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Year 2020, Volume: 3 Issue: 1, 81 - 94, 15.04.2020
https://doi.org/10.38001/ijlsb.624435

Abstract

References

  • 1. Hashem, A., et al., The interaction between arbuscular mycorrhizal fungi and endophytic bacteria enhances plant growth of Acacia gerrardii under salt stress. Frontiers in Plant Sciences, 2016. 7:p.1089.
  • 2. Ahmad, P., et al., Roles of enzymatic and nonenzymatic antioxidants in plants during abiotic stress. Critical Reviews in Biotechnology, 2010. 30: p. 161–175.
  • 3. Groppa, M.D., et al., Cadmium modulates NADPH oxidase activity and expression in sunflower leaves. Biologia Plantarum, 2012. 56: p. 167–171.
  • 4. Kazan, K. Auxin and the integration of environmental signals into plant root development. Annals of Botany, 2013. 112: p. 1655–1665
  • 5. Hu, Y.F., et al., Cadmium interferes with maintenance of auxin homeostasis in Arabidopsis seedlings. Journal of Plant Physiology, 2013. 170: p. 965–975.
  • 6. Egamberdieva, D. and Z. Kucharova, Selection for root colonising bacteria stimulating wheat growth in saline soils. Biology Fertiliters Soils, 2009. 45: p. 561–573.
  • 7. Khan, M.I.R., M. Asgher, and N.A. Khan, Alleviation of salt-induced photosynthesis and growth inhibition by salicylic acid involves glycine betaine and ethylene in mungbean (Vigna radiata L.). Plant Physiology and Biochemistry, 2014. 80: p. 67–74.
  • 8. Khan, A.L., et al.,. Endophytic fungi: a source of gibberellins and crop resistance to abiotic stress. Critical Reviews Biotechnology, 2013. 35: p. 62–74.
  • 9. Berg, G., et al., Biocontrol and osmoprotection for plants under saline conditions. In Molecular Microbial Ecology of the Rhizosphere, ed. F. J. de Bruijn (Hoboken, NJ: Wiley-Blackwell) 2013.
  • 10. Asaf, S., et al., Bacterial endophytes from arid land plants regulate endogenous hormone content and promote growth in crop plants: an example of Sphingomonas sp. and Serratia marcescens. Journal of Plant Interactions, 2017. 12: p. 31–38.
  • 11. Kudoyarova, G.R., et al., Cytokinin producing bacteria stimulate amino acid deposition by wheat roots. Plant Physiology and Biochemistry, 2014. 83: p. 285–291.
  • 12. Sgroy, V., et al., Isolation and characterization of endophytic plant growth-promoting (PGPB) or stress homeostasis-regulating (PSHB) bacteria associated to the halophyte Prosopis strombulifera. Applied Microbiology and Biotechnology, 2009. 85: p. 371–381.
  • 13. Pereira, S.I.A., et al., Endophytic culturable bacteria colonizing Lavandula dentata L. plants: isolation, characterization and evaluation of their plant growth-promoting activities. Ecological Engineering, 2016. 87: p. 91–97.
  • 14. Mendes, R., P., Garbeva, and J.M. Raaijmakers, The rhizosphere microbiome: significance of plant beneficial, plant pathogenic, and human pathogenic microorganisms. FEMS Microbiology Reviews, 2013. 37: p. 634–663.
  • 15. Sorty, A.M., et al., Effect of plant growth promoting bacteria associated with halophytic weed (Psoralea corylifolia L.) on germination and seedling growth of wheat under saline conditions. Applied Biochemistry and Biotechnology, 2016.180: p. 872–882.
  • 16. Egamberdieva, D., et al., Antimicrobial activity of medicinal plants correlates with the proportion of antagonistic endophytes. Frontiers in Microbiology, 2017. 8:p. 199.
  • 17. Cho, S.T., et al., Genome analysis of Pseudomonas fluorescens PCL1751: a rhizobacterium that controls root diseases and alleviates salt stress for its plant host. PLOS ONE, 2015. 10: p. 140231.
