INVESTIGADORES
DOGI Cecilia Ana
artículos
Título:
Adsorption of ochratoxin A and zearalenone by Saccharomyces cerevisiae strains and its relation with cell wall thickness
Autor/es:
ARMANDO, ROMINA; PIZZOLITO, ROMINA; DOGI CECILIA; CRISTOFOLINI, ANDREA; MERKIS, CECILIA; DALCERO, ANA; CAVAGLIERI, LILIA
Revista:
JOURNAL OF APPLIED MICROBIOLOGY
Editorial:
WILEY-BLACKWELL PUBLISHING, INC
Referencias:
Lugar: Londres; Año: 2012 vol. 113 p. 256 - 264
ISSN:
1364-5072
Resumen:
Aims: to examine Saccharomyces cerevisae strains, with previously reported beneficial properties and aflatoxin B1 binding capacity, for their ability to reduce ochratoxin A (OTA) and zearalenone (ZEA) and to study the relation between cell wall thickness and detoxificant ability of yeast strains. Methods and Results: mycotoxin binding assay at different toxin concentrations and the effect of gastrointestinal conditions on mycotoxin binding were evaluated. Ultrastructural studies of yeast cells were performed by transmission electronic microscopy. All tested strains were capable to reduce OTA and ZEA. Saccharomyces cerevisiae RC012 and RC016 showed the highest OTA reduction percentage, whereas RC009 and RC012 strains showed the highest ZEA reduction percentages. Cell diameter/cell wall thickness relation showed a correlation between cell wall amount and mycotoxin reduction ability. After exposure to gastrointestinal conditions, a significant increase in the mycotoxin binding was observed. Conclusions: all tested Saccharomyces cerevisiae strains were able to reduce OTA and ZEA and a physical adsorption would be the main mechanism involved in ochratoxin A and ZEA reduction. Gastrointestinal conditions would enhance adsorption and not decrease the mycotoxin-adsorbent interactions. Significance and Impact of Study: live strains with mycotoxin binding ability and beneficial properties are potentially probiotics to be included in animal feed. Previous and present results, suggest that RC008 and RC016 strains are the most promising candidates for functional feed product development.