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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%">Martinez-Montero, M. E.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Martinez, J.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Engelmann, Florent</style>
          </author>
        </authors>
      </contributors>
      <titles>
        <title>Cryopreservation of sugarcane somatic embryos</title>
        <secondary-title>Cryo-Letters</secondary-title>
      </titles>
      <pages>229-242</pages>
      <keywords>
        <keyword>Somatic embryos</keyword>
        <keyword>Sugarcane</keyword>
        <keyword>Vitrification</keyword>
        <keyword>Encapsulation-vitrification</keyword>
        <keyword>Droplet-vitrification</keyword>
      </keywords>
      <dates>
        <year>2008</year>
      </dates>
      <call-num>fdi:010042701</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>Cryo-Letters</full-title>
      </periodical>
      <isbn>0143-2044</isbn>
      <accession-num>ISI:000257824900006</accession-num>
      <number>3</number>
      <urls>
        <related-urls>
          <url>https://www.documentation.ird.fr/hor/fdi:010042701</url>
        </related-urls>
        <pdf-urls>
          <url>https://www.documentation.ird.fr/intranet/publi/2008/08/010042701.pdf</url>
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      </urls>
      <volume>29</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <abstract>in this paper, we compared three vitrification-based cryopreservation techniques, viz. vitrification, encapsulation-vitrification and droplet-vitrification for cryopreserving sugarcane somatic embryos. Viability of somatic embryos was evaluated by measuring electrolyte leakage and by regrowth on recovery medium. Droplet-vitrification was the most efficient technique. Optimal conditions included loading with a solution containing 1.5 M glycerol and 0.3 M sucrose for 30 min at 25 degrees C, treatment with the PVS2 solution for 20-40 min at 0 degrees C followed by rapid immersion in liquid nitrogen of clumps of somatic embryos placed in microdroplets of cryoprotectant solution. Under such conditions, viability of cryopreserved somatic embryos reached 55 %.</abstract>
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      <custom1>UR188</custom1>
      <custom7>Cuba</custom7>
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