nitric oxide reductases in Ralstonia eutropha and Synechocystis sp. and, like those
13 ar-native, "frozen-hydrated" state in intact Ralstonia eutropha cells.
14  When grown in contact with these catalysts, Ralstonia eutropha consumed the produced H2 to synthesiz
15 NAD(+)-reducing [NiFe] hydrogenase (SH) from Ralstonia eutropha couples the reversible cleavage of H2
16 or two model organisms, the 'Proteobacteria' Ralstonia eutropha (epsilon = 19.0 per mille) and Rhodob
17 drogenases in the lithoautotrophic bacterium Ralstonia eutropha for bioplastic formation, discover th
18 toglutarate (alpha-KG)-dioxygenase (TfdA) in Ralstonia eutropha (formerly Alcaligenes eutrophus) JMP1
19                                The bacterium Ralstonia eutropha forms cytoplasmic granules of polyhyd
20                          Here we report that Ralstonia eutropha H16 (Cupriavidus necator ATCC 17699)
21                                              Ralstonia eutropha H16 is capable of growth and polyhydr
22                                The bacterium Ralstonia eutropha H16 synthesizes polyhydroxybutyrate (
23  [NiFe] hydrogenase (MBH) supports growth of Ralstonia eutropha H16 with H2 as the sole energy source
24 chemolithoautotroph Cupriavidus necator H16 (Ralstonia eutropha H16) by characterizing the proxy proc
25 engineered a lithoautotrophic microorganism, Ralstonia eutropha H16, to produce isobutanol and 3-meth
26 NAD(+)-reducing [NiFe]-hydrogenase (SH) from Ralstonia eutropha H16.
27                      Here the phasin PhaP of Ralstonia eutropha has been analyzed with regard to its
28         Here, the full heterotrimeric MBH of Ralstonia eutropha, including the membrane-integral cyto
29 lectrochemical system in which the bacterium Ralstonia eutropha is used to efficiently convert CO2, a
30                                              Ralstonia eutropha JMP134 2,4,6-trichlorophenol (2,4,6-T
31                                              Ralstonia eutropha JMP134 can grow on several chlorinate
32        Here we have tested the effect of the Ralstonia eutropha PhaR protein on the regulation of Pha
33                                              Ralstonia eutropha produces both the homopolymer poly-be
34 ne-bound [NiFe]-hydrogenase from the aerobe, Ralstonia eutropha, reacts reversibly with O2 even durin
35 orage, and degradation in the model organism Ralstonia eutropha remains limited.
36 ogenase (SH) of aerobic beta-proteobacterium Ralstonia eutropha strain H16 to accomplish ambient, ele
37                                              Ralstonia eutropha (syn.
38 etoglutarate dioxygenase and 27% identity to Ralstonia eutropha TfdA, a herbicide-degrading enzyme.
39 ed a segment of S. meliloti DNA which allows Ralstonia eutropha to grow on the alpha-glucosides sucro
40 ss I PhaC from Cupriavidus necator (formerly Ralstonia eutropha) to 1.80 A resolution.
41  from Cupriavidus necator (formerly known as Ralstonia eutropha) to catalyze the reverse of the physi
42 acellular PHB depolymerase gene (phaZ1) from Ralstonia eutropha was identified.
43                                Surprisingly, Ralstonia eutropha was the dominant group.
44 ce that were fed with (15)N hydrolysate from Ralstonia eutropha, we identified 12 326 nonredundant un
45    Here we show that the aerobic H2 oxidizer Ralstonia eutropha, which produces active [NiFe]-hydroge