Exploring the Phosphate Solubilising Rhizobacteria isolated from Wild Musa Rhizosphere and their Efficacy on Growth Promotion of Phaseolus vulgaris
DOI:
https://doi.org/10.18006/2024.12(5).742.755Keywords:
Biofertilizer, IAA production, PGPR, Phosphate solubilisation, Siderophore production, Wild Musa rhizosphereAbstract
Plant growth-promoting rhizobacteria (PGPR) are recognized for enhancing plant growth, protecting against pathogens, and boosting productivity. The present study focused on isolating PGPR from the rhizosphere of wild Musa, screening for growth-promoting traits, and assessing their effects on the growth of Phaseolus vulgaris L. A total of 20 strains were isolated and evaluated for their capacity to solubilize phosphate, produce indole-3-acetic acid (IAA), synthesize siderophores, and their tolerance to salt and heavy metals. Among 20 isolates, four most effective isolates were selected and based on 16S rRNA sequencing these isolates were identified as: Burkholderia cepacia (RZ27), Agrobacterium larrymoorei (RZ23), Pseudomonas taiwanensis (RZ5), and Pseudomonas orientalis (RZ3). P. orientalis exhibited the highest phosphate solubilization ability (222.17 µg/ml), followed closely by B. cepacia (222.80 µg/ml), A. larrymoorei (71.57 µg/ml), and P. taiwanensis (19.20 µg/ml). Isolate RZ27 demonstrated the greatest salt tolerance at 14%, followed by RZ5 and RZ23 (10% each) and RZ3 (6%). Notably, only isolate RZ23 produced IAA, while all isolates except RZ27 could produce siderophores. The highest siderophore production was recorded with RZ23 (33.34% siderophore production unit, SPU), followed by RZ3 (29.07 SPU) and RZ5 (27.20 SPU). A. larrymoorei and P. orientalis showed the highest chromium tolerance (1840 µg/ml), followed by B. cepacia (1810 µg/ml) and P. taiwanensis (1300 µg/ml). There was a noticeable enhancement in plant growth when P. vulgaris was inoculated with the PGPR strains. Among the four isolates, RZ3 significantly increased both shoot and root lengths and biomass compared to the control; meanwhile, isolate RZ23 improved shoot fresh weight. These findings suggest that these isolates have the potential to be used as bioinoculants to improve plant development.
References
Akhtar, N., Ilyas, N., Yasmin, H., Sayyed, R.Z., Hasnain, Z., AElsayed, E., & El Enshasy, H. A. (2021). Role of Bacillus cereus in improving the growth and phytoextractability of Brassica nigra (L.) K. Koch in chromium contaminated soil. Molecules, 26(6), 1569. https://doi.org/10.3390/molecules26061569
Alexander, D.B., & Zuberer, D.A. (1991) Use of chrome azurol S reagents to evaluate siderophore production by rhizosphere bacteria. Biology and Fertility of Soils, 12, 39-45. https://doi.org/10.1007/BF00369386
Bakhshandeh, E., Rahimian, H., Pirdashti, H., & Nematzadeh, G.A. (2014). Phosphate solubilization potential and modeling of stress tolerance of rhizobacteria from rice paddy soil in northern Iran. World Journal of Microbiology & Biotechnology, 30(9), 2437–2447. https://doi.org/10.1007/s11274-014-1669-1
Bouzar, H., & Jones, J.B. (2001). Agrobacterium larrymoorei sp. nov., a pathogen isolated from aerial tumours of Ficus benjamina. International Journal of Systematic and Evolutionary Microbiology, 51(3), 1023–1026. https://doi.org/10.1099/00207713-51-3-1023
Chen, Y.P., Rekha, P.D., Arun, A.B., Shen, F.T., Lai, W.A., & Young, C.C. (2006). Phosphate solubilizing bacteria from subtropical soil and their tricalcium phosphate solubilizing abilities. Applied Soil Ecology, 34(1), 33-41. https://doi.org/10.1016/j.apsoil.2005.12.002
Deb, C.R., & Tatung, M. (2024). Siderophore producing bacteria as biocontrol agent against phytopathogens for a better environment: a review. South African Journal of Botany, 165, 153-162. https://doi.org/10.1016/j.sajb.2023.12.031.
