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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Method
Establishing a Role for Bacterial Cellulose in Environmental Interactions: Lessons Learned from Diverse Biofilm-Producing Proteobacteria
Augimeri, R. V., Varley, A., & Strap, J. L. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01282 · Cited by 128
“IAA metabolism and degradation (Leveau and Lindow, 2005; Leveau and Gerards, 2008) has been observed in other bacteria and recently reviewed (Duca et al., 2014).”
Background
Production of Indole-3-Acetic Acid via the Indole-3-Acetamide Pathway in the Plant-Beneficial Bacterium Pseudomonas chlororaphis O6 Is Inhibited by ZnO Nanoparticles but Enhanced by CuO Nanoparticles
Dimkpa, C. O., Zeng, J., McLean, J., Britt, D. W., Zhan, J., & Anderson, A. (2011) · Applied and Environmental Microbiology · doi:10.1128/aem.07424-11 · Cited by 117
“One biofertilizer, the phytohormone indole-3-acetic acid (IAA), is important in microbe-microbe and microbe-plant signaling and promotes growth in a variety of plant species (1, 3, 4, 9, 14, 16, 17, 19, 24, 26, 32, 36, 40).”
Indole-3-Acetic Acid (IAA) Production in Symbiotic and Non-Symbiotic Nitrogen-Fixing Bacteria and its Optimization by Taguchi Design
Shokri, D., & Emtiazi, G. (2010) · Current Microbiology · doi:10.1007/s00284-010-9600-y · Cited by 114
“The IAA produced by bacteria colonizing the rhizosphere of plants is proposed to act in conjunction with endogenous IAA in plant to stimulate cell proliferation, elongation, and enhancement of host’s uptake of minerals and nutrients from the soil [9, 11 , 16, 19].”
Background
Production of the Phytohormone Indole-3-Acetic Acid by Estuarine Species of the Genus Vibrio
Gutierrez, C. K., Matsui, G. Y., Lincoln, D. E., & Lovell, C. R. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.02072-08 · Cited by 111
“Responses to increasing IAA concentrations advance from the stimulation of primary root tissue to the development of lateral and adventitious roots and finally to the complete cessation of root growth (1, 6, 16, 29, 32, 37, 44).”
Background
Comparative Study between Exogenously Applied Plant Growth Hormones versus Metabolites of Microbial Endophytes as Plant Growth-Promoting for Phaseolus vulgaris L.
Ismail, M., Amin, M. A., Eid, A., Hassan, S., Mahgoub, H. A. M., Lashin, I. I., Abdelwahab, A. T., Azab, E., Gobouri, A., Elkelish, A. A., et al. (2021) · Cells · doi:10.3390/cells10051059 · Cited by 110
“The extracellular applications of both IAA and IAA-producing strains was used as a source of exogenous IAA [96].”
Method
Characterization of N2-fixing plant growth promoting endophytic and epiphytic bacterial community of Indian cultivated and wild rice (Oryza spp.) genotypes
Banik, A., Mukhopadhaya, S. K., & Dangar, T. K. (2015) · Planta · doi:10.1007/s00425-015-2444-8 · Cited by 116
Deep evolutionary origins of neurobiology: Turning the essence of 'neural' upside-down
Baluška, F., & Mancuso, S. (2009) · Communicative & Integrative Biology · doi:10.4161/cib.2.1.7620 · Cited by 127
Citrus plants exude proline and phytohormones under abiotic stress conditions
Vives-Peris, V., Gómez-Cadenas, A., & Pérez-Clemente, R. (2017) · Plant Cell Reports · doi:10.1007/s00299-017-2214-0 · Cited by 99
Beneficial Endophytic Bacterial Populations Associated With Medicinal Plant Thymus vulgaris Alleviate Salt Stress and Confer Resistance to Fusarium oxysporum
Mohamad, O. A. A., Ma, J.-B., Liu, Y.-H., Zhang, D.-Y., Hua, S.-F., Bhute, S., Hedlund, B., Li, W.-J., & Li, L. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.00047 · Cited by 97
Formula diet driven microbiota shifts tryptophan metabolism from serotonin to tryptamine in neonatal porcine colon
Saraf, M. K., Piccolo, B. D., Bowlin, A. K., Mercer, K. E., LeRoith, T., Chintapalli, S. V., Shankar, K., Badger, T. M., & Yeruva, L. (2017) · Microbiome · doi:10.1186/s40168-017-0297-z · Cited by 105
“Indole acetic acid (IAA) concentration was measured by using Salkowski method [19, 20].”
