Ryecyanatines A and B and ryecarbonitrilines A and B, substituted cyanatophenol, cyanatobenzo[1,3]dioxole, and benzo[1,3]dioxolecarbonitriles from rye (Secale cereale L.) root exudates: Novel metabolites with allelopathic activity on Orobanche seed germination and radicle growth
Ryecyanatines A (1) and B and ryecarbonitrilines A (3) and B, were isolated from rye (Secale cereale L.) root exudates. 1 inhibits the radicle growth of O. crenata, O. cumana and O. minor, while 3 specifically stimulates O. cumana seeds germination. [Display omitted] •A cyanatophenol, cyanato- and c...
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description | Ryecyanatines A (1) and B and ryecarbonitrilines A (3) and B, were isolated from rye (Secale cereale L.) root exudates. 1 inhibits the radicle growth of O. crenata, O. cumana and O. minor, while 3 specifically stimulates O. cumana seeds germination. [Display omitted]
•A cyanatophenol, cyanato- and carbonitrile-benzo[1,3]dioxoles, were isolated from rye.•A carbonitrile-benzo[1,3]dioxole stimulates O. cumana seed germination.•A cyanatophenol inhibits radicle growth of O. crenata, O. cumana and O. minor.•The two bioactive metabolites could be used as broomrapes natural eco-friendly herbicides.
Orobanche and Phelipanche species (the broomrapes) are root parasitic plants, some of which represent serious weed problems causing heavy yield losses on important crops. Current control relies on the use of certain agronomic practices, resistant crop varieties, and herbicides, albeit success has been marginal. Agronomic practices such as the use of allelopathic species in intercropping or cover crops, or the use of direct seedling over residues of allelopathic species incorporate the principle of allelopathy exerted by molecules exuded from roots or released by crop residues to control broomrapes. In addition, the isolation of natural substances from root exudates of plants with potential to inhibit broomrape development opens the door to the design of new herbicides based on natural and benign sources. Ryecyanatines A and B and ryecarbonitrilines A and B, the first new substituted cyanatophenol, substituted cyanatobenzo[1,3]dioxole, and the latter two new substituted benzo[1,3]dioxolecarbonitriles were isolated from rye (Secale cereale L.) root exudates. They were characterized as 4-cyanato-2-methoxyphenol, 2-cyanato-benzo[1,3]dioxole, 2-methoxybenzo[1,3]dioxole-5-carbonitrile and benzo[1,3]dioxole-2-carbonitrile by spectroscopic (essentially NMR and HRESI MS spectra) methods. These compounds were investigated for allelopathic activity on Orobanche germination and development. Ryecarbonitriline A induced germination of Orobanche cumana seeds, and this germination can be considered as suicidal because O. cumana does not parasite rye roots and cannot survive without host resources beyond germination stage. In addition, ryecyanatine A promotes a rapid cessation of O. cumana, Orobanche crenata and Orobanche minor radicle growth with the promotion of a layer of papillae at the radicle tip in O. cumana and O. crenata hampering the contact of the parasite to the host. Ryecar |
doi_str_mv | 10.1016/j.phytochem.2014.10.034 |
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•A cyanatophenol, cyanato- and carbonitrile-benzo[1,3]dioxoles, were isolated from rye.•A carbonitrile-benzo[1,3]dioxole stimulates O. cumana seed germination.•A cyanatophenol inhibits radicle growth of O. crenata, O. cumana and O. minor.•The two bioactive metabolites could be used as broomrapes natural eco-friendly herbicides.
