ライフサイエンスコーパス: Bacillus

1 The success of Bacillus amyloliquefaciens as a biological control agent

2 Gram-positive bacteria like Bacillus and phytopathogen Rhodococcus fascians showed i

3 and rapidly evaluate lignin degradation for Bacillus and Vibrio strains.

4 Widespread release of Bacillus anthracis (anthrax) or Yersinia pestis (plague)

5 nsis (F. tularensis) subspecies novicida and Bacillus anthracis (B. anthracis) Sterne, surrogates for

6 onal DABs are present in the human pathogens Bacillus anthracis and Vibrio cholerae.

7 Bacillus anthracis is a spore-forming, Gram-positive bac

8 amma-glutamic acid (PGA) capsule produced by Bacillus anthracis is composed entirely of d-isomer glut

9 Bacillus anthracis is the causative agent of anthrax dis

10 NEI supplementation also promoted anti-Bacillus anthracis protective antigen (PA) neutralizing

11 Population exposure to Bacillus anthracis spores could cause mass casualties re

12 Since the intentional release of Bacillus anthracis spores through the U.S.

13 tional anthrax, a disease caused by inhaling Bacillus anthracis spores, leads to respiratory distress

14 ) is a protease virulence factor produced by Bacillus anthracis that is required for its pathogenicit

15 Bacillus anthracis, a spore-forming gram-positive bacter

16 Francisella tularensis, Bacillus anthracis, and Yersinia pestis are tier 1 selec

17 Anthrax lethal toxin (LT), produced by Bacillus anthracis, comprises a receptor-binding moiety,

18 AtxA, the master virulence gene regulator of Bacillus anthracis, is a PRD-Containing Virulence Regula

19 ylococcus aureus, Enterococcus faecalis, and Bacillus anthracis, on samples similar to those in real-

20 occus aureus, as well as Yersinia pestis and Bacillus anthracis, organisms of biodefense interest.

21 Bacillus anthracis, the causative agent of anthrax, disp

22 Bacillus anthracis, the etiological agent of anthrax, is

23 ema toxins are critical virulence factors of Bacillus anthracis.

24 Detection of HSA, Bacillus atrophaeus (BG spores), MS2 bacteriophage and E

25 2) on three different spore strains , namely Bacillus atrophaeus, Bacillus subtilis and Geobacillus s

26 lted in the enrichment of specific taxa with Bacillus being the most enriched.

27 Bacillus benzeovorans assisted and supported growth of r

28 ic pathogens, including those from the genus Bacillus, Brucella, Coxiella, and others, in bushmeat.

29 e systemic disease caused by a gram-positive bacillus called Tropheryma whipplei.

30 We generated a recombinant Bacillus Calmette-Guerin ([BCG] BCG-disA-OE) that overex

31 ow efficacy of the only licensed TB vaccine, Bacillus Calmette-Guerin (BCG) against pulmonary TB.

32 ed immunity, by the antituberculosis vaccine bacillus Calmette-Guerin (BCG) contributes to protection

33 Using Mycobacterium bovis bacillus Calmette-Guerin (BCG) cultures and TB-positive

34 sed in humans as a vaccine for tuberculosis, Bacillus Calmette-Guerin (BCG) has been suggested as a p

35 Bacillus Calmette-Guerin (BCG) immunotherapy for bladder

36 sibility, safety, and immunogenicity of live bacillus Calmette-Guerin (BCG) in a lung-oriented contro

37 Bacillus Calmette-Guerin (BCG) is the only licensed vacc

38 BACKGROUNDThe antituberculosis vaccine bacillus Calmette-Guerin (BCG) reduces overall infant mo

39 c regression showed that old age, absence of bacillus Calmette-Guerin (BCG) scar, presence of donor-s

40 In Taiwan, the inoculation of Bacillus Calmette-Guerin (BCG) Tokyo-172 strain vaccine

41 Bacillus Calmette-Guerin (BCG) vaccination induces varia

42 sted a negative association between national bacillus Calmette-Guerin (BCG) vaccination policy and th

43 The Mycobacterium bovis Bacillus Calmette-Guerin (BCG) vaccine is administered p

44 The Bacillus Calmette-Guerin (BCG) vaccine provides protecti

45 ccination with the phosphoantigen-containing bacillus Calmette-Guerin (BCG) vaccine.

