Skip to main content

Plausible Role of Plant Growth-Promoting Rhizobacteria in Future Climatic Scenario

  • Chapter
  • First Online:

Abstract

Increasing agro-productivity for feeding growing world population under present climatic scenario requires optimizing the use of resources and adopting the sustainable agriculture methods. This can be achieved by using plant-beneficial bacteria. Target of achieving sustainable agriculture implies the use of varieties that are resistant to disease and tolerant to stress and having desired nutrition value. This can be effectively achieved through the use of rhizospheric microflora including bacteria, fungi, algae, etc. Among these, plant growth-promoting rhizobacteria (PGPR) have been seen as reliable and most promising bioinoculants for promoting plant growth and controlling phytopathogen without causing environmental deterioration. Application of PGPR as bioinoculants can help in achieving the target of global agricultural productivity to feed the world’s booming population, which is expected to become 9 billion by 2050. However, to be useful and effective bioinoculants, PGPR strains should be competent in their habitat, safe to the environment, helpful in plant nutrition and biocontrol, compatible with useful soil rhizobacteria, and tolerant to a variety of stress factors and show broad spectrum activity. In the context of the above scenario, this chapter focusses on the use of PGPR to increase agro-productivity and as one of the vital drivers of the agro-economy. In this review we focus on the modes of action of PGPR and their role in environmental protection and agricultural sustainability under increasing climatic variations.

This is a preview of subscription content, log in via an institution.

Buying options

Chapter
USD   29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD   149.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Hardcover Book
USD   199.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Learn about institutional subscriptions

References

  • Alarcon, M. V., Lloret, P. G., Iglesias, D. J., Talon, M., & Salguero, J. (2012). Comparison of growth responses to auxin 1-naphthaleneacetic acid and the ethylene precursor 1-aminocyclopropane-1-carboxilic acid in maize seedling root. Acta Biologica Cracoviensia Series Botanica, 54, 16–23.

    Google Scholar 

  • Aloni, R., Aloni, E., Langhans, M., & Ullrich, C. I. (2006). Role of cytokinin and auxin in shaping root architecture: Regulating vascular differentiation, lateral root initiation, root apical dominance and root gravitropism. Annals of Botany, 97, 883–893.

    Article  CAS  Google Scholar 

  • Ashraf, M. (1994). Organic substances responsible for salt tolerance in Eruca sativa. Biologia Plantarum, 36, 255–259.

    Article  CAS  Google Scholar 

  • Ashraf, M., Hasnain, S., Berge, O., & Mahmood, T. (2004). Inoculating wheat seedlings with exopolysaccharide-producing bacteria restricts sodium uptake and stimulates plant growth under salt stress. Biology and Fertility of Soils, 40, 157–162.

    CAS  Google Scholar 

  • Ashrafuzzaman, M., Hossen, F. A., Ismail, M. R., Hoque, A., Islam, M. Z., Shahidullah, S. M., & Meon, S. (2009). Efficiency of plant growth-promoting rhizobacteria (PGPR) for the enhancement of rice growth. African Journal of Biotechnology, 8(7), 1247–1252.

    CAS  Google Scholar 

  • Babalola, O. O., Osir, E. O., Sanni, A. I., Odhiambo, G. D., & Bulimo, W. D. (2003). Amplification of 1-amino-cyclopropane-1-carboxylic (ACC) deaminase from plant growth promoting rhizobacteria in striga-infested soil. African Journal of Biotechnology, 2, 157–160.

    Article  CAS  Google Scholar 

  • Barka, E. A., Nowak, J., & Clément, C. (2006). Enhancement of chilling resistance of inoculated grapevine plantlets with a plant growth-promoting rhizobacterium, Burkholderia phytofirmans strain PsJN. Applied and Environmental Microbiology, 72, 7246–7252.

