Antifungal activity of metals-flavonoid complexes against fungi with agronomic interest

• Autores: Burgos, Soledad; Alarcón, Rosana; Cristobal, Hector Antonio; Celiz, Gustavo
• Año de publicación: 2020
• Idioma: inglés
• Tipo de recurso: documento de conferencia
• Materia: METAL FLAVONOID COMPLEX; ANTIFUNGAL ACTIVITY; PHYTOPATHOGENIC AGRONOMIC FUNGI
• Institución: Consejo Nacional de Investigaciones Científicas y Técnicas

Phytopathogenic fungi are organisms which cause disease in plants; they affect agricultural production generating large economic losses in diverse crops. The need to found new environmental friendly fungicides has led researchers to search for compounds that satisfise this concept. Naringin (NAR) and naringenin (NGE) are flavonoids obtained from wastes of the Citrus industry, with diverse biological properties. These flavonoids have the capability to form complexes with ion transition metals. Currently, the study of the antifungal properties of metal-flavonoid complexes is practically unexplored. In this work, the antifungal activity of some metal-flavonoid complexes was evaluated against three phytopathogenic fungi.This activity was quantitatively evaluated by contact assay using potato dextrose agar as culture medium. In Sclerotium rolfsii, solutions of Cu(II)-NGE (62 mmol/L), Cu(II)-NAR (32 mmol/L), Ni(II)-NAR (32 mmol/L) and Mn(II)-NAR (14 mmol/L) complexes were tested. In addition, flavonoids NGE (124 mmol/L) and NAR (64 mmol/L) were assayed alone. For Rhizoctonia solani and Sclerotinia sclerotiorum, Cu(II)-NAR (32 and 16 mmol/L), NAR (64 and 32 mmol/L) and CuSO4.5H2O (32 and 16 mmol/L) solutions were tested. To prepare this solutions N,N-dimethylformamide/water 10 % (v/v) have been used as solvent. This bioassay was realized using a fully randomized design with five replicates for each treatment.Our results shown that S. rolfsii was higly inhibited by Ni(II)-NAR complex (91 %), followed by Cu(II)-NGE (72 %), Mn(II)-NAR (36 %) and Cu(II)-NAR (3 %), whereas NGE alone caused only 24 % of inhibition and NAR did not present antifungal activity. Solutions of Fe(III)-NAR (40 mmol/L), Co(II)-NAR (24 mmol/L) and Cr(III)-NAR (6 mmol/L) were also tested, but they did not exhibit activity. S. sclerotiorum was not hibited by none of the compounds assayed. For R. solani, only the solution of Cu(II)SO4.5H2O at 32 mmol/L caused significant inhibition (16 %).In conclusion, this study is probably the first reported about the antifundal activity of this kind of compounds, and it demostrate that some of these coordination compounds have potential as new environmental friendly fungicides.
Fil: Burgos, Soledad. Universidad Nacional de Salta. Facultad de Ciencias Naturales; Argentina
Fil: Alarcón, Rosana. Universidad Nacional de Salta. Facultad de Ciencias Naturales; Argentina
Fil: Cristobal, Hector Antonio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Investigaciones para la Industria Química. Universidad Nacional de Salta. Facultad de Ingeniería. Instituto de Investigaciones para la Industria Química; Argentina. Universidad Nacional de Salta. Facultad de Ciencias Naturales; Argentina
Fil: Celiz, Gustavo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Investigaciones para la Industria Química. Universidad Nacional de Salta. Facultad de Ingeniería. Instituto de Investigaciones para la Industria Química; Argentina. Universidad Nacional de Salta. Facultad de Ciencias Exactas; Argentina
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