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Norway spruce (Picea abies) genetic transformation with modified Cry3A gene of Bacillus thuringiensis
J. Bříza, D. Pavingerová, J. Vlasák, H. Niedermeierová,
Jazyk angličtina Země Polsko
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Directory of Open Access Journals
od 2003
Free Medical Journals
od 1977 do 2018
ROAD: Directory of Open Access Scholarly Resources
od 1997
PubMed
23888296
Knihovny.cz E-zdroje
- MeSH
- Agrobacterium tumefaciens genetika MeSH
- Bacillus thuringiensis genetika MeSH
- bakteriální proteiny genetika MeSH
- endotoxiny genetika MeSH
- genetická transkripce MeSH
- genetické vektory MeSH
- geneticky modifikované rostliny * MeSH
- hemolyziny genetika MeSH
- jedle embryologie genetika MeSH
- promotorové oblasti (genetika) MeSH
- semena rostlinná genetika růst a vývoj MeSH
- somatická embryogeneze rostlin MeSH
- transformace genetická MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Modified versions of the Cry3A gene of Bacillus thuringiensis (Bt) were transferred into Norway spruce (Picea abies). Both the biolistic approach and Agrobacterium tumefaciens mediated procedure were employed for transformation of embryogenic tissue (ET) cultures. The latter method proved to be more efficient yielding 70 transgenic embryogenic tissue lines compared with 18 lines obtained by biolistics. The modified Cry3A genes were driven by a 35S promoter and the nptII screenable selection marker gene was used in all vectors. The transgenic ETs were molecularly characterized and converted into mature somatic embryos. Germinating embryos formed plantlets which were finally planted into perlite and their Cry3A gene transcription activities were demonstrated by RT-PCR.
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- $a Modified versions of the Cry3A gene of Bacillus thuringiensis (Bt) were transferred into Norway spruce (Picea abies). Both the biolistic approach and Agrobacterium tumefaciens mediated procedure were employed for transformation of embryogenic tissue (ET) cultures. The latter method proved to be more efficient yielding 70 transgenic embryogenic tissue lines compared with 18 lines obtained by biolistics. The modified Cry3A genes were driven by a 35S promoter and the nptII screenable selection marker gene was used in all vectors. The transgenic ETs were molecularly characterized and converted into mature somatic embryos. Germinating embryos formed plantlets which were finally planted into perlite and their Cry3A gene transcription activities were demonstrated by RT-PCR.
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