Cited by 286Plant-Microbe Interactions and ImmunityLegume Nitrogen Fixing SymbiosisPlant Molecular Biology Research

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Utilization of the Plant Hormone Indole-3-Acetic Acid for Growth by Pseudomonas putida Strain 1290

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Leveau, Johan H. J., Lindow, Steven E.·2005·Applied and Environmental Microbiology

DOI 10.1128/aem.71.5.2365-2371.2005

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Abstract

We have isolated from plant surfaces several bacteria with the ability to catabolize indole-3-acetic acid (IAA). One of them, isolate 1290, was able to utilize IAA as a sole source of carbon, nitrogen, and energy. The strain was identified by its 16S rRNA sequence as Pseudomonas putida . Activity of the enzyme catechol 1,2-dioxygenase was induced during growth on IAA, suggesting that catechol is an intermediate of the IAA catabolic pathway. This was in agreement with the observation that the oxygen uptake by IAA-grown P. putida 1290 cells was elevated in response to the addition of catechol. The inability of a catR mutant of P. putida 1290 to grow at the expense of IAA also suggests a central role for catechol as an intermediate in IAA metabolism. Besides being able to destroy IAA, strain 1290 was also capable of producing IAA in media supplemented with tryptophan. In root elongation assays, P. putida strain 1290 completely abolished the inhibitory effect of exogenous IAA on the elongation of radish roots. In fact, coinoculation of roots with P. putida 1290 and 1 mM concentration of IAA had a positive effect on root development. In coinoculation experiments on radish roots, strain 1290 was only partially able to alleviate the inhibitory effect of bacteria that in culture overproduce IAA. Our findings imply a biological role for strain 1290 as a sink or recycler of IAA in its association with plants and plant-associated bacteria.

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A model for the lowering of plant ethylene concentrations by plant growth-promoting bacteria
Glick, B. R., Penrose, D. M., & Li, J. (1998) · Journal of Theoretical Biology · doi:10.1006/jtbi.1997.0532 · Cited by 1,466 · cited 1×
“A very similar phenomenon has been reported for a number of rhizobacteria that express the enzyme 1-aminocyclopropane-1-carboxylate deaminase and are capable of lowering the plant endogenous levels of another plant hormone, ethylene (12).”
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Andreae, W. A., and M. W. H. van Ysselstein. 1960. Studies on 3-indoleacetic acid metabolism. VI. 3-Indoleacetic acid uptake and metabolism by pea roots and epicotyls. Plant Physiol.35:225-232. · DOI
Bouillenne-Walrand, M., C. Leyh, and T. Gaspar. 1963. Mise en évidence d'un protecteur de l'acide beta indol-acétique dans un extrait de feuilles de Zea mays L. Bull. Soc. R. Sci. Liege4:262-268.
10.1128/aem.62.11.4121-4128.1996 · DOI
10.1128/AEM.64.9.3256-3263.1998 · DOI
Bruckner, B., and D. Blechschmidt. 1991. The gibberellin fermentation. Crit. Rev. Biotechnol.11:163-192. · DOI
10.1093/nar/gkg039 · DOI
10.3109/10408419509113531 · DOI
Davies, P. J. 1995. The plant hormone concept: concentration, sensitivity, and transport, p. 13-18. In P. J. Davies (ed.), Plant hormones: physiology, biochemistry, and molecular biology. Kluwer Academic Publishers, Dordrecht, The Netherlands.
10.1128/AEM.64.7.2710-2715.1998 · DOI
Dullaart, J. 1970. The bioproduction of indole-3-acetic acid and related compounds in root nodules and roots of Lupinus luteus and by its microbial symbiont. Acta Bot. Neerl.19:573-615. · DOI
10.1128/jb.173.15.4897-4901.1991 · DOI
10.1128/jb.170.5.2367-2373.1988 · DOI
10.1128/aem.61.2.793-796.1995 · DOI
10.1104/pp.115.3.865 · DOI
Hutzinger, O., and T. Kosuge. 1968. Microbial synthesis and degradation of indole 3-acetic acid. III. The isolation and characterization of indole-3-acetyl-epsilon-l-lysine. Biochemistry7:601-605. · DOI
10.1128/AEM.65.6.2685-2690.1999 · DOI
10.1128/jb.177.20.5762-5766.1995 · DOI
10.1046/j.1462-2920.2002.00370.x · DOI
King, E. O., M. K. Ward, and D. E. Raney. 1954. Two simple media for the demonstration of pyocyanin and fluorescein. J. Lab. Clin. Med.44:301-307.
10.1016/S0966-842X(00)01732-7 · DOI
Leveau, J., and S. Lindow. 2001. Appetite of an epiphyte: quantitative monitoring of bacterial sugar consumption in the phyllosphere. Proc. Natl. Acad. Sci. USA6:3446-3453.
