Modulation of Secondary Metabolites: A Halotolerance Strategy of Plant Growth Promoting Rhizobacteria Against Sodium Chloride Stress.
Journal
Current microbiology
ISSN: 1432-0991
Titre abrégé: Curr Microbiol
Pays: United States
ID NLM: 7808448
Informations de publication
Date de publication:
Dec 2021
Dec 2021
Historique:
received:
17
02
2020
accepted:
30
08
2021
pubmed:
6
10
2021
medline:
19
11
2021
entrez:
5
10
2021
Statut:
ppublish
Résumé
An experiment was conducted to evaluate the role of bacterial secondary metabolites against induced salt stress. Five bacterial strains were isolated from three different habitats: Khewra salt range, oily sludge field in Chakwal, and garden soil of Quaid-i-Azam University Islamabad, Pakistan. The 16S rRNA gene and BLAST analysis of bacterial strains showed 99% sequence similarity with Pseudomonas putida AMUPP-2 (KM435273), Lysinibacillus sphaericus OUG29GKBB (KM972671), Bacillus pumilus MB431 (KP723538) isolated from salt range, Pseudomonas fluorescens B8 (KF010368) from garden soil and Exiguobacterium aurantiacum SPD2 (KX121703) from oily sludge, respectively. Pseudomonas fluorescens produced 294.98 µg/g of proline in the M9 medium supplemented with 125 mM NaCl, but its growth rate was decreased from 1.81 to 0.37. The P. putida showed faster growth rate even than control at 125 mM NaCl. B. pumilus and L. sphaericus did not show any decline in growth rate up to 100 mM NaCl. The synthesis of new amino acids were recorded at 125 mM NaCl stress, e.g., Pro, Leu, Arg in P. fluorescens and L. sphaericus, Pro, Lys, Phe, Ala in P. putida, Lys, Ala in B. pumilus, Met, Val, and Ala in E. aurantiacum. Liquid chromatography-mass spectrometry analysis of ethyl acetate extract of P. putida and L. sphaericus demonstrated that NaCl (125mM) induced the production of 3-oxo-C
Identifiants
pubmed: 34609577
doi: 10.1007/s00284-021-02647-x
pii: 10.1007/s00284-021-02647-x
doi:
Substances chimiques
RNA, Ribosomal, 16S
0
Sodium Chloride
451W47IQ8X
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
4050-4059Informations de copyright
© 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
Références
Shigyo N, Umeki K, Hirao T (2019) Plant functional diversity and soil properties control elevational diversity gradients of soil bacteria. FEMS Microbiol Ecol 95(4):fiz025. https://doi.org/10.1093/femsec/fiz025
doi: 10.1093/femsec/fiz025
pubmed: 30816915
Verma M, Mishra J, Arora NK (2019) Plant growth-promoting rhizobacteria: diversity and applications. In: Environmental Biotechnology for sustainable future. Springer, Singapore, pp 129-173. https://doi.org/10.1007/978-981-10-7284-06
Etesami H, Beattie GA (2017) Plant-microbe interactions in adaptation of agricultural crops to abiotic stress conditions. In: Probiotics and Plant Health. Springer, Singapore, pp 163-200. https://doi.org/10.1007/978-981-10-3473-2_7
Vaidya S, Dev K, Sourirajan A (2018) Distinct osmoadaptation strategies in the strict halophilic and halotolerant bacteria isolated from Lunsu saltwater body of Northwest Himalayas. Curr Microbiol 75(7):888–895. https://doi.org/10.1007/s00284-018-1462-8
doi: 10.1007/s00284-018-1462-8
pubmed: 29480323
Gunde-Cimerman N, Plemenitaš A, Oren A (2018) Strategies of adaptation of microorganisms of the three domains of life to high salt concentrations. FEMS Microbiol Rev 42(3):353–375. https://doi.org/10.1093/femsre/fuy009
doi: 10.1093/femsre/fuy009
pubmed: 29529204
Kindzierski V, Raschke S, Knabe N, Siedler F, Scheffer B, Pflüger-Grau K, Kunte HJ (2017) Osmoregulation in the halophilic bacterium Halomonas elongata: a case study for integrative systems biology. PloS One 12(1):e0168818. https://doi.org/10.1371/journal.pone.0168818
