Cited by 67Plant-Microbe Interactions and ImmunityMicrobial bioremediation and biosurfactantsBacterial Genetics and Biotechnology

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Functional Characterization of the Bacterial iac Genes for Degradation of the Plant Hormone Indole-3-Acetic Acid

Scott, Jeness C., Greenhut, Isaac V., Leveau, Johan H. J.·2013·Journal of Chemical Ecology

Abstract

Pseudomonas putida 1290 is a model organism for the study of bacterial degradation of the plant hormone indole-3-acetic acid (IAA). This property is encoded by the iac gene cluster. Insertional inactivation and/or deletion of individual iac genes and heterologous expression of the gene cluster in Escherichia coli were combined with mass spectrometry to demonstrate that iac-based degradation of IAA is likely to involve 2-hydroxy-IAA, 3-hydroxy-2-oxo-IAA, and catechol as intermediates. The first gene of the cluster, iacA encodes for the first step in the pathway, and also can convert indole to indoxyl to produce the blue pigment indigo. Transcriptional profiling of iac genes in P. putida 1290 revealed that they were induced in the presence of IAA. Based on results with an iacR knockout, we propose that this gene codes for a repressor of iacA expression and that exposure to IAA relieves this repression. Transformation of P. putida KT2440 (which cannot degrade IAA) with the iac gene cluster conferred the ability to grow on IAA as a sole source of carbon and energy, but not the ability to chemotaxi towards IAA. We could show such tactic response for P. putida 1290, thus representing the first demonstration of bacterial chemotaxis towards IAA. We discuss the ecological significance of our findings, and specifically the following question: under what circumstances do bacteria with the ability to degrade, recognize, and move towards IAA have a selective advantage?

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1007/s10886-013-0324-x

Cites

1 of 1 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • The reduction in IAA can be explained by consumption of the acid by the yeast in the stationary phase of cell growth.

    “This can be explained by the consumption of the acid by the yeast in the stationary phase of cell growth, as reported in the literature regarding studies on microorganisms that oxidize IAA (Faure et al. 2009; Scott et al. 2013; Zuniga et al. 2013).”

    From Phosphate solubilization and indole acetic acid production by rhizosphere yeast Torulaspora globosa: improvement of culture conditions for better performance in vitro (2022) · cites this paper as Scott et al. 2013

    The Results (p. 7) show that IAA fell to near the detection limit in cultures of E. coli carrying the full iac gene cluster, supporting microbial degradation of IAA. The study concerns bacteria, however; it does not establish that yeast consumes IAA during stationary-phase growth. (LLM, conf=0.88)

    Experimental — accuracy not yet measured

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Flagged first, then by citations