10.1128/jb.178.23.6824-6832.1996 · DOI
Libbert, E., and H. Risch. 1969. Interactions between plants and epiphytic bacteria regarding their auxin metabolism. V. Isolation and identification of the IAA-producing and -destroying bacteria from pea plants. Physiol. Plantarum22:51-58. · DOI
Libbert, E., S. Wichner, U. Schiewer, H. Risch, and W. Kaiser. 1966. The influence of epiphytic bacteria on auxin metabolism. Planta68:327-344. · DOI
10.1094/PHYTO.1998.88.11.1149 · DOI
10.1046/j.1364-3703.2003.00178.x · DOI
Mino, Y. 1970. Studies on the destruction of indole-3-acetic acid by a species of Arthrobacter. IV. Decomposition products. Plant Cell Physiol.11:129-138. · DOI
Nielsen, S. V. S., L. A. Egebo, and B. Jochimsen. 1988. Bradyrhizobial indoleacetic acid metabolism and its significance for root nodule development, p. 151-152. In R. Palacios and D. P. S. Verma (ed.), Molecular genetics of plant-microbe interactions. APS Press, St. Paul, Minn.
Nissl, D., and M. H. Zenk. 1969. Evidence against induction of protein synthesis during auxin-induced initial elongation of Avena coleoptiles. Planta89:323-341. · DOI
10.1007/BF00035068 · DOI
10.1139/m96-032 · DOI
10.1128/AEM.68.8.3795-3801.2002 · DOI
10.1046/j.1365-3040.2003.00956.x · DOI
Proctor, M. H. 1958. Bacterial dissimilation of indoleacetic acid: a new route of breakdown of the indole nucleus. Nature181:1345.
10.1073/pnas.0400659101 · DOI · Paper page
Rigaud, T., C. Soutygrosset, R. Raimond, J. P. Mocquard, and P. Juchault. 1991. Feminizing endocytobiosis in the terrestrial crustacean Armadillidium vulgare Latr (Isopoda): recent acquisitions. Endocytobiosis Cell Res.7:259-273.
Riviere, J., and B. Berthier. 1964. Action des microorganismes de la rhizosphère sur la croissance du blé. III. Isolement et identification des bacteries dégradant l'acide indole-3-acétique. Ann. Inst. Pasteur3:250-256.
10.1073/pnas.87.15.5797 · DOI
Ronen, Z., A. Abeliovich, and A. Nejidat. 1997. Biodegradation of alkylpyridines by bacteria isolated from a polluted subsurface. Biodegradation8:357-361. · DOI
Rosendahl, L., and B. U. Jochimsen. 1995. In vitro indole-3-acetic acid uptake in symbiosomes from soybean (Glycine max L) root nodules. Symbiosis19:99-110.
10.1139/m93-095 · DOI
10.1128/aem.62.8.2910-2914.1996 · DOI
Tomaszewski, M., and K. V. Thimann. 1966. Interactions of phenolic acids, metallic ions, and chelating agents on auxin-induced growth. Plant Physiol.41:1443-1454. · DOI
Tsubokura, S., Y. Sakamoto, and K. Ichihara. 1961. The bacterial decomposition of indoleacetic acid. J. Biochem.49:38-42.
10.1128/AEM.64.11.4185-4193.1998 · DOI
Wichner, S. 1968. Beziehungen zwischen Pflanzen und epiphytischen Bakterien hinsichtlich ihres Auxinstoffwechsels. IV. IES-Zerstoerung und Produktion von Inhibitoren der IES-Oxydase durch epiphytische Bakterien. Flora Abt. A159:141-166.
Wichner, S., and E. Libbert. 1964. Hinweise zur Exoenzym-Natur einer IES-Oxydase. Naturwissenschaften51:268.
Wichner, S., and E. Libbert. 1968. Interactions between plants and epiphytic bacteria regarding their auxin metabolism. I. Detection of IAA-producing epiphytic bacteria and their role in long duration experiments on tryptophan metabolism in plant homogenates. Physiol. Plant21:227-241. · DOI
Wichner, S., and E. Libbert. 1968. Interactions between plants and epiphytic bacteria regarding their auxin metabolism. II. Influence of IAA-producing epiphytic bacteria on short-term IAA production from tryptophan in plant extracts. Physiol. Plant21:500-509. · DOI

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Background
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“As controls, we used P. putida KT2440 (Nelson et al., 2002), P. putida 1290 (Leveau and Lindow, 2005), Escherichia coli TOP10 (Life Technologies), Collimonas arenae Cal35 (Wu et al., 2015), Collimonas fungivorans Ter331 (de Boer et al., 2004) and Cal2 (Uroz et al., 2014), and Pantoea agglomerans…”
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“IAA is the major auxin in plants which regulate many important physiological processes including the tissue differentiation, cell enlargement, and division and responses to light and gravity [7].”
