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                <text>&lt;strong&gt;The mandelate pathway, an alternative to the PAL pathway for the synthesis of benzenoids in yeast&lt;/strong&gt;</text>
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                <text>Benzenoid-derived metabolites act as precursors for a wide variety of products&amp;nbsp; involved in essential metabolic roles in eukaryotic cells. They are synthesised in&amp;nbsp; plants and some fungi through the phenylalanine ammonia lyase (PAL) or tyrosine&amp;nbsp; ammonia lyase (TAL) pathways. Ascomycete yeasts and animals both lack the&amp;nbsp; capacity for PAL/TAL pathways, and metabolic reactions leading to benzenoid&amp;nbsp; synthesis in these organisms have remained incompletely known for decades. Here&amp;nbsp; we show genomic, transcriptomic and metabolomic evidence that yeasts use a&amp;nbsp; mandelate pathway to synthesise benzenoids, with some similarities to pathways&amp;nbsp; used by bacteria. We conducted feeding experiments using a synthetic&amp;nbsp; fermentation medium that contained either 13C-phenylalanine or 13C-tyrosine and,&amp;nbsp; using methylbenzoylphosphonate (MBP) to inhibit benzoylformate decarboxylase,&amp;nbsp; we were able to accumulate intracellular intermediates in the yeast Hanseniaspora&amp;nbsp; vineae. To further confirm this pathway, we tested three mutants in separate&amp;nbsp; fermentation experiments with deletions in the key genes putatively proposed to&amp;nbsp; form benzenoids (Saccharomyces cerevisiae aro10&amp;Delta;, dld1&amp;Delta; and dld2&amp;Delta;). Our results&amp;nbsp; elucidate the mechanism of benzenoid synthesis in yeast through phenylpyruvate&amp;nbsp; linked with the mandelate pathway to produce benzyl alcohol and 4- hydroxybenzaldehyde from the aromatic amino acids, phenylalanine and tyrosine,&amp;nbsp; as well as sugars. These results provide an explanation for the origin of the&amp;nbsp; benzoquinone ring, 4-hydroxybenzoate, and suggest Aro10p has benzoylformate&amp;nbsp; and 4-hydroxybenzoylformate decarboxylase functions in yeast.&amp;nbsp; Keywords: phenylpyruvate pathway, yeast, benzyl alcohol, Hanseniaspora vineae, 4-&amp;nbsp; hydroxybenzoic acid, benzoylformate decarboxylase, ARO10, coenzyme Q.</text>
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                <text>Applied and Environmental Microbiology, 2020. -- p. 1-38</text>
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                <text>&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt; (Por favor lea este aviso antes de abrir los documentos u objetos) &lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho de autor&lt;/strong&gt; sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006) ADVERTENCIA - La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.</text>
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                <text>A versatile palladium-catalyzed tandem synthetic sequence to afford E-stilbenes libraries has been developed. Excellent regio- and stereocontrol have been achieved by means of the sequence of Hiyama and Heck cross-couplings. Undesirable homocoupling byproducts were avoided employing immobilized substrates.</text>
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                <text>BIBLIOGRAFIA NACIONAL QUIMICA</text>
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                <text>2015</text>
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          <element elementId="87">
            <name>Abstract</name>
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                <text>Aza and oxo Diels&amp;ndash;Alder reactions using enantiopure cis-cyclohexadienediols were studied. These dienediols were obtained from the biotransformation of monosubstituted arenes using bacterial dioxygenases (toluene and benzoate dioxygenases). Ethyl glyoxylate and its N-tosyl imine were used as dienophiles to afford the corresponding hetero Diels&amp;ndash;Alder bicyclic adducts with excellent regio- and stereoselectivities. Quantum chemical calculations at the B3LYP/6-31+G(d,p) level of theory were performed to rationalize the observed selectivities especially the stereochemical aspects of the cycloadditions. The synthetic importance of these adducts is highlighted for the preparation of enantiopure 2,2,3,4,5,6-hexasubstituted piperidine and tetrahydropyran from toluene</text>
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            <name>Creator</name>
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                <text>&lt;strong&gt;Pazos, Mariana&lt;/strong&gt;</text>
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              <elementText elementTextId="350314">
                <text>&lt;strong&gt;Mart&amp;iacute;nez, Sebasti&amp;aacute;n&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Vila, Mar&amp;iacute;a Agustina&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Rodr&amp;iacute;guez, Paola&lt;/strong&gt;</text>
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                <text>&lt;a title="Curriculum Vitae" href="http://buscadores.anii.org.uy/buscador_sni/exportador/ExportarPdf?hash=f31ba94f764507db0d42d457038dd734" target="_blank"&gt;&lt;strong&gt;Veiga, Nicolas&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>&lt;a title="Curriculum Vitae" href="http://buscadores.anii.org.uy/buscador_sni/exportador/ExportarPdf?hash=502f70a0642a910f5abf0e0d5c853b61" target="_blank"&gt;&lt;strong&gt;Seoane, Gustavo&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>&lt;strong&gt;Carrera, Ignacio&lt;/strong&gt;</text>
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                <text>Tetrahedron: Asymmetry v. 26, no. 24, 2015. -- p. 1436-1447</text>
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            <name>Publisher</name>
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              <elementText elementTextId="350321">
                <text>Elsevier</text>
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              <elementText elementTextId="350322">
                <text>2015</text>
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          <element elementId="47">
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                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;br /&gt; &lt;br /&gt; (Por favor lea este aviso antes de abrir los documentos u objetos)&lt;br /&gt; &lt;br /&gt; &lt;strong&gt;La legislaci&amp;oacute;n uruguaya&lt;/strong&gt; protege el derecho de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes&lt;br /&gt; &lt;br /&gt; (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006 LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;br /&gt; &lt;br /&gt; &lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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            <name>Format</name>
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                <text>PDF</text>
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              <elementText elementTextId="350325">
                <text>Ingl&amp;eacute;s</text>
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                <text>Art&amp;iacute;culo</text>
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                <text>doi:10.1016/j.tetasy.2015.10.015</text>
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        <name>Dioxigenasa</name>
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        <name>Esterioquímica</name>
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        <name>Hidrocarburos aromáticos</name>
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