ライフサイエンスコーパス: insecticidal

1 O) prequalifies LLINs that remain adequately insecticidal 3 years after deployment.

2 The insecticidal action involves blocking the lambda-aminobu

3 and cellular mechanisms associated with the insecticidal action of Bacillus thuringiensis (Bt) Cry t

4 oduced by Bacillus thuringiensis (Bt) exerts insecticidal action upon binding to BT-R1, a cadherin re

5 in the molecular bases of Bt specificity and insecticidal action.

6 ivermectin, describing its anthelmintic and insecticidal actions and recent studies that have sought

7 ever, there remains the need for alternative insecticidal actives due to emerging insect resistance t

8 Insecticidal activities of the mutant toxins on Manduca

9 pecificity of dsRNA targeting DvSSJ1 mRNA on insecticidal activities was also evaluated in diet bioas

10 embrane insertion and also in haemolytic and insecticidal activities.

11 have been reported to have antimicrobial and insecticidal activities.

12 ssues expressing cholesterol oxidase exerted insecticidal activity against boll weevil larvae.

13 in exhibited N-acetylglucosamine-binding and insecticidal activity against cowpea weevil, indicating

14 o10, Asn27, and Arg35, that are critical for insecticidal activity against flies (Musca domestica) an

15 crystal protein (Cry51Aa2) was reported with insecticidal activity against Lygus spp.

16 Parigidin-br1 showed potent insecticidal activity against neonate larvae of Lepidopt

17 xin B, independently contributed to the oral insecticidal activity against Southern corn rootworm.

18 n in mature potato tubers, and it has potent insecticidal activity against the corn rootworm.

19 nd (b) proteins confer upon Escherichia coli insecticidal activity against the lepidopteran insect la

20 ese variants revealed that Cyt1Aa exerts its insecticidal activity and hemolysis through different me

21 Excellent target site selectivity with high insecticidal activity and low toxicity to mammals were a

22 This study aimed to define insecticidal activity and neurophysiological impacts of

23 a Drosophila snakeskin (ssk) ortholog, show insecticidal activity and significant plant protection f

24 lants expressing dsRNA targeting dvssj1 show insecticidal activity and significant plant protection f

25 Their potent insecticidal activity arises from selectively activating

26 t behavior, but have not elucidated links to insecticidal activity at the molecular and cellular leve

27 Furthermore, insecticidal activity correlated with the resistance to

28 elated to the use of this peptide to enhance insecticidal activity of Bt toxin-based biopesticides an

29 We conclude that the insecticidal activity of G. biloba extracts can be attri

30 Much of the insecticidal activity of GSII is attributable to the lar

31 Together, these results establish that insecticidal activity of GSII is functionally linked to

32 The nature of the insecticidal activity of Photorhabdus bacteria was inves

33 injected into Mamestra brassicae larvae, the insecticidal activity of the Hv1a/GNA fusion protein was

34 ntermediates and one IVM hybrid retained the insecticidal activity of the parental molecule, clarifyi

35 Insecticidal activity of the recombinant proteins correl

36 osomal targeting, dramatically increased the insecticidal activity of this protein.

37 rotein products either have antimicrobial or insecticidal activity or are involved in the synthesis o

38 ntly identified class of proteins conferring insecticidal activity to several bacteria within the Ent

39 A preliminary study of the contact insecticidal activity toward fruit flies (Drosophila mel

40 acid substitutions in Cry51Aa2 that increase insecticidal activity towards Lygus spp. by >200-fold.

41 gna is the first transgene to exhibit insecticidal activity towards sap-sucking insects in an

42 -steroidal agonists of 20E and exhibit their insecticidal activity via interaction with the ecdystero

43 different rGSII proteins were evaluated for insecticidal activity when added to the diet of the cowp

44 cetylglucosamine-specific legume lectin, has insecticidal activity when fed to the cowpea weevil, Cal

45 ) bioefficacy and chemical content (residual insecticidal activity) and (2) protective efficacy for v

46 nd medical use (including anti-bacterial and insecticidal activity).

47 on of antibiotics abolished B. thuringiensis insecticidal activity, and reestablishment of an Enterob

48 They are well known for their insecticidal activity, contribution to bitterness in cit

49 g procedures to select variants with greater insecticidal activity, illustrating the potential of pha

50 eudotuberculosis progenitor included loss of insecticidal activity, increased resistance to antibacte

51 The Hairpinless mutant was devoid of insecticidal activity, indicating the functional importa

52 he microcapsule formulation exhibited higher insecticidal activity, resulting in a larval mortality o

53 step for membrane insertion, haemolysis and insecticidal activity.

