Probiotic assisted drought tolerance in green gram: A novel strategy for sustainable agriculture
DOI:
https://doi.org/10.14719/pst.6497Keywords:
antioxidant enzymes, biopriming, drought tolerance, green gram, nodule associated plant probiotics, root nodules, stomatal morphologyAbstract
Drought stress is a critical factor that limits crop growth and yield. Biopriming has emerged as an effective and eco-friendly method to mitigate drought stress and enhance plant growth. This study evaluated the impact of nodule-associated plant probiotics (NAPP) on green gram seeds through treatments such as biopriming, coating and their combination of biopriming + coating along with hydropriming and uninoculated seeds served as a control in both in vivo and pot experiments. The study demonstrated that a combination of 6 mL biopriming + 4 mL coated seeds significantly improved the speed of germination (33%), germination percentage (16%), total seedling length (31%), dry weight (29%), seed vigor index (50%) compared uninoculated seeds. In the pot experiment, seeds treated with the combination of biopriming + coating were planted in different drought conditions viz., severe drought (40% water holding capacity, WHC), moderate drought (70% WHC) and controlled conditions (100% WHC). Combining biopriming + coated seeds showed a higher photosynthetic rate and relative water content, significantly improving plant growth under drought stress and optimal conditions. The biochemical study found that combining biopriming + coated seeds considerably increased proline content, total soluble protein and antioxidant enzymes under drought stress and control conditions. Furthermore, the combination significantly increased yield components, including the number of seeds, pods, 100-seed weight and root nodules, under both control and drought stress conditions. Principal component analysis (PCA) confirmed the modulation of growth, root nodules, antioxidant enzymes and yield components by combining biopriming and coating. It also showed reduced electrical leakage (EL) in green gram under drought stress conditions.
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Wen W, Timmermans J, Chen Q, van Bodegom PM. A review of remote sensing challenges for food security with respect to salinity and drought threats. Remote Sens. 2020;13(1):6. https://doi.org/10.3390/rs13010006
Jahan MS, Shu S, Wang Y, Hasan MM, El-Yazied AA, Alabdallah NM, et al. Melatonin pretreatment confers heat tolerance and repression of heat-induced senescence in tomato through the modulation of ABA- and GA-mediated pathways. Front Plant Sci. 2021;650955. https://doi.org/10.3389/fpls. 2021.650955
Oshunsanya SO, Nwosu NJ, Li Y. Abiotic stress in agricultural crops under climatic conditions. In: Jhariya M, Banerjee A, Meena R, Yadav D, editors. Sustainable agriculture, forest and environmental management. Singapore: Springer; 2019. https://doi.org/10.1007/978-981-13-6830-1_3
Nawaz H, Hussain N, Ahmed N, Javaiz AL. Efficiency of seed bio-priming technique for healthy mung bean productivity under terminal drought stress. J Integr Agric. 2021;20(1):87-99. https://doi.org/10.1016/S2095-3119(20)63184-7
Mehta A, Bhardwaj N. Phytotoxic effect of industrial effluents on seed germination and seedling growth of Vigna radiata and Cicer arietinum. Global J of Biol, Biotech and Biochem. 2012;1(1):1?5.
