ライフサイエンスコーパス: Bacillus

1 and host-pathogen interactions of the genus Bacillus.

2 Pseudomonas, Acinetobacter, Burkholderia and Bacillus.

3 lective agar (BCSA) and a standard acid-fast bacillus (AFB) culture method for the isolation of nontu

4 ions in the gyrA and gyrB genes of acid-fast bacillus (AFB) smear-positive sediments or of M. tubercu

5 yotic NaVs NsVBa (nonselective voltage-gated Bacillus alcalophilus) and NaChBac (bacterial sodium cha

6 Thermophilic Bacillus altitudinis immobilized nanodiamond was used as

7 Heterotrophic Bacillus amyloliquefaciens associated with edible red se

8 Recently, a microcin C homologue from Bacillus amyloliquefaciens containing a longer peptide p

9 We established Bacillus amyloliquefaciens LoaP as a paradigm for this p

10 characterised three orthologues of BslA from Bacillus amyloliquefaciens, Bacillus licheniformis and B

11 Bacteria of the genera Bacillus and Clostridium form highly resistant spores, w

12 ones of many gram-positive bacteria, such as Bacillus and Streptococcus, are small, linear peptides s

13 rikingly from those governing sporulation of Bacillus and Streptomyces, suggesting that Myxococcus ev

14 uring to illustrate the relationship between Bacillus and YTC.

15 community relevant spore-forming pathogens, Bacillus anthracis and Clostridium difficile.

16 Therefore, the abilities of Bacillus anthracis and Escherichia coli gyrase and topoi

17 The lung is the terminal target of Bacillus anthracis before death, whatever the route of i

18 ng glycans on spores, whereas others such as Bacillus anthracis do not.

19 Bacillus anthracis edema toxin (ET) consists of protecti

20 he most prevalent form of naturally acquired Bacillus anthracis infection, which is associated with e

21 Bacillus anthracis is a sporulating Gram-positive bacter

22 Bacillus anthracis is a tier 1 select agent with the pot

23 Escherichia coli, Staphylococcus aureus, and Bacillus anthracis particles.

24 tion between the human CMG2 receptor and the Bacillus anthracis protective antigen (PA) is essential

25 the interaction between macrophage cells and Bacillus anthracis spores is of significant importance w

26 , we demonstrate that PHB deficiency impairs Bacillus anthracis sporulation through diminishing the e

27 se anthrax lethal factor (LF) is secreted by Bacillus anthracis to promote disease virulence through

28 elements (29 nt), a fluoride riboswitch from Bacillus anthracis(48 nt), and a frame-shifting element

29 res of the Bacillus cereus group (B. cereus, Bacillus anthracis, and Bacillus thuringiensis) are surr

30 strains of the Bacillus cereus group, i.e., Bacillus anthracis, Bacillus cereus, Bacillus mycoides,

31 uccessfully implemented for the detection of Bacillus anthracis, botulinum B, and tularemia in comple

32 solution that the active form of DAPDC from Bacillus anthracis, Escherichia coli, Mycobacterium tube

33 During high-impact events involving Bacillus anthracis, such as the Amerithrax incident of 2

34 Bacillus anthracis, the anthrax agent, is a member of th

35 Bacillus anthracis, the causative agent of anthrax, is a

36 threatening disease caused by infection with Bacillus anthracis, which expresses lethal factor and th

37 Forty-six distinct strains of Bacillus anthracis, Yersinia pestis, Francisella tularen

38 x using recombinant protective Ag (rPA) from Bacillus anthracis.

39 th inductive strains of Cellulophaga lytica, Bacillus aquimaris and Staphylococcus warneri were under

40 effect of sterilization process on spores of Bacillus atrophaeus.

41 opper oxidase (MCO) MnxG protein from marine Bacillus bacteria plays an essential role in producing M

42 Gene knockouts of the Bacillus C-methyltransferase and the 4-reductase confirm

43 uced by both tuberculosis (TB) infection and bacillus Calmette Guerin (BCG) vaccination.