54 y1Ab adsorbed to a selected HA retained full insecticidal activity.

55 ce of parigidin-br1, consistent with in vivo insecticidal activity.

56 -produced XptB1 and XptC1 had high levels of insecticidal activity.

57 y 60 base-pairs (bp) are required for DvSSJ1 insecticidal activity.

58 ding mechanism occurs, which is critical for insecticidal activity.

59 ) is an indole diterpene fungal product with insecticidal activity.

60 Proteolytic processing was shown to enhance insecticidal activity.

61 be responsible for the observed increase of insecticidal activity.

62 ivity mode as anticancer, antimicrobial, and insecticidal agents.

63 are a class of natural products with potent insecticidal and anticancer activities.

64 erial, antifungal, antimalarial, anticancer, insecticidal and herbicidal activities through the selec

65 otect plants and are promising candidates as insecticidal and nematocidal agents in agriculture.

66 nes and is reported to have antinociceptive, insecticidal, and anthelmintic activity.

67 EOs have repellent, insecticidal, and growth-reducing effects on a variety o

68 drocrepenynic acids that display antifungal, insecticidal, and nematicidal properties are distributed

69 Destruxins are a class of insecticidal, anti-viral, and phytotoxic cyclic depsipep

70 ng insects, which are generally resistant to insecticidal Bacillus thuringiensis (Bt) proteins, have

71 mbrella and penknife models hypothesize that insecticidal Bacillus thuringiensis Cry toxins partition

72 Binding of the insecticidal Bacillus thuringiensis Cry1Ac toxin to the

73 over the potential for insect resistance to insecticidal Bacillus thuringiensis toxins expressed in

74 re-forming proteins found in a wide range of insecticidal bacteria and some mammalian pathogens.

75 Bacillus thuringiensis (Bt) is an insecticidal bacterium that has successfully been used a

76 ndomized controlled trial testing the use of insecticidal bait on cockroach counts and asthma morbidi

77 ht to test the use of a single intervention, insecticidal bait, to reduce cockroach exposure in the h

78 The strategic placement of insecticidal bait, which is inexpensive, has low toxicit

79 Long-lasting insecticidal bed nets (LLINs) protect humans from malari

80 ince then, progress has stalled(2), and with insecticidal bednets losing efficacy against pyrethroid-

81 ct as a quantitative trait locus controlling insecticidal C-glycosyl flavone level in maize silks, an

82 thway and the first step in the formation of insecticidal C-glycosyl flavones.

83 al properties for possible antimicrobial and insecticidal candidates.

84 oteins represents the major component of the insecticidal capability of the bacterium Bacillus thurin

85 me, aphids have developed resistance to many insecticidal classes.

86 DeltaBbPacC mutant also did not produce the insecticidal compound dipicolinic acid, however, product

87 ts in growth, stress resistance, and oxalate/insecticidal compound production, only a small decrease

88 Effective new insecticidal compounds with minimal adverse effects on h

89 which include the use of essential oil-based insecticidal compounds, have been proposed for their con

90 for several classes of natural and synthetic insecticidal compounds.

91 th field populations surviving ten times the insecticidal concentration required to kill susceptible

92 With insecticidal control options dwindling, research on clic

93 t insecticide rotation or utilization of non-insecticidal control tactics could be part of an effecti

94 Bacillus thuringiensis produces insecticidal Cry and Cyt proteins that are toxic to diff

95 ption is a key process affecting the fate of insecticidal Cry proteins (Bt toxins), produced by genet

96 ize crop was genetically modified to express insecticidal Cry proteins derived from Bacillus thuringi

97 he familiar three-domain arrangement seen in insecticidal Cry proteins.

98 for target insects of Bacillus thuringiensis insecticidal Cry toxins is largely determined by toxin a

99 The insecticidal Cry toxins produced by Bacillus thuringiens

100 Crops producing insecticidal crystal (Cry) proteins from Bacillus thurin

101 ment with a synthetic Bacillus thuringiensis insecticidal crystal protein gene (Bt cryIAc) driven by

102 of action of several Bacillus thuringiensis insecticidal crystal proteins (Cry) is reviewed and test

103 insect larvae largely through the action of insecticidal crystal proteins and is commonly deployed a

104 The insecticidal crystal proteins produced by Bacillus thuri

105 step in understanding the mode of action of insecticidal crystal toxins from Bacillus thuringiensis

106 nting strategies to delay pest adaptation to insecticidal cultivars are reviewed.