doi: 10.1371/journal.pone.0168818
pubmed: 28081159
pmcid: 5231179
León MJ, Hoffmann T, Sánchez-Porro C, Heider J, Ventosa A, Bremer E (2018) Compatible solute synthesis and import by the moderate halophile Spiribacter salinus: physiology and genomics. Front Microbiol 9:108. https://doi.org/10.3389/fmicb.2018.00108
doi: 10.3389/fmicb.2018.00108
pubmed: 29497403
pmcid: 5818414
Deole R, Hoff WD (2020) A potassium chloride to glycine betaine osmoprotectant switch in the extreme halophile Halorhodospira halophila. Sci Rep 10(1):1–10. https://doi.org/10.1038/s41598-020-59231-9
doi: 10.1038/s41598-020-59231-9
Imhoff JF, Rahn T, Kunzel S, Keller A, Neulinger SC (2021) Osmotic adaptation and compatible solute biosynthesis of phototrophic bacteria as revealed from genome analyses. Microorganisms 9(1):46. https://doi.org/10.3390/microorganisms9010046
doi: 10.3390/microorganisms9010046
Chen JH, Chi MC, Lin MG, Lin LL, Wang TF (2015) Beneficial effect of sugar osmolytes on the refolding of guanidine hydrochloride-denatured trehalose-6-phosphate hydrolase from Bacillus licheniformis. Biomed Res Int 4:1–9. https://doi.org/10.1155/2015/806847
doi: 10.1155/2015/806847
Marchant R (2019) The future of microbial biosurfactants and their applications. In: Microbial biosurfactants and their environmental and industrial applications. CRC Press/Taylor and Francis Group, pp 364-370. https://doi.org/10.1201/b21950-14
Mnif I, Ghribi D (2015) Review lipopeptides biosurfactants: mean classes and new insights for industrial, biomedical, and environmental applications. Pept Sci 104(3):129–147. https://doi.org/10.1002/bip.22630
doi: 10.1002/bip.22630
Ines M, Dhouha G (2015) Lipopeptide surfactants: production, recovery and pore forming capacity. Peptides 71:100–112. https://doi.org/10.1002/bip.22630
doi: 10.1002/bip.22630
pubmed: 26189973
Loeschcke A, Thies S (2015) Pseudomonas putida: A versatile host for the production of natural products. Appl Microbiol Biotechnol 99(15):6197–6214. https://doi.org/10.1007/s00253-015-6745-4
doi: 10.1007/s00253-015-6745-4
pubmed: 26099332
pmcid: 4495716
Saha M, Sarkar S, Sarkar B, Sharma BK, Bhattacharjee S, Tribedi P (2016) Microbial siderophores and their potential applications: a review. Environ Sci Pollut Res 23(5):3984–3999. https://doi.org/10.1007/s11356-015-4294-0
doi: 10.1007/s11356-015-4294-0
Ullah A, Bano A (2019) Role of PGPR in the reclamation and revegetation of saline land. Pak J Bot 51(1): 27-35. https://doi.org/10.30848/pjb2019-1(43 )
Aryal S (2018) Gram staining: principle, procedure, interpretation, examples and animation
Steel KJ (1961) The oxidase reaction as a taxonomic tool. Microbiol 25(2):297–306. https://doi.org/10.1099/00221287-25-2-297
doi: 10.1099/00221287-25-2-297
Smith PB (1981) Biochemical tests for identification of medical bacteria. MacFadden JF, Williams W, Baltimore 1980 (edn), pp 527. Int J Syst Evol Microbiol 31(1):108-108. https://doi.org/10.1099/00207713-31-1-108
Montville TJ (1983) Dual-substrate plate diffusion assay for proteases. Appl Environ Microbiol 45(1):200–204. https://doi.org/10.1128/aem.45.1.200-204.1983
doi: 10.1128/aem.45.1.200-204.1983
pubmed: 6337548
pmcid: 242253
Ertugrul S, Donmez G, Takaç S (2007) Isolation of lipase producing Bacillus sp. from olive mill wastewater and improving its enzyme activity. J Hazard Mat 149(3):720–724. https://doi.org/10.1016/j.jhazmat.2007.04.034
doi: 10.1016/j.jhazmat.2007.04.034
Barrow G, Feltham RKA (2004) Cowan and steel’s manual for the identification of medical bacteria. Cambridge Univ Press. https://doi.org/10.1017/cbo9780511527104
doi: 10.1017/cbo9780511527104
