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Gene Review

cheD  -  methyl-accepting chemotaxis protein

Agrobacterium fabrum str. C58

 
 
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Disease relevance of cheD

  • Like homologous sugar-binding proteins in Escherichia coli, ChvE was required for chemotaxis toward galactose and several other sugars [1].
  • Swimming against the tide: chemotaxis in Agrobacterium [2].
  • Characterization of a sugar-binding protein from Azospirillum brasilense mediating chemotaxis to and uptake of sugars [3].
 

High impact information on cheD

  • A chromosomally-determined chemotaxis system causes the bacterium to be attracted into the rhizosphere by chemoattractants in plant exudates [2].
  • Chemotaxis in bacteria is an excellent model for signal transduction processes [2].
  • The protein, designated as SbpA (sugar binding protein A), is involved in the uptake of D-galactose and functions in the chemotaxis of A. brasilense towards several sugars, including D-galactose, L-arabinose and D-fucose [3].
  • Downstream of traS is a gene encoding a truncated, defective chemoreceptor whose expression abolished chemotaxis [4].
  • A. tumefaciens C58C1 containing Ti-plasmids with Tn5 insertions in virB, C, D or E exhibited marked chemotaxis towards acetosyringone [5].
 

Chemical compound and disease context of cheD

 

Biological context of cheD

 

Associations of cheD with chemical compounds

  • We have found that R. meliloti RCR2011 exhibits positive chemotaxis towards luteolin [11].
  • Insertion mutations in the palK and palE genes showed the necessity of these genes for bacterial growth and chemotaxis with palatinose as the carbon source, but no inhibition of tumorigenesis was observed [12].
  • The acc locus from the Ti plasmid pTiC58 confers utilization of and chemotaxis toward agrocinopines A and B (A+B), as well as susceptibility to a highly specific antiagrobacterial antibiotic, agrocin 84 [13].
  • The presence of naringenin but not apigenin abolished chemotaxis of R. meliloti towards luteolin [11].
  • The determinants for chemotaxis to these opines were localized to the regions of the octopine- and nopaline-type Ti plasmids coding for transport and catabolism of that opine [14].

References

  1. Sugars induce the Agrobacterium virulence genes through a periplasmic binding protein and a transmembrane signal protein. Cangelosi, G.A., Ankenbauer, R.G., Nester, E.W. Proc. Natl. Acad. Sci. U.S.A. (1990) [Pubmed]
  2. Swimming against the tide: chemotaxis in Agrobacterium. Shaw, C.H. Bioessays (1991) [Pubmed]
  3. Characterization of a sugar-binding protein from Azospirillum brasilense mediating chemotaxis to and uptake of sugars. Van Bastelaere, E., Lambrecht, M., Vermeiren, H., Van Dommelen, A., Keijers, V., Proost, P., Vanderleyden, J. Mol. Microbiol. (1999) [Pubmed]
  4. Activity of the quorum-sensing regulator TraR of Agrobacterium tumefaciens is inhibited by a truncated, dominant defective TraR-like protein. Zhu, J., Winans, S.C. Mol. Microbiol. (1998) [Pubmed]
  5. virA and virG are the Ti-plasmid functions required for chemotaxis of Agrobacterium tumefaciens towards acetosyringone. Shaw, C.H., Ashby, A.M., Brown, A., Royal, C., Loake, G.J., Shaw, C.H. Mol. Microbiol. (1988) [Pubmed]
  6. 3-Ketoglycoside-mediated metabolism of sucrose in E. coli as conferred by genes from Agrobacterium tumefaciens. Schuerman, P.L., Liu, J.S., Mou, H., Dandekar, A.M. Appl. Microbiol. Biotechnol. (1997) [Pubmed]
  7. Ti plasmid-specified chemotaxis of Agrobacterium tumefaciens C58C1 toward vir-inducing phenolic compounds and soluble factors from monocotyledonous and dicotyledonous plants. Ashby, A.M., Watson, M.D., Loake, G.J., Shaw, C.H. J. Bacteriol. (1988) [Pubmed]
  8. Requirement for chemotaxis in pathogenicity of Agrobacterium tumefaciens on roots of soil-grown pea plants. Hawes, M.C., Smith, L.Y. J. Bacteriol. (1989) [Pubmed]
  9. Assessment of bioavailability of soil-sorbed atrazine. Park, J.H., Feng, Y., Ji, P., Voice, T.C., Boyd, S.A. Appl. Environ. Microbiol. (2003) [Pubmed]
  10. A chemotaxis cluster from Agrobacterium tumefaciens. Wright, E.L., Deakin, W.J., Shaw, C.H. Gene (1998) [Pubmed]
  11. Chemotaxis of Rhizobium meliloti to the plant flavone luteolin requires functional nodulation genes. Caetano-Anollés, G., Crist-Estes, D.K., Bauer, W.D. J. Bacteriol. (1988) [Pubmed]
  12. Structural and functional analysis of a putative gene cluster for palatinose transport on the linear chromosome of Agrobacterium tumefaciens MAFF301001. De Costa, D.M., Suzuki, K., Yoshida, K. J. Bacteriol. (2003) [Pubmed]
  13. Characterization of the acc operon from the nopaline-type Ti plasmid pTiC58, which encodes utilization of agrocinopines A and B and susceptibility to agrocin 84. Kim, H., Farrand, S.K. J. Bacteriol. (1997) [Pubmed]
  14. Opine catabolic loci from Agrobacterium plasmids confer chemotaxis to their cognate substrates. Kim, H., Farrand, S.K. Mol. Plant Microbe Interact. (1998) [Pubmed]
 
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