Background
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“Indole acetic acid production The efficacy of isolates for (IAA) production was determined by the colorimetric technique (Leveau and Lindow, 2005).”
Method
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Genomic flank-sequencing of plasposon insertion sites for rapid identification of functional genes.
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Self-citation
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“This result was consistent with that of Leveau and Lindow [31], which indicated that the lowest concentration of IAA (1 nmol/l) significantly stimulated radish root growth compared with higher concentrations (1 µmol/l and 1 mmol/l) and control (without IAA).”
Result
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“Plant growth-promoting rhizobacteria (PGPR) are known for production and degradation of the phytohormone auxin, leading to enhanced root growth (Leveau and Lindow, 2005; Spaepen et al., 2014; Finkel et al., 2020).”
Background
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“2004; Leveau and Lindow 2005; Yoolong et al.”
The Mexican giant maize of Jala landrace harbour plant-growth-promoting rhizospheric and endophytic bacteria
Rios-Galicia, B., Villagómez-Garfias, C., la Vega-Camarillo, E. D., Guerra-Camacho, J., Medina-Jaritz, N., Arteaga-Garibay, R., Villa-Tanaca, L., & Hernández-Rodríguez, C. (2021) · 3 Biotech · doi:10.1007/s13205-021-02983-6 · Cited by 17
Interactions in Soil-Microbe-Plant System: Adaptation to Stressed Agriculture
Shilev, S., Azaizeh, H., Vassilev, N. B., Georgiev, D., & Babrikova, I. (2019) · Springer eBooks · doi:10.1007/978-981-13-8391-5_6 · Cited by 26
Characterization of the IAA-Producing and -Degrading Pseudomonas Strains Regulating Growth of the Common Duckweed (Lemna minor L.)
Popržen, T., Nikolić, I., Krstić-Milošević, D., Uzelac, B., Trifunović-Momčilov, M. M., Marković, M., & Radulović, O. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242417207 · Cited by 16
“%) agar plates with 8.3 mM sodium-benzoate or 5 mM IAA as the sole carbon source, according to Scott et al. (2013) [38].”
BackgroundMethodInfluential
Screening of Rhizobacteria for Plant Growth Promotion and Their Tolerance to Drought Stress
Putrie, R. F. W., Wahyudi, A., Nawangsih, A. A., & Husen, E. (2013) · doi:10.5454/mi.7.3.2 · Cited by 16
Complete genome analysis of sugarcane root associated endophytic diazotroph Pseudomonas aeruginosa DJ06 revealing versatile molecular mechanism involved in sugarcane development
Guo, D.-J., Singh, P., Yang, B., Singh, R., Verma, K., Sharma, A., Khan, Q., Qin, Y.-Z., Chen, T., Song, X.-P., et al. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1096754 · Cited by 15
“The secretion of IAA is another direct plant-promoting characteristic of PGPBs such as P. fluorescens (Gravel et al., 2007), P. aeruginosa TQ3 (Khare and Arora, 2010), and P. putida1290 (Leveau and Lindow, 2005).”
Background
In acid-aminopyrimidine continuum: experimental and computational studies of furan tetracarboxylate-2-aminopyrimidinium salt
Garg, U., Azim, Y., & Alam, M. (2021) · RSC Advances · doi:10.1039/d1ra01714d · Cited by 15
Phyllospheric plant growth promoting bacteria
Wagi, S., & Ahmed, A. (2017) · doi:10.15406/jbmoa.2017.05.00119 · Cited by 15
Role of novel fungus Lasiodiplodia sp. JAS12 and plant growth promoting bacteria Klebsiella pneumoniae JAS8 in mineralization of endosulfan and its metabolites
Abraham, J., & Silambarasan, S. (2014) · doi:10.1016/j.ecoleng.2014.05.029 · Cited by 15
Strategies for Characterization of Agriculturally Important Bacteria
Szilagyi-Zecchin, V. J., Mógor, Á. F., & Figueiredo, G. G. O. (2016) · Springer eBooks · doi:10.1007/978-81-322-2647-5_1 · Cited by 14
Root development is maintained by specific bacteria-bacteria interactions within a complex microbiome
Finkel, O., Salas-González, I., Castrillo, G., Law, T. F., Conway, J., Jones, C. D., & Dangl, J. (2019) · bioRxiv · doi:10.1101/645655 · Cited by 14
Rhodotorula mucilaginosa YR29 is able to accumulate Pb2+ in vacuoles: a yeast with bioremediation potential
Paz, G. Á.-D., Martínez-Gutiérrez, H., Ramírez-Granillo, A., López-Villegas, E., Medina-Canales, M., & Rodríguez-Tovar, A. (2023) · World Journal of Microbiology & Biotechnology · doi:10.1007/s11274-023-03675-4 · Cited by 14
Synthesis of Chitosan Microparticles Encapsulating Bacterial Cell-Free Supernatants and Indole Acetic Acid, and Their Effects on Germination and Seedling Growth in Tomato (Solanum lycopersicum)
Gonzalez-Montfort, T. S., Almaraz-Abarca, N., Pérez-y-Terrón, R., Ocaranza-Sánchez, E., & Rojas-López, M. (2022) · International Journal of Analytical Chemistry · doi:10.1155/2022/2182783 · Cited by 14
Antimycotal Activity of Collimonas Isolates and Synergy-Based Biological Control of Fusarium Wilt of Tomato
Doan, H., Maharaj, N., Kelly, K., Miyao, E., Davis, R., & Leveau, J. (2020) · Phytobiomes Journal · doi:10.1094/pbiomes-05-19-0027-r · Cited by 14
“Escherichia coli TOP10 (Invitrogen) and Pseudomonas putida 1290 (Leveau and Lindow 2005) were used as non-Collimonas controls.”
