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Research Articles

Early Access

Application of nitrogen-fixing, phosphate and potassium-solubilising rhizosphere bacteria as potential biofertilisers for maize

DOI
https://doi.org/10.14719/pst.13728
Submitted
19 January 2026
Published
02-07-2026
Versions

Abstract

The national demand for maize in Indonesia reached 14.46 million tons in 2023 and is expected to continue increasing in 2024 and 2025. To meet this growing demand, efforts to improve maize production are essential. Fertilisation is a key factor in enhancing crop productivity. However, the efficiency of nitrogen uptake from chemical NPK fertilisers is relatively low, with only 30–40 % absorbed by plants. At the same time, the remainder is lost to the environment through ammonia volatilisation and nitrate leaching. Biofertilisers containing consortia of nitrogen-fixing,  phosphate-solubilising and potassium-solubilising bacteria offer a promising alternative to reduce nitrogen loss and improve nutrient availability for maize growth. In this study, bacteria were isolated from the maize rhizosphere and roots, yielding a total of 29 isolates, comprising 12 phosphate-solubilising bacteria, 8 potassium-solubilising bacteria and 9 nitrogen-fixing bacteria. The isolate NBP2NB exhibited the highest phosphate-solubilising ability, while AKT2 demonstrated the highest potassium-solubilising capacity. Pathogenicity tests confirmed that none of the 29 isolates showed pathogenic effects on maize seedlings. In planta evaluation of bacterial consortia significantly improved maize growth compared with the control treatments, as reflected by vegetative and generative growth parameters. These findings indicate that bacterial consortia derived from the maize rhizosphere have potential aspects as biofertilisers for sustainably enhancing maize productivity.

 

