ライフサイエンスコーパス: proteobacteria

1 anisms within the phylum of M (in this case, Proteobacteria).

2 unreported ejection of polar motors by gamma-proteobacteria.

3 -oxidizing genes under sulfide stress in the Proteobacteria.

4 h the phyla Anaerolinea, Ignavibacteria, and Proteobacteria.

5 ectors encoded predominantly by 15 genera of Proteobacteria.

6 ability is probably widespread among aquatic proteobacteria.

7 ription factor CuxR in plant symbiotic alpha-proteobacteria.

8 tinal sites were dominated by Firmicutes and Proteobacteria.

9 acteroidetes, Firmicutes, Actinobacteria and Proteobacteria.

10 a(13)C taxa, with methane-metabolizing gamma-proteobacteria.

11 present in beta-, gamma-, delta- and epsilon-proteobacteria.

12 ately drawn from the phyla Bacteroidetes and Proteobacteria.

13 Fusobacteria, Firmicutes, Actinobacteria and Proteobacteria.

14 red community dominated by Acidobacteria and Proteobacteria.

15 bacteria, NBs are found exclusively in gamma-proteobacteria.

16 rides reduced the prevalence of inflammatory Proteobacteria.

17 LB), is a non culturable member of the alpha-proteobacteria.

18 teins from beta-, gamma-, delta- and epsilon-proteobacteria.

19 ran-2-yl) nonanoate (9D5-FuFA), in two alpha-proteobacteria.

20 nolytic gene clusters from Bacteroidetes and Proteobacteria.

21 free-living and obligate intracellular alpha-proteobacteria.

22 ed with the Alphaproteobacteria class of the Proteobacteria.

23 system which is highly conserved among gamma-proteobacteria.

24 f Paracoccus denitrificans and related alpha-proteobacteria.

25 H was primarily represented by heterotrophic Proteobacteria.

26 tivity over the ATPase turnover in the alpha-proteobacteria.

27 ed Bacteroidetes and Firmicutes with reduced Proteobacteria.

28 ly related to the genera Paracoccus of alpha-Proteobacteria.

29 is widespread and conserved among the gamma-proteobacteria.

30 on of TH17-related genes was associated with Proteobacteria.

31 bserved between biopsy eosinophil values and Proteobacteria.

32 from cyanobacteria, mitochondria arose from proteobacteria.

33 DNA binding protein conserved in most gamma-proteobacteria.

34 evolved more recently as a direct target in Proteobacteria.

35 Bacilli (Firmicutes), and in alpha and beta Proteobacteria.

36 control of plant diseases caused by diverse Proteobacteria.

37 erial community dominated by beta- and gamma-Proteobacteria.

38 mechanism of F1F0-ATPase regulation in alpha-proteobacteria.

39 his has not been demonstrated in other alpha-proteobacteria.

40 d in bacteria as phylogenetically distant as proteobacteria.

41 n and growth rate among 13 strains of marine Proteobacteria.

42 ccinyl-CoA in non-plant eukaryotes and alpha-proteobacteria.

43 en known to play a role in osmoregulation in proteobacteria.

44 16S rRNA processing in both alpha- and gamma-proteobacteria.

45 of Bacteroidetes and increased abundance of Proteobacteria.

46 longer in alpha-proteobacteria than in gamma-proteobacteria.

47 vation of multiple PPIase domains in SurA in proteobacteria.

48 n and fecal level of calprotectin) and fecal Proteobacteria.

49 n homeostasis in Rhizobium and related alpha-proteobacteria.

50 annotated PIMT proteins present in the alpha-proteobacteria.

51 itize fungi or Leviviridae, which may infect Proteobacteria.

52 bacterial species but not in beta- and gamma-proteobacteria.

53 terial phyla Firmicutes, Actinobacteria, and Proteobacteria.

54 teria, and AMH showing higher Firmicutes and Proteobacteria.

55 re mainly attributed to members of the phyla Proteobacteria (14% to 68%), Firmicutes (26% to 41%), Ac

56 bushmeat samples include Firmicutes (67.8%), Proteobacteria (18.4%), Cyanobacteria (8.9%), and Bacter

57 ther SE or LE showed persistent expansion of Proteobacteria (2 log difference, P < 0.01).