MethodSelf-citation
KARAKTERISASI BAKTERI PENGHASIL ASAM INDOL ASETAT DAN PENGARUHNYA TERHADAP VIGOR BENIH PADI
Lestari, P., Suryadi, Y., Susilowati, D., Priyatno, T. P., & Samudra, I. M. (2015) · doi:10.14203/beritabiologi.v14i1.1859 · Cited by 14
“Sesuai pendapat sebelumnya (Patten and Glick, 2002; Leveau and Lindow, 2004) bahwa peningkatan pertumbuhan akar tanaman merupakan salah satu tanda utama tanaman tersebut telah diinokulasi oleh bakteri Bedasarkan analisis molekuler, semua amplikon ke tiga isolat berukuran 1.400-1.600 bp (Gambar 2),…”
BackgroundInfluential
Pseudomonas fluorescent and its ability to promote root formation of olive microshoots
Peyvandi, M., Farahani, F., Mazinani, M., Noormohamadi, Z., Ataii, S., & Asgharzade, A. (2010) · doi:10.22069/ijpp.2012.682 · Cited by 14
“, 2001), Pseudomonas putida (Leveau and Lindow, 2005) which stimulate the growth of roots can produce at least small amounts of the auxin indole 3-acetic acid (IAA).”
Background
Heavy toxic sludge tolerance in microalgae: Effect of energy generation metabolisms from C. humicola under IAA applications
Zhao, J., Yang, Y., Li, R., Song, M., Yin, D., Ye, X., & Chen, X. (2024) · Journal of Cleaner Production · doi:10.1016/j.jclepro.2024.140620 · Cited by 12
Transcriptional response of Pseudomonas aeruginosa to a phosphate-deficient Lolium perenne rhizosphere
Zyśko, A., Sanguin, H., Hayes, A., Wardleworth, L., Zeef, L. A. H., Sim, A., Paterson, E., Singh, B. K., & Kertesz, M. (2011) · Plant and Soil · doi:10.1007/s11104-011-1060-z · Cited by 13
“In addition, catechol is an intermediate in degradation of the plant hormone indole-3-acetic acid (Leveau and Lindow 2005), and tryptophan, but we were unable to detect enhanced levels of either of these compounds in the exudates from P-limited plants.”
Background
The Azospirillum genus and the cultivation of vegetables. A review
Vendruscolo, E., & de Lima, S. D. (2021) · Base · doi:10.25518/1780-4507.19175 · Cited by 13
“It should be noted that IAA is present in all plants and has the most important role in their growth and development, allowing cell stretching and division, tissue differentiation, phototropism, gravitropism, and defensive responses (Leveau & Lindow, 2005).”
Effectiveness of Plant Growth-Promoting Rhizobacteria in Phytoremediation of Chromium Stressed Soils
Gupta, P., Rani, R., Chandra, A., Varjani, S., & Kumar, V. (2018) · doi:10.1007/978-981-10-7413-4_16 · Cited by 13
Invisible Inhabitants of Plants and a Sustainable Planet: Diversity of Bacterial Endophytes and their Potential in Sustainable Agriculture
Alam, M., Pandit, B., Moin, A., & Iqbal, U. N. (2024) · Indian Journal of Microbiology · doi:10.1007/s12088-024-01225-6 · Cited by 12
“The reverse activity, i.e., degradation of IAA by some endophytes, like Pseudomonas putida 1290 and Bradyrhizobium japonicum E109, have also been reported to affect plant growth [161, 162].”
