ライフサイエンスコーパス: Bacillus thuringiensis

1 us species, including Bacillus anthracis and Bacillus thuringiensis.

2 complexes formed with the AHL lactonase from Bacillus thuringiensis.

3 rates as catalyzed by the AHL lactonase from Bacillus thuringiensis.

4 e Cry family of toxins (including Cry4Ba) of Bacillus thuringiensis.

5 is related to the 3-domain crystal toxins of Bacillus thuringiensis.

6 nked to resistance against Cry1Ac toxin from Bacillus thuringiensis.

7 acis Sterne strain and its genetic relative, Bacillus thuringiensis.

8 the insecticidal capability of the bacterium Bacillus thuringiensis.

9 otile, or nonmotile/quorum-sensing-deficient Bacillus thuringiensis.

10 sts among B. anthracis, Bacillus cereus, and Bacillus thuringiensis.

11 he pore-forming Crystal toxin family made by Bacillus thuringiensis.

12 ance in the YHD2 strain to Cry1Ac toxin from Bacillus thuringiensis.

13 ties that produce a toxin from the bacterium Bacillus thuringiensis.

14 y1A toxins of the entomopathogenic bacterium Bacillus thuringiensis.

15 rom corn engineered to express proteins from Bacillus thuringiensis.

16 ent derived from the gram-positive bacterium Bacillus thuringiensis.

17 lity to the Cry3Aa insecticidal protein from Bacillus thuringiensis.

18 ghly selective antimicrobial activity toward Bacillus thuringiensis.

19 press insecticidal Cry proteins derived from Bacillus thuringiensis.

20 intron that resides in the recA gene of the Bacillus thuringiensis 03058-36 bacteriophage.

21 , Bacillus cereus D-17, B. cereus 43881, and Bacillus thuringiensis 33679, contained sequences that w

22 38 isolates), Bacillus mycoides (1 isolate), Bacillus thuringiensis (53 isolates from 17 serovars), a

23 The gene encoding AsbF from Bacillus thuringiensis 97-27 was overexpressed in an Esc

24 has been isolated from supernatant fluids of Bacillus thuringiensis AB88 cultures.

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

26 Much like a homologous AHL lactonase from Bacillus thuringiensis, AiiB appears to be a metal-depen

27 Enterotoxin-producing Bacillus thuringiensis also gave positive results with P

28 rom large plasmids of Bacillus anthracis and Bacillus thuringiensis and are probably involved in plas

29 of a PapR pentapeptide as normally occurs in Bacillus thuringiensis and B. cereus can be mimicked by

30 ly used to explore two PAB isolates, namely, Bacillus thuringiensis and B. subtilis from rhizospheric

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

32 Copper, and Zinc, to heat, and to pathogens Bacillus thuringiensis and Staphylococcus epidermidis, a

33 al system: the Gram-positive insect pathogen Bacillus thuringiensis and the larvae of the diamondback

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

35 n species of the B. cereus group, B. cereus, Bacillus thuringiensis, and Bacillus mycoides, were each

36 Bt, is found on the large pBtoxis plasmid in Bacillus thuringiensis, and interacts via its extended C

37 vitro: Escherichia coli, Bacillus subtilis, Bacillus thuringiensis, and Mycobacterium smegmatis.

38 Bacillus anthracis, Bacillus cereus, and Bacillus thuringiensis are closely related gram-positive

39 Cry toxins produced by the bacterium Bacillus thuringiensis are effective biological insectic

40 Crystal (Cry) proteins made by the bacterium Bacillus thuringiensis are pore-forming toxins that spec

41 y needed, and crystal (Cry) proteins made by Bacillus thuringiensis are promising new candidates.

42 Cry proteins produced by Bacillus thuringiensis are selective biodegradable insec

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

44 ogenic strains such as Erwinia carotovora or Bacillus thuringiensis, are blocked in the anterior midg

45 ion experimentally, rare codons encoded by a Bacillus thuringiensis (B.t.) toxin gene (cryIA(c)) or a

46 t is well established that the expression of Bacillus thuringiensis (B.t.) toxin genes in higher plan

47 xamples of this problem are the cry genes of Bacillus thuringiensis (B.t.), which encode the insectic

48 are desorbed from spores of Bacillus cereus, Bacillus thuringiensis, Bacillus subtilis, and Bacillus

49 process, we imaged purified Bacillus cereus, Bacillus thuringiensis, Bacillus subtilis, and Clostridi

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

51 ilization of resistant varieties, and use of Bacillus thuringiensis-based preparations.

