IAA (Indole-3-Acetic Acid) Production by ACC Deaminase-Producing Rhizobacteria Isolated from Peanut Rhizosphere
DOI:
https://doi.org/10.33394/bioscientist.v14i3.20039Keywords:
ACC deaminase, IAA production dynamics, peanut, PGPR, rhizobacteriaAbstract
This study aimed to evaluate the indole-3-acetic acid (IAA)-producing capacity of rhizobacterial isolates obtained from the rhizosphere of peanut (Arachis hypogaea L.) and previously identified as ACC deaminase-producing bacteria under in vitro conditions. IAA production was assessed qualitatively and quantitatively. Qualitative detection was performed using the colorimetric Salkowski reagent assay, whereas quantitative determination was conducted spectrophotometrically by comparing sample absorbance values with an IAA standard curve. The results showed that all six rhizobacterial isolates, together with Escherichia coli used as a reference strain, exhibited IAA-producing activity, although the estimated IAA concentrations varied among isolates and incubation periods. Among the tested rhizobacteria, isolate I9 exhibited the highest IAA concentration, reaching 34.75 ppm after three days of incubation, and showed an overall increasing production trend during the incubation period. These findings demonstrate that the ACC deaminase-positive rhizobacterial isolates examined in this study also possess IAA-producing capacity, although their production profiles differ among isolates. The combined potential for IAA production and ACC deaminase activity suggests that these isolates warrant further evaluation as plant growth-promoting rhizobacteria (PGPR) for improving plant growth and development.
References
Advinda, L., Fifendy, M., Anhar, A., Leilani, I., & Sahara, A. L. (2018). Pertumbuhan stek horizontal batang jarak pagar (Jatropha curcas L.) yang diintroduksi dengan pseudomonad fluoresen. Eksakta, 19(1), 68–75. https://doi.org/10.24036/eksakta/vol19-iss1/129
Astriani, M., & Murtiyaningsih, H. (2018). Pengukuran indole-3-acetic acid (IAA) pada Bacillus sp. dengan penambahan L-tryptofan. Bioeduscience, 2(2), 116–121. https://doi.org/10.29405/j.bes/22116-1212233
Bal, H. B., Das, S., Dangar, T. K., & Adhya, T. K. (2013). ACC deaminase and IAA producing growth promoting bacteria from the rhizosphere soil of tropical rice plants. Journal of Basic Microbiology, 53(12), 972–984. https://doi.org/10.1002/jobm.201200445
Bhattacharyya, P. N., & Jha, D. K. (2012). Plant growth-promoting rhizobacteria (PGPR): Emergence in agriculture. World Journal of Microbiology and Biotechnology, 28, 1327–1350. https://doi.org/10.1007/s11274-011-0979-9
Dewi, T. K., Suryanggono, J., & Agustiyani, D. (2016). Isolasi dan uji aktivitas bakteri penghasil hormon tumbuh IAA (indole-3-acetic acid) dan bakteri perombak protein dari tanah pertanian Tual, Maluku Tenggara. Prosiding Seminar Nasional Masyarakat Biodiversitas Indonesia, 2(2), 271–276. https://doi.org/10.13057/psnmbi/m020226
Gang, S., Sharma, S., Saraf, M., Buck, M., & Schumacher, J. (2019). Analysis of indole-3-acetic acid (IAA) production in Klebsiella by LC-MS/MS and the Salkowski method. Bio-Protocol, 9(9), e3230. https://doi.org/10.21769/BioProtoc.3230
Gordon, A. S., & Weber, R. P. (1951). Colorimetric estimation of indoleacetic acid. Plant Physiology, 26(1), 192–195.