  • 18. Etesami, H., H.A. Alikhani, and H.M. Hosseini, Indole-3-acetic acid (IAA) production trait, a useful screening to select endophytic and rhizosphere competent bacteria for rice growth promoting agents. MethodsX, 2015. 2: p. 72–78.
  • 19. Tsavkelova, E.A., et al., Orchid-associated bacteria produce indole-3-acetic acid, promote seed germination, and increase their microbial yield in response to exogenous auxin. Archives of Microbiology, 2007.188: p. 655–664.
  • 20. Piccoli, P., et al., An endophytic bacterium isolated from roots of the halophyte Prosopis strombulifera produces ABA, IAA, gibberellins A1 and A3 and jasmonic acid in chemically-defined culture medium. Plant Growth Regulation, 2011. 64: p. 207–210.
  • 21. de Santi Ferrara, F.I., et al., Endophytic and rhizospheric enterobacteria isolated from sugar cane have different potentials for producing plant growth-promoting substances. Plant Soil, 2012. 353:p. 409–417.
  • 22. Mishra, S.K., et al., Characterisation of Pseudomonas spp. and Ochrobactrum sp. isolated from volcanic soil. Antonie Van Leeuwenhoek, 2017. 110: p. 253–270.
  • 23. Karadeniz, A., Ş.Topçuoğlu, and S. İnan, Auxin, gibberellin, cytokinin and abscisic acid production in some bacteria. World Journal of Microbiology and Biotechnology, 2006. 22: p. 1061–1064.
  • 24. Grobkinsky, D.K., et al., Cytokinin production by Pseudomonas fluorescens G20-18 determines biocontrol activity against Pseudomonas syringae in Arabidopsis. Scientific Reports, 2016. 6: p. 23310.
  • 25. Ahmad, I., et al., Differential effects of plant growth-promoting rhizobacteria on maize growth and cadmium uptake. Journal of Plant Growth Regulation, 2016. 35: p. 303–315.
  • 26. Naz, I., A. Bano, and T. Ul-Hassan, Isolation of phytohormones producing plant growth promoting rhizobacteria from weeds growing in Khewra salt range, Pakistan and their implication in providing salt tolerance to Glycine max L. African Journal of Biotechnology, 2009. 8: p. 5762–5766.
  • 27. Gutierrez-Manero, F.J., et. al., The plant growth promoting rhizobacteria Bacillus pumilus and Bacillus licheniformis produce high amounts of physiologically active gibberellins. Physiologia Plantarum, 2001. 111: p. 206–211
  • 28. Bottini, R., F. Cassan, and P. Piccoli, Gibberellin production by bacteria and its involvement in plant growth promotion and yield increase. Applied Microbiology and Biotechnology, 2004. 65: p. 497–503.
  • 29. Salomon, M.V., et al., Bacteria isolated from roots and rhizosphere of Vitis vinifera retard water losses, induce abscisic acid accumulation and synthesis of defense-related terpenes in in vitro cultured grapevine. Physiologia Plantarum, 2014. 51: p. 359–374.
  • 30. Forchetti, G., et al., Endophytic bacteria in sunflower (Helianthus annuus L.) isolation, characterization, and production of jasmonates and abscisic acid in culture medium. Applied Microbiology and Biotechnology, 2007. 76: p. 1145–1152.
  • 31. Hayat, S., et al., Growth of tomato (Lycopersicon esculentum) in response to salicylic acid under water stress. Journal of Plant Interactions, 2008. 3: p. 297–304.
  • 32. Shutsrirung, A., et al., Diversity of endophytic actinomycetes in mandarin grown in northern Thailand, their phytohormone production potential and plant growth promoting activity. Soil Science and Plant Nutrtion, 2013. 59: p. 322–330.
