<?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>1665-2738</journal-id>
<journal-title><![CDATA[Revista mexicana de ingeniería química]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. Mex. Ing. Quím]]></abbrev-journal-title>
<issn>1665-2738</issn>
<publisher>
<publisher-name><![CDATA[Universidad Autónoma Metropolitana, División de Ciencias Básicas e Ingeniería]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1665-27382007000300007</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[El ABTS&#8226;+ agente oxidante de diversos compuestos químicos y su mecanismo de reciclado entre la lacasa y el sustrato]]></article-title>
<article-title xml:lang="en"><![CDATA[The ABTS&#8226;+ an oxidant agent of different chemical compounds and its recycling process between laccase susbtrate]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Solís-Oba]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Bárzana]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[García-Garibay]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<xref ref-type="aff" rid="A03"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Viniegra-González]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<xref ref-type="aff" rid="A03"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Instituto Politécnico Nacional Centro de Investigación en Biotecnología Aplicada ]]></institution>
<addr-line><![CDATA[Tepetitla de Lardizabal Tlaxcala]]></addr-line>
<country>México</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Universidad Nacional Autónoma de México Facultad de Química ]]></institution>
<addr-line><![CDATA[México D.F.]]></addr-line>
<country>México</country>
</aff>
<aff id="A03">
<institution><![CDATA[,Universidad Autónoma Metropolitana Unidad Iztapalapa Departamento de Biotecnología ]]></institution>
<addr-line><![CDATA[México D.F.]]></addr-line>
<country>México</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2007</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2007</year>
</pub-date>
<volume>6</volume>
<numero>3</numero>
<fpage>275</fpage>
<lpage>281</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1665-27382007000300007&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1665-27382007000300007&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1665-27382007000300007&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[La lacasa comercial obtenida de Myceliophtera termophila y expresada sobre Aspergillus oryzae se empleó para producir un cation radical estable y muy activo del mediador químico ABTS (ácido 2,2'-azino-bis-(3-etillbenzotiazolin-6-sulfonico) con el fin de probar la factibilidad de emplearlo como un intermediario para la oxidación de una variedad de compuestos aromáticos en ausencia de la enzima. Se demostró que el catión radical ABTS&#8226;+ por si mismo oxidó al azul índigo, ácido tánico, ácido gálico, azul brillante G, azul de Coomassie, naranja 7 y p-cresol. La reacción de oxidación reveló cambios importantes en sus espectros de absorción en la región del espectro visible. Se demostró también que la oxidación de estos compuestos por la mezcla de lacasa y ABTS se puede efectuar de forma cíclica, de tal forma que la velocidad de reacción fue 94 veces mayor para el índigo, 17 veces mayor para el azul brillante G, 34 veces mayor para el naranja 7 y 5 veces mayor para el p-cresol, comparado con usar el mediador o la lacasa en forma individual. Estos resultados muestran la factibilidad de un esquema de reciclado para la oxidación final de una variedad de compuestos orgánicos en los cuales la enzima no este directamente en contacto con el mismo y que se efectúe a través del mediador ABTS&#8226;+.