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Abstract
A large number of morphologically normal, fertile, transgenic rice plants were obtained
by co-cultivation of rice tissues with Agrobacterium tumefaciens. The efficiency of
transformation was similar to that obtained by the methods used routinely for transformation
of dicotyledons with the bacterium. Stable integration, expression and inheritance
of transgenes were demonstrated by molecular and genetic analysis of transformants
in the R0, R1 and R2 generations. Sequence analysis revealed that the boundaries of
the T-DNA in transgenic rice plants were essentially identical to those in transgenic
dicotyledons. Calli induced from scutella were very good starting materials. A strain
of A. tumefaciens that carried a so-called 'super-binary' vector gave especially high
frequencies of transformation of various cultivars of japonica rice that included
Koshihikari, which normally shows poor responses in tissue culture.