Research works printed but not linked: 31

  1. Alemayehu D, Gordon LM, O’Mahony MM, O’Leary ND, Dobson AD (2004) Cloning and functional analysis by gene disruption of a novel gene involved in indigo production and fluoranthene metabolism in Pseudomonas alcaligenes PA-10. FEMS Microbiol Lett 239:285–293 · DOI
  2. Cho M, Lee OR, Ganguly A, Cho HT (2007) Auxin-signaling: short and long. J Plant Biol 50:79–89 · DOI
  3. Dodd IC, Zinovkina NY, Safronova VI, Belimov AA (2010) Rhizobacterial mediation of plant hormone status. Annal Appl Biol 157:361–379 · DOI
  4. Enya J, Shinohara H, Yoshida S, Negishi TTH, Suyama K, Tsushima S (2007) Culturable leaf-associated bacteria on tomato plants and their potential as biological control agents. Microb Ecol 53:524–536 · DOI
  5. Faure D, Vereecke D, Leveau JHJ (2009) Molecular communication in the rhizosphere. Plant Soil 321:279–303 · DOI · Paper page
  6. Fiehn O, Wohlgemuth G, Scholz M (2005) Setup and annotation of metabolomic experiments by integrating biological and mass spectrometric metadata. Data Integr Life Sci Proc 3615:224–239 · DOI
  7. Fiehn O, Wohlgemuth G, Scholz M, Kind T, Lee DY, Lu Y, Moon S, Nikolau B (2008) Quality control for plant metabolomics: reporting MSI-compliant studies. Plant J 53:691–704 · DOI
  8. Garcia-Gomez E, Gonzalez-Pedrajo B, Camacho-Arroyo I (2013) Role of sex steroid hormones in bacterial-host interactions. Biomed Res Int 2013:928290 · DOI
  9. Glickmann E, Dessaux Y (1995) A critical examination of the specificity of the Salkowski reagent for indolic compounds produced by phytopathogenic bacteria. Appl Environ Microbiol 61:793–796 · DOI
  10. Gray WM (2004) Hormonal regulation of plant growth and development. PLoS Biol 2:E311 · DOI
  11. Harwood CS, Nichols NN, Kim MK, Ditty JL, Parales RE (1994) Identification of the pcaRKF gene cluster from Pseudomonas putida: involvement in chemotaxis, biodegradation, and transport of 4-hydroxybenzoate. J Bacteriol 176:6479–6488 · DOI
  12. Heeb S, Itoh Y, Nishijyo T, Schnider U, Keel C, Wade J, Walsh U, O’Gara F, Haas D (2000) Small, stable shuttle vectors based on the minimal pVS1 replicon for use in gram-negative, plant-associated bacteria. Mol Plant Microbe Interact 13:232–237 · DOI
  13. Jensen JB, Egsgaard H, Vanonckelen H, Jochimsen BU (1995) Catabolism of indole-3-acetic acid and 4-chloroindole-3-acetic and 5-chloroindole-3-acetic acid in Bradyrhizobium japonicum. J Bacteriol 177:5762–5766 · DOI
  14. King EO, Ward MK, Raney DE (1954) Two simple media for the demonstration of pyocyanin and fluorescein. J Lab Clin Med 44:301–307
  15. Krell T, Lacal J, Munoz-Martinez F, Reyes-Darias JA, Cadirci BH, Garcia-Fontana C, Ramos JL (2011) Diversity at its best: bacterial taxis. Environ Microbiol 13:1115–1124 · DOI
  16. Lee JT, Jayaraman A, Wood TK (2007) Indole is an inter-species biofilm signal mediated by SdiA. BMC Microbiol 7:15 · DOI
  17. Leveau JHJ, Gerards S (2008) Discovery of a bacterial gene cluster for catabolism of the plant hormone indole 3-acetic acid. FEMS Microbiol Ecol 65:238–250 · DOI
  18. Lin GH, Chen HP, Huang JH, Liu TT, Lin TK, Wang SJ, Tseng CH, Shu HY (2012) Identification and characterization of an indigo-producing oxygenase involved in indole 3-acetic acid utilization by Acinetobacter baumannii. A Van Leeuw J Microb 101:881–890 · DOI
  19. Ljung K, Hull AK, Kowalczyk M, Marchant A, Celenza J, Cohen JD, Sandberg G (2002) Biosynthesis, conjugation, catabolism and homeostasis of indole-3-acetic acid in Arabidopsis thaliana. Plant Mol Biol 50:309–332 · DOI
  20. Miller WG, Leveau JHJ, Lindow SE (2000) Improved gfp and inaZ broad-host-range promoter-probe vectors. Mol Plant Microbe Interact 13:1243–1250 · DOI
  21. Monier JM, Lindow SE (2004) Frequency, size, and localization of bacterial aggregates on bean leaf surfaces. Appl Environ Microbiol 70:346–355 · DOI
  22. Nelson KE, Weinel C, Paulsen IT, Dodson RJ, Hilbert H, dos Santos VAPM, Fouts DE, Gill SR, Pop M, Holmes M et al (2002) Complete genome sequence and comparative analysis of the metabolically versatile Pseudomonas putida KT2440. Environ Microbiol 4:799–808 · DOI
  23. Ostin A, Kowalyczk M, Bhalerao RP, Sandberg G (1998) Metabolism of indole-3-acetic acid in Arabidopsis. Plant Physiol 118:285–296 · DOI
  24. Parales RE, Luu RA, Chen GY, Liu X, Wu V, Lin P, Hughes JG, Nesteryuk V, Parales JV, Ditty JL (2013) Pseudomonas putida F1 has multiple chemoreceptors with overlapping specificity for organic acids. Microbiology Published online ahead of print(doi: 10.1099/mic.0.065698-0 ) · DOI
  25. Patten CL, Glick BR (1996) Bacterial biosynthesis on indole-3-acetic acid. Can J Microbiol 42:207–220 · DOI
  26. Perera IC, Grove A (2010) Molecular mechanisms of ligand-mediated attenuation of DNA binding by MarR family transcriptional regulators. J Mol Cell Biol 2:243–254 · DOI
  27. Pfaffl MW (2001) A new mathematical model for relative quantification in real-time RT-PCR. NAR 29:e45 · DOI · Paper page
  28. Providenti MA, Wyndham RC (2001) Identification and functional characterization of CbaR, a MarR-Like modulator of the cbaABC-encoded chlorobenzoate catabolism pathway. Appl Environ Microbiol 67:3530–3541 · DOI
  29. Reinecke DM, Bandurski RS (1981) Metabolic Conversion of C-14-Labeled Indole-3-Acetic-Acid to C-14-Labeled Oxindole-3-Acetic Acid. Biochem Bioph Res Co 103:429–433 · DOI
  30. Spaepen S, Vanderleyden J, Remans R (2007) Indole-3-acetic acid in microbial and microorganism-plant signaling. FEMS Microbiol Rev 31:425–448 · DOI · Paper page
  31. Stein SE (1999) An integrated method for spectrum extraction and compound identification from gas chromatography/mass spectrometry data. J Am Soc Mass Spectr 10:770–781 · DOI

Cited by

Sorted by citations

Metadata

Authors
Scott, J. C., Greenhut, I. V., & Leveau, J. H. J.
Affiliations
University of California, Davis (US)
Corresponding author
Leveau, Johan H. J.
Venue
Journal of Chemical Ecology
Published
2013-07
Volume
39
Issue
7
Pages
942-951
ISSN
  • 0098-0331 (ISSN-L)
  • 1573-1561
OpenAlex
W2097385676
Cited by
67
References
1
Citations by year
2026: 2 · 2025: 9 · 2024: 7 · 2023: 6 · 2022: 9 · 2021: 7 · 2020: 9 · 2019: 4 · 2018: 3 · 2017: 2 · 2016: 1 · 2015: 3 · 2014: 5
FWCI
3.62
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Chemical Ecology (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • U.S. Department of Agriculture
  • University of California, Davis
Topics
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant-Microbe Interactions and Immunity
  • Physical Sciences › Environmental Science › Pollution › Microbial bioremediation and biosurfactants
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
Keywords
indole-3-acetic acid, Pseudomonas putida, catechol, indigo biosynthesis, indoxyl, transcriptional regulation, chemotaxis, plant growth-promoting bacteria
MeSH terms
Chemotaxis, Escherichia coli, Genes, Bacterial, Indoleacetic Acids, Phenotype, Plasmids, Gene Expression, Pseudomonas putida

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review