Department of Agriculture and Farmers Welfare [Internet]. Government of India. [Cited 2023]. Available from: https://agriwelfare.gov.in/
Farooq M, Hussain M, Siddique KHM. Drought stress in wheat during flowering and grain-filling periods. Crit Rev Plant Sci. 2014;33(4):331-49. https://doi.org/10.1080/07352689.2014.875291
Rashid A, Harris D, Hollington P, Rafiq M. Improving the yield of mung bean (Vigna radiata) in the Northwest frontier province of Pakistan using on-farm seed priming. Exp Agric. 2004;40(2):233-44. https://doi.org/10.1017/S0014479703 001539
Raja SRT, Thangappan S, Uthandi S. Non-rhizobial nodule-associated bacteria (NAB) from black gram (Vigna mungo L.) and their possible role in plant growth promotion. Madras Agric J. 2019;106(7-9):451-59. https://doi.org/10.29321/MAJ.2019.000291
Thanuja GK, Annadurai B, Thankappan S, Uthandi S. Non-rhizobial endophytic (NRE) yeasts assist nodulation of Rhizobium in root nodules of black gram (Vigna mungo L.). Arch Microbiol. 2020;202(10):2739-49. https://doi.org/10.1007/ s00203-020-01983-z
Rakholiya KD, Kaneria MJ, Singh SP, Vora VD, Sutaria GS. Biochemical and proteomics analysis of the plant growth-promoting rhizobacteria in stress conditions. In: Singh R, Kothari R, Koringa P, Singh S, editors. Understanding host-microbiome interactions - an omics approach. Singapore: Springer; 2017. p. 227–45. https://doi.org/10.1007/978-981-10-5050-3_14
Dudeja S, Giri R, Saini R, Suneja Madan P, Kothe E. Interaction of endophytic microbes with legumes. J Basic Microbiol. 2012;52(3):248-60. https://doi.org/10. 1002/jobm.201100063
Woomer PL, Karanja N, Kisamuli SM, Murwira M, Bala A. A revised manual for rhizobium methods and standard protocols [Internet]. 2011 [cited 2024 Oct 23]: 69 p. Available from: www.N2Africa.org
Muniyappan VK, Sundaralingam K, Sivakumar U, Geetha V, Jerlin R, Shobana N, et al. Enhancing plant resilience and drought stress in green gram through seed priming with nodule associated plant probiotics. Plant Sci Today. 2024;11(4);1406-14. https://doi.org/10.14719/pst.4603
ISTA. International rules for seed testing. In: Seed science and technology. Bassersdorf, Switzerland: International Seed Testing Association; 2019.
Abdul-Baki AA, Anderson JD. Vigor determination in soybean seed by multiple criteria. Crop Sci. 1973;13(5):630-33. https://doi.org/10.2135/cropsci1973.00111 83X001300060013x
Barrs H, Weatherly P. Physiological indices for high yield potential in wheat. Indian J Plant Physiol. 1962;25:352-57.
Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976;72:248-54. https://doi.org/10.1006/abio.1976.9999
Bates LS, Waldren R, Teare I. Rapid determination of free proline for water-stress studies. Plant Soil. 1973;39:205-07. https://doi.org/10.1007/BF00018060
Wu W, Zhang Q, Ervin EH, Yang Z, Zhang X. Physiological mechanism of enhancing salt stress tolerance of perennial ryegrass by 24-epibrassinolide. Front Plant Sci. 2017; 8:1017. https://doi.org/10.3389/fpls.2017.01017
Arnon DI. Copper enzymes in isolated chloroplasts: Polyphenoloxidase in Beta vulgaris. Plant Physiol. 1949;24:1-15. https://doi.org/10.1104/pp.24.1.1
Giannopolitis CN, Ries SK. Superoxide dismutases: I. Occurrence in higher plants. Plant Physiol. 1977; 59:309-14. https://doi.org/10.1104/pp.59.2.309
Aebi H. Catalase in vitro. Methods Enzymol. 1984;105:121–26. https://doi.org/10.1016/S0076-6879(84)05016-3
Malik CP, Singh MB. Plant enzymology and histo enzymology. New Delhi: Kalyani Publishers; 1980. p. 286.
Mia MB, Shamsuddin Z, Mahmood M. Effects of rhizobia and plant growth-promoting bacteria inoculation on germination and seedling vigor of lowland rice. Afr J Biotechnol. 2012;11:3758-65. https://doi.org/10.5897/AJB09.1337
Huang H, Ullah F, Zhou DX, Yi M, Zhao Y. Mechanisms of ROS regulation of plant development and stress responses. Front Plant Sci. 2019 Jun 25;10:800. https://doi.org/10.3389/fpls.2019.00800
Sharma P, Bhatt A, Jyoti B. Effect of seed bio-priming with microbial inoculants on plant growth, yield and yield-contributing characters in soybean (Glycine max L. Merril). Int J Econ Plants. 2018;5:53-58. https://doi.org/10.239 10/IJEP/2018.5.2.0214
Annadurai B, Kennedy ZJ, Uthandi S. Drought tolerant Rhizobium sp. VRE1 induced osmotic stress tolerance, seed germination and seedling vigor in black gram (Vigna mungo L.). Inter J of Ecol and Environ Sci. 2020;2:37-42.
