Literature DB >> 11446302

Can simultaneous inhibition of seedling growth and stimulation of rhizosphere bacterial populations provide evidence for phytotoxin transfer from plant residues in the bulk soil to the rhizosphere of sensitive species?

K Staman1, U Blum, F Louws, D Robertson.   

Abstract

In order to demonstrate that allelopathic interactions are occurring, one must, among other things, demonstrate that putative phytotoxins move from plant residues on or in the soil, the source, through the bulk soil to the root surface, a sink, by way of the rhizosphere. We hypothesized that the incorporation of phytotoxic plant residues into the soil would result in a simultaneous inhibition of seedling growth and a stimulation of the rhizosphere bacterial community that could utilize the putative phytotoxins as a sole carbon source. If true and consistently expressed, such as relationship would provide a means of establishing the transfer of phytotoxins from residue in the soil to the rhizosphere of a sensitive species under field conditions. Presently, direct evidence for such transfer is lacking. To test this hypothesis, cucumber seedlings were grown in soil containing various concentrations of wheat or sunflower tissue. Both tissue types contain phenolic acids, which have been implicated as allelopathic phytotoxins. The level of phytotoxicity of the plant tissues was determined by the inhibition of pigweed seedling emergence and cucumber seedling leaf area expansion. The stimulation of cucumber seedling rhizosphere bacterial communities was determined by the plate dilution frequency technique using a medium containing phenolic acids as the sole carbon source. When sunflower tissue was incorporated into autoclaved (to reduce the initial microbial populations) soil, a simultaneous inhibition of cucumber seedling growth and stimulation of the community of phenolic acid utilizing rhizosphere bacteria occurred. Thus, it was possible to observe simultaneous inhibition of cucumber seedlings and stimulation of phenolic acid utilizing rhizosphere bacteria, and therefore provide indirect evidence of phenolic acid transfer from plant residues in the soil to the root surface. However, the simultaneous responses were not sufficiently consistent to be used as a field screening tool but were dependent upon the levels of phenolic acids and the bulk soil and rhizosphere microbial populations present in the soil. It is possible that this screening procedure may be useful for phytotoxins that are more unique than phenolic acids.

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Year:  2001        PMID: 11446302     DOI: 10.1023/a:1010362221390

Source DB:  PubMed          Journal:  J Chem Ecol        ISSN: 0098-0331            Impact factor:   2.626


  14 in total

1.  Inhibition of pitted morning glory (Ipomoea lacunosa L.) and certain other weed species by phytotoxic components of wheat (Triticum aestivum L.) straw.

Authors:  R A Liebl; A D Worsham
Journal:  J Chem Ecol       Date:  1983-08       Impact factor: 2.626

2.  On the variability of chlorogenic acid concentration.

Authors:  Roger Del Moral
Journal:  Oecologia       Date:  1972-09       Impact factor: 3.225

3.  Stress modification of allelopathy ofHelianthus annuus L. debris on seedling biomass production ofAmaranthus retroflexus L.

Authors:  A B Hall; U Blum; R C Fites
Journal:  J Chem Ecol       Date:  1983-08       Impact factor: 2.626

4.  Plate-dilution frequency technique for assay of microbial ecology.

Authors:  R F Harris; L E Sommers
Journal:  Appl Microbiol       Date:  1968-02

5.  Phytotoxicity of acetic acid produced in the anaerobic decomposition of wheat straw.

Authors:  J M Lynch
Journal:  J Appl Bacteriol       Date:  1977-02

Review 6.  Benzoxazinones: cyclic hydroxamic acids found in plants.

Authors:  J I Willard; D Penner
Journal:  Residue Rev       Date:  1976

7.  Relationships between chemical structure and inhibitory activity of C6 through C 9 volatiles emitted by plant residues.

Authors:  J M Bradow
Journal:  J Chem Ecol       Date:  1991-11       Impact factor: 2.626

8.  Mechanism by which noninhibitory concentrations of glucose increase inhibitory activity ofp-coumaric acid on morning-glory seedling biomass accumulation.

Authors:  K J Pue; U Blum; T M Gerig; S R Shafer
Journal:  J Chem Ecol       Date:  1995-06       Impact factor: 2.626

9.  Modification of allelopathic effects ofp-coumaric acid on morning-glory seedling biomass by glucose, methionine, and nitrate.

Authors:  U Blum; T M Gerig; A D Worsham; L D King
Journal:  J Chem Ecol       Date:  1993-12       Impact factor: 2.626

10.  Effects of mixtures of phenolic acids on leaf area expansion of cucumber seedlings grown in different pH portsmouth A1 soil materials.

Authors:  U Blum; T M Gerig; S B Weed
Journal:  J Chem Ecol       Date:  1989-10       Impact factor: 2.626

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  3 in total

Review 1.  Phenolic acids act as signaling molecules in plant-microbe symbioses.

Authors:  Santi M Mandal; Dipjyoti Chakraborty; Satyahari Dey
Journal:  Plant Signal Behav       Date:  2010-04-07

2.  Root-secreted allelochemical in the noxious weed Phragmites australis deploys a reactive oxygen species response and microtubule assembly disruption to execute rhizotoxicity.

Authors:  Thimmaraju Rudrappa; Justin Bonsall; John L Gallagher; Denise M Seliskar; Harsh P Bais
Journal:  J Chem Ecol       Date:  2007-10       Impact factor: 2.626

3.  Production of indole acetic acid by Pseudomonas sp.: effect of coinoculation with Mesorhizobium sp. Cicer on nodulation and plant growth of chickpea (Cicer arietinum).

Authors:  Deepak K Malik; Satyavir S Sindhu
Journal:  Physiol Mol Biol Plants       Date:  2011-01-13
  3 in total

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