Bates LS, Waldren RP, Teare ID (1973) Rapid determination of free proline for water-stress studies. Plant Soil 39(1):205–207. https://doi.org/10.1007/bf00018060
doi: 10.1007/bf00018060
Triplett EW (2007). Prospects for significant nitrogen fixation in grasses from bacterial endophytes. In: Associative and endophytic nitrogen-fixing bacteria and cyanobacterial associations. Springer, Dordrecht, pp 303-314. https://doi.org/10.1007/1-4020-3546-2_13
Ramadoss D, Lakkineni VK, Bose P, Ali S, Annapurna K (2013) Mitigation of salt stress in wheat seedlings by halotolerant bacteria isolated from saline habitats. Springerplus 2(1):6. https://doi.org/10.1186/2193-1801-2-6
doi: 10.1186/2193-1801-2-6
pubmed: 23449812
pmcid: 3579424
Wratten SJ, Wolfe MS, Andersen RJ, Faulkner DJ (1977) Antibiotic metabolites from a marine pseudomonad. Antimicrobe Agents Chemother 11(3):411–414. https://doi.org/10.1128/aac.11.3.411
doi: 10.1128/aac.11.3.411
Cheng HR, Jiang N (2006) Extremely rapid extraction of DNA from bacteria and yeasts. Biotechnol lett 28(1):55–59. https://doi.org/10.1007/s10529-005-4688-z
doi: 10.1007/s10529-005-4688-z
pubmed: 16369876
Janda JM, Abbott SL (2007) 16S rRNA gene sequencing for bacterial identification in the diagnostic laboratory: pluses, perils, and pitfalls. J Clin Microbiol 45(9):2761–2764. https://doi.org/10.1128/jcm.01228-07
doi: 10.1128/jcm.01228-07
pubmed: 17626177
pmcid: 2045242
Kumar S, Stecher G, Tamura K (2016) MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol Biol Evol 33(7):1870–1874. https://doi.org/10.1093/molbev/msw054
doi: 10.1093/molbev/msw054
pubmed: 27004904
pmcid: 27004904
Berga M, Zha Y, Székely AJ, Langenheder S (2017) Functional and compositional stability of bacterial meta communities in response to salinity changes. Front. Microbiol 8:948. https://doi.org/10.3389/fmicb.2017.00948
doi: 10.3389/fmicb.2017.00948
pubmed: 28642735
pmcid: 5463035
Chun SC, Paramasivan M, Chandrasekaran M (2018) Proline accumulation influenced by osmotic stress in arbuscular mycorrhizal symbiotic plants. Front. Microbiol 9:2525. https://doi.org/10.3389/fmicb.2018.02525
doi: 10.3389/fmicb.2018.02525
pubmed: 30459731
pmcid: 6232873
El Moukhtari A, Cabassa-Hourton C, Farissi M, Savouré A (2020) How does proline treatment promote salt stress tolerance during crop plant development? Front Plant Sci 11:1127. https://doi.org/10.3389/fpls.2020.01127
doi: 10.3389/fpls.2020.01127
pubmed: 32793273
pmcid: 7390974
Leung, D. W. (2015). Relationship between changes in contents of nitric oxide and amino acids particularly proline in plants under abiotic stress. In: Reactive oxygen species and oxidative damage in plants under stress, Springer, Cham, pp 341-352. https://doi.org/10.1007/978-3-319-20421-5_14
Qiu XM, Sun YY, Ye XY, Li ZG (2020) Signaling role of glutamate in plants. Front Plant Sci 10:1743. https://doi.org/10.3389/fpls.2019.01743
doi: 10.3389/fpls.2019.01743
pubmed: 32063909
pmcid: 6999156
Sharma A, Shahzad B, Rehman A, Bhardwaj R, Landi M, Zheng B (2019) Response of phenylpropanoid pathway and the role of polyphenols in plants under abiotic stress. Molecules 24(13):2452. https://doi.org/10.3390/molecules24132452
doi: 10.3390/molecules24132452
pmcid: 6651195
Martínez Y, Li X, Liu G, Bin P, Yan W, Mas D, Yin Y (2017) The role of methionine on metabolism, oxidative stress and diseases. J Amino Acids 49(12):2091–2098. https://doi.org/10.1007/s00726-017-2494-2
doi: 10.1007/s00726-017-2494-2
Kang Y, Hwang I (2018) Glutamate uptake is important for osmoregulation and survival in the rice pathogen Burkholderia glumae. PloS One 13(1):e0190431. https://doi.org/10.1371/journal.pone.0190431
doi: 10.1371/journal.pone.0190431
pubmed: 29293672
