ライフサイエンスコーパス: Bacillus subtilis

1 ate membrane synthesis with cell division in Bacillus subtilis.

2 e development in the Gram-positive bacterium Bacillus subtilis.

3 pathway in the Gram-positive model bacterium Bacillus subtilis.

4 master regulator of nitrogen assimilation in Bacillus subtilis.

5 ins from Methylosinus trichosporium OB3b and Bacillus subtilis.

6 of ciprofloxacin and marbofloxacin via HPTLC-Bacillus subtilis.

7 merases found in the Gram-positive bacterium Bacillus subtilis.

8 manganese ions in both Escherichia coli and Bacillus subtilis.

9 rowing bacteria such as Escherichia coli and Bacillus subtilis.

10 letely abrogates mismatch repair activity in Bacillus subtilis.

11 ics from other species such as subtilin from Bacillus subtilis.

12 pression vector for antibiotic production in Bacillus subtilis.

13 bacterium tuberculosis and the yuk system of Bacillus subtilis.

14 asement layer assembly during sporulation in Bacillus subtilis.

15 g to pellicle formation in the Gram-positive Bacillus subtilis.

16 tase small alarmone synthetase 1 (SAS1) from Bacillus subtilis.

17 c-di-AMP is an essential second messenger in Bacillus subtilis.

18 me from the highly selective RppH present in Bacillus subtilis.

19 that activate expression of biofilm genes in Bacillus subtilis.

20 growth of the Gram-positive model bacterium Bacillus subtilis.

21 urified PG sacculi obtained from E. coli and Bacillus subtilis.

22 ble for completing chromosome segregation in Bacillus subtilis.

23 es produced by the ubiquitous soil bacterium Bacillus subtilis.

24 than those encoded on the leading strand in Bacillus subtilis.

25 ryptophan biosynthetic (trpEDCFBA) operon in Bacillus subtilis.

26 of the model organisms Escherichia coli and Bacillus subtilis.

27 iron/manganese homeostasis in the bacterium Bacillus subtilis.

28 scherichia coli, Pseudomonas aeruginosa, and Bacillus subtilis.

29 obial agents when incubated with E. coli and Bacillus subtilis.

30 tor YjbH and ATP-dependent protease ClpXP in Bacillus subtilis.

31 r represses many genes during sporulation of Bacillus subtilis.

32 for growth under gluconeogenic conditions in Bacillus subtilis.

33 eliminated its antibiotic properties against Bacillus subtilis.

34 A and the nucleoid-associated protein Rok of Bacillus subtilis.

35 e states of the PP2C phosphatase SpoIIE from Bacillus subtilis.

36 el the mature PG in whole bacterial cells of Bacillus subtilis.

37 ein, YonO, encoded by the SPbeta prophage of Bacillus subtilis.

38 ights the dynamic nature of ParB networks in Bacillus subtilis.

39 rient extraction from Bacillus megaterium by Bacillus subtilis.

40 to describe a mechanism for MV formation in Bacillus subtilis.

41 an those in the Gram-positive model organism Bacillus subtilis.

42 t was reported that many bacteria, including Bacillus subtilis [1], Escherichia coli [2], and Pseudom

43 ith soil bacteria (Pseudomonas putida F1 and Bacillus subtilis 168).

44 d growth of the Gram-positive model organism Bacillus subtilis 168, WTA is lost from the cell wall in

45 nthetic gene cluster from the marine isolate Bacillus subtilis 1779.

46 nges are needed for the L-form transition in Bacillus subtilis [7].

47 During spore formation in Bacillus subtilis a transenvelope complex is assembled a

48 S) technology to study environmental fate of Bacillus subtilis, a widely used BCA, focusing on its di

49 ms) or exposed to a single strain probiotic (Bacillus subtilis) added to the water.

