<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>1405-888X</journal-id>
<journal-title><![CDATA[TIP. Revista especializada en ciencias químico-biológicas]]></journal-title>
<abbrev-journal-title><![CDATA[TIP]]></abbrev-journal-title>
<issn>1405-888X</issn>
<publisher>
<publisher-name><![CDATA[Universidad Nacional Autónoma de México, Facultad de Estudios Superiores Zaragoza]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1405-888X2017000200015</article-id>
<article-id pub-id-type="doi">10.1016/j.recqb.2017.04.002</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Obtención de dehidrodiisoeugenol por dimerización de isoeugenol con cultivos celulares de Bouvardia ternifolia (trompetilla)]]></article-title>
<article-title xml:lang="en"><![CDATA[Dehidrodiisoeugenol by dimerization of isoeugenol with cell culture of Bouvardia ternifolia]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Hernández-Vázquez]]></surname>
<given-names><![CDATA[Liliana]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Olivera-Flores]]></surname>
<given-names><![CDATA[Ma. Teresa de Jesús]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Luna]]></surname>
<given-names><![CDATA[Héctor]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Navarro-Ocaña]]></surname>
<given-names><![CDATA[Arturo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad Autónoma Metropolitana Unidad Xochimilco Departamento de Sistemas Biológicos]]></institution>
<addr-line><![CDATA[Ciudad de México México]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Universidad Nacional Autónoma de México Laboratorio de Cultivos Vegetales, Facultad de Química, Departamento de Bioquímica]]></institution>
<addr-line><![CDATA[ Ciudad de México]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Universidad Nacional Autónoma de México Facultad de Química Departamento de Alimentos y Biotecnología]]></institution>
<addr-line><![CDATA[ Ciudad de México]]></addr-line>
<country>Mexico</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2017</year>
</pub-date>
<volume>20</volume>
<numero>2</numero>
<fpage>15</fpage>
<lpage>22</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1405-888X2017000200015&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1405-888X2017000200015&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1405-888X2017000200015&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen Los cultivos celulares de Bouvardia ternifolia fueron usados como catalizadores en la reacción de acoplamiento oxidativo de isoeugenol. El compuesto dimérico dehidrodiisoeugenol se obtuvo con 77 % de rendimiento cuando se usó el sobrenadante obtenido de un cultivo de células en suspensión, que poseía actividad de peroxidasa. La conversión procede en condiciones suaves de reacción y al adicionar el peróxido de hidrógeno disminuye el rendimiento en la obtención del dehidrodiisoeugenol.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract Cell cultures of Bouvardia ternifolia were used as catalyst for the oxidative coupling of isoeugenol, to produce dehydrodiisoeugenol, a dimer, 77% isolated yield, when using the supernatat from the cell cultures suspension having peroxidase activity. The biotransformation proceeded under very mild conditions. It was observed that an increase in the amount of hydrogen peroxide decreases the yield.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[acoplamiento oxidativo]]></kwd>
<kwd lng="es"><![CDATA[Bouvardia ternifolia]]></kwd>
<kwd lng="es"><![CDATA[cultivo celular]]></kwd>
<kwd lng="es"><![CDATA[dehidrodiisoeugenol]]></kwd>
<kwd lng="es"><![CDATA[isoeugenol]]></kwd>
<kwd lng="en"><![CDATA[oxidative coupling]]></kwd>
<kwd lng="en"><![CDATA[Bouvardia ternifolia]]></kwd>
<kwd lng="en"><![CDATA[cell culture]]></kwd>
<kwd lng="en"><![CDATA[dehidrodiisoeugenol]]></kwd>
<kwd lng="en"><![CDATA[isoeugenol]]></kwd>
</kwd-group>
</article-meta>
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