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   <subfield code="a">Agrobacterium -mediated high frequency transformation in dwarf recalcitrant rice cultivars</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[P. Kant, S. Kant, R. Jain, V. Chaudhury]</subfield>
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   <subfield code="a">The Agrobacterium-mediated transformation was done in rice (Oryza sativa L. var. indica) cv. HKR126 and elite cross-bred cv. Pusa Basmati1 (PB1), using strain LBA4404 containing pCAMBIA1300 cloned with gene cassettes; potato proteinase inhibitor and Bacillus thuringiensis endotoxin (plasmid JDW53) or mannitol-1-phosphate dehydrogenase (plasmid RKJ108). Co-cultivation with scutellar-calli derived from mature seeds showed stable and highly efficient transformation. In cvs. HKR126 and PB1, 35 % and 41 % of hygromycin resistant calli were obtained. The transformation efficiency in PB1 (22.0 %) was much higher than in HKR126 (12.5 %). Similarly, PB1 had higher plant regeneration efficiency than HKR126. The shoots regenerated per callus were, 3-4 in HKR126 and 5-6 in PB1. The transformation efficiency with pRKJ108 (18.6 %) was higher than pJDW53 (15.9 %). Polymerase chain reaction (PCR) analysis showed the presence of transgenes in regenerated transgenic plants of both cultivars.</subfield>
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   <subfield code="a">Institute of Experimental Botany, ASCR, 2007</subfield>
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   <subfield code="a">Bacillus thuringiensis endotoxin</subfield>
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   <subfield code="a">napthaleneacetic acid</subfield>
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   <subfield code="a">2,4-D : 2,4-dichlorophenoxyacetic acid</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">MS medium : Murashige and Skoog's medium</subfield>
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   <subfield code="a">NAA : 1-napthaleneacetic acid</subfield>
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   <subfield code="a">Kant</subfield>
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   <subfield code="u">J. Blaustein Institutes for Desert Research, Department of Dryland Biotechnologies, Ben-Gurion University of the Negev, 84990, Midreshet Ben-Gurion, Israel</subfield>
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