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1                                              R. eutropha is engineered to heterologously express an e
2                                              R. eutropha phaC PHA synthase and phaP phasin gene repla
3                                              R. eutropha strains with phaR, phaC, and/or phaP deletio
4 binant PhaP, antibodies against PhaP, and an R. eutropha phaP deletion strain have been generated for
5 tributed to the beta-ketothiolase encoded by R. eutropha phbA.
6 tentially offers a means to use and engineer R. eutropha for efficient chemical production coupled wi
7 s with the wild-type (H16) and an engineered R. eutropha strain for short- and or medium-chain-length
8 e ETC to regenerate NADH/NADPH, facilitating R. eutropha's biomass synthesis from CO(2).
9 down assays with crude protein extracts from R. eutropha Re2058/pCB113, followed by liquid chromatogr
10 ion of candidate PHB depolymerase genes from R. eutropha, namely, phaZ2 and phaZ3, and their characte
11  of conserved cysteine residues in HypD from R. eutropha was investigated.
12 bktB, which encodes a beta-ketothiolase from R. eutropha that is capable of forming beta-ketovaleryl-
13 f PhaZ2 and PhaZ3 was examined by generating R. eutropha H16 deletion strains (Delta phaZ1, Delta pha
14 tion of HoxR protein from its original host, R. eutropha, revealed only low protein amounts.
15  is the limiting step in PHB biosynthesis in R. eutropha H16 during nitrogen-limited growth on fructo
16 ding these enzymatic steps was discovered in R. eutropha and has been well studied.
17 ent physiological and ecological function in R. eutropha.
18 lglycerol and fatty acid catabolism genes in R. eutropha.
19 tify two new candidate depolymerase genes in R. eutropha: phaZ2 and phaZ3.
20 hts into the regulation of PHA metabolism in R. eutropha, uncovering specific interactions of novel t
21 ntly created genus Ralstonia, which includes R. eutropha, R. pickettii, and R. solanacearum.
22 iven proton motive force are integrated into R. eutropha's native electron transport chain (ETC).
23 s permit uptake of radiolabeled sucrose into R. eutropha cells.
24                     Moreover, engineering of R. eutropha enabled production of the fusel alcohol isop
25 tially supports the emulsion-based growth of R. eutropha on plant oils.
26 compare whole-cell gene expression levels of R. eutropha H16 during growth and polyhydroxyalkanoate p
27            Analysis of a phcA-null mutant of R. eutropha showed that phcA (and probably Phc) positive
28 le beta-oxidation operon deletion mutants of R. eutropha could grow using palm oil or crude palm kern
29                We also demonstrate that some R. eutropha produce an extracellular factor that complem
30                           We could show that R. eutropha DNA-binding xenobiotic response element-fami
31      Although our data strongly suggest that R. eutropha has a functional Phc-like system and support
32                     The results suggest that R. eutropha has evolved a regulatory mechanism that can
33 n blot hybridization analysis suggested that R. eutropha harbours other Phc components, such as PhcB
34 I synthases revealed similar residues in the R. eutropha synthase.
35               Sequencing and analysis of the R. eutropha genome revealed putative isologs for each of
36                              Transfer of the R. eutropha phaR, phaP, and PHA biosynthesis (phaCAB) ge
37         These primers and PCR methods on the R. eutropha genome were used to identify two new candida
38                               Similarly, the R. eutropha phcA mutant was unaffected in siderophore pr
39                These studies reveal that the R. eutropha synthase possesses an essential catalytic dy
40 l system splits water to supply electrons to R. eutropha via the Mtr outer-membrane route.