<?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>0187-7380</journal-id>
<journal-title><![CDATA[Revista fitotecnia mexicana]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. fitotec. mex]]></abbrev-journal-title>
<issn>0187-7380</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Mexicana de Fitogenética A.C.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0187-73802023000100033</article-id>
<article-id pub-id-type="doi">10.35196/rfm.2023.1.33</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Regeneración in vitro de plantas de Prosthechea vitellina (Lindley) W. E. Higging por organogenesis directa]]></article-title>
<article-title xml:lang="en"><![CDATA[In vitro Regeneration of Prosthechea vitellina (Lindley) W. E. Higgins plants by direct organogenesis]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Mora-Cruz]]></surname>
<given-names><![CDATA[Yazmín]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[López-Peralta]]></surname>
<given-names><![CDATA[María Cristina Guadalupe]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Hernández-Meneses]]></surname>
<given-names><![CDATA[Eleodoro]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Cruz-Huerta]]></surname>
<given-names><![CDATA[Nicacio]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,aff1  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>México</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,aff2  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>México</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Tecológico Nacional de México Campus de la Región Sierra ]]></institution>
<addr-line><![CDATA[Teapa Tabasco]]></addr-line>
<country>México</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>03</month>
<year>2023</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>03</month>
<year>2023</year>
</pub-date>
<volume>46</volume>
<numero>1</numero>
<fpage>33</fpage>
<lpage>40</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S0187-73802023000100033&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S0187-73802023000100033&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S0187-73802023000100033&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN Prosthechea vitellina (Lindley) W. E. Higgins es una orquídea epífita endémica de México con valor ornamental y económico; está sujeta a protección especial por la NOM-059-SEMARNAT-2010 debido al comercio ilegal y la destrucción de su hábitat. El cultivo de tejidos vegetales in vitro es una opción para rescate, conservación y propagación masiva de especies amenazadas. El objetivo del presente estudio fue determinar las condiciones óptimas in vitro para regenerar plantas por organogénesis directa y aclimatarlas. El proceso se inició con plántulas germinadas in vitro, y en las etapas sucesivas se evaluó la concentración de sales del medio MurashigeSkoog (MS, 50 y 100 %), carbón activado, 6-benciladenina (BA, 1.1-2.2 mg L-1), ácido naftalenacético (ANA, 0.19-0.38 mg L-1), ácido indolacético (AIA, 0.18-0.36 mg L-1) y ácido indolbutírico (AIB, 0.5-2.0 mg L-1). En la etapa de aclimatación se evaluaron plantas enraizadas in vitro de 5 y 7 cm en diferentes sustratos. Los experimentos se establecieron en un diseño completamente al azar y los datos obtenidos se sometieron a un ANDEVA. En la etapa de inducción la mayor cantidad de brotes (2.03) se obtuvo con 2.2 mg L-1 de BA y 0.19 mg L-1 de ANA. En la multiplicación se produjeron 2.5 brotes con 1.0 mg L-1 de BA y 0.25 mg L-1 de AIA a las ocho semanas de cultivo. El alargamiento mayor de brotes (2.16 cm) se logró con MS 50 % y 0.5 g L-1 de carbón activado. En el enraizamiento el mayor número de raíces se produjo con 2.0 mg L-1 de AIB, generando 5.27 raíces por planta. En la aclimatación, la supervivencia fue de 100 %, con plantas de 7 cm en corteza de pino. El protocolo desarrollado aporta un método para la propagación de esta orquídea con fines de rescate, conservación, reintroducción y aprovechamiento comercial.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[SUMMARY Prosthechea vitellina (Lindley) W.E. Higgins is an epiphytic orchid endemic to Mexico with ornamental and economic value; it is subject to special protection by NOM-059-SEMARNAT-2010 due to illegal trade and destruction of its habitat. In vitro plant tissue culture is an option for rescue, conservation and massive propagation of endangered species. The aim of the present study was to determine optimal in vitro conditions to regenerate plants by direct organogenesis and acclimatize them. The process started with germinated seedlings in vitro, and in successive stages the concentration of salts of the Murashige-Skoog medium (MS, 50 and 100 %), activated charcoal, 6-benzyl adenine (BA, 1.1-2.2 mg L-1), naphthaleneacetic acid (ANA, 0.19-0.38 mg L-1), indoleacetic acid (IAA, 0.18-0.36 mg L-1) and indole butyric acid (IBA, 0.52.0 mg L-1). In the acclimatization stage, 5 and 7-cm in vitro rooted plants were evaluated on different substrates. The experiments were established in a completely randomized design and the data obtained were subjected to ANOVA. At the induction stage, the largest number of shoots (2.03) were obtained with 2.2 mg L-1 of BA and 0.19 mg L-1 of ANA. At multiplication, 2.5 shoots were produced with 1.0 mg L-1 of BA and 0.25 mg L-1 of IAA at eight weeks of culture. The largest elongation of shoots (2.16 cm) was achieved with MS 50 % and 0.5 g L-1 of activated charcoal. At rooting, the largest number of roots occurred with 2.0 mg L-1 of IBA, generating 5.27 roots per plant. In acclimatization, survival was 100 %, with 7-cm plants on pine bark. The developed protocol provides a method for the propagation of this orchid for rescue, conservation, reintroduction and commercial use.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Prosthechea vitellina]]></kwd>
<kwd lng="es"><![CDATA[endémica]]></kwd>
<kwd lng="es"><![CDATA[micropropagación]]></kwd>
<kwd lng="es"><![CDATA[morfogénesis]]></kwd>
<kwd lng="es"><![CDATA[organogénesis]]></kwd>
<kwd lng="es"><![CDATA[orquídea]]></kwd>
<kwd lng="en"><![CDATA[Prosthechea vitellina]]></kwd>
<kwd lng="en"><![CDATA[endemic]]></kwd>
<kwd lng="en"><![CDATA[micropropagation]]></kwd>
<kwd lng="en"><![CDATA[morphogenesis]]></kwd>
<kwd lng="en"><![CDATA[orchid]]></kwd>
<kwd lng="en"><![CDATA[organogenesis]]></kwd>
</kwd-group>
</article-meta>
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