new class of mealybug pheromones: a hemiterpene ester in the sex pheromone of Crisicoccus matsumotoi
Mealybugs, which include several agricultural pests, are small sap feeders covered with a powdery wax. They exhibit clear sexual dimorphism; males are winged but fragile and short lived, whereas females are windless and less mobile. Thus, sex pheromones emitted by females facilitate copulation and r...
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Veröffentlicht in: | Die Naturwissenschaften 2012-07, Vol.99 (7), p.567-574 |
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creator | Tabata, Jun Narai, Yutaka Sawamura, Nobuo Hiradate, Syuntaro Sugie, Hajime |
description | Mealybugs, which include several agricultural pests, are small sap feeders covered with a powdery wax. They exhibit clear sexual dimorphism; males are winged but fragile and short lived, whereas females are windless and less mobile. Thus, sex pheromones emitted by females facilitate copulation and reproduction by serving as a key navigation tool for males. Although the structures of the hitherto known mealybug pheromones vary among species, they have a common structural motif; they are carboxylic esters of monoterpene alcohols with irregular non-head-to-tail linkages. However, in the present study, we isolated from the Matsumoto mealybug, Crisicoccus matsumotoi (Siraiwa), a pheromone with a completely different structure. Using gas chromatography–mass spectrometry and nuclear magnetic resonance spectroscopy, we identified the pheromone as 3-methyl-3-butenyl 5-methylhexanoate. Its attractiveness to males was confirmed in a series of field trapping experiments involving comparison between the isolated natural product and a synthetic sample. This is the first report of a hemiterpene mealybug pheromone. In addition, the acid moiety (5-methylhexanoate) appears to be rare in insect pheromones. |
doi_str_mv | 10.1007/s00114-012-0935-z |
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They exhibit clear sexual dimorphism; males are winged but fragile and short lived, whereas females are windless and less mobile. Thus, sex pheromones emitted by females facilitate copulation and reproduction by serving as a key navigation tool for males. Although the structures of the hitherto known mealybug pheromones vary among species, they have a common structural motif; they are carboxylic esters of monoterpene alcohols with irregular non-head-to-tail linkages. However, in the present study, we isolated from the Matsumoto mealybug, Crisicoccus matsumotoi (Siraiwa), a pheromone with a completely different structure. Using gas chromatography–mass spectrometry and nuclear magnetic resonance spectroscopy, we identified the pheromone as 3-methyl-3-butenyl 5-methylhexanoate. Its attractiveness to males was confirmed in a series of field trapping experiments involving comparison between the isolated natural product and a synthetic sample. This is the first report of a hemiterpene mealybug pheromone. 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They exhibit clear sexual dimorphism; males are winged but fragile and short lived, whereas females are windless and less mobile. Thus, sex pheromones emitted by females facilitate copulation and reproduction by serving as a key navigation tool for males. Although the structures of the hitherto known mealybug pheromones vary among species, they have a common structural motif; they are carboxylic esters of monoterpene alcohols with irregular non-head-to-tail linkages. However, in the present study, we isolated from the Matsumoto mealybug, Crisicoccus matsumotoi (Siraiwa), a pheromone with a completely different structure. Using gas chromatography–mass spectrometry and nuclear magnetic resonance spectroscopy, we identified the pheromone as 3-methyl-3-butenyl 5-methylhexanoate. Its attractiveness to males was confirmed in a series of field trapping experiments involving comparison between the isolated natural product and a synthetic sample. This is the first report of a hemiterpene mealybug pheromone. In addition, the acid moiety (5-methylhexanoate) appears to be rare in insect pheromones.</description><subject>alcohols</subject><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>copulation</subject><subject>Environment</subject><subject>esters</subject><subject>Esters - chemistry</subject><subject>Esters - isolation & purification</subject><subject>Esters - pharmacology</subject><subject>Female</subject><subject>females</subject><subject>gas chromatography</subject><subject>Gas Chromatography-Mass Spectrometry</subject><subject>Hemiptera - chemistry</subject><subject>Hemiptera - drug effects</subject><subject>Hemiptera - physiology</subject><subject>insect pheromones</subject><subject>Life Sciences</subject><subject>Male</subject><subject>males</subject><subject>mass spectrometry</subject><subject>monoterpenoids</subject><subject>nuclear magnetic resonance spectroscopy</subject><subject>Original Paper</subject><subject>pests</subject><subject>Pseudococcidae</subject><subject>Sex Attractants - chemistry</subject><subject>Sex Attractants - isolation & purification</subject><subject>Sex Attractants - pharmacology</subject><subject>sex