Ferreira, M.J., Silva, H., & Cunha, A. (2019). Siderophore-producing rhizobacteria as a promising tool for empowering plants to cope with iron limitation in saline soils: a review. Pedosphere, 29(4), 409-420. https://doi.org/10.1016/S1002-0160(19)60810-6
Giannelli, G., Potestio, S., & Visioli, G. (2023). The contribution of PGPR in salt stress tolerance in crops: unravelling the molecular mechanisms of cross-talk between plant and bacteria. Plants, 12(11), 2197. https://doi.org/10.3390/plants12112197
Hadjouti, R., Oulebsir-Mohandkaci, H., Farida, B., & Furze, J. (2022). Enhancing agriculture recovery of Phaseolus vulgaris L. and Cucurbita pepo L. with Olea europaea L. plant growth promoting rhizobacteria. Soil Research, 60, 850-863. https://doi.org/10.1071/SR21320
Hider, R.C., & Kong, X. (2010). Chemistry and biology of siderophores. Nature Product Reports, 27(5), 637-57. https://doi.org/10.1039/b906679a.
Janaki, M., Kirupanantha-Rajan, P., Senthil-Nathan, S., Stanley-Raja, V., Al Farraj, D.A., Aljeidi, R.A., & Arokiyaraj, S. (2024). Beneficial role of Burkholderia cepacia in heavy metal bioremediation in metal-polluted soils and enhance the tomato plant growth. Biocatalysis and Agricultural Biotechnology, 57, 103032. https://doi.org/10.1016/j.bcab.2024.103032
Kang, S.M., Shahzad, R., Bilal, S., Khan, A.L., You, Y.H., Lee, W.H., Ryu, H.L., Lee, K.E., & Lee, I.J. (2017). Metabolism-mediated induction of zinc tolerance in Brassica rapa by Burkholderia cepacia CS2-1. Journal of Microbiology, 55(12), 955–965. https://doi.org/10.1007/s12275-017-7305-7
Khanna, K., Jamwal, V.L., Gandhi, S.G., Ohri, P., & Bhardwaj, R. (2019). Metal resistant PGPR lowered Cd uptake and expression of metal transporter genes with improved growth and photosynthetic pigments in Lycopersicon esculentum under metal toxicity. Scientific Reports, 9(1), 5855. https://doi.org/10.1038/s41598-019-41899-3
Khurana, A., & Kumar, V. (2022). State of Biofertilizers and Organic Fertilizers in India, Centre for Science and Environment, New Delhi, India.
Li, X., Sun, P., Zhang, Y., Jin, C., & Guan, C. (2020). A novel PGPR strain Kocuria rhizophilaY1 enhances salt stress tolerance in maize by regulating phytohormone levels, nutrient acquisition, redox potential, ion homeostasis, photosynthetic capacity and stress-responsive genes expression. Environmental and Experimental Botany, 174(3), 104023. https://doi.org/10.1016/j.envexpbot.2020.104023
Li, Z., Henawy, A.R., Halema, A.A., Fan, Q., Duanmu, D., & Huang, R. (2022). A wild rice rhizobacterium Burkholderia cepacia BRDJ enhances nitrogen use efficiency in rice. International Journal of Molecular Sciences, 23(18), 10769. https://doi.org/10.3390/ijms231810769
Mazhar, R., Ilyas, N., Arshad, M., Khalid, A., & Hussain, M. (2020). Isolation of heavy metal-tolerant PGPR strains and amelioration of chromium effect in wheat in combination with biochar. Iranian Journal of Science and Technology, Transactions A: Science, 44, 1-12. https://doi.org/10.1007/s40995-019-00800-7
Megu, M., Paul, A. & Deb, C.R. (2024a). Isolation and screening of stress tolerant and plant growth promoting root nodulating rhizobial bacteria from some wild legumes of Nagaland, India. South African Journal of Botany, 168, 260-269. https://doi.org/10.1016/j.sajb.2024.03.021
Megu, M., Paul, A. & Deb, C.R. (2024b). Potential nitrogen fixing rhizobia isolated from some wild legumes of Nagaland based on RAPD with nif-directed primer and their biochemical activities. Journal of Experimental Biology and Experimental Science, 12(4), 388-605. http://dx.doi.org/10.18006/2024.12(4).588.605
Mishra, P., Mishra, J., & Arora, N.K. (2023). Salt tolerant Pseudomonas taiwanensis PWR-1 in combination with a reduced dose of mineral fertilizers improves the nutritional and antioxidant properties of wheatgrass grown in saline soil. World Journal of Microbiology & Biotechnology, 40(1), 11. https://doi.org/10.1007/s11274-023-03806-x
Molinaro, A., De Castro, C., Lanzetta, R., Parrilli, M., Raio, A., & Zoina, A. (2003). Structural elucidation of a novel core oligosaccharide backbone of the lipopolysaccharide from the new bacterial species Agrobacterium larrymoorei. Carbohydrate Research, 338(23), 2721–2730. https://doi.org/10.1016/s0008-6215(03)00316-1