52 w approach was employed aiming at the use of Bacillus thuringiensis Berliner, a strain commercially a

53 expressing toxins derived from the bacterium Bacillus thuringiensis (Bt maize) exhibited declining pr

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

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

56 7702) spores in presence of large amounts of Bacillus thuringiensis (BT) and Bacillus cereus (BC) is

57 nsecticidal proteins from the soil bacterium Bacillus thuringiensis (Bt) are becoming a cornerstone o

58 he insecticidal crystal proteins produced by Bacillus thuringiensis (Bt) are broadly used to control

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

60 crops that produce insecticidal toxins from Bacillus thuringiensis (Bt) are grown widely for pest co

61 secticidal toxins derived from the bacterium Bacillus thuringiensis (Bt) are grown worldwide to manag

62 Cry) proteins produced by the soil bacterium Bacillus thuringiensis (Bt) are harmless to vertebrates,

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

64 has long been known that toxins produced by Bacillus thuringiensis (Bt) are stored in the bacterial

65 insecticides derived from the soil bacterium Bacillus thuringiensis (Bt) are the most widely used bio

66 The protein toxins produced by Bacillus thuringiensis (Bt) are the most widely used nat

67 neered to produce insecticidal proteins from Bacillus thuringiensis (Bt) are used globally to manage

68 Toxins from the bacterium Bacillus thuringiensis (Bt) are used widely for insect c

69 ing insecticidal proteins from the bacterium Bacillus thuringiensis (Bt) are useful for pest control,

70 nic crops producing insecticidal toxins from Bacillus thuringiensis (Bt) are widely used for pest con

71 nic crops producing insecticidal toxins from Bacillus thuringiensis (Bt) are widely used to control p

72 lis (Hubner), to a commercial formulation of Bacillus thuringiensis (Bt) Berliner toxin, Dipel ES, ap

73 currently available insecticidal toxins from Bacillus thuringiensis (Bt) Berliner, currently the most

74 resistance in insects to the bioinsecticide Bacillus thuringiensis (Bt) can be dramatically reduced

75 c crops producing insecticidal proteins from Bacillus thuringiensis (Bt) can benefit agriculture, but

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

77 dal delta-endotoxins from the soil bacterium Bacillus thuringiensis (Bt) caused much public interest.

78 ing insecticidal crystal (Cry) proteins from Bacillus thuringiensis (Bt) control important lepidopter

79 ields in Arizona show that use of transgenic Bacillus thuringiensis (Bt) cotton reduced insecticide u

80 ese species are not controlled by commercial Bacillus thuringiensis (Bt) cotton varieties resulting i

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

82 ults are illustrated with examples involving Bacillus thuringiensis (Bt) crops and antibiotic use in

83 Transgenic Bacillus thuringiensis (Bt) crops play an increasing rol

84 r lepidopteran pest and target of transgenic Bacillus thuringiensis (Bt) crops, between 2002 and 2017

85 ed the ecological consequences of transgenic Bacillus thuringiensis (Bt) crops, debates continue rega

86 are either sprayed or produced by transgenic Bacillus thuringiensis (Bt) crops.

87 Genetically engineered crops expressing Bacillus thuringiensis (Bt) Cry toxins have transformed

88 s associated with the insecticidal action of Bacillus thuringiensis (Bt) Cry toxins.

89 Bacillus thuringiensis (Bt) Cry34Ab1/Cry35Ab1 are binary

90 Bacillus thuringiensis (Bt) crystal proteins are pore-fo

91 cern that corn pollen, engineered to express Bacillus thuringiensis (Bt) endotoxin, might travel beyo

92 rops that produce insecticidal proteins from Bacillus thuringiensis (Bt) entails refuges of plants th

93 The Cry1Ab toxin produced by Bacillus thuringiensis (Bt) exerts insecticidal action u

94 ps have been engineered to express toxins of Bacillus thuringiensis (Bt) for insect control.