Microbial communities in the phyllosphere
Leveau, J. (2007) · Blackwell Publishing Ltd eBooks · doi:10.1002/9780470988718.ch11 · Cited by 95
Self-citation
Endophytes from maize with plant growth promotion and biocontrol activity under drought stress
Sandhya, V., Shrivastava, M., Ali, S. Z., & Vurukonda, S. S. K. P. (2017) · Russian Agricultural Sciences · doi:10.3103/s1068367417010165 · Cited by 132
Diversity and Taxonomic Distribution of Endophytic Bacterial Community in the Rice Plant and Its Prospective
Ali, M., Ali, Q., Sohail, M. A., Ashraf, M. F., Saleem, M. H., Hussain, S., & Zhou, L. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221810165 · Cited by 105
“[146] reported that Pseudomonas putida strain 1290 displayed an effective role in IAA degradation to enhance plant growth, such as elongation of the radish (Raphanus sativus) roots through eliminating the inhibitory effects of exogenous IAA.”
Background
Tryptophan, thiamine and indole-3-acetic acid exchange between Chlorella sorokiniana and the plant growth-promoting bacterium Azospirillum brasilense
Palacios, O. A., Gómez-Anduro, G. A., Yoav Bashan, A., & de‐Bashan, L. E. (2016) · FEMS Microbiology Ecology · doi:10.1093/femsec/fiw077 · Cited by 90
“Indole acetaldehyde can be used to support the growth of the PGPB Pseudomonas putida in a minimal medium (Leveau and Lindow 2005).”
DddY, a periplasmic dimethylsulfoniopropionate lyase found in taxonomically diverse species of Proteobacteria
Curson, A. R. J., Sullivan, M. J., Todd, J. D., & Johnston, A. W. B. (2011) · The ISME Journal · doi:10.1038/ismej.2010.203 · Cited by 94
Genome Sequence of Azospirillum brasilense CBG497 and Comparative Analyses of Azospirillum Core and Accessory Genomes provide Insight into Niche Adaptation
Wisniewski-Dyé, F., Lozano, L., Acosta-Cruz, E., Borland, S., Drogue, B., Prigent-Combaret, C., Rouy, Z., Barbe, V., Herrera, A. M., González, V., et al. (2012) · Genes · doi:10.3390/genes3040576 · Cited by 85
“IAA catabolism has been characterized in some rhizobacteria such as Pseudomonas putida, and relies on the presence of the iac locus (for IAA catabolism) constituted of 10 genes with coding similarity to enzymes acting on indole or amidated aromatics and to proteins with regulatory or unknown function [44,45].”
Understanding the physiology of Lactobacillus plantarum at zero growth
Goffin, P., van de Bunt, B., Giovane, M., Leveau, J. H. J., Höppener‐Ogawa, S., Teusink, B., & Hugenholtz, J. (2010) · Molecular Systems Biology · doi:10.1038/msb.2010.67 · Cited by 75
Self-citation
The Plant Growth-Promoting Rhizobacterium Variovorax boronicumulans CGMCC 4969 Regulates the Level of Indole-3-Acetic Acid Synthesized from Indole-3-Acetonitrile
Sun, S.-L., Yang, W.-L., Fang, W.-W., Zhao, Y.-X., Guo, L., & Dai, Y.-J. (2018) · Applied and Environmental Microbiology · doi:10.1128/aem.00298-18 · Cited by 81
“Apart from synthesizing IAA, some PGPR, such as Pseudomonas, Arthrobacter, and Bradyrhizobium, can degrade IAA and use it as a carbon and nitrogen source (10, 11).”
