Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2002 Aug;68(8):3795-801.
doi: 10.1128/AEM.68.8.3795-3801.2002.

Role of Pseudomonas putida indoleacetic acid in development of the host plant root system

Affiliations

Role of Pseudomonas putida indoleacetic acid in development of the host plant root system

Cheryl L Patten et al. Appl Environ Microbiol. 2002 Aug.

Abstract

Many plant-associated bacteria synthesize the phytohormone indoleacetic acid (IAA). While IAA produced by phytopathogenic bacteria, mainly by the indoleacetamide pathway, has been implicated in the induction of plant tumors, it is not clear whether IAA synthesized by beneficial bacteria, usually via the indolepyruvic acid pathway, is involved in plant growth promotion. To determine whether bacterial IAA enhances root development in host plants, the ipdc gene that encodes indolepyruvate decarboxylase, a key enzyme in the indolepyruvic acid pathway, was isolated from the plant growth-promoting bacterium Pseudomonas putida GR12-2 and an IAA-deficient mutant constructed by insertional mutagenesis. The canola seedling primary roots from seeds treated with wild-type P. putida GR12-2 were on average 35 to 50% longer than the roots from seeds treated with the IAA-deficient mutant and the roots from uninoculated seeds. In addition, exposing mung bean cuttings to high levels of IAA by soaking them in a suspension of the wild-type strain stimulated the formation of many, very small, adventitious roots. Formation of fewer roots was stimulated by treatment with the IAA-deficient mutant. These results suggest that bacterial IAA plays a major role in the development of the host plant root system.

PubMed Disclaimer

Figures

FIG. 1.
FIG. 1.
Alignment of indolepyruvate decarboxylase (IPDC) amino acid sequences from P. putida GR12-2 (Pp), E. cloacae FERM BP-1529 (Ec), E. herbicola 299R (Eh), and A. brasilense Sp245 (Ab) and pyruvate decarboxylase (PDC) amino acid sequences from Z. mobilis (Zm) and S. cerevisiae (Sc). Asterisks indicate identical amino acids; colons and periods indicate strongly and weakly conserved amino acids, respectively.

References

    1. Abdel-Salam, M. S., and W. Klingmüller. 1987. Transposon Tn5 mutagenesis in Azosprillum lipoferum: isolation of indoleacetic acid mutants. Mol. Gen. Genet. 210:165-170.
    1. Alvarez, R., S. J. Nissen, and E. G. Sutter. 1989. Relationship between indole-3-acetic acid levels in apple (Malus pumila Mill.) rootstocks cultured in vitro and adventitious root formation in the presence of indole-3-butyric acid. Plant Physiol. 89:439-443. - PMC - PubMed
    1. Barbieri, P., and E. Galli. 1993. Effect on wheat root development of inoculation with an Azospirillum brasilense mutant with altered indole-3-acetic acid production. Res. Microbiol. 144:69-75. - PubMed
    1. Beyerler, M., P. Michaux, C. Keel, and D. Haas. 1997. Effect of enhanced production of indole-3-acetic acid by the biological control agent Pseudomonas fluorescens CHA0 on plant growth, p. 310-312. In A. Ogoshi, K. Kobayashi, Y. Homma, F. Kodama, N. Kondo, and S. Akino (ed.), Plant growth-promoting rhizobacteria: present status and future prospects. OECD, Paris, France.
    1. Brandl, M. T., and S. E. Lindow. 1996. Cloning and characterization of a locus encoding an indolepyruvate decarboxylase involved in indole-3-acetic acid synthesis in Erwinia herbicola. Appl. Environ. Microbiol. 62:4121-4128. - PMC - PubMed

Publication types

MeSH terms

Associated data

LinkOut - more resources