ライフサイエンスコーパス: Actinobacteria

1 ith a preferential enrichment for members of Actinobacteria.

2 onds to disulfide stress in the cytoplasm of Actinobacteria.

3 r of steroid responsiveness, correlated with Actinobacteria.

4 ry, along with higher relative abundances of Actinobacteria.

5 utes sequences and reducing the abundance of Actinobacteria.

6 n folding pathway may be a common feature in Actinobacteria.

7 d by Streptomyces coelicolor A3(2) and other actinobacteria.

8 cofactor found in methanogens and in various actinobacteria.

9 ing c-di-AMP signaling to ion homeostasis in Actinobacteria.

10 cholesterol and bile acids, respectively, in actinobacteria.

11 ine steric gates, in many taxa of the phylum Actinobacteria.

12 RbpA plays a key role in the sigma cycle in actinobacteria.

13 Mycobacterium tuberculosis (Mtb) and related actinobacteria.

14 n profiles of antibiotics and other drugs in actinobacteria.

15 es that infect bacterial hosts in the phylum Actinobacteria.

16 genes analogous to those observed in related actinobacteria.

17 for the selective inhibition of archaea and actinobacteria.

18 GH51 in the genomes of eleven members of the actinobacteria.

19 Streptomyces, a related group of filamentous Actinobacteria.

20 hed for the related thiol (mycothiol) in the Actinobacteria.

21 HemQ from Bacillus subtilis and a number of Actinobacteria.

22 e closely related to elements found in other actinobacteria.

23 t role in the antibiotic resistance in other actinobacteria.

24 ranscription factor conserved in Proteo- and Actinobacteria.

25 on and modulating cell shape in pleiomorphic actinobacteria.

26 thermophilic soil bacterium that belongs to Actinobacteria.

27 eubacterial topoisomerases found largely in Actinobacteria.

28 pecies of proteobacteria, cyanobacteria, and actinobacteria.

29 icrobiomes from snail tank were dominated by Actinobacteria.

30 odopsin (MR) genes predominant in non-marine actinobacteria.

31 rmicutes, Bacteroidetes, Proteobacteria, and Actinobacteria.

32 ounds, which coincided with proliferation of Actinobacteria.

33 GCs, suggesting the occurrence of RiPPs from actinobacteria.

34 metabolic trait is also observed within the Actinobacteria.

35 homologs are found scattered throughout the Actinobacteria.

36 s the obligate III(2)IV(2) supercomplex from actinobacteria.

37 etwork that is encoded in Proteobacteria and Actinobacteria.

38 Saccharibacteria, grow as epibionts on host Actinobacteria.

39 myces, which is the largest genus within the Actinobacteria.

40 Rhodospirillales), Gammaproteobacteria, and Actinobacteria.

41 aribacteria species are epibionts of diverse Actinobacteria.

42 cteria, as well as uncultured Firmicutes and Actinobacteria.

43 ), with fewer Firmicutes, Bacteroidetes, and Actinobacteria.

44 cts produced by Streptomyces and Salinispora actinobacteria.

45 gy to search for novel thioamidated RiPPs in Actinobacteria.

46 y different numbers of homologous operons in Actinobacteria.

47 inated by Proteobacteria, Bacteroidetes, and Actinobacteria.

48 atterns in other phylogenetic groups such as Actinobacteria.

49 es have been predicted in proteobacteria and actinobacteria.

50 communities dominated by Proteobacteria and Actinobacteria.

51 30%), unclassified bacteria (~ 24 to ~ 35%), Actinobacteria (~ 0.01 to ~ 11%) and Cyanobacteria (less

52 ntrast, Firmicutes (47% vs 63%, P = .17) and Actinobacteria (10% vs 14%, P = .36) were found more fre

53 99% +/- 0.29), Firmicutes (11.45% +/- 0.51), Actinobacteria (10.21% +/- 0.37) and Cyanobacteria (1.96

54 and increased that of partially ligninolytic Actinobacteria (+24%) on decaying fine roots.