Oo, K., Win, T., Khai, A., & Fu, P. (2020). Isolation, screening and molecular characterization of multifunctional plant growth promoting rhizobacteria for a sustainable agriculture. American Journal of Plant Sciences, 11. 773-792. https://doi.org/10.4236/ajps.2020.116055
Ortiz, J., Soto, J., Almonacid, L., Fuentes, A., Campos-Vargas, R., & Arriagada, C. (2019). Alleviation of metal stress by Pseudomonas orientalis and Chaetomium cupreum strains and their effects on Eucalyptus globulus growth promotion. Plant and Soil, 436(1-2), 449-461. https://doi.org/10.1007/s11104-019-03946-w
Pande, A., Pandey, P., Mehra, S., Singh, M., & Kaushik, S. (2017). Phenotypic and genotypic characterization of phosphate solubilizing bacteria and their efficiency on the growth of maize. Journal of Genetic Engineering & Biotechnology, 15(2), 379–391. https://doi.org/10.1016/j.jgeb.2017.06.005
Payne, S.M. (1993). Iron acquisition in microbial pathogenesis. Trends in Microbiology, 1(2), 66–69. https://doi.org/10.1016/0966-842x(93)90036-q
Pereira, S.I.A., Abreu, D., Moreira, H., Vega, A., & Castro, P.M.L. (2020). Plant growth-promoting rhizobacteria (PGPR) improve the growth and nutrient use efficiency in maize (Zea mays L.) under water deficit conditions. Heliyon, 6(10), e05106. https://doi.org/10.1016/j.heliyon.2020.e05106
Pongener, B., Deb, C.R. & Paul, A. (2024). Prospecting beneficial microsymbiont associated with root nodules of crop legumes of North-Eastern India, Nagaland. Proceedings of National Academy of Sciences, India Section B: Plant Science, 94(4), 835-843. https://doi.org/10.1007/s40011-024-01601-8
Prasad, S., Yadav, K.K., Kumar, S., Gupta, N., Cabral-Pinto, M.M.S., Rezania, S., Radwan, N., & Alam, J. (2021). Chromium contamination and effect on environmental health and its remediation: a sustainable approaches. Journal of Environmental Management, 285, 112174. https://doi.org/10.1016/j.jenvman.2021.112174
Qingwei, Z., Lushi, T., Yu, Z., Yu, S., Wanting, W., Jiangchuan, W., Xiaolei, D., Xuejiao, H., & Bilal, M. (2023). Isolation and characterization of phosphate-solubilizing bacteria from rhizosphere of poplar on road verge and their antagonistic potential against various phytopathogens. BMC Microbiology, 23(1), 221. https://doi.org/10.1186/s12866-023-02953-3
Rana, A., Saharan, B., Joshi, M., Prasanna, R., Kumar, K., & Nain, L. (2011). Identification of multi-trait PGPR isolates and evaluating their potential as inoculants for wheat. Annals of Microbiology, 61(4), 893–900. https://doi.org/10.1007/s13213-011-0211-z
Sarkar, A., Pramanik, K., Mitra, S., Soren, T., & Maiti, T.K. (2018). Enhancement of growth and salt tolerance of rice seedlings by ACC deaminase-producing Burkholderia sp. MTCC12259. Journal of Plant Physiology, 231, 434-442. https://doi.org/10.1016/j.jplph.2018.10.010
Sanchez-Gonzalez, M.E., Mora-Herrera, M.E., Wong-Villarreal, A., De La Portilla-López, N., Sanchez-Paz, L., Lugo, J., Vaca-Paulín, R., Del Aguila, P., & Yañez-Ocampo, G. (2022). Effect of pH and carbon source on phosphate solubilization by bacterial strains in Pikovskaya medium. Microorganisms, 11(1), 49. https://doi.org/10.3390/microorganisms11010049
Sharma, A., Dev, K., Sourirajan, A., & Choudhary, M. (2021a). Isolation and characterization of salt-tolerant bacteria with plant growth-promoting activities from saline agricultural fields of Haryana, India. Journal of Genetic Engineering & Biotechnology, 19(1), 99. https://doi.org/10.1186/s43141-021-00186-3
Sharma, S., Shah, R., Rathod, Z., Jain, R., Lucie, K., & Saraf, M. (2021b). Isolation of heavy metal tolerant rhizobacteria from Zawarminesarea, Udaipur, Rajasthan, India. Bioscience Biotechnology Research Communications. 13, 233-238. https://doi.org/10.3390/plants9010100
Shultana, R., Kee Zuan, A. T., Yusop, M.R., & Saud, H.M. (2020). Characterization of salt-tolerant plant growth-promoting rhizobacteria and the effect on growth and yield of saline-affected rice. PloSOne, 15(9), e0238537. https://doi.org/10.1371/ journal.pone.0238537
Tatung, M., & Deb, C.R. (2021). Plant growth promotion by rhizobacteria: a potential tool for sustainable agriculture. In C.R. Deb & A. Paul (Eds.), Bioresources and Sustainable Livelihood of Rural India (pp 29-49). Mittal Publications, New Delhi, India.
