Sex pheromone in the moth Heliothis virescens is produced as a mixture of two pools: de novo and via precursor storage in glycerolipids

Most species of moths use a female-produced volatile sex pheromone, typically produced via de novo fatty acid synthesis in a specialized gland, for communication among mates. While de novo biosynthesis of pheromone (DNP) is rapid, suggesting transient precursor acids, substantial amounts of pheromon...

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Veröffentlicht in:Insect biochemistry and molecular biology 2017-08, Vol.87, p.26-34
Hauptverfasser: Foster, Stephen P., Anderson, Karin G., Casas, Jérôme
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Casas, Jérôme
description Most species of moths use a female-produced volatile sex pheromone, typically produced via de novo fatty acid synthesis in a specialized gland, for communication among mates. While de novo biosynthesis of pheromone (DNP) is rapid, suggesting transient precursor acids, substantial amounts of pheromone precursor (and other) acids are stored, predominantly in triacylglycerols in the pheromone gland. Whether these stored acids are converted to pheromone later or not has been the subject of some debate. Using a tracer/tracee approach, in which we fed female Heliothis virescens U-13C-glucose, we were able to distinguish two pools of pheromone, in which precursors were temporally separated (after and before feeding on labeled glucose): DNP synthesized from a mixed tracer/tracee acetyl CoA pool after feeding, and pheromone made from precursor acids primarily synthesized before feeding, which we call recycled precursor fat pheromone (RPP). DNP titer varied from high (during scotophase) to low (photophase) and with presence/absence of pheromone biosynthesis activating neuropeptide (PBAN), in accord with native pheromone titer previously observed. By contrast, RPP was constant throughout the photoperiod and did not change with PBAN presence/absence. The amount of RPP (6.3–10.3 ng/female) was typically much lower than that of DNP, especially during the scotophase (peak DNP, 105 ng/female). We propose an integral role for stored fats in pheromone biosynthesis, in which they are hydrolyzed and re-esterified throughout the photoperiod, with a small proportion of liberated precursor acyl CoAs being converted to pheromone. During the sexually active period, release of PBAN results in increased flux of glucose (from trehalose) and hydrolyzed acids entering the mitochondria, producing acetyl CoA precursor for de novo fat and pheromone biosynthesis. [Display omitted] •Tracer-tracee method demonstrates two routes for pheromone biosynthesis in moth Heliothis virescens.•De novo-produced pheromone (DNP) varies during the photophase, while recycled precursor fat pheromone (RPP) does not.•DNP is PBAN dependent, while RPP production is not.•RPP production is essential for gland function, but contributes little to pheromonal communication.
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While de novo biosynthesis of pheromone (DNP) is rapid, suggesting transient precursor acids, substantial amounts of pheromone precursor (and other) acids are stored, predominantly in triacylglycerols in the pheromone gland. Whether these stored acids are converted to pheromone later or not has been the subject of some debate. Using a tracer/tracee approach, in which we fed female Heliothis virescens U-13C-glucose, we were able to distinguish two pools of pheromone, in which precursors were temporally separated (after and before feeding on labeled glucose): DNP synthesized from a mixed tracer/tracee acetyl CoA pool after feeding, and pheromone made from precursor acids primarily synthesized before feeding, which we call recycled precursor fat pheromone (RPP). DNP titer varied from high (during scotophase) to low (photophase) and with presence/absence of pheromone biosynthesis activating neuropeptide (PBAN), in accord with native pheromone titer previously observed. By contrast, RPP was constant throughout the photoperiod and did not change with PBAN presence/absence. The amount of RPP (6.3–10.3 ng/female) was typically much lower than that of DNP, especially during the scotophase (peak DNP, 105 ng/female). We propose an integral role for stored fats in pheromone biosynthesis, in which they are hydrolyzed and re-esterified throughout the photoperiod, with a small proportion of liberated precursor acyl CoAs being converted to pheromone. During the sexually active period, release of PBAN results in increased flux of glucose (from trehalose) and hydrolyzed acids entering the mitochondria, producing acetyl CoA precursor for de novo fat and pheromone biosynthesis. 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By contrast, RPP was constant throughout the photoperiod and did not change with PBAN presence/absence. The amount of RPP (6.3–10.3 ng/female) was typically much lower than that of DNP, especially during the scotophase (peak DNP, 105 ng/female). We propose an integral role for stored fats in pheromone biosynthesis, in which they are hydrolyzed and re-esterified throughout the photoperiod, with a small proportion of liberated precursor acyl CoAs being converted to pheromone. During the sexually active period, release of PBAN results in increased flux of glucose (from trehalose) and hydrolyzed acids entering the mitochondria, producing acetyl CoA precursor for de novo fat and pheromone biosynthesis. [Display omitted] •Tracer-tracee method demonstrates two routes for pheromone biosynthesis in moth Heliothis virescens.•De novo-produced pheromone (DNP) varies during the photophase, while recycled precursor fat pheromone (RPP) does not.•DNP is PBAN dependent, while RPP production is not.