コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 was with the membrane-bound hydrogenase from Rhodospirillum rubrum.
2 cell curvature in the photosynthetic species Rhodospirillum rubrum.
3 se domains of GlnD from Escherichia coli and Rhodospirillum rubrum.
4 r used in the anaerobic energy metabolism of Rhodospirillum rubrum.
5 imilar to those measured for native LH1 from Rhodospirillum rubrum.
6 ription of genes involved in CO oxidation in Rhodospirillum rubrum.
7 of the genes responsible for CO oxidation in Rhodospirillum rubrum.
8 oA is a dimeric CO-sensing heme protein from Rhodospirillum rubrum.
9 n identified in the photosynthetic bacterium Rhodospirillum rubrum.
10 rotein transcription factor of the bacterium Rhodospirillum rubrum.
11 d previously in the photosynthetic bacterium Rhodospirillum rubrum.
12 mely, Rb. sphaeroides, P. denitrificans, and Rhodospirillum rubrum.
13 ired for utilizing CO as an energy source in Rhodospirillum rubrum.
14 of carbon monoxide dehydrogenase (CODH) from Rhodospirillum rubrum.
15 nsformed by plasmids carrying dra genes from Rhodospirillum rubrum.
16 reductase ADP-ribosyltransferase (DRAT) from Rhodospirillum rubrum.
17 but resembles that of the CO sensor CooA of Rhodospirillum rubrum.
18 ethanosarcina barkeri, Escherichia coli, and Rhodospirillum rubrum.
19 of CO to CO(2) in the phototrophic bacterium Rhodospirillum rubrum.
20 ructures, including the form II homolog from Rhodospirillum rubrum.
21 complex (LH1) of Rhodobacter sphaeroides or Rhodospirillum rubrum.
22 hate for nonmevalonate isoprene synthesis in Rhodospirillum rubrum.
23 the carbon monoxide dehydrogenase (CODH) of Rhodospirillum rubrum.
24 es in the spiral-shaped alphaproteobacterium Rhodospirillum rubrum again reveal a close association o
25 adenosine and 5'-methylthioadenosine in both Rhodospirillum rubrum and Extraintestinal Pathogenic Esc
26 e consisting of alpha and beta subunits from Rhodospirillum rubrum and gamma subunit from spinach chl
28 regulatory system, has been characterized in Rhodospirillum rubrum and other nitrogen-fixing bacteria
29 the nonsulfur purple photosynthetic bacteria Rhodospirillum rubrum and Rhodobacter sphaeroides, conta
31 ylene formation in the phototrophic bacteria Rhodospirillum rubrum and Rhodopseudomonas palustris In
32 he photosynthetic, nitrogen-fixing bacterium Rhodospirillum rubrum and the analysis of the roles of G
33 the highest identity with the cbbM gene from Rhodospirillum rubrum, and analysis of the inferred amin
34 quired cofactor for anaerobic respiration in Rhodospirillum rubrum, and it is also found in several h
36 the same mean diameter as the LH1 rings from Rhodospirillum rubrum ( approximately 90 A) and therefor
37 Nitrogen fixation is tightly regulated in Rhodospirillum rubrum at two different levels: transcrip
38 ammaC) and the cloned alpha subunit from the Rhodospirillum rubrum ATP synthase (alphaR) was assemble
39 n monoxide-sensing transcription factor from Rhodospirillum rubrum, binds CO at a reduced (Fe(II)) he
40 n monoxide-sensing transcription factor from Rhodospirillum rubrum, binds CO through a heme moiety re
41 urple nonsulfur photosynthetic bacteria like Rhodospirillum rubrum can acquire electrons by multiple
42 Carbon monoxide dehydrogenase (CODH) from Rhodospirillum rubrum catalyzes both the oxidation of CO
43 , reduced, and CO-bound reduced forms of the Rhodospirillum rubrum CO oxidation transcriptional activ
45 Fe, whereas the same cluster in enzymes from Rhodospirillum rubrum (CODH(Rr)) and Moorella thermoacet
46 Carbon-monoxide dehydrogenase (CODH) from Rhodospirillum rubrum contains two metal centers: a Ni-X
47 tal-binding site on the inner surface of the Rhodospirillum rubrum encapsulated ferritin at the inter
48 ginine hydrolases from mammalian tissues and Rhodospirillum rubrum exhibit three regions of similarit
49 entoxin-insensitive photosynthetic bacterium Rhodospirillum rubrum F(1) (RrF(1)), was stimulated but
50 d together with alpha and beta subunits from Rhodospirillum rubrum F1 into a hybrid photosynthetic F1
