Plant growth promoting bacteria Bacillus subtilis promote growth and physiological parameters of Zingiber officinale Roscoe
DOI:
https://doi.org/10.14719/pst.2021.8.1.997Keywords:
Plant, Bacterial inoculation, Plant height, Transpiration rate, Chlorophyll contentAbstract
Ginger (Zingiber officinale Roscoe) is an important medicinal crop grown for its aromatic rhizome which is used as a spice, food, flavouring agent and medicine. It has been characterised for its hypoglycemic, hypotensive, antioxidant and antibiotic properties. This study was conducted to determine the impact of plant growth-promoting potential of bacterial strain Bacillus subtilis L2 on plant growth and physiological properties of ginger. The experiment was carried out in randomised block design with three replications in pot experiments. The plants were grown in greenhouse conditions for three months. The results showed that at 8 and 12 weeks after planting (WAP) bacterial inoculation increased plant height, leaf length, number of leaves per plant and leaf width. Inoculation with B. subtilis L2 significantly increased plant height by 16, 20 and 18% compared to control at 4, 8 and 12 WAP. At 8 and 12 WAP, leaf length significantly raised by B. subtilis L2 as compared to uninoculated control. B. subtilis L2 significantly increased the number of leaves per plant and leaf width by 30 and 21% respectively when comparing with non-inoculated plants at 8 WAP. The percentage increase in chlorophyll content resulted from the inoculation with B. subtilis L2 over the control was 10.5%, 15.5% and 18.4% at 4, 8 and 12 WAP respectively. It is concluded that there is a significant positive effect of inoculation with B. subtilis L2 on the growth of ginger. B. subtilis L2 strain can be used as a potential agent or bio-fertiliser for stimulation of ginger growth.
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References
Ebadi M. Pharmacodynamics basis of herbal medicine. 2nd ed. Boca Raton: Taylor and Francis Group; 2006. https://doi.org/10.1201/9781420006452
Khare CP. Indian Medicinal Plants: An Illustrated Dictionary. Springer-Verlag New York; 2007.
Banerjee S, Mullick HI, Banerjee J, Ghosh A. Zingiber officinale: ‘A natural gold’. Int J Pharmaceutical Bio-Sci. 2011;2:283-94.
Duke JA. Handbook of Medicinal Herbs. Boca Raton: CRC press; 2002. https://doi.org/10.1201/9781420040463
Grzanna R, Lindmark L, Frondoza CG. Ginger - a herbal medicinal product with broad anti-inflammatory actions. Journal of Medicinal Food. 2005;8(2):125-32. https://doi.org/ 10.1089/jmf.2005.8.125
Zadeh JB, Kor NM. Physiological and pharmaceutical effects of Ginger (Zingiber officinale Roscoe) as a valuable medicinal plant. European Journal of Experimental Biology. 2014;4(1):87-90.
Al-Amin ZM, Thomson M, Al-Qattan KK, Peltonen-Shalaby R, Ali M. Anti-diabetic and hypolipidaemic properties of ginger (Zingiber officinale) in streptozotocin-induced diabetic rats. British Journal of Nutrition. 2006;96(4):660-66. https://doi.org/ 10.1079/bjn20061849
Andlauer W, Fürst P. Nutraceuticals: a piece of history, present status and outlook. Food Research International. 2002;35(2-3):171-86.
Liu Y, Liu J, Zhang Y. Research Progress on Chemical Constituents of Zingiber officinale Roscoe. BioMed Research International. 2019. https://doi.org/10.1155/2019/5370823
Shuhua L. Contents of nitrate, nitrite, vitamin C, organic acid and total sugar of Zingiber officinale in plastic greenhouse. Journal of Anhui Agricultural Sciences. 2006;34(14):33-46.
Zhang YF, Ma ZC. Ingredients and applications of ginger. Chemistry Teaching, 2012;8:73-80.