58 ominated by three phyla: Firmicutes (62.9%), Proteobacteria (29.9%) and Fusobacteria (9.6%).

59 nt phyla, followed by Bacteroidetes (13.6%), Proteobacteria (3.6%), and Fusobacteria (2.5%).

60 In gamma-proteobacteria, 3-'5' exoribonucleases comprise up to ei

61 he microbiota (90%), whereas in digesta both Proteobacteria (47%) and Firmicutes (38%) showed high ab

62 rity), primarily from Firmicutes (92.6%) and Proteobacteria (6.9%), via 16S rRNA gene amplicon sequen

63 e chicken blood microbiota were dominated by Proteobacteria (60.58% +/- 0.65) followed by Bactroidete

64 nce of Firmicutes and increased abundance of Proteobacteria - a shift in community structure which ha

65 ovel lineages of podoviruses infecting alpha-proteobacteria, a bacterial class critical to oceanic ca

66 ase subgroup 1beta in tested alpha- and beta-proteobacteria, a branched-chain aminotransferase in tes

67 en substrates that correlates with increased Proteobacteria abundance, including Pseudomonas.

68 Porphyromonas gingivalis or ligature, gamma-proteobacteria accumulate and stimulate host immune resp

69 ial sequences were related to Cyanobacteria, Proteobacteria, Actinobacteria and Bacteriodetes previou

70 "and "F-type" which were highly abundant in Proteobacteria, Actinobacteria and Firmicutes, respectiv

71 The microbiome was dominated by Proteobacteria, Actinobacteria, Bacteroidetes, Chlorofle

72 The metagenomic analysis showed that Proteobacteria, Actinobacteria, Bacteroidetes, Cyanobact

73 Firmicutes increased sharply, whereas Proteobacteria, Actinobacteria, Cyanobacteria and Acidob

74 They commonly occurred in the phyla of Proteobacteria, Actinobacteria, Firmicutes, and Cyanobac

75 in the relative abundance of Firmicutes and Proteobacteria after treatment.

76 rent classes within the Gram-negative phylum Proteobacteria: Agrobacterium tumefaciens (syn.

77 In delta-proteobacteria, an additional cysteine tRNA with an 8/4

78 Chloroflexi and Crenarchaeota, but lower for Proteobacteria and Actinobacteria in highly contaminated

79 oportion of oxygen-tolerant organisms of the Proteobacteria and Actinobacteria phyla associated with

80 Heterotrophic Proteobacteria and Actinobacteria were isolated from Lak

81 ession of these genes have been predicted in proteobacteria and actinobacteria.

82 bited low diversity communities dominated by Proteobacteria and Actinobacteria.

83 f GapR, which are ubiquitous among the alpha-proteobacteria and are encoded on multiple bacteriophage

84 Proteobacteria and Bacteroidetes persisted in WD-fed FXR

85 Proteobacteria and Bacteroidetes rhodopsins were the mos

86 Snail microbiomes were dominated by Proteobacteria and Bacteroidetes while water microbiomes

87 The soybean rhizosphere was enriched in Proteobacteria and Bacteroidetes, and had relatively low

88 ory system is conserved throughout the gamma-proteobacteria and controls key pathways in central carb

89 on is typified by both expansions in aerobic Proteobacteria and decreases in anaerobic Firmicutes and

90 ortunistic pathogens belonging to the phylum Proteobacteria and Enterococcus genus have also been lin

91 and phylogenetic diversity, was dominated by Proteobacteria and Euryarchaeota and was significantly e

92 al changes following ZVI exposure, with more Proteobacteria and fewer Bacteroidetes in the ZVI-amende

93 partum was dominated by inversely correlated Proteobacteria and Firmicutes, and exhibited discrete co

94 unities are dominated by the bacterial phyla Proteobacteria and Firmicutes.

95 arget genes for TaoR family members in other Proteobacteria and Firmicutes.