51 (fMetTrpArg) of the LH1 alpha-polypeptide of Rhodospirillum rubrum form a cluster that is most likely
52 hesis of polyhydroxyalkanoates (PHAs) in the Rhodospirillum rubrum genome revealed by the occurrence
55 -S carbon monoxide dehydrogenase (CODH) from Rhodospirillum rubrum has been determined to 2.8-A resol
56 reductase ADP-ribosyltransferase (DRAT) from Rhodospirillum rubrum has been investigated with a cross
57 nifH mutant of the photosynthetic bacterium Rhodospirillum rubrum has been purified and characterize
58 (RC-LH1) of the purple non- sulfur bacterium Rhodospirillum rubrum have been formed from detergent-so
59 In carbon monoxide dehydrogenase (CODH) from Rhodospirillum rubrum, histidine 265 was replaced with v
60 he CO-sensing transcriptional activator from Rhodospirillum rubrum, in which CO binding to its heme p
61 arbon monoxide, the photosynthetic bacterium Rhodospirillum rubrum induces expression of proteins whi
64 O enzyme from the nonsulfur purple bacterium Rhodospirillum rubrum is also able to function as an eno
65 BluB protein of the photosynthetic bacterium Rhodospirillum rubrum is necessary and sufficient for ca
66 tations that correct such growth problems in Rhodospirillum rubrum mutants lacking P(II) proteins.
69 ly partially understood, and we show that in Rhodospirillum rubrum one P(II) homolog, GlnJ, has highe
71 Here we show that denatured RuBisCO from Rhodospirillum rubrum populates a stable, nonaggregating
73 smus quadricauda proteins, and Cu binding to Rhodospirillum rubrum proteins and pigments are shown.
74 CO-responsive transcription factor CooA from Rhodospirillum rubrum provides evidence on the nature of
75 he CO-sensing transcriptional regulator from Rhodospirillum rubrum, reacts with NO to form a five-coo
78 onoxide dehydrogenase in the proteobacterium Rhodospirillum rubrum requires three accessory proteins,
80 in the purple bacteria (Chromatium vinosum, Rhodospirillum rubrum, Rhodobacter sphaeroides, and Rhod
81 of Rhodobacter sphaeroides (sph beta 31) or Rhodospirillum rubrum (rr beta 31) could form subunit-ty
82 eminate CO rebinding in two CooA homologues, Rhodospirillum rubrum (RrCooA) and Carboxydothermus hydr
84 t RuBP accumulation can impede the growth of Rhodospirillum rubrum (Rs. rubrum) and Rhodopseudomonas
85 of carbon monoxide dehydrogenase (CODH) from Rhodospirillum rubrum show that CODH is mostly inactive
86 chia coli, thermophilic Bacillus strain PS3, Rhodospirillum rubrum, spinach chloroplasts, and the cya
87 rogenase reductases also were expressed in a Rhodospirillum rubrum strain that lacked its endogenous
90 NAD(H) binding alpha1 subunit (domain I) of Rhodospirillum rubrum TH have been determined at 1.8 A r
91 is a CO-sensing transcription activator from Rhodospirillum rubrum that binds specific DNA sequences
92 hat the H(+)-pyrophosphatase (H(+)-PPase) of Rhodospirillum rubrum, the first enzyme of this type tha
94 e-based sensor CooA regulates the ability of Rhodospirillum rubrum to grow on CO as an energy source.
95 ining transcriptional activator that enables Rhodospirillum rubrum to sense and grow on CO as a sole
97 dI and dIII (the dI(2)dIII(1) complex) from Rhodospirillum rubrum transhydrogenase catalyzes fast si
98 in the NAD(H)-binding component (dI) of the Rhodospirillum rubrum transhydrogenase was substituted w
99 designated H2NADH) bound to isolated dI from Rhodospirillum rubrum transhydrogenase with similar affi
101 ing homodimeric transcription activator from Rhodospirillum rubrum, undergoes a conformational change
102 Carbon monoxide dehydrogenase (CODH) from Rhodospirillum rubrum utilizes three types of Fe-S clust
104 hanism of the transcription factor CooA from Rhodospirillum rubrum was studied through a systematic m
105 protein from the CO dehydrogenase system of Rhodospirillum rubrum, was purified by immobilized metal
106 mutations and metabolomics in the bacterium Rhodospirillum rubrum, we show here that Rubisco concurr
107 ctase-activating glycohydrolase (DRAG), from Rhodospirillum rubrum, were shown to be sensitive to the
108 purified from the chromatophore membranes of Rhodospirillum rubrum with a 3,464-fold purification and