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dc.contributor.author
Travaini, Maria L  
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Sosa, Gustavo M.  
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Ceccarelli, Eduardo Augusto  
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Walter, Helmut  
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Cantrell, Charles L.  
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Carrillo, Nestor Jose  
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Dayan, Franck E.  
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Meepagala, Kumudini M.  
dc.contributor.author
Duke, Stephen O.  
dc.date.available
2018-07-23T17:44:34Z  
dc.date.issued
2016-12  
dc.identifier.citation
Travaini, Maria L; Sosa, Gustavo M.; Ceccarelli, Eduardo Augusto; Walter, Helmut; Cantrell, Charles L.; et al.; Khellin and Visnagin, Furanochromones from Ammi visnaga (L.) Lam., as Potential Bioherbicides; American Chemical Society; Journal of Agricultural and Food Chemistry; 64; 50; 12-2016; 9475-9487  
dc.identifier.issn
0021-8561  
dc.identifier.uri
http://hdl.handle.net/11336/52842  
dc.description.abstract
Plants constitute a source of novel phytotoxic compounds to be explored in searching for effective and environmentally safe herbicides. From a previous screening of plant extracts for their phytotoxicity, a dichloromethane extract of Ammi visnaga (L.) Lam. was selected for further study. Phytotoxicity-guided fractionation of this extract yielded two furanochromones, khellin and visnagin, for which herbicidal activity had not been described before. Khellin and visnagin were phytotoxic to model species lettuce (Lactuca sativa) and duckweed (Lemna paucicostata), with IC50 values ranging from 110 to 175 μM. These compounds also inhibited the growth and germination of a diverse group of weeds at 0.5 and 1 mM. These weeds included five grasses [ryegrass (Lolium multiflorum), barnyardgrass (Echinocloa crus-galli), crabgrass (Digitaria sanguinalis), foxtail (Setaria italica), and millet (Panicum sp.)] and two broadleaf species [morningglory (Ipomea sp.) and velvetleaf (Abutilon theophrasti)]. During greenhouse studies visnagin was the most active and showed significant contact postemergence herbicidal activity on velvetleaf and crabgrass at 2 kg active ingredient (ai) ha-1. Moreover, its effect at 4 kg ai ha-1 was comparable to the bioherbicide pelargonic acid at the same rate. The mode of action of khellin and visnagin was not a light-dependent process. Both compounds caused membrane destabilization, photosynthetic efficiency reduction, inhibition of cell division, and cell death. These results support the potential of visnagin and, possibly, khellin as bioherbicides or lead molecules for the development of new herbicides.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
American Chemical Society  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Ammi Visnaga  
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Bioherbicide  
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Furanochromone  
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Herbicide  
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Khellin  
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Phytotoxin  
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Visnagin  
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Otras Biotecnología Agropecuaria  
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Biotecnología Agropecuaria  
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CIENCIAS AGRÍCOLAS  
dc.title
Khellin and Visnagin, Furanochromones from Ammi visnaga (L.) Lam., as Potential Bioherbicides  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2018-07-23T12:55:00Z  
dc.journal.volume
64  
dc.journal.number
50  
dc.journal.pagination
9475-9487  
dc.journal.pais
Estados Unidos  
dc.journal.ciudad
Washington  
dc.description.fil
Fil: Travaini, Maria L. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Biología Molecular y Celular de Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Biología Molecular y Celular de Rosario; Argentina. Investigaciones Biológicas en Agroquímicos Rosario S.A.; Argentina  
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Fil: Sosa, Gustavo M.. Investigaciones Biológicas en Agroquímicos Rosario S.A.; Argentina  
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Fil: Ceccarelli, Eduardo Augusto. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Biología Molecular y Celular de Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Biología Molecular y Celular de Rosario; Argentina  
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Fil: Walter, Helmut. AgroField Consulting; Alemania  
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Fil: Cantrell, Charles L.. Natural Products Utilization Research Unit; Estados Unidos  
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Fil: Carrillo, Nestor Jose. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Biología Molecular y Celular de Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Biología Molecular y Celular de Rosario; Argentina  
dc.description.fil
Fil: Dayan, Franck E.. Natural Products Utilization Research Unit; Estados Unidos  
dc.description.fil
Fil: Meepagala, Kumudini M.. Natural Products Utilization Research Unit; Estados Unidos  
dc.description.fil
Fil: Duke, Stephen O.. Natural Products Utilization Research Unit; Estados Unidos  
dc.journal.title
Journal of Agricultural and Food Chemistry  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/https://dx.doi.org/10.1021/acs.jafc.6b02462  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/acs.jafc.6b02462