body: <record xmlns="http://www.openarchives.org/OAI/2.0/">
                          <header>
                              <identifier>oai:research.chalmers.se:504700</identifier>
                              <datestamp>2018-12-19T10:29:07Z</datestamp>
                              <setSpec>openaire</setSpec>
                          </header>
                          <metadata>
                              <oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" 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:title>The Synthetic Potential of Fungal Feruloyl Esterases: A Correlation with Current Classification Systems and Predicted Structural Properties</dc:title>
                                  <dc:identifier>https://research.chalmers.se/en/publication/504700</dc:identifier>
                                  <dc:date>2018</dc:date>
                                              <dc:creator>Cerullo, Gabriella</dc:creator>
                                              <dc:creator>Hüttner, Silvia</dc:creator>
                                              <dc:creator>Uthoff, Stefan</dc:creator>
                                              <dc:creator>Dilokpimol, Adiphol</dc:creator>
                                              <dc:creator>Iancu, Laura</dc:creator>
                                              <dc:creator>Varriale, Simona</dc:creator>
                                              <dc:creator>Antonopoulou, Io</dc:creator>
                                              <dc:creator>Mäkelä, Miia</dc:creator>
                                              <dc:creator>Faraco, Vincenza</dc:creator>
                                              <dc:creator>Hildén, Kristiina</dc:creator>
                                              <dc:creator>Steinbüchel, Alexander</dc:creator>
                                              <dc:creator>Jütten, Peter</dc:creator>
                                              <dc:creator>Piechot, Alexander</dc:creator>
                                              <dc:creator>Olsson, Lisbeth</dc:creator>
                                              <dc:creator>Vries, Ronald P. de</dc:creator>
                                              <dc:creator>Rova, Ulrika</dc:creator>
                                              <dc:creator>Christakopoulos, Paul</dc:creator>
                                                  <dc:subject>Bioprocess Technology</dc:subject>
                                                  <dc:subject>Biocatalysis and Enzyme Technology</dc:subject>
                                                  <dc:subject>Organic Chemistry</dc:subject>
                                              <dc:subject>glyceryl ferulate</dc:subject>
                                              <dc:subject>feruloyl esterase</dc:subject>
                                              <dc:subject>antioxidants</dc:subject>
                                              <dc:subject>prenyl caffeate</dc:subject>
                                              <dc:subject>phylogenetic classification</dc:subject>
                                              <dc:subject>prenyl ferulate</dc:subject>
                                              <dc:subject>sugar esters</dc:subject>
                                              <dc:subject>butyl ferulate</dc:subject>
                                              <dc:subject>transesterification</dc:subject>
                                              <dc:subject>l-arabinose ferulate</dc:subject>
                                          <dc:description>Twenty-eight fungal feruloyl esterases (FAEs) were evaluated for their synthetic abilities in a ternary system of n-hexane: t-butanol: 100 mM MOPS-NaOH pH 6.0 forming detergentless microemulsions. Five main derivatives were synthesized, namely prenyl ferulate, prenyl caffeate, butyl ferulate, glyceryl ferulate, and l-arabinose ferulate, offering, in general, higher yields when more hydrophilic alcohol substitutions were used. Acetyl xylan esterase-related FAEs belonging to phylogenetic subfamilies (SF) 5 and 6 showed increased synthetic yields among tested enzymes. In particular, it was shown that FAEs belonging to SF6 generally transesterified aliphatic alcohols more efficiently while SF5 members preferred bulkier l-arabinose. Predicted surface properties and structural characteristics were correlated with the synthetic potential of selected tannase-related, acetyl-xylan-related, and lipase-related FAEs (SF1-2, -6, -7 members) based on homology modeling and small molecular docking simulations.</dc:description>
                                                                  <dc:relation>info:eu-repo/grantAgreement/EC/FP7/613868//Optimized esterase biocatalysts for cost-effective industrial production (OPTIBIOCAT)/</dc:relation>
                                                  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.3390/catal8060242</dc:relation>
                                          <dc:type>info:eu-repo/semantics/article</dc:type>
                                          <dc:source>Catalysts (2073-4344) vol.8(2018)</dc:source>
                                                      <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:language>eng</dc:language>
                                  <dc:audience>Researchers</dc:audience>
                                  <dc:format>application/pdf</dc:format>
                              </oai_dc:dc>
                          </metadata>
                      </record>