Pattnaik S, Dash D, Mohapatra S, Pattnaik M, Marandi AK, Das S, Samantaray DP. Improvement of rice plant productivity by native Cr (VI) reducing and plant growth-promoting soil bacteria Enterobacter cloacae. Chemosphere. 2020;240:124895. https://doi.org/10.1016/j.chemosphere.2019.124895
Woo OG, Kim H, Kim J-S, Keum HL, Lee K-C, Sul WJ, Lee J-H. Bacillus subtilis strain GOT9 confers enhanced tolerance to drought and salt stresses in Arabidopsis thaliana and Brassica campestris. Plant Physiol Biochem. 2020;148:359-67. https://doi.org/10.1016/j.plaphy.2020.01.032
Singh M, Singh PK. Enhancing growth and drought tolerance in tomato through arbuscular mycorrhizal symbiosis. Rodriguesia. 2024;75:e00482024. https://doi.org/10.1590/2175-7860202475079
Monisha S. Studies on harnessing the potential of bioinoculants for the management of abiotic and biotic stress in black gram [Vigna mungo (L.) Hepper) [Doctoral dissertation]. Tamil Nadu Agricultural University, Coimbatore; 2023.
Zhang Z, Cao B, Gao S, Xu K. Grafting improves tomato drought tolerance through enhancing photosynthetic capacity and reducing ROS accumulation. Protoplasma. 2019;256:1013-24. https://doi.org/10.1007/s00709-019-01357-3
Xia D, Zhou H, Wang Y, Li P, Fu P, Wu B, He Y. How rice organs are colored: The genetic basis of anthocyanin biosynthesis in rice. Crop J. 2021;9:598-608. https://doi.org/10.1016/j.cj.2021.03.013
Sivakumar R, Nandhitha G, Chandrasekaran P, Boominathan P, Senthilkumar M. Impact of pink pigmented facultative methylotroph and PGRs on water status, photosynthesis, proline and NR activity in tomato under drought. Int J Curr Microbiol App Sci. 2017;6:1640-51. https://doi.org/10.20546/ijcmas.2017.606.192
Vardharajula S, Ali SZ, Grover M, Reddy G, Bandi V. Drought-tolerant plant growth-promoting Bacillus spp. Effect on growth, osmolites and antioxidant status of maize under drought stress. J Plant Interact. 2011;6:1-14. https://doi.org/10. 1080/17429145.2010.535178
Mutava RN, Prince SJK, Syed NH, Song L, Valliyodan B, Chen W, Nguyen HT. Understanding abiotic stress tolerance mechanisms in soybean: A comparative evaluation of soybean response to drought and flooding stress. Plant Physiol Biochem. 2015;86:109-20. https://doi.org/10.1016/j.plaphy.2014.11.010
Zhao W, Sun Y, Kjelgren R, Liu X. Response of stomatal density and bound gas exchange in leaves of maize to soil water deficit. Acta Physiol Plant. 2015;37:1-9. https://doi.org/10.1007/s11738-014-1704-8
Zafar-ul-Hye M, Danish S, Abbas M, Ahmad M, Munir TM. ACC deaminase producing PGPR Bacillus amyloliquefaciens and Agrobacterium fabrum along with biochar improve wheat productivity under drought stress. Agron. 2019;9:343. https://doi.org/10.3390/agronomy9070343
Brito C, Dinis LT, Moutinho-Pereira J, Correia CM. Drought stress effects and olive tree acclimation under a changing climate. Plants. 2019;8:232. https://doi.org/10.3390 /plants8070232
Nemeskeri E, Molnar K, Vigh R, Nagy J, Dobos A. Relationships between stomatal behaviour, spectral traits and water use and productivity of green peas (Pisum sativum L.) in dry seasons. Acta Physiol Plant. 2015;37:1-16. https://doi.org/10.1007 /s11738-015-1776-0
