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            <subfield code="a">10.1128/AEM.00623-13</subfield>
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            <subfield code="a">eng</subfield>
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        <datafield tag="100" ind1=" " ind2=" ">
            <subfield code="0">(orcid)0000-0002-5895-2157</subfield>
            <subfield code="a">Gayán, E.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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        <datafield tag="245" ind1=" " ind2=" ">
            <subfield code="a">Mechanism of the synergistic inactivation of Escherichia coli by UV-C light at mild temperatures</subfield>
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        <datafield tag="260" ind1=" " ind2=" ">
            <subfield code="c">2013</subfield>
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            <subfield code="a">UV light only penetrates liquid food surfaces to a very short depth, thereby limiting its industrial application in food pasteurization. One promising alternative is the combination of UV light with mild heat (UV-H), which has been demonstrated to produce a synergistic bactericidal effect. The aim of this article is to elucidate the mechanism of synergistic cellular inactivation resulting from the simultaneous application of UV light and heat. The lethality of UV-H treatments remained constant below ~45ºC, while lethality increased exponentially as the temperature increased. The percentage of synergism reached a maximum (40.3%) at 55ºC. Neither the flow regimen nor changes in the dose delivered by UV lamps contributed to the observed synergism. UV-H inactivation curves of the parental Escherichia coli strain obtained in a caffeic acid selective recovery medium followed a similar profile to those obtained with uvrA mutant cells in a nonselective medium. Thermal fluidification of membranes and synergistic lethal effects started around 40 to 45ºC. Chemical membrane fluidification with benzyl alcohol decreased the UV resistance of the parental strain but not that of the uvrA mutant. These results suggest that the synergistic lethal effect of UV-H treatments is due to the inhibition of DNA excision repair resulting from the membrane fluidification caused by simultaneous heating.</subfield>
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            <subfield code="u">http://www.europeana.eu/rights/rr-f/</subfield>
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            <subfield code="a">3.952</subfield>
            <subfield code="b">2013</subfield>
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            <subfield code="a">MICROBIOLOGY</subfield>
            <subfield code="b">24 / 119 = 0.202</subfield>
            <subfield code="c">2013</subfield>
            <subfield code="d">Q1</subfield>
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            <subfield code="a">BIOTECHNOLOGY &amp; APPLIED MICROBIOLOGY</subfield>
            <subfield code="b">30 / 165 = 0.182</subfield>
            <subfield code="c">2013</subfield>
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        <datafield tag="700" ind1=" " ind2=" ">
            <subfield code="0">(orcid)0000-0002-7971-4828</subfield>
            <subfield code="a">Mañas, P.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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        <datafield tag="700" ind1=" " ind2=" ">
            <subfield code="0">(orcid)0000-0003-2430-858X</subfield>
            <subfield code="a">Álvarez, I.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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        <datafield tag="700" ind1=" " ind2=" ">
            <subfield code="0">(orcid)0000-0002-1902-0648</subfield>
            <subfield code="a">Condón, S.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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            <subfield code="1">2008</subfield>
            <subfield code="2">780</subfield>
            <subfield code="a">Universidad de Zaragoza</subfield>
            <subfield code="b">Dpto. Produc.Animal Cienc.Ali.</subfield>
            <subfield code="c">Área Tecnología de Alimentos</subfield>
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        <datafield tag="773" ind1=" " ind2=" ">
            <subfield code="g">79, 14 (2013), 4465-4473</subfield>
            <subfield code="p">Appl. environ. microbiol.</subfield>
            <subfield code="t">APPLIED AND ENVIRONMENTAL MICROBIOLOGY</subfield>
            <subfield code="x">0099-2240</subfield>
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