Guo, D., Kong, S., Chu, X., Li, X., & Pan, H. (2019). De novo biosynthesis of indole-3-acetic acid in engineered Escherichia coli. Journal of Agricultural and Food Chemistry, 67(29), 8186–8190. https://doi.org/10.1021/acs.jafc.9b02048
Jaya, D. K., Susilowati, L. E., Arifin, Z., Iwandaka, A., & Martini, E. (2024). The population and isolates of potential ACC deaminase-producing rhizobacteria from rhizospheric soil of peanut under different moisture level. Jurnal of Research in Science Education, 9(1), 8366–8375. https://doi.org/10.29303/jppipa.v10i11.7818
Karnwal, A. (2009). Production of indole acetic acid by fluorescent Pseudomonas in the presence of L-tryptophan and rice root exudates. Journal of Plant Pathology, 91(1), 61–63. https://doi.org/10.4454/jpp.v91i1.624
Kravchenko, L. V., Azarova, T. S., Makarova, N. M., & Tikhonovich, I. A. (2004). The effect of tryptophan present in plant root exudates on the phytostimulating activity of rhizobacteria. Microbiology, 73(2), 156–158. https://doi.org/10.1023/B:MICI.0000023982.76684.9d
Lebrazi, S., Niehaus, K., Bednarz, H., Fadli, M., Chraibi, M., & Fikri-Benbrahim, K. (2020). Screening and optimization of indole-3-acetic acid production and phosphate solubilization by rhizobacterial strains isolated from Acacia cyanophylla root nodules and their effects on its plant growth. Journal of Genetic Engineering and Biotechnology, 18, Article 71. https://doi.org/10.1186/s43141-020-00090-2
Li, M., Guo, R., Yu, F., Chen, X., Zhao, H., Li, H., & Wu, J. (2018). Indole-3-acetic acid biosynthesis pathways in the plant-beneficial bacterium Arthrobacter pascens ZZ21. International Journal of Molecular Sciences, 19(2), 443. https://doi.org/10.3390/ijms19020443
McFarland, J. M. (1907). The nephelometer: An instrument for estimating the number of bacteria in suspensions used for calculating the opsonic index and for vaccines. Journal of the America Medial Accosiation, 49(14), 1176–1178. https://doi.org/10.1001/jama.1907.25320140022001f
Melo, J., Carolino, M., Carvalho, L., Correia, P., Tenreiro, R., Chaves, S., Meleiro, A. I., de Souza, S. B., Dias, T., Cruz, C., & Ramos, A. C. (2016). Crop management as a driving force of plant growth promoting rhizobacteria physiology. SpringerPlus, 5(1), Article 1574. https://doi.org/10.1186/s40064-016-3232-z
Nonhebel, H. M. (2015). Tryptophan-independent indole-3-acetic acid synthesis: Critical evaluation of the evidence. Plant Physiology, 169(2), 1001–1005. https://doi.org/10.1104/pp.15.01091
Patten, C. L., & Glick, B. R. (1996). Bacterial biosynthesis of indole-3-acetic acid. Canadian Journal of Microbiology, 42, 207–220. https://doi.org/10.1139/m96-032
Ratnaningsih, H. R., Noviana, Z., Dewi, T. K., Loekito, S., Wiyono, S., Gafur, A., & Antonius, S. (2023). IAA and ACC deaminase producing-bacteria isolated from the rhizosphere of pineapple plants grown under different abiotic and biotic stresses. Heliyon, 9(6), e16306. https://doi.org/10.1016/j.heliyon.2023.e16306
Rini, I. A., Oktaviani, I., Asril, M., Agustin, R., & Frima, F. K. (2020). Isolasi dan karakterisasi bakteri penghasil IAA (indole acetic acid) dari rhizosfer tanaman akasia (Acacia mangium). Agro Bali: Agricultural Journal, 3(2), 210–219. https://doi.org/10.37637/ab.v3i2.619
Roopa, S., Mishra, T., Bhattacharya, S., Bhadra, A., Raj, S., Shrivastava, R., & Patil, S. J. (2023). Role of IAA in plant growth, development, and interaction with other phytohormones. European Chemical Bulletin, 12(5), 5293–5297. https://doi.org/10.48047/ecb/2023.12.si5a.0448
Wahyudi, A. T., Astuti, R. P., Widyawati, A., Meryandini, A., & Nawangsih, A. A. (2011). Characterization of Bacillus sp. strains isolated from rhizosphere of soybean plants for their use as potential plant growth for promoting rhizobacteria. Journal of Microbiology and Antimicrobials, 3(2), 34–40. https://academicjournals.org/JMA
Wu, C. H., Bernard, S. M., Andersen, G. L., & Chen, W. (2009). Developing microbe-plant interactions for applications in plant-growth promotion and disease control, production of useful compounds, remediation and carbon sequestration. Microbial Biotechnology, 2(4), 428–440. https://doi.org/10.1111/j.1751-7915.2009.00109.x
Zahroya, I. U., Mubarik, N. R., & Tjahjoleksono, A. (2020). Isolation and characterization of indole-3-acetic acid producing bacteria from red onion rhizosphere. IOP Conference Series: Earth and Environmental Science, 457, 012046. https://doi.org/10.1088/1755-1315/457/1/012046
Zerrouk, I. Z., Rahmoune, B., Khelifi, L., Mounir, K., & Baluska, F. (2019). Algerian Sahara PGPR confers maize root tolerance to salt and aluminum toxicity via ACC deaminase and IAA. Acta Physiologiae Plantarum, 41, Article 91. https://doi.org/10.1007/s11738-019-2881-2
Zhang, P., Jin, T., Sahu, S. K., Xu, J., Shi, Q., Liu, H., & Wang, Y. (2019). The distribution of tryptophan-dependent indole-3-acetic acid synthesis pathways in bacteria unravelled by large-scale genomic analysis. Molecules, 24(7), 1411. https://doi.org/10.3390/molecules24071411
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