ライフサイエンスコーパス: Bacillus subtilis

1 ompared to its bacterial homolog RNase J1 of Bacillus subtilis.

2 lation in the sole RNR of the model organism Bacillus subtilis.

3 ivision site in the Gram-positive bacterium, Bacillus subtilis.

4 Escherichia coli W, Yarrowia lipolytica, or Bacillus subtilis.

5 m in ICEBs1 from the Gram-positive bacterium Bacillus subtilis.

6 oding topoisomerase I in the model bacterium Bacillus subtilis.

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

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

9 rowing bacteria such as Escherichia coli and Bacillus subtilis.

10 scherichia coli, Pseudomonas aeruginosa, and Bacillus subtilis.

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

12 partner-switching pathway, best described in Bacillus subtilis.

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

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

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

16 rient extraction from Bacillus megaterium by Bacillus subtilis.

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

18 ative Escherichia coli and the Gram-positive Bacillus subtilis.

19 ate membrane synthesis with cell division in Bacillus subtilis.

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

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

22 master regulator of nitrogen assimilation in Bacillus subtilis.

23 ensor" in YfkE, a bacterial CAX homolog from Bacillus subtilis.

24 (GlcNAc) could be balanced and optimized in Bacillus subtilis.

25 g activation of the DNA damage checkpoint in Bacillus subtilis.

26 tide secreted by the Gram-positive bacterium Bacillus subtilis.

27 mer's ligand-free structure in the mesophile Bacillus subtilis.

28 -negative Escherichia coli and Gram-positive Bacillus subtilis.

29 ned against Escherichia coli K-12 (G(-)) and Bacillus subtilis 1046 (G(+)).

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

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

32 In Bacillus subtilis, 2 proteins initiate coat assembly: Sp

33 Here, we explore the interaction between Bacillus subtilis 3610 and Pseudomonas chlororaphis PCL1

34 tron microscopy structure of RbgA bound to a Bacillus subtilis 50S subunit assembly intermediate (45S

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

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

37 Previously, we characterized the Bacillus subtilis acetylome and found that the essential

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

39 cle sequencing approach to Escherichia coli, Bacillus subtilis, Agrobacterium tumefaciens, and Mesopl

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

41 dCACHE domains of histidine kinase KinD from Bacillus subtilis and diguanylate cyclase rpHK1S-Z16 fro

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

43 monstrated using two model organisms, namely Bacillus subtilis and Escherichia coli, and by developin

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

45 spore strains , namely Bacillus atrophaeus, Bacillus subtilis and Geobacillus stearothermophilus, ha

46 of the lipid-binding domains of DivIVA from Bacillus subtilis and GpsB from several species share a

47 ST is successfully applied for Gram-positive Bacillus subtilis and Gram-negative Escherichia coli as

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

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

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

51 t with XPRT from the Gram-positive bacterium Bacillus subtilis and inhibit XPRT activity by competing

52 at biofilm-forming bacterial lawns including Bacillus subtilis and Pseudomonas aeruginosa strongly al

53 as Escherichia coli, Salmonella typhimurium, Bacillus subtilis and Saccharomyces cerevisiae have pinp

54 ion and network recovery using examples from Bacillus subtilis and Saccharomyces cerevisiae, and show

55 spiro-fermentative microorganisms, including Bacillus subtilis and Saccharomyces cerevisiae.

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

57 lling potassium uptake in the model organism Bacillus subtilis and several other bacteria.