96 in both bloom and control samples with Alpha-proteobacteria and Gamma-proteobacteria being the predom

97 Data showed that the dominant alpha-proteobacteria and gamma-proteobacteria communities in b

98 ccus and a negative association with percent Proteobacteria and Haemophilus.

99 ride, a cell wall component of Gram-negative Proteobacteria and known inducer of lupus in mice, into

100 ersity and an altered composition, with more Proteobacteria and less Bacteroidetes compared with heal

101 lacking -7T appear to be widespread in alpha-proteobacteria and may have evolved away from consensus

102 corticosteroids alone led to enrichment for Proteobacteria and members of other phyla.

103 ned on a normal diet (including increases in Proteobacteria and striking decreases in Bacterioidetes)

104 ugh MapZ orthologs/homologs is widespread in proteobacteria and that the use of allosterically regula

105 by a reduction in the relative abundance of Proteobacteria and Verrucomicrobia (specifically Akkerma

106 bligate methanotrophs belonging to the Phyla Proteobacteria and Verrucomicrobia require oxygen for re

107 ent decrease in Gram-negative Bacteroidetes, Proteobacteria and Verrucomicrobia.

108 real growth phenotype datasets for E. coli, proteobacteria and yeast.

109 ce of Bacteroidetes, followed by Firmicutes, Proteobacteria, and Actinobacteria phyla.

110 obiota devoid of opportunistic pathogens and Proteobacteria, and conventional SPF mice that harbor a

111 s of other P. putida strains, in other gamma-Proteobacteria, and in beta- and alpha-Proteobacteria, f

112 ded in a wide range of host-associated alpha-proteobacteria, and it is likely that the VtlR genetic s

113 found that CrsR is conserved in many aquatic proteobacteria, and most of the time it is associated wi

114 ly increased the abundance of Firmicutes and Proteobacteria, and reduced the content of Bacteroidetes

115 .g., Bacteroides, Bacillus, Firmicutes, beta-proteobacteria, and Spirochetes) were significantly elev

116 terized by increased numbers of Akkermansia, Proteobacteria, and TM7 in the GF diet group.

117 tified a core earthworm community comprising Proteobacteria ( approximately 50%) and Actinobacteria (

118 spectroscopic properties Nap from different Proteobacteria are phylogenetically distinct.

119 gamma-Proteobacteria are produced in the majority of mixed fun

120 N2 fixation rates indicates that these gamma-proteobacteria are unlikely to be responsible for previo

121 n oral, nasal, stool, skin, and vagina, with Proteobacteria as the dominant phylum (60 %).

122 is CbiX can generally be identified in alpha-proteobacteria as the terminal enzyme of siroheme biosyn

123 tial, including members of Bacteroidetes and Proteobacteria, as well as several poorly characterized

124 on in the gut--Bacteroidetes, Firmicutes and Proteobacteria--as well as one aerobic pathogen (Staphyl

125 al classes that are active in the gut (gamma-Proteobacteria, Bacilli and Actinobacteria), all of whic

126 ne phyla, among which the most abundant were Proteobacteria, Bacteroidetes and Chloroflexi.

127 und six phyla of amoeba-associated bacteria: Proteobacteria, Bacteroidetes, Actinobacteria, Chlamydia

128 otic microbial assemblages were dominated by Proteobacteria, Bacteroidetes, and Actinobacteria.

129 een the microbiome of CM and H milk in phyla Proteobacteria, Bacteroidetes, Firmicutes and Actinobact

130 bacteria in C. elegans habitats, with phyla Proteobacteria, Bacteroidetes, Firmicutes, and Actinobac

131 otolerant taxa from the phyla Euryarchaeota, Proteobacteria, Balneolaeota, Bacteroidetes and Rhodothe

132 The proteobacteria Bdellovibrio bacteriovorus and Micavibrio

133 omposition of the ileal bacterial community (Proteobacteria became the most abundant species).

134 samples with Alpha-proteobacteria and Gamma-proteobacteria being the predominant classes detected.

