References
- Libbert E, Risch H. 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 Plant. 1969;22:51-58. https://doi.org/10.1111/j.1399-3054.1969.tb07840.x
- Ruanpanun P, Tangchitsomkid N, Hyde KD, et al. Actinomycetes and fungi isolated from plant-parasitic nematode infested soils: screening of the effective biocontrol potential, indole-3-acetic acid and siderophore production. World J Microbiol Biotechnol. 2010;26:1569-1578. https://doi.org/10.1007/s11274-010-0332-8
- Limtong S, Koowadjanakul N. Yeasts from phylloplane and their capability to produce indole-3-acetic acid. World J Microbiol Biotechnol. 2012;28:3323-3335. https://doi.org/10.1007/s11274-012-1144-9
- Mano Y, Nemoto K. The pathway of auxin biosynthesis in plants. J Exp Bot. 2012;63:2853-2872. https://doi.org/10.1093/jxb/ers091
- Spaepen S, Vanderleyden J, Remans R. Indole-3-acetic acid in microbial and microorganism-plant signaling. FEMS Microbiol Rev. 2007;31:425-448. https://doi.org/10.1111/j.1574-6976.2007.00072.x
- Duca D, Lorv J, Patten CL, et al. Indole-3-acetic acid in plant-microbe interactions. Antonie Van Leeuwenhoek. 2014;106:85-125. https://doi.org/10.1007/s10482-013-0095-y
- Zakharova EA, Shcherbakov AA, Brudnik VV, et al. Biosynthesis of indole-3-acetic acid in Azospirillum brasilense. Insights from quantum chemistry. Eur J Biochem. 1999;259:572-576. https://doi.org/10.1046/j.1432-1327.1999.00033.x
- Xin G, Glawe D, Doty SL. Characterization of three endophytic, indole-3-acetic acid-producing yeasts occurring in Populus trees. Mycol Res. 2009;113:973-980. https://doi.org/10.1016/j.mycres.2009.06.001
- Limtong S, Kaewwichian R, Yongmanitchai W, et al. Diversity of culturable yeasts in phylloplane of sugarcane in Thailand and their capability to produce indole-3-acetic acid. World J Microbiol Biotechnol. 2014;30:1785-1796. https://doi.org/10.1007/s11274-014-1602-7
- Nutaratat P, Srisuk N, Arunrattiyakorn P, et al. Plant growth-promoting traits of epiphytic and endophytic yeasts isolated from rice and sugar cane leaves in Thailand. Fungal Biol. 2014;118:683-694. https://doi.org/10.1016/j.funbio.2014.04.010
- Fu S-F, Sun P-F, Lu H-Y, et al. Plant growth-promoting traits of yeasts isolated from the phyllosphere and rhizosphere of Drosera spatulata Lab. Fungal Biol. 2016;120:433-448. https://doi.org/10.1016/j.funbio.2015.12.006
- El-Tarabily KA. Suppression of Rhizoctonia solani diseases of sugar beet by antagonistic and plant growth-promoting yeasts. J Appl Microbiol. 2004;96:69-75. https://doi.org/10.1046/j.1365-2672.2003.02043.x
- Nutaratat P, Srisuk N, Arunrattiyakorn P, et al. Indole-3-acetic acid biosynthetic pathways in the basidiomycetous yeast Rhodosporidium paludigenum. Arch Microbiol. 2016;198:429-437. https://doi.org/10.1007/s00203-016-1202-z
- Rao RP, Hunter A, Kashpur O, et al. Aberrant synthesis of indole-3-acetic acid in Saccharomyces cerevisiae triggers morphogenic transition, a virulence trait of pathogenic fungi. Genetics. 2010;185:211. https://doi.org/10.1534/genetics.109.112854
- Sun P-F, Fang W-T, Shin L-Y, et al. Indole-3-acetic acid-producing yeasts in the phyllosphere of the carnivorous plant Drosera indica L. Plos One. 2014;9:e114196. https://doi.org/10.1371/journal.pone.0114196
- Surussawadee J, Khunnamwong P, Srisuk N, et al. Papiliotrema siamense f.a., sp. nov., a yeast species isolated from plant leaves. Int J Syst Evol Microbiol. 2014;64:3058-3062. https://doi.org/10.1099/ijs.0.065607-0
- Nutaratat P, Amsri W, Srisuk N, et al. Indole-3-acetic acid production by newly isolated red yeast Rhodosporidium paludigenum. J Gen Appl Microbiol. 2015;61:1-9. https://doi.org/10.2323/jgam.61.1
- Mujahid M, Sasikala C, Ramana CV. Production of indole-3-acetic acid and related indole derivatives from L-tryptophan by Rubrivivax benzoatilyticus JA2. Appl Microbiol Biotechnol. 2011;89:1001-1008. https://doi.org/10.1007/s00253-010-2951-2
- Kulkarni GB, Sanjeevkumar S, Kirankumar B, et al. Indole-3-acetic acid biosynthesis in Fusarium delphinoides strain GPK, a causal agent of wilt in chickpea. Appl Biochem Biotechnol. 2013;169:1292-1305. https://doi.org/10.1007/s12010-012-0037-6