55 und that in the deep-dentin carious lesions, Actinobacteria (35.8%) and Firmicutes (31.2%) were the m

56 teria (14% to 68%), Firmicutes (26% to 41%), Actinobacteria (6 to 23%) and Bacteroidetes (1% to 21%).

57 ed by their ecological roles in nature, make Actinobacteria a promising group for the bioenergy indus

58 In the actinobacteria, a class of muralytic enzymes - the 'resu

59 ces coelicolor is the model organism for the actinobacteria, a group of high-GC Gram-positive bacteri

60 conserved only among the mycolata family of actinobacteria, a group of intracellularly surviving bac

61 Actinobacteria, a large bacterial phylum that includes t

62 ere we show that in Streptomyces, a genus of Actinobacteria abundant in soil and symbiotic niches, th

63 s [Bacteroidota] (> 50% relative abundance), Actinobacteria [Actinomycetota], or Proteobacteria [Pseu

64 n the gut (gamma-Proteobacteria, Bacilli and Actinobacteria), all of which are predicted to participa

65 s subgroup, MtrB, is widely conserved in the actinobacteria, along with its presumed cognate response

66 nated by a core microbiome of taxa including Actinobacteria, Alpha-, Beta-, and Gammaproteobacteria,

67 t in a wide diversity of bacteria, including Actinobacteria, alpha-,beta-, and gamma-proteobacteria,

68 We found that soil-inhabiting, free-living Actinobacteria also harbor as many as 12 TA pairs.

69 derate asthma were significantly enriched in Actinobacteria, although the largest differences observe

70 usters have been most commonly identified in Actinobacteria and a few other bacteria.

71 roidetes, and had relatively lower levels of Actinobacteria and Acidobacteria compared with bulk soil

72 re related to Cyanobacteria, Proteobacteria, Actinobacteria and Bacteriodetes previously identified i

73 after 1 week were Firmicutes, but by 7 weeks Actinobacteria and Bacteroidetes were also dominant.

74 ge, were associated with higher abundance of Actinobacteria and Bifidobacteriaceae, and lower abundan

75 esentatives of other mycolic acid containing actinobacteria and can thus be equated with the rank of

76 clades related to Bacteroidetes, Firmicutes, Actinobacteria and Chloroflexi were ubiquitously found i

77 onded positively to AMF, while taxa from the Actinobacteria and Comamonadaceae responded negatively t

78 ing YcaO and TfuA proteins are widespread in Actinobacteria and encode a highly diverse landscape of

79 sed growth form include hyphal tip growth in actinobacteria and filamentous fungi and pollen tube dev

80 Herein, we show that the Actinobacteria and Firmicutes (high-GC and low-GC Gram-p

81 The phyla Actinobacteria and Firmicutes were more abundant in the

82 proteobacteria, and Gram-positive bacteria (actinobacteria and firmicutes).

83 hich were highly abundant in Proteobacteria, Actinobacteria and Firmicutes, respectively.

84 tional orthologs of Rv2179c are prevalent in actinobacteria and found in bacteria as phylogenetically

85 fects were prominent in Acidobacteria, while Actinobacteria and Gammaroteobacteria communities were a

86 ta provide novel insight on cell division in actinobacteria and highlights a new class of potential d

87 yldiaminopimelate aminotransferase in tested actinobacteria and in the beta-proteobacterium Nitrosomo

88 pathway, MutS-MutL are absent in almost all Actinobacteria and many Archaea.

89 conserved in bacteria belonging to the phyla Actinobacteria and Nitrospira.

90 of spatial and temporal dynamics for SAR11, Actinobacteria and OCS116 in the North Atlantic by demon

91 cuss what is known about this pathway in the actinobacteria and offer insights into why an essential

92 phil recovery post-HCT, the presence of oral Actinobacteria and oral Firmicutes in stool was positive

93 lecular exchanges between termite-associated actinobacteria and pathogenic fungi, we uncovered a rema

94 Mycothiol (MSH) is the major thiol in Actinobacteria and plays a role analogous to that of glu

95 trait is widespread among soil bacteria with Actinobacteria and Proteobacteria, specifically Betaprot

96 dies, particularly in relative abundances of Actinobacteria and Proteobacteria.