    Article  CAS  Google Scholar 

  • Barnawal, D., Bharti, N., Maji, D., Chanotiya, C. S., & Kalra, A. (2012). 1-Aminocyclopropane-1-carboxylic acid (ACC) deaminase-containing rhizobacteria protect Ocimum sanctum plants during waterlogging stress via reduced ethylene generation. Plant Physiology and Biochemistry, 58, 227–235.

    Article  CAS  Google Scholar 

  • Bartel, B. (1997). Auxin biosynthesis. Annual Review of Plant Biology, 48, 51–66.

    Article  CAS  Google Scholar 

  • Belimov, A. A., Safronova, V. I., & Mimura, T. (2002). Response of spring rape (Brassica napus var. oleifera L.) to inoculation with plant growth promoting rhizobacteria containing 1-aminocyclopropane-1-carboxylate deaminase depends on nutrient status of the plant. Canadian Journal of Microbiology, 48, 189–199.

    Article  CAS  Google Scholar 

  • Belimov, A. A., Hontzeas, N., Safronova, V. I., Demchinskaya, S. V., Piluzza, G., Bullitta, S., & Glick, B. R. (2005). Cadmium-tolerant plant growth-promoting bacteria associated with the roots of Indian mustard (Brassica juncea L. Czern.). Soil Biology and Biochemistry, 37, 241–250.

    Article  CAS  Google Scholar 

  • Beneduzi, A., Ambrosini, A., & Passaglia, L. M. (2012). Plant growth-promoting rhizobacteria (PGPR): Their potential as antagonists and biocontrol agents. Genetics and Molecular Biology, 35, 1044–1051.

    Article  CAS  Google Scholar 

  • Bensalim, S., Nowak, J., & Asiedu, S. K. (1998). A plant growth promoting rhizobacterium and temperature effects on performance of 18 clones of potato. American Journal of Potato Research, 75, 145–152.

    Article  Google Scholar 

  • Bhattacharyya, P. N., & Jha, D. K. (2012). Plant growth-promoting rhizobacteria (PGPR): Emergence in agriculture. World Journal of Microbiology and Biotechnology, 28, 1327–1350.

    Article  CAS  Google Scholar 

  • Blumer, C., & Haas, D. (2000). Mechanism, regulation, and ecological role of bacterial cyanide biosynthesis. Archives of Microbiology, 173, 170–177.

    Article  CAS  Google Scholar 

  • Boughammoura, S., Chemek, M., Mimouna, S. B., Banni, M., & Messaoudi, I. (2017). Involvement of Zn depletion in cd-induced toxicity on prenatal bone formation in rat. Biology of Trace Elements Research in Press, 180(1), 70–80. https://doi.org/10.1007/s12011-017-0981-7.

    Article  CAS  Google Scholar 

  • Burdman, S., Jurkevitch, E., & Okon, Y. (2000). Recent advances in the use of plant growth promoting rhizobacteria (PGPR) in agriculture. In Microbial interactions in agriculture and forestry (Vol. 2, pp. 229–250).

    Google Scholar 

  • Castric, P. A. (1977). Glycine metabolism by Pseudomonas aeruginosa: Hydrogen cyanide biosynthesis. Journal of Bactriology, 130, 826–831.

    CAS  Google Scholar 

  • Castric, P. (1994). Influence of oxygen on the Pseudomonas aeruginosa hydrogen cyanide synthase. Current Microbiology, 29, 19–21.

    Article  CAS  Google Scholar 

  • Cattelan, A. M., Aversa, S. M. L., Zanchetta, M., Meneghetti, F., De Rossi, A., & Chieco-Bianchi, L. (1999). Regression of AIDS-related Kaposi’s sarcoma following antiretroviral therapy with protease inhibitors: Biological correlates of clinical outcome. European Journal of Cancer, 35, 1809–1815.

    Article  CAS  Google Scholar 

  • Cazorla, F. M., Duckett, S. B., Bergström, E. T., Noreen, S., Odijk, R., Lugtenberg, B. J., Thomas-Oates, J. E., & Bloemberg, G. V. (2006). Biocontrol of avocado dematophora root rot by antagonistic Pseudomonas fluorescens PCL1606 correlates with the production of 2-hexyl 5-propyl resorcinol. Molecular Plant-Microbe Interactions, 19, 418–428.