46 Mtb- specific antigens and live bacillus Calmette-Guerin (BCG) were used as stimuli, wit

47 e, but how the current tuberculosis vaccine, bacillus Calmette-Guerin (BCG), impacts early immunity i

48 al cDC1s was also observed during S. aureus, bacillus Calmette-Guerin (BCG), or E. coli infection, as

49 reatment and vaccination, in particular with Bacillus Calmette-Guerin (BCG), remain the main strategi

50 Bacillus Calmette-Guerin (BCG), the only licensed TB vac

51 Mycobacterium bovis bacillus Calmette-Guerin (BCG), the only TB vaccine in c

52 Treatments include intravesical maintenance Bacillus Calmette-Guerin (mBCG) and radical cystectomy (

53 -SPOT.TB, and TST (with adjustment for prior bacillus Calmette-Guerin [BCG] vaccination).Measurements

54 sl resulted in increased Mycobacterium bovis bacillus Calmette-Guerin and Mycobacterium tuberculosis

55 Bacillus Calmette-Guerin instillation after removal of t

56 Bacillus Calmette-Guerin therapy fails in >50% of cases,

57 haride motifs within AM and its functions in bacillus Calmette-Guerin vaccination and/or in controlle

58 d for comparison of the efficacy of standard bacillus Calmette-Guerin vaccination as well as novel TB

59 The only available vaccine, BCG (Bacillus Calmette-Guerin), is given intradermally and ha

60 of Helicobacter pylori, Mycobacterium bovis bacillus Calmette-Guerin, and Citrobacter rodentium and

61 ent tuberculosis (TB) vaccine trial to boost bacillus Calmette-Guerin-mediated anti-TB immunity despi

62 omized study to determine the feasibility in Bacillus Calmette-Guerin-naive patients.

63 In bacillus Calmette-Guerin-vaccinated subjects and those w

64 action, such as intravesical instillation of Bacillus Calmette-Guerin.

65 ehenate or infected with Mycobacterium bovis bacillus Calmette-Guerin.

66 tuberculosis; the vaccine strain of M. bovis Bacillus Calmette-Guerin; and M. kansasii to demonstrate

67 Bacteria of the genera Pseudomonas and Bacillus can promote plant growth and protect plants fro

68 n the decades following the discovery of the bacillus causing typhoid, in 1880, understanding of the

69 A Bacillus cereus BREX system provides resistance to sever

70 coli signal recognition particle RNA and the Bacillus cereus crcB fluoride riboswitch.

71 For pathogenic Gram-positive targets (Bacillus cereus group, Enterococcus spp., Enterococcus f

72 domonas fluorescens, Salmonella enterica and Bacillus cereus has not been previously reported.

73 from the neglected human foodborne pathogen Bacillus cereus is an activator of the NLRP3 inflammasom

74 as conducted to evaluate the inactivation of Bacillus cereus spore in mesquite flour with intense pul

75 es of the UDP-glucuronic acid epimerase from Bacillus cereus The geometry of the substrate-NAD(+) int

76 sted (D(10) of 42.8 s at 65 degrees C) while Bacillus cereus was the most resistant pathogen to irrad

77 ospira, Escherichia coli, Bacillus subtilis, Bacillus cereus) were identified via the modeling techni

78 lococcus aureus, Listeria monocytogenes, and Bacillus cereus, using the well diffusion assay.

79 HBL), produced by the gram-positive pathogen Bacillus cereus.

80 is highly conserved among the human pathogen Bacillus cereus.

81 The single-domain GH11 glycosidase from Bacillus circulans (BCX) is involved in the degradation

82 doxanthomonas-Streptomyces-Saccharopolyspora-Bacillus clausii) highly predictive of long-term survivo

83 ficantly different from that of an acid-fast bacillus culture (AFC) which includes both MGIT and Midd

84 can take many forms, including formation of Bacillus endospores, Streptomyces exospores, and metabol

85 oadings of oral bacteria (e.g., Bacteroides, Bacillus, Firmicutes, beta-proteobacteria, and Spirochet

86 MhsT of Bacillus halodurans is a transporter of hydrophobic amin

87 The OLE RNA of the alkaliphile Bacillus halodurans is highly expressed and naturally in

88 a crucial role in the structural dynamics of Bacillus halodurans YidC2.