Modulation of the Wheat Seed-Borne Bacterial Community by Herbaspirillum seropedicae RAM10 and Its Potential Effects for Tryptophan Metabolism in the Root Endosphere
Carril, P., Cruz, J., Serio, C. D., Pieraccini, G., Bessai, S. A., Tenreiro, R., & Cruz, C. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.792921 · Cited by 12
“In agreement with this hypothesis, previous studies have shown that bacterial degradation of IAA, and not only its production, is often required for full plant growth promotion and root development (Leveau and Lindow, 2005; Zúñiga et al., 2013).”
Result
Plant Probiotics for Nutrient Acquisition by Agriculturally Important Grasses: A Comprehensive Review of the Science and the Application
Swift, R., Denton, M., & Melino, V. J. (2019) · Annual Plant Reviews online · doi:10.1002/9781119312994.apr0697 · Cited by 12
The plant growth promoting bacterium Bacillus sp. CaSUT007 produces phytohormone and extracellular proteins for enhanced growth of cassava
Buensanteai, N., Sompong, M., Thamnu, K., Athinuwat, D., Brauman, A., & Plassard, C. (2013) · doi:10.5897/ajmr12.1839 · Cited by 12
“The peak concentrations of IAA detected in the indole extract of CaSUT007 were higher than that reported for any other strains of plant growth promoting bacteria (Araujo et al., 2005; Leveau and Lindow, 2005; Kang et al., 2006).”
Background
Molecular Characterization of Pseudomonas spp. Isolated from Root Nodules of Various Leguminous Plants of Shekhawati Region, Rajasthan, India
Issar, S., Sharma, S., Choudhary, D., Gautam, H., & Gaur, R. (2012) · doi:10.4236/ajps.2012.31005 · Cited by 12
Synthesis and Degradation of the Phytohormone Indole-3-Acetic Acid by the Versatile Bacterium Paraburkholderia xenovorans LB400 and Its Growth Promotion of Nicotiana tabacum Plant
Vega-Celedón, P., Castillo-Novales, D., Bravo, G., Cárdenas, F., Romero-Silva, M. J., & Seeger, M. (2024) · Plants · doi:10.3390/plants13243533 · Cited by 11
“Plants 2024 , 13 , 3533 2 of 22 Indole-3-acetic acid (IAA) is a phytohormone that serves as the primary endogenous auxin in higher plants, influencing various physiological processes such as cell division, elongation, tissue differentiation, phototropism, gravitropism, and defensive responses [4,5].”
Desert truffle mycorrhizosphere harbors organic acid releasing plant growth–promoting rhizobacteria, essentially during the truffle fruiting season
Arenas, F., López-García, Á., Berná, L. M., Morte, A., & Navarro-Ródenas, A. (2022) · Mycorrhiza · doi:10.1007/s00572-021-01067-w · Cited by 11
“2005; Leveau and Lindow 2005) at 30 °C for 2 days in a shaking incubator, at 100 rpm. Bacterial cells were removed from the culture broth by centrifugation (1.5 mL of bacterial suspension).”
Influential
Comparison of IAA Production by Shallot Rhizosphere Isolated Bacteria in Solid and Liquid Media and Their Effect on Shallot Plant Growth
Kafrawi, Nildayanti, Zahraeni, K., & Baharuddin, B. (2017) · doi:10.4172/1948-5948.1000375 · Cited by 11
“, Alcaligenes faecalis and Cyanobacteria [1,3].”
Background
QS-type bacterial signal molecules of nonpeptide origin
Shpakov, A. (2009) · Microbiology · doi:10.1134/s0026261709020015 · Cited by 11
“Pseudomonas putida is known to use the plant hormone indolyl-3-acetic acid as an energy source and to incorporate it into its metabolic pathways [68].”
Background
Bacteria Associated with Orchid Roots
Tsavkelova, E. (2011) · doi:10.1007/978-3-642-20332-9_11 · Cited by 11
“Auxin accumulation in the culture medium reached its maximum during the stationary phase of bacterial growth (Tsavkelova et al. 2005, 2007a) that has also been shown for diverse plant-associated Pseudomonas, Azospirillum, Arthrobacter and Agrobacterium strains (Tien et al. 1979; Cacciari et al. 1989; Olyunina and Shab…”
BackgroundInfluential
Roles of β-Indole Acetic Acid (IAA) Producing Endophytic Bacteria on the Recovery of Plant Growth and Survival Ability of Sugarcane Infected White Leaf Disease (SWLD)
Nguyen, T. K., Mai, D. T. H., Hiu, B. L., Dưong, C. A., Nguyễn, C. N. B., Nguyễn, N. M., Nguyen, M., & Nguyễn, Q. B. (2022) · Current Microbiology · doi:10.1007/s00284-022-03091-1 · Cited by 10
“Bacterial IAA producers (BIPs) interfere with these processes by input of IAA into the plant’s auxin pool [51].”