pheromones</subject><subject>sexual dimorphism</subject><subject>trapping</subject><issn>0028-1042</issn><issn>1432-1904</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1v1DAQhi1ERbeFH8AFfOQSOv5IvOkNrYBWqtQD9Gw5zng3VRIvnkRt99fXqxR64-SR_LyvZh7GPgr4KgDMBQEIoQsQsoBalcXhDVsJrWQhatBv2QpArgsBWp6yM6L7TNemrN-xUylNKdaVWbF2xAfue0fEY-ADuv6pmbd8v8MUhzgiXXLHdzh0E6Y9jsiR8sS7kU875ISPr-ixYJM66nz0fiY-uInmIU6xe89OgusJP7y85-zux_ffm6vi5vbn9ebbTeG10lNhyko7A3lu60YF5duAlWkq06Ipy6B1rdZel8FLNG3r1xpN1ZgGsAZAY4I6Z1-W3n2Kf-a8qR068tj3bsQ4kxUgNdS5BjIqFtSnSJQw2H3qBpeeMmSPcu0i12a59ijXHnLm00v93AzY_kv8tZkBuQCUv8YtJnsf5zTmk__b-nkJBRet22aB9u6XBKEzWakSpHoGScyPoQ</recordid><startdate>20120701</startdate><enddate>20120701</enddate><creator>Tabata, Jun</creator><creator>Narai, Yutaka</creator><creator>Sawamura, Nobuo</creator><creator>Hiradate, Syuntaro</creator><creator>Sugie, Hajime</creator><general>Springer-Verlag</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20120701</creationdate><title>new class of mealybug pheromones: a hemiterpene ester in the sex pheromone of Crisicoccus matsumotoi</title><author>Tabata, Jun ; Narai, Yutaka ; Sawamura, Nobuo ; Hiradate, Syuntaro ; Sugie, Hajime</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c434t-7564a70434d9b3f3cdfe67b67de755f44938c45fc2e7ddc84e76b7b0e900e77f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>alcohols</topic><topic>Animals</topic><topic>Biomedical and Life Sciences</topic><topic>copulation</topic><topic>Environment</topic><topic>esters</topic><topic>Esters - chemistry</topic><topic>Esters - isolation & purification</topic><topic>Esters - pharmacology</topic><topic>Female</topic><topic>females</topic><topic>gas chromatography</topic><topic>Gas Chromatography-Mass Spectrometry</topic><topic>Hemiptera - chemistry</topic><topic>Hemiptera - drug effects</topic><topic>Hemiptera - physiology</topic><topic>insect pheromones</topic><topic>Life Sciences</topic><topic>Male</topic><topic>males</topic><topic>mass spectrometry</topic><topic>monoterpenoids</topic><topic>nuclear magnetic resonance spectroscopy</topic><topic>Original Paper</topic><topic>pests</topic><topic>Pseudococcidae</topic><topic>Sex Attractants - chemistry</topic><topic>Sex Attractants - isolation & purification</topic><topic>Sex Attractants - pharmacology</topic><topic>sex pheromones</topic><topic>sexual dimorphism</topic><topic>trapping</topic><toplevel>online_resources</toplevel><creatorcontrib>Tabata, Jun</creatorcontrib><creatorcontrib>Narai, Yutaka</creatorcontrib><creatorcontrib>Sawamura, Nobuo</creatorcontrib><creatorcontrib>Hiradate, Syuntaro</creatorcontrib><creatorcontrib>Sugie, Hajime</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Die Naturwissenschaften</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tabata, Jun</au><au>Narai, Yutaka</au><au>Sawamura, Nobuo</au><au>Hiradate, Syuntaro</au><au>Sugie, Hajime</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>new class of mealybug pheromones: a hemiterpene ester in the sex pheromone of Crisicoccus matsumotoi</atitle><jtitle>Die Naturwissenschaften</jtitle><stitle>Naturwissenschaften</stitle><addtitle>Naturwissenschaften</addtitle><date>2012-07-01</date><risdate>2012</risdate><volume>99</volume><issue>7</issue><spage>567</spage><epage>574</epage><pages>567-574</pages><issn>0028-1042</issn><eissn>1432-1904</eissn><abstract>Mealybugs, which include several agricultural pests, are small sap feeders covered with a powdery wax. They exhibit clear sexual dimorphism; males are winged but fragile and short lived, whereas females are windless and less mobile. Thus, sex pheromones emitted by females facilitate copulation and reproduction by serving as a key navigation tool for males. Although the structures of the hitherto known mealybug pheromones vary among species, they have a common structural motif; they are carboxylic esters of monoterpene alcohols with irregular non-head-to-tail linkages. However, in the present study, we isolated from the Matsumoto mealybug, Crisicoccus matsumotoi (Siraiwa), a pheromone with a completely different structure. Using gas chromatography–mass spectrometry and nuclear magnetic resonance spectroscopy, we identified the pheromone as 3-methyl-3-butenyl 5-methylhexanoate. Its attractiveness to males was confirmed in a series of field trapping experiments involving comparison between the isolated natural product and a synthetic sample. 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subjects | alcohols Animals Biomedical and Life Sciences copulation Environment esters Esters - chemistry Esters - isolation & purification Esters - pharmacology Female females gas chromatography Gas Chromatography-Mass Spectrometry Hemiptera - chemistry Hemiptera - drug effects Hemiptera - physiology insect pheromones Life Sciences Male males mass spectrometry monoterpenoids nuclear magnetic resonance spectroscopy Original Paper pests Pseudococcidae Sex Attractants - chemistry Sex Attractants - isolation & purification Sex Attractants - pharmacology sex pheromones sexual dimorphism trapping |
title | new class of mealybug pheromones: a hemiterpene ester in the sex pheromone of Crisicoccus matsumotoi |
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