- Ricardo C-L, Campos-Reales N, Elmerich C, et al. Physiological evidence for differently regulated tryptophan-dependent pathways for indole-3-acetic acid synthesis in Azospirillum brasilense. Mol Gen Genet. 2000;264:521-530. https://doi.org/10.1007/s004380000340
- Tanaka E, Tanaka C, Ishihara A, et al. Indole-3-acetic acid biosynthesis in Aciculosporium take, a causal agent of witches' broom of bamboo. J Gen Plant Pathol. 2003;69:1-6. https://doi.org/10.1007/s10327-002-0002-2
- Reineke G, Heinze B, Schirawski J, et al. Indole-3-acetic acid (IAA) biosynthesis in the smut fungus Ustilago maydis and its relevance for increased IAA levels in infected tissue and host tumour formation. Mol Plant Pathol. 2008;9:339-355. https://doi.org/10.1111/j.1364-3703.2008.00470.x
- Hilbert M, Voll LM, Ding Y, et al. Indole derivative production by the root endophyte Piriformospora indica is not required for growth promotion but for biotrophic colonization of barley roots. New Phytol. 2012;196:520-534. https://doi.org/10.1111/j.1469-8137.2012.04275.x
- Krause K, Henke C, Asiimwe T, et al. Biosynthesis and secretion of indole-3-acetic acid and its morphological effects on Tricholoma vaccinum-spruce ectomycorrhiza. Appl Environ Microbiol. 2015;81:7003-7011. https://doi.org/10.1128/AEM.01991-15
- Mashiguchi K, Tanaka K, Sakai T, et al. The main auxin biosynthesis pathway in Arabidopsis. Proc Natl Acad Sci USA. 2011;108:18512-18517. https://doi.org/10.1073/pnas.1108434108
- Zhao Y. Auxin biosynthesis. Arabidopsis book. 2014;12:e0173. https://doi.org/10.1199/tab.0173
- Brandi M, Clark EM, Lindow SE. Characterization of the indole-3-acetic acid (IAA) biosynthetic pathway in an epiphytic strain of Erwinia herbicola and IAA production in vitro. Can J Microbiol. 1996;42:586-592. https://doi.org/10.1139/m96-079
- Spaepen S, Vanderleyden J. Auxin and plantmicrobe interactions. Cold Spring Harb Perspect Biol. 2011;3:a001438. https://doi.org/10.1101/cshperspect.a001438
- Stes E, Prinsen E, Holsters M, et al. Plant-derived auxin plays an accessory role in symptom development upon Rhodococcus fascians infection. Plant J. 2012;70:513-527. https://doi.org/10.1111/j.1365-313X.2011.04890.x
- Koga J, Adachi T, Hidaka H. IAA Biosynthetic pathway from tryptophan via indole-3-pyruvic acid in Enterobacter cloacae. Agric Biol Chem. 1991;55:701-706. https://doi.org/10.1271/bbb1961.55.701
- Brown HM, Purves WK. Indole acetaldehyde reductase of Cucumis sativus L: kinetic properties and role in auxin biosynthesis. Plant Physiol. 1980;65:107-113. https://doi.org/10.1104/pp.65.1.107
- Koshiba T, Saito E, Ono N, et al. Purification and properties of flavin- and molybdenum-containing aldehyde oxidase from coleoptiles of maize. Plant Physiol. 1996;110:781-789. https://doi.org/10.1104/pp.110.3.781
- Zhao Y. Auxin biosynthesis: a simple two-step pathway converts tryptophan to indole-3-acetic acid in plants. Mol Plant. 2012;5:334-338. https://doi.org/10.1093/mp/ssr104
Cited by
- Auxins of microbial origin and their use in agriculture vol.104, pp.20, 2020, https://doi.org/10.1007/s00253-020-10890-8
- Auxin-producing fungal endophytes promote growth of sunchoke vol.16, 2019, https://doi.org/10.1016/j.rhisph.2020.100271
- Halotolerant Endophytic Bacterium Serratia rubidaea ED1 Enhances Phosphate Solubilization and Promotes Seed Germination vol.11, pp.3, 2021, https://doi.org/10.3390/agriculture11030224
- Culturable Yeasts as Biofertilizers and Biopesticides for a Sustainable Agriculture: A Comprehensive Review vol.10, pp.5, 2019, https://doi.org/10.3390/plants10050822
- Natural Indoles From the Bacterium Pseudovibrio denitrificans P81 Isolated From a Marine Sponge, Aaptos Species vol.16, pp.9, 2021, https://doi.org/10.1177/1934578x211033735
- Diversity of the Tryptophanase Gene and Its Evolutionary Implications in Living Organisms vol.9, pp.10, 2019, https://doi.org/10.3390/microorganisms9102156
- Large scale production of indole-3-acetic acid and evaluation of the inhibitory effect of indole-3-acetic acid on weed growth vol.11, pp.1, 2019, https://doi.org/10.1038/s41598-021-92305-w