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  <titleInfo>
    <title>Expression of Foreign Genes in Dunaliella by Electroporation</title>
  </titleInfo>
  <name type="personal">
    <namePart>Sun, Y.</namePart>
  </name>
  <name type="personal">
    <namePart>Yang, Z.</namePart>
  </name>
  <name type="personal">
    <namePart>Gao, X.</namePart>
  </name>
  <name type="personal">
    <namePart>Li, Q.</namePart>
  </name>
  <name type="personal">
    <namePart>Zhang, Q.</namePart>
  </name>
  <name type="personal">
    <namePart>Xu, Z.</namePart>
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  <abstract>An electroporation procedure has been described for introducing plasmid DNA into Dunaliella salina cells. By this procedure, a bulk of plasmid DNA was delivered into the cells and retained for at least 3 d. Reverse transcriptase polymerase chain reaction (RT-PCR)and sequencing analyses indicated that the transcription and pre-mRNA splicing of ble gene (contributing the Zeocin resistance)were detected in the cells as early as 1 h after the electroporation. Individual colonies could retain the resistance to 10 mg/L Zeocin for at least 6 mo. Subsequent Southern blot analysis showed the existence of introduced plasmid DNA inside these colonies. However, most of the cells (approx 90</abstract>
  <subject>
    <topic>DUNALIELLA SALINA</topic>
  </subject>
  <subject>
    <topic>ELECTROPORATION</topic>
  </subject>
  <subject>
    <topic>BLE GENE</topic>
  </subject>
  <subject>
    <topic>ZEOCIN</topic>
  </subject>
  <subject>
    <topic>EPISOMAL DNA</topic>
  </subject>
  <relatedItem type="series">
    <titleInfo>
      <title>Molecular Biotechnology, 30, p.185-192, 2005</title>
    </titleInfo>
  </relatedItem>
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