50 One of the most studied riboswitches is the Bacillus subtilis adenine-responsive pbuE riboswitch, wh

51 -off" activities of both FMN riboswitches in Bacillus subtilis, allowing rib gene expression even in

52 ode-of-action study using the model organism Bacillus subtilis and different assays, including proteo

53 nique to the staphylococci, as homologs from Bacillus subtilis and Enterococcus faecalis retain this

54 inst other Gram-positive bacteria, including Bacillus subtilis and Enterococcus faecalis, and drug-se

55 ated three species of TDB, Escherichia coli, Bacillus subtilis and Enterococcus faecalis, from the gu

56 he silver loaded membranes on model bacteria Bacillus subtilis and Escherichia coli.

57 flagellar filaments from both Gram-positive Bacillus subtilis and Gram-negative Pseudomonas aerugino

58 eV was examined in distantly related species Bacillus subtilis and Helicobacter pylori, but its role

59 sduction in the initiation of sporulation in Bacillus subtilis and in bacterial two-component systems

60 Bacillus subtilis and its closest relatives have multipl

61 interact with the same peptides and include Bacillus subtilis and other Gram-positive clamps.

62 reated knockdowns of every essential gene in Bacillus subtilis and probed their phenotypes.

63 to no experimentally observed PPI, including Bacillus subtilis and Salmonella enterica which are pred

64 ties against gram-positive bacteria, such as Bacillus subtilis and Staphylococcus aureus, and gram-ne

65 the Gram-positive, peritrichous-flagellated Bacillus subtilis and the Gram-negative, polar-flagellat

66 inant of size in the Gram-positive bacterium Bacillus subtilis and the single-celled eukaryote Saccha

67 re involved in important bacterial diseases (Bacillus subtilis and Vibrio cholera, respectively).

68 ne modeling and experimental analyses of the Bacillus subtilis and Vibrio harveyi quorum-sensing netw

69 ngle bacterial cells that undergo symmetric (Bacillus subtilis) and asymmetric (Caulobacter crescentu

70 in model bacteria such as Escherichia coli, Bacillus subtilis, and Caulobacter crescentus.

71 wth of Escherichia coli, Micrococcus luteus, Bacillus subtilis, and Klebsiella pneumoniae at a minima

72 udomonas aeruginosa, Listeria monocytogenes, Bacillus subtilis, and Staphylococcus aureus were compar

73 serovar Typhimurium, Pseudomonas aeruginosa, Bacillus subtilis, and Staphylococcus epidermidis at the

74 Here, we use the ComQXPA system of Bacillus subtilis as a model system, to show that pherot

75 es, we have employed the repressor AraR from Bacillus subtilis as a model system.

76 bacitracin resistance system BceRS-BceAB of Bacillus subtilis as an example.

77 e monitors behavior of fluorescently labeled Bacillus subtilis as it colonizes the root of Arabidopsi

78 ally long untranslated region of the cotH in Bacillus subtilis, as well as upstream regions of certai

79 logical samples is demonstrated using living Bacillus subtilis ATCC 49760 colonies on agar plates.

80 pact of ceragenin CSA-13 on spores formed by Bacillus subtilis (ATCC 6051), we performed the series o

81 ested against Escherichia coli (E. coli) and Bacillus subtilis (B. subtilis) by bacterial growth on t

82 Salmonella typhimurium (S. typhimurium) and Bacillus subtilis (B. subtilis) were examined and observ

83 The GP12 protein from the Bacillus subtilis bacteriophage varphi29 has been implic

84 gral component of the packaging motor in the Bacillus subtilis bacteriophage varphi29 is a viral geno

85 ect combination with Aliivibrio fischeri and Bacillus subtilis bioassays.

86 mediated electrical signaling generated by a Bacillus subtilis biofilm can attract distant cells.

