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      <ref-type name="Journal Article">17</ref-type>
      <contributors>
        <authors>
          <author>D. Tekdal</author>
          <author>S. Cetiner</author>
        </authors>
      </contributors>
      <titles>
        <title>IN-OVULE EMBRYO CULTURE OF Thermopsis turcica</title>
        <secondary-title>Journal of Animal and Plant Sciences</secondary-title>
        <alt-title>JAPS</alt-title>
      </titles>
      <dates><year>2014</year><pub-dates><date>2014/12/01</date></pub-dates></dates>
      <volume>24</volume>
      <number>6</number>
      <pages>1673-1679</pages>
      <isbn>1018-7081</isbn>
      <electronic-resource-num>NA</electronic-resource-num>
      <abstract>&lt;p&gt;The possibility of micropropagation for the endangered&amp;nbsp;&lt;em&gt;Thermopsis turcica&amp;nbsp;&lt;/em&gt;wasinvestigated through an fruit ovule-embryo culture. This technique prevents embryo degradation at the early development stage, shortens breeding time, and enables efficient propagation of many plants from a single embryo, thus avoiding for breaking seed dormancy. Although a number of efficient propagation protocols of&amp;nbsp;&lt;em&gt;T. turcica&amp;nbsp;&lt;/em&gt;has been reported for multiple shoot induction and plantlet regeneration from the seeds of&amp;nbsp;&lt;em&gt;T. turcica&lt;/em&gt;, to date no publication exists on any protocol on embryo culture of&amp;nbsp;&lt;em&gt;T. turcica&lt;/em&gt;. This paper reports on the optimisation of protocols for culturing of&amp;nbsp;&lt;em&gt;T.&lt;/em&gt;&amp;nbsp;&lt;em&gt;turcica&lt;/em&gt;&amp;nbsp;fruit embryos. The protocol for embryo culture used in this research consisted of cracking the fruit, pitting it to remove the seed, excising the ovule-embryo from the seed, placing it on the medium modified from established Fabaceae embryo tissue culture media, extracting embryos from ovular integuments, and culturing. In the present study, extracted ovule-embryos were cultured on a Murashige and Skoog&amp;rsquo;s medium supplemented with Zeatin (0.5 mg L-1), Giberellic acid &amp;nbsp;(0.5 mg L-1), and Indole-3-acetic acid (0.2 mg L-1). Excised embryos from the ovular integuments were maintained on Giberellic acid-free MS medium. During culturing, cotyledons began to arise and grow plantlets. Regenerated plantles were rooted on a MS medium with Indole-3-butyric acid (2.0 mg L-1). These results show that embryo culture technique can be an alternative ex-situ conservation technique for&amp;nbsp;&lt;em&gt;in vitro&lt;/em&gt;&amp;nbsp;propagation of the threatened rare plant species&amp;nbsp;&lt;em&gt;T. turcica&lt;/em&gt;.&lt;/p&gt;</abstract>
      <keywords><keyword>Micropropagation, fabaceae, seed, rare plant species, tissue culture media</keyword></keywords>
      <publisher>Pakistan Agricultural Scientists Forum</publisher>
      <urls><related-urls><url>https://thejaps.org.pk/AbstractView.aspx?mid=2014-JAPS-240</url></related-urls></urls>
    </record>
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