References

  1. 1. Direktorat Pakan. Pemanfaatan jagung lokal oleh industri pakan. Buku Jagung. 2024;5.
  2. 2. Marsono E. Luas panen dan produksi jagung di Indonesia 2024 (angka tetap). Badan Pus Stat. 2025;2(16):15.
  3. 3. Komalasari WB. Analisis kinerja perdagangan jagung. Anal Kinerja Perdagang Jagung. 2024;14:70.
  4. 4. Badan Pusat Statistik. Luas panen dan produksi jagung di Indonesia 2022 (angka sementara). Ber Resmi Stat. 2023;74:1–16.
  5. 5. Jumadi O, Hartono H, Masniawati A, Iriany RN, Makkulawu AT, Inubushi K. Emissions of nitrous oxide and methane from rice field after granulated urea application with nitrification inhibitors and zeolite under different water managements. Paddy Water Environ. 2019;17(4):715–24. https://doi.org/10.1007/s10333-019-00724-3
  6. 6. James EK, Olivares FL, Baldani JI, Döbereiner J. Herbaspirillum, an endophytic diazotroph colonising vascular tissue in leaves of Sorghum bicolour L. Moench. J Exp Bot. 1997;48(308):785–97. https://doi.org/10.1093/jxb/48.3.785
  7. 7. Rodríguez H, Fraga R. Phosphate solubilising bacteria and their role in plant growth promotion. Biotechnol Adv. 1999;17(4–5):319–39. https://doi.org/10.1016/S0734-9750(99)00014-2
  8. 8. Etesami H, Emami S, Alikhani HA. Potassium solubilising bacteria (KSB): mechanisms, promotion of plant growth and future prospects - a review. J Soil Sci Plant Nutr. 2017;17(4):897–911. https://doi.org/10.4067/S0718-95162017000400005
  9. 9. Sayed ET, Eisa T, Mohamed HO, Abdelkareem MA, Allagui A, Alawadhi H, et al. Direct urea fuel cells: challenges and opportunities. J Power Sources. 2019;417:159–75. https://doi.org/10.1016/j.jpowsour.2018.12.024
  10. 10. IFA. 2023 IFA medium-term outlook report. 2023 Jun. https://www.ifastat.org/market-outlooks
  11. 11. Bahtiar, Arsyad M, Salman D, Azrai M, Tenrirawe A, Yasin M, et al. Promoting the new superior variety of national hybrid maize: improve farmer satisfaction to enhance production. Agriculture. 2023;13(1):174. https://doi.org/10.3390/agriculture13010174
  12. 12. Sansinenea E. Bacillus spp.: as plant growth-promoting bacteria. In: Secondary metabolites of plant growth-promoting rhizomicroorganisms. Singapore: Springer; 2019. p. 225–37. https://doi.org/10.1007/978-981-13-5862-3_11
  13. 13. Syafruddin S, Djaenuddin N, Irmadamayanti A, Najamuddin E, Arief R, Muis A, et al. Rhizobacteria consortium as a biofertiliser to enhance yield, nutrient use and fertiliser efficiency in maize. Bragantia. 2025;84:e20240196. https://doi.org/10.1590/1678-4499.20240196
  14. 14. Utami DS, Nugraha DR, Setiawati MR, Simarmata T. Assessment of the synergistic effects of selected native plant growth-promoting bacteria in farmers extract organic-biofertiliser formulations for enhancing maize growth. J Ecol Eng. 2025;26(4):171–81. https://doi.org/10.12911/22998993/199870
  15. 15. Kruščić K, Jelušić A, Hladnik M, Janakiev T, Anđelković J, Bandelj D, et al. The influence of bacterial inoculants and a biofertiliser on maize cultivation and the associated shift in bacteriobiota during the growing season. Plants. 2025;14(12):1753. https://doi.org/10.3390/plants14121753
  16. 16. Arsita R, Karim H, Hala Y, Iriany N, Jumadi O. Isolation and identification of nitrogen-fixing bacteria in the corn rhizosphere (Zea mays L.) originating from Jeneponto Regency, South Sulawesi. IOP Conf Ser Earth Environ Sci. 2020;484(1):012051. https://doi.org/10.1088/1755-1315/484/1/012051
  17. 17. Haswania, Karim H, Azis AA, Iriany N, Jumadi O. Isolation and characterisation of phosphate solubilising bacteria from corn rhizosphere. IOP Conf Ser Earth Environ Sci. 2021;911(1):012063. https://doi.org/10.1088/1755-1315/911/1/012063
  18. 18. Mirsam H, Kalqutny SH, Suriani, Aqil M, Azrai M, Pakki S, et al. Indigenous fungi from corn as a potential plant growth promoter and its role in Fusarium verticillioides suppression on corn. Heliyon. 2021;7(9):e07926. https://doi.org/10.1016/j.heliyon.2021.e07926
  19. 19. Sarkar P, Chourasia R. Bioconversion of organic solid wastes into biofortified compost using a microbial consortium. Int J Recycl Org Waste Agric. 2017;6(4):321–34. https://doi.org/10.1007/s40093-017-0180-8
  20. 20. Klement Z. Rapid detection of the pathogenicity of phytopathogenic pseudomonads. Nature. 1963;199(4890):299–300. https://doi.org/10.1038/199299b0
  21. 21. Hayashi TY, Sakamoto K. A rapid method for determination of nitrate in soil by hydrazine reduction procedure. Jpn J Soil Sci Plant Nutr. 1997;68:322–26. https://doi.org/10.20710/dojo.68.3_322
  22. 22. Mirsam H, Suriani, Aqil M, Azrai M, Efendi R, Muliadi A, et al. Molecular characterisation of indigenous microbes and its potential as a biological control agent of Fusarium stem rot disease (Fusarium verticillioides) on maize. Heliyon. 2022;8(12):e11960. https://doi.org/10.1016/j.heliyon.2022.e11960