87 We discovered that two Bacillus subtilis biofilm communities undergoing metabol

88 Bacillus subtilis biofilm formation relies on the assemb

89 uch an internal conflict within a microbial (Bacillus subtilis) biofilm community: cells in the biofi

90 Humphries et al. show that Bacillus subtilis biofilms utilize potassium production

91 Formation of Bacillus subtilis biofilms, consisting of cells encapsul

92 sorption of Hg(II), Cd(II), and Au(III) onto Bacillus subtilis biomass with an elevated concentration

93 n atomic model of an l,d-transpeptidase from Bacillus subtilis bound to its natural substrate, the in

94 e-forming enzyme lumazine synthase (LS) from Bacillus subtilis (BsLS), for example, encapsulates ribo

95 not required for normal planktonic growth of Bacillus subtilis but is essential for robust biofilm fo

96 has been observed in swarms of the bacterium Bacillus subtilis, but the underlying molecular mechanis

97 in the model organisms Escherichia coli and Bacillus subtilis by following diauxic growth curves, as

98 Bacillus subtilis can enter three developmental pathways

99 Here we show that Bacillus subtilis can kill and prey on Bacillus megateri

100 Here, the authors show that Bacillus subtilis can kill and prey on Bacillus megateri

101 The bacterium Bacillus subtilis can respond to sudden nutrient limitat

102 Bacaucin, a novel cyclic lipopeptide from Bacillus subtilis CAU21, is reported.

103 l organisms, which include Escherichia coli, Bacillus subtilis, Caulobacter crescentus, and Myxococcu

104 re we investigate the mechanism by which the Bacillus subtilis cell-division inhibitor, MciZ (mother

105 reduction of membrane fluidity both in live Bacillus subtilis cells and in model membranes.

106 Sporulating Bacillus subtilis cells assemble a multimeric membrane c

107 nhibits initiation of replication in diploid Bacillus subtilis cells committed to the developmental p

108 Here, we show that Bacillus subtilis cells lacking all 10 MOP superfamily m

109 ation, we analyzed changes in mRNA levels in Bacillus subtilis cells with and without dnaA, using eng

110 e to growing rod-shaped Escherichia coli and Bacillus subtilis cells, we demonstrate that the cells c

111 Bacillus subtilis CheD plays an important role in chemot

112 unravel the higher-order organization of the Bacillus subtilis chromosome and its dynamic rearrangeme

113 ocated on the prophage-like region P6 of the Bacillus subtilis chromosome.

114 how, in contrast, that a sluggish variant of Bacillus subtilis CM, in which a cationic active-site ar

115 Bacillus subtilis competence-induced RecA, SsbA, SsbB, a

116 ructures of the HK:RR complex DesK:DesR from Bacillus subtilis, comprising snapshots of the phosphotr

117 In Bacillus subtilis, condensin is loaded at centromeric pa

118 sdRS are paralogous two-component systems in Bacillus subtilis controlling the response to antimicrob

119 neered for expression of the ribAGH genes of Bacillus subtilis converts isotope-labeled purine supple

120 the CVs and the log total count of bacteria (Bacillus subtilis) could be established using the equati

121 ficity of the E. coli enzyme relative to its Bacillus subtilis counterpart and provides a framework f

122 iscuity of EcRppH differentiates it from its Bacillus subtilis counterpart, which has a strict RNA se

123 a randomly chosen pole during sporulation in Bacillus subtilis creates unequal sized daughter cells w

124 emical and mutational analysis, we show that Bacillus subtilis delta binds to DNA immediately upstrea

125 Here, we show that Bacillus subtilis delta could also function as a transcr

126 es along with the prototypic enzyme Sfp from Bacillus subtilis demonstrated their varying specificiti

127 ofilms formed by the Gram-positive bacterium Bacillus subtilis depend on the production of the secret

128 Bacillus subtilis differentiates into a state of compete

129 roduced in the model Gram-positive bacterium Bacillus subtilis differs from Lipid II found in Gram-ne

130 During sporulation, Bacillus subtilis divides around the nucleoid near one c

131 posed technique was applied for detection of Bacillus subtilis DNA samples and detection limit of 10p

132 Here we show that FliW of Bacillus subtilis does not bind to the same residues of

133 how that the classical chemoreceptor TlpA of Bacillus subtilis does not localize according to the con

134 that arginine phosphorylation is induced in Bacillus subtilis during oxidative stress.