97 I)(2)-NrdF, prototypical of the enzymes from actinobacteria and proteobacteria.

98 es from the phyla Bacteroidetes, Firmicutes, Actinobacteria and Proteobacteria.

99 ances in the phyla Fusobacteria, Firmicutes, Actinobacteria and Proteobacteria.

100 ty communities that are markedly enriched in Actinobacteria and specific families from other phyla, n

101 Firmicutes, Fusobacteria, Bacteriodetes, and Actinobacteria) and 24 genera were altered in unstabiliz

102 eneficial bacteria, such as Bifidobacterium (Actinobacteria) and Akkermansia (Verrucomicrobia).

103 .e. fungi, Gram-positive bacteria (including actinobacteria) and Gram-negative bacteria] in temperate

104 ith a significant increase of Firmicutes and Actinobacteria, and a decrease of Bacteroidetes and Fuso

105 se, 52 also lack homologs in closely related actinobacteria, and are termed "Frankia-specific." The g

106 ity showed that some species of Chloroflexi, Actinobacteria, and candidate phylum AD3 (or Dormibacter

107 ction is conserved in members of Firmicutes, Actinobacteria, and Deinococcus-Thermus, but not in Prot

108 ngly, RIN-mediated effects on root exudates, Actinobacteria, and disease suppression were evident fro

109 Engraftment of some Actinobacteria, and engraftment or loss of Proteobacteri

110 for targeted protein degradation in archaea, Actinobacteria, and eukaryotes.

111 vorable taxa Psychrobacter, Corynebacterium, Actinobacteria, and Neisseria were the signature taxa of

112 ificant increase in Firmicutes, numerical in Actinobacteria, and numerical decrease in Proteobacteria

113 ed mostly of the bacterial phyla Firmicutes, Actinobacteria, and Proteobacteria.

114 s, an overall increase in Proteobacteria and Actinobacteria, and reduced richness.

115 robia compared to the small intestine, while Actinobacteria, and superphylum Patescibacteria were pre

116 e revealed that at least some members of the Actinobacteria (another phylum of Gram-positive bacteria

117 on during spore germination, and that in the actinobacteria, any signaling function associated with s

118 in the FRI and NH groups, Proteobacteria and Actinobacteria appeared more prevalent, respectively.

119 sing Proteobacteria ( approximately 50%) and Actinobacteria ( approximately 30%), with lower abundanc

120 The actinomycetes, although not all the Actinobacteria, are easy to isolate from the marine envi

121 ria (beta-proteobateria), Bacteroidetes, and Actinobacteria as the main taxa despite the cyanobacteri

122 omologous ACAD gene pairs are found in other Actinobacteria, as well as Proteobacteria.

123 n disrupts the drought-induced enrichment of Actinobacteria, as well as their improvement in host phe

124 Actinobacteria, Bacilli, and many Gammaproteobacteria ta

125 ivars, with higher differential abundance of Actinobacteria, Bacteroidetes and Proteobacteria in tall

126 for temperature and xerotolerance (including Actinobacteria, Bacteroidetes and Proteobacteria); is po

127 um level, altering the relative abundance of Actinobacteria, Bacteroidetes, and Firmicutes.

128 assigned to the Proteobacteria, Firmicutes, Actinobacteria, Bacteroidetes, and Fusobacteria phyla.

129 n was more diverse, with lineages from OP11, Actinobacteria, Bacteroidetes, and Proteobacteria found

130 D includes 619 taxa in 13 phyla, as follows: Actinobacteria, Bacteroidetes, Chlamydiae, Chloroflexi,

131 microbiome was dominated by Proteobacteria, Actinobacteria, Bacteroidetes, Chloroflexi and many uncl

132 genomic analysis showed that Proteobacteria, Actinobacteria, Bacteroidetes, Cyanobacteria, and Firmic

133 y of a diverse group of taxa affiliated with Actinobacteria, Bacteroidetes, Firmicutes and Proteobact