107 Experience with classically bred, insecticidal cultivars has demonstrated that a solid und

108 plant's three major classes of JA-inducible insecticidal defenses, we demonstrate that the choice of

109 fly of maize genetically modified to express insecticidal delta-endotoxins from the soil bacterium Ba

110 The Bacillus thuringiensis insecticidal delta-endotoxins have a three-domain struct

111 Despite high commercial interest in insecticidal dsRNA, information on resistance to dsRNA i

112 sk assessment of transgenic maize expressing insecticidal dsRNA.

113 The insecticidal, ecotoxicological properties and the mode o

114 Although an overwhelming insecticidal effect against Anopheles stephensi mosquito

115 Besides its strong insecticidal effect on mosquito vectors of the disease,

116 ne the repellent, oviposition-deterrent, and insecticidal effects of C. fioriniae on D. suzukii.

117 ring their algogenic effects in mice, potent insecticidal effects, and high levels of sequence conser

118 , Metarhizium anisopliae, has broad-spectrum insecticidal effects.

119 ade it possible to significantly improve the insecticidal efficacy of fungi and their tolerance to ad

120 After 4 years of use, the insecticidal efficacy of the LLINs was diminished to bel

121 e compounds that have shown anthelmintic and insecticidal (endectocidal) activity.

122 ith malaria, compared to those that survived insecticidal exposure.

123 n factor responsible for the accumulation of insecticidal flavones in maize (Zea mays) silks and red

124 iotic stress tolerance, independent of their insecticidal function.

125 VIP3-insecticidal gene homologues have been detected in appro

126 The anti-metabolic or insecticidal gene, arcelin (Arl) was isolated, cloned an

127 A novel vegetative insecticidal gene, vip3A(a), whose gene product shows ac

128 a soybean transgenic for a highly expressed insecticidal gene.

129 This might he achieved by adding insecticidal genes to the fungus, an approach considered

130 in complex (tc) genes of Photorhabdus encode insecticidal, high molecular weight Tc toxins.

131 This varies among species and is affected by insecticidal irritancy.

132 inhibitors offering a new mode of action for insecticidal malaria vector control.

133 is and swelling of cells, consistent with an insecticidal mechanism involving membrane disruption.

134 and diverse family of natural products, the insecticidal metabolite (+)-brevianamide A is particular

135 bility of the metabolic engineering of these insecticidal metabolites in plants and microbes.

136 The standard theory of its anthelmintic and insecticidal mode of action is that it is a selective po

137 is independent of the accumulation of major insecticidal molecules.

138 enes, including the potent antimicrobial and insecticidal monoterpene 3-carene.

139 geting the anticancer, antiinflammatory, and insecticidal natural product (+/-)-rocaglamide.

140 eles gambiae is targeted and killed by small insecticidal net barriers positioned above a standard be

141 women attending ANC, as well as long-lasting insecticidal net distribution targeted towards first-tim

142 mly allocated to receive either long-lasting insecticidal nets (LLINs) alone or LLINs in combination

143 nt vector control interventions-long-lasting insecticidal nets (LLINs) and indoor residual spraying (

144 Long-lasting insecticidal nets (LLINs) and indoor residual spraying (

145 ugh indoor insecticides such as long-lasting insecticidal nets (LLINs) and indoor residual spraying m

146 Long-lasting insecticidal nets (LLINs) and indoor residual spraying o

147 Long-lasting insecticidal nets (LLINs) are believed to have helped to

148 Long-lasting insecticidal nets (LLINs) are the primary malaria preven

149 oor residual spraying (IRS) and long-lasting insecticidal nets (LLINs) are the primary tools for mala

150 o dual-active ingredient (a.i.) long-lasting insecticidal nets (LLINs) compared to pyrethroid-only LL

151 hether the use of repellent and long-lasting insecticidal nets (LLINs) could reduce malaria more than

152 r over 4 years following a mass long-lasting insecticidal nets (LLINs) distribution in Tanzania.

153 rethroid based products such as long-lasting insecticidal nets (LLINs) has created mosquito populatio

154 Two billion long-lasting insecticidal nets (LLINs) have been procured for malaria

155 largely due to distribution of long-lasting insecticidal nets (LLINs)(5), with many SSA countries ha

156 ), programmatically distributed long-lasting insecticidal nets (LLINs), and standard case management.