    Article  CAS  Google Scholar 

  • Chaiharn, M., & Lumyong, S. (2009). Phosphate solubilization potential and stress tolerance of rhizobacteria from rice soil in northern Thailand. World Journal of Microbiology and Biotechnology, 25, 305–314.

    Article  CAS  Google Scholar 

  • Chen, Y., Yan, F., Chai, Y., Liu, H., Kolter, R., Losick, R., & Guo, J. H. (2013). Biocontrol of tomato wilt disease by Bacillus subtilis isolates from natural environments depends on conserved genes mediating biofilm formation. Environmental Microbiology, 15, 848–864.

    Article  Google Scholar 

  • Cheng, Z., Park, E., & Glick, B. R. (2007). 1-Aminocyclopropane-1-carboxylate (ACC) deaminase from Pseudomonas putida UW4 facilitates the growth of canola in the presence of salt. Canadian Journal of Microbiology, 53(7), 912–918.

    Article  CAS  Google Scholar 

  • Chin-A-Woeng, T. F., Bloemberg, G. V., & Lugtenberg, B. J. (2003). Phenazines and their role in biocontrol by Pseudomonas bacteria. The New Phytologist, 157, 503–523.

    Article  CAS  Google Scholar 

  • Compant, S., Duffy, B., Nowak, J., Clément, C., & Barka, E. A. (2005a). Use of plant growth-promoting bacteria for biocontrol of plant diseases: Principles, mechanisms of action, and future prospects. Applied and Environmental Microbiology, 71, 4951–4959.

    Article  CAS  Google Scholar 

  • Compant, S., Reiter, B., Sessitsch, A., Nowak, J., Clément, C., & Barka, E. A. (2005b). Endophytic colonization of Vitis vinifera L. by plant growth-promoting bacterium Burkholderia sp. strain PsJN. Applied and Environmental Microbiology, 71, 1685–1693.

    Article  CAS  Google Scholar 

  • Davies, W. J., & Hartung, W. (2004). Has extrapolation from biochemistry to crop functioning worked to sustain plant production under water scarcity. In Proceeding of the fourth International crop Science Congress (Vol. 26).

    Google Scholar 

  • de Souza, J. T., Weller, D. M., & Raaijmakers, J. M. (2003). Frequency, diversity and activity of 2, 4-diacetylphloroglucinol producing fluorescent Pseudomonas spp. in Dutch take-all decline soils. Phytopathology, 93, 54–63.

    Article  Google Scholar 

  • Dell’Amico, E., Cavalca, L., & Andreoni, V. (2008). Improvement of Brassica napus growth under cadmium stress by cadmium-resistant rhizobacteria. Soil Biology and Biochemistry, 40, 74–84.

    Article  CAS  Google Scholar 

  • Dunne, C., Crowley, J. J., Moënne-Loccoz, Y., Dowling, D. N., & O’Gara, F. (1997). Biological control of Pythium ultimum by Stenotrophomonas maltophilia W81 is mediated by an extracellular proteolytic activity. Microbiology, 143, 3921–3931.

    Article  CAS  Google Scholar 

  • Egamberdieva D, Lugtenberg B (2014) Use of plant growth-promoting rhizobacteria to alleviate salinity stress in plants. In Use of microbes for the alleviation of soil stresses (Vol. 1, pp. 73–96). New York: Springer.

    Google Scholar 

  • Ezziyyani, M., Requena, M. E., Egea-Gilabert, C., & Candela, M. E. (2007). Biological control of phytophthora root rot of pepper using Trichoderma harzianum and Streptomyces rochei in combination. Journal of Phytopathology, 155, 342–349.

    Article  CAS  Google Scholar 

  • Figueiredo, M. V. B., Martinez, C. R., Burity, H. A., & Chanway, C. P. (2008). