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1 A after integration of this oxygen-respiring eubacterium.
2 phic merger between an archaebacterium and a eubacterium.
3 a, generated hydrogen sulfide to protect the eubacterium, a heterotrophic swimmer comparable to Spiro
7 tilizing bacteria producing butyrate, namely Eubacterium and Anaerostipes species, supported by incre
8 cluster resembling that from a gram-positive eubacterium and the other resembling a eubacterial V nit
9 roides, Oscillospira, Blautia, Ruminococcus, Eubacterium, and Christensenella species in the RS4 grou
10 nella, Tannerella, Streptococcus, Atopobium, Eubacterium, and Treponema were elevated in disease.
11 dy, the PilT homologue from the thermophilic eubacterium Aquifex aeolicus was cloned, overexpressed,
14 , CBM65A and CBM65B, derived from EcCel5A, a Eubacterium cellulosolvens endoglucanase, bind to a rang
17 M. smegmatis as the first known example of a eubacterium containing both Lon and a complete 20S prote
18 occus faecium, E. coli, Streptococcus avium, Eubacterium contortum, Peptostreptococcus productus, and
19 , and a Ro ortholog enhances survival of the eubacterium Deinococcus radiodurans after ultraviolet ir
20 s homolog encoded by the radiation-resistant eubacterium Deinococcus radiodurans and show that DNA bi
22 orthologue of Ro in the radiation-resistant eubacterium Deinococcus radiodurans contributes to survi
23 that a Ro protein in the radiation-resistant eubacterium Deinococcus radiodurans participates in ribo
26 all eukaryotic genomes whereas the number of eubacterium-derived genes is much more variable, suggest
27 rchaebacterium Methanococcus jannaschii, the eubacterium Escherichia coli, and the nematode, Caenorha
31 noma infections included those in the genera Eubacterium, Flavobacterium, Kocuria, Microbacterium, an
32 of Lactobacillus bulgaricus, a gram-positive eubacterium, for the conversion by an amidotransferase o
33 genera Capnocytophaga, Cytophaga, Dialister, Eubacterium, Fusobacterium, Gemella, Mogibacterium, Pept
34 coccus cristatus, Capnocytophaga gingivalis, Eubacterium IR009, Campylobacter rectus, and Lachnospira
35 ance of a bacterial group composed mostly of Eubacterium limosum in the validation set was associated
36 entified in the obligate anaerobic bacterium Eubacterium limosum, is composed of five previously unch
37 ns, and co-occurrence analysis revealed that Eubacterium minutum was correlated with Prevotella inter
38 We have shown that the genetically tractable eubacterium Mycobacterium smegmatis contains a 20S prote
40 a (86%/62%), Campylobacter rectus (90%/76%), Eubacterium nodatum (64%/30%), Prevotella intermedia (58
41 associated with periodontitis, whereas high Eubacterium nodatum titers were associated with periodon
42 e (which included Actinomyces naeslundii and Eubacterium nodatum) was inversely associated (OR = 0.93
43 ae, Prevotella intermedia, Parvimonas micra, Eubacterium nodatum, and Campylobacter gracilis, a signi
45 This genome fusion between a deep branching eubacterium, possibly an ancestor of the cyanobacterium
46 We describe properties of the recently found eubacterium proton pump from Exiguobacterium sibiricum (
47 lostridium, Lactobacillus, Ruminococcus, and Eubacterium, ranging from 4% to 19% relative abundance).
48 ridium coccoides (cluster XIVa), C coccoides-Eubacterium rectale (cluster XIVab), Bacteroidetes, and
49 relative abundance of Bacteroides, Roseburia-Eubacterium rectale and Bifidobacterium and an increase
50 inished genome sequences were generated from Eubacterium rectale and E. eligens, which belong to Clos
51 n some cases, discrete subspecies (e.g., for Eubacterium rectale and Prevotella copri) or continuous
53 t also known as the Clostridium coccoides or Eubacterium rectale group, contains species that have ev
61 thensis (37.9%), Capnocytophaga sp. (36.9%), Eubacterium saburreum (32.7%), Campylobacter rectus (17.
62 species (Cs), Porphyromonas gingivalis (Pg), Eubacterium saburreum (Es), and Fusobacterium nucleatum
64 lifactor alocis, Treponema lecithinolyticum, Eubacterium saphenum, Desulfobulbus sp./OT041, and Mogib
65 5 from the TM7 phylum, and the named species Eubacterium saphenum, Porphyromonas endodontalis, Prevot
66 tructures of the THF-sensing domain from the Eubacterium siraeum riboswitch in the ligand-bound and u
68 to an alpha-hydroxysteroid dehydrogenase of Eubacterium sp. strain VPI 12708, a 25-kDa protein corre
71 ntermedia/nigrescens, Bacteroides forsythus, Eubacterium species, Campylobacter species, Fusobacteriu
72 were analyzed by differential isolation and eubacterium-specific PCR-denaturing gradient gel electro
73 ter spp., Selenomonas spp., Catonella morbi, Eubacterium spp., Filifactor alocis, Parvimonas micra, P
75 lum, a phylotype (clone BS095) of Dialister, Eubacterium sulci, a phylotype (clone DR034) of the uncu
77 etrans is a gram-positive, endospore-forming eubacterium that apparently is a member of the Bacillus-
78 otes as a fusion of an archaebacterium and a eubacterium that could not have been observed using phyl
81 properties of HU from the hyperthermophilic eubacterium Thermotoga maritima are shown here to differ
82 show here that HU from the hyperthermophilic eubacterium Thermotoga maritima HU bends DNA and constra
84 adenylosuccinate lyase from the thermophilic eubacterium Thermotoga maritima, the archaebacterial lya
85 tone-like protein from the hyperthermostable eubacterium Thermotoga maritima, TmHU as an efficient ge
87 de dismutase from the extremely thermophilic eubacterium Thermus thermophilus has been cloned and exp
90 exporter from the thermophilic Gram-negative eubacterium Thermus thermophilus; it is homologous to va
93 equence of strain 195 indicated that it is a eubacterium without close affiliation to any known group
94 ured Lachnospiraceae (Firmicutes) related to Eubacterium xylanophilum and Butyrivibrio spp. were stro
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