Background
Trichoderma Enhances Net Photosynthesis, Water Use Efficiency, and Growth of Wheat (Triticum aestivum L.) under Salt Stress
Oljira, A. M., Hussain, T., Waghmode, T., Zhao, H.-C., Sun, H.-Y., Liu, X., Wang, X., & Liu, B.-B. (2020) · Microorganisms · doi:10.3390/microorganisms8101565 · Cited by 75
“When used in seed treatment, beneficial root-colonizing microbes that secrete IAA can potentially manipulate the plant’s endogenous pool of IAA, contributing to host tolerance to the harmful effects of environmental stress [64,65].”
Background
Plant growth‐promoting effects of native Pseudomonas strains on Mentha piperita (peppermint): an in vitro study
Santoro, M. V., Cappellari, L. D. R., Giordano, W. F., & Banchio, E. (2015) · Plant Biology · doi:10.1111/plb.12351 · Cited by 87
The magic and menace of metagenomics: prospects for the study of plant growth-promoting rhizobacteria
Leveau, J. H. J. (2007) · European Journal of Plant Pathology · doi:10.1007/s10658-007-9186-9 · Cited by 70
“…clones can be measured using high-pressure liquid chromatography or colorimetric assays (Bric et al. 1991; Omer et al. 2004; Radwan et al. 2002; Leveau and Lindow 2005), while cytokinins and their metabolites are detectable in supernatants by e.g. immunoaffinity chromatography (Timmusk et al.…”
BackgroundMethodSelf-citation
Large scale production of indole-3-acetic acid and evaluation of the inhibitory effect of indole-3-acetic acid on weed growth
Bunsangiam, S., Thongpae, N., Limtong, S., & Srisuk, N. (2021) · Scientific Reports · doi:10.1038/s41598-021-92305-w · Cited by 72
Diversity of phytobeneficial traits revealed by whole‐genome analysis of worldwide‐isolated phenazine‐producing Pseudomonas spp.
Biessy, A., Novinscak, A., Blom, J., Léger, G., Thomashow, L. S., Cazorla, F. M., Jošić, D., & Filion, M. (2018) · Environmental Microbiology · doi:10.1111/1462-2920.14476 · Cited by 78
Microbial Degradation of Indole and Its Derivatives
Arora, P., Sharma, A., & Bae, H. (2015) · Journal of Chemistry · doi:10.1155/2015/129159 · Cited by 70
“Catechol is also detected as a metabolite of indole-3-acetic acid degradation by Pseudomonas putida 1290 [81], Pseudomonas sp.”
Background
The birth of a giant: evolutionary insights into the origin of auxin responses in plants
Carrillo‐Carrasco, V. P., Hernández‐García, J., Mutte, S. K., & Weijers, D. (2023) · The EMBO Journal · doi:10.15252/embj.2022113018 · Cited by 79
“Yet, these responses may also be part of a more general metabolic homeostasis system, which would agree with the idea of IAA being used as a carbon source for bacteria (Jensen et al , 1995; Leveau & Lindow, 2005; Donoso et al , 2016; Conway et al , 2022).”
Biological roles of indole-3-acetic acid in Acinetobacter baumannii.
Lin, H.-R., Shu, H.-Y., & Lin, G.-H. (2018) · Microbiology Research · doi:10.1016/j.micres.2018.08.004 · Cited by 67
Functional Characterization of the Bacterial iac Genes for Degradation of the Plant Hormone Indole-3-Acetic Acid
Scott, J. C., Greenhut, I. V., & Leveau, J. H. J. (2013) · Journal of Chemical Ecology · doi:10.1007/s10886-013-0324-x · Cited by 67
“This bacterium originally was isolated from pear tree foliage and it efficiently exploits IAA as a nutrient source (Leveau and Lindow 2005).”