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

59 ved in osmolyte transport in species such as Bacillus subtilis and Streptococcus pneumoniae, but whet

60 Application of this methodology to Bacillus subtilis and Streptomyces coelicolor revealed h

61 ug ABC transporters, the homodimer BmrA from Bacillus subtilis and the heterodimer PatA/PatB from Str

62 is found exclusively in Firmicutes including Bacillus subtilis and the opportunistic pathogens Clostr

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

64 tator complexes from Clostridium sporogenes, Bacillus subtilis and Vibrio mimicus, allowing interpret

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

66 We test the system against Gram-positive (Bacillus subtilis) and Gram-negative (Escherichia coli)

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

68 nhibit biofilms by Pseudomonas aeruginosa or Bacillus subtilis, and inhibited biofilms by S. aureus t

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

70 s Staphylococcus aureus, Streptococcus spp., Bacillus subtilis, and Mycobacterium spp. have demonstra

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

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

73 bosomes in the Gram-positive model bacterium Bacillus subtilis, and that this 'runaway transcription'

74 od-shaped bacterium like Escherichia coli or Bacillus subtilis, and the genome typically carries 20 o

75 anslation is uncoupled from transcription in Bacillus subtilis, arguing that bacteria utilize very di

76 We identify the potassium importer KimA from Bacillus subtilis as a member of the KUP family, demonst

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

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

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

80 agement in the Gram-positive model bacterium Bacillus subtilis as proof-of-principle precedent.

81 ned how each affects the growth and width of Bacillus subtilis as well as the mechanical anisotropy a

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

83 t E. coli strains at lower UV-B doses, while Bacillus subtilis ATCC 6633 was more resistant to the tr

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

85 avin on the antimicrobial activities against Bacillus subtilis (ATCC 6633) and two strains of Escheri

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

87 strains, four (Nitrospira, Escherichia coli, Bacillus subtilis, Bacillus cereus) were identified via

88 re identified by 16S-rRNA gene sequencing as Bacillus subtilis, Bacillus thuringiensis, and Bacillus

89 rns to form in a model multicellular system, Bacillus subtilis bacterial biofilms.

90 ying life cycle progression in the bacterium Bacillus subtilis, based on hundreds of previously acqui

91 ect combination with Aliivibrio fischeri and Bacillus subtilis bioassays.

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

93 We discovered that two Bacillus subtilis biofilm communities undergoing metabol

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

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

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

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

98 PlsX is a peripheral membrane enzyme in Bacillus subtilis, but how it associates with the membra

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

100 rt that a similar function is carried out in Bacillus subtilis by CpgA, a checkpoint protein known to

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

102 Bacillus subtilis can enter three developmental pathways

103 sors for model bacteria Escherichia coli and Bacillus subtilis can go to 0.5119 and 1.69 cells/mL, re

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

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

106 Bacillus subtilis can measure the activity of the enzyme

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

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

109 Here, we find that non-sporulating Bacillus subtilis cells can survive deep starvation cond

110 We applied microSPLiT to >25,000 Bacillus subtilis cells sampled at different growth stag

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

112 by measuring membrane potential dynamics of Bacillus subtilis cells, we show that actively growing b

113 to distinct clusters in Escherichia coli and Bacillus subtilis cells.

114 ynamics of three replisomal proteins in live Bacillus subtilis cells: the two replicative DNA polymer

115 In Bacillus subtilis, cells lacking all four PBPs with tran

116 et of essential sequence elements within the Bacillus subtilis chromosome origin unwinding region.

117 For bacteria tested (Staphylococcus aureus, Bacillus subtilis, Clostridium perfringens, Escherichia

118 nes CodY protein was functionally similar to Bacillus subtilis CodY when expressed in B. subtilis cel

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

120 transcriptional regulatory network (TRN) of Bacillus subtilis coordinates cellular functions of fund

121 Solution NMR structures of the homologous Bacillus subtilis CopL, together with phylogenetic analy

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

123 lly characterize S. aureus homologues of the Bacillus subtilis cystine transporters TcyABC and TcyP.

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

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

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

127 Bacillus subtilis differentiates into a state of compete

128 he marquee features of a cell fate switch in Bacillus subtilis-discrete states, multigenerational inh

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

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

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

132 iously described a novel regulatory logic in Bacillus subtilis enabling the cell to directly monitor

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

134 Bacillus subtilis encodes two functionally redundant D,L

135 rent elements, we compared the activities of Bacillus subtilis, Escherichia coli, and Mycobacterium t

136 f model systems (Aspergillus penicillioides; Bacillus subtilis; Escherichia coli; Eurotium amstelodam

137 Bacillus subtilis exhibited a reduction in bioleaching e

138 The Gram-positive bacterium Bacillus subtilis exhibits complex spatial and temporal

139 We observe that when Bacillus subtilis exits rapid growth, a subpopulation of

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

141 The Bacillus subtilis extracytoplasmic function sigma factor

142 Bacillus subtilis flagella are not only required for loc

143 ains tested, however no effect was found for Bacillus subtilis for up to 80 mJ/cm(2) UV-B.

