A Bacterial Transgene for Catalase Protects Translation of D1 Protein - AlTaweel, Khaled
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Abstract The pBI101-katE binary vector harboring katE gene derived from Escherichia coli and driven by the promoter of the Rubisco small subunit gene of tomato, rbcS3C, was isolated and molecular characterized then transformed into competent cells using the heat chock method. The binary vector was transformed into competent Agrobacterium tumefaciens cells by two ways; the first way via the tri-parental mating method, and the second one by the electroporation method. The pBI101-katE construct was introduced into a dwarf tomato via Agrobacterium tumefaciens-mediated transformation. And also the…mehr

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Produktbeschreibung
Abstract The pBI101-katE binary vector harboring katE gene derived from Escherichia coli and driven by the promoter of the Rubisco small subunit gene of tomato, rbcS3C, was isolated and molecular characterized then transformed into competent cells using the heat chock method. The binary vector was transformed into competent Agrobacterium tumefaciens cells by two ways; the first way via the tri-parental mating method, and the second one by the electroporation method. The pBI101-katE construct was introduced into a dwarf tomato via Agrobacterium tumefaciens-mediated transformation. And also the construct was introduced into a tobacco by biolistic bombardment.Putative transgenic plants were regenerated and further screened by using PCR. PCR analysis of T1 plants from the independent calli revealed the presence of katE and nptII genes.
Autorenporträt
Khaled AlTaweel, Faculty of Pharmacy, University of Manitoba, Winnipeg, Manitoba, CanadaPhD in Genetic Engineering & Functional Genomics, Osaka Prefecture University, Japan.Research Associate in Gene expression of nerve growth factor .Faculty of Pharmacy, University of Manitoba, Canada