Background
Identification and functional characterization of olfactory indolergic receptors in Drosophila melanogaster.
Ruel, D. M., Vainer, Y. G., Yakir, E., & Bohbot, J. (2021) · Insect Biochemistry and Molecular Biology · doi:10.1016/j.ibmb.2021.103651 · Cited by 9
New Zn(II) coordination polymer of indole-3-acetic acid, a plant-growth promoting hormone: Crystal structure, spectroscopic characterization, DFT calculations and microbiological activity
Szmigiel-Bakalarz, K., Skoczyńska, A., Lewańska, M., Günther, D., Oeckler, O., Malik-Gajewska, M., Michalska, D., & Morzyk-Ociepa, B. (2020) · doi:10.1016/j.poly.2020.114582 · Cited by 9
The effect of phytohormones on the growth, cellulose production and pellicle properties of Gluconacetobacter xylinus ATCC 53582
Qureshi, O., Sohail, H., Latos, A., & Strap, J. (2013) · doi:10.4081/aab.2013.s1.e7 · Cited by 9
Beneficial interactions in the rhizosphere
Hol, W. H. G., de Boer, W., & Medina, A. (2014) · doi:10.1007/978-94-017-8890-8_3 · Cited by 9
Microbiomes in action: multifaceted benefits and challenges across academic disciplines
Soth, S., Hampton, J. G., Alizadeh, H., Wakelin, S. A., & Mendoza‐Mendoza, A. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1550749 · Cited by 12
Improvement of Trimethylamine Uptake by Euphorbia milii: Effect of Inoculated Bacteria
Siswanto, D., & Thiravetyan, P. (2016) · doi:10.11594/jtls.06.02.11 · Cited by 8
Interactions between Indole-3-acetic Acid Producing Acinetobacter sp. SW5 and Growth of Tomato Plant
Kwon, H.-D., & Song, H.-G. (2014) · doi:10.7845/kjm.2014.4050 · Cited by 8
“The effects and action mechanisms of IAA in plants and biosynthetic pathways of IAA in plants and bacteria have been well known (Patten and Glick, 2002; Leveau and Lindow, 2005; Spaepen and Vanderleyden, 2011).”
Background
Alleviating arsenic stress affecting the growth of Vigna radiata through the application of Klebsiella strain ASBT-KP1 isolated from wastewater
Prasad, M., Madhavan, A., Babu, P., Salim, A., Subhash, S., Nair, B. G., & Pal, S. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1484069 · Cited by 7
“PGP bacteria stimulate plant growth directly by synthesizing the hormone IAA, which controls many physiological functions such as tissue differentiation, root initiation, cell enlargement and division, and phototropism (Leveau and Lindow, 2005).”
Auxin-Mediated Modulation of Maize Rhizosphere Microbiome: Insights from Azospirillum Inoculation and Indole-3-Acetic Acid Treatment
Coniglio, A., Larama, G., Nievas, S., Cale, N. L., Mora, V., Torres, D., López, G., Donadío, F., Rodríguez, B., Marin, A., et al. (2024) · Journal of soil science and plant nutrition · doi:10.1007/s42729-024-02013-3 · Cited by 7
“Interest-ingly, when IAA is present in high concentrations, auxin-degrading bacteria can interfere with this negative chemical signaling restoring root growth (Finkel et al. 2020; Leveau and Lindow 2005).”
Molecular Analysis of Indole and Skatole Decomposition Metabolism in Acinetobacter piscicola p38 Utilizing Biochemical and Omics Approaches
Wang, Z., Sun, J., Yang, P., Zhang, W., Jiang, Y., Liu, Q., Yang, Y., Hao, R., Guo, G., Huo, W., et al. (2024) · Microorganisms · doi:10.3390/microorganisms12091792 · Cited by 8
“…shown that various bacteria, such as Acinetobacter baumannii [17], Paraburkholderia phytoﬁrmans [18], Enterobacter soli [19], Pseudomonas putida [20], and Caballeronia glathei [14], have the ability to degrade N-heterocyclic compounds, and oxygenases have been conﬁrmed to play a key initial…”
Background
Coupled treatment of wet-dry alternation irrigation and seedling-promoting fertilizer has a beneficial effect on the rhizosphere microbial community profile and regenerating physiology of ratoon rice
Chen, H.-F., Yang, Y., Yang, X., Pang, X.-M., Shao, C.-H., Li, Z., Fang, C.-X., & Lin, W.-X. (2023) · Plant growth regulation (Print) · doi:10.1007/s10725-023-00986-2 · Cited by 7
“The secretion of ABA or IAA into the rhizosphere could be a mechanism for plants to select microbes capable of using these as a carbon source (Leveau et al. 2005; Belimov et al. 2014 ).”