95 ess insecticidal proteins from the bacterium Bacillus thuringiensis (Bt) has become widely adopted in

96 vegetative insecticidal protein Vip3Aa from Bacillus thuringiensis (Bt) has been produced by transge

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

98 For over 100 years, Bacillus thuringiensis (Bt) has been used as an agricult

99 gut-active toxins such as those derived from Bacillus thuringiensis (Bt) have been successfully used

100 rystalline (Cry) proteins from the bacterium Bacillus thuringiensis (Bt) have been used extensively t

101 xpressing insecticidal proteins derived from Bacillus thuringiensis (Bt) have been used to manage WCR

102 ing insecticidal proteins from the bacterium Bacillus thuringiensis (Bt) have controlled and reduced

103 co-expressing two new delta-endotoxins from Bacillus thuringiensis (Bt) have demonstrated protection

104 neered to produce insecticidal proteins from Bacillus thuringiensis (Bt) have many benefits and are i

105 uce insecticidal proteins from the bacterium Bacillus thuringiensis (Bt) have revolutionized pest man

106 ansgenes encoding insecticidal proteins from Bacillus thuringiensis (Bt) in crop plants is a well-est

107 n threat to the long-term use of toxins from Bacillus thuringiensis (Bt) in transgenic plants.

108 cens MYb115 that is known to protect against Bacillus thuringiensis (Bt) infection.

109 Cry1B.3 and Cry1Da_7 are Bacillus thuringiensis (Bt) insecticidal proteins, where

110 Bacillus thuringiensis (Bt) insecticidal toxins bind to

111 Despite the prominent and worldwide use of Bacillus thuringiensis (Bt) insecticidal toxins in agric

112 Bacillus thuringiensis (Bt) is a widely used microbial i

113 Bacillus thuringiensis (Bt) is an insecticidal bacterium

114 The soil bacterium Bacillus thuringiensis (Bt) is the most successfully use

115 s for commercial production of two cry1Ab/Ac Bacillus thuringiensis (Bt) lines, China made a great le

116 secticidal toxins derived from the bacterium Bacillus thuringiensis (Bt) places intense selective pre

117 ihood that monarch larvae will be exposed to Bacillus thuringiensis (Bt) pollen, we studied milkweed

118 effectiveness of insecticidal proteins from Bacillus thuringiensis (Bt) produced by transgenic crops

119 mechanisms in a WCR strain resistant to the Bacillus thuringiensis (Bt) protein eCry3.1Ab using dsRN

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

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

122 The global reliance on Bacillus thuringiensis (Bt) proteins for controlling lep

123 Transgenic crops that produce Bacillus thuringiensis (Bt) proteins for pest control ar

124 Transgenic crops producing Bacillus thuringiensis (Bt) proteins have become a prima

125 Transgenic crops producing Bacillus thuringiensis (Bt) proteins kill key insect pes

126 hich are generally resistant to insecticidal Bacillus thuringiensis (Bt) proteins, have emerged as a

127 epidopteran larvae, and are also involved in Bacillus thuringiensis (Bt) protoxin activation and prot

128 ton that produces insecticidal proteins from Bacillus thuringiensis (Bt) relies on refuges of host pl

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

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

131 Transgenic crops that produce toxins from Bacillus thuringiensis (Bt) to control insects are grown

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

133 With the increase of resistance to Bacillus thuringiensis (Bt) toxin in transgenic cotton p

134 ducted to establish the relative toxicity of Bacillus thuringiensis (Bt) toxins and pollen from Bt co

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

136 e to genetically modified crops that produce Bacillus thuringiensis (Bt) toxins are based primarily o

137 Transgenic plants expressing Bacillus thuringiensis (Bt) toxins are currently being d

138 enic plants producing environmentally benign Bacillus thuringiensis (Bt) toxins are deployed increasi

139 Transgenic crops that produce Bacillus thuringiensis (Bt) toxins are grown widely for

140 Fitness costs associated with resistance to Bacillus thuringiensis (Bt) toxins critically impact the

141 genetic studies of insect adaptation to the Bacillus thuringiensis (Bt) toxins expressed by currentl

142 Although transgenic crops expressing Bacillus thuringiensis (Bt) toxins have been used succes

143 sts threatens the continued effectiveness of Bacillus thuringiensis (Bt) toxins in sprays and transge

144 Understanding how Bacillus thuringiensis (Bt) toxins interact with protein

145 Transgenic crops producing Bacillus thuringiensis (Bt) toxins kill some key insect

146 Transgenic crops producing Bacillus thuringiensis (Bt) toxins kill some key insect

147 g insect pests from developing resistance to Bacillus thuringiensis (Bt) toxins produced by transgeni

148 tinued success of transgenic crops producing Bacillus thuringiensis (Bt) toxins that kill pests.

