ライフサイエンスコーパス: sex pheromone

1 s of all 16 stereoisomers of the pine sawfly sex pheromone.

2 processing of information about the female's sex pheromone.

3 and tested the key compounds in V. velutina sex pheromone.

4 component that also acts as a long-distance sex pheromone.

5 for processing of sensory information about sex pheromones.

6 s long-distance signaling via female-emitted sex pheromones.

7 to information about social signals such as sex pheromones.

8 ize or otherwise enhance insect responses to sex pheromones.

9 cussed with special reference to research on sex pheromones.

10 diverse defensive secretions to function as sex pheromones.

11 tudied in insects with a particular focus on sex pheromones.

12 lence determinants can be induced by peptide sex pheromones.

13 ng volatile semiochemicals that mimic female sex pheromones.

14 d in both the emission and the perception of sex pheromones.

15 Although the ability to sense sex pheromones [1, 2, 3] is likely to be important for i

16 ter, several hydrocarbons including the male sex pheromone 11-cis-vaccenyl acetate (cVA) and female-s

17 l signals of females [2-7], especially their sex pheromones [8-11].

18 by disrupting male-female communication with sex pheromones, a technique known as mating disruption.

19 with an estimated half-life in vivo for the sex pheromone and a behavioral antagonist of approximate

20 6- to 7-day-old males released twice as much sex pheromone and acquired another mate in less than hal

21 ings provide a mechanism for the origin of a sex pheromone and show that sensory exploitation changes

22 , as moths use precise blends of odorants as sex pheromones and are skillful at tracking them in spit

23 The current study demonstrates that the sex pheromones and receptors of Schizophyllum, when expr

24 any fish species employ hormonal products as sex pheromones, and these cues are often mixtures that a

25 Since the female and male sex pheromones are biosynthetically related in this and

26 ls, such that the emission and perception of sex pheromones are precisely coordinated in this species

27 pests of agricultural crops, but the use of sex pheromones as attractants is limited by male multipl

28 ted to the female-specific production of the sex pheromones ascr#1 and ascr#9.

29 worker ovary development; it also acts as a sex pheromone, attracting drones during mating flights.

30 eptide (PBAN) was identified that stimulated sex pheromone biosynthesis in a lepidopteran moth.

31 ction of PBAN has become well understood for sex pheromone biosynthesis in moths.

32 evealed a serial of differentially expressed sex pheromone biosynthesis-associated proteins at the di

33 nd to be expressed during the key periods of sex pheromone biosynthesis.

34 n genes that function as key players in moth sex pheromone biosynthesis.

35 saturated fatty acids is a common feature of sex pheromone biosynthetic pathways in the Lepidoptera.

36 The biosynthesis of female moth sex pheromone blends is controlled by a number of differ

37 w this might impact the establishment of new sex pheromone blends within a species.

38 and subsequently PBAN-induced production of sex pheromone, bombykol.

39 s elegantly demonstrated by the reception of sex pheromone by the Japanese beetle.

40 o perfect its chemical mimicry of pollinator sex pheromones by escape from deleterious pleiotropy, su

41 est the qualification of the two steroids as sex pheromones by examining whether they communicate gen

42 h periphery and antennal lobes, reception of sex pheromones by moth ORs suggests that their labeled l

43 AD1 confers a mating response to the peptide sex pheromone cAD1 secreted by plasmid-free strains of E

44 g response to the recipient-produced peptide sex pheromone cAD1.

45 M373 encode a mating response to the peptide sex pheromones cAD1 and cAM373 respectively.

46 onjugative mating response to an octapeptide sex pheromone (cAD1) secreted by plasmid-free strains.

47 s a conjugative mating response to a peptide sex pheromone, cAD1, secreted by plasmid-free bacteria.

48 sponse induced by exposure to an octapeptide sex pheromone, cAD1, secreted by plasmid-free enterococc

49 s of Enterococcus faecalis secrete a peptide sex pheromone, cAD1, which specifically induces a mating

50 The sex pheromone cAM373 of Enterococcus faecalis and the re

51 aecalis that encodes a response to a peptide sex pheromone, cAM373, secreted by plasmid-free (recipie

52 It is found that disruptive doses of sex pheromone can have a marked influence upon male moth

53 donor cells occurs in response to a peptide sex pheromone, cCF10, secreted by recipients.

54 males by other males through the use of the sex pheromone CH503.