135 attern emerged with Bacteria from the phylum Proteobacteria being the prominent taxon among the fores

136 largely conserved at the phylum level, with Proteobacteria (beta-proteobateria), Bacteroidetes, and

137 complex microbial communities ex vivo, with Proteobacteria blooming and Bacteroidetes declining in t

138 FadR is extraordinarily conserved in gamma-proteobacteria but has migrated.

139 minated by Actinobacteria, Cyanobacteria and Proteobacteria but were heavily impacted by climate vari

140 e with more Actinobacteria, Fusobacteria and Proteobacteria, but fewer Bacteroidetes, Firmicutes and

141 plants include nitrogen-fixing Gram-negative proteobacteria called rhizobia that are able to interact

142 ow here that the evolution of gene blocks in proteobacteria can be described by a small set of events

143 in the sediments were facultative anaerobic Proteobacteria capable of coping with OAI-associated red

144 d in three main groups: select heterotrophic Proteobacteria, chemoautotrophic Thaumarchaeota, and pho

145 e bacteria in the clouds belong to the gamma-Proteobacteria class, among which the Pseudomonas genus

146 e of which are human pathogens, across three Proteobacteria classes, three other phyla and in Thermop

147 Perturbations eliciting an expansion of Proteobacteria coincided with ectopic lesions and tissue

148 the dominant alpha-proteobacteria and gamma-proteobacteria communities in bulk soil and root endosph

149 in Actinobacteria, and numerical decrease in Proteobacteria compared to control.

150 hereas 90 to 99% of promoters from non-alpha-proteobacteria contained -7T.

151 In gamma-proteobacteria, CsrA activity is competitively antagoniz

152 Proteobacteria, Cyanobacteria, and Bacteroidetes dominat

153 d with trend for higher Bifidobacterium, and Proteobacteria decrease accounted for Enterobacteriaceae

154 in all steps while the relative abundance of Proteobacteria decreased as processing progressed.

155 y increased abundance of the bacterial phyla Proteobacteria, Deferribacteres, and TM7, among which th

156 Firmicutes (appearance of Erysipelotrichi), Proteobacteria (Desulfovibrionales) and Verrucomicrobia,

157 mation, and had already evolved before alpha-proteobacteria developed into mitochondria.

158 sputum total leukocyte values (predominantly Proteobacteria) differed markedly from those associated

159 Mic60 homologues from alpha-proteobacteria display the same membrane deforming activ

160 Proteobacteria dominance and lower diversity was associa

161 ysis showed significant associations between Proteobacteria dominance and the neutrophil activation p

162 Proteobacteria dominance was associated with increased m

163 20) identify harbored bacteriophages among a Proteobacteria-dominant community unique to toddlers wit

164 Proteobacteria dominated in immature stages while Firmic

165 In mucosa, Proteobacteria dominated the microbiota (90%), whereas i

166 63; 95% CI, 1.22-5.32; P = 0.015), and gamma-proteobacteria domination of fecal microbiota (HR, 2.64;

167 5% CI, 1.42-31.80; P = 0.016), whereas gamma-proteobacteria domination predicted PCs postengraftment

168 Postengraftment PCs and gamma-proteobacteria domination were predictive of mortality.

169 The mechanisms enabling the outgrowth of Proteobacteria during inflammation are incompletely unde

170 hat in contrast to other characterised Gamma-proteobacteria, E. coli Sxy is positively autoregulated

171 A few species in the class of gamma-proteobacteria encode a cytoplasmic N-glycosylation syst

172 However, the observation that proteobacteria encode a large number of GGDEF proteins,

173 ctinobacteria, Bacteroidetes, Firmicutes and Proteobacteria (especially Roseobacter of its alpha line

174 specificity are widespread in all classes of Proteobacteria, except Deltaproteobacteria, and in flowe

175 ocathode bacterial community was enriched in Proteobacteria, exoelectrogens, and putative producers o

176 Antibiotic treatment, leading to Proteobacteria expansion, further enhanced gluten-induce

177 microbial diversity reduction occurred with Proteobacteria expansion.