149 ansgenic crop pyramids producing two or more Bacillus thuringiensis (Bt) toxins that kill the same in

150 st resistance threatens the effectiveness of Bacillus thuringiensis (Bt) toxins used in transgenic an

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

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

153 ect resistance to transgenic crops producing Bacillus thuringiensis (Bt) toxins, nearby "refuges" of

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

155 ect control by transgenic crops that produce Bacillus thuringiensis (Bt) toxins.

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

157 ing insecticidal proteins from the bacterium Bacillus thuringiensis (Bt) were first commercialized in

158 ing insecticidal proteins from the bacterium Bacillus thuringiensis (Bt) were grown on over 13 millio

159 Bacillus thuringiensis (Bt) were used for biosynthesis o

160 istance to insecticidal proteins produced by Bacillus thuringiensis (Bt) would decrease our ability t

161 ng insecticidal proteins from the bacterium, Bacillus thuringiensis (Bt), are revolutionizing agricul

162 c crops producing insecticidal proteins from Bacillus thuringiensis (Bt), the "pyramid" strategy uses

163 xic effect of the entomopathogenic bacterium Bacillus thuringiensis (Bt), which delay the evolution o

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

165 Two Bacillus thuringiensis (Bt)-resistant strains of the Ind

166 hydrolysates of water-soluble proteins from Bacillus thuringiensis (Bt)-transgenic (Aristis-Bt) and

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

168 nt mode of action from that of proteins from Bacillus thuringiensis (Bt).

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

170 ered to produce an insecticidal protein from Bacillus thuringiensis (Bt).

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

172 ants are based on insecticidal proteins from Bacillus thuringiensis (Bt).

173 t produce insecticidal proteins derived from Bacillus thuringiensis (Bt).

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

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

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

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

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

179 Here, we report that TLPs from Bacillus thuringiensis (BtTLP) and Methanosarcina acetiv

180 closely related species Bacillus cereus and Bacillus thuringiensis, but the patterns differed.

181 rously evaluate the mechanism of PI-PLC from Bacillus thuringiensis by examining the functional and s

182 atidylinositol-specific phospholipase C from Bacillus thuringiensis can be activated by nonsubstrate

183 atidylinositol-specific phospholipase C from Bacillus thuringiensis catalyzes the cleavage of the pho

184 sitol-specific phospholipase C (PI-PLC) from Bacillus thuringiensis catalyzes the hydrolysis of phosp

185 insecticidal protein 3) family proteins from Bacillus thuringiensis convey toxicity to species within

186 on (Gossypium hirsutum L.), transformed with Bacillus thuringiensis Cry genes (Bt G. hirsutum) that c

187 Bacillus thuringiensis Cry protein exerts its toxic effe

188 enknife models hypothesize that insecticidal Bacillus thuringiensis Cry toxins partition into the api

189 We showed that several putative Bacillus thuringiensis Cry1A receptors, including the 12

190 cadherin protein Bt-R(1a) is a receptor for Bacillus thuringiensis Cry1A toxins in Manduca sexta.

191 Bacillus thuringiensis Cry1Aa insecticidal protein is th

192 Binding of the insecticidal Bacillus thuringiensis Cry1Ac toxin to the putative rece

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

194 s of the three surface loops in domain II of Bacillus thuringiensis CryIIIA delta-endotoxin has been

195 s or deletions of domain II loop residues of Bacillus thuringiensis delta-endotoxin CryIAb were const

196 Here, we report a Bacillus thuringiensis delta-endotoxin, Cry14Ab, that co

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

198 ays using bee larvae and the insect pathogen Bacillus thuringiensis demonstrated that paenilamicins o

199 usion construct between cry11A with p20 from Bacillus thuringiensis did not express Cry11A protein in

200 ting of corn genetically modified to produce Bacillus thuringiensis endotoxin has led to speculation

201 sitol-specific phospholipase C (PI-PLC) from Bacillus thuringiensis exhibits 'interfacial activation'

202 sitol-specific phospholipase C (PI-PLC) from Bacillus thuringiensis exhibits several types of interfa

203 as useful alternatives to those derived from Bacillus thuringiensis for expression in insect-resistan