Orobanche and Phelipanche species (the broomrapes) are root parasitic plants, some of which represent serious weed problems causing heavy yield losses on important crops. Current control relies on the use of certain agronomic practices, resistant crop varieties, and herbicides, albeit success has been marginal. Agronomic practices such as the use of allelopathic species in intercropping or cover crops, or the use of direct seedling over residues of allelopathic species incorporate the principle of allelopathy exerted by molecules exuded from roots or released by crop residues to control broomrapes. In addition, the isolation of natural substances from root exudates of plants with potential to inhibit broomrape development opens the door to the design of new herbicides based on natural and benign sources. Ryecyanatines A and B and ryecarbonitrilines A and B, the first new substituted cyanatophenol, substituted cyanatobenzo[1,3]dioxole, and the latter two new substituted benzo[1,3]dioxolecarbonitriles were isolated from rye (Secale cereale L.) root exudates. They were characterized as 4-cyanato-2-methoxyphenol, 2-cyanato-benzo[1,3]dioxole, 2-methoxybenzo[1,3]dioxole-5-carbonitrile and benzo[1,3]dioxole-2-carbonitrile by spectroscopic (essentially NMR and HRESI MS spectra) methods. These compounds were investigated for allelopathic activity on Orobanche germination and development. Ryecarbonitriline A induced germination of Orobanche cumana seeds, and this germination can be considered as suicidal because O. cumana does not parasite rye roots and cannot survive without host resources beyond germination stage. In addition, ryecyanatine A promotes a rapid cessation of O. cumana, Orobanche crenata and Orobanche minor radicle growth with the promotion of a layer of papillae at the radicle tip in O. cumana and O. crenata hampering the contact of the parasite to the host. Ryecarbonitriline B also displayed the same activity although being less active than ryecyanatine A and mainly restricted to O. cumana.</description><identifier>ISSN: 0031-9422</identifier><identifier>EISSN: 1873-3700</identifier><identifier>DOI: 10.1016/j.phytochem.2014.10.034</identifier><identifier>PMID: 25468713</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Allelopathy ; Benzodioxoles - chemistry ; Benzodioxoles - isolation & purification ; Environmental Sciences ; Germination - drug effects ; Herbicides - chemistry ; Herbicides - isolation & purification ; Life Sciences ; Molecular Structure ; Nitriles - chemistry ; Nitriles - isolation & purification ; Orobanche ; Orobanche - drug effects ; Parasitic weeds ; Phenols - chemistry ; Phenols - isolation & purification ; Pheromones - chemistry ; Plant Exudates - chemistry ; Plant Roots - chemistry ; Plant Weeds - drug effects ; Root exudates ; Ryecarbonitrilines A and B ; Ryecyanatines A and B ; Secale - chemistry ; Secale cereale ; Seed germination/inhibition ; Seeds - growth & development ; Vegetal Biology</subject><ispartof>Phytochemistry (Oxford), 2015-01, Vol.109, p.57-65</ispartof><rights>2014 Elsevier Ltd</rights><rights>Copyright © 2014 Elsevier Ltd. All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-ce1cc8410a91595611d8d5f9526cacba614177bf9ccb9c771af53894b5acee103</citedby><cites>FETCH-LOGICAL-c405t-ce1cc8410a91595611d8d5f9526cacba614177bf9ccb9c771af53894b5acee103</cites><orcidid>0000-0002-1551-4237 ; 0000-0001-9110-1656</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.phytochem.2014.10.034$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,4024,27923,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25468713$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.inrae.fr/hal-02633526$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Cimmino, Alessio</creatorcontrib><creatorcontrib>Fernández-Aparicio, Mónica</creatorcontrib><creatorcontrib>Avolio, Fabiana</creatorcontrib><creatorcontrib>Yoneyama, Koichi</creatorcontrib><creatorcontrib>Rubiales, Diego</creatorcontrib><creatorcontrib>Evidente, Antonio</creatorcontrib><title>Ryecyanatines A and B and ryecarbonitrilines A and B, substituted cyanatophenol, cyanatobenzo[1,3]dioxole, and benzo[1,3]dioxolecarbonitriles from rye (Secale cereale L.) root exudates: Novel metabolites with allelopathic activity on Orobanche seed germination and radicle growth</title><title>Phytochemistry (Oxford)</title><addtitle>Phytochemistry</addtitle><description>Ryecyanatines A (1) and B and ryecarbonitrilines A (3) and B, were isolated from rye (Secale cereale L.) root exudates. 1 inhibits the radicle growth of O. crenata, O. cumana and O. minor, while 3 specifically stimulates O. cumana seeds germination. [Display omitted]
•A cyanatophenol, cyanato- and carbonitrile-benzo[1,3]dioxoles, were isolated from rye.•A carbonitrile-benzo[1,3]dioxole stimulates O. cumana seed germination.•A cyanatophenol inhibits radicle growth of O. crenata, O. cumana and O. minor.•The two bioactive metabolites could be used as broomrapes natural eco-friendly herbicides.