Asnani VE, Verma RJ. Antioxidative effect of rhizome of Zingiber officinale on paraben induced lipid peroxidation: an in-vitro study. Acta Pol Pharm. 2007;64(1):35-37.
Prasad S, Tyagi AK. Ginger and its constituents: role in prevention and treatment of gastrointestinal cancer. Gastroenterology Research and Practice. 2015 Jan 1. https://doi.org/10.1155/2015/142979.
Zhang F, Ma N, Gao YF, Sun LL, Zhang JG. Therapeutic effects of 6?gingerol, 8?gingerol and 10?gingerol on dextran sulfate sodium?induced acute ulcerative colitis in rats. Phytotherapy Research. 2017;31(9):1427-32. https://doi.org/10.1002/ptr.5871
Yadav IC, Devi NL, Syed JH, Cheng Z, Li J, Zhang G, Jones KC. Current status of persistent organic pesticides residues in air, water and soil, and their possible effect on neighbouring countries: a comprehensive review of India. Science of the Total Environment. 2015;511:123-37. https://doi.org/ 10.1016/j.scitotenv.2014.12.041
Elkoca E, Kantar F, Sahin F. Influence of nitrogen fixing and phosphorus solubilising bacteria on the nodulation, plant growth and yield of chickpea. Journal of Plant Nutrition. 2006; 31(1):157-71. https://doi.org/10.1080/01904160701742097
Sayyed RZ, Patel PR, Shaikh SS. Plant growth promotion and root colonisation by EPS producing Enterobacter sp. RZS5 under heavy metal contaminated soil. Indian Journal of Experimental Biology. 2015;53:116-23.
Jabborova D, Wirth S, Kannepalli A, Narimanov A, Desouky S, Davranov K, Sayyed RZ, El Enshasy H, Malek RA, Syed A, Bahkali AH. Co-Inoculation of Rhizobacteria and Biochar Application Improves Growth and Nutrientsin Soybean and Enriches Soil Nutrients and Enzymes. Agronomy. 2020;10(8):1142.https://doi.org/10.3390/agronomy10081142
Sayyed RZ, Badgujar MD, Sonawane HM, Mhaske MM, Chincholkar SB. Production of microbial iron chelators (siderophores) by fluorescent Pseudomonads. Indian Journal of Biotechnology. 2005;4:484-90.
Mohamed HI, Gomaa EZ. Effect of plant growth promoting Bacillus subtilis and Pseudomonas fluorescens on growth and pigment composition of radish plants (Raphanus sativus) under NaCl stress. Photosynthetica. 2012;50(2):263-72. https://doi.org/ 10.1007/s11099-012-0032-8
Glick BR. Bacteria with ACC deaminase can promote plant growth and help to feed the world. Microbiological Research. 2014;169:30-39. http://dx.doi.org/10.1016/j.micres.2013.09.009
Egamberdieva D, Jabborova D. Efficiency of phytohormone-producing Pseudomonas to improve salt stress tolerance in Jew’s Mallow (Corchorus olitorius L.). Plant-growth-promoting Rhizobacteria (PGPR) and Medicinal Plants Springer International Publishing Switzerland. 2015;201-13. https://doi.org/ 10.1007/978-3-319-13401-7_9
Egamberdieva D, Jabborova D, Hashem A. Pseudomonas induces salinity tolerance in cotton (Gossypium hirsutum) and resistance to Fusarium root rot through the modulation of indole-3-acetic acid. Saudi Journal of Biological Sciences. 2015;22(6):773-79. https://doi.org/10.1016/j.sjbs.2015.04.019
Jabborova DP, Narimanov AA, Enakiev YI, Davranov KD. Effect of Bacillus subtilis 1 strain on the growth and development of wheat (Triticum aestivum L.) under saline condition. Bulgarian Journal of Agricultural Science. 2020;26(4):744-47.
Jabborova D, Davranov K. Effect of phosphorus and nitrogen concentrations on root colonisation of Soybean (Glycine max L.) by Bradyrhizobium japonicum and Pseudomonas putida. International Journal of Advanced Biotechnology and Research (IJBR), 2015;6:418.