204 rulated and vegetative Bacillus subtilis and Bacillus thuringiensis from irradiated lysates were reco

205 pest insects using MCAs, including viruses, Bacillus thuringiensis, fungi, and entomopathogenic nema

206 s were constructed by insertion of lacZ into Bacillus thuringiensis genes encoding PI-PLC (plcA) and

207 ing result that individual dormant spores of Bacillus thuringiensis grow and shrink in response to in

208 erine lactone hydrolase (AHL lactonase) from Bacillus thuringiensis has been determined, by using sin

209 sitol-specific phospholipase C (PI-PLC) from Bacillus thuringiensis has been solved to 1.8A resolutio

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

211 second (designated InhA) is a homolog of the Bacillus thuringiensis immune inhibitor A.

212 sing (18)O, (2)H, and the AHL lactonase from Bacillus thuringiensis implicate an addition-elimination

213 proteins and resistance to Cry1Ac toxin from Bacillus thuringiensis in the tobacco budworm (Heliothis

214 Specificity for target insects of Bacillus thuringiensis insecticidal Cry toxins is largel

215 microprojectile bombardment with a synthetic Bacillus thuringiensis insecticidal crystal protein gene

216 model of the mechanism of action of several Bacillus thuringiensis insecticidal crystal proteins (Cr

217 The Bacillus thuringiensis insecticidal delta-endotoxins hav

218 main II, loop 2 residues, 368RRPFNIGI375, of Bacillus thuringiensis insecticidal protein CryIAb.

219 t pests on crops depend on the expression of Bacillus thuringiensis insecticidal proteins, most of wh

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

221 The soil bacterium Bacillus thuringiensis is a pathogen of insects and nema

222 Bacillus thuringiensis is a widely used bacterial entomo

223 sitol-specific phospholipase C (PI-PLC) from Bacillus thuringiensis is an allosteric enzyme with both

224 Bacillus thuringiensis is an insect pathogen that is wid

225 Here, the gene for an AHL lactonase from Bacillus thuringiensis is cloned, and the protein is exp

226 Bacillus thuringiensis is the most widely applied biolog

227 f action of insecticidal crystal toxins from Bacillus thuringiensis is their partitioning into membra

228 Bacillus thuringiensis is widely used as a biological pe

229 sence of a Bt toxin-encoding plasmid defines Bacillus thuringiensis isolates.

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

231 We evaluated two biolarvicides, VectoBac (Bacillus thuringiensis israelensis (Bti)) and VectoMax (

232 y characterized an operon, named Bti_pse, in Bacillus thuringiensis israelensis ATCC 35646, which enc

233 the 3D elemental distribution present within Bacillus thuringiensis israelensis spores.

234 one biological warfare agent (BWA) simulant, Bacillus thuringiensis kurstaki.

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

236 sitol-specific phospholipase C (PI-PLC) from Bacillus thuringiensis , often depend on lipid-specific

237 cts of calcium and Cry1Ab toxin, produced by Bacillus thuringiensis, on the adhesive properties of BB

238 Recently, a plasmid stability cassette on Bacillus thuringiensis pBtoxis encoding a putative FtsZ/

239 aments of TubZ protein (TubZ filaments) from Bacillus thuringiensis pBtoxis plasmid with their centro

240 group I intron in the DNA polymerase gene of Bacillus thuringiensis phage Bastille.

241 nd cIP hydrolysis to inositol 1-phosphate by Bacillus thuringiensis phosphatidylinositol-specific pho

242 The Bacillus thuringiensis phosphatidylinositol-specific pho

243 ssociation of a peripheral membrane protein, Bacillus thuringiensis phosphatidylinositol-specific pho

244 Bacillus thuringiensis phosphatidylinositol-specific pho

245 se conclusions were affirmed in studies with Bacillus thuringiensis phosphatidylinositol-specific pho

246 Bacillus thuringiensis phosphatidylinositol-specific pho

247 For Bacillus thuringiensis PI-PLC these interactions are syn

248 For Bacillus thuringiensis PI-PLC, a small amount of phospha

249 correlated motions between the two halves of Bacillus thuringiensis PI-PLC, and Pro(245) variants sho

250 During sporulation, Bacillus thuringiensis produces inclusions comprised of

251 Bacillus thuringiensis produces insecticidal Cry and Cyt

252 During sporulation, Bacillus thuringiensis produces intracellular, crystalli

253 Bacillus thuringiensis secretes the virulence factor pho

254 k that helps discriminate B. atrophaeus from Bacillus thuringiensis spores grown in rich media is [N(

255 etic germination and heterogeneity of single Bacillus thuringiensis spores in an aqueous solution by

256 work, we investigate the chemical changes of Bacillus thuringiensis spores treated with sporicidal ag

257 orm (Helicoverpa zea) has been isolated from Bacillus thuringiensis strain AB88.

