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. (January 2015)
- Record Type:
- Journal Article
- 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. (January 2015)
- Main 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
- Authors:
- Cimmino, Alessio
Fernández-Aparicio, Mónica
Avolio, Fabiana
Yoneyama, Koichi
Rubiales, Diego
Evidente, Antonio - Abstract:
- Graphical 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, while3 specifically stimulates O. cumana seeds germination. Highlights: 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. Abstract: 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, theGraphical 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, while3 specifically stimulates O. cumana seeds germination. Highlights: 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. Abstract: 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 . … (more)
- Is Part Of:
- Phytochemistry. Volume 109(2015:J )
- Journal:
- Phytochemistry
- Issue:
- Volume 109(2015:J )
- Issue Display:
- Volume 109 (2015)
- Year:
- 2015
- Volume:
- 109
- Issue Sort Value:
- 2015-0109-0000-0000
- Page Start:
- 57
- Page End:
- 65
- Publication Date:
- 2015-01
- Subjects:
- Parasitic weeds -- Orobanche -- Seed germination/inhibition -- Secale cereale -- Root exudates -- Ryecyanatines A and B -- Ryecarbonitrilines A and B
Botanical chemistry -- Periodicals
Biochemistry -- Periodicals
Botany -- Periodicals
Chimie végétale -- Périodiques
572.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00319422 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.phytochem.2014.10.034 ↗
- Languages:
- English
- ISSNs:
- 0031-9422
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6489.800000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 6016.xml