157 raying of insecticides (IRS) or long-lasting insecticidal nets (LLINs), can be highly effective at re

158 onventional and next-generation long-lasting insecticidal nets (LLINs), determined resistance profile

159 ramatic loss of efficacy of all long-lasting insecticidal nets (LLINs), including piperonyl butoxide

160 e indoor residual spraying with long-lasting insecticidal nets (LLINs), the two studies assessing the

161 ica through the distribution of long-lasting insecticidal nets (LLINs).

162 e-based control tools including long lasting insecticidal nets (LLINs).

163 io (Innovate), which included longer-lasting insecticidal nets and expansion of seasonal malaria chem

164 currently relies on the use of long-lasting insecticidal nets together with intermittent preventive

165 oor Residual Sprays) and LLINs (Long Lasting Insecticidal Nets) are the cornerstone for vector contro

166 ght include the distribution of long-lasting insecticidal nets, intermittent preventive treatment for

167 gnant women with high uptake of long-lasting insecticidal nets, IPTp-DP is cost-effective in areas wi

168 or resistance to pyrethroids in long-lasting insecticidal nets, which has prompted calls for a return

169 been effectively controlled by long-lasting insecticidal nets.

170 Cost per hammock, including insecticidal netting, sewing, transport, and distributio

171 molecules, and it is highly specific for the insecticidal p.p'DDT [1,1,1-trichloro-2,2-bis(p-chloroph

172 ts (BBnets), regular bednets with a vertical insecticidal panel to target mosquitoes above the bednet

173 ted with an electrostatic coating that binds insecticidal particles through polarity.

174 In the present study, we isolated an insecticidal peptide (Ae1a) from venom of the African sp

175 Hm-3 is an insecticidal peptide toxin consisting of 35 amino acid r

176 dramatically enhancing the oral activity of insecticidal peptides and proteins.

177 nagement, a diverse range of insect-specific insecticidal peptides remains an untapped resource for p

178 an incredibly rich source of disulfide-rich insecticidal peptides that have been tuned over millions

179 are potentially important genetic leads for insecticidal peptides.

180 ng characteristics, we hypothesized that the insecticidal pharmacophore influences neonicotinoid sorp

181 thoxy-2H-1,4-benzoxazin-3(4H)-one), a potent insecticidal phytotoxin produced by poaceous plants.

182 First-generation insecticidal PIPs were Cry proteins expressed in GM crop

183 the development and regulation of transgenic insecticidal plants.

184 delta-HXTXs were repurposed from an initial insecticidal predatory function to a role in defending a

185 e compounds with fungicidal, acaricidal, and insecticidal properties because of their strong inhibiti

186 his study was carried out to investigate the insecticidal properties of Beauveria bassiana, Metarhizi

187 sea indica(1) and has potent antifeedant and insecticidal properties.

188 d by transgenic Bt corn producing the Cry1Fa insecticidal protein (event TC1507).

189 ransgenic corn that produces a Bt vegetative insecticidal protein (Vip).

190 n family, VgrG1, that contained a vegetative insecticidal protein (VIP-2) domain at its carboxyl-term

191 ties with the catalytic domain of vegetative insecticidal protein 2 (VIP2), an actin ADP-ribosyltrans

192 Among these are type VI secretion systems, insecticidal protein complexes, and bacteriocins.

193 s, 368RRPFNIGI375, of Bacillus thuringiensis insecticidal protein CryIAb.

194 transgenes has resulted in the formation of insecticidal protein crystals or inclusion bodies of pha

195 ctron micrographs showed the presence of the insecticidal protein folded into cuboidal crystals.

196 eties of cotton bio-engineered to produce an insecticidal protein from Bacillus thuringiensis (Bt).

197 es of one pest species in one country to one insecticidal protein from Bacillus thuringiensis (Bt).

198 ly used biopesticide in agriculture, and its insecticidal protein genes are the primary transgenes us

199 pressing Bacillus thuringiensis (Bt)-derived insecticidal protein genes have been commercially availa

200 uding GFP, YFP, mOrange and mStrawberry) and insecticidal protein genes in Flavobacterium strains.

