Statistical optimization of culture conditions for biomass production of probiotic gut-borne Saccharomyces cerevisiae strain able to reduce fumonisin B1

Aim: To evaluate the ability of probiotic Saccharomyces cerevisiae RC016 strain to reduce fumonisin B1 (FB1) in vitro and to optimize the culture conditions for the growth of the yeast employing surface response methodology. Methods and Results: Using Plackett-Burman screening designs (PBSD) and cen...

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Autor principal: Armando, M.R
Otros Autores: Galvagno, M.A, Dogi, C.A, Cerrutti, P., Dalcero, A.M, Cavaglieri, L.R
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2013
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Acceso en línea:Registro en Scopus
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024 7 |2 cas  |a fumonisin B1, 116355-83-0; molasses, 68476-78-8; Carbon, 7440-44-0; Culture Media; Fumonisins; Nitrogen, N762921K75; fumonisin B1, 116355-83-0 
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030 |a JAMIF 
100 1 |a Armando, M.R. 
245 1 0 |a Statistical optimization of culture conditions for biomass production of probiotic gut-borne Saccharomyces cerevisiae strain able to reduce fumonisin B1 
260 |c 2013 
270 1 0 |m Cavaglieri, L.R.; Departamento de Microbiología e Inmunología, Universidad Nacional de Río Cuarto, Ruta 36 km.601, 5800 Río Cuarto, Córdoba, Argentina; email: lcavaglieri@arnet.com.ar 
506 |2 openaire  |e Política editorial 
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504 |a Armando, M.R., Pizzolitto, R.P., Dogi, C.A., Cristofolini, A., Merkis, C., Poloni, V., Dalcero, A.M., Cavaglieri, L.R., Adsorption of ochratoxin A and zearalenone by potential probiotic Saccharomyces cerevisiae strains and its relation with cell wall thickness (2012) J Appl Microbiol, 113, pp. 256-264 
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504 |a Dal Bello, G.M., Monaco, C.I., Simon, M.R., Biological control of seedling blight of wheat caused by Fusarium graminearum with beneficial rhizosphere microorganisms (2002) World J Microbiol Biotechnol, 18, pp. 627-636 
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504 |a Diamond, H., Cooke, B.M., Preliminary studies on biological control of the Fusarium ear blight complex of wheat (2003) Crop Prot., 22, pp. 99-107 
504 |a Dogi, C.A., Armando, R., Ludueña, R., Moreno de LeBlanc, A., Rosa, C.A., Dalcero, A., Cavaglieri, L., Saccharomyces cerevisiae strains retain their viability and aflatoxin B1 binding ability under gastrointestinal conditions and improve ruminal fermentation (2011) Food Addit Contam Part A Chem Anal Control Expo Risk Assess, 28, pp. 1705-1711 
504 |a Doko, M.B., Rapior, S., Visconti, A., Schjoth, J.E., Incidence and Levels of Fumonisin Contamination in Maize Genotypes Grown in Europe and Africa (1995) J Agric Food Chem, 43, pp. 429-434 
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504 |a Khan, N.I., Schisler, D.A., Boehm, M.J., Slininger, P.J., Bothast, R.J., Selection and evaluation of microorganisms for biocontrol of Fusarium head blight of wheat incited by Gibberella zeae (2001) Plant Dis, 85, pp. 1253-1258 
504 |a Lamprecht, S.C., Marasas, W.F.O., Alberts, J.F., Cawood, M.E., Gelderblom, W.C.A., Shepherd, G.S., Thiel, P.G., Calitz, F.J., Phytotoxicity of fumonisins and TA-toxin to corn and tomato (1994) Phytopathology, 84, pp. 383-391 
504 |a Luz, W.C.D., Stockwell, C.A., Bergstrom, G.C., Biological control of Fusarium graminearum (2003) Fusarium Head Blight of Wheat and Barley, pp. 381-394. , ed. Leonard, K.J. and Bushnell, W.R. St Paul, MN: American Phytopathological Society, APS Press 
504 |a Montgomery, D.C., (2001) Design and Analysis of Experiments, , New York: Marcel Dekker 
504 |a Niderkorn, V., Boudra, H., Morgavi, D.P., Binding of Fusarium mycotoxins by fermentative bacteria in vitro (2006) J Appl Microbiol, 101, pp. 849-856 