InfluentialSelf-citation
Biochemical and Genetic Bases of Indole-3-Acetic Acid (Auxin Phytohormone) Degradation by the Plant-Growth-Promoting Rhizobacterium Paraburkholderia phytofirmans PsJN
Donoso, R., Leiva-Novoa, P., Zúñiga, A., Timmermann, T., Recabarren‐Gajardo, G., & González, B. (2016) · Applied and Environmental Microbiology · doi:10.1128/aem.01991-16 · Cited by 63
“An anaerobic auxin degradation pathway has been proposed in Azoarcus evansii and Aromatoleum aromaticum (8), and complete aerobic degradation of this auxin has been reported in Bradyrhizobium (9, 10); Pseudomonas (11); Burkholderia, Rhodococcus, and Sphingomonas (12); and Acinetobacter (13) species.”
BackgroundInfluential
Grapevine (Vitis vinifera) Crown Galls Host Distinct Microbiota
Faist, H., Keller, A., Hentschel, U., & Deeken, R. (2016) · Applied and Environmental Microbiology · doi:10.1128/aem.01131-16 · Cited by 84
Synergistic plant–microbe interactions between endophytic bacterial communities and the medicinal plant Glycyrrhiza uralensis F.
Li, L., Mohamad, O., Ma, J.-B., Friel, A. D., Su, Y.-G., Wang, Y., Musa, Z., Liu, Y.-H., Hedlund, B., & Li, W.-J. (2018) · Antonie van Leeuwenhoek · doi:10.1007/s10482-018-1062-4 · Cited by 61
“Some studies have reported that endophytic bacteria isolated from medicinal plants produced indole-3-acetic acid (IAA) (Khan et al. 2014), which is involved in stimulation of plant growth by stimulating cell enlargement, division, differentiation, and gene regulation (Leveau and Lindow 2005).”
Background
Towards a better greener future - an alternative strategy using biofertilizers. I: Plant growth promoting bacteria
Basu, S., Rabara, R., & Negi, S. (2017) · Plant Gene · doi:10.1016/j.plgene.2017.07.004 · Cited by 65
Endophytic fungi Aspergillus spp. reduce fusarial wilt disease severity, enhance growth, metabolism and stimulate the plant defense system in pepper plants
Attia, M. S., Salem, M., & Abdelaziz, A. (2022) · Biomass Conversion and Biorefinery · doi:10.1007/s13399-022-03607-6 · Cited by 59
“The ability of fungi to create indole acetic acid (IAA) was established by the technique described by Leveau and Lin-dow [39].”
Bacterial catabolism of indole-3-acetic acid
Laird, T. S., Flores, N., & Leveau, J. (2020) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-020-10938-9 · Cited by 58
Self-citation
Anti-fungal activity of bacterial endophytes associated with legumes against Fusarium solani: Assessment of fungi soil suppressiveness and plant protection induction
Bahroun, A., Jousset, A., Mhamdi, R., Mrabet, M., & Mhadhbi, H. (2017) · doi:10.1016/j.apsoil.2017.10.025 · Cited by 54
Biogenic Gold Nanoparticle Supplementation to Plant Beneficial Pseudomonas monteilii was Found to Enhance its Plant Probiotic Effect
Panichikkal, J., Thomas, R., John, J. C., & Radhakrishnan, E. (2019) · Current Microbiology · doi:10.1007/s00284-019-01649-0 · Cited by 53
Significance of Microbial Interactions in the Mycorrhizosphere
Bending, G. D., Aspray, T. J., & Whipps, J. M. (2006) · Advances in applied microbiology · doi:10.1016/s0065-2164(06)60004-x · Cited by 51
“However, as the ECM fungus L. bicolor also produces IAA, it is not clear what contribution bacterially produced IAA has on enhancing this symbiosis.”
BackgroundInfluential
Statistical optimization for improved indole-3-acetic acid (iaa) production by Pseudomonas aeruginosa and demonstration of enhanced plant growth promotion
Sasirekha, B., & Shivakumar, S. (2012) · doi:10.4067/s0718-95162012005000038 · Cited by 51
“The IAA produced by bacteria colonizing the rhizosphere of the plants is proposed to act in conjunction with endogenous IAA in plant to stimulate cell proliferation, elongation, and enhancement of host’s uptake of minerals and nutrients from the soil (Suzuki and Oyaizu, 2003; Leveau and Lindow, 2005).”