  • 33. Vijayabharathi, R., A. Sathya, and S. Gopalakrishnan, A Renaissance in plant growth-promoting and biocontrol agents by endophytes. In Microbial Inoculants in Sustainable Agricultural Productivity, eds D. P. Singh, H. B. Singh, and R. Prabha (New Delhi: Springer), 2016. p. 37–61.
  • 34. Ruanpanun, P., et al., Actinomycetes and fungi isolated from plant-parasitic nematode infested soils: screening of the effective biocontrol potential, indole-3-acetic acid and siderophore production. World J. Microbiology and Biotechnology, 2010. 26: p.1569–1578.
  • 35. Yandigeri, M.S., et al., 2012. Drought-tolerant endophytic actinobacteria promote growth of wheat (Triticum aestivum) under water stress conditions. Plant Growth Regulation. 68: p. 411–420.
  • 36. Nabti, E., et al., A Halophilic and osmotolerant Azospirillum brasilense strain from algerian soil restores wheat growth under saline conditions. Engineering in Life Sciences, 2007. 7: p. 354–360.
  • 37. Hidri, R., et al., Impact of microbial inoculation on biomass accumulation by Sulla carnosa provenances, and in regulating nutrition, physiological and antioxidant activities of this species under non-saline and saline conditions. Journal of Plant Physiology, 2016. 201: p. 28–41.
  • 38. Indiragandhi, P., et al., Characterization of plant growth-promoting traits of bacteria isolated from larval guts of diamondback moth Plutella xylostella (Lepidoptera: Plutellidae). Current Microbiology, 2008. 56: p. 327–333.
  • 39. Khan, A.L., et al., Gibberellins producing endophytic Aspergillus fumigatus sp. LH02 influenced endogenous phytohormonal levels, isoflavonoids production and plant growth in salinity stress. Process Biochemistry, 2011. 46: p. 440–447.
  • 40. Egamberdieva, D., et al., Bacteria able to control foot and root rot and to promote growth of cucumber in salinated soils. Biology Fertiliters Soils, 2011. 47: p.197–205.
  • 41. Egamberdieva, D., et al., Coordination between Bradyrhizobium and Pseudomonas alleviates salt stress in soybean through altering root system architecture. Journal of Plant Interactions, 2017. 12: p. 100–107.
  • 42. Liu, Y., et al., Effect of IAA produced by Klebsiella oxytoca Rs-5 on cotton growth under salt stress. Journal of General and Applied Microbiology, 2013. 59:p. 59–65.
  • 43. Ngumbi, E., and J. Kloepper, Bacterial-mediated drought tolerance: current and future prospects. Applied Soil Ecology, 2014. 105: p. 109–125.
  • 44. Singh, R.P., and P.N. Jha, A halotolerant bacterium Bacillus licheniformis HSW-16 augments induced systemic tolerance to salt stress in wheat plant (Triticum aestivum). Frontiers in Plant Science, 2016. 7: p. 1890.
  • 45. Zaheer, A., et al., Association of plant growth-promoting Serratia spp. with the root nodules of chickpea. Research in Microbiology, 2016. 167: p. 510–520.
  • 46. Egamberdieva, D., et al., High incidence of plant growth-stimulating bacteria associated with the rhizosphere of wheat grown on salinated soil in Uzbekistan. Environmental Microbiology, 2008. 10: p. 1-9.
  • 47. Forchetti, G., et al., Endophytic bacteria improve seedling growth of sunflower under water stress, produce salicylic acid, and inhibit growth of pathogenic fungi. Currents Microbiology, 2010. 61: p. 485–493.
  • 48. Shahzad, R., Inoculation of abscisic acid-producing endophytic bacteria enhances salinity stress tolerance in Oryza sativa. Journal Environmental and Experimental Botany, 2017. 136: p. 68–77.
