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      <dc:title>Protein recovery from pot ale, a whisky by-product</dc:title>
      <dc:creator>Bagés Estopà, Sara</dc:creator>
      <dc:subject>Àrees temàtiques de la UPC::Enginyeria agroalimentària::Indústries agroalimentàries::Biotecnologia alimentària</dc:subject>
      <dc:subject>Àrees temàtiques de la UPC::Enginyeria química::Química orgànica::Compostos orgànics</dc:subject>
      <dc:subject>Feeds –- Biotechnology</dc:subject>
      <dc:subject>Saccharomyces cerevisiae -– Biotechnology</dc:subject>
      <dc:subject>Enginyeria de proteïnes</dc:subject>
      <dc:subject>Pinsos -- Biotecnologia</dc:subject>
      <dc:subject>Llevat de cervesa -- Biotecnologia</dc:subject>
      <dc:subject>Protein engineering</dc:subject>
      <dc:description>The objective of this research is to recover yeast protein from pot ale, a whisky by-product. Different yeast disruption methods were tested: enzymatic disruption, glass beads, the commercial reagent Y-PER plus, autolysis, sonication, homogenization and combination of mechanical and non-mechanical methods. This work was focused on the enzymatic disruption and combined method; the effect of different enzymes, enzyme concentration and time on protein recovery was studied. The optimal extraction method was the pot ale incubation with 1000 ppm Rohalase® BX and 0.015M EDTA followed by homogenization at 500 bars, which increases the protein recovery yield up to 50% compared with homogenization. The hydrolysis of yeast in pot ale permits the recovery of high quality proteins, which can be used as food or feed grade.</dc:description>
      <dc:date>2012-11</dc:date>
      <dc:type>Master thesis</dc:type>
      <dc:rights>Restricted access - author's decision</dc:rights>
      <dc:publisher>Universitat Politècnica de Catalunya</dc:publisher>
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