Abstract

Agrobacterium was identified as the agent causing the plant tumor, crown gall over 100 years ago. Since then, studies have resulted in many surprising observations. Armin Braun demonstrated that Agrobacterium infected cells had unusual nutritional properties, and that the bacterium was necessary to start the infection but not for continued tumor development. He developed the concept of a tumor inducing principle (TIP), the factor that actually caused the disease. Thirty years later the TIP was shown to be a piece of a tumor inducing (Ti) plasmid excised by an endonuclease. In the next 20 years, most of the key features of the disease were described. The single-strand DNA (T-DNA) with the endonuclease attached is transferred through a type IV secretion system into the host cell where it is likely coated and protected from nucleases by a bacterial secreted protein to form the T-complex. A nuclear localization signal in the endonuclease guides the transferred strand (T-strand), into the nucleus where it is integrated randomly into the host chromosome. Other secreted proteins likely aid in uncoating the T-complex. The T-DNA encodes enzymes of auxin, cytokinin, and opine synthesis, the latter a food source for Agrobacterium. The genes associated with T-strand formation and transfer (vir) map to the Ti plasmid and are only expressed when the bacteria are in close association with a plant. Plant signals are recognized by a two-component regulatory system which activates vir genes. Chromosomal genes with pleiotropic functions also play important roles in plant transformation. The data now explain Braun’s old observations and also explain why Agrobacterium is nature’s genetic engineer. Any DNA inserted between the border sequences which define the T-DNA will be transferred and integrated into host cells. Thus, Agrobacterium has become the major vector in plant genetic engineering.

Highlights

  • After analyzing 124 insertions for tumor formation and beta-galactosidase in bacteria grown in the presence of plant cells, they divided the vir region into six complementation groups: virA, virB, virC, virD, virE, and virG (Stachel and Nester, 1986)

  • All associated with the wound site on a plant are important in vir gene induction. These include a number of different phenolic compounds, a variety of monosaccharides which are components of plant cell walls and act through a binding protein encoded on the bacterial chromosome (ChvE) and acidic conditions which are required at several steps in the induction process

  • SUMMARY It is unusual that the study of a single organism can reveal a unique biological system, contribute to an understanding of fundamental biological principles and lead to the development of an entirely new industry

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Summary

Introduction

After analyzing 124 insertions for tumor formation and beta-galactosidase in bacteria grown in the presence of plant cells, they divided the vir region into six complementation groups: virA, virB, virC, virD, virE, and virG (Stachel and Nester, 1986). These include a number of different phenolic compounds, a variety of monosaccharides which are components of plant cell walls and act through a binding protein encoded on the bacterial chromosome (ChvE) and acidic conditions which are required at several steps in the induction process.

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