134 tified, with most sequences belonging to the Actinobacteria, Bacteroidetes, Firmicutes and Proteobact

135 phyla were shared between the uterine sites: Actinobacteria, Bacteroidetes, Firmicutes, and Proteobac

136 ree mice, using cultured commensals from the Actinobacteria, Bacteroidetes, Firmicutes, and Proteobac

137 ganisms covering seven phyla (Acidobacteria, Actinobacteria, Bacteroidetes, Firmicutes, Nitrospirae,

138 Five phyla (Firmicutes, Actinobacteria, Bacteroidetes, Proteobacteria, and Fusob

139 This study focused on actinobacteria because they are keystone species in terr

140 oteobacteria, Bacteroidetes, Firmicutes, and Actinobacteria being most abundant.

141 a 3'-->5' exonuclease highly conserved among Actinobacteria, Beta-, Delta- and Gammaproteobacteria-as

142 pport the monophyly of the cyanobacteria and actinobacteria but not the proteobacteria, lending suppo

143 insights in the evolution of cell shapes in Actinobacteria, but also lead to medical interventions t

144 us to eukaryotic ubiquitination, proteins in actinobacteria can be post-translationally modified in a

145 num-dependent catechol dehydroxylases in gut Actinobacteria catalyze the removal of para-hydroxyl gro

146 ted bacteria: Proteobacteria, Bacteroidetes, Actinobacteria, Chlamydiae, Firmicutes, and Acidobacteri

147 lative abundance of some bacteria, including Actinobacteria, Chloroflexi, and Saccharibacteria, was i

148 fied in the phyla Firmicutes, Thermotogales, Actinobacteria, Chloroflexi, Deinococcus-Thermus, and Pr

149 onging to the Roseobacter, OCS116 and marine Actinobacteria clades were enriched in the eddy core and

150 asmatales and M. thermoautotrophicus, and in Actinobacteria compared to Halobacteriales.

151 acquired via horizontal transfer from marine Actinobacteria, conferring an adaptive advantage that mi

152 treptomyces coelicolor that is widespread in actinobacteria confirmed another example of d-allo-l-MeL

153 anisms and symbionts of herbivorous animals, Actinobacteria contribute to the global carbon cycle thr

154 s increased sharply, whereas Proteobacteria, Actinobacteria, Cyanobacteria and Acidobacteria decrease

155 Stone microbiomes were dominated by Actinobacteria, Cyanobacteria and Proteobacteria but wer

156 d abundance in Verrocomicrobia but decreased Actinobacteria, Cyanobacteria, and Firmicutes as well as

157 Applying Seq2PKS to Actinobacteria datasets, we discover biosynthetic gene c

158 increasing the relative abundance of phylum Actinobacteria, decreasing the relative abundance of Fus

159 obacteria, delta-Proteobacteria, Clostridia, Actinobacteria, Deinococcus-Thermus species and DNAs fro

160 n (Gammaproteobacteria, Alphaproteobacteria, Actinobacteria) developed in the SOAs, initiating a succ

161 g molecular techniques and metagenomics, and actinobacteria emerge as an often significant, sometimes

162 Most Actinobacteria encode a small transmembrane protein, who

163 ioneuston) in these systems were depleted in Actinobacteria, enriched in either Betaproteobacteria or

164 iverse as cyanobacteria, proteobacteria, and actinobacteria exhibit wholesale substitution of aminoad

165 ain HTCC2649 is a novel marine member of the Actinobacteria, family Intrasporangiaceae, and is closel

166 scovered sequences unique to clades, such as Actinobacteria, Firmicutes and gamma-Proteobacteria, and

167 At school age, many new Actinobacteria, Firmicutes, and Bacteroidetes bacterial

168 nly occurred in the phyla of Proteobacteria, Actinobacteria, Firmicutes, and Cyanobacteria in bacteri

169 Three phyla (Actinobacteria, Firmicutes, and Proteobacteria) accounte

170 The main phyla in all samples were Actinobacteria, Firmicutes, and Proteobacteria.

171 istributed among species within the phyla of Actinobacteria, Firmicutes, and Proteobacteria.