Inoculation effects of growthpromoting bacteria on corn root architecture: influence of nitrogen levels, bacterial populations, and plant genotypes
Dias, A. C., Alves, G. C., da Silva, T. F. R., & Reis, V. M. (2023) · Revista Brasileira de Ciência do Solo · doi:10.36783/18069657rbcs20230059 · Cited by 7
Rhizosphere Bacteria from Coastal Sand Dunes and Their Applications in Agriculture
Godinho, A., & Bhosle, S. (2013) · doi:10.1007/978-3-642-37241-4_4 · Cited by 7
Indole-Acetic Acid Promotes Ammonia Removal Through Heterotrophic Nitrification, Aerobic Denitrification With Mixed Enterobacter sp. Z1 and Klebsiella sp. Z2
Zhang, Y.-X., Xu, Q., Wang, G.-J., & Shi, K.-X. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.929036 · Cited by 6
Applications of Beneficial Microbe in Arid and Semiarid Agroecosystem: IAA-Producing Bacteria
Zarea, M. (2019) · Microbiome in Plant Health and Disease · doi:10.1007/978-981-13-8495-0_5 · Cited by 6
Plant-Microbe Interactions: Current Perspectives of Mechanisms Behind Symbiotic and Pathogenic Associations
Akram, M., Shahid, M., Tahir, M., Mehmood, F., & Ijaz, M. (2017) · doi:10.1007/978-981-10-5813-4_6 · Cited by 6
Synergetic Effect of Rhizosphere Bacteria Isolates and Composted Manure on Fusarium Wilt Disease of Tomato Plants
Lachisa, L., & Dabassa, A. (2016) · doi:10.3923/jm.2016.20.27 · Cited by 6
Phosphate solubilization and indole acetic acid production by rhizosphere yeast Torulaspora globosa: improvement of culture conditions for better performance in vitro
Albertini, J., Rocha, R. K., Bastos, R. G., Ceccato-Antonini, S. R., & Rosa-Magri, M. M. (2022) · 3 Biotech · doi:10.1007/s13205-022-03322-z · Cited by 5
“Microorganisms use various mechanisms for complete biodegradation (mineralization) or transformation of indole compounds into other compounds, such as catechol (Leveau and Lindow 2005), indole-3-aldehyde (Arora and Bae 2014), 3-methylindole (Arora et al.”
Background
Enterobacter soli Strain AF-22b-4245: Study of the Genome and the Effect on Wheat Growth
Sokolova, E., Mishukova, O., Khlistun, I. V., Tromenschleger, I., Chumanova, E., & Voronina, E. (2025) · Microbiology Research · doi:10.3390/microbiolres16020034 · Cited by 5
A Comprehensive Approach Combining Short-Chain Polyphosphate and Bacterial Biostimulants for Effective Nutrient Solubilization and Enhanced Wheat Growth
Bourak, K., Oulkhir, F. E., Maghnia, F. Z., Massart, S., Biskri, L., Jijakli, M. H., & Allaoui, A. (2024) · Microorganisms · doi:10.3390/microorganisms12071423 · Cited by 5
“The amount of IAA (indole-3-acetic acid) produced by PSB strains was measured by cultivating them in Trypticase soy broth (TSB) broth, containing 0.1% L-tryptophan, which acts as a precursor for IAA synthesis [37].”
MethodInfluential
Comparative study of availability of vitamins from Leea macrophylla Roxb.
Jadhao, K., Wadekar, M., & Mahalkar, M. S. (2019) · doi:10.13005/bbra · Cited by 6
Endophytic Microbiomes: Biodiversity, Current Status, and Potential Agricultural Applications
Ghiasian, M. (2020) · doi:10.1007/978-981-15-3208-5_3 · Cited by 5
Medicinal Plant-Associated Microbes as a Source of Protection and Production of Crops
Mohamad, O. A. A., Ma, J., Liu, Y., Li, L., Hatab, S. R., & Li, W. (2019) · Microorganisms for sustainability · doi:10.1007/978-981-13-9566-6_10 · Cited by 6
Bacterial auxin catabolism as a driver of plant growth promotion and rhizosphere colonization fitness.
Roca, A., Gorts, J., & Matilla, M. A. (2025) · Microbiology Research · doi:10.1016/j.micres.2025.128431 · Cited by 4
Label-Free Quantitative Proteomic Analysis of the Global Response to Indole-3-Acetic Acid in Newly Isolated Pseudomonas sp. Strain LY1
Zhao, S., Chen, X., Sun, Q., Wang, F., Hu, C.-H., Guo, L.-Z., Bai, J., & Yu, H. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.694874 · Cited by 4
“IAAdegrading strain, Pseudomonas putida 1290, could abolish the inhibitory effect to roots caused by exogenous IAA (Leveau and Lindow, 2005).”