135 Given that Bacillus halodurans and Bacillus subtilis encode AsnRS for Asn-tRNA(Asn) formati

136 The Gram-positive bacterium Bacillus subtilis encodes three diadenylate cyclases tha

137 is an IMMP that cleaves Pro-sigma(K) during Bacillus subtilis endospore formation.

138 ised as riboswitch identifiers and tested on Bacillus subtilis, Escherichia coli, and Synechococcus e

139 We report that the Bacillus subtilis exopolysaccharide (EPS) is a signaling

140 Recombinant ferrochelatase (BsFECH) from Bacillus subtilis expressed in Escherichia coli BL21(DE3

141 Bacillus subtilis expresses numerous iron importers, but

142 ssential in the Gram-positive model organism,Bacillus subtilis, facilitated a global analysis of inte

143 Bacillus subtilis flagella are not only required for loc

144 The Gram-positive bacterium Bacillus subtilis forms biofilms that exhibit a characte

145 When starved, the Gram-positive bacterium Bacillus subtilis forms durable spores for survival.

146 To survive starvation, the bacterium Bacillus subtilis forms durable spores.

147 The spore-forming bacterium Bacillus subtilis frequently experiences high osmolarity

148 e show that fumarase of the model prokaryote Bacillus subtilis (Fum-bc) is induced upon DNA damage, c

149 in the mouse model and is an ortholog of the Bacillus subtilis Fur- and PerR-regulated Fe(II) efflux

150 illus cereus which, when integrated into the Bacillus subtilis genome, confers resistance to a broad

151 sing complementation analysis in a series of Bacillus subtilis gerD mutants, we demonstrated that alt

152 During sporulation in Bacillus subtilis, germinant receptors assemble in the i

153 om small angle X-ray scattering data for the Bacillus subtilis glyQS T-box riboswitch in complex with

154 g conditions on the growth of Gram-positive (Bacillus subtilis), Gram-negative (Escherichia coli) bac

155 s paralicheniformis 9945a DISARM system into Bacillus subtilis has rendered the engineered bacteria p

156 tral role in maintaining iron homeostasis in Bacillus subtilis Here we utilized FrvA, a high-affinity

157 1 function appeared to be conserved with the Bacillus subtilis homologue, and resistance to oxidative

158 uired for efficient germination of spores in Bacillus subtilis; however, the mechanism by which CotH

159 By dispersing swimming Bacillus subtilis in a liquid crystalline environment wi

160 n of TiO2 NPs increased the cell survival of Bacillus subtilis in autolysis-inducing buffer by 0.5 to

161 cture of inactive mutant (D88N) of RecU from Bacillus subtilis in complex with a 12 base palindromic

162 artian surface regolith, vegetative cells of Bacillus subtilis in Martian analogue environments lost

163 Here, we report a pathway in Bacillus subtilis in which regulated cell death maintain

164 ase secreted by the non-pathogenic bacterium Bacillus subtilis, induces plasma clotting by proteolyti

165 hat the YcgR homolog MotI (formerly DgrA) of Bacillus subtilis inhibits motility like a molecular clu

166 The differentiation of the bacterium Bacillus subtilis into a dormant spore is among the most

167 sed to re-engineer the PreQ1 riboswitch from Bacillus subtilis into an orthogonal OFF-switch.