  • 49. Marulanda, A., J.M. Barea, and R. Azcon, Stimulation of plant growth and drought tolerance by native microorganisms (AM fungi and bacteria) from dry environments: mechanisms related to bacterial effectiveness. Journal of Plant Growth Regulation, 2009. 28: p. 115–124.
  • 50. Raza, A., and M. Faisal, Growth promotion of maize by desiccation tolerant Micrococcus luteus-chp37 isolated from Cholistan desert, Pakistan. Australian Journal of Crop Science, 2013. 7: p. 1693–1698.
  • 51. Cereus, C., R.J. Sueldo, and C.A. Barassi, Water relations and yield in Azospirillum inoculated wheat exposed to drought in yield. Canadian Journal of Botany, 2004. 82: p. 273-281.
  • 52. Lavania, M., and C. Nautiyal, Solubilization of tricalcium phosphate by temperature and salt tolerant Serratia marcescens NBRI1213 isolated from alkaline soils. African Journal of Microbiology Research, 2013. 7: p. 4403–4413.
  • 53. Park, Y.G., et al., Bacillus aryabhattai SRB02 tolerates oxidative and nitrosative stress and promotes the growth of soybean by modulating the production of phytohormones. PLOS ONE, 2017. 12: p. 1-28.
  • 54. Dourado, M.N., et al., Burkholderia sp. SCMS54 reduces cadmium toxicity and promotes growth in tomato. Annals Applied Biology, 2013. 163: p. 494–507.
  • 55. Islam, F., et al., Combined ability of chromium (Cr) tolerant plant growth promoting bacteria (PGPB) and salicylic acid (SA) in attenuation of chromium stress in maize plants. Plant Physiology and Biochemistry, 2016. 108: p. 456–467.
  • 56. Burd, G., D.G. Dixon, and B.R. Glick, Plant growth promoting bacteria that decrease heavy metal toxicity in plants. Canadian Journal of Microbiology, 2000. 46: p. 237-245.
  • 57. Cardinale, M., et al., Paradox of plant growth promotion potential of rhizobacteria and their actual promotion effect on growth of barley (Hordeum vulgare L.) under salt stress. Microbiology Research, 2015. 181: p. 22–32.
  • 58. Upadhyay, S.K., et al., Impact of PGPR inoculation on growth and antioxidant status of wheat under saline conditions. Plant Biology, 2012. 14: p. 605–611.
  • 59. Bianco, C., and R. Defez, Medicago truncatula improves salt tolerance when nodulated by an indole-3-acetic acid-overproducing Sinorhizobium meliloti strain. Journal of Experimental Botany, 2009. 60: p. 3097–3107.
  • 60. Ma, Y., M. Rajkumar, and H. Fritas, Inoculation of plant growth promoting bacterium Achromobacter xylosoxidans strain Ax10 for the improvement of copper phytoextraction by Brassica juncea. Journal of Environmental Management, 2008. 90: p. 831–837.
  • 61. Zaidi, S., et al., Significance of Bacillus subtilis strain SJ-101 as a bioinoculant for concurrent plant growth promotion and nickel accumulation in Brassica juncea. Chemosphere, 2006. 64: p. 991–997.
  • 62. Khan, W.U., et al., Application of Bacillus megaterium MCR-8 improved phytoextraction and stress alleviation of nickel in Vinca rosea. International Journal of Phytoremediation, 2017. 19: p. 813–824.
  • 63. Nadeem, S.M., et al., The role of mycorrhizae and plant growth promoting rhizobacteria (PGPR) in improving crop productivity under stressful environments. Biotechnology Advances 2014. 32: p. 429–448.
  • 64. Egamberdieva, D., et al., Endophytic bacteria improve plant growth, symbiotic performance of chickpea (Cicer arietinum L.) and induce suppression of root rot caused by Fusarium solani under salt stress. Frontiers in Microbiology, 2017.. 8: p. 1887