55 selection pressure on the long-range female sex pheromone channel and consequently affect the evolut

56 of insects, host plant influences on insect sex pheromone communication may be important aspects of

57 Sex pheromone communication, acting as a prezygotic barr

58 on insect physiology and behavior, including sex pheromone communication, that reflect strategies by

59 orGOBP2 and BmorABPx all bind to the B. mori sex pheromone component (10E,12Z)-hexadecadien-1-ol (bom

60 less responsive than groomed antennae to the sex pheromone component periplanone-B, as well as to the

61 They are also sex pheromone components of the female Zeleboria.

62 silkmoth, Bombyx mori, female moths emit two sex pheromone components, bombykol and bombykal, but onl

63 Ostrinia species with structurally different sex pheromone components.

64 ,000 moth species (Lepidoptera) that produce sex pheromones comprising communication channels used in

65 In moths, females emit a species-specific sex pheromone, consisting of a blend of biochemically re

66 The Drosophila sex pheromone cVA elicits different behaviors in males a

67 edge of how insects are actually affected by sex pheromones deployed throughout a crop so as to disru

68 Lepidopteran insects use sex pheromones derived from fatty acids in their species

69 In that context, moth sex-pheromone desaturase genes seem to be evolving under

70 genomes indicates that the evolution of moth sex pheromone desaturases in general is much more comple

71 results from published studies on other moth sex pheromone desaturases.

72 e biosynthetic pathway for production of the sex pheromone disparlure, 2-methyl-7R,8S-epoxy-octadecan

73 Sex pheromones facilitate reproduction by attracting pot

74 Animals often use sex pheromones for mate choice and reproduction.

75 We specifically produce multicomponent sex pheromones for two species.

76 e other neuron is tuned to (S)-japonilure, a sex pheromone from a closely related species and a behav

77 d expression of a single desaturase from the sex pheromone gland of the light brown apple moth, Epiph

78 In moths, more long-range female sex pheromones have been identified than in any other an

79 ommunication in cockroaches: Each long-range sex pheromone identified to date from different genera b

80 tode mating, suggesting that MMB might mimic sex pheromone in Caenorhabditis species.

81 lms alters the induction of conjugation by a sex pheromone in E. faecalis.

82 The biosynthesis and release of sex pheromone in female moths are regulated by pheromone

83 We show that darcin, an involatile protein sex pheromone in male mouse urine, can rapidly condition

84 , and the first chemical identification of a sex pheromone in the eusocial hornets.

85 We tested the hypothesis that the male sex pheromone in the noctuid moth Heliothis virescens pe

86 n gynes (reproductive females) produced this sex pheromone in the sixth intersegmental sternal glands

87 Additionally, certain iridoids are used as sex pheromones in agriculturally important species of ap

88 usible explanation for opposing responses to sex pheromones in male and female flies.

89 Other insects produce or release sex pheromones in response to particular host plant cues

90 ys release a bile acid that acts as a potent sex pheromone, inducing preference and searching behavio

91 family in moth species mediates conspecific sex pheromone information for sexual behaviour.

92 Such semisynthetic preparation of sex pheromones is a novel and cost-effective way of prod

93 (more 5,9-C27:2 and less 7,11-C27:2, female sex pheromone isomers).

94 rally by their responses to subtly different sex pheromone isomers, (E)-12- and (Z)-12-tetradecenyl a

95 ecades after the discovery of the first moth sex pheromone, little is known about the molecular mecha

96 f both pheromone emission and orientation to sex pheromone may explain, at least in part, an observed

97 ic control of the emission and perception of sex pheromones must be tightly coadapted, and yet we sti

98 ell known for their exquisite sensitivity to sex pheromone odorants, molecular mechanisms underlying

99 All 16 stereoisomers of the sex pheromone of pine sawfly (3,7,11-trimethylundecanol

100 The irregular monoterpenoid sex pheromone of Pseudococcus longispinus and its enanti

101 d in a short synthesis of a component of the sex pheromone of the Californian red scale beetle.

102 by producing a chemical cue that mimics the sex pheromone of the female bee.

103 The sex pheromone of the German cockroach, Blattella germani

104 te configurations to both enantiomers of the sex pheromone of the longtailed mealybug, an irregular m

105 ompounds that together constitute the female sex pheromone of the pink hibiscus mealybug (PHM), Macon

106 ila melanogaster, is highly sensitive to the sex pheromone of the silkworm moth, bombykol.

107 g, we have identified the genes encoding the sex pheromones of the heterothallic species Neurospora c

108 lants are acetylated to mimic the respective sex pheromones of the small ermine moths Yponomeuta evon

109 nvestigated the effect of an oriental beetle sex pheromone on the development and behavior of the nem

110 ted females were less responsive to the male sex pheromone or unable to use it as a cue at all.

111 the number of trapped male moths exposed to sex pheromones or by the number of trapped male and fema

112 acquire host plant compounds and use them as sex pheromones or sex pheromone precursors.