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

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

146 ed CTT to assembly and enzymatic activity of Bacillus subtilis FtsZ (Bs-FtsZ).

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

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

149 tion (RNET-seq), we analyzed RNAP pausing in Bacillus subtilis genome-wide and identified an extensiv

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

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

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

153 For contamination rule-out targets (Bacillus subtilis group, Corynebacterium, Cutibacterium

154 The gram-positive bacterium Bacillus subtilis has become a model organism for studyi

155 cterial species such as Escherichia coli and Bacillus subtilis has provided a vast amount of knowledg

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

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

158 1 function appeared to be conserved with the Bacillus subtilis homologue, and resistance to oxidative

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

160 py enabled in situ and real-time tracking of Bacillus subtilis in a forward osmosis system with space

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

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

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

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

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

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

167 Starvation of Bacillus subtilis initiates endosporulation involving fo

168 o determine how the initiation proteins from Bacillus subtilis interact with each other.

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

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

171 Biofilm formation by Bacillus subtilis is a communal process that culminates

172 Bacillus subtilis is an important bacterium for understa

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

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

175 ribosome-binding resistance factor VmlR from Bacillus subtilis is localized to the cytoplasm, ruling

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

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

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

179 , chromosome cycle and division mechanism of Bacillus subtilis L-forms.

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

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

182 rate at 1.9 angstrom resolution and those of Bacillus subtilis LCP enzymes, TagT, TagU, and TagV, in

183 or depleting oxygen enables L-form growth in Bacillus subtilis, Listeria monocytogenes and Staphyloco

184 ycan synthases from three bacterial species (Bacillus subtilis, Listeria monocytogenes and Streptococ

185 determined the crystallographic structure of Bacillus subtilis LS (SacB) in complex with a levan-type

186 hes, including the riboswitch present in the Bacillus subtilis metI gene, which encodes cystathionine

187 The Bacillus subtilis MntR metalloregulatory protein senses

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

189 ll as the entire set of Escherichia coli and Bacillus subtilis mRNAs, we showed that 3'UTR variabilit

190 omosomally encoded RNase HII and RNase HIII, Bacillus subtilis NCIB 3610 encodes a previously unchara

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

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

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

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

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

196 rminal phosphate moieties as orthophosphate (Bacillus subtilis) or pyrophosphate (Escherichia coli) t

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

198 dicted structural features was identified in Bacillus subtilis over a decade ago, but its structure a

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

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

201 Bacillus subtilis ParB forms multimeric networks involvi

202 Bacillus subtilis PdaC (BsPdaC) is a membrane-bound, mul

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

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

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

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

207 The conjugative Bacillus subtilis plasmid pLS20 uses quorum sensing to d

208 Bacillus subtilis possess two protein lipoylation pathwa

209 Like many eukaryotes and some bacteria, Bacillus subtilis primarily utilizes oxygen during respi

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

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

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

213 The Bacillus subtilis protein regulator of the gabTD operon

214 Endospore formation in Bacillus subtilis provides an ideal model system for stu

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

216 We find that Bacillus subtilis rapidly inhibits Bacillus megaterium g

217 However, PG from Bacillus subtilis reduced infection >10,000-fold, while

218 Exopolysaccharide (EPS) from the probiotic Bacillus subtilis reduces bacterial burden and inflammat

219 m tumefaciens, or the plant growth promoting Bacillus subtilis, relative to controls.

