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New Approaches to Agrobacterium tumefaciens-Mediated Gene Transfer to Plants

Mustafa Yıldız, Murat Aycan, Sunjung Park

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Abstract

Agrobacterium tumefaciens, a plant pathogen, is commonly used as a vector for the introduction of foreign genes into plants and consequent regeneration of transgenic plants. A. tumefaciens naturally infects the wound sites in dicotyledonous plants and induces diseases known as crown gall. The bacterium has a large plasmid that induces tumor induction, and for this reason, it was named tumor-inducing (Ti) plasmid. The expression of T-DNA genes of Ti-plasmid in plant cells causes the formation of tumors at the infection site. The molecular basis of Agrobacterium-mediated transformation is the stable integration of a DNA sequence (T-DNA) from Ti (tumor-inducing) plasmid of A. tumefaciens into the plant genome. A. tumefaciens-mediated transformation has some advantages compared with direct gene transfer methods such as integration of low copy number of T-DNA into plant genome, stable gene expression, and transformation of large size DNA segments. That is why manipulations of the plant, bacteria and physical conditions have been applied to increase the virulence of bacteria and to increase the transformation efficiency. Preculturing explants before inoculation, modification of temperature and medium pH, addition chemicals to inoculation medium such as acetosyringone, changing bacterial density, and co-cultivation period, and vacuum infiltration have been reported to increase transformation. In this chapter, four new transformation protocols that can be used to increase the transformation efficiency via A. tumefaciens in most plant species are described.

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Agrobacterium tumefaciens, a plant pathogen, is commonly used as a vector for the introduction of foreign genes into plants and consequent regeneration of transgenic plants. A. tumefaciens naturally infects the wound sites in dicotyledonous plants and induces diseases known as crown gall. The bacterium has a large plasmid that induces tumor induction, and for this reason, it was named tumor-inducing (Ti) plasmid. The expression of T-DNA genes of Ti-plasmid in plant cells causes the formation of tumors at the infection site. The molecular basis of Agrobacterium-mediated transformation is the stable integration of a DNA sequence (T-DNA) from Ti (tumor-inducing) plasmid of A. tumefaciens into the plant genome. A. tumefaciens-mediated transformation has some advantages compared with direct gene transfer methods such as integration of low copy number of T-DNA into plant genome, stable gene expression, and transformation of large size DNA segments. That is why manipulations of the plant, bacteria and physical conditions have been applied to increase the virulence of bacteria and to increase the transformation efficiency. Preculturing explants before inoculation, modification of temperature and medium pH, addition chemicals to inoculation medium such as acetosyringone, changing bacterial density, and co-cultivation period, and vacuum infiltration have been reported to increase transformation. In this chapter, four new transformation protocols that can be used to increase the transformation efficiency via A. tumefaciens in most plant species are described.

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Available abstract

Agrobacterium tumefaciens, a plant pathogen, is commonly used as a vector for the introduction of foreign genes into plants and consequent regeneration of transgenic plants. A. tumefaciens naturally infects the wound sites in dicotyledonous plants and induces diseases known as crown gall. The bacterium has a large plasmid that induces tumor induction, and for this reason, it was named tumor-inducing (Ti) plasmid. The expression of T-DNA genes of Ti-plasmid in plant cells causes the formation of tumors at the infection site. The molecular basis of Agrobacterium-mediated transformation is the stable integration of a DNA sequence (T-DNA) from Ti (tumor-inducing) plasmid of A. tumefaciens into the plant genome. A. tumefaciens-mediated transformation has some advantages compared with direct gene transfer methods such as integration of low copy number of T-DNA into plant genome, stable gene expression, and transformation of large size DNA segments. That is why manipulations of the plant, bacteria and physical conditions have been applied to increase the virulence of bacteria and to increase the transformation efficiency. Preculturing explants before inoculation, modification of temperature and medium pH, addition chemicals to inoculation medium such as acetosyringone, changing bacterial density, and co-cultivation period, and vacuum infiltration have been reported to increase transformation. In this chapter, four new transformation protocols that can be used to increase the transformation efficiency via A. tumefaciens in most plant species are described.

Key concepts: Agrobacterium tumefaciens, Transfer DNA, Biology, Ti plasmid, Plasmid, Transformation (genetics), Acetosyringone, Agrobacterium

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