172 Among the actinobacteria four Micrococcus species produced MSH, bu

173 the non-legume Parasponia (Cannabaceae), and actinobacteria Frankia, which are able to interact with

174 bacteria, alphabetagamma-Proteobacteria, and Actinobacteria (Frankia) and provide strong support for

175 bial biosynthetic potential and diversity of actinobacteria from Pobitora Wildlife Sanctuary and Kazi

176 t the DNA damage response in Mtb and related actinobacteria function via distinct pathways as compare

177 and unrelated to stool microbiome with more Actinobacteria, Fusobacteria and Proteobacteria, but few

178 bacterial phyla: Firmicutes, Proteobacteria, Actinobacteria, Fusobacterium, and Bacteroidetes, with t

179 Actinobacteria generate a large number of structurally d

180 In conclusion, intestinal Actinobacteria generate BH4.

181 NDPUMA in a systematic investigation of 7635 Actinobacteria genomes, suggesting that NRP chemical div

182 lies Ruminococcaceae and Turicibacteraceae), Actinobacteria (genus Bifidobacterium) and Bacteroidetes

183 Cholesterol catabolism by actinobacteria has been extensively studied.

184 Members of the Corynebacterineae suborder of Actinobacteria have a unique cell surface architecture a

185 ividual phages infecting hosts in the phylum Actinobacteria have been sequenced and grouped into Clus

186 qlH lack a classical RecQ, though many other Actinobacteria have both RqlH and RecQ.

187 Actinobacteria have frequently been reported in the Ande

188 Small molecules produced by Actinobacteria have played a prominent role in both drug

189 l and could be seen attached to their larger Actinobacteria hosts.

190 phosphatase PstP is conserved throughout the Actinobacteria in a genetic locus related to cell wall s

191 narchaeota, but lower for Proteobacteria and Actinobacteria in highly contaminated samples.

192 by the exclusive presence of Pseudonocardia (Actinobacteria) in the biofilm and the absence of Limnob

193 the development of communities dominated by Actinobacteria including members of the genera Mycobacte

194 iB-like family that is widely distributed in actinobacteria including the notoriously persistent path

195 fferent phyla, being especially prevalent in Actinobacteria (including M. tuberculosis) and Proteobac

196 fferent phyla, being especially prevalent in Actinobacteria (including M. tuberculosis).

197 In many gram-positive Actinobacteria, including Actinomyces oris and Corynebac

198 in the majority of bacterial species outside Actinobacteria, including Escherichia coli.

199 e holoenzyme and stimulates transcription in actinobacteria, including Streptomyces coelicolor and My

200 -associated protein conserved throughout the actinobacteria, including the antibiotic-producing Strep

201 ecies do not possess proteasome systems, the actinobacteria, including the human pathogen Mycobacteri

202 In the actinobacteria, including the streptomycetes and mycobac

203 nsia, whereas in fast-fermenting simulations Actinobacteria increased with trend for higher Bifidobac

204 Actinobacteria is a goldmine for the discovery of abunda

205 The ancient phylum Actinobacteria is composed of phylogenetically and physi

206 The culturability of several actinobacteria is controlled by resuscitation-promoting

207 This study establishes that actinobacteria isolated from the poorly explored Indo-Bu

208 In many Actinobacteria it is the sole annotated serine threonine

209 rganisms is a monotopic membrane protein, in actinobacteria, it is a polytopic protein with three tra

210 nd in KEGG, from plants, fungi, metazoa, and actinobacteria; KEGG contains pathways not found in Meta

211 e only cell division-associated protein from Actinobacteria known to interact with the conserved C-te

212 tage than that found in the genomes of other actinobacteria, legume endosymbionts, and plant pathogen

213 Actinobacteria like Streptomyces and Mycobacterium lack

214 the DnaK sequences from Halobacteriales and Actinobacteria likely reflects common biases in their am

215 Abundant freshwater Actinobacteria lineages, in particular Rhodoluna sp., we

216 In contrast to most other actinobacteria, M. luteus encodes only one resuscitation

217 dates, and confirmation of indigenous marine actinobacteria, make exciting discoveries even more like

218 rature, and propose that LTA biosynthesis in Actinobacteria might be fundamentally different to that

219 tion experiments showed that three different Actinobacteria (Mycobacterium smegmatis, Streptomyces li

220 hed near the genic termini of the pathogenic Actinobacteria, Mycobacterium tuberculosis.