Bitki gelişimini Teşvik Eden Rizobakteriler tarafından Üretilen Metabolitler ve Bitki Gelişimine Etkileri

Year 2020, Volume: 3 Issue: 1, 81 - 94, 15.04.2020
https://doi.org/10.38001/ijlsb.624435

Abstract



Çevresel stres bitki
gelişimini olumsuz etkiler. Kuraklık, tuzluluk, ağır metaller, sıcaklık gibi
abiyotik faktörler bitkisel verimin azalmasına neden olurlar. Mikroorganizmalar
tarafından üretilen metabolitler en önemli bitki gelişme düzenleyicilerindendir.
Strese karşı bitki savunma mekanizmalarını stimüle ederler. Rizosfer
bakterileri oksin, sitokinin, gibberellin, etilen ve absisik asit gibi bitki
hormonlarını üreterek bitki gelişimini teşvik ederler. Mineral fosfatın ve
diğer besin maddelerinin çözünmesi, strese karşı direncin arttırılmasında,
toprak agregatlarının stabilizasyonunda ve toprağın organik madde içeriğinin
iyileştirilmesine yardımcı olurlar. Bu derlemede, bitkilerin stres toleransını
indükleyen  rizobakteriler tarafından
üretilen metabolitler ile ilgili yapılan çalışmalar özetlenmiştir.