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[The commercial enzyme laccase cloned from Myceliophtera termophila and expressed in Aspergillus oryzae was used to produce an active, stable and oxidized form of the chemical mediator ABTS (2,2'-azino-bis-(3-ethylbenzothiazoline-6-sulphonic acid)) in order to test the feasibility of using the monocation ABTS&#8226;+ as a recyclable intermediate for the oxidation of a variety of aromatic chemicals in the absence of the enzyme. It was shown that ABTS&#8226;+, by itself, oxidized, indigo blue, tannic and galic acids, brilliant blue G, Coomassie blue, orange 7 and p-cresol. Oxidation was assessed by important changes in their visible absorption spectra. It was also shown that oxidation of these compounds by a mixture of ABTS and laccase can be done in a cyclic manner, such a way the oxidation rate was 94 times higher for indigo, 17 times for brilliant blue G, 34 times for orange 7 and 5 times higher for p-cresol compared with using the mediator or the laccase alone. Those results show the feasibility of a recycling scheme for the final oxidation of a wide variety of aromatic compounds in which the enzyme is not directly in contact with the compound but through the intermediate ABTS&#8226;+.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[ABTS]]></kwd>
<kwd lng="es"><![CDATA[reciclado]]></kwd>
<kwd lng="es"><![CDATA[oxidación]]></kwd>
<kwd lng="es"><![CDATA[colorantes]]></kwd>
<kwd lng="es"><![CDATA[lacasa]]></kwd>
<kwd lng="en"><![CDATA[ABTS]]></kwd>
<kwd lng="en"><![CDATA[recycling]]></kwd>
<kwd lng="en"><![CDATA[oxidation]]></kwd>
<kwd lng="en"><![CDATA[dyes]]></kwd>
<kwd lng="en"><![CDATA[lacction]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="justify"><font face="verdana" size="4">Biotecnolog&iacute;a</font></p>     <p align="justify"><font face="verdana" size="4">&nbsp;</font></p>     <p align="center"><font face="verdana" size="4"><b>El ABTS<sup>&bull;+</sup> agente oxidante de diversos compuestos qu&iacute;micos y su mecanismo de reciclado entre la lacasa y el sustrato</b></font></p>     <p align="center"><font face="verdana" size="2">&nbsp;</font></p>     <p align="center"><font face="verdana" size="3"><b>The ABTS<sup>&bull;+</sup> an oxidant agent of different chemical compounds and its recycling process between laccase susbtrate</b></font></p>     <p align="center"><font face="verdana" size="2">&nbsp;</font></p>     <p align="center"><font face="verdana" size="2"><b>M. Sol&iacute;s&#150;Oba<sup>1*</sup>, E. B&aacute;rzana<sup>2</sup>, M. Garc&iacute;a&#150;Garibay<sup>3</sup> y G. Viniegra&#150;Gonz&aacute;lez<sup>3</sup></b></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><i><i><sup>1</sup></i> Centro de Investigaci&oacute;n en Biotecnolog&iacute;a Aplicada del Instituto Polit&eacute;cnico Nacional, Carretera Estatal <i>Santa In&eacute;s Tecuexcomac&#150;Tepetitla Km 1.5, Tepetitla de Lardizabal, Tlaxcala, CP. 90700, M&eacute;xico. <i>* Autor para la correspondencia: E&#150;mail: </i></i></i><a href="mailto:msolis@ipn.mx">msolis@ipn.mx</a><i><i> <i>Tel. 57 29 63 00 ext 87810, Fax 57 29 63 00 ext 87826</i></i></i></font></p>     <p align="justify"><font face="verdana" size="2"><i><sup>2</sup> Facultad de Qu&iacute;mica, Universidad Nacional Aut&oacute;noma de M&eacute;xico, <i>Ciudad Universitaria, M&eacute;xico D.F., M&eacute;xico.</i></i></font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2"><i><sup>3 </sup>Departamento de Biotecnolog&iacute;a, Universidad Aut&oacute;noma Metropolitana Unidad Iztapalapa Av. San Rafael </i><i>  Atlixco No. 186, Col. Vicentina, M&eacute;xico D.F., M&eacute;xico.</i></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2">Recibido 2 de Junio 2007    <br> Aceptado 31 de Octubre 2007</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Resumen</b></font></p>     <p align="justify"><font face="verdana" size="2">La lacasa comercial obtenida de <i>Myceliophtera termophila </i>y expresada sobre <i>Aspergillus oryzae </i>se emple&oacute; para producir un cation radical estable y muy activo del mediador qu&iacute;mico ABTS (&aacute;cido 2,2'&#150;azino&#150;bis&#150;(3&#150;etillbenzotiazolin&#150;6&#150;sulfonico) con el fin de probar la factibilidad de emplearlo como un intermediario para la oxidaci&oacute;n de una variedad de compuestos arom&aacute;ticos en ausencia de la enzima. Se demostr&oacute; que el cati&oacute;n radical ABTS<sup>&bull;+</sup> por si mismo oxid&oacute; al azul &iacute;ndigo, &aacute;cido t&aacute;nico, &aacute;cido g&aacute;lico, azul brillante G, azul de Coomassie, naranja 7 y p&#150;cresol. La reacci&oacute;n de oxidaci&oacute;n revel&oacute; cambios importantes en sus espectros de absorci&oacute;n en la regi&oacute;n del espectro visible. Se demostr&oacute; tambi&eacute;n que la oxidaci&oacute;n de estos compuestos por la mezcla de lacasa y ABTS se puede efectuar de forma c&iacute;clica, de tal forma que la velocidad de reacci&oacute;n fue 94 veces mayor para el &iacute;ndigo, 17 veces mayor para el azul brillante G, 34 veces mayor para el naranja 7 y 5 veces mayor para el p&#150;cresol, comparado con usar el mediador o la lacasa en forma individual. Estos resultados muestran la factibilidad de un esquema de reciclado para la oxidaci&oacute;n final de una variedad de compuestos org&aacute;nicos en los cuales la enzima no este directamente en contacto con el mismo y que se efect&uacute;e a trav&eacute;s del mediador ABTS<sup>&bull;+</sup>.</font></p>     <p align="justify"><font face="verdana" size="2"><b>Palabras clave: </b>ABTS, reciclado, oxidaci&oacute;n, colorantes, lacasa.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Abstract</b></font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">The commercial enzyme laccase cloned from <i>Myceliophtera termophila </i>and expressed in <i>Aspergillus oryzae </i>was used to produce an active, stable and oxidized form of the chemical mediator ABTS (2,2'&#150;azino&#150;bis&#150;(3&#150;ethylbenzothiazoline&#150;6&#150;sulphonic acid)) in order to test the feasibility of using the monocation ABTS<sup>&bull;+</sup> as a recyclable intermediate for the oxidation of a variety of aromatic chemicals in the absence of the enzyme. It was shown that ABTS<sup>&bull;+</sup>, by itself, oxidized, indigo blue, tannic and galic acids, brilliant blue G, Coomassie blue, orange 7 and p&#150;cresol. Oxidation was assessed by important changes in their visible absorption spectra. It was also shown that oxidation of these compounds by a mixture of ABTS and laccase can be done in a cyclic manner, such a way the oxidation rate was 94 times higher for indigo, 17 times for brilliant blue G, 34 times for orange 7 and 5 times higher for p&#150;cresol compared with using the mediator or the laccase alone. Those results show the feasibility of a recycling scheme for the final oxidation of a wide variety of aromatic compounds in which the enzyme is not directly in contact with the compound but through the intermediate ABTS<sup>&bull;+</sup>.</font></p>     <p align="justify"><font face="verdana" size="2"><b>Keywords: </b>ABTS, recycling, oxidation, dyes, lacction.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><a href="/pdf/rmiq/v6n3/v6n3a7.pdf" target="_blank">DESCARGAR ART&Iacute;CULO EN FORMATO PDF</a></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Referencias</b></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">Bourbonnais R., Paice M. (1990). Oxidation of non&#150;phenolic substrates. An expanded role for laccase   in   lignin   biodegradation. <i>FEBS </i><i>Letters 267, </i>99&#150;102.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=8531164&pid=S1665-2738200700030000700001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">Bourbonnais R., Paice M., Freiermuth B., Bodie E., Borneman S. (1997). Reactivities of various mediators and laccases with Kraft pulp and lignin model compounds, <i>Applied and Environmental Microbiology, </i>4627&#150;4632.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=8531166&pid=S1665-2738200700030000700002&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --> </font></p>     ]]></body>
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<person-group person-group-type="author">
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<article-title xml:lang="en"><![CDATA[Oxidation of non-phenolic substrates. An expanded role for laccase in lignin biodegradation]]></article-title>
<source><![CDATA[FEBS Letters]]></source>
<year>1990</year>
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