ライフサイエンスコーパス: Ralstonia eutropha

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1 -dependent FdsABG formate dehydrogenase from Ralstonia eutropha.

2 now rigorously tested for the phasin PhaP of Ralstonia eutropha.

3 Wautersia eutropha, formerly known as Ralstonia eutropha, a gram-negative bacterium, accumulat

4 ng frame (ORF) encoding a homolog of NosX of Ralstonia eutropha, a putative maturation factor of nitr

5 -pathogenic, facultative chemolithoautotroph Ralstonia eutropha (Alcaligenes eutrophus) that fully co

6 III polyhydroxybutyrate (PHB) synthases from Ralstonia eutropha and Chromatium vinosum, respectively,

7 lysis that the purified HypCD complexes from Ralstonia eutropha and Escherichia coli carry in additio

8 y recently reported for similar enzymes from Ralstonia eutropha and Hydrogenovibrio marinus, two supe

9 he highest 16S rRNA gene similarity was with Ralstonia eutropha and Ralstonia solanacearum.

10 identity with the nitric oxide reductases in Ralstonia eutropha and Synechocystis sp. and, like those

11 ar-native, "frozen-hydrated" state in intact Ralstonia eutropha cells.

12 When grown in contact with these catalysts, Ralstonia eutropha consumed the produced H2 to synthesiz

13 NAD(+)-reducing [NiFe] hydrogenase (SH) from Ralstonia eutropha couples the reversible cleavage of H2

14 toglutarate (alpha-KG)-dioxygenase (TfdA) in Ralstonia eutropha (formerly Alcaligenes eutrophus) JMP1

15 The bacterium Ralstonia eutropha forms cytoplasmic granules of polyhyd

16 Ralstonia eutropha H16 is capable of growth and polyhydr

17 The bacterium Ralstonia eutropha H16 synthesizes polyhydroxybutyrate (

18 [NiFe] hydrogenase (MBH) supports growth of Ralstonia eutropha H16 with H2 as the sole energy source

19 engineered a lithoautotrophic microorganism, Ralstonia eutropha H16, to produce isobutanol and 3-meth

20 NAD(+)-reducing [NiFe]-hydrogenase (SH) from Ralstonia eutropha H16.

21 Here the phasin PhaP of Ralstonia eutropha has been analyzed with regard to its

22 Here, the full heterotrimeric MBH of Ralstonia eutropha, including the membrane-integral cyto

23 lectrochemical system in which the bacterium Ralstonia eutropha is used to efficiently convert CO2, a

24 Ralstonia eutropha JMP134 2,4,6-trichlorophenol (2,4,6-T

25 Ralstonia eutropha JMP134 can grow on several chlorinate

26 Here we have tested the effect of the Ralstonia eutropha PhaR protein on the regulation of Pha

27 Ralstonia eutropha produces both the homopolymer poly-be

28 ne-bound [NiFe]-hydrogenase from the aerobe, Ralstonia eutropha, reacts reversibly with O2 even durin

29 ogenase (SH) of aerobic beta-proteobacterium Ralstonia eutropha strain H16 to accomplish ambient, ele

30 etoglutarate dioxygenase and 27% identity to Ralstonia eutropha TfdA, a herbicide-degrading enzyme.

31 ed a segment of S. meliloti DNA which allows Ralstonia eutropha to grow on the alpha-glucosides sucro

32 ss I PhaC from Cupriavidus necator (formerly Ralstonia eutropha) to 1.80 A resolution.

33 from Cupriavidus necator (formerly known as Ralstonia eutropha) to catalyze the reverse of the physi

34 acellular PHB depolymerase gene (phaZ1) from Ralstonia eutropha was identified.

35 Surprisingly, Ralstonia eutropha was the dominant group.

36 Here we show that the aerobic H2 oxidizer Ralstonia eutropha, which produces active [NiFe]-hydroge

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