Background
Diverse MarR bacterial regulators of auxin catabolism in the plant microbiome
Conway, J., Walton, W., Salas-González, I., Law, T. F., Lindberg, C., Crook, L., Kosina, S., Fitzpatrick, C. R., Lietzan, A., Northen, T., et al. (2022) · Nature Microbiology · doi:10.1038/s41564-022-01244-3 · Cited by 50
Phytoprotective influence of bacteria on growth and cadmium accumulation in the aquatic plant Lemna minor.
Stout, L., Dodova, E. N., Tyson, J., & Nüsslein, K. (2010) · Water Research · doi:10.1016/j.watres.2010.07.073 · Cited by 50
Bacillus thuringiensis beyond insect biocontrol: plant growth promotion and biosafety of polyvalent strains
Raddadi, N., Cherif, A., Ouzari, H., Marzorati, M., Brusetti, L., Boudabous, A., & Daffonchio, D. G. (2007) · Annals of Microbiology · doi:10.1007/bf03175344 · Cited by 55
“…al., 2003b), autolysins (Raddadi et al., 2004, 2005), lactonases (Dong et al., 2002), siderophores, β-1,3-glucanase, chitinases, antibiotics and hydrogene cyanide and to the ability to degrade indole-3-acetic acid (IAA) (protect the plant from high-IAA-producing bacteria) (Leveau and Lindow, 2005).”
Background
Characterization of IAA Production by the Mangrove Cyanobacterium Phormidium sp. MI405019 and Its Influence on Tobacco Seed Germination and Organogenesis
Boopathi, T., Balamurugan, V., Gopinath, S., & Sundararaman, M. (2013) · Journal of Plant Growth Regulation · doi:10.1007/s00344-013-9342-8 · Cited by 48
“Chlorophyll content and production of IAA were quantitatively analyzed at 24-h intervals using the Salkowski method (Leveau and Lindow 2005).”
Method
Protective role of plant growth-promoting fungi Aspergillus chevalieri OP593083 and Aspergillus egyptiacus OP593080 as biocontrol approach against Alternaria leaf spot disease of Vicia faba plant
Daigham, G. E., Mahfouz, A. Y., Abdelaziz, A., Nofel, M. M., & Attia, M. S. (2023) · Biomass Conversion and Biorefinery · doi:10.1007/s13399-023-04510-4 · Cited by 45
“The efficacy of isolates for (IAA) production was determined by the colorimetric technique according to Leveau and Lin-dow [22].”
Transcriptional Response and Plant Growth Promoting Activity of Pseudomonas fluorescens DR397 under Drought Stress Conditions
Nishu, S. D., No, J., & Lee, T. (2022) · Microbiology spectrum · doi:10.1128/spectrum.00979-22 · Cited by 45
“elongation, cell division, and enlargement under drought stress (15).”
Background
Biocontrol potential of plant growth-promoting rhizobacteria (PGPR) against Sclerotiorum rolfsii diseases on sugar beet (Beta vulgaris L.)
Farhaoui, A., Adadi, A., Tahiri, A., Alami, N. E., Khayi, S., Mentag, R., Ezrari, S., Nabil, R., Mokrini, F., Belabess, Z., et al. (2022) · Physiological and molecular plant pathology · doi:10.1016/j.pmpp.2022.101829 · Cited by 45
Beneficial native bacteria improve survival and mycorrhization of desert truffle mycorrhizal plants in nursery conditions
Navarro-Ródenas, A., Berná, L., Lozano-Carrillo, C., Andrino, A., & Morte, A. (2016) · Mycorrhiza · doi:10.1007/s00572-016-0711-6 · Cited by 44
“For this, the isolates were cultivated in a NB medium supplemented with 3 g/l of tryptophan (Ahmad et al. 2005; Leveau and Lindow 2005) at 28 °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).”