Sagar A, Sayyed RZ, Ramteke PW, Sharma S, Marraiki N, Elgorban AM, Syed A. ACC deaminase and antioxidant enzymes producing halophilic Enterobacter sp. PR14 promotes the growth of rice and millets under salinity stress. Physiology and Molecular Biology of Plants. 2020;26(9):1847-54. https://doi.org/10.1007/s12298-020-00852-9
Masciarelli O, Llanes A, Luna V. A new PGPR co-inoculated with Bradyrhizobium japonicum enhances soybean nodulation. Microbiological Research. 2014;169(7-8):609-15. https://doi.org/10.1016/j.micres.2013.10.001
Egamberdieva D, Wirth S, Jabborova D, Räsänen LA, Liao H. Coordination between Bradyrhizobium and Pseudomonas alleviates salt stress in soybean through altering root system architecture. Journal of Plant Interactions. 2017;12(1):100-07. https://doi.org/10.1080/17429145.2017.1294212
Egamberdieva D, Jabborova D, Berg G. Synergistic interactions between Bradyrhizobium japonicum and the endophyte Stenotrophomonas rhizophila and their effects on growth and nodulation of soybean under salt stress. Plant and Soil. 2016;405(1-2):35-45.
Egamberdieva D, Jabborova D, Wirth SJ, Alam P, Alyemeni MN, Ahmad P. Interactive effects of nutrients and Bradyrhizobium japonicum on the growth and root architecture of soybean (Glycine max L.). Frontiers in Microbiology. 2018;9:1000. https://doi.org/10.3389/fmicb.2018.01000
Jabborova DP, Enakiev YI, Davranov KD, Begmatov SA. Effect of co-inoculation with Bradyrhizobium japonicum and Pseudomonas putida on root morph-architecture traits, nodulation and growth of soybean in response to phosphorus supply under hydroponic conditions. Bulgarian Journal of Agricultural Science. 2018;24(6):1004-11.
Kashem MA, Mian MH and Rahman MF. Effect of Bradyrhizobium on the yield of mungbean (Vigna radiata L.) grown in Ganges Tidal floodplain soil. Journal of Agricultural Research. 2000;33(38):407.
Raza W, Akhtar MJ, Arshad M, Yousaf S. Growth, nodulation and yield of mungbean (Vigna radiata L.) as influenced by coinoculation with rhizobium and plant growth promoting rhizobacteria. Pakistan Journal of Agricultural Sciences. 2004;41(3/4):125.
Dinesh R, Anandaraj M, Kumar A, Srinivasan V, Bini YK., Subila KP, Aravind R, Hamza S. Effects of plant growth-promoting rhizobacteria and NPK fertilizers on biochemical and microbial properties of soils under ginger (Zingiber officinale) cultivation. Agricultural Research Volume. 2013;2:346–53. https://doi.org/10.1007/s40003-013-0080-8
Kumar A, Vandana, Singh M, Singh PP, Singh SK, Singh PK, Pandey KD. Isolation of plant growth promoting rhizobacteria and their impact on growth and curcumin content in Curcuma longa L. Biocatalysis and Agricultural Biotechnology. 2016;8:1-7. https://doi.org/10.1016/j.bcab.2016.07.002
Fritze D. Taxonomy of the genus Bacillus and related genera: the aerobic endospore-forming bacteria. Phytopathology. 2004;94(11):1245-48. https://doi.org/10.1094/PHYTO.2004.94.11.1245
Patel S, Jinal HN, Amaresan N. Isolation and characterisation of drought resistance bacteria for plant growth promoting properties and their effect on chilli (Capsicum annuum) seedling under salt stress. Biocatalysis and Agricultural Biotechnology. 2017;12:85-89. https://doi.org/10.1016/j.bcab.2017.09.002
Qiao J, Yu X, Liang X, Liu Y, Borriss R, Liu Y. Addition of plant-growth-promoting Bacillus subtilis PTS-394 on tomato rhizosphere has no durable impact on composition of root microbiome. BMC microbiology. 2017;17(1):131. https://doi.org/10.1186/s12866-017-1039-x
Pikovskaya RI. Mobilisation of phosphorus in soil in connection with vital activity of some microbial species. Mikrobiologiya. 1948;17:362-70.