168 We show that interaction of Bacillus subtilis IP SpoIVFB with its substrate Pro-sigm

169 Sporulation by Bacillus subtilis is a cell density-dependent response t

170 Messenger RNA decay in Bacillus subtilis is accomplished by a combination of ex

171 The bistably expressed K-state of Bacillus subtilis is characterized by two distinct featu

172 Sporulation in Bacillus subtilis is governed by a cascade of alternativ

173 Entry into sporulation in Bacillus subtilis is governed by a phosphorelay in which

174 Bacillus subtilis is intensively studied as a model orga

175 Biofilm formation by Bacillus subtilis is largely governed by a circuit in wh

176 Conjugation of plasmid pLS20 from Bacillus subtilis is limited to a time window between ea

177 Translation elongation factor P (EF-P) in Bacillus subtilis is required for a form of surface migr

178 Bacillus subtilis is the best studied spore-former and w

179 Since the origin of pimelic acid in Bacillus subtilis is unknown, (13) C-NMR studies were ca

180 ied, genetically tractable endospore-former, Bacillus subtilis, is an ideal subject for laboratory ev

181 y surfing" still occurs in mutant strains of Bacillus subtilis lacking flagella.

182 We show that biofilm formation by Bacillus subtilis, Lactobacillus rhamnosus and Pseudomon

183 Here we report that Bacillus subtilis LonA specifically degrades the master

184 In Bacillus subtilis, many adaptive genes are under the neg

185 The Bacillus subtilis MntR metalloregulatory protein senses

186 es affecting biofilm formation phenotypes in Bacillus subtilis modify community structure to the same

187 the present study, the kinetic properties of Bacillus subtilis MraY (BsMraY) were investigated by flu

188 In Bacillus subtilis, nitrogen homeostasis is controlled by

189 , we report on the native redox partners for Bacillus subtilis NOS (bsNOS) and a novel chimera that p

190 The crystal structure of Bacillus subtilis NrnA reveals a dynamic bi-lobal archit

191 genome-wide 3' end-mapping on an engineered Bacillus subtilis NusA depletion strain, we show that we

192 ssivity by suppressing RNAP pausing, whereas Bacillus subtilis NusG dramatically stimulates pausing a

193 What Bacillus subtilis offered was endless fascinating biolog

194 on the impact of a model soil microorganism, Bacillus subtilis, on the fate of pristine and already s

195 o the growth medium (termed 'High Sulfhydryl Bacillus subtilis' or HSBS) was compared to that onto B.

196 of sulfhydryl sites (termed 'Low Sulfhydryl Bacillus subtilis' or LSBS) and to sorption onto a comme

197 prokaryotic cells such as Escherichia coli, Bacillus subtilis, or Caulobacter crescentus.

198 onella enterica, the Gram-positive bacterium Bacillus subtilis, or Mycobacterium marinum.

199 s of high resolution structures of QueG from Bacillus subtilis Our structure of QueG bound to a tRNA(

200 (U51) in the P4 helix of circularly permuted Bacillus subtilis P RNA with 4-thiouridine, 4-deoxyuridi

201 proposed intermolecular interactions in the Bacillus subtilis ParB (BsSpo0J) and characterized their

202 ngle-molecule approaches, we discovered that Bacillus subtilis ParB (Spo0J) is able to trap DNA loops

203 is work, we have investigated the binding of Bacillus subtilis ParB to DNA in vitro using a variety o

204 In addition, nine Bacillus subtilis PBP-null mutants were evaluated with t

205 Recently, the participation of Bacillus subtilis PfeT, a P1B4-ATPase, in cytoplasmic Fe

206 AR9 is a giant Bacillus subtilis phage whose uracil-containing double-s

207 Here, we uncover roles for the Bacillus subtilis PhoP regulon genes glpQ and phoD as en

208 novel derivative of ct6A found in tRNAs from Bacillus subtilis, plants and Trypanosoma brucei.