113 at either promote upwind flight (conspecific sex pheromones) or inhibit it (interspecific antagonists

114 array and qPCR, we identified four candidate sex pheromone Ors (AmOr10, -11, -18, and -170) from the

115 ggregation substance proteins encoded by the sex pheromone plasmid family of Enterococcus faecalis ha

116 ntial for high-efficiency conjugation of the sex pheromone plasmids and also serve as virulence facto

117 The sex pheromone plasmids in Enterococcus faecalis are one

118 Aggregation substance proteins encoded by sex pheromone plasmids increase the virulence of Enteroc

119 Aggregation substance (AS) on the sex pheromone plasmids of E. faecalis has been implicate

120 at GPAT acts to regulate the biosynthesis of sex pheromone precursor, TAG, thus influencing PBAN-indu

121 ction of this protein in the biosynthesis of sex pheromone precursor, triacylglcerol (TAG), and subse

122 ular mechanism regarding the biosynthesis of sex pheromone precursor.

123 compounds and use them as sex pheromones or sex pheromone precursors.

124 The sex pheromone present in the pre-ovulatory urine of fema

125 One neuron specifically detects the sex pheromone produced by conspecific females (R,Z)-5-(-

126 In Drosophila melanogaster, the sex pheromone produced by males, cis-vaccenyl acetate (c

127 A "mate-sensing" peptide sex pheromone produced by recipient cells is detected by

128 The sex pheromone-producing gland in adult females was ident

129 et to modulate the timing of onset of female sex pheromone production and mating.

130 recursor, TAG, thus influencing PBAN-induced sex pheromone production and subsequent mating behavior.

131 les serve as a signal for males, acting as a sex pheromone proxy for females concealed within plant t

132 PBPs are involved in sex pheromone reception by the antennae of male moths.

133 A sex pheromone receptor BmOR1 is specifically tuned to bo

134 In vitro, ECB(Z) odorant receptor 3 (OR3), a sex pheromone receptor expressed in male antennae, respo

135 e first direct evidence that a member of the sex pheromone receptor family in moth species mediates c

136 pheromone substances have been identified as sex pheromone receptors in various moth species.

137 w the specificity of more broadly responsive sex pheromone receptors may provide a mechanism that con

138 s class IIa bacteriocin MC4-1 encoded by the sex pheromone-responding, multiple-antibiotic resistance

139 prgX, a gene proposed to negatively regulate sex pheromone response of the E.faecalis plasmid, pCF10.

140 pHKK703 is an approx. 55-kb putative sex pheromone-response plasmid that is required for conj

141 rating that it is the receptor that mediates sex pheromone responses in male silkmoths.

142 various positions and configurations, called sex pheromones (SPs).

143 Odorant receptors (ORs) for sex pheromone substances have been identified as sex phe

144 gories: male-biased genes for key enzymes in sex-pheromone synthesis and female-biased genes for gene

145 is the first genetic analysis of a potential sex pheromone system in a commensal oral streptococcal s

146 tate plasmid exchange as part of a bacterial sex pheromone system.

147 dry season males produced significantly less sex pheromones than wet season males, partly due to accl

148 nded cockroaches, Supella longipalpa, emit a sex pheromone that attracts males from a distance.

149 ete multiple peptides representing different sex pheromones that induce mating responses by bacteria

150 y in production of the major female-specific sex pheromones (the 7,11-C27 and -C29 dienes) and a chan

151 ns, particularly the 7-alkenes, in an insect sex pheromone to attract and elicit mating behavior in i

152 Male moths use species-specific sex pheromones to identify and orientate toward conspeci

153 Here we produce moth sex pheromone, using Nicotiana benthamiana as a plant fa

154 ed; they include two genes encoding a fungal sex pheromone (Vir1 and Vir2), a gene encoding an extrac

155 the orientation responses of adult males to sex pheromone were also significantly inhibited by these

156 , signals corresponding to two male-specific sex pheromones were detected in the ejaculatory bulb, a

157 and thus appear to be part of the C. elegans sex pheromone, whereas higher concentrations induce deve

158 the secretions of sting-associated glands as sex pheromones, whereas a variety of nonhymenopterous sp

159 emale P. lata emit a volatile, long-distance sex pheromone, which, once identified and synthesized, c

160 roxy-4-decanolide (RS) as component of their sex pheromone while only N. vitripennis (Nv), employs ad

161 esents the details of the FMS of pine sawfly sex pheromones with an emphasis on identification and so

162 t receptors (ORs) to detect species-specific sex pheromones with remarkable sensitivity and selectivi

163 tudies have suggested the existence of human sex pheromones, with particular interest in two human st

164 up, and males often display with close-range sex pheromones, yet odor-based post-copulatory mate guar