178 Family Enterobacteriaceae (phylum Proteobacteria), family Lactobacillaceae, and genus Bact

179 t bacterial phyla (Spirochaetes, Firmicutes, Proteobacteria, Fibrobacteres and Bacteroidetes) althoug

180 o the previously characterized fusobacteria, proteobacteria, firmicutes, and bacteroidetes.

181 distributed among diverse clades, including Proteobacteria, Firmicutes, and Methanomicrobia, with De

182 All oral microbiomes were dominated by Proteobacteria, Firmicutes, Bacteroidetes and Fusobacter

183 exi/Cyanobacteria, and finally Bacteroidetes/Proteobacteria/Firmicutes.

184 dicate that multi-domain proteins evolved in Proteobacteria for specific functions in maintaining cel

185 gamma-Proteobacteria, and in beta- and alpha-Proteobacteria, for example, in genomes of Enterobacteri

186 rom OP11, Actinobacteria, Bacteroidetes, and Proteobacteria found in high relative abundance across a

187 ti MCE domain-containing proteins evolved in Proteobacteria from single-domain proteins.

188 The relative abundance of Proteobacteria, Gammaproteobacteria, Enterobacteriales,

189 eterocystous cyanobacteria and heterotrophic proteobacteria had the genetic potential for N2 fixation

190 lation in Caulobacter, indicating that alpha-proteobacteria have retained HvyA activity.

191 nt homology to Francisella tularensis (gamma-proteobacteria) have been characterized in several tick

192 itional analysis revealed lower abundance of Proteobacteria, higher abundance of Firmicutes, along wi

193 PTS(Ntr) is widely conserved in proteobacteria, highlighting its global importance.

194 wo PPIase domains is common in SurA in later proteobacteria, implying an evolutionary advantage for t

195 e found in the genomes of other marine alpha-proteobacteria, implying lipid renovation is a common st

196 detected in association with an expansion of Proteobacteria in both UC and CD, while expression of li

197 e and gene neighborhood of T4aP secretins in Proteobacteria in comparison with VcPilQ.

198 well as a dramatic increase of Gram-negative Proteobacteria in HFD+BDL versus CTRL+BDL mice.

199 revealed unique, competition-based roles for Proteobacteria in multiple distinct habitats.

200 mounts of Lactobacillus resp. low amounts of Proteobacteria in SBS patients with preservation of colo

201 the proportion of the phylum Firmicutes and Proteobacteria in stool was significantly decreased and

202 undance of Actinobacteria, Bacteroidetes and Proteobacteria in tall cultivars, compared with a higher

203 observed a significantly higher abundance of Proteobacteria in the anterior nares in non-SSTI partici

204 wever, there was an increase in abundance of Proteobacteria in the congestive heart failure group (p

205 revealed decreased Firmicutes and increased Proteobacteria in ulcerated sites, as compared with heal

206 earance of relic structures in diverse gamma-proteobacteria including Plesiomonas shigelloides, Vibri

207 0 orthologues are found in a subset of alpha-proteobacteria, including Agrobacterium tumefaciens Usin

208 ke protein are widespread in gamma- and beta-proteobacteria, including human, animal, and plant patho

209 is an important nutrient for several alpha-2 Proteobacteria, including N2-fixing plant endosymbionts

210 nd BisDC is widespread among Gamma- and Beta-proteobacteria, including various pathogenic strains, hi

211 genetic level, Bacteroidetes decreased while Proteobacteria increased in the CRS group at the phylum

212 A higher abundance of genus Bosea (phylum Proteobacteria) increased with stage.

213 ites, but CsrA in bacteria outside the gamma-proteobacteria is antagonized by a protein called FliW.