pmcid: 5749808
Fatma M, Masood A, Per TS, Khan NA (2016) Nitric oxide alleviates salt stress inhibited photosynthetic performance by interacting with sulfur assimilation in mustard. Front Plant Sci 7:521. https://doi.org/10.3389/fpls.2016.00521
doi: 10.3389/fpls.2016.00521
pubmed: 27200007
pmcid: 4842777
Kang SM, Radhakrishnan R, Lee SM, Park YG, Kim AY, Seo CW, Lee IJ (2015) Enterobacter sp. SE992-induced regulation of amino acids, sugars, and hormones in cucumber plants improves salt tolerance. Acta Physiol. Plant 37(8):1–10. https://doi.org/10.1007/s11738-015-1895-7
doi: 10.1007/s11738-015-1895-7
Han M, Zhang C, Suglo P, Sun S, Wang M, Su T (2021) l-Aspartate: an essential metabolite for plant growth and stress acclimation. Molecules 26(7):1887. https://doi.org/10.3390/molecules26071887
doi: 10.3390/molecules26071887
pubmed: 33810495
pmcid: 8037285
Hartmann A (2020) Quorum sensing N-acyl-homoserine lactone signal molecules of plant beneficial Gram-negative rhizobacteria support plant growth and resistance to pathogens. Rhizosphere 16:100258. https://doi.org/10.1016/j.rhisph.2020.100258
doi: 10.1016/j.rhisph.2020.100258
Monnier N, Furlan A, Botcazon C, Dahi A, Mongelard G, Cordelier S, Rippa S (2018) Rhamnolipids from Pseudomonas aeruginosa are elicitors triggering Brassica napus protection against Botrytis cinerea without physiological disorders. Front Plant Sci 9:1170. https://doi.org/10.3389/fpls.2018.01170
doi: 10.3389/fpls.2018.01170
pubmed: 30135699
pmcid: 6092566
Mozejko-Ciesielska J, Szacherska K, Marciniak P (2019) Pseudomonas species as producers of eco-friendly polyhydroxyalkanoates. J Polym Environ 27(6):1151–1166. https://doi.org/10.1007/s10924-019-01422-1
doi: 10.1007/s10924-019-01422-1
Van der Veen JN, Kennelly JP, Wan S, Vance JE, Vance DE, Jacobs RL (2017) The critical role of phosphatidylcholine and phosphatidylethanolamine metabolism in health and disease. Biochem Biophys Acta Biomemb 9:1558–1572. https://doi.org/10.1016/j.bbamem.2017.04.006
doi: 10.1016/j.bbamem.2017.04.006
Suresh P, Varathraju G, Shanmugaiah V, Almaary KS, Elbadawi YB, Mubarak A (2021) Partial purification and characterization of 2, 4-diacetylphloroglucinol producing Pseudomonas fluorescens VSMKU3054 against bacterial wilt disease of tomato. Saudi J Biol Sci 28(4):2155–2167. https://doi.org/10.1016/j.sjbs.2021.02.073
doi: 10.1016/j.sjbs.2021.02.073
pubmed: 33911932
pmcid: 8071909
Rush TA, Puech-Pagès V, Bascaules A, Jargeat P, Maillet F, Haouy AAne JM, (2020) Lipo-chitooligosaccharides as regulatory signals of fungal growth and development. Nat Commun 11(1):1–10. https://doi.org/10.1038/s41467-020-17615-5
doi: 10.1038/s41467-020-17615-5
Siliakus MF, van der Oost J, Kengen SW (2017) Adaptations of archaeal and bacterial membranes to variations in temperature, pH and pressure. Extremophiles 21(4):651–670. https://doi.org/10.1007/s00792-017-0939-x
doi: 10.1007/s00792-017-0939-x
pubmed: 28508135
pmcid: 5487899
Rudolf JD, Alsup TA, Xu B, Li Z (2021) Bacterial terpenome. Nat Product Rep. https://doi.org/10.1039/D0NP00066C
doi: 10.1039/D0NP00066C
Koo YM, Heo AY, Choi HW (2020) Salicylic acid as a safe plant protector and growth regulator. Plant Pathol J 36(1):1. https://doi.org/10.5423/PPJ.RW.12.2019.0295
doi: 10.5423/PPJ.RW.12.2019.0295
pubmed: 32089657
pmcid: 32089657
Ma X, Zheng J, Zhang X, Hu Q, Qian R (2017) Salicylic acid alleviates the adverse effects of salt stress on Dianthus superbus (Caryophyllaceae) by activating photosynthesis, protecting morphological structure, and enhancing the antioxidant system. Front Plant Sci 8:600. https://doi.org/10.3389/fpls.2017.00600
doi: 10.3389/fpls.2017.00600
pubmed: 28484476
pmcid: 5399920