Orobanche and Phelipanche species (the broomrapes) are root parasitic plants, some of which represent serious weed problems causing heavy yield losses on important crops. Current control relies on the use of certain agronomic practices, resistant crop varieties, and herbicides, albeit success has been marginal. Agronomic practices such as the use of allelopathic species in intercropping or cover crops, or the use of direct seedling over residues of allelopathic species incorporate the principle of allelopathy exerted by molecules exuded from roots or released by crop residues to control broomrapes. In addition, the isolation of natural substances from root exudates of plants with potential to inhibit broomrape development opens the door to the design of new herbicides based on natural and benign sources. Ryecyanatines A and B and ryecarbonitrilines A and B, the first new substituted cyanatophenol, substituted cyanatobenzo[1,3]dioxole, and the latter two new substituted benzo[1,3]dioxolecarbonitriles were isolated from rye (Secale cereale L.) root exudates. They were characterized as 4-cyanato-2-methoxyphenol, 2-cyanato-benzo[1,3]dioxole, 2-methoxybenzo[1,3]dioxole-5-carbonitrile and benzo[1,3]dioxole-2-carbonitrile by spectroscopic (essentially NMR and HRESI MS spectra) methods. These compounds were investigated for allelopathic activity on Orobanche germination and development. Ryecarbonitriline A induced germination of Orobanche cumana seeds, and this germination can be considered as suicidal because O. cumana does not parasite rye roots and cannot survive without host resources beyond germination stage. In addition, ryecyanatine A promotes a rapid cessation of O. cumana, Orobanche crenata and Orobanche minor radicle growth with the promotion of a layer of papillae at the radicle tip in O. cumana and O. crenata hampering the contact of the parasite to the host. Ryecarbonitriline B also displayed the same activity although being less active than ryecyanatine A and mainly restricted to O. cumana.</description><subject>Allelopathy</subject><subject>Benzodioxoles - chemistry</subject><subject>Benzodioxoles - isolation & purification</subject><subject>Environmental Sciences</subject><subject>Germination - drug effects</subject><subject>Herbicides - chemistry</subject><subject>Herbicides - isolation & purification</subject><subject>Life Sciences</subject><subject>Molecular Structure</subject><subject>Nitriles - chemistry</subject><subject>Nitriles - isolation & purification</subject><subject>Orobanche</subject><subject>Orobanche - drug effects</subject><subject>Parasitic weeds</subject><subject>Phenols - chemistry</subject><subject>Phenols - isolation & purification</subject><subject>Pheromones - chemistry</subject><subject>Plant Exudates - chemistry</subject><subject>Plant Roots - chemistry</subject><subject>Plant Weeds - drug effects</subject><subject>Root exudates</subject><subject>Ryecarbonitrilines A and B</subject><subject>Ryecyanatines A and B</subject><subject>Secale - chemistry</subject><subject>Secale cereale</subject><subject>Seed germination/inhibition</subject><subject>Seeds - growth & development</subject><subject>Vegetal Biology</subject><issn>0031-9422</issn><issn>1873-3700</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUk1v1DAQDQhEl8KZG_jYSruLHeeT21IBRVpRiY8TQpYzmTReOfFiO9uGX4-z264qceDikd97M89jvSh6w-iSUZa93Sy37egNtNgtY8qSgC4pTx5HM1bkfMFzSp9EM0o5W5RJHJ9Ez53bUErTNMueRSdxmmRFzvjs0auvI8Ioe-lVj46siOxr8n5_2sBIW5leeav0Q3pO3FA5r_zgsSaHdrNtsTd6fn-tsP9jfrI5_1Urc2s0zve9_8APLIJBY003GZOzb4HRSAAtTnW9PCfWGE_wdqilR_eOfDE71KRDLyujVYDIjfItkVqjNlvpWwVEglc75UdienJlTSX78GXEYXj2NdpOTXsHar-urBUEp2trbnz7InraSO3w5V09jX58_PD94nKxvvr0-WK1XkBCU78AZABFwqgsWVqmGWN1UadNmcYZSKhkxhKW51VTAlQl5DmTTcqLMqlSCYiM8tPo_DC3lVpsreqkHYWRSlyu1mLCaJxxHsbtWNCeHbRba34P6LzolAPUWvZoBidYxpO4iLOYB2l-kII1zllsjrMZFVOCxEYcEySmBE1ESFDofH1nMlQd1se--8gEweogwPAtO4VWOFDYA9bKInhRG_Vfk797wOHF</recordid><startdate>201501</startdate><enddate>201501</enddate><creator>Cimmino, Alessio</creator><creator>Fernández-Aparicio, Mónica</creator><creator>Avolio, Fabiana</creator><creator>Yoneyama, Koichi</creator><creator>Rubiales, Diego</creator><creator>Evidente, Antonio</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>1XC</scope><orcidid>https://orcid.org/0000-0002-1551-4237</orcidid><orcidid>https://orcid.org/0000-0001-9110-1656</orcidid></search><sort><creationdate>201501</creationdate><title>Ryecyanatines