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   <subfield code="a">Improved genetic transformation protocol for cork oak ( Quercus suber L.)</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Rubén Álvarez, Ricardo Ordás]</subfield>
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   <subfield code="a">An optimized protocol for Agrobacterium tumefaciens-mediated transformation of mature Quercus suberL. embryogenic masses is reported. In this work several variables were tested. Plant genotype, explant type and time elapsed between the last subculture and inoculation, i.e. the explant preculture period, were found to be very important. Interaction between inoculum density and cocultivation period influenced the transformation efficiency as well. A transformation efficiency (i.e. percentage of the inoculated explants that yielded independent transgenic embryogenic lines) of up to 43% was obtained, greatly improving the previously described method for plant transformation of adult-selected cork oak. It was also shown that this protocol could be applied to various genotypes.</subfield>
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   <subfield code="a">Springer Science+Business Media B.V., 2007</subfield>
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   <subfield code="a">Somatic embryogenesis</subfield>
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   <subfield code="a">Tree genetic transformation</subfield>
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   <subfield code="a">GE : number of GUS spots per inoculated explant three weeks after the inoculation</subfield>
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   <subfield code="a">IG : percentage of inoculated explants showing GUS spots three weeks after the inoculation</subfield>
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   <subfield code="a">MSSH : expression-proliferation medium</subfield>
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   <subfield code="a">Npt II : neomycin phosphotransferase gene II</subfield>
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   <subfield code="a">OD600nm : optical density of the bacterial cultures at 600nm</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
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