Effectiveness of UV-C light assisted by mild heat on Saccharomyces cerevisiae KE 162 inactivation in carrot-orange juice blend studied by flow cytometry and transmission electron microscopy

The aim of this study was to analyze the effectiveness of UV-C light (0–10.6 kJ/m2) assisted by mild heat treatment (50 °C) on the inactivation of Saccharomyces cerevisiae KE 162 in peptone water and fresh carrot-orange juice blend (pH: 3.8; 9.8°Brix; 707 NTU; absorption coefficient: 0.17 cm−1). Yea...

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Autor principal: García Carrillo, M.
Otros Autores: Ferrario, M., Guerrero, S.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: Academic Press 2018
Acceso en línea:Registro en Scopus
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030 |a FOMIE 
100 1 |a García Carrillo, M. 
245 1 0 |a Effectiveness of UV-C light assisted by mild heat on Saccharomyces cerevisiae KE 162 inactivation in carrot-orange juice blend studied by flow cytometry and transmission electron microscopy 
260 |b Academic Press  |c 2018 
270 1 0 |m Guerrero, S.; Departamento de Industrias, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad UniversitariaArgentina; email: sguerrero@di.fcen.uba.ar 
506 |2 openaire  |e Política editorial 
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520 3 |a The aim of this study was to analyze the effectiveness of UV-C light (0–10.6 kJ/m2) assisted by mild heat treatment (50 °C) on the inactivation of Saccharomyces cerevisiae KE 162 in peptone water and fresh carrot-orange juice blend (pH: 3.8; 9.8°Brix; 707 NTU; absorption coefficient: 0.17 cm−1). Yeast induced damage by single UV-C and mild heat (H) and the combined treatment UV-C/H, was investigated by flow cytometry (FC) and transmission electron microscopy (TEM). When studying induced damage by FC, cells were labeled with fluorescein diacetate (FDA) and propidium iodide (PI) to monitor membrane integrity and esterase activity. UV-C/H provoked up to 4.7 log-reductions of S. cerevisiae; whereas, only 2.6–3.3 log-reductions were achieved by single UV-C and H treatments. FC revealed a shift with treatment time from cells with esterase activity and intact membrane to cells with permeabilized membrane. This shift was more noticeable in peptone water and UV-C/H treated juice. In the UV-C treated juice, double stained cells were detected, suggesting the possibility of being sub-lethally damaged, with compromised membrane but still metabolically active. TEM images of treated cells revealed severe damage, encompassing coagulated inner content, disorganized lumen and cell debris. FC and TEM provided additional information regarding degree and type of damage, complementing information revealed by the traditional plate count technique. © 2018 Elsevier Ltd  |l eng 
536 |a Detalles de la financiación: Agencia Nacional de Promoción Científica y Tecnológica 
536 |a Detalles de la financiación: Universidad de Buenos Aires, 2013-X045 
536 |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas 
536 |a Detalles de la financiación: 310/2015 
536 |a Detalles de la financiación: Inter-American Development Bank 
536 |a Detalles de la financiación: The authors would like to acknowledge the financial support from Universidad de Buenos Aires ( 2013-X045 Project), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) ( 2012-289 Project), Instituto Nacional de la Yerba Mate (INYM) (N° 69, Resol. 310/2015 ) and Agencia Nacional de Promoción Científica y Tecnológica (ANPCyT) ( 2015-0401 Project) of Argentina and from Banco Interamericano de Desarrollo . Appendix A 
593 |a Departamento de Industrias, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, C.A.B.A., 1428, Argentina 
593 |a Member of Consejo Nacional de Investigaciones Científicas y Técnicas de la República Argentina, Argentina 
593 |a Scholar of Consejo Nacional de Investigaciones Científicas y Técnicas de la República Argentina, Argentina 
690 1 0 |a FLOW CYTOMETRY 
690 1 0 |a MILD HEAT 
690 1 0 |a TRANSMISSION ELECTRON MICROSCOPY 
690 1 0 |a UV-C LIGHT 
690 1 0 |a CARROT 
690 1 0 |a CHEMISTRY 
690 1 0 |a EVALUATION STUDY 
690 1 0 |a FLOW CYTOMETRY 
690 1 0 |a FOOD PRESERVATION 
690 1 0 |a FRUIT AND VEGETABLE JUICE 
690 1 0 |a GROWTH, DEVELOPMENT AND AGING 
690 1 0 |a HEAT 
690 1 0 |a MICROBIAL VIABILITY 
690 1 0 |a MICROBIOLOGY 
690 1 0 |a PROCEDURES 
690 1 0 |a RADIATION RESPONSE 
690 1 0 |a SACCHAROMYCES CEREVISIAE 
690 1 0 |a SWEET ORANGE 
690 1 0 |a TRANSMISSION ELECTRON MICROSCOPY 
690 1 0 |a ULTRASTRUCTURE 
690 1 0 |a ULTRAVIOLET RADIATION 
690 1 0 |a CITRUS SINENSIS 
690 1 0 |a DAUCUS CAROTA 
690 1 0 |a FLOW CYTOMETRY 
690 1 0 |a FOOD PRESERVATION 
690 1 0 |a FRUIT AND VEGETABLE JUICES 
690 1 0 |a HOT TEMPERATURE 
690 1 0 |a MICROBIAL VIABILITY 
690 1 0 |a MICROSCOPY, ELECTRON, TRANSMISSION 
690 1 0 |a SACCHAROMYCES CEREVISIAE 
690 1 0 |a ULTRAVIOLET RAYS 
700 1 |a Ferrario, M. 
700 1 |a Guerrero, S. 
773 0 |d Academic Press, 2018  |g v. 73  |h pp. 1-10  |p Food Microbiol.  |x 07400020  |w (AR-BaUEN)CENRE-4767  |t Food Microbiology 
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