209 Deletion of the Bacillus subtilis pnpA gene, encoding the major 3' exonu

210 For vitamin B2 (riboflavin), GM Bacillus subtilis production strains have been developed

211 analysis of the cellular toxicity caused by Bacillus subtilis prophage SPbeta-encoded toxin BsrG rev

212 ein PBP 2B is a key cell division protein in Bacillus subtilis proposed to have a specific catalytic

213 ) from the probiotic spore-forming bacterium Bacillus subtilis protects mice from acute colitis induc

214 A striking example is the self-inserting Bacillus subtilis protein Mistic, which is involved in b

215 The Bacillus subtilis protein regulator of the gabTD operon

216 Bacillus subtilis provides a model for the coordinate re

217 The crystal structure of Bacillus subtilis PrsA reveals a central catalytic parvu

218 Inactivation of Bacillus subtilis pxpA, pxpB, or pxpC genes slowed growt

219 gicidal lipopeptide class of surfactins from Bacillus subtilis QST713, and the detergent octyl glucos

220 We find that Bacillus subtilis rapidly inhibits Bacillus megaterium g

221 Here we investigated the importance of Bacillus subtilis RecD2 helicase to genome integrity.

222 Bacillus subtilis regulates flagellar assembly using bot

223 Bacillus subtilis responds to peptide stress by releasin

224 he crystal structure of unliganded CodY from Bacillus subtilis revealing a 10-turn alpha-helix linkin

225 effect of induced liquid state fermentation (Bacillus subtilis, Rhizopus oryzae, Saccharomyces cerevi

226 Although Bacillus subtilis riboswitches have been shown to contro

227 We show that Bacillus subtilis RoxS, a major trans-acting sRNA shared

228 We identified three RNA structures in the Bacillus subtilis rplJL leader transcript that function

229 Bacillus subtilis seems to have redundant genes, bioI an

230 major low-molecular-weight thiol compound in Bacillus subtilis, serves as an important zinc buffer in

231 ments on pellicles, or floating biofilms, of Bacillus subtilis showed that while they are multiplying

232 yloA of the model bacterium Bacillus subtilis shows high homology to genes encoding

233 f labor of two cell types that appear during Bacillus subtilis sliding motility.

234 ule fluorescence microscopy to visualize how Bacillus subtilis SMC (BsSMC) interacts with flow-stretc

235 In the bacterium Bacillus subtilis, SMC-condensin complexes are topologic

236 to predict the disinfection efficiency of a Bacillus subtilis spore culture.

237 of Escherichia coli, bacteriophage MS2, and Bacillus subtilis spores as surrogates for pathogens und

238 We show that in hamsters immunized with Bacillus subtilis spores expressing a carboxy-terminal s

239 Bacillus subtilis spores were exposed to germinants for

240 In Bacillus subtilis spores, the coat contains over 70 dist

241 ate a functional role for the arrangement of Bacillus subtilis sporulation network genes on opposite

242 During Bacillus subtilis sporulation, chromosome copy number is

243 During Bacillus subtilis sporulation, segregating sister chromo

244 me translocation and membrane fission during Bacillus subtilis sporulation.

245 Bacteriophage phi29 from Bacillus subtilis starts replication of its terminal pro

246 eolyticus str 115 in a genetically tractable Bacillus subtilis strain to parse the processing steps o

247 Recently, a Bacillus subtilis strain was isolated in which the essen

248 Bacillus subtilis strains lacking the Rv1422 homologue y

249 Some pesticides contain Bacillus subtilis strains that produce lipopeptide famil

250 Spores of Bacillus megaterium and Bacillus subtilis strains were harvested shortly after r

251 PrsA homologues encoded by Bacillus subtilis, Streptococcus pyogenes, Streptococcus

252 EF-P-encoding gene (efp) primarily supports Bacillus subtilis swarming differentiation, whereas EF-P

253 BisI (G(m5)C downward arrow NGC) is found in Bacillus subtilis T30.

254 function, we created a ileS(T233P) mutant of Bacillus subtilis that allows tRNA(Ile) mischarging whil

255 Here we show in Bacillus subtilis that cooperative interactions in a spa

256 YphC and YsxC are GTPases in Bacillus subtilis that facilitate the assembly of the 50

257 o-component sigma factor YvrI and YvrHa from Bacillus subtilis that independently contributes to the

258 thermore, it has been shown in the bacterium Bacillus subtilis that loss of RER increases spontaneous

