Abstract
The objective of the investigation was to improve phosphate solubilization in tomato plants by Bacillus licheniformis, a rhizobacterium that promotes plant growth. Ultraviolet (UV) radiation, Ethyl methanesulfonate (EMS) and Ethidium bromide (EtBr) mutagenesis produced twenty-one mutants. Phosphate solubilization was higher in the PM7 (physical mutant) (121.00 g mL−1) than in the wild type (82.00 g mL−1). PM7 showed high antifungal activity against Phytophthora capsici, Fusarium oxysporum and Dematophora necatrix besides increased siderophore production and HCN production. In a net-house experiment, PM7 improved root and shoot parameters, P assimilation and soil P availability in tomato plants. This study demonstrates the potential of PM7 as an effective rhizobacterium for enhancing nutrient availability and plant growth.
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs42770-024-01453-4/MediaObjects/42770_2024_1453_Fig1_HTML.png)
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs42770-024-01453-4/MediaObjects/42770_2024_1453_Fig2_HTML.png)
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs42770-024-01453-4/MediaObjects/42770_2024_1453_Fig3_HTML.png)
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs42770-024-01453-4/MediaObjects/42770_2024_1453_Fig4_HTML.png)
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs42770-024-01453-4/MediaObjects/42770_2024_1453_Fig5_HTML.png)
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs42770-024-01453-4/MediaObjects/42770_2024_1453_Fig6_HTML.png)
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs42770-024-01453-4/MediaObjects/42770_2024_1453_Fig7_HTML.png)
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs42770-024-01453-4/MediaObjects/42770_2024_1453_Fig8_HTML.png)
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs42770-024-01453-4/MediaObjects/42770_2024_1453_Fig9_HTML.png)
![](http://media.springernature.com/m312/springer-static/image/art%3A10.1007%2Fs42770-024-01453-4/MediaObjects/42770_2024_1453_Fig10_HTML.png)
References
Khan AA, Jilani G, Akhtar MS, Naqvi SMS (2009) Phosphorus solubilizing bacteria: occurrence, mechanisms, and their role in crop production. J Agric Biol Sci 1:48–58
Rodriguez H, Fraga R (1999) Phosphate solubilizing bacteria and their role in plant growth promotion. Biotechnol Adv 17:319–339. https://doi.org/10.1016/s0734-9750(99)00014-2
Rinu K, Pandey A (2001) Slow and steady phosphate solubilization by a psychrotolerant strain of Paecilomyces hepiali (MTCC 9621). World J Microbiol Biotechnol 27:1055–1062. https://doi.org/10.1007/s11274-010-0550-0
Reyes I, Baziramakenga R, Bernier L, Antoun H (2001) Solubilization of phosphate rocks and minerals by a wild-type strain and two UV-induced mutants of Penicillium rugulosum. Soil Biol Biochem 33:1741–1747
Karpagam T, Nagalakshmi PK (2014) Isolation and characterization of phosphate solubilizing microbes from agricultural soil. Int J Curr Microbiol App Sci 3:601–614
Vessey JK (2003) Plant growth promoting rhizobacteria as biofertilizers. Plant Soil 255(2):571–586. https://doi.org/10.1023/A:1026037216893
Chaiharn M, Chunhaleuchanon S, Kozo A, Lumyong S (2008) Screening of rhizobacteria for their plant growth promoting activities. KMITL Sci Technol 81:18–23
Vyas P, Gulati A (2009) Organic acid production in vitro and plant growth promotion in maize under controlled environment by phosphate solubilizing fluorescent Pseudomonas. BMC Microbiol 9:174. https://doi.org/10.1186/1471-2180-9-174
Chen YP, Rekha PD, Arun AB (2006) Phosphate solubilizing bacteria from subtropical soil and their tri-calcium phosphate solubilizing abilities. Appl Soil Ecol 34:33–41. https://doi.org/10.1016/j.apsoil.2005.12.002
Miller JH (1972) Experiments in molecular genetics. Cold Spring Harbor Laboratory Press, US, pp 352–355
Achal V, Savant VV, Reddy MS (2007) Phosphate solubilization by a wild type strain and UV-induced mutants of Aspergillus tubingensis. Soil Biol Biochem 39:695–699
Bray RH, Kurtz LT (1945) Determination of total organic and available forms of phosphorus in soils. Curr Sci 59:39–45
Schwyn B, Neilands JB (1987) Universal chemical assay for the detection and determination of siderophores. Curr Sci 160:47–56
Bakker AW, Schippers B (1987) Microbial cyanide production in the rhizosphere in relation to potato yield reduction and Pseudomonas spp.-mediated plant growth-stimulation. Soil Biol Biochem 19(4):451–457
Vincent JM (1947) Distortion of fungal hyphae in the presence of certain inhibitors. Nature 159:850. https://doi.org/10.1038/159850b0
Olsen SR, Cole CV, Watanabe FS, Dean LA (1954) Circular. US Department of Agriculture, Washington, DC
