Literature DB >> 3430596

Characterization of Agrobacterium tumefaciens virulence proteins induced by the plant factor acetosyringone.

P Engström1, P Zambryski, M Van Montagu, S Stachel.   

Abstract

The Ti plasmid virulence (vir) loci encode functions essential for the transfer of the T-DNA element from Agrobacterium tumefaciens to plant cells. The expression of these loci is specifically signaled by plant phenolics such as acetosyringone. Here, we characterize the protein products that are induced in Agrobacterium grown in the presence of acetosyringone. More than 10 to 15 proteins are induced in strains harboring different Ti plasmids. Two general classes of acetosyringone-induced proteins are observed, encoded either within or outside the vir region. Synthesis of both classes of proteins requires acetosyringone and the products of the vir regulatory genes A and G. Those proteins encoded outside the vir region define a novel category of proteins, the virulence-related proteins, which are both chromosomally and Ti plasmid-encoded. The molecular weight and subcellular localization of several pTiA6 vir-induced proteins are identified. The most abundant induced protein has a molecular weight of 65,000, and is the single product of the virE locus; this protein distributes into both cell envelope and soluble fractions. Three proteins with molecular weights of approximately 33,000, 80,000 and 25,000 fractionate with the cell envelope and are encoded by genes within the 5' half of the virB locus. The envelope localization of the virB proteins suggests that they play a role in directing T-DNA transfer events that occur at the bacterial surface.

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Year:  1987        PMID: 3430596     DOI: 10.1016/0022-2836(87)90470-0

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  46 in total

Review 1.  Two-way chemical signaling in Agrobacterium-plant interactions.

Authors:  S C Winans
Journal:  Microbiol Rev       Date:  1992-03

Review 2.  Unraveling the secret lives of bacteria: use of in vivo expression technology and differential fluorescence induction promoter traps as tools for exploring niche-specific gene expression.

Authors:  Hans Rediers; Paul B Rainey; Jos Vanderleyden; René De Mot
Journal:  Microbiol Mol Biol Rev       Date:  2005-06       Impact factor: 11.056

3.  Identification of different agrobacterium strains isolated from the same forest nursery.

Authors:  M F Michel; A C Brasileiro; C Depierreux; L Otten; F Delmotte; L Jouanin
Journal:  Appl Environ Microbiol       Date:  1990-11       Impact factor: 4.792

Review 4.  Agrobacterium in the genomics age.

Authors:  Stanton B Gelvin
Journal:  Plant Physiol       Date:  2009-05-13       Impact factor: 8.340

5.  Stimulation of Agrobacterium tumefaciens T-DNA transfer by overdrive depends on a flanking sequence but not on helical position with respect to the border repeat.

Authors:  C E Shurvinton; W Ream
Journal:  J Bacteriol       Date:  1991-09       Impact factor: 3.490

6.  High-efficiency Agrobacterium rhizogenes-mediated transformation of heat inducible sHSP18.2-GUS in Nicotiana tabacum.

Authors:  Shih-Cheng Chen; Hui-Wen Liu; Kung-Ta Lee; Takashi Yamakawa
Journal:  Plant Cell Rep       Date:  2006-07-28       Impact factor: 4.570

7.  pSa causes oncogenic suppression of Agrobacterium by inhibiting VirE2 protein export.

Authors:  L Y Lee; S B Gelvin; C I Kado
Journal:  J Bacteriol       Date:  1999-01       Impact factor: 3.490

8.  A nontransformable Triticum monococcum monocotyledonous culture produces the potent Agrobacterium vir-inducing compound ethyl ferulate.

Authors:  E Messens; R Dekeyser; S E Stachel
Journal:  Proc Natl Acad Sci U S A       Date:  1990-06       Impact factor: 11.205

9.  The mating pair formation system of plasmid RP4 defined by RSF1010 mobilization and donor-specific phage propagation.

Authors:  M Lessl; D Balzer; K Weyrauch; E Lanka
Journal:  J Bacteriol       Date:  1993-10       Impact factor: 3.490

10.  Genetic complementation analysis of the Agrobacterium tumefaciens virB operon: virB2 through virB11 are essential virulence genes.

Authors:  B R Berger; P J Christie
Journal:  J Bacteriol       Date:  1994-06       Impact factor: 3.490

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