Acetosyringone promotes high efficiency transformation of Arabidopsis thaliana explants by Agrobacterium tumefaciens
- 1 January 1987
- journal article
- conference paper
- Published by Springer Nature in Plant Molecular Biology
- Vol. 8 (4) , 291-298
- https://doi.org/10.1007/bf00021308
Abstract
High frequency transformation of Arabidopsis thaliana leaf explants has been obtained using a disarmed Ti plasmid containing the coding region of a neomycin phosphotransferase gene (NPT II) as a selectable marker. The rate of transformation ranged from 55 to 63 percent when acetosyringone (AS), a natural wound response molecule, was added to an Agrobacterium tumefaciens culture prior to incubation with leaf segments. Without acetosyringone, the transformation rate was approximately 2 to 3 percent. Calli resistant to G418 were regenerated into mature flowering plants in the presence of 10 μg/ml G418. Southern analysis and neomycin phosphotransferase assays confirmed the insertion and expression of the NPT II gene in regenerated Arabidopsis plants.Keywords
This publication has 29 references indexed in Scilit:
- The mutants of ArabidopsisTrends in Genetics, 1986
- Transformation of Tobacco, Tomato, Potato, and Arabidopsis thaliana Using a Binary Ti Vector SystemPlant Physiology, 1986
- Characterization of the genome of Arabidopsis thalianaJournal of Molecular Biology, 1986
- Temporal requirement for phytohormone balance in the control of organogenesis in vitroDevelopmental Biology, 1985
- Arabidopsis thaliana and Plant Molecular GeneticsScience, 1985
- A Simple and General Method for Transferring Genes into PlantsScience, 1985
- Involvement of circular intermediates in the transfer of T-DNA from Agrobacterium tumefaciens to plant cellsNature, 1985
- Right 25 by terminus sequence of the nopaline t-DNA is essential for and determines direction of DNA transfer from Agrobacterium to the plant genomeCell, 1984
- Induction and in vitro culture of Arabidopsis Thaliana crown gall tumoursPlant Science Letters, 1979
- A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue CulturesPhysiologia Plantarum, 1962