The Sex Pheromone of the Mediterranean Flour Moth

Lachrymatory factor synthase (LFS), an enzyme essential for the synthesis of the onion lachrymatory factor (propanethial S-oxide), was identified in 2002. This was the first reported enzyme involved in the production of thioaldehyde S-oxides via an intra-molecular H⁺ substitution reaction, and we therefore attempted to identify the catalytic amino acid residues of LFS as the first step in elucidating the unique catalytic reaction mechanism of this enzyme. A comparison of the LFS cDNA sequences among lachrymatory Allium plants, a deletion analysis and site-directed mutagenesis enabled us to identify two amino acids (Arg71 and Glu88) that were indispensable to the LFS activity. Homology modeling was performed for LFS/23–169 on the basis of the template structure of a pyrabactin resistance 1-like protein (PYL) which had been selected from a BLASTP search on SWISS-MODEL against LFS/23–169. We identified in the modeled structure of LFS a pocket corresponding to the ligand-binding site in PYL, and Arg71 and Glu88 were located in this pocket.     

5,7-Dodecadien-1-ol: Candidate for the Sex Pheromone of the Pine Moth

Ferredoxin-nitrite reductase (EC 1.7.7.1), an enzyme which catalyzes the 6-electron reduction of nitrite to ammonia, has been isolated from Spinacia oleracea. The isolated enzyme was homogeneous by disc electrophoresis with polyacrylamide gel. The molecular weight of the enzyme was estimated to be 86,000 by Ultrogel AcA 34 gel filtration. In the oxidized form, the enzyme had absorption maxima at 278, 388 (Soret band), 573 (α band) and 690 nm, indicating that siroheme is directly involved in the catalysis of nitrite reduction. This absorption spectrum was modified by sulfite, hydroxylamine and cyanide. The enzyme exhibited electron paramagnetic resonance signals with g values of 6.9 and 5.2, which are characteristic of a high spin Fe³⁺ -siroheme in the molecule. These signals disappeared upon the addition of dithionite or nitrite. This isolated enzyme also contained four moles of labile sulfide and 7 g-atoms of iron per 86,000 g of protein.     

A New Synthesis of (E,E)-8, 10-Dodecadien-1-ol,Sex Pheromone of Codling Moth

A methanol-utilizing bacterium, which produced red to pink pigments and assimilated methanol via icl^- serine pathway, was isolated from soil and tentatively designated as Pseudomonas MS 31. This bacterium produced L-serine when glycine was added to the growth medium at the late exponential phase of growth. The cells showed high L-serine degradation activity. Chelating agents and some metal ions, which inhibited L-serine degradation, stimulated the L-serine accumulation. In the presence of 0.1 ? 1 mM EDTA, o-phenanthroline, 8-hydroxyquinoline, α,α'-dipyridyl, cobalt sulfate or nickel sulfate, this bacterium produced 0.7?2.1mg L-serine from 4mg glycine per ml culture.     

Synthesis of (S,E)-1-Methyl-9-dodecenyl Acetate,the Sex Pheromone of the Hessian Fly,Mayetiola destructor

(S,E)-1-Methyl-9-dodecenyl acetate (1), the sex pheromone of the Hessian fly, was synthesized by starting from ethyl (S)-3-hydroxybutanoate (2).     

Synthesis of Both the Enantiomers of (2Z, 6Z)-2,6-Nonadien-4-olide,the Possible Male-Secreted Sex Pheromone from a Pyralid Moth,Aphomia gularis Zeller

Both the enantiomers (~96% e.e.) of (2Z, 6Z)-2,6-nonadien-4-olide, a possible pheromone of Aphomia gularis, were synthesized by resolving an acetylenic intermediate.     

Sex Pheromone Composition and Male Trapping of the Peach Fruit Moth,Carposina sasakii (Matsumura) (Lepidoptera: Carposinidae) in Korea

Sex pheromone composition, mating behavior, and field trapping were analyzed for the peach fruit moth, Carposina sasakii(Matsumura) to develop a monitoring system with its sex pheromone. The upwind flying response of males to female was the most frequent at 4th to 5th hr after lights-off. The highest mating rate was seen at 5th hr after lights-off. The extract of female abdominal tip was analyzed with gas chromatography and proved to have two compounds, (Z)-7-eicosen-11-one and (Z)-7-nonadecen-11-one. In field-trapping, however, a lure containing (Z)-7-eicosen-11-one only showed the highest attractivity.     

Synthesis of (S,E)-1-Methyl-9-dodecenyl Acetate,the Sex Pheromone of the Hessian Fly,Mayetiola destructor,by Lipase-catalyzed Enantioselective Hydrolysis

(S,E)-1-Methyl-9-dodecenyl acetate [(S)-8], the sex pheromone of the hessian fly, Mayetiola destructor, was synthesized in a highly enantiomerically pure form by Pseudomonas cepacia lipase-catalyzed hydrolysis.     