44 For the population of patients for whom bacillus Calmette-Guerin (BCG) has failed, the type of f

45 Bacillus Calmette-Guerin (BCG) osteitis was more common

46 dder cancer (NMIBC) are either refractory to bacillus Calmette-Guerin (BCG) treatment or may experien

47 We estimated the association between bacillus Calmette-Guerin (BCG) vaccination and childhood

48 Studies have suggested that Bacillus Calmette-Guerin (BCG) vaccination may reduce th

49 adults before and after primary or secondary bacillus Calmette-Guerin (BCG) vaccination were assessed

50 Bacillus Calmette-Guerin (BCG) vaccine is widely used fo

51 Vaccinations studied comprised Bacillus Calmette-Guerin (BCG) vaccine, Triple vaccine,

52 avesical immunotherapy instillation with the bacillus Calmette-Guerin (BCG) vaccine.

53 mber of WCV candidates, based on recombinant bacillus Calmette-Guerin (BCG), attenuated Mycobacterium

54 hat regulate tuberculosis susceptibility and bacillus Calmette-Guerin (BCG)-induced immunity are most

55 matis (M. smegmatis) and Mycobacterium bovis Bacillus Calmette-Guerin (BCG).

56 ein report that M. tuberculosis and M. bovis bacillus Calmette-Guerin infection down-regulated the ex

57 A enhanced nonpathogenic Mycobacterium bovis bacillus Calmette-Guerin intracellular survival, downreg

58 and evaluated as alternatives to traditional Bacillus Calmette-Guerin needles and syringes for the ad

59 d culture status of index cases, the age and bacillus Calmette-Guerin vaccination status of contacts,

60 D4(+) T cells induced by Mycobacterium bovis bacillus Calmette-Guerin vaccination.

61 production after stimulation with live BCG (Bacillus Calmette-Guerin), and a second locus on chromos

62 M. bovis bacillus Calmette-Guerin-primed sanroque T cells transfe

63 7 years, he underwent cystoprostatectomy for bacillus Calmette-Guerin-refractory, high-grade noninvas

64 with CD154 expression by CD4(+) T cells from bacillus Calmette-Guerin-vaccinated mice and show that h

65 In addition to multiple virulence factors, Bacillus cereus a pathogen that causes food poisoning an

66 Bacillus cereus AlkD is the only DNA glycosylase known t

67 ylococcus aureus, Leuconostoc mesenteroides, Bacillus cereus and Enterococcus faecalis proving its an

68 phages, like GIL16 or Bam35, whose hosts are Bacillus cereus and related Gram-positive bacteria.

69 se structure were linked to spore glycans in Bacillus cereus ATCC 14579 and ATCC 10876.

70 xamined the conformational properties of the Bacillus cereus beta-lactamase II in the presence of che

71 at the dynamics of an anthrax-causing agent, Bacillus cereus biovar anthracis, in a tropical rainfore

72 tion rate, and recombination tract length of Bacillus cereus from a whole genome alignment.

73 The spores of the Bacillus cereus group (B. cereus, Bacillus anthracis, an

74 sis of 16S rRNA genes from 50 strains of the Bacillus cereus group, i.e., Bacillus anthracis, Bacillu

75 The exosporium of the Bacillus cereus group, including the anthrax pathogen, c

76 we demonstrate the quantitative detection of Bacillus cereus in buffer medium and Escherichia coli in

77 or rupture of dormant spores of B. subtilis, Bacillus cereus or Bacillus megaterium, although germina

78 racis, the anthrax agent, is a member of the Bacillus cereus sensu lato group, which includes invasiv

79 Treatment of cells with Bacillus cereus sphingomyelinase (bSMase) increases the

80 cum, ColT from C. tetani, and ColQ1 from the Bacillus cereus strain Q1, while showing negligible acti

81 llus cereus group, i.e., Bacillus anthracis, Bacillus cereus, Bacillus mycoides, and Bacillus thuring

82 Antimicrobial properties on tester strains (Bacillus cereus, Escherichia coli, Staphylococcus aureus

83 racts inhibited the growth of gram-positive (Bacillus cereus, Staphylococcus aureus, Listeria monocyt

84 s of the commercial beta-galactosidases from Bacillus circulans, Kluyveromyces lactis and Aspergillus

85 Expansins facilitate plant colonization by Bacillus, Clavibacter, and Trichoderma species, a list l

86 pzX in Bacillus could represent a trait shared by many spore-pr

87 MIC values from different bacterial genera (Bacillus, Cupriavidus, Klebsiella, Ochrobactrum, Paeniba

88 ed to represent a novel species of the genus Bacillus, for which the name Bacillus oryziterrae sp. no

89 RefZ is conserved across the Bacillus genus and remains functional as an inhibitor of

90 Given that Bacillus halodurans and Bacillus subtilis encode AsnRS f

91 complex sequence-activity landscapes for the Bacillus halodurans I-C (Cascade), Escherichia coli I-E

92 BH0236 from Bacillus halodurans is a multimodular beta-1,3-glucanase

93 structure of an amide-modified RNA-DNA with Bacillus halodurans RNase H1.