258 e role as a receptor for the Cry4Ba toxin of Bacillus thuringiensis strain israelensis.

259 ive genome hybridization of 19 B. cereus and Bacillus thuringiensis strains against a B. anthracis DN

260 It has been reported that Cry5B-producing Bacillus thuringiensis strains can infect C. elegans and

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

262 sequenced B. cereus, Bacillus anthracis, and Bacillus thuringiensis strains.

263 Bacillus thuringiensis subsp.

264 most potent toxins produced by mosquitocidal Bacillus thuringiensis subsp.

265 the action of three bacterial mosquitocides, Bacillus thuringiensis subsp.

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

267 Bacillus thuringiensis subsp. israelensis produces cryst

268 ly identified a minireplicon of pBtoxis from Bacillus thuringiensis subsp. israelensis that contained

269 Cry4Ba, isolated from Bacillus thuringiensis subsp. israelensis, is specifical

270 Cry11Ba produced by Bacillus thuringiensis subsp. jegathesan is an active to

271 oxin CytB, found in parasporal inclusions of Bacillus thuringiensis subspecies kyushuensis, is a memb

272 Strains of Bacillus thuringiensis such as B. thuringiensis subsp. i

273 ence was almost identical to one detected in Bacillus thuringiensis that also bound the E2 subunit bu

274 n Bacillus anthracis and the insect pathogen Bacillus thuringiensis, the former being used as a biolo

275 trains of Bacillus cereus, and 12 strains of Bacillus thuringiensis; the gyrA gene was analyzed by th

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

277 l structure of an engineered PLC enzyme from Bacillus thuringiensis to 2.1 A resolution.

278 la xylostella, resistant to the biopesticide Bacillus thuringiensis, to estimate the costs of resista

279 sitol-specific phospholipase C (PI-PLC) from Bacillus thuringiensis toward PI vesicles has been inves

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

281 gans bre-1 gene was isolated in a screen for Bacillus thuringiensis toxin-resistant (bre) mutants to

282 similar to the effects seen with exposure to Bacillus thuringiensis toxin.

283 Pectobacterium atrosepticum (ToxIN(Pa)) and Bacillus thuringiensis (ToxIN(Bt)) that ToxI RNAs are hi

284 ential for insect resistance to insecticidal Bacillus thuringiensis toxins expressed in transgenic pl

285 ed in detail the binding sites that comprise Bacillus thuringiensis tubC, visualized the TubRC comple

286 found in spores of either Bacillus cereus or Bacillus thuringiensis, two species that are the most ph

287 closely related species Bacillus cereus and Bacillus thuringiensis typically produce beta-lactamases

288 cloacae, Pseudomonas pseudoalcaligenes, and Bacillus thuringiensis under either inorganic (calcium p

289 nce factors (crystal toxins) in the pathogen Bacillus thuringiensis using diamondback moth larvae (Pl

290 The microbial larvicide VectoMax combining Bacillus thuringiensis var israelensis (Bti) and Bacillu

291 It is generally believed that Bacillus thuringiensis var. israelensis (Bti) biopestici

292 Bacillus thuringiensis var. israelensis (Bti) satisfies

293 The cytolytic delta-endotoxin Cyt1A from Bacillus thuringiensis var. israelensis is used in comme

294 ects of a novel 20-kDa protein isolated from Bacillus thuringiensis var. thuringiensis (BTp20) parasp

295 re we characterize a protein (TubZ) from the Bacillus thuringiensis virulence plasmid pBtoxis, which

296 p protection applications since approval for Bacillus thuringiensis was granted in 1961.

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

298 lcR-deficient mutants of Bacillus cereus and Bacillus thuringiensis were constructed by insertional i

299 of Bacillus cereus, Bacillus anthracis, and Bacillus thuringiensis when strains were grown in a defi

300 Bacillus thuringiensis, which is well known as an entomo