Synthesis and Characterization of Hexadecadienyl Compounds with a Conjugated Diene System,Sex Pheromone of the Persimmon Fruit Moth and Related Compounds

Hexadecadien-1-ol and the derivatives (acetate and aldehyde) with a conjugated diene system have recently been identified from a pheromone gland extract of the persimmon fruit moth (Stathmopoda masinissa), a pest insect of persimmon fruits distributed in East Asia. The alcohol and acetate showed their base peaks at m/z 79 in a GC-MS analysis by electron impact ionization, but the aldehyde produced a unique base peak at m/z 84, suggesting a 4,6-diene structure. To confirm this inference, four geometrical isomers of each 4,6-hexadecadienyl compound were synthesized by two different routes in which one of two double bonds was furnished in a highly stereoselective manner. Separation of the two isomers synthesized together by each route was facilely accomplished by preparative HPLC. Their mass spectra coincided well with those of natural components, indicating that they were available for use as authentic standards for determining the configuration of the natural pheromone. Furthermore, other hexadecadienyl compounds, including the conjugated diene system between the 3- and 10-positions, were synthesized to accumulate the spectral data of pheromone candidates. 5,7-Hexadecadienal interestingly showed the base peak at m/z 80; meanwhile, the base peaks of its alcohol and acetate were detected at m/z 79 like the corresponding 4,6-dienes. The base peaks of all 6,8-, 7,9-, and 8,10-dienes universally appeared at m/z 67 like 9,11-, 10,12-, and 13,15-dienes, the spectra of which have already been published. Although 3,5-hexadecadienal was not prepared, base peaks at m/z 67 and 79 were recorded for the alcohol and acetate, respectively.     

Synthesis of Both the Enantiomers of 3-Octanol,the Pheromone of Various Species of Ants

(2S,3R,1′S,2′S)-Serricorole (1) and (2S,3R,1′R)-serricorone (2), sex pheromone components of the cigarette beetle (Lasioderma serricorne F.), were synthesized, starting from the enantiomers of methyl 3-hydroxypentanoate. The stereochemistry of the naturally occurring 1 was determined to be 2S,3R,1′S,2′S, and that of 2 to be 2S,3R,1′RS by comparing between the CD spectra of the natural and synthetic samples.     

Calling Behavior and Rhythms of Sex Pheromone Production in the Black Cutworm Moth in China

The hourly and daily variation of calling behavior and sex pheromone production by the female black cutworm moth, Agrotis ypsilon (Rottemberg), were investigated. Both calling behavior and titers of five sex pheromone components showed distinct diel rhythms, and peak periods of calling and pheromone titer were synchronous. Females began to call on the first night after eclosion and called mainly during the second half of the scotophase. The percentage of females calling increased in 1 to 3-d-old females and decreased in 3 to 7-d-old females. Females advanced their calling time with increasing age (1 to 7 d). GC-MS analysis of hexane extracts of pheromone glands revealed that the titers of the five sex pheromone components were very low on the first night after eclosion, but increased sharply and peaked on the third night. Titers decreased greatly with increasing age (3 to 7 d), but from the onset of the scotophase to 4.5 h into scotophase, titers remained invariate. However, from 4.5 to 7 h, pheromone titers, especially that of the primary component Z7-12:Ac, increased sharply and peaked. After the peak, the titers decreased greatly at 8 h, and thereafter decreased gradually to the level before 4.5 h. The quantity of each component almost reached zero after lights-on.     

Synthesis and Characterization of 3,13- and 2,13-Octadecadienyl Compounds for Identification of the Sex Pheromone Secreted by a Clearwing Moth,Nokona pernix

Several geometrical isomers of 3,13- and 2,13-octadecadien-1-ols and their acetates were synthesized starting from 1,8-octanediol or 1,9-nonanediol utilizing acetylene coupling reactions. In addition to commercially available compounds, all geometrical isomers of each dienyl compound were analyzed by NMR and GC-MS to accumulate chemical data for studies of sex pheromones secreted from clearwing moths classified into the family Sesiidae of Lepidoptera. Although acetoxy derivatives of the 3,13- and 2,13-dienes showed almost the same mass spectra, the alcohols were distinguished by comparing the relative intensities of [M?18]⁺ at m?z 248, indicating direct differentiation of the two positional isomers without derivatization. Furthermore, each geometrical isomer eluted from a high-polar GC column with a different retention time. Base on these data, a pheromone gland extract of a sesiid moth, Nokona pernix, was analyzed by GC-EAD and GC-MS, and two EAG-active components were identified, viz., the (3E,13Z)- and (3Z,13Z)-isomers of 3,13-octadecadien-1-ol in a ratio of 9:1. In the field, the synthetic compounds mixed in 9:1 ratio attracted N. pernix males well, while a single component scarcely attracted the males. The number of attracted males peaked in the middle of June, and a small second peak was observed in August.     

