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1 R. rubrum puf interposon mutants do not form intracytopl
3 f the redox dependence of CO(2) reduction by R. rubrum CODH show that (1) CODH is unable to catalyze
4 the gas-sensing regulation mechanism used by R. rubrum CooA and its homologs in other organisms, we c
5 Instead, under aerobic growth conditions, R. rubrum RLP employs another intermediate of the MSP, 5
6 recently described hybrid enzyme containing R. rubrum alpha and beta subunits and the CF1 gamma subu
10 I) and Escherichia coli (ecI), and dIII from R. rubrum (rrIII) and E. coli (ecIII) were overexpressed
12 -fold more efficient than DraT purified from R. rubrum, but with a similar K(m) value for NAD(+).
13 an be functionally promiscuous, RuBisCO from R. rubrum is not promiscuous for either of the known RLP
14 We then examined the ability of RuBisCO from R. rubrum to catalyze both of the RLP-catalyzed reaction
15 thionine in polyamine biosynthesis; however, R. rubrum lacks the classical methionine salvage pathway
18 required for activation of NifA activity in R. rubrum, GlnK and GlnJ do not appear to be involved in
20 When examined for physiological effects in R. rubrum, these GlnB* variants activated NifA in the pr
23 The effect of the lack of bluB function in R. rubrum was reflected by the impaired ability of a Del
25 resence of functional, yet separate, MSPs in R. rubrum under both aerobic (chemoheterotrophic) and an
29 causative basis for the poor growth seen in R. rubrum mutants lacking P(II) and presumably in mutant
31 r uptake and accumulation of (63)Ni(2+) into R. rubrum and to observe the effect of mutations in the
33 DPH (H2NADPH) bound very tightly to isolated R. rubrum dIII, but the rate constant for dissociation w
34 ne encoding the RLP abolishes the ability of R. rubrum to utilize 5'-methylthioadenosine as a sole su
35 The identification of the acidocalcisomes of R. rubrum was carried out by using transmission electron
37 s, we studied the heterologous expression of R. rubrum draTG in Klebsiella pneumoniae glnB and glnK m
38 PHA accumulation in enhancing the fitness of R. rubrum was indicated by the relationship between PHA
40 these results suggest that the H(+)-PPase of R. rubrum has two distinct roles depending on its locati
42 e results indicate that the C(red1) state of R. rubrum CODH (E(m) = -110 mV; g(zyx)() = 2.03, 1.88, 1
43 mplete genome sequence of a mutant strain of R. rubrum (F11), which cannot grow anaerobically and doe
44 ucture is also compared to the structures of R. rubrum domain I with NAD bound (PDB code 1F8G) and wi
48 ibiting low (<20%) activity with 87% reduced R. rubrum Fe protein relative to activity with fully oxi
49 ependent transcription of the CooA-regulated R. rubrum promoter PcooF in vitro, which indicates that
50 ast few dissimilar residues from the related R. rubrum homolog increased the enzyme's kcat for carbox
53 quired to sustain CO-dependent growth of the R. rubrum mutants demonstrated different phenotypes: whe
56 e generated a deletion mutant from wild-type R. rubrum by the targeted replacement of rquA with a gen
59 ibe several in vivo feeding experiments with R. rubrum used for the identification of RQ biosynthetic
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