220 SPO1 bacteriophage infection of Bacillus subtilis results in comprehensive remodeling of

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

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

223 Although Bacillus subtilis riboswitches have been shown to contro

224 We structurally analyzed Bacillus subtilis RNAP-delta-HelD complexes.

225 In Bacillus subtilis, robust biofilm formation requires lar

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

227 oelectron microscopy (cryo-EM) structures of Bacillus subtilis RQC complexes representing different A

228 encoding a bacterial (p)ppGpp synthetase in Bacillus subtilis, sasA, exhibits high levels of extrins

229 Bacillus subtilis seems to have redundant genes, bioI an

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

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

232 catalytic, and DNA-binding properties of the Bacillus subtilis SMC complex.

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

234 ated the crystal structures of AimR from the Bacillus subtilis SPbeta phage in its apo form, bound to

235 logically distinct Staphylococcus aureus and Bacillus subtilis species, using live cells and purified

236 Assembly of the Bacillus subtilis spore coat involves over 80 proteins w

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 r-resolution time-lapse imaging of wild-type Bacillus subtilis spores, which contain low numbers of g

240 Here, we visualize Bacillus subtilis sporulation using cryo-electron tomogr

241 During Bacillus subtilis sporulation, chromosome copy number is

242 During Bacillus subtilis sporulation, segregating sister chromo

243 Here we present a crystal structure of Bacillus subtilis SsbA bound to ssDNA.

244 In some bacteria, including Bacillus subtilis strain 168, both WTA and LTA are glyce

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

246 romic sequence GACGmAG within the genomes of Bacillus subtilis strains.

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

248 collective behavior phases which develop as Bacillus subtilis swarms expand over five orders of magn

249 M structures of Geobacillus kaustophilus and Bacillus subtilis T-box-tRNA complexes, detailing their

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

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

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

253 in genetic backgrounds of S. pneumoniae and Bacillus subtilis that exhibit Mn2+ sensitivity, reveali

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

255 an antibiotic specific DNA repair pathway in Bacillus subtilis that is composed of a previously uncha

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

257 ed exopolysaccharide (EPS) from a probiotic, Bacillus subtilis, that induces anti-inflammatory macrop

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

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

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

261 In the Gram-positive model bacterium, Bacillus subtilis, the final maturation steps of the two

262 In Bacillus subtilis, the forespore protein SpoIIQ and the

263 In Bacillus subtilis, the interaction stimulates the endonu

264 discovered that in biofilms of the bacterium Bacillus subtilis, the propagation of an electrical sign

265 In Bacillus subtilis, the RNAP delta subunit and NTPase Hel

266 ts a wide variety of states is the bacterium Bacillus subtilis, the subject of this Primer.

267 In Bacillus subtilis, these properties are influenced by th

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

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

270 for membrane coating were investigated with Bacillus subtilis to achieve the most efficient removal

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

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

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

274 In Bacillus subtilis, UgtP synthesises the glucolipid precu

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

276 domain (GSR(apt)) of the xpt-pbuX operon in Bacillus subtilis Unlike what had been observed in prote

277 The Gram-positive bacterium Bacillus subtilis uses serine not only as a building blo

278 te a long history of genetic manipulation of Bacillus subtilis using auxotrophic markers, the genes i

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

280 Spx-recognition motif previously defined in Bacillus subtilis was identified in the promoters of Spx

281 eudomonas putida, Staphylococcus aureus, and Bacillus subtilis was observed when the assay was perfor

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 Using Bacillus subtilis, we identified factors that revealed t

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 nterobacter sp., Pseudomonas aeruginosa, and Bacillus subtilis when they are confined within a thin l

289 recently elucidated in Escherichia coli and Bacillus subtilis where fatty acid synthesis plus dedica

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

296 of the delta subunit of RNA polymerase from Bacillus subtilis whose unfolded domain is highly charge

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

298 production of PLY endowed the nonpathogenic Bacillus subtilis with the ability to trigger neutrophil

299 terial community composed of five strains of Bacillus subtilis, with each strain producing a variant

300 Here, we demonstrate that the Bacillus subtilis YciC zinc metallochaperone (here renam