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      <ref-type name="Journal Article">17</ref-type>
      <work-type>ACL : Articles dans des revues avec comité de lecture répertoriées par l'AERES</work-type>
      <contributors>
        <authors>
          <author>
            <style face="normal" font="default" size="100%">Jiang, Q. B.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Ma, Y. Z.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Zhong, C. L.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Zeng, B. S.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Zhang, Y.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Pinyopusarerk, K.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Bogusz, Didier</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Franche, Claudine</style>
          </author>
        </authors>
      </contributors>
      <titles>
        <title>Optimization of the conditions for Casuarina cunninghamiana Miq. genetic transformation mediated by Agrobacterium tumefaciens</title>
        <secondary-title>Plant Cell Tissue and Organ Culture</secondary-title>
      </titles>
      <pages>195-204</pages>
      <keywords>
        <keyword>Actinorhizal plant</keyword>
        <keyword>Casuarina cunninghamiana</keyword>
        <keyword>Agrobacterium tumefaciens</keyword>
        <keyword>Genetic transformation</keyword>
        <keyword>Frankia</keyword>
      </keywords>
      <dates>
        <year>2015</year>
      </dates>
      <call-num>fdi:010064063</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>Plant Cell Tissue and Organ Culture</full-title>
      </periodical>
      <isbn>0167-6857</isbn>
      <accession-num>ISI:000351524900017</accession-num>
      <number>1</number>
      <electronic-resource-num>10.1007/s11240-014-0694-y</electronic-resource-num>
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          <url>https://www.documentation.ird.fr/hor/fdi:010064063</url>
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          <url>https://www.documentation.ird.fr/intranet/publi/2015/04/010064063.pdf</url>
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      <volume>121</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <abstract>Using epicotyl fragments of the actinorhizal tree Casuarina cunninghamiana and the disarmed strain of Agrobacterium tumefaciens C58C1 (pGV2260) containing the pBIN19-35S-GUSINT binary vector, a method for the genetic transformation of C. cunninghamiana was established. Transformed cells were initially selected for 2 weeks on nutrient medium supplemented with kanamycin 20 mg L-1 during callus induction, and then subcultured with 50 mg L-1 until adventitious bud and shoot differentiation. Different factors involved in the early stages of the T-DNA transfer process were studied. Agrobacterium-mediated DNA delivery was most successful when epicotyl fragments excised from 45-day-old seedlings were co-cultivated with an exponentially growing culture of A. tumefaciens at an OD600nm of 0.3, for 5 days in the presence of 50 mu M of acetosyringone. Kanamycin resistant calli were observed on 88.89 % of the explants and transgenic rooted C. cunninghamiana plants were obtained in 6 months. Evidence of genetic transformation was demonstrated by -glucuronidase histochemical assays and polymerase chain reaction analyses. The possibility to obtain transgenic nitrogen-fixing nodules after inoculation by the soil actinomycete Frankia was established.</abstract>
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      <custom7>Chine</custom7>
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