89 mising candidate for human gene editing from Bacillus hisashii, BhCas12b.

90 y entertained by the SPbeta prophage and its Bacillus host, ensuring both stable prophage maintenance

91 Bacillus improved wheat survival in all stress condition

92 Bacillus is known to be heat tolerant.

93 hort of contemporary, clinical Gram-negative bacillus isolates from 3 U.S. academic medical centers (

94 the orphan transcriptional factor LutR from Bacillus licheniformis is an endogenous sensor of the la

95 nd crude ethyl acetate extracts of PUFSTP35 (Bacillus licheniformis KT921419) displayed strong antica

96 lution-phase structure of apo-BlLPMO10A from Bacillus licheniformis, along with solution-phase struct

97 erminal domain (NTD) of the A subunit of the Bacillus megaterium GerK(3) GR, revealing two distinct g

98 ytochrome P450 monooxygenase (P450(BM3) from Bacillus megaterium, CYP102A1) has promiscuous activity

99 engineering of a scCO(2)-tolerant strain of Bacillus megaterium, previously isolated from formation

100 cillus subtilis, Bacillus thuringiensis, and Bacillus megaterium, respectively.

101 he phage G host is a Lysinibacillus, and not Bacillus megaterium: identity of host proteins in our ma

102 ion was isolated from soil and identified as Bacillus mojavensis based on the 16S rRNA gene sequencin

103 zation of bacteria affiliated with the genus Bacillus Moreover, both leaf and systemic root metabolom

104 Bacillus phages use a communication system, termed "arbi

105 Recently members of Bacillus phages were found to utilize a small peptide (6

106 the epsilon subunit of F(0)F(1)-ATPase from Bacillus PS3.

107 o identified viable Bacillus zhangzhouensis, Bacillus pumilus, and Bacillus spp. in the upper troposp

108 oculture (Pseudomonas poae, Pseudomonas sp., Bacillus pumilus., Pantoea agglomerance., Microbacterium

109 iotransformation of nitrogenous compounds in Bacillus sp. cells as the plausible cause of the inducib

110 , the site-saturation mutagenesis library of Bacillus sp. MN chitosanase consisting of 167 muteins, e

111 In detail, an aldoxime dehydratase from Bacillus sp. OxB-1 was used as a biocatalyst for a dehyd

112 lococcus sp. isolates were also inhibited by Bacillus sp. strains in TTC presence, to a lesser extent

113 study we investigate the effects of a mixed Bacillus species (B. licheniformis and B. amyloliquefaci

114 ferent transcription factor family where two Bacillus species plus bacterial and archaeal thermophile

115 -isomer glutamic acid, whereas nonpathogenic Bacillus species produce mixed d-, l-isomer PGAs.

116 te immune cells than PGAs from nonpathogenic Bacillus species, resulting in failure to induce a robus

117 respectively with pGpp, ppGpp and pppGpp in Bacillus species.

118 ective against a lethal challenge of inhaled bacillus spores at 3 and 28 weeks after vaccination.

119 Germination of Bacillus spores is induced by the interaction of specifi

120 The combinations of Bacillus spp and Enterococcus spp, and 1 or more Bifidob

121 cillus zhangzhouensis, Bacillus pumilus, and Bacillus spp. in the upper troposphere.

122 lso exhibits notable differences relative to Bacillus spp., where spore formation has been more exten

123 The inhibition of other Bacillus strains by Bacillunoic acids extended the antim

124 ditions, suggesting that these salt tolerant Bacillus strains exhibit PGP traits only in the presence

125 inhibiting properties of potential probiotic Bacillus strains isolated from fermented brine mango pic

126 e that the collection of 58 plant endophytic Bacillus strains represents an important genomic resourc

127 Among a total of 368 culturable isolates, 58 Bacillus strains were identified from which the 16 most

128 When the 16 Bacillus strains were tested on the non-host plant Arabi

129 e strongest activity against closely related Bacillus strains, the ABC transporter exported the toxic