A and B and ryecarbonitrilines A and B, substituted cyanatophenol, cyanatobenzo[1,3]dioxole, and benzo[1,3]dioxolecarbonitriles from rye (Secale cereale L.) root exudates: Novel metabolites with allelopathic activity on Orobanche seed germination and radicle growth</title><author>Cimmino, Alessio ; Fernández-Aparicio, Mónica ; Avolio, Fabiana ; Yoneyama, Koichi ; Rubiales, Diego ; Evidente, Antonio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c405t-ce1cc8410a91595611d8d5f9526cacba614177bf9ccb9c771af53894b5acee103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Allelopathy</topic><topic>Benzodioxoles - chemistry</topic><topic>Benzodioxoles - isolation & purification</topic><topic>Environmental Sciences</topic><topic>Germination - drug effects</topic><topic>Herbicides - chemistry</topic><topic>Herbicides - isolation & purification</topic><topic>Life Sciences</topic><topic>Molecular Structure</topic><topic>Nitriles - chemistry</topic><topic>Nitriles - isolation & purification</topic><topic>Orobanche</topic><topic>Orobanche - drug effects</topic><topic>Parasitic weeds</topic><topic>Phenols - chemistry</topic><topic>Phenols - isolation & purification</topic><topic>Pheromones - chemistry</topic><topic>Plant Exudates - chemistry</topic><topic>Plant Roots - chemistry</topic><topic>Plant Weeds - drug effects</topic><topic>Root exudates</topic><topic>Ryecarbonitrilines A and B</topic><topic>Ryecyanatines A and B</topic><topic>Secale - chemistry</topic><topic>Secale cereale</topic><topic>Seed germination/inhibition</topic><topic>Seeds - growth & development</topic><topic>Vegetal Biology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cimmino, Alessio</creatorcontrib><creatorcontrib>Fernández-Aparicio, Mónica</creatorcontrib><creatorcontrib>Avolio, Fabiana</creatorcontrib><creatorcontrib>Yoneyama, Koichi</creatorcontrib><creatorcontrib>Rubiales, Diego</creatorcontrib><creatorcontrib>Evidente, Antonio</creatorcontrib><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><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Phytochemistry (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cimmino, Alessio</au><au>Fernández-Aparicio, Mónica</au><au>Avolio, Fabiana</au><au>Yoneyama, Koichi</au><au>Rubiales, Diego</au><au>Evidente, Antonio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ryecyanatines A and B and ryecarbonitrilines A and B, substituted cyanatophenol, cyanatobenzo[1,3]dioxole, and benzo[1,3]dioxolecarbonitriles from rye (Secale cereale L.) root exudates: Novel metabolites with allelopathic activity on Orobanche seed germination and radicle growth</atitle><jtitle>Phytochemistry (Oxford)</jtitle><addtitle>Phytochemistry</addtitle><date>2015-01</date><risdate>2015</risdate><volume>109</volume><spage>57</spage><epage>65</epage><pages>57-65</pages><issn>0031-9422</issn><eissn>1873-3700</eissn><abstract>Ryecyanatines A (1) and B and ryecarbonitrilines A (3) and B, were isolated from rye (Secale cereale L.) root exudates. 1 inhibits the radicle growth of O. crenata, O. cumana and O. minor, while 3 specifically stimulates O. cumana seeds germination. [Display omitted]
•A cyanatophenol, cyanato- and carbonitrile-benzo[1,3]dioxoles, were isolated from rye.•A carbonitrile-benzo[1,3]dioxole stimulates O. cumana seed germination.•A cyanatophenol inhibits radicle growth of O. crenata, O. cumana and O. minor.•The two bioactive metabolites could be used as broomrapes natural eco-friendly herbicides.