BackgroundInfluential
IMPACTO DE AZOSPIRILLUM BRASILENSE, UNA RIZOBACTERIA QUE ESTIMULA LA PRODUCCIÓN DEL ÁCIDO INDOL-3-ACÉTICO COMO EL MECANISMO DE MEJORA DEL CRECIMIENTO DE LAS PLANTAS EN LOS CULTIVOS AGRÍCOLAS
Licea-Herrera, J. I., Quiroz-Velásquez, J. D., & Hernández-Mendoza, J. L. (2020) · Revista Boliviana de Química · doi:10.34098/2078-3949.37.1.5 · Cited by 4
“Una de las principales fitohormonas producidas por Azospirillum es el ácido-3-indol acético (AIA), auxina que controla diversos procesos fisiológicos [40].”
Background
Adverse Effects of Salt Stress on Rootability of Rosmarinus officinalis Cuttings and their Alleviation by Indole-3-Butyric Acid (IBA) and Bacillus subtilis
Abdelrahman, S. (2019) · doi:10.21608/ejoh.2019.18698.1121 · Cited by 4
“IAA produced by the bacteria works in conjunction with the internal auxin plant to stimulate root proliferation and division of cells and nutrient uptake from the rooting substrate (Leveau and Lindow, 2005).”
BackgroundResultInfluential
Finished Genome Sequence of the Indole-3-Acetic Acid-Catabolizing Bacterium Pseudomonas putida 1290
Laird, T. S., & Leveau, J. (2019) · Microbiology Resource Announcements · doi:10.1128/mra.00519-19 · Cited by 4
Self-citation
Exploration And Screening For Endophytic Microbes Of Maize Plant Root Against Fusarium Verticillioides
Jahuddin, R., Jamila, Awaluddin, & Suriani (2018) · doi:10.23960/j.hptt.11857-64 · Cited by 4
“…level. physiological processes in plant by means of introducing IAA they produce to the plant, making the plant more sensitive in changing the endogenic IAA concentration with the result that it supports lateral root and adventive root forming and primary root elongation (Leveau & Lindow, 2005).”
Background
ENHANCED FABA BEAN GROWTH BY COMBINED INOCULATION WITH Rhizobium STRAINS AND Pseudomonas ﬂuorescens PF-23932 STRAIN AS A PLANT GROWTH PROMOTING RHIZOBACTERIA
Sayed, A. E., El-Sanosy, A. S., & Nassef, M. (2015) · doi:10.21608/jacb.2015.48475 · Cited by 4

Authors: Leveau, J. H. J., & Lindow, S. E.
Affiliations: Netherlands Institute of Ecology (NL)
University of California, Berkeley (US)
ORCID: Leveau, Johan H. J.
Lindow, Steven E.
Venue: Applied and Environmental Microbiology
Publisher: American Society for Microbiology
Published: 2005-05
Volume: 71
Issue: 5
Pages: 2365-2371
ISSN: 0099-2240 (ISSN-L)
1098-5336
DOI: 10.1128/aem.71.5.2365-2371.2005
OpenAlex: W2143648038
Cited by: 286
References: 58
Citations by year: 2026: 4 · 2025: 11 · 2024: 21 · 2023: 15 · 2022: 25 · 2021: 22 · 2020: 20 · 2019: 21 · 2018: 13 · 2017: 22 · 2016: 15 · 2015: 13 · 2014: 11 · 2013: 16 · 2012: 9
FWCI: 8.82
Type: journal article
Language: en
Open access: green
europepmc.org
Licence: journals.asm.org/non-commercial-tdm-license (tdm)
Locations: Applied and Environmental Microbiology (publishedVersion)
Europe PMC (PubMed Central) (publishedVersion)
PubMed (publishedVersion)
PubMed Central (publishedVersion)
Data Archiving and Networked Services (DANS) (submittedVersion)
KNAW research portal (Royal Academy of Art and Sciences (KNAW)) (submittedVersion)
Funders: Nederlandse Organisatie voor Wetenschappelijk Onderzoek (863.03.005)
Topics: Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant-Microbe Interactions and Immunity
Life Sciences › Agricultural and Biological Sciences › Plant Science › Legume Nitrogen Fixing Symbiosis
Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
Keywords: indole-3-acetic acid, Pseudomonas putida, catechol 1,2-dioxygenase, root elongation, radish, plant growth-promoting bacteria, plant-associated bacteria
MeSH terms: Base Sequence, Culture Media, Indoleacetic Acids, Molecular Sequence Data, Phylogeny, RNA, Ribosomal, 16S, Pseudomonas putida, Plant Roots

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Utilization of the Plant Hormone Indole-3-Acetic Acid for Growth by Pseudomonas putida Strain 1290

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