ライフサイエンスコーパス: insecticidal

1 The insecticidal action involves blocking the lambda-aminobu

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

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

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

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

6 Insecticidal activities of the mutant toxins on Manduca

7 embrane insertion and also in haemolytic and insecticidal activities.

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

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

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

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

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

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

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

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

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

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

18 Their potent insecticidal activity arises from selectively activating

19 Furthermore, insecticidal activity correlated with the resistance to

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

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

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

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

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

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

26 Insecticidal activity of the recombinant proteins correl

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

44 Proteolytic processing was shown to enhance insecticidal activity.

45 step for membrane insertion, haemolysis and insecticidal activity.

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

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

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

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

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

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

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

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

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

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

56 Binding of the insecticidal Bacillus thuringiensis Cry1Ac toxin to the

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

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

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

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

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

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

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

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

65 al properties for possible antimicrobial and insecticidal candidates.

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

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

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

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

70 for several classes of natural and synthetic insecticidal compounds.

71 With insecticidal control options dwindling, research on clic

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

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

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

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

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

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

78 The insecticidal Cry toxins produced by Bacillus thuringiens

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

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

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

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

83 The insecticidal crystal proteins produced by Bacillus thuri

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

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

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

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

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

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

90 The insecticidal, ecotoxicological properties and the mode o

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

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

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

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

95 iotic stress tolerance, independent of their insecticidal function.

96 VIP3-insecticidal gene homologues have been detected in appro

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

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

99 a soybean transgenic for a highly expressed insecticidal gene.

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

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

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

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

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

105 is independent of the accumulation of major insecticidal molecules.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

127 are potentially important genetic leads for insecticidal peptides.

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

129 the development and regulation of transgenic insecticidal plants.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

152 Vip3A insecticidal proteins are secreted without N-terminal pr

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

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

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

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

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

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

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

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

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

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

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

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

165 Transgenic plants expressing insecticidal proteins from the bacterium Bacillus thurin

166 Transgenic plants expressing insecticidal proteins from the bacterium Bacillus thurin

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

168 Transgenic plants producing insecticidal proteins from the bacterium Bacillus thurin

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

170 Insecticidal proteins from the soil bacterium Bacillus t

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

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

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

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

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

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

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

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

179 d Photorhabdus spp. bacteria represent novel insecticidal proteins.

180 istance to other Bt crops expressing similar insecticidal proteins.

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

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

183 Acylsugars are insecticidal specialized metabolites produced in the gla

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

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

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

187 Insecticidal spider-venom peptides are promising candida

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

203 partners XptB1 and XptC1 producing the full insecticidal toxin.

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

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

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

207 Cry1A insecticidal toxins bind sequentially to different larva

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

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

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

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

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

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

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

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

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

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

218 t pests to transgenic host plants containing insecticidal toxins.

219 greatly improve the durability of transgenic insecticidal toxins.

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

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