•RPP production is essential for gland function, but contributes little to pheromonal communication.</description><subject>acetyl coenzyme A</subject><subject>Age Factors</subject><subject>Animal biology</subject><subject>Animals</subject><subject>Biochemistry</subject><subject>Biochemistry, Molecular Biology</subject><subject>biosynthesis</subject><subject>Chemical communication</subject><subject>fatty acids</subject><subject>Female</subject><subject>females</subject><subject>glucose</subject><subject>Glucose - metabolism</subject><subject>Heliothis virescens</subject><subject>hydrolysis</subject><subject>Invertebrate Zoology</subject><subject>Lepidoptera</subject><subject>Life Sciences</subject><subject>Mass isotopomer distribution analysis</subject><subject>mitochondria</subject><subject>moths</subject><subject>Moths - metabolism</subject><subject>Neuropeptides - metabolism</subject><subject>Noctuidae</subject><subject>pheromone biosynthesis activating neuropeptide</subject><subject>Photoperiod</subject><subject>photophase</subject><subject>scotophase</subject><subject>Sex Attractants - biosynthesis</subject><subject>sex pheromones</subject><subject>Stable isotope</subject><subject>Tracer/tracee</subject><subject>trehalose</subject><subject>Trehalose - metabolism</subject><subject>triacylglycerols</subject><subject>Triglycerides - metabolism</subject><issn>0965-1748</issn><issn>1879-0240</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc9u1DAQhy0EokvhBTggH-GQMM46_oO4VBWwSCv1UDhbjjPpepXEwU6W9gl4bbxs6bE9jWx9vxl7PkLeMigZMPFxX_pmaMoKmCxBlAD8GVkxJXUBFYfnZAVa1AWTXJ2RVyntIRO8li_JWaUE00LoFflzjbd02mEMQxiR-pHOO6RDmHd0g73P1Sd68BGTwzHRfJhiaBeHLbWJWjr423mJSENH59-BTiH06RNtkY7hEKgd2xy2OYNuiSlEmuYQ7c2_QTf9nctzez_5Nr0mLzrbJ3xzX8_Jz69fflxuiu3Vt--XF9vCcSHnooHaMa6rBpi1XGklGg6ASmgUVee064R1UjRCtZy3zgmUjVpXWnLWqc7J9Tn5cOq7s72Zoh9svDPBerO52JrjHVS1XDMNB5bZ9yc2f_nXgmk2g89r6Hs7YliSqfJC65oLqJ9EmWYg9ZopldHqhLoYUorYPTyDgTl6NXtz9GqOXg0Ik63l0Lv7_kszYPsQ-S8yA59PAOblHTxGk5zHMXvK7txs2uAf6_8Xy4K0gQ</recordid><startdate>20170801</startdate><enddate>20170801</enddate><creator>Foster, Stephen P.</creator><creator>Anderson, Karin G.</creator><creator>Casas, Jérôme</creator><general>Elsevier Ltd</general><general>Elsevier</general><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><scope>7S9</scope><scope>L.6</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0003-1666-295X</orcidid></search><sort><creationdate>20170801</creationdate><title>Sex pheromone in the moth Heliothis virescens is produced as a mixture of two pools: de novo and via precursor storage in glycerolipids</title><author>Foster, Stephen P. ; 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While de novo biosynthesis of pheromone (DNP) is rapid, suggesting transient precursor acids, substantial amounts of pheromone precursor (and other) acids are stored, predominantly in triacylglycerols in the pheromone gland. Whether these stored acids are converted to pheromone later or not has been the subject of some debate. Using a tracer/tracee approach, in which we fed female Heliothis virescens U-13C-glucose, we were able to distinguish two pools of pheromone, in which precursors were temporally separated (after and before feeding on labeled glucose): DNP synthesized from a mixed tracer/tracee acetyl CoA pool after feeding, and pheromone made from precursor acids primarily synthesized before feeding, which we call recycled precursor fat pheromone (RPP). DNP titer varied from high (during scotophase) to low (photophase) and with presence/absence of pheromone biosynthesis activating neuropeptide (PBAN), in accord with native pheromone titer previously observed. By contrast, RPP was constant throughout the photoperiod and did not change with PBAN presence/absence. The amount of RPP (6.3–10.3 ng/female) was typically much lower than that of DNP, especially during the scotophase (peak DNP, 105 ng/female). We propose an integral role for stored fats in pheromone biosynthesis, in which they are hydrolyzed and re-esterified throughout the photoperiod, with a small proportion of liberated precursor acyl CoAs being converted to pheromone. During the sexually active period, release of PBAN results in increased flux of glucose (from trehalose) and hydrolyzed acids entering the mitochondria, producing acetyl CoA precursor for de novo fat and pheromone biosynthesis. [Display omitted] •Tracer-tracee method demonstrates two routes for pheromone biosynthesis in moth Heliothis virescens.•De novo-produced pheromone (DNP) varies during the photophase, while recycled precursor fat pheromone (RPP) does not.•DNP is PBAN dependent, while RPP production is not.•RPP production is essential for gland function, but contributes little to pheromonal communication.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>28619669</pmid><doi>10.1016/j.ibmb.2017.06.004</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-1666-295X</orcidid><oa>free_for_read</oa></addata></record>
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subjects acetyl coenzyme A
Age Factors
Animal biology
Animals
Biochemistry
Biochemistry, Molecular Biology
biosynthesis
Chemical communication
fatty acids
Female
females
glucose
Glucose - metabolism
Heliothis virescens
hydrolysis
Invertebrate Zoology
Lepidoptera
Life Sciences
Mass isotopomer distribution analysis
mitochondria
moths
Moths - metabolism
Neuropeptides - metabolism
Noctuidae
pheromone biosynthesis activating neuropeptide
Photoperiod
photophase
scotophase
Sex Attractants - biosynthesis
sex pheromones
Stable isotope
Tracer/tracee
trehalose
Trehalose - metabolism
triacylglycerols
Triglycerides - metabolism
title Sex pheromone in the moth Heliothis virescens is produced as a mixture of two pools: de novo and via precursor storage in glycerolipids
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