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Novel Floral Scent Compounds from Night-Blooming Araceae Pollinated by Cyclocephaline Scarabs (Melolonthidae, Cyclocephalini)
Nocturnal flowering plants often release strong scents to attract their pollinators. Among night active flower visitors are cyclocephaline scarab beetles, which have been demonstrated to respond to uncommon volatile organic compounds released in high amounts by their host plants. In Araceae, the mol...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6469606/ https://www.ncbi.nlm.nih.gov/pubmed/30229355 http://dx.doi.org/10.1007/s10886-018-1018-1 |
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author | Maia, Artur Campos D. Grimm, Christopher Schubert, Mario Etl, Florian Gonçalves, Eduardo Gomes Do Amaral Ferraz Navarro, Daniela Maria Schulz, Stefan Dötterl, Stefan |
author_facet | Maia, Artur Campos D. Grimm, Christopher Schubert, Mario Etl, Florian Gonçalves, Eduardo Gomes Do Amaral Ferraz Navarro, Daniela Maria Schulz, Stefan Dötterl, Stefan |
author_sort | Maia, Artur Campos D. |
collection | PubMed |
description | Nocturnal flowering plants often release strong scents to attract their pollinators. Among night active flower visitors are cyclocephaline scarab beetles, which have been demonstrated to respond to uncommon volatile organic compounds released in high amounts by their host plants. In Araceae, the molecular structure of several such compounds is yet to be unveiled. We investigated headspace floral scent samples of Philodendron squamiferum, Thaumatophyllum mello-baretoanum, and Xanthosoma hylaeae by a variety of approaches, leading to the identification of novel compounds. Dehydrojasmone, (Z)-4-methylene-5-(pent-2-en-1-yl)cyclopent-2-en-1-one (1), (Z)-3-methylene-2-(pent-2-en-1-yl)cyclopentyl acetate (isojasmyl acetate, 3), and (E)-4,8-dimethylnona-1,3,7-trien-5-yl acetate (4) had not been previously reported, while full analytical data of the recently described (Z)-3-methylene-2-(pent-2-en-1-yl)cyclopentan-1-ol (isojasmol, 2) are presented here. All these compounds are derived from more common precursors, (Z)-jasmone and (E)-4,8-dimethyl-1,3,7-nonatriene, likely through biosynthetic “post-processing”. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10886-018-1018-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6469606 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-64696062019-05-03 Novel Floral Scent Compounds from Night-Blooming Araceae Pollinated by Cyclocephaline Scarabs (Melolonthidae, Cyclocephalini) Maia, Artur Campos D. Grimm, Christopher Schubert, Mario Etl, Florian Gonçalves, Eduardo Gomes Do Amaral Ferraz Navarro, Daniela Maria Schulz, Stefan Dötterl, Stefan J Chem Ecol Article Nocturnal flowering plants often release strong scents to attract their pollinators. Among night active flower visitors are cyclocephaline scarab beetles, which have been demonstrated to respond to uncommon volatile organic compounds released in high amounts by their host plants. In Araceae, the molecular structure of several such compounds is yet to be unveiled. We investigated headspace floral scent samples of Philodendron squamiferum, Thaumatophyllum mello-baretoanum, and Xanthosoma hylaeae by a variety of approaches, leading to the identification of novel compounds. Dehydrojasmone, (Z)-4-methylene-5-(pent-2-en-1-yl)cyclopent-2-en-1-one (1), (Z)-3-methylene-2-(pent-2-en-1-yl)cyclopentyl acetate (isojasmyl acetate, 3), and (E)-4,8-dimethylnona-1,3,7-trien-5-yl acetate (4) had not been previously reported, while full analytical data of the recently described (Z)-3-methylene-2-(pent-2-en-1-yl)cyclopentan-1-ol (isojasmol, 2) are presented here. All these compounds are derived from more common precursors, (Z)-jasmone and (E)-4,8-dimethyl-1,3,7-nonatriene, likely through biosynthetic “post-processing”. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10886-018-1018-1) contains supplementary material, which is available to authorized users. Springer US 2018-09-19 2019 /pmc/articles/PMC6469606/ /pubmed/30229355 http://dx.doi.org/10.1007/s10886-018-1018-1 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Article Maia, Artur Campos D. Grimm, Christopher Schubert, Mario Etl, Florian Gonçalves, Eduardo Gomes Do Amaral Ferraz Navarro, Daniela Maria Schulz, Stefan Dötterl, Stefan Novel Floral Scent Compounds from Night-Blooming Araceae Pollinated by Cyclocephaline Scarabs (Melolonthidae, Cyclocephalini) |
title | Novel Floral Scent Compounds from Night-Blooming Araceae Pollinated by Cyclocephaline Scarabs (Melolonthidae, Cyclocephalini) |
title_full | Novel Floral Scent Compounds from Night-Blooming Araceae Pollinated by Cyclocephaline Scarabs (Melolonthidae, Cyclocephalini) |
title_fullStr | Novel Floral Scent Compounds from Night-Blooming Araceae Pollinated by Cyclocephaline Scarabs (Melolonthidae, Cyclocephalini) |
title_full_unstemmed | Novel Floral Scent Compounds from Night-Blooming Araceae Pollinated by Cyclocephaline Scarabs (Melolonthidae, Cyclocephalini) |
title_short | Novel Floral Scent Compounds from Night-Blooming Araceae Pollinated by Cyclocephaline Scarabs (Melolonthidae, Cyclocephalini) |
title_sort | novel floral scent compounds from night-blooming araceae pollinated by cyclocephaline scarabs (melolonthidae, cyclocephalini) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6469606/ https://www.ncbi.nlm.nih.gov/pubmed/30229355 http://dx.doi.org/10.1007/s10886-018-1018-1 |
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