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   <subfield code="a">Agrobacterium -mediated transformation of Cry1C, Cry2A and Cry9C genes into Gossypium hirsutum and plant regeneration</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[X. Guo, C. Huang, S. Jin, S. Liang, Y. Nie, X. Zhang]</subfield>
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   <subfield code="a">Three constructs harbouring novel Bacillus thuringiensis genes (Cry1C, Cry2A, Cry9C) and bar gene were transformed into four upland cotton cultivars, Ekangmian10, Emian22, Coker201 and YZ1 via Agrobacterium-mediated transformation. With the bar gene as a selectable marker, about 84.8 % of resistant calli have been confirmed positive by polymerase chain reaction (PCR) tests, and totally 50 transgenic plants were regenerated. The insertions were verified by means of Southern blotting. Bioassay showed 80 % of the transgenic plantlets generated resistance to both herbicide and insect. We optimized conditions for improving the transformation efficiency. A modified in vitro shoot-tip grafting technique was introduced to help entire transplantation. This result showed that bar gene can replace antibiotic marker genes (ex. npt II gene) used in cotton transformation.</subfield>
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   <subfield code="a">Institute of Experimental Botany, ASCR, 2007</subfield>
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   <subfield code="a">Agrobacterium tumefaciens</subfield>
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   <subfield code="a">AS : acetosyringone</subfield>
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   <subfield code="a">EC : embryogenic callus</subfield>
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   <subfield code="a">npt II : neomycin phosphotransferase</subfield>
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   <subfield code="a">AS : acetosyringone</subfield>
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   <subfield code="a">MSB : Murashige and Skoog (1962) medium with B5 (Gamborg et al. 1968) vitamins</subfield>
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   <subfield code="a">PAT : phosphinothricin acetyltransferase</subfield>
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   <subfield code="t">Biologia Plantarum</subfield>
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