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        <dc:title>Plant regeneration from embryogenic cell suspension cultures of wild sorghum (Sorghum dimidiatum Stapf.)</dc:title>
        <dc:creator>Mythili, P K</dc:creator>
        <dc:creator>Seetharama, N</dc:creator>
        <dc:creator>Reddy, V D</dc:creator>
        <dc:subject>Sorghum</dc:subject>
        <dc:description>A simple and efficient protocol is described for regeneration of wild sorghum (Sorghum dimidiatum) from cell suspension cultures. Fast-growing cell suspensions were established from shoot-meristem-derived callus. Plating of the suspension on Murashige and Skoog agar medium supplemented with 2.5 mg 1-1 2,4-dichlorophen-oxyacetic acid (2,4-D) resulted in the formation of embryogenic calli. High-frequency (80%) somatic embryogenesis from small cell clusters (300-400 micrometer) was observed when the cultures were initially maintained in liquid medium with reduced levels of 2,4-D (0.25 mg l-1), followed by transfer to regeneration medium. Direct plating of these small clusters on regeneration medium or transfer to liquid regeneration medium containing kinetin and 6-benzylaminopurine resulted in the development of mature somatic embryos and plantlets. The regenerants developed to maturity and were all phenotypically and cytologically norma.</dc:description>
        <dc:publisher>Springer Verlag</dc:publisher>
        <dc:date>1999</dc:date>
        <dc:type>Article</dc:type>
        <dc:type>PeerReviewed</dc:type>
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        <dc:language>en</dc:language>
        <dc:identifier>http://oar.icrisat.org/1824/1/PlCellRep18%28424-428_1999.pdf</dc:identifier>
        <dc:identifier>  Mythili, P K and Seetharama, N and Reddy, V D  (1999) Plant regeneration from embryogenic cell suspension cultures of wild sorghum (Sorghum dimidiatum Stapf.).  Plant Cell Reports, 18 (5).  pp. 424-428.      </dc:identifier>
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