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

156 Bacillus subtilis can measure the activity of the enzyme

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

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

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

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

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

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

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

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

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

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

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

168 Bacillus subtilis encodes two functionally redundant D,L

169 Bacillus subtilis exhibited a reduction in bioleaching e

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

171 The Bacillus subtilis extracytoplasmic function sigma factor

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

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

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

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

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

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

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

179 Starvation of Bacillus subtilis initiates endosporulation involving fo

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

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

182 Bacillus subtilis is an important bacterium for understa

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

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

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

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

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

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

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

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

191 Bacillus subtilis ParB forms multimeric networks involvi

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

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

194 Bacillus subtilis possess two protein lipoylation pathwa

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

244 In Bacillus subtilis, robust biofilm formation requires lar

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

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

247 In Bacillus subtilis, the interaction stimulates the endonu

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

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

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

251 In Bacillus subtilis, these properties are influenced by th

252 In Bacillus subtilis, UgtP synthesises the glucolipid precu

253 Using Bacillus subtilis, we identified factors that revealed t

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

270 igment (prodigiosin)-producing Gram-negative bacillus that is naturally found in soil and water.

271 c crops producing insecticidal proteins from Bacillus thuringiensis (Bt) are cultivated extensively,

272 rops that produce insecticidal proteins from Bacillus thuringiensis (Bt) can suppress pests and reduc

273 d-evolved resistance of this species to Cry1 Bacillus thuringiensis (Bt) proteins expressed in maize

274 he risks of increased transgene silencing of Bacillus thuringiensis (Bt) rice under elevated CO(2).

275 WCR populations with resistance to Bacillus thuringiensis (Bt) toxins utilized in commercia

276 , thereby countering the virulence effect of Bacillus thuringiensis (Bt) toxins.

277 An encapsulated formulation of Bacillus thuringiensis (Bt) was produced by the Pickerin

278 Bacillus thuringiensis (Bt) were used for biosynthesis o

279 neered to produce insecticidal proteins from Bacillus thuringiensis (Bt).

280 y stages of adaptation to toxins produced by Bacillus thuringiensis (Bt).

281 uce insecticidal proteins from the bacterium Bacillus thuringiensis (Bt).

282 rops that produce insecticidal proteins from Bacillus thuringiensis (Bt).

283 lactis, and 4 strains of the entomopathogen Bacillus thuringiensis After 14 generations of host sele

284 synthesized (anatase and rutile) through the Bacillus thuringiensis and phase mixture can increase th

285 mbrane-binding properties of both species to Bacillus thuringiensis Cry1Ea toxin.

286 ize lines expressing various Cry toxins from Bacillus thuringiensis have been adopted as a management

287 ytica, EhFNT, and also show that BtFdhC from Bacillus thuringiensis is a functional formate transport

288 rotoxins produced by mosquitocidal bacterium Bacillus thuringiensis israelensis (Bti) that has been s

289 Bacillus thuringiensis subsp. israelensis produces cryst

290 n did not affect susceptibility of larvae to Bacillus thuringiensis toxin, but significantly decrease

291 Bacillus thuringiensis var. israelensis (Bti) satisfies

292 tode Caenorhabditis elegans and its pathogen Bacillus thuringiensis We combined experimental evolutio

293 (Pseudomonas fluorescens) and Gram-positive (Bacillus thuringiensis) bacterial species were monitored

294 S-rRNA gene sequencing as Bacillus subtilis, Bacillus thuringiensis, and Bacillus megaterium, respect

295 ecular changes connected with the ability of Bacillus velezensis 5113 to mediate abiotic stress toler

296 his study, a plant beneficial rhizobacterium Bacillus velezensis SQR9 was discovered to produce novel

297 clostridium, Haloimpatiens, Clostridium, and Bacillus were dominating in the bioreactors.

298 Seedlings treated with Bacillus were exposed to heat, cold/freezing or drought

299 lla, Salmonella, Yersinia, Mycobacterium and Bacillus-yet are relatively non-toxic to mammalian cells

300 ture-based detections also identified viable Bacillus zhangzhouensis, Bacillus pumilus, and Bacillus