Hashem A, Kumar A, Al-Dbass AM, Alqarawi AA, Al-Arjani ABF, Singh G, et al. Arbuscular mycorrhizal fungi and biochar improve drought tolerance in chickpea. Saudi J Biol Sci. 2019;26:614-24. https://doi.org/10.1016/j.sjbs.2018.11.005
Ren C, Li Z, Song P, Wang Y, Liu W, Zhang L, et al. Overexpression of a grape MYB transcription factor gene VhMYB2 increases salinity and drought tolerance in Arabidopsis thaliana. Int J Mol Sci. 2023;24:10743. https://doi.org/10.3390/ijms241310743
Hasanuzzaman M, Bhuyan MB, Zulfiqar F, Raza A, Mohsin SM, Mahmud JA, et al. Reactive oxygen species and antioxidant defense in plants under abiotic stress: Revisiting the crucial role of a universal defense regulator. Antioxidants. 2020;9:681. https://doi.org/10.3390/antiox9080681
Singh M, Chauhan A, Srivastava DK, Singh PK. Arbuscular mycorrhizal fungi promote growth and enhance the accumulation of bioactive compounds in tomato (Solanum lycopersicum L.) Biologia Futura. 2024;75:251-57. https://doi.org/10.1007/s42977-024-00214-6
Saleem M, Fariduddin Q, Castroverde CDM. Salicylic acid: A key regulator of redox signalling and plant immunity. Plant Physiol Biochem. 2021;168:381-97. https://doi.org/10.1016/j.plaphy.2021.10.011
Samanta S, Seth CS, Roychoudhury A. The molecular paradigm of reactive oxygen species (ROS) and reactive nitrogen species (RNS) with different phytohormone signaling pathways during drought stress in plants. Plant Physiol Biochem. 2023;206:108259. https://doi.org/10.1016/j.plaphy.2023.108259
Chew O, Whelan J, Millar AH. Molecular definition of the ascorbate-glutathione cycle in Arabidopsis mitochondria reveals dual targeting of antioxidant defenses in plants. J Biol Chem. 2003;278(47):46869-77. https://doi.org/10.1074/ jbc.M307525200
Ahmad M, Zahir ZA, Khalid M, Nazli F, Arshad M. Efficacy of Rhizobium and Pseudomonas strains to improve physiology, ionic balance and quality of mung bean under salt-affected conditions on farmer's fields. Plant Physiol Biochem. 2013;63:170-76. https://doi.org/10.1016/j.plaphy.2012.11.024
Fatema MK, Mamun MAA, Sarker U, Hossain MS, Mia MAB, Roychowdhury R, et al. Assessing morpho-physiological and biochemical markers of soybean for drought tolerance potential. Sustain. 2023;15:1427. https://doi.org/10.3390/su15021427
Khan AL, Hamayun M, Radhakrishnan R, Waqas M, Kang SM, Kim YH, et al. Mutualistic association of Paecilomyces formosus LHL10 offers thermotolerance to Cucumis sativus. Antonie van Leeuwenhoek. 2012;101:267-79. https://doi.org/10.1007/s10482-011-9630-x
Abd Allah EF, Hashem A, Alqarawi AA, Bahkali AH, Alwhibi MS. Enhancing growth performance and systemic acquired resistance of medicinal plant Sesbania sesban (L.) Merr using arbuscular mycorrhizal fungi under salt stress. Saudi J Biol Sci. 2015;22(2):274-83. https://doi.org/10.1016/j.sjbs.2015.03.004

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Copyright (c) 2025 V Vijaya Geetha, Vinoth Kumar Muniyappan, K Sundaralingam, A Thanga Hemavathy, U Sivakumar, C Vanitha, T Murugeshwari, S Mohan Kumar, A Arun, V S Kavinesh

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