In vitro removal of ochratoxin A by two strains of Saccharomyces cerevisiae and their performances under fermentative and stressing conditions
Article first published online: 15 OCT 2013
© 2013 The Society for Applied Microbiology
Journal of Applied Microbiology
Volume 116, Issue 1, pages 60–70, January 2014
How to Cite
Petruzzi, L., Bevilacqua, A., Baiano, A., Beneduce, L., Corbo, M.R. and Sinigaglia, M. (2014), In vitro removal of ochratoxin A by two strains of Saccharomyces cerevisiae and their performances under fermentative and stressing conditions. Journal of Applied Microbiology, 116: 60–70. doi: 10.1111/jam.12350
- Issue published online: 16 DEC 2013
- Article first published online: 15 OCT 2013
- Accepted manuscript online: 25 SEP 2013 02:16AM EST
- Manuscript Accepted: 13 SEP 2013
- Manuscript Revised: 28 AUG 2013
- Manuscript Received: 21 MAY 2013
- DAP addition;
- ochratoxin A;
- Saccharomyces cerevisiae;
The aim of this research was to study the effect of time, temperature, sugar content and addition of diammonium phosphate (DAP) on ochratoxin A (OTA) removal by two strains of Saccharomyces cerevisiae using a completely randomized design.
Methods and Results
The strains were grown in a medium containing OTA (2 μg l−1), two sugar levels (200 and 250 g l−1), with or without DAP (300 mg l−1), and incubated at 25–30°C. The yeasts were able to decrease the toxin amount by c. 70%, with the highest removing effect observed after 3 days at 30°C in the presence of 250 g l−1 of sugars and with DAP; after 10 days, the toxin was partially released into the medium. The strains produced high ethanol and glycerol contents, showed high tolerance to single/combined stress conditions and possessed β-d-glucosidase, pectinase and xylanase activities.
Ochratoxin A removal was affected by time, temperature, sugar and addition of DAP. Moreover, the phenomenon was reversible.
Significance and Impact of the Study
Ochratoxin A removal could be an interesting trait for the selection of promising strains; however, the strains removing efficiently the toxin could release it back; thus, the selection of the starter should take into account both the removal and the binding ability of OTA.