Synthesis of the Enantiomers of (Z)-5-(1-Octenyl)oxacyclopentan-2-one,a Sex Pheromone of the Cupreous Chafer Beetle,Anomala cuprea Hope

Glutaminase (EC 3.5.1.2) was isolated from Pseudomonas nitroreducens IFO 12694 grown on 0.6% sodium glutamate as a nitrogen source (325-fold purification, 13% yield). The molecular weight of the enzyme was estimated to be 40,000 by gel filtration and SDS-gel electrophoresis. The enzyme hydro-lyzed glutamine optimally at pH 9, and its K_m was 6.5 mm. d-Glutamine, γ-glutamyl p-nitroanilide, γ-glutamylmethylamide, γ-glutamylethylamide (theanine), and glutathione showed respectively 107, 85, 78, 74, and 82% reactivity of glutamine. Zn²⁺, Ni²⁺, Cd²⁺, Co²⁺, Fe²⁺, and Cu²⁺ repressed the enzyme activity strongly.

Glutaminase formed γ-glutamylhydroxamate in the reaction mixture containing glutamine and hydroxylamine (transferring reaction). The optimum pH of the transferring reaction was 7–8, and the K_m for glutamine and hydroxylamine were 4 mm and 120 mm, respectively. γ-Glutamyl derivatives hydrolyzable by glutaminase showed reactivity for the transferring reaction. Methylamine or ethylamine was replaceable for hydroxylamine with 3 or 8% reactivity. The effect of divalent cations was not so striking as in the hydrolyzing reaction.     

Isolation and Identification of the Female Sex Pheromone of the Potato Tuberworm Moth,Phthorimaea operculella (Zeller)

The sex pheromone produced by adult females of the potato tuberworm moth was isolated from unmated female moths reared in the laboratory. The gas Chromatographic and mass spectrometric data suggested the pheromone to be a tridecatrienyl acetate. The isolated pheromone was subjected to partial hydrogenation with hydrazine and hydrogen peroxide and subsequent ozonolysis to produce a mixture of ω-acetoxy-alkanals. They were identified by mass Chromatographic technique as 4-acetoxy-butanal, 7-acetoxy-heptanal, and 10-acetoxy-decanal respectively. Consequently, the pheromone was identified as 4,7,10-tridecatrienyl acetate except the geometric configuration.     

(5Z, 7E)-5,7-Dodecadien-1-ol: Female Sex Pheromone of the Pine Moth Dendrolimus spectabilis Butler

The sex pheromone of the pine moth Dendrolimus spectabilis Butler was tentatively identified as 5,7-dodecadien-l-ol by the use of the electroantennogram technique. Analyses of abdominal tip extracts of virgin females by gas-liquid chromatography and mass spectroscopy showed the presence of a (5Z, 7E)-isomer and a (5E, 7E)-isomer in the ratio of about ca. 5:1. In field examinations with four synthetic isomers of 5,7-dodecadien-l-ol, only traps baited with the (5Z, 7E)-isomer captured an appreciable numbers of male moths.     

小地老虎中国种群性信息素的成分鉴定及田间试验（英文）

研究了小地老虎中国种群的性信息素组分,3日龄处女蛾单腺体性信息素提取物中性信息素的含量非常低。GC和GC-MS分析表明,小地老虎性信息素含有5种成分：顺-7-12碳乙酸酯（A）、顺-9-14碳乙酸酯（B）、顺-11-16碳乙酸酯（C）、顺-5-10碳乙酸酯（D）和顺-8-12碳乙酸酯（E）。它们的含量分别为：（0.245±0.098）、（0.080±0.031）、（0.089±0.03）、(0.085±0.031)和 (0.105±0.065)ng, 这5种物质的百分比分别为40.451±13.66、13.176±5.279、14.943±5.142、14.392±6.10和17.225±9.792,前3种物质的百分比为58.75±9.429、18.91±7.539和22.34±7.209。田间试验表明,性信息素单一组分均未诱到雄蛾,AB以3∶1的比例配成的诱芯对雄蛾有一定的引诱活性,一个诱捕器平均诱捕到2.6头。ABC组分以3∶1∶1的比例配成的诱芯对雄蛾引诱活性显著增强,一个诱捕器平均诱捕量为7.40头,是AB（3∶1）诱芯的2.8倍。诱芯中性信息素的含量对诱蛾活性有明显的影响,在剂量为200 µg时的平均诱捕量最高。     

Synthesis of the Deuterated Sex Pheromone Components of the Grape Borer,Xylotrechus pyrrhoderus

Adult males of the grape borer, Xylotrechus pyrrhoderus, secrete (S)-2-hydroxy-3-octanone [(S)-1] and (2S,3S)-2,3-octanediol [(2S,3S)-2] from their nota of prothoraces as sex pheromone components. Their structural similarity suggests that one of them is the biosynthetic precursor of the other component. In order to confirm the biochemical conversion, deuterated derivatives of both components were synthesized by starting from a Wittig reaction between hexanal and an ylide derived from D₅-iodoethane and ending with enantiomeric resolution by chiral HPLC. The molecular ions of 1 and 2 could scarcely be detected by using a GC-MS analysis, and the labeled compounds showed similar mass spectra to the unlabeled pheromone components. However, several fragment ions, including four deuterium atoms, were observed in the mass spectra of their acetate derivatives, indicating that the conversion could be confirmed by examining a compound with the diagnostic ions after acetylation of the volatiles collected from insects treated with the labeled precursors.