259 For the Gram-positive bacterium Bacillus subtilis the process involves the differentiati

260 t a promoter resembling the pyrG promoter of Bacillus subtilis The structure reveals that the reitera

261 stingly, in the Gram-positive model organism Bacillus subtilis, the competence master regulator ComK

262 the guanine-sensing xpt-pbuX riboswitch from Bacillus subtilis, the conformation of the full-length t

263 g inactivation for both Escherichia coli and Bacillus subtilis, the described membrane assemblies wit

264 In Bacillus subtilis, the forespore protein SpoIIQ and the

265 In the well-studied spore-former Bacillus subtilis, the highly conserved sigma(E) , SpoII

266 In Bacillus subtilis, the nucleoid occlusion protein Noc bi

267 During sporulation in Bacillus subtilis, the only convex (positively curved) s

268 In Bacillus subtilis, the proteolytic adaptor protein MecA

269 In Bacillus subtilis, the RNase Mini-III is integral to 23S

270 Here we report that, in Bacillus subtilis, this complex is functional in the abs

271 In addition, bioimaging studies against Bacillus subtilis through confocal fluorescence microsco

272 e histidine-kinase that allows the bacterium Bacillus subtilis to adjust the levels of unsaturated fa

273 vestigated the ability of the soil bacterium Bacillus subtilis to discriminate kin from nonkin in the

274 ling strategy in the gram-positive bacterium Bacillus subtilis to investigate the nanoscale structure

275 that controls the general stress response of Bacillus subtilis to uncover widely relevant general des

276 Repression by the Bacillus subtilis transcription factor Zur requires Zn(I

277 CodY and ScoC are Bacillus subtilis transcriptional regulators that contro

278 We studied the Bacillus subtilis trp 5'-UTR (untranslated region), whic

279 During times of environmental insult, Bacillus subtilis undergoes developmental changes leadin

280 Thus, we propose that Bacillus subtilis utilizes the same nanotube apparatus i

281 reduction of 2-cyclohexen-1-one by YqjM from Bacillus subtilis was selected as the model system.

282 of the same genus Bacillus licheniformis and Bacillus subtilis, was confirmed via leave-one-out cross

283 Applied to a real data set from Bacillus subtilis we demonstrate it's ability to detecti

284 of sigma1.1 from the Gram-positive bacterium Bacillus subtilis We found that B. subtilis sigma1.1 is

285 cherichia coli, Mycobacterium smegmatis, and Bacillus subtilis), we show that the frequency of TAG an

286 Extending this analysis to Bacillus subtilis, we isolated a novel benzamide-depende

287 set of these clusters in Escherichia coli or Bacillus subtilis, we show that they encode pyrazinones

288 nt layers of the envelope stress response of Bacillus subtilis when challenged with the lipid II cycl

289 pendent control of spxA2 was accomplished in Bacillus subtilis, where deletion analysis uncovered two

290 BslA is a protein secreted by Bacillus subtilis which forms a hydrophobic film that co

291 a quality control pathway was discovered in Bacillus subtilis which monitors the assembly of the spo

292 those from psychotropic microorganisms (e.g. Bacillus subtilis), which produce enzymes under refriger

293 triking example is the competence circuit in Bacillus subtilis, which exhibits much larger noise in t

294 rom Pseudomonas stutzeri and a protease from Bacillus subtilis, which were immobilized in octyl-glyox

295 SSF was carried out by Bacillus subtilis, whilst LSF was performed either by na

296 ineered several modular Escherichia coli and Bacillus subtilis whole-cell-based biosensors which inco

297 of various lengths, including swarm cells), Bacillus subtilis (wild-type and a mutant with fewer fla

298 dge is completely hydrolyzed, whereas PGN of Bacillus subtilis with meso-diaminopimelic acid directly

299 l activity against Staphylococcus aureus and Bacillus subtilis with MICs ranging from 5.5 to 17 muM.

300 he guanine and adenine riboswitches from the Bacillus subtilis xpt gene encoding xanthine phosphoribo