  23. 23. Kirkman JH, Basker A, Surapaneni A, Mac Gregor AN. Potassium in the soil of New Zealand-a review. N Z J Agric Res. 1994;37(2):207–27. https://doi.org/10.1080/00288233.1994.9513059
  24. 24. Irawati AFC, Mutaqin KH, Suhartono MT, Sastro Y, Sulastri N, Widodo N. The exploration and effect of endophytic fungus isolated from chilli’s root to growth of chilli seedling. J Hortik. 2017;27(1):105. https://doi.org/10.21082/jhort.v27n1.2017.p105-112
  25. 25. Goldstein AH. Bacterial solubilization of mineral phosphates: historical perspective and future prospects. Am J Altern Agric. 1986;1(2):51–7. https://doi.org/10.1017/S0889189300000886
  26. 26. Meena VS, Maurya BR, Verma JP, Meena RS. Potassium solubilising microorganisms for sustainable agriculture. New Delhi: Springer; 2016. https://doi.org/10.1007/978-81-322-2776-2
  27. 27. Vincentz M, Moureaux T, Leydecker MT, Vaucheret H, Caboche M. Regulation of nitrate and nitrite reductase expression in Nicotiana plumbaginifolia leaves by nitrogen and carbon metabolites. Plant J. 1993;3:315–24. https://doi.org/10.1111/j.1365-313X.1993.tb00183.x
  28. 28. Migge A, Becker TW. In tobacco leaves, the genes encoding the nitrate-reducting or the ammonium-assimilating enzymes are regulated differently by external nitrogen sources. Plant Physiol Biochem. 1996;34:665–71.
  29. 29. Atilio JB, Causin HF. The central role of amino acids on nitrogen utilisation and plant growth. J Plant Physiol. 1996;149:358–62. https://doi.org/10.1016/S0176-1617(96)80134-9
  30. 30. Tilahun T, Minale L, Alemayehu A, Abreham M. Maize fertiliser response at the major maize growing areas of northwest Ethiopia. In: Proceedings of the 1st Annual Regional Conference on Completed Crop Research Activities; 2006 Aug 14–17; Bahir Dar, Ethiopia. Bahir Dar: Amhara Regional Agricultural Research Institute; 2006.
  31. 31. Ebelhar SA, Varsa EC. Tillage and potassium placement effects on potassium utilisation by corn and soybean. Commun Soil Sci Plant Anal. 2000;31:11–4. https://doi.org/10.1080/00103620009370591
  32. 32. Zhang ZY, Wang QL, Li ZH, Duan LS, Tian XL. Effects of potassium deficiency on root growth of cotton seedlings and its physiological mechanisms. Acta Agron Sin. 2009;35(4):718–23. https://doi.org/10.1016/S1875-2780(08)60079-6
  33. 33. Li JT, Zhong XL, Wang F, Zhao QG. Effect of poultry litter and livestock manure on soil physical and biological indicators in a rice-wheat rotation system. Plant Soil Environ. 2011;57(8):351–56. https://doi.org/10.17221/233/2010-PSE
  34. 34. Chaturvedi. Peranan pupuk N, P, dan K pada budidaya pertanian. Jakarta: Penebar Swadaya; 2005. p. 75–6.
  35. 35. Gardner FP, Pearce RB, Mitchell RL. Fisiologi tanaman budidaya. Susilo H, translator. Jakarta: UI Press; 1991.
  36. 36. Radkowski A, Radkowska I, Bocianowski J, Cyplik A, Wolski K, Bujak H. Effect of amino acids and effective microorganisms on meadow silage chemical composition. Agronomy. 2021;11(6):1198. https://doi.org/10.3390/agronomy11061198
  37. 37. Moe LA. Amino acids in the rhizosphere: from plants to microbes. Am J Bot. 2013;100(9):1692–705. https://doi.org/10.3732/ajb.1300033
  38. 38. Ma L, Yang L, Liu W, Zhang Y, Zhou Q, Wu Z, et al. Effects of root exudates on rhizosphere bacteria and nutrient removal in pond-ditch circulation systems (PDCSs) for rural wastewater treatment. Sci Total Environ. 2021;782:147282. https://doi.org/10.1016/j.scitotenv.2021.147282
  39. 39. Afridi MS, Kumar A, Javed MA, Dubey A, Medeiros FHV, Santoyo G. Harnessing root exudates for plant microbiome engineering and stress resistance in plants. Microbiol Res. 2024;279:127564. https://doi.org/10.1016/j.micres.2023.127564
  40. 40. Fitzpatrick TB, Chapman LM. The importance of thiamine (vitamin B1) in plant health: from crop yield to biofortification. J Biol Chem. 2020;295(34):12002–013. https://doi.org/10.1074/jbc.REV120.010918
  41. 41. Hessler T, Huddy RJ, Sachdeva R, Lei S, Harrison STL, Diamond S, et al. Vitamin interdependencies predicted by metagenomics-informed network analyses and validated in microbial community microcosms. Nat Commun. 2023;14:4768. https://doi.org/10.1038/s41467-023-40360-4
  42. 42. Luo D, Shi J, Li M, Chen J, Wang T, Zhang Q, et al. Consortium of phosphorus-solubilising bacteria promotes maize growth and changes the microbial community composition of rhizosphere soil. Agronomy. 2024;14(7):1535. https://doi.org/10.3390/agronomy14071535
  43. 43. Tang A, Haruna AO, Majid NMA, Jalloh MB. Effects of selected functional bacteria on maize growth and nutrient use efficiency. Microorganisms. 2020;8(6):854. https://doi.org/10.3390/microorganisms8060854
  44. 44. Khati P, Mishra PK, Pal RS, Kant L. Enhancing maize growth and drought resilience by synergistic application of plant growth promoting rhizobacteria. Sci Rep. 2025;15:45440. https://doi.org/10.1038/s41598-025-29110-2

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