References

  • 1. Hashem, A., et al., The interaction between arbuscular mycorrhizal fungi and endophytic bacteria enhances plant growth of Acacia gerrardii under salt stress. Frontiers in Plant Sciences, 2016. 7:p.1089.
  • 2. Ahmad, P., et al., Roles of enzymatic and nonenzymatic antioxidants in plants during abiotic stress. Critical Reviews in Biotechnology, 2010. 30: p. 161–175.
  • 3. Groppa, M.D., et al., Cadmium modulates NADPH oxidase activity and expression in sunflower leaves. Biologia Plantarum, 2012. 56: p. 167–171.
  • 4. Kazan, K. Auxin and the integration of environmental signals into plant root development. Annals of Botany, 2013. 112: p. 1655–1665
  • 5. Hu, Y.F., et al., Cadmium interferes with maintenance of auxin homeostasis in Arabidopsis seedlings. Journal of Plant Physiology, 2013. 170: p. 965–975.
  • 6. Egamberdieva, D. and Z. Kucharova, Selection for root colonising bacteria stimulating wheat growth in saline soils. Biology Fertiliters Soils, 2009. 45: p. 561–573.
  • 7. Khan, M.I.R., M. Asgher, and N.A. Khan, Alleviation of salt-induced photosynthesis and growth inhibition by salicylic acid involves glycine betaine and ethylene in mungbean (Vigna radiata L.). Plant Physiology and Biochemistry, 2014. 80: p. 67–74.
  • 8. Khan, A.L., et al.,. Endophytic fungi: a source of gibberellins and crop resistance to abiotic stress. Critical Reviews Biotechnology, 2013. 35: p. 62–74.
  • 9. Berg, G., et al., Biocontrol and osmoprotection for plants under saline conditions. In Molecular Microbial Ecology of the Rhizosphere, ed. F. J. de Bruijn (Hoboken, NJ: Wiley-Blackwell) 2013.
  • 10. Asaf, S., et al., Bacterial endophytes from arid land plants regulate endogenous hormone content and promote growth in crop plants: an example of Sphingomonas sp. and Serratia marcescens. Journal of Plant Interactions, 2017. 12: p. 31–38.
  • 11. Kudoyarova, G.R., et al., Cytokinin producing bacteria stimulate amino acid deposition by wheat roots. Plant Physiology and Biochemistry, 2014. 83: p. 285–291.
  • 12. Sgroy, V., et al., Isolation and characterization of endophytic plant growth-promoting (PGPB) or stress homeostasis-regulating (PSHB) bacteria associated to the halophyte Prosopis strombulifera. Applied Microbiology and Biotechnology, 2009. 85: p. 371–381.
  • 13. Pereira, S.I.A., et al., Endophytic culturable bacteria colonizing Lavandula dentata L. plants: isolation, characterization and evaluation of their plant growth-promoting activities. Ecological Engineering, 2016. 87: p. 91–97.
  • 14. Mendes, R., P., Garbeva, and J.M. Raaijmakers, The rhizosphere microbiome: significance of plant beneficial, plant pathogenic, and human pathogenic microorganisms. FEMS Microbiology Reviews, 2013. 37: p. 634–663.
  • 15. Sorty, A.M., et al., Effect of plant growth promoting bacteria associated with halophytic weed (Psoralea corylifolia L.) on germination and seedling growth of wheat under saline conditions. Applied Biochemistry and Biotechnology, 2016.180: p. 872–882.
  • 16. Egamberdieva, D., et al., Antimicrobial activity of medicinal plants correlates with the proportion of antagonistic endophytes. Frontiers in Microbiology, 2017. 8:p. 199.
  • 17. Cho, S.T., et al., Genome analysis of Pseudomonas fluorescens PCL1751: a rhizobacterium that controls root diseases and alleviates salt stress for its plant host. PLOS ONE, 2015. 10: p. 140231.
  • 18. Etesami, H., H.A. Alikhani, and H.M. Hosseini, Indole-3-acetic acid (IAA) production trait, a useful screening to select endophytic and rhizosphere competent bacteria for rice growth promoting agents. MethodsX, 2015. 2: p. 72–78.
  • 19. Tsavkelova, E.A., et al., Orchid-associated bacteria produce indole-3-acetic acid, promote seed germination, and increase their microbial yield in response to exogenous auxin. Archives of Microbiology, 2007.188: p. 655–664.
  • 20. Piccoli, P., et al., An endophytic bacterium isolated from roots of the halophyte Prosopis strombulifera produces ABA, IAA, gibberellins A1 and A3 and jasmonic acid in chemically-defined culture medium. Plant Growth Regulation, 2011. 64: p. 207–210.
  • 21. de Santi Ferrara, F.I., et al., Endophytic and rhizospheric enterobacteria isolated from sugar cane have different potentials for producing plant growth-promoting substances. Plant Soil, 2012. 353:p. 409–417.
  • 22. Mishra, S.K., et al., Characterisation of Pseudomonas spp. and Ochrobactrum sp. isolated from volcanic soil. Antonie Van Leeuwenhoek, 2017. 110: p. 253–270.