201 Bacillus thuringiensis Cry1Aa insecticidal protein is the most active known B. thuring

202 ains led to the discovery of a two-component insecticidal protein named AfIP-1A/1B from an Alcaligene

203 olesterol oxidase represents a novel type of insecticidal protein with potent activity against the co

204 Here we describe an insecticidal protein, designated IPD072Aa, that is isola

205 The crystal structure of the Gram-negative insecticidal protein, GNIP1Aa, has been solved at 2.5- a

206 Thus, introduction of an insecticidal proteinase inhibitor gene into cereal plant

207 Combining two or more insecticidal proteins active against the same target pes

208 pression is restricted to sporulation, Vip3A insecticidal proteins are expressed in the vegetative st

209 Vip3A insecticidal proteins are secreted without N-terminal pr

210 illus thuringiensis (B.t.), which encode the insecticidal proteins commonly referred to as B.t. toxin

211 een Cry34Ab1/Cry35Ab1 and coleopteran active insecticidal proteins Cry3Aa, Cry6Aa, and Cry8Ba on west

212 ed genetically engineered crops that produce insecticidal proteins derived from Bacillus thuringiensi

213 Crops genetically engineered to produce insecticidal proteins from Bacillus thuringiensis (Bt) a

214 Transgenic crops producing insecticidal proteins from Bacillus thuringiensis (Bt) a

215 Widely grown transgenic crops producing insecticidal proteins from Bacillus thuringiensis (Bt) c

216 Transgenic crops that produce insecticidal proteins from Bacillus thuringiensis (Bt) c

217 resistance to transgenic crops that produce insecticidal proteins from Bacillus thuringiensis (Bt) e

218 Crops genetically engineered to produce insecticidal proteins from Bacillus thuringiensis (Bt) h

219 nce in pests can reduce the effectiveness of insecticidal proteins from Bacillus thuringiensis (Bt) p

220 esistance to transgenic cotton that produces insecticidal proteins from Bacillus thuringiensis (Bt) r

221 est resistance to transgenic crops producing insecticidal proteins from Bacillus thuringiensis (Bt),

222 he benefits of transgenic crops that produce insecticidal proteins from Bacillus thuringiensis (Bt).

223 ect-resistant transgenic plants are based on insecticidal proteins from Bacillus thuringiensis (Bt).

224 s of crops genetically engineered to produce insecticidal proteins from Bacillus thuringiensis (Bt).

225 ncreased, because transgenic crops producing insecticidal proteins from Bt are being grown commercial

226 ation of gene expression, and genes encoding insecticidal proteins from other organisms, particularly

227 and planting of cotton engineered to produce insecticidal proteins from the bacterium Bacillus thurin

228 Transgenic plants producing insecticidal proteins from the bacterium Bacillus thurin

229 Transgenic maize engineered to express insecticidal proteins from the bacterium Bacillus thurin

230 Transgenic plants expressing insecticidal proteins from the bacterium Bacillus thurin

231 Transgenic plants expressing insecticidal proteins from the bacterium Bacillus thurin

232 Crops genetically engineered to produce insecticidal proteins from the bacterium Bacillus thurin

233 sustainability of transgenic crops producing insecticidal proteins from the bacterium Bacillus thurin

234 Transgenic plants expressing insecticidal proteins from the bacterium, Bacillus thuri

235 Insecticidal proteins from the soil bacterium Bacillus t

236 delta-endotoxins (Bt toxins) are widely used insecticidal proteins in engineered crops that provide a

237 roborate different mode-of-actions for other insecticidal proteins including Cry34Ab1/35Ab1, Cry6Aa1,

238 Engineering genes encoding insecticidal proteins into crop plants offers numerous b

239 Our work indicates that insecticidal proteins obtained from a non-Bt bacterial s

240 Evolution of pest resistance to insecticidal proteins produced by Bacillus thuringiensis

241 t cotton was genetically modified to produce insecticidal proteins targeting Lepidopteran pests and i

242 ringiensis (Bt) Cry34Ab1/Cry35Ab1 are binary insecticidal proteins that are co-expressed in transgeni

243 teins has highlighted an urgent need for new insecticidal proteins with different modes or sites of a

244 h little sequence similarity exists to known insecticidal proteins, efficacy tests using WCR populati

245 s (BBTV) were used for the expression of two insecticidal proteins, Hadronyche versuta (Blue Mountain

246 on the expression of Bacillus thuringiensis insecticidal proteins, most of which permeabilize the me

247 and Cry1Da_7 are Bacillus thuringiensis (Bt) insecticidal proteins, whereas the Vip3Cb1 protein is de

248 d Photorhabdus spp. bacteria represent novel insecticidal proteins.