Tatung, M., & Deb, C.R. (2023). Isolation, characterization, and investigation on potential multi-trait plant growth promoting rhizobacteria from wild banana (Musa itinerans) rhizospheric soil. Journal of Pure and Applied Microbiology, 17(3), 1578-1590. https://doi.org/10.22207/JPAM.17.3.19
Tatung, M., & Deb, C.R. (2024a). Screening and characterization of heavy metal tolerant rhizobacteria from wild Musa rhizosphere from coal mining area of Changki, Nagaland, India and assessment of their growth promoting potential under Cd/Cu contaminated conditions. South African Journal of Botany, 165, 217-227. https://doi.org/10.1016/j.sajb.2023.12.039.
Tatung, M., & Deb, C. R. (2024b). Bacterial siderophores as potential biocontrol agent against phytopathogens. In C.R. Deb, Talijungla & N. Puro (Eds.), Bioresources: Conservation and Sustainability. (pp 423-436). Mittal Publications, New Delhi, India.
Uebersax, M.A., Cichy, K.A., Gomez, F.E., Porch, T.G., Heitholt, J., Osorno, J.M., Kamfwa, K., Snapp, S.S., & Bales, S. (2023). Dry beans (Phaseolus vulgaris L.) as a vital component of sustainable agriculture and food security—a review. Legume Science, 5(1), e155. https://doi.org/10.1002/leg3.155
Wang, C., Wang, H., Li, Y., Li, Q., Yan, W., Zhang, Y., Wu, Z., & Zhou, Q. (2021). Plant growth-promoting rhizobacteria isolation from rhizosphere of submerged macrophytes and their growth-promoting effect on Vallisneria natans under high sediment organic matter load. Microbial Biotechnology, 14(2), 726–736. https://doi.org/10.1111/1751-7915.13756
Yadav, J.S., Sharma, R.K., Yadav, J., Tiwari, S., Kumar, U., Singh, P.K., & Kumar, I. (2022). Isolation, identification, and characterization of cadmium resistant rhizobacterial isolates from long-term waste water irrigated soils. Journal of Scientific Research, 66(1), 201-208. https://doi.org/10.37398/JSR.2022.660122
Yaghoubi, K.M., Strafella, S., Filannino, P., Minervini, F., & Crecchio, C. (2024). Importance of lactic acid bacteria as an emerging group of plant growth-promoting rhizobacteria in sustainable agroecosystems. Applied Sciences, 14, 1798. https://doi.org/10.3390/ app14051798
Yamini, P., Gopalakrishnan, R., Prasad, S., Karkuvelraja, R., Commerce, C.T., & Biodiversity, M. (2021). Isolation and identification of indole acetic acid (IAA) producing bacteria from organic soil: investigating its efficacy on plant growth. Journal of University of Shanghai for Science and Technology, 23, 1294-1312. https://doi.org/10.51201/jusst/21/06443
Young J. M. (2004). Renaming of Agrobacterium larrymoorei Bouzar and Jones 2001 as Rhizobium larrymoorei (Bouzar and Jones 2001) comb. nov. International journal of systematic and evolutionary microbiology, 54(Pt 1), 149. https://doi.org/10.1099/ijs.0.02870-0
You, M., Fang, S., MacDonald, J., Xu, J., & Yuan, Z.C. (2020). Isolation and characterization of Burkholderia cenocepacia CR318, a phosphate solubilizing bacterium promoting corn growth. Microbiological Rresearch, 233, 126395. https://doi.org/10.1016/j.micres.2019.126395
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