221 cluded Acidobacteria (groups 6, 17, and 22), Actinobacteria (Nocardioides and Illumatobacter), Bacter

222 western and eastern regions of the gyre, and Actinobacteria, OCS116 and members of the Roseobacter li

223 ty structure varies across the gyre and that Actinobacteria, OCS116, and members of the Roseobacter c

224 We identified shifts in SAR11, Actinobacteria, OCS116, SAR86, SAR116 and members of the

225 an extended genus of metabolically versatile Actinobacteria of considerable biotechnological interest

226 For example, actinobacteria of the genus Streptomyces form multicellu

227 Filamentous actinobacteria of the genus Streptomyces have a complex

228 wer lakes (Erie, Ontario), in part due to an Actinobacteria oligotype (acI-C2) that averaged 7.7% of

229 eriaceae; ammonium enriched for oligotrophic Actinobacteria OM1 and Gammaproteobacteria KI89A clades

230 Moreover, despite both belonging to Actinobacteria, only 21 P450 families were common, and 1

231 er Symbiobacterium thermophilum belongs with Actinobacteria or Firmicutes.

232 Actinobacteria OTUs showed particularly strong correlati

233 in two phyla (Proteobacteria [p = 0.01] and Actinobacteria [p = 0.02]) and two families (Moraxellace

234 ad more sequences in Firmicutes and fewer in Actinobacteria phyla and more sequences in the genera Ba

235 tolerant organisms of the Proteobacteria and Actinobacteria phyla associated with rectal mucosa, comp

236 followed by Firmicutes, Proteobacteria, and Actinobacteria phyla.

237 n bacteria belonging to the Spirochaetes and Actinobacteria phyla.

238 oups/species belonging to Proteobacteria and Actinobacteria phyla; however, similar to abiotic foulan

239 am negative Proteobacteria and gram positive Actinobacteria phyla; the bacterial genera that showed t

240 h favorable response are confined within the Actinobacteria phylum and the Lachnospiraceae/Ruminococc

241 In the Actinobacteria phylum, we found several Actinomadura, Ac

242 TPS-2-producing bacteria as belonging to the Actinobacteria phylum.

243 e Proteobacteria, Firmicutes, Bacteroidetes, Actinobacteria, Planctomycetes, Acidobacteria, Nitrospin

244 Actinobacteria possess unique ways to regulate the oxogl

245 olecular identification indicated that these actinobacteria predominantly belonged to genus Streptomy

246 Actinobacteria produce numerous antibiotics and other sp

247 nobacteria and algae while Acidobacteria and Actinobacteria proportions were higher in epipsammic hab

248 Based on metaproteomic analysis, Actinobacteria, Proteobacteria, and Firmicutes phyla dom

249 mbers of six phyla, Firmicutes, Bacteroides, Actinobacteria, Proteobacteria, Fusobacteria, and TM7, w

250 Here we provide evidence that, in Actinobacteria, pupylation plays a crucial role in this

251 e composition showed a lower Fusobacteria to Actinobacteria ratio in OCD cases.

252 Filamentous Actinobacteria, recently renamed Actinomycetia, are the

253 2-oxoglutarate dehydrogenase complex (ODH), actinobacteria rely on a two-in-one protein (OdhA) in wh

254 However, examination of Firmicutes and Actinobacteria reveals that PspA orthologs associate wit

255 etes rhodopsins were the most abundant while Actinobacteria rhodopsins, or actinorhodopsins, were com

256 s one of the smallest genomes of free-living actinobacteria sequenced to date, comprising a single ci

257 Streptomyces and Mycobacterium of the phylum Actinobacteria show no sign of similarity.

258 verification successfully identified several actinobacteria species which were not previously known t

259 Actinobacteria spp. exhibited trends with treatment.

260 etermine the more flexible rod-like shape in actinobacteria such as Mycobacterium species are unknown

261 Filamentous actinobacteria such as Streptomyces undergo two distinct

262 se was conserved among the Frankia and other actinobacteria such as Streptomyces.