249 esent in non-seed plants, none include these insecticidal proteins.

250 transgenic plants harbouring genes encoding insecticidal proteins.

251 istance to other Bt crops expressing similar insecticidal proteins.

252 In this work, we characterized 2 novel insecticidal proteins; Vip3Ab1 and Vip3Bc1.

253 With the discovery of insecticidal resistance in some populations frequently t

254 link between reduced miRNA expression and an insecticidal resistance phenotype through reduced target

255 Acylsugars are insecticidal specialized metabolites produced in the gla

256 These proteins display unique insecticidal spectra and have differential rates of proc

257 As baculoviruses usually have a narrow insecticidal spectrum, knowing the mechanisms by which t

258 ith antibiofilm, antimalarial, anti-protist, insecticidal, spermicidal, chemotactic, wound healing, a

259 Insecticidal spider-venom peptides are promising candida

260 The side chain of the insecticidal steroid petuniasterone D was synthesized by

261 typically associated with alterations to the insecticidal target-site or with gene expression variati

262 as such, are emerging novel therapeutic and insecticidal targets.

263 n suppression approaches, genetic analogs of insecticidal techniques that reduce the number of insect

264 , is in good physical condition, and remains insecticidal, thereby providing protection against vecto

265 ral homology between the cubozoan toxins and insecticidal three-domain Cry toxins (delta-endotoxins)

266 ian angiotensin-converting enzyme (ACE), are insecticidal to larvae of the mosquitoes, Aedes aegypti

267 Vip3A represents a novel class of proteins insecticidal to lepidopteran insect larvae.

268 tivation of cockroach Na(V) channels and was insecticidal to sheep blowflies.

269 osquito control methods include a variety of insecticidal tools that target adults or juveniles.

270 CsTx-1 and CT1-long are insecticidal toward Drosophila flies and destroys Escher

271 Domain I of the Cry1Ab insecticidal toxic protein has seven alpha-helices and i

272 However, there was concern about insecticidal toxicity against the algal population of so

273 t of Lepidopteran insects susceptible to the insecticidal toxin complex.

274 These genes encode large insecticidal toxin complexes with little homology to oth

275 contains a cluster of genes with homology to insecticidal toxin encoding genes of the insect pathogen

276 i engineered to produce the B. thuringiensis insecticidal toxin killed gypsy moth larvae irrespective

277 glyphosate herbicides and to produce its own insecticidal toxin, maize GE to resist glyphosate, soybe

278 is very similar to that of the Bacillus Cry insecticidal toxin-like proteins, despite the low sequen

279 partners XptB1 and XptC1 producing the full insecticidal toxin.

280 ary plant-protectant gene (PPPG) encoding an insecticidal toxin.

281 consequence of virulence factors, including insecticidal toxins and enzymes that degrade the insect

282 ative autotransporters, and several possible insecticidal toxins and hemolysins.

283 Cry1A insecticidal toxins bind sequentially to different larva

284 Bacillus thuringiensis (Bt) insecticidal toxins bind to receptors on midgut epitheli

285 g of crops genetically engineered to produce insecticidal toxins derived from the bacterium Bacillus

286 of genetically engineered crops that produce insecticidal toxins derived from the bacterium Bacillus

287 Genetically engineered crops that produce insecticidal toxins from Bacillus thuringiensis (Bt) are

288 Transgenic crops producing insecticidal toxins from Bacillus thuringiensis (Bt) are

289 Transgenic crops producing insecticidal toxins from Bacillus thuringiensis (Bt) are

290 worldwide use of Bacillus thuringiensis (Bt) insecticidal toxins in agriculture, knowledge of the mec

291 s (including adhesins, secretion systems and insecticidal toxins).

292 to a lifestyle in which pathways to produce insecticidal toxins, degrading enzymes to digest the ins

293 dely used bacterial entomopathogen producing insecticidal toxins, some of which are expressed in inse

294 t pests to transgenic host plants containing insecticidal toxins.

295 greatly improve the durability of transgenic insecticidal toxins.

296 y capacity of pests for adaptive response to insecticidal traits in crops.

297 tive, have the potential to improve existing Insecticidal Treated Bednets (ITNs), by reducing the qua

298 repeated rounds of universal distribution of insecticidal treated nets in Tororo District, eastern Ug

299 licoverpa zea, is a major target pest of the insecticidal Vip3Aa protein used in pyramided transgenic

300 It is potently insecticidal when injected into a wide variety of insect