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   <subfield code="a">Production of herbicide-resistant transgenic sweet potato plants through Agrobacterium tumefaciens method</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Hye Choi, Thummala Chandrasekhar, Hyo-Yeon Lee, Kyung-Moon Kim]</subfield>
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   <subfield code="a">Transgenic herbicide-resistant sweet potato plants [Ipomoea batatas (L.) Lam.] were produced through Agrobacterium-mediated transformation system. Embryogenic calli derived from shoot apical meristems were infected with Agrobacterium tumefaciens strain EHA105 harboring the pCAMBIA3301 vector containing the bar gene encoding phosphinothricin N-acetyltransferase (PAT) and the gusA gene encoding β-glucuronidase (GUS). The PPT-resistant calli and plants were selected with 5 and 2.5mgl−1 PPT, respectively. Soil-grown plants were obtained 28-36weeks after Agrobacterium-mediated transformation. Genetic transformation of the regenerated plants growing under selection was demonstrated by PCR, and Southern blot analysis revealed that one to three copies of the transgene were integrated into the plant genome of each transgenic plant. Expression of the bar gene in transgenic plants was confirmed by RT-PCR and application of herbicide. Transgenic plants sprayed with Basta containing 900mgl−1 of glufosinate ammonium remained green and healthy. The transformation frequency was 2.8% determined by herbicide application which was high when compared to our previous biolistic method. In addition, possible problems with multiple copies of transgene were also discussed. We therefore report here a successful and reliable Agrobacterium-mediated transformation of the bar gene conferring herbicide-resistance and this method may be useful for routine transformation and has the potential to develop new varieties of sweet potato with several important genes for value-added traits such as enhanced tolerance to the herbicide Basta.</subfield>
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   <subfield code="a">Springer Science+Business Media B.V., 2007</subfield>
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   <subfield code="a">Agrobacterium tumefaciens</subfield>
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   <subfield code="a">bar</subfield>
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   <subfield code="a">Basta</subfield>
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   <subfield code="a">Ipomoea batatas</subfield>
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   <subfield code="a">Transformation</subfield>
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   <subfield code="a">AS : Acetosyringone</subfield>
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   <subfield code="a">BAP : 6-Benzylaminopurine</subfield>
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   <subfield code="a">CPM : Callus-proliferating medium</subfield>
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   <subfield code="a">2,4-D : 2,4-Dichlorophenoxyacetic acid</subfield>
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   <subfield code="a">GUS : β-Glucuronidase</subfield>
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   <subfield code="a">MES : 2-(N-morpholino) ethanesulfonic acid</subfield>
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   <subfield code="a">MS : Murashige and Skoog (1962)</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">PAT : Phosphinothricin N-acetyltransferase</subfield>
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   <subfield code="a">PPT : Phosphinothricin</subfield>
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   <subfield code="a">RT-PCR : Reverse transcriptase-PCR</subfield>
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   <subfield code="a">YEP : Yeast extract and peptone</subfield>
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   <subfield code="t">Plant Cell, Tissue and Organ Culture</subfield>
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   <subfield code="g">91/3(2007-12-01), 235-242</subfield>
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