<?xml version="1.0" encoding="UTF-8"?>
<collection>
<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1016/j.ifset.2018.04.012</dc:identifier><dc:language>eng</dc:language><dc:creator>Martínez, J.M.</dc:creator><dc:creator>Delso, C.</dc:creator><dc:creator>Angulo, J.</dc:creator><dc:creator>Álvarez, I.</dc:creator><dc:creator>Raso, J.</dc:creator><dc:title>Pulsed electric field-assisted extraction of carotenoids from fresh biomass of Rhodotorula glutinis</dc:title><dc:identifier>ART-2018-106425</dc:identifier><dc:description>The aim of this study was to demonstrate the potential of PEF for inducing autolysis of R. glutinis, with the purpose of designing a more efficient and ecofriendly carotenoid extraction process: an extraction from fresh biomass, using cheaper, non-toxic, environmental-friendly solvents. Propidium iodide uptake and release of intracellular components revealed the irreversible electroporation of R. glutinis by PEF. Flow cytometry measurements detected morphological changes in PEF-treated R. glutinis cells during incubation caused by the autolysis triggering effect of electroporation. After submitting the fresh biomass to a PEF treatment (15 kV/cm, 150 µs) that irreversibly electroporated more than the 90% of the cells, ethanol proved ineffective for extracting carotenoids from fresh biomass of R. glutinis. However, after incubating the PEF-treated fresh biomass for 24 h at 20 °C in a pH 7 buffer, ca. 240 µg/g d.w. of carotenoids were recovered after 1 h of extraction in ethanol. The highest amount of carotenoids extracted (375 µg/g d.w.) from the PEF-treated cells of R. glutinis was obtained after having incubated them at 25 °C for 24 h in a medium of pH 8.0. The improvement in carotenoid extraction by incubating the R. glutinis cells after PEF treatment seems to be caused by PEF-triggered autolysis, which tends to disrupt the association of carotenoids with other molecules present in the cytoplasm, and causes a degradation of the cell wall.</dc:description><dc:date>2018</dc:date><dc:source>http://zaguan.unizar.es/record/135891</dc:source><dc:doi>10.1016/j.ifset.2018.04.012</dc:doi><dc:identifier>http://zaguan.unizar.es/record/135891</dc:identifier><dc:identifier>oai:zaguan.unizar.es:135891</dc:identifier><dc:identifier.citation>INNOVATIVE FOOD SCIENCE &amp; EMERGING TECHNOLOGIES 47 (2018), 421-427</dc:identifier.citation><dc:rights>All rights reserved</dc:rights><dc:rights>http://www.europeana.eu/rights/rr-f/</dc:rights><dc:rights>info:eu-repo/semantics/closedAccess</dc:rights></dc:dc>

</collection>