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520 3 |a Aim: To evaluate the ability of probiotic Saccharomyces cerevisiae RC016 strain to reduce fumonisin B1 (FB1) in vitro and to optimize the culture conditions for the growth of the yeast employing surface response methodology. Methods and Results: Using Plackett-Burman screening designs (PBSD) and central composite designs (CCD), an optimized culture medium containing (g l-1) fermentable sugars provided by sugar cane molasses (CMs), yeast extract (YE) and (NH4)2HPO4 (DAP) was formulated. The S. cerevisiae RC016 strain showed the greatest binding at all assayed FB1 concentration. The CMs, YE, DAP concentrations and incubation time influenced significantly the biomass of S. cerevisiae RC016. Conclusion: A combination of CMs 17%; YE 4·61 g l-1 and incubation time 60 h was optimum for maximum biomass of S. cerevisiae RC016. Significance and Impact of the Study: The importance of this work lies in the search for live strains with both probiotic and fumonisin B1 decontamination properties that could be sustainably produced in a medium just containing cheap carbon, nitrogen and phosphorus sources and would be included in a novel product to animal feed. © 2013 The Society for Applied Microbiology.  |l eng 
593 |a Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Agencia Córdoba Ciencia (ACC), Ciudad autónoma de Buenos Aires, Argentina 
593 |a Departamento de Microbiología e Inmunología, Universidad Nacional de Río Cuarto, Río Cuarto, Argentina 
593 |a Consejo Nacional de Investigaciones Científicas y Tecnológicas (CONICET), Ciudad autónoma de Buenos Aires, Argentina 
593 |a Departamento de Ingeniería Química, Pabellón de Industrias, Universidad de Buenos Aires, Ciudad autónoma de Buenos Aires, Argentina 
593 |a Instituto de Investigaciones Biotecnológicas, CONICET, UNSAM, Buenos Aires, Argentina 
690 1 0 |a BIOMASS PRODUCTION 
690 1 0 |a CANE MOLASSES 
690 1 0 |a FUMONISIN B1 
690 1 0 |a SACCHAROMYCES CEREVISIAE 
690 1 0 |a STATISTICAL OPTIMIZATION 
690 1 0 |a FUMONISIN B1 
690 1 0 |a MOLASSES 
690 1 0 |a PROBIOTIC AGENT 
690 1 0 |a BIOASSAY 
690 1 0 |a BIOMASS 
690 1 0 |a CONCENTRATION (COMPOSITION) 
690 1 0 |a FERMENTATION 
690 1 0 |a GROWTH RATE 
690 1 0 |a OPTIMIZATION 
690 1 0 |a PROBIOTICS 
690 1 0 |a STATISTICAL ANALYSIS 
690 1 0 |a TOXIC ORGANISM 
690 1 0 |a YEAST 
690 1 0 |a ARTICLE 
690 1 0 |a BATCH FERMENTATION 
690 1 0 |a BINDING ASSAY 
690 1 0 |a BIOMASS PRODUCTION 
690 1 0 |a BIOREACTOR 
690 1 0 |a CHEMICAL STRUCTURE 
690 1 0 |a CULTURE MEDIUM 
690 1 0 |a FUNGAL STRAIN 
690 1 0 |a FUNGUS CULTURE 
690 1 0 |a FUNGUS GROWTH 
690 1 0 |a IN VITRO STUDY 
690 1 0 |a INCUBATION TIME 
690 1 0 |a NONHUMAN 
690 1 0 |a RESPONSE SURFACE METHOD 
690 1 0 |a SACCHAROMYCES CEREVISIAE 
690 1 0 |a SUGARCANE 
690 1 0 |a ANIMAL FEED 
690 1 0 |a BIOMASS 
690 1 0 |a BIOREACTORS 
690 1 0 |a CULTURE MEDIA 
690 1 0 |a FERMENTATION 
690 1 0 |a FUMONISINS 
690 1 0 |a INDUSTRIAL MICROBIOLOGY 
690 1 0 |a MODELS, STATISTICAL 
690 1 0 |a MOLASSES 
690 1 0 |a NITROGEN 
690 1 0 |a PROBIOTICS 
690 1 0 |a SACCHAROMYCES CEREVISIAE 
690 1 0 |a SACCHARUM 
690 1 0 |a ANIMALIA 
690 1 0 |a SACCHAROMYCES CEREVISIAE 
690 1 0 |a SACCHARUM 
650 1 7 |2 spines  |a CARBON 
700 1 |a Galvagno, M.A. 
700 1 |a Dogi, C.A. 
700 1 |a Cerrutti, P. 
700 1 |a Dalcero, A.M. 
700 1 |a Cavaglieri, L.R. 
773 0 |d 2013  |g v. 114  |h pp. 1338-1346  |k n. 5  |p J. Appl. Microbiol.  |x 13645072  |w (AR-BaUEN)CENRE-5421  |t Journal of Applied Microbiology 
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856 4 0 |u https://doi.org/10.1111/jam.12144  |y DOI 
856 4 0 |u https://hdl.handle.net/20.500.12110/paper_13645072_v114_n5_p1338_Armando  |y Handle 
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