MethodInfluential
Growth promotion of Vigna mungo (L.) by Pseudomonas spp. exhibiting auxin production and ACC-deaminase activity
Noreen, S., Ali, B., & Hasnain, S. (2012) · Annals of Microbiology · doi:10.1007/s13213-011-0277-7 · Cited by 43
“It has been previously reported that bacteria produced the highest concentrations of IAA during stationary phase cultures (Leveau and Lindow 2005).”
Background
Exogenous naringenin improved digestible protein accumulation and altered morphology via VrPIN and auxin redistribution in Vigna radiata
Sharma, P., Kumar, V., Khosla, R., & Guleria, P. (2020) · 3 Biotech · doi:10.1007/s13205-020-02428-6 · Cited by 41
A dynamic rhizosphere interplay between tree roots and soil bacteria under drought stress
Oppenheimer‐Shaanan, Y., Jakoby, G., Starr, M. L., Karliner, R., Eilon, G., Itkin, M., Malitsky, S., & Klein, T. (2022) · eLife · doi:10.7554/elife.79679 · Cited by 73
Isolation and characterization of novel soil- and plant-associated bacteria with multiple phytohormone-degrading activities using a targeted methodology
Nascimento, F., Glick, B. R., & Rossi, M. (2019) · Access Microbiology · doi:10.1099/acmi.0.000053 · Cited by 40
Bacteria from wheat and cucurbit plant roots metabolize PAHs and aromatic root exudates: Implications for rhizodegradation
Ely, C., & Smets, B. (2017) · International journal of phytoremediation · doi:10.1080/15226514.2017.1303805 · Cited by 40
Rhizospheric Phosphate Solubilizing Bacillus atrophaeus GQJK17 S8 Increases Quinoa Seedling, Withstands Heavy Metals, and Mitigates Salt Stress
Mahdi, I., Fahsi, N., Hafidi, M., Benjelloun, S., Allaoui, A., & Biskri, L. (2021) · doi:10.3390/su13063307 · Cited by 39
Isolation, identification and characterization of phenolic acid‐degrading bacteria from soil
Wang, Y., Zhang, W., Zhang, Z.-F., Wang, W.-H., Xu, S.-F., & He, X.-F. (2020) · Journal of Applied Microbiology · doi:10.1111/jam.14956 · Cited by 39
“…these, Pseudomonas sp., including P. putida, P. fluorescens, P. syringae, P. mendocina and P. aeruginosa, are considered to be the best bacterial agents for enhancing plant growth and yield (Patten and Glick 1996; Leveau and Lindow 2005; Kohler et al. 2010; Kochar et al. 2011; Goswami et al. 2015).”
Background
Continuous production of indole-3-acetic acid by immobilized cells of Arthrobacter agilis
Ozdal, M., Ozdal, O. G., Sezen, A., Algur, O. F., & Kurbanoglu, E. B. (2017) · 3 Biotech · doi:10.1007/s13205-017-0605-0 · Cited by 39
“Leveau and Lindow (2005) reported degradation of IAA to catechol by Pseudomonas putida.”
Background
Identification of New Metabolites of Bacterial Transformation of Indole by Gas Chromatography-Mass Spectrometry and High Performance Liquid Chromatography
Arora, P. K., & Bae, H. (2014) · International Journal of Analytical Chemistry · doi:10.1155/2014/239641 · Cited by 38
“Leveau and Lindow [22] studied catabolism of indole-3-acetic acid by Pseudomonas putida strain 1290 that degraded indole-3-acetic acid via formation of catechol.”
Background
Halotolerant Endophytic Bacterium Serratia rubidaea ED1 Enhances Phosphate Solubilization and Promotes Seed Germination
Mahdi, I., Hafidi, M., Allaoui, A., & Biskri, L. (2021) · Agriculture · doi:10.3390/agriculture11030224 · Cited by 38
“5% of L-tryptophan and incubated at 28 ± 2 ◦C for 11 days under shaking of 150 rpm [55].”
Method
Genomics as a potential tool to unravel the rhizosphere microbiome interactions on plant health
Priya, P., Aneesh, B. P., & Harikrishnan, K. (2021) · Journal of Microbiological Methods · doi:10.1016/j.mimet.2021.106215 · Cited by 56

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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