94 ) and NaChBac (bacterial sodium channel from Bacillus halodurans) (IC50 = 112 nM and 30 nM, respectiv

95 drophobic amino acid transporter (MhsT) from Bacillus halodurans, have been resolved in novel inward-

96 ved macrophages following infection with the bacillus in vitro.

97 Fortunately, the leprosy bacillus is sensitive to several antibiotics.

98 ive attenuated Bacille Calmette-Guerin (BCG) bacillus is the only licensed vaccine for tuberculosis p

99 ues of BslA from Bacillus amyloliquefaciens, Bacillus licheniformis and Bacillus pumilus as well as a

100 h other, including members of the same genus Bacillus licheniformis and Bacillus subtilis, was confir

101 l species was shown with ternary mixtures of Bacillus licheniformis, Escherichia coli JM109, and Lact

102 tment with a DNA-degrading enzyme, NucB from Bacillus licheniformis, strongly inhibited the accumulat

103 ering of the unexplored, extreme alkaliphile Bacillus marmarensis as a platform for new bioprocesses

104 Tyrosinase from Bacillus megaterium (TyrBm) was previously used to modul

105 provide evidence of nutrient extraction from Bacillus megaterium by Bacillus subtilis.

106 that Bacillus subtilis can kill and prey on Bacillus megaterium by delivering a toxin and extracting

107 of OXT-A has been linked to a plasmid-borne Bacillus megaterium gene cluster that contains four gene

108 find that Bacillus subtilis rapidly inhibits Bacillus megaterium growth by delivering the tRNase toxi

109 ures and biochemical characterization of the Bacillus megaterium HD domain phosphohydrolase OxsA, inv

110 Here, we show that a soil bacterial isolate, Bacillus megaterium Sb5, promotes plant infection by Phy

111 nt spores of B. subtilis, Bacillus cereus or Bacillus megaterium, although germinated B. subtilis spo

112 that Bacillus subtilis can kill and prey on Bacillus megaterium.

113 , including characteristics of the causative bacillus Mycobacterium leprae: the long incubation perio

114 , i.e., Bacillus anthracis, Bacillus cereus, Bacillus mycoides, and Bacillus thuringiensis These spec

115 We predicted the disorder propensities of Bacillus naganoensis pullulanase (PUL) using the bioinfo

116 The soil-dwelling opportunistic bacterium Bacillus nematocida B16 uses a "Trojan horse" mechanism

117 amily DNase and other DHH family nanoRNases, Bacillus NrnA has gained an extended substrate-binding p

118 ssion of Mycobacterium leprae, the causative bacillus of the disease.

119 es of the genus Bacillus, for which the name Bacillus oryziterrae sp. nov. is proposed.

120 Engineering the Bacillus paralicheniformis 9945a DISARM system into Baci

121 myloliquefaciens, Bacillus licheniformis and Bacillus pumilus as well as a paralogue from B. subtilis

122 e isolated an As(III)-methylating bacterium, Bacillus sp. CX-1, and identified a gene encoding a S-ad

123 Overall, gemfibrozil exposure in Bacillus sp. GeD10 increased the abundance of several en

124 BlarsM is constitutively expressed in Bacillus sp. Heterologous expression of BlarsM conferred

125 The active Mn oxidase in Bacillus sp. PL-12, Mnx, is a complex composed of a mult

126 RNA gene sequence similarity) is the closest Bacillus species according to 16S rRNA gene comparison.

127 ubtilis, and dormant spores of several other Bacillus species by incubation on bSi wafers with and wi

128 acids and glucose by two Pseudomonas and one Bacillus species isolated from ground water.

129 sulfhydryl site concentrations for the three Bacillus species studied, the elevated glucose concentra

130 quirements for this developmental process in Bacillus species.

131 whereas Coagulase negative Staphylococci and Bacillus spp. are common causes of post-operative and po

132 cteria from the family Hyphomicrobiaceae and Bacillus spp., respectively.