263 us with Thermotoga, and Halobacteriales with Actinobacteria, suggesting that the three archaeal types

264 ly of the cyanobacteria, proteobacteria, and actinobacteria, supporting vertical descent.

265 ases of Mycobacterium, a genus of the phylum Actinobacteria that includes the human pathogen Mycobact

266 ructures enable the identification of 90 new actinobacteria that may be regulated by butenolides, two

267 compounds, primarily from cyanobacteria and actinobacteria, that illustrate the tremendous potential

268 rculosis, Rhodococcus jostii RHA1, and other Actinobacteria, the cholesterol and 4-AD catabolic gene

269 cteroidetes, Firmicutes, Proteobacteria, and Actinobacteria, the four most common phyla of gut bacter

270 Among Actinobacteria, the four-gene module occurred only in tu

271 h domain organisation are widely found among Actinobacteria, the functional role of ECFs with a fused

272 In Actinobacteria, the thioviridamide-like molecules are a

273 rase present in Mycobacteriaceae and related Actinobacteria, this subfamily of type IA topoisomerase

274 t that land plant TAL genes are derived from Actinobacteria through an ancient horizontal gene transf

275 logs in Leotiomyceta fungi were derived from Actinobacteria through an independent HGT event, forming

276 pression of an eight-gene operon encoding an actinobacteria-type H2-uptake [NiFe]-hydrogenase.

277 Our results reveal the structure of an Actinobacteria-unique insert of the RNAP beta' subunit.

278 alphaproteobacteria, gammaproteobacteria and actinobacteria used a methionine methylation pathway ind

279 In contrast, aerobic actinobacteria utilize systems comprised of independentl

280 10 major subclades within the Flavobacteria, Actinobacteria, Verrucomicrobia and Proteobacteria (incl

281 a dominated the fermentation medium, and the Actinobacteria was associated with the matrix of maize d

282 r sequences found in organisms of the phylum Actinobacteria was investigated.

283 a group of related vOTUs predicted to infect actinobacteria was shown to be significantly enriched in

284 In addition, Firmicutes and Actinobacteria were also the abundant phyla in the given

285 Heterotrophic Proteobacteria and Actinobacteria were isolated from Lake Matano, Indonesia

286 A total of 107 actinobacteria were isolated, of which 77 exhibited sign

287 s belonging to Firmicutes, Bacteroidetes and Actinobacteria were present in the copepod guts througho

288 Recently, these actinobacteria were shown to harbor self-resistance prop

289 Compared to CTRLs, in NAFLD patients Actinobacteria were significantly increased and Bacteroi

290 ti and Tsokar showed that Proteobacteria and Actinobacteria were the dominant phyla in all samples.

291 ed as LD12 (Alphaproteobacteria) and acI-B1 (Actinobacteria), were among the most abundant in every s

292 s and Mycobacterium, belonging to the phylum Actinobacteria, were studied owing to their contrasting

293 ortunistic pathogens from the Firmicutes and Actinobacteria, which exhibit a Gram-positive type of ce

294 cases of Mycobacteria, a genus of the phylum Actinobacteria, which includes the human pathogen Mycoba

295 for lipid aminoacylation, conserved in many Actinobacteria, which results in formation of Ala-PG and

296 This enzyme is a large monomer in actinobacteria, while it is constituted of two subunits

297 roteobacteria, Bacteroidetes, Firmicutes and Actinobacteria with an inclusion of 68.04% previously un

298 Spearman's analysis negatively correlated Actinobacteria with cecal cholesterol, intestinal and pl

299 nalysis of nucleic acid sequences placed the actinobacteria within the proteobacteria, supporting lat

300 Some analyses place the cyanobacteria and actinobacteria within the proteobacteria, which suggests