Bric JM, Bostock RM, Silverstone SE. Rapid in-situ assay for indoleacetic acid production by bacteria immobilised on a nitrocellulose membrane. Applied and Environmental Microbiology. 1991;57(2):535-38. https://doi.org/10.1128/AEM.57.2.535-538.1991
Patel PR, Shaikh SS, Sayyed RZ. Modified chrome azurol S method for detection and estimation of siderophores having affinity for metal ions other than iron. Environmental Sustainability. 2018;1(1):81-87. https://doi.org/10.1007/s42398-018-0005-3
Khan F, Asif M, Khan A, Tariq M, Ansari T, Shariq M, Siddiqui MA. Evaluation of the nematicidal potential of some botanicals against root-knot nematode, Meloidogyne incognita infected carrot: In-vitro and greenhouse study. Current Plant Biology. 2019;20:1001152. https://doi.org/10.1016/j.cpb.2019.100115
Egamberdieva D, Jabborova D. Improvement of cotton production in arid saline soils by beneficial microbes. In Crop Yields: Production, Management Practices and Impact of Climate Change. 2013;109-22.
Egamberdieva D, Jabborova D, Wirth S. Alleviation of salt stress in legumes by co-inoculation with Pseudomonas and Rhizobium. In: Plant Microbe Symbiosis: Fundamentals and Advances. New Delhi: Springer. 2013;291-303.
Meliani A, Bensoltane A, Benidire L, Oufdou K. Plant growth-promotion and IAA secretion with Pseudomonas fluorescens and Pseudomonas putida. Research & Reviews: Journal of Botanical Sciences. 2017;6(2):16-24.
Pandya ND, Desai PV, Sayyed RZ. Antifungal and phytohormone production ability of plant growth promoting rhizobacteria associated with the rhizosphere of sugarcane. World Journal of Microbiology and Biotechnology. 2011;13(1):112-16.
Jabborova D, Annapurna K, Fayzullaeva M, Sulaymonov K, Kadirova D, Jabbarov Z, Sayyed R. Isolation and characterisation of endophytic bacteria from ginger (Zingiber officinale Rosc.). Annals of Phytomed. 2020;9:116-21.
Singh M, Khan MM, Naeem M. Effect of nitrogen on growth, nutrient assimilation, essential oil content, yield and quality attributes in Zingiber officinale Rosc. Journal of the Saudi Society of Agricultural Sciences. 2016;15(2):171-78. https://doi.org/10.1016/j.jssas.2014.11.002
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 Physiology and Biochemistry. 2013 Feb 1;63:170-76. https://doi.org/10.1016/j.plaphy.2012.11.024
Barnawal D, Bharti N, Maji D, Chanotiya CS, Kalra A. ACC deaminase-containing Arthrobacter protophormiae induces NaCl stress tolerance through reduced ACC oxidase activity and ethylene production resulting in improved nodulation and mycorrhisation in Pisum sativum. Journal of Plant Physiology. 2014;171(11):884-94. https://doi.org/10.1016/j.jplph.2014.03.007
Kang SM, Radhakrishnan R, Khan AL, Kim MJ, Park JM, Kim BR, Shin DH, Lee IJ. Gibberellin secreting Rhizobacterium, Pseudomonas putida H-2-3 modulates the hormonal and stress physiology of soybean to improve the plant growth under saline and drought conditions. Plant Physiology and Biochemistry. 2014;84:115-24. https://doi.org/10.1016/j.plaphy.2014.09.001
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