Orobanche and Phelipanche species (the broomrapes) are root parasitic plants, some of which represent serious weed problems causing heavy yield losses on important crops. Current control relies on the use of certain agronomic practices, resistant crop varieties, and herbicides, albeit success has been marginal. Agronomic practices such as the use of allelopathic species in intercropping or cover crops, or the use of direct seedling over residues of allelopathic species incorporate the principle of allelopathy exerted by molecules exuded from roots or released by crop residues to control broomrapes. In addition, the isolation of natural substances from root exudates of plants with potential to inhibit broomrape development opens the door to the design of new herbicides based on natural and benign sources. Ryecyanatines A and B and ryecarbonitrilines A and B, the first new substituted cyanatophenol, substituted cyanatobenzo[1,3]dioxole, and the latter two new substituted benzo[1,3]dioxolecarbonitriles were isolated from rye (Secale cereale L.) root exudates. They were characterized as 4-cyanato-2-methoxyphenol, 2-cyanato-benzo[1,3]dioxole, 2-methoxybenzo[1,3]dioxole-5-carbonitrile and benzo[1,3]dioxole-2-carbonitrile by spectroscopic (essentially NMR and HRESI MS spectra) methods. These compounds were investigated for allelopathic activity on Orobanche germination and development. Ryecarbonitriline A induced germination of Orobanche cumana seeds, and this germination can be considered as suicidal because O. cumana does not parasite rye roots and cannot survive without host resources beyond germination stage. In addition, ryecyanatine A promotes a rapid cessation of O. cumana, Orobanche crenata and Orobanche minor radicle growth with the promotion of a layer of papillae at the radicle tip in O. cumana and O. crenata hampering the contact of the parasite to the host. Ryecarbonitriline B also displayed the same activity although being less active than ryecyanatine A and mainly restricted to O. cumana.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>25468713</pmid><doi>10.1016/j.phytochem.2014.10.034</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-1551-4237</orcidid><orcidid>https://orcid.org/0000-0001-9110-1656</orcidid></addata></record> |
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ispartof | Phytochemistry (Oxford), 2015-01, Vol.109, p.57-65 |
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language | eng |
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source | MEDLINE; Elsevier ScienceDirect Journals Complete |
subjects | Allelopathy Benzodioxoles - chemistry Benzodioxoles - isolation & purification Environmental Sciences Germination - drug effects Herbicides - chemistry Herbicides - isolation & purification Life Sciences Molecular Structure Nitriles - chemistry Nitriles - isolation & purification Orobanche Orobanche - drug effects Parasitic weeds Phenols - chemistry Phenols - isolation & purification Pheromones - chemistry Plant Exudates - chemistry Plant Roots - chemistry Plant Weeds - drug effects Root exudates Ryecarbonitrilines A and B Ryecyanatines A and B Secale - chemistry Secale cereale Seed germination/inhibition Seeds - growth & development Vegetal Biology |
title | Ryecyanatines A and B and ryecarbonitrilines A and B, substituted cyanatophenol, cyanatobenzo[1,3]dioxole, and benzo[1,3]dioxolecarbonitriles from rye (Secale cereale L.) root exudates: Novel metabolites with allelopathic activity on Orobanche seed germination and radicle growth |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T23%3A56%3A47IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_hal_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Ryecyanatines%20A%20and%20B%20and%20ryecarbonitrilines%20A%20and%20B,%20substituted%20cyanatophenol,%20cyanatobenzo%5B1,3%5Ddioxole,%20and%20benzo%5B1,3%5Ddioxolecarbonitriles%20from%20rye%20(Secale%20cereale%20L.)%20root%20exudates:%20Novel%20metabolites%20with%20allelopathic%20activity%20on%20Orobanche%20seed%20germination%20and%20radicle%20growth&rft.jtitle=Phytochemistry%20(Oxford)&rft.au=Cimmino,%20Alessio&rft.date=2015-01&rft.volume=109&rft.spage=57&rft.epage=65&rft.pages=57-65&rft.issn=0031-9422&rft.eissn=1873-3700&rft_id=info:doi/10.1016/j.phytochem.2014.10.034&rft_dat=%3Cproquest_hal_p%3E1634282623%3C/proquest_hal_p%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1634282623&rft_id=info:pmid/25468713&rft_els_id=S0031942214004385&rfr_iscdi=true |