214 pe mutants in a number of curved and helical Proteobacteria is beginning to suggest possible mechanis

215 (including Actinobacteria, Bacteroidetes and Proteobacteria); is populated by photosynthetic Cyanobac

216 achnospiraceae/Clostridiales), the second by Proteobacteria (Klebsiella/Enterobacter), the third by B

217 al mucosal tissue, and fusobacteria and beta-Proteobacteria levels increased with advancing cancer st

218 o-Bacteroidetes ratios and endotoxin-bearing Proteobacteria levels-but also maintains intestinal barr

219 ifferently than what was described for other proteobacteria like Escherichia coli We argue that this

220 with their own genome that arose from alpha-proteobacteria living within single-celled Archaea more

221 In several Proteobacteria, LuxI-type enzymes catalyze the biosynthe

222 obacteriaceae family of human gut-associated Proteobacteria maintain a GUS operon under the transcrip

223 clear that T2S is largely restricted to the Proteobacteria, occurring in many, but not all, genera i

224 a similar Hg(II) uptake mechanism within the proteobacteria of accidental Hg(II) transport through he

225 roteins encoded in the genomes of other beta-proteobacteria of the Azoarcus/Thauera group further sug

226 Proteobacteria often co-ordinate responses to carbon sou

227 f the variation in the relative abundance of Proteobacteria on the skin of healthy individuals, suppo

228 Samples were classified as Proteobacteria or Firmicutes (phylum level) and Haemophi

229 Fusobacteria (p < 0.007) and epsilon- Proteobacteria (p < 0.01) were enriched on tumour when c

230 utes (P </=0.001), fusobacteria (P = 0.003), proteobacteria (P </=0.001), synergistetes (P = 0.04), a

231 D11c(+) macrophages from mucus in two phyla (Proteobacteria [p = 0.01] and Actinobacteria [p = 0.02])

232 Most bacteria within the Bacteroidetes and Proteobacteria phyla were already present at 5 weeks aft

233 biosis, with expansion of the Firmicutes and Proteobacteria phyla, near elimination of Bacteroidetes,

234 tinobacteria, Bacteroidetes, Firmicutes, and Proteobacteria phyla, we found that potent Nod-like rece

235 profoundly significant increase in taxa from Proteobacteria phylum in comparison to healthy subjects.

236 d after supplementation with a member of the Proteobacteria phylum, an enteroadherent Escherichia col

237 reased at exacerbation were primarily of the Proteobacteria phylum, including nontypical COPD pathoge

238 sociated with a concomitant reduction in the Proteobacteria phylum.

239 ce the evolution of the system through gamma-Proteobacteria, pinpointing key evolutionary events that

240 of some functional microorganisms, including Proteobacteria, Planctomycetales, Acinetobacter, Pseudom

241 However, many proteobacteria possess LuxR receptors, yet lack any LuxI

242 educed microbiome diversity, associated with Proteobacteria (predominantly Haemophilus) dominance, is

243 ellicle biofilms formed by Bacteroidetes and Proteobacteria (predominantly of the alpha and gamma cla

244 Conversely, in the upper airways, Proteobacteria prime immunity through IL-17A, but K. pne

245 n isolate of the SAR11 clade of marine alpha-proteobacteria, produces methane from MPn, stoichiometri

246 (Terrimonas and Flavobacterium) and diverse Proteobacteria (Pseudomonadaceae, Sphingomonadaceae, and

247 ere determined for two model organisms, the 'Proteobacteria' Ralstonia eutropha (epsilon = 19.0 per m

248 cterization revealed a high Bacteroidetes to Proteobacteria ratio in healthy animals.

249 Fatty acid biosynthesis in alpha- and gamma-proteobacteria requires two functionally distinct dehydr

250 r enrichment or reductions of Firmicutes and Proteobacteria, respectively, at a false discovery rate

251 ding Actinobacteria, alpha-,beta-, and gamma-proteobacteria, revealing a common role of this Amadori

252 apples and reconstructed microbiomes: alpha-Proteobacteria-rich communities promote proliferation, w

253 SAH was associated with increased Proteobacteria (SAH 14% vs. HDC 7% and SAH vs. HC 2%, P

254 Photorhabdus luminescens in 25 diverse gamma-Proteobacteria species.

255 among soil bacteria with Actinobacteria and Proteobacteria, specifically Betaproteobacteria and Gamm

256 In alpha-proteobacteria, strict regulation of cell cycle progress

257 bic bacteria and an expansion of facultative Proteobacteria such as commensal E. coli.