133 In Bacillus spp., where PHB biosynthesis precedes the forma

134 ric trp RNA-binding Attenuation Protein from Bacillus stearothermophilus using nearest-neighbor stati

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

152 ect combination with Aliivibrio fischeri and Bacillus subtilis bioassays.

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

154 We discovered that two Bacillus subtilis biofilm communities undergoing metabol

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

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

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

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

159 Bacillus subtilis can enter three developmental pathways

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

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

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

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

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

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

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

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

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

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

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

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

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

173 Bacillus subtilis flagella are not only required for loc

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

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

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

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

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

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

180 1 function appeared to be conserved with the Bacillus subtilis homologue, and resistance to oxidative

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

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

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

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

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

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

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

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

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

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

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

192 The Bacillus subtilis MntR metalloregulatory protein senses

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

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

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

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

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

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

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

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

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

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

203 The Bacillus subtilis protein regulator of the gabTD operon

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

205 We find that Bacillus subtilis rapidly inhibits Bacillus megaterium g

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

207 Although Bacillus subtilis riboswitches have been shown to contro

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

209 Bacillus subtilis seems to have redundant genes, bioI an

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

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

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

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

214 During Bacillus subtilis sporulation, chromosome copy number is

215 During Bacillus subtilis sporulation, segregating sister chromo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

253 In Bacillus subtilis, the forespore protein SpoIIQ and the

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

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

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

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

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

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

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

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

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

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

264 rient extraction from Bacillus megaterium by Bacillus subtilis.

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

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

267 ate membrane synthesis with cell division in Bacillus subtilis.

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

269 rowing bacteria such as Escherichia coli and Bacillus subtilis.

270 scherichia coli, Pseudomonas aeruginosa, and Bacillus subtilis.

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

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

273 in their positioning relative to oriC across Bacillus, suggesting that the function of the RBMs is bo

274 rice expressing cry genes from the bacterium Bacillus thuringiensis (Bt rice) is highly resistant to

275 GO) in the protective effect of olive oil on Bacillus thuringiensis (Bt) after being exposed to UV ra

276 The insecticidal Cry toxins produced by Bacillus thuringiensis (Bt) are increasingly important i

277 idae species are not sensitive to commercial Bacillus thuringiensis (Bt) cotton, resulting in signifi

278 Cry1Ie protein derived from Bacillus thuringiensis (Bt) has been proposed as a promi

279 Although crop plants that produce Bacillus thuringiensis (Bt) proteins can limit insect in

280 expressing three crystal (Cry) proteins from Bacillus thuringiensis (Bt) tested the impact of CDS rec

281 Cry6Aa1 is a Bacillus thuringiensis (Bt) toxin active against nematod

282 and the impacts of elevated CO2 on exogenous Bacillus thuringiensis (Bt) toxins and transgene express

283 Since transgenic crops expressing Bacillus thuringiensis (Bt) toxins were first released,

284 Crops expressing Bacillus thuringiensis (Bt)-derived insecticidal protein

285 one country to one insecticidal protein from Bacillus thuringiensis (Bt).

286 ing insecticidal proteins from the bacterium Bacillus thuringiensis (Bt).

287 umed to be environmentally friendly, such as Bacillus thuringiensis (Bt).

288 secticidal toxins derived from the bacterium Bacillus thuringiensis (Bt).

289 The Bacillus thuringiensis delta-endotoxins (Bt toxins) are

290 Bacillus thuringiensis is a widely used bacterial entomo

291 ntroduction of genes isolated from different Bacillus thuringiensis strains to express Cry-type toxin

292 Two mosquitocidal bacteria, Bacillus thuringiensis subsp. israelensis (Bti) and Lysi

293 cis, Bacillus cereus, Bacillus mycoides, and Bacillus thuringiensis These species have 11 to 14 rRNA

294 us group (B. cereus, Bacillus anthracis, and Bacillus thuringiensis) are surrounded by a paracrystall

295 ontaining transgenes from the soil bacterium Bacillus thuringiensis; next-generation double-stranded

296 Understanding the factors which allow the bacillus to control responses to host stress and mechani

297 and in a mixture with a different species of Bacillus to test non-specific interference using a porta

298 branes (e.g., eukaryotic cells, membranes of Bacillus vegetative cells).

299 In conclusion, Bacillus was strongly associated with YTC.

300 The plague bacillus Yersinia pestis is unique among the pathogenic