Literature DB >> 3884588

Strain-specific chemotaxis of Azospirillum spp.

B Reinhold, T Hurek, I Fendrik.   

Abstract

Chemotactic responses of three Azospirillum strains originating from different host plants were compared to examine the possible role of chemotaxis in the adaptation of these bacteria to their respective hosts. The chemotaxis to several sugars, amino acids, and organic acids was determined qualitatively by an agar plate assay and quantitatively by a channeled-chamber technique. High chemotactic ratios, up to 40, were obtained with the latter technique. The chemotactic response did not rely upon the ability of the bacteria to metabolize the attractant. Rather, it depended on the attractant concentration and stereoconfiguration. Chemotaxis was found to be strain specific. Differences were particularly observed between a wheat isolate and strains originating from the C4-pathway plants maize and Leptochloa fusca. In contrast to the other two strains, the wheat isolate was strongly attracted to D-fructose, L-aspartate, citrate, and oxalate. The other strains showed maximal attraction to L-malate. The chemotactic responses to organic acids partially correlate with the exudation of these acids by the respective host plants. Additionally, a heat-labile, high-molecular-weight attractant was found in the root exudates of L. fusca, which specifically attracted the homologous Azospirillum strain. It is proposed that strain-specific chemotaxis probably reflects an adaptation of Azospirillum spp. to the conditions provided by the host plant and contributes to the initiation of the association process.

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Year:  1985        PMID: 3884588      PMCID: PMC218973          DOI: 10.1128/jb.162.1.190-195.1985

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  13 in total

Review 1.  Chemotaxis in bacteria.

Authors:  J Adler
Journal:  Annu Rev Biochem       Date:  1975       Impact factor: 23.643

2.  Chemotaxis of Zoospores for Root Exudates.

Authors:  G A Zentmyer
Journal:  Science       Date:  1961-05-19       Impact factor: 47.728

3.  Control of the receptor for galactose taxis in Salmonella typhimurium.

Authors:  M Fahnestock; D E Koshland
Journal:  J Bacteriol       Date:  1979-02       Impact factor: 3.490

4.  A method for measuring chemotaxis and use of the method to determine optimum conditions for chemotaxis by Escherichia coli.

Authors:  J Adler
Journal:  J Gen Microbiol       Date:  1973-01

5.  Survival value of chemotaxis in mixed cultures.

Authors:  W K Pilgram; F D Williams
Journal:  Can J Microbiol       Date:  1976-12       Impact factor: 2.419

6.  Relationships between Carbon Dioxide, Malate, and Nitrate Accumulation and Reduction in Corn (Zea mays L.) Seedlings.

Authors:  C A Neyra; R H Hageman
Journal:  Plant Physiol       Date:  1976-12       Impact factor: 8.340

7.  Chemotaxis toward sugars in Escherichia coli.

Authors:  J Adler; G L Hazelbauer; M M Dahl
Journal:  J Bacteriol       Date:  1973-09       Impact factor: 3.490

8.  Chemical detection of microbial prey by bacterial predators.

Authors:  I Chet; S Fogel; R Mitchell
Journal:  J Bacteriol       Date:  1971-06       Impact factor: 3.490

9.  Chemotaxis of Rhizobium spp. to a Glycoprotein Produced by Birdsfoot Trefoil Roots.

Authors:  W W Currier; G A Strobel
Journal:  Science       Date:  1977-04-22       Impact factor: 47.728

10.  [Chemotaxis of Azospirillum lipoferum and Azospirillum brasiliensis toward Gramineae root exudates. I. Corn, wheat and sorghum activity].

Authors:  R A Alvarez-Morales; A Lemos-Pastrana
Journal:  Rev Latinoam Microbiol       Date:  1980 Jul-Sep
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  27 in total

1.  Role of a ferredoxin gene cotranscribed with the nifHDK operon in N(2) fixation and nitrogenase "switch-off" of Azoarcus sp. strain BH72.

Authors:  T Egener; D E Martin; A Sarkar; B Reinhold-Hurek
Journal:  J Bacteriol       Date:  2001-06       Impact factor: 3.490

2.  Energy taxis is the dominant behavior in Azospirillum brasilense.

Authors:  G Alexandre; S E Greer; I B Zhulin
Journal:  J Bacteriol       Date:  2000-11       Impact factor: 3.490

Review 3.  Chemotaxis signaling systems in model beneficial plant-bacteria associations.

Authors:  Birgit E Scharf; Michael F Hynes; Gladys M Alexandre
Journal:  Plant Mol Biol       Date:  2016-01-21       Impact factor: 4.076

Review 4.  Use of plant growth-promoting bacteria for biocontrol of plant diseases: principles, mechanisms of action, and future prospects.

Authors:  Stéphane Compant; Brion Duffy; Jerzy Nowak; Christophe Clément; Essaïd Ait Barka
Journal:  Appl Environ Microbiol       Date:  2005-09       Impact factor: 4.792

5.  Cross-reaction of predominant nitrogen-fixing bacteria with enveloped, round bodies in the root interior of kallar grass.

Authors:  B Reinhold; T Hurek; I Fendrik
Journal:  Appl Environ Microbiol       Date:  1987-04       Impact factor: 4.792

6.  Effects of Partial O(2) Pressure, Partial CO(2) Pressure, and Agitation on Growth Kinetics of Azospirillum lipoferum under Fermentor Conditions.

Authors:  E Paul; D Mulard; P Blanc; J Fages; G Goma; A Pareilleux
Journal:  Appl Environ Microbiol       Date:  1990-11       Impact factor: 4.792

7.  Chemotaxis of azospirillum species to aromatic compounds.

Authors:  G Lopez-de-Victoria; C R Lovell
Journal:  Appl Environ Microbiol       Date:  1993-09       Impact factor: 4.792

8.  Root-to-Root Travel of the Beneficial Bacterium Azospirillum brasilense.

Authors:  Y Bashan; G Holguin
Journal:  Appl Environ Microbiol       Date:  1994-06       Impact factor: 4.792

9.  Close association of azospirillum and diazotrophic rods with different root zones of kallar grass.

Authors:  B Reinhold; T Hurek; E G Niemann; I Fendrik
Journal:  Appl Environ Microbiol       Date:  1986-09       Impact factor: 4.792

10.  Root-Zone-Specific Oxygen Tolerance of Azospirillum spp. and Diazotrophic Rods Closely Associated with Kallar Grass.

Authors:  T Hurek; B Reinhold; I Fendrik; E G Niemann
Journal:  Appl Environ Microbiol       Date:  1987-01       Impact factor: 4.792

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