  • 23. Karadeniz, A., Ş.Topçuoğlu, and S. İnan, Auxin, gibberellin, cytokinin and abscisic acid production in some bacteria. World Journal of Microbiology and Biotechnology, 2006. 22: p. 1061–1064.
  • 24. Grobkinsky, D.K., et al., Cytokinin production by Pseudomonas fluorescens G20-18 determines biocontrol activity against Pseudomonas syringae in Arabidopsis. Scientific Reports, 2016. 6: p. 23310.
  • 25. Ahmad, I., et al., Differential effects of plant growth-promoting rhizobacteria on maize growth and cadmium uptake. Journal of Plant Growth Regulation, 2016. 35: p. 303–315.
  • 26. Naz, I., A. Bano, and T. Ul-Hassan, Isolation of phytohormones producing plant growth promoting rhizobacteria from weeds growing in Khewra salt range, Pakistan and their implication in providing salt tolerance to Glycine max L. African Journal of Biotechnology, 2009. 8: p. 5762–5766.
  • 27. Gutierrez-Manero, F.J., et. al., The plant growth promoting rhizobacteria Bacillus pumilus and Bacillus licheniformis produce high amounts of physiologically active gibberellins. Physiologia Plantarum, 2001. 111: p. 206–211
  • 28. Bottini, R., F. Cassan, and P. Piccoli, Gibberellin production by bacteria and its involvement in plant growth promotion and yield increase. Applied Microbiology and Biotechnology, 2004. 65: p. 497–503.
  • 29. Salomon, M.V., et al., Bacteria isolated from roots and rhizosphere of Vitis vinifera retard water losses, induce abscisic acid accumulation and synthesis of defense-related terpenes in in vitro cultured grapevine. Physiologia Plantarum, 2014. 51: p. 359–374.
  • 30. Forchetti, G., et al., Endophytic bacteria in sunflower (Helianthus annuus L.) isolation, characterization, and production of jasmonates and abscisic acid in culture medium. Applied Microbiology and Biotechnology, 2007. 76: p. 1145–1152.
  • 31. Hayat, S., et al., Growth of tomato (Lycopersicon esculentum) in response to salicylic acid under water stress. Journal of Plant Interactions, 2008. 3: p. 297–304.
  • 32. Shutsrirung, A., et al., Diversity of endophytic actinomycetes in mandarin grown in northern Thailand, their phytohormone production potential and plant growth promoting activity. Soil Science and Plant Nutrtion, 2013. 59: p. 322–330.
  • 33. Vijayabharathi, R., A. Sathya, and S. Gopalakrishnan, A Renaissance in plant growth-promoting and biocontrol agents by endophytes. In Microbial Inoculants in Sustainable Agricultural Productivity, eds D. P. Singh, H. B. Singh, and R. Prabha (New Delhi: Springer), 2016. p. 37–61.
  • 34. Ruanpanun, P., et al., Actinomycetes and fungi isolated from plant-parasitic nematode infested soils: screening of the effective biocontrol potential, indole-3-acetic acid and siderophore production. World J. Microbiology and Biotechnology, 2010. 26: p.1569–1578.
  • 35. Yandigeri, M.S., et al., 2012. Drought-tolerant endophytic actinobacteria promote growth of wheat (Triticum aestivum) under water stress conditions. Plant Growth Regulation. 68: p. 411–420.
  • 36. Nabti, E., et al., A Halophilic and osmotolerant Azospirillum brasilense strain from algerian soil restores wheat growth under saline conditions. Engineering in Life Sciences, 2007. 7: p. 354–360.
  • 37. Hidri, R., et al., Impact of microbial inoculation on biomass accumulation by Sulla carnosa provenances, and in regulating nutrition, physiological and antioxidant activities of this species under non-saline and saline conditions. Journal of Plant Physiology, 2016. 201: p. 28–41.
  • 38. Indiragandhi, P., et al., Characterization of plant growth-promoting traits of bacteria isolated from larval guts of diamondback moth Plutella xylostella (Lepidoptera: Plutellidae). Current Microbiology, 2008. 56: p. 327–333.
  • 39. Khan, A.L., et al., Gibberellins producing endophytic Aspergillus fumigatus sp. LH02 influenced endogenous phytohormonal levels, isoflavonoids production and plant growth in salinity stress. Process Biochemistry, 2011. 46: p. 440–447.
  • 40. Egamberdieva, D., et al., Bacteria able to control foot and root rot and to promote growth of cucumber in salinated soils. Biology Fertiliters Soils, 2011. 47: p.197–205.
  • 41. Egamberdieva, D., et al., Coordination between Bradyrhizobium and Pseudomonas alleviates salt stress in soybean through altering root system architecture. Journal of Plant Interactions, 2017. 12: p. 100–107.