Jackson ML (1973) Soil chemical analysis. Prentice Hall, New Delhi, pp 106–203
Guleria S, Walia A, Chauhan A (2013) Mutagenesis of alkalophilic Cellulosimicrobium sp. CKMX1 for hyper-production of cellulose-free xylanase in solid state fermentation of apple pomace. Proc Natl Acad Sci India Sect B Biol Sci 85:241–252. https://doi.org/10.1007/s40011-013-0273-8
Tripura C, Sashidhar B, Podile AR (2007) Ethyl methanesulfonate mutagenesis-enhanced mineral phosphate solubilization by groundnut-associated Serratia marcescens GPS-5. Curr Microbiol 54:79–84
Gupta R, Singal R, Shankar A, Kuhad RC, Saxena RK (1994) A modified plate assay for screening phosphate solubilizing microorganisms. J Gen Appl Microbiol 40:255–260. https://doi.org/10.2323/jgam.40.255
Blumer C, Haas D (2000) Mechanism, regulation and ecological role of bacterial cyanide biosynthesis. Arch Microbiol 173(3):170–177. https://doi.org/10.1007/s002039900127
Dey R, Pal KK, Bhatt DM, Chauhan SM (2004) Growth promotion and yield enhancement of peanut (Arachis hypogae L.) by application of plant growth promoting rhizobacterial. Microbiol Res 159(4):371–394. https://doi.org/10.1016/j.micres.2004.08.004
Beneduzi A, Ambrosini A, Passaglia LM (2012) Plant growth-promoting rhizobacteria (PGPR): their potential as antagonists and biocontrol agents. Genet Mol Biol 35:1044–1051. https://doi.org/10.1590/s1415-47572012000600020
Reddy, P.P. (2014). Mechanisms of Biocontrol. In: Plant Growth Promoting Rhizobacteria for Horticultural Crop Protection. Springer, New Delhi. https://doi.org/10.1007/978-81-322-1973-6_4
Katiyar V, Goel R (2004) Siderophore mediated plant growth promotion at low temperature by mutant of fluorescent Pseudomonad. Plant Growth Regul 42:239–244. https://doi.org/10.1023/B:GROW.0000026477.10681.d2
Ramirez AR, Abarca E, Aquilar UG, Jones HPM, Barboza JE (2004) Antifungal activity of Bacillus thuringiensis chitinase and its potential for the biocontrol of phytopathogenic fungi in soyabean seeds. J Food Sci 69(5):131–134. https://doi.org/10.1111/j.1365-2621.2004.tb10721.x
Cazorla FM, Romero D, Garcia AP (2007) Isolation and characterization of antagonistic Bacillus subtilis strains from avocado rhizoplane displaying biocontrol activity. J Appl Microbiol 103:1950–1959
Nautiyal CS (1999) An efficient microbiological growth medium for screening phosphate solubilizing microorganisms. FEMS Microbiol Lett 17:265–270. https://doi.org/10.1111/j.1574-6968.1999.tb13383.x
Kumar V, Behl RK, Narula N (2001) Establishment of phosphate-solubilizing strains of Azotobacter chroococcum in the rhizosphere and their effect on wheat cultivars under greenhouse conditions. Microbiol Res 156:87–93. https://doi.org/10.1078/0944-5013-00081
Sivasakthi S, Saranraj P, Sujatha D (2015) Mutation based strain improvement of PGPR isolates (Pseudomonas fluorescens and Bacillus subtilis) for the improvement of growth and yield of paddy (Oryza sativa L.). American-Eurasian J Agric Environ Sci 15(8):1591–1601. https://doi.org/10.5829/idosi.aejaes.2015.15.8.94149
Mohamed HM, Ibrahim EMA (2011) Effect of inoculation with Bacillus polymyxa mutants on growth, phosphorus and iron uptake by tomato (Lycopersicon esculentum L.) in calcareous soils. Int J Soil Sci 6:176–187. https://doi.org/10.3923/ijss.2011.176.187
Trivedi P, Sa T (2008) Pseudomonas corrugata (NRRL B-30409) mutants increased phosphate solubilization, organic acid production, and plant growth at lower temperatures. Curr Microbiol 56:140–144. https://doi.org/10.1007/s00284-007-9058-8
Yu X, Liu X, Zhu TH, Liu GH, Mao C (2011) Isolation and characterization of phosphate solubilization bacteria from walnut and their effect on growth and phosphorus mobilization. Biol Fertil Soils 47:437–446
Acknowledgements
The authors are thankful to the Department of Basic Sciences, Microbiology section, Dr. Yashwant Singh Parmar, University of Horticulture and Forestry, Nauni, Solan, H.P, India for providing necessary facilities to conduct this work.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of interest
The authors declare that they have no conflicts of interest.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Responsible Editor: Admir Giachini
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Kumar, G., Chauhan, A., Bhardwaj, S. et al. Enhancing Phosphate Uptake and Antifungal Activity in Tomato Plants via Bacillus licheniformis Mutagenesis: Evaluating Growth Parameters. Braz J Microbiol (2024). https://doi.org/10.1007/s42770-024-01453-4
Received:
Accepted:
Published:
DOI: https://doi.org/10.1007/s42770-024-01453-4