258 Airway infection with Proteobacteria such as P. aeruginosa was associated with

259 Many proteobacteria, such as Escherichia coli, contain two ma

260 oidaceae was reduced, whereas Firmicutes and Proteobacteria, such as Ruminococcaceae, Lachnospiraceae

261 in various archaea, cyanobacteria, and some proteobacteria, such as the enterobacterium, Serratia sp

262 yanobacteria) and copiotrophic (e.g., phylum Proteobacteria) taxa were apparent through substantial c

263 Three phyla, Proteobacteria, Tenericutes and TM7, and 11 genera, incl

264 The pre-16S species is longer in alpha-proteobacteria than in gamma-proteobacteria.

265 and classes Anaerolineae, Delta- and Gamma- Proteobacteria than the deeper sections, indicating that

266 Rok, an analog of H-NS from gamma-proteobacteria that affects chromosome architecture and

267 Micavibrio aeruginosavorus are Gram-negative proteobacteria that are obligate predators of other Gram

268 ecies of non-pathogenic and pathogenic gamma-proteobacteria that infect different hosts, including hu

269 cter jejuni, organisms from three classes of Proteobacteria that live in diverse environments, from f

270 minase in fluorescent pseudomonads and other proteobacteria that we termed PtaA for "periplasmic tran

271 0 bacterial isolates belonging to the phylum Proteobacteria that were enriched from north temperate l

272 In Escherichia coli and other gamma-proteobacteria, the PhoQ-PhoP two-component signaling sy

273 i, Salmonella enterica, and many other gamma-proteobacteria, the transcription factor Crl positively

274 samples had a greater than 10% abundance of Proteobacteria, there were only 19/196 (10%) positive cu

275 environmental mats of sulfur-oxidizing gamma-Proteobacteria (Thiothrix).

276 om obligate to facultative anaerobes such as Proteobacteria This microbial imbalance can contribute t

277 a administration led to a decreased ratio of Proteobacteria to Bacteroidetes, decreased presence of H

278 widespread molecular weapon deployed by many Proteobacteria to target effectors/toxins into both euka

279 Widely found in animal and plant-associated proteobacteria, type VI secretion systems (T6SSs) are po

280 we show that while SurA homologues in early proteobacteria typically contain one or no PPIase domain

281 Many proteobacteria use AHL to coordinate virulence and biofi

282 In the IBD group, Firmicutes, Proteobacteria, Verrucomicrobia, and Fusobacteria were s

283 this response has been well characterized in proteobacteria, very little is known about the effectors

284 RNA gene sequencing, we observed that phylum Proteobacteria was most abundant in normal (n = 8), norm

285 An increase in the relative abundance of Proteobacteria was observed in the posttransplantation s

286 Proteobacteria was the most dominant phylum in all sampl

287 of copper response are conserved through the Proteobacteria, we propose a cell-wide view of copper de

288 The abundances of Fusobacteria and Proteobacteria were also remarkably increased in asympto

289 of Firmicutes were markedly reduced, whereas Proteobacteria were enriched in the mfec and cad1(S205F)

290 In mice lacking RELMbeta, Proteobacteria were present in the inner mucus layer and

291 ominant phyla (Bacteroidetes, Firmicutes and Proteobacteria) were similar.

292 e Actinobacteria, and engraftment or loss of Proteobacteria, were related to better disease outcomes

293 acteria, and Deinococcus-Thermus, but not in Proteobacteria, where (p)ppGpp regulates RNA polymerase

294 In contrast, the alpha-proteobacteria which include important plant and mammali

295 KO also had reduced Firmicutes and increased Proteobacteria, which could be reversed by Abx.

296 e highly diverse CO(2) fixation machinery of Proteobacteria will facilitate their successful implemen

297 RCDI patients were dominated by Proteobacteria with Escherichia coli and Klebsiella most

298 s alone primarily decreased the abundance of Proteobacteria, with the prolonged suppression of some m

299 As can directly modulate mRNA degradation in Proteobacteria without interfering with translation.

300 TLR1 promotes acute enteric infection by the proteobacteria Yersinia enterocolitica.