  • 42. Liu, Y., et al., Effect of IAA produced by Klebsiella oxytoca Rs-5 on cotton growth under salt stress. Journal of General and Applied Microbiology, 2013. 59:p. 59–65.
  • 43. Ngumbi, E., and J. Kloepper, Bacterial-mediated drought tolerance: current and future prospects. Applied Soil Ecology, 2014. 105: p. 109–125.
  • 44. Singh, R.P., and P.N. Jha, A halotolerant bacterium Bacillus licheniformis HSW-16 augments induced systemic tolerance to salt stress in wheat plant (Triticum aestivum). Frontiers in Plant Science, 2016. 7: p. 1890.
  • 45. Zaheer, A., et al., Association of plant growth-promoting Serratia spp. with the root nodules of chickpea. Research in Microbiology, 2016. 167: p. 510–520.
  • 46. Egamberdieva, D., et al., High incidence of plant growth-stimulating bacteria associated with the rhizosphere of wheat grown on salinated soil in Uzbekistan. Environmental Microbiology, 2008. 10: p. 1-9.
  • 47. Forchetti, G., et al., Endophytic bacteria improve seedling growth of sunflower under water stress, produce salicylic acid, and inhibit growth of pathogenic fungi. Currents Microbiology, 2010. 61: p. 485–493.
  • 48. Shahzad, R., Inoculation of abscisic acid-producing endophytic bacteria enhances salinity stress tolerance in Oryza sativa. Journal Environmental and Experimental Botany, 2017. 136: p. 68–77.
  • 49. Marulanda, A., J.M. Barea, and R. Azcon, Stimulation of plant growth and drought tolerance by native microorganisms (AM fungi and bacteria) from dry environments: mechanisms related to bacterial effectiveness. Journal of Plant Growth Regulation, 2009. 28: p. 115–124.
  • 50. Raza, A., and M. Faisal, Growth promotion of maize by desiccation tolerant Micrococcus luteus-chp37 isolated from Cholistan desert, Pakistan. Australian Journal of Crop Science, 2013. 7: p. 1693–1698.
  • 51. Cereus, C., R.J. Sueldo, and C.A. Barassi, Water relations and yield in Azospirillum inoculated wheat exposed to drought in yield. Canadian Journal of Botany, 2004. 82: p. 273-281.
  • 52. Lavania, M., and C. Nautiyal, Solubilization of tricalcium phosphate by temperature and salt tolerant Serratia marcescens NBRI1213 isolated from alkaline soils. African Journal of Microbiology Research, 2013. 7: p. 4403–4413.
  • 53. Park, Y.G., et al., Bacillus aryabhattai SRB02 tolerates oxidative and nitrosative stress and promotes the growth of soybean by modulating the production of phytohormones. PLOS ONE, 2017. 12: p. 1-28.
  • 54. Dourado, M.N., et al., Burkholderia sp. SCMS54 reduces cadmium toxicity and promotes growth in tomato. Annals Applied Biology, 2013. 163: p. 494–507.
  • 55. Islam, F., et al., Combined ability of chromium (Cr) tolerant plant growth promoting bacteria (PGPB) and salicylic acid (SA) in attenuation of chromium stress in maize plants. Plant Physiology and Biochemistry, 2016. 108: p. 456–467.
  • 56. Burd, G., D.G. Dixon, and B.R. Glick, Plant growth promoting bacteria that decrease heavy metal toxicity in plants. Canadian Journal of Microbiology, 2000. 46: p. 237-245.
  • 57. Cardinale, M., et al., Paradox of plant growth promotion potential of rhizobacteria and their actual promotion effect on growth of barley (Hordeum vulgare L.) under salt stress. Microbiology Research, 2015. 181: p. 22–32.
  • 58. Upadhyay, S.K., et al., Impact of PGPR inoculation on growth and antioxidant status of wheat under saline conditions. Plant Biology, 2012. 14: p. 605–611.
  • 59. Bianco, C., and R. Defez, Medicago truncatula improves salt tolerance when nodulated by an indole-3-acetic acid-overproducing Sinorhizobium meliloti strain. Journal of Experimental Botany, 2009. 60: p. 3097–3107.
  • 60. Ma, Y., M. Rajkumar, and H. Fritas, Inoculation of plant growth promoting bacterium Achromobacter xylosoxidans strain Ax10 for the improvement of copper phytoextraction by Brassica juncea. Journal of Environmental Management, 2008. 90: p. 831–837.
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There are 64 citations in total.

Details

Primary Language Turkish
Subjects Soil Sciences and Ecology
Journal Section Review Articles
Authors

Çiğdem Küçük

Ahmet Almaca

Publication Date April 15, 2020
Published in Issue Year 2020 Volume: 3 Issue: 1

Cite

EndNote Küçük Ç, Almaca A (April 1, 2020) Bitki gelişimini Teşvik Eden Rizobakteriler tarafından Üretilen Metabolitler ve Bitki Gelişimine Etkileri. International Journal of Life Sciences and Biotechnology 3 1 81–94.



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