Biodegradation of glyphosate by wild yeasts

Authors

  • M. Cristina Romero Cátedra de Micología Médica e Industrial “Dr. Pablo Negroni“, Fac. de Ciencias Veterinarias, Universidad Nacional de La Plata, Argentina
  • Enso H Reinoso Cátedra de Micología Médica e Industrial “Dr. Pablo Negroni“, Fac. de Ciencias Veterinarias, Universidad Nacional de La Plata, Argentina
  • A. Moreno Kiernan Facultad de Ciencias Agrarias y Forestales, Universidad Nacional de La Plata. Argentina
  • Susana Córdoba Cátedra de Micología Médica e Industrial “Dr. Pablo Negroni“, Fac. de Ciencias Veterinarias, Universidad Nacional de La Plata, Argentina

DOI:

https://doi.org/10.33885/sf.2004.3.924

Keywords:

Candida krusei, Yarrowia lipolytica, environmental technologies, glyphosate degradation, CN P sources

Abstract

Glifosate detoxification by wild yeasts were studied from colonies isolated of treated
and non treated soils with the herbicide. Seventy seven yeast colonies were obtained from
treated soils and 38 from non treated samples, being Candida kruseis and Yarrowia lipolytica the
dominant species in each group, respectively. Y. lipolytica showed a longer lag phase and
degradation began 6 days from incubation, while in C. kruseis after 3 days from incubation with
a higher total uptake of the herbicide (66 vs. 42.5%). Both species were cultivated in enriched
media with phosphate, gliphosate or aminomethylphosphonic acid (AMPA) in order to obtain
active strains cultivated on substrates with organophosphonates as C and P sources. Enriched
cultures increased the mycelial density of the yeasts, although the phosphate presence
inhibited the gliphosate breakdown. The presence of mycoflora adapted to degrade glyphosate
and its metabolites was confirmed, therefore wild yeasts could be significant in natural
detoxification processes, specially in the bioremediation of agricultural areas polluted with
organophosphonates.

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How to Cite

Romero, M. C., Reinoso, E. H., Moreno Kiernan, A., & Córdoba, S. (2016). Biodegradation of glyphosate by wild yeasts. Scientia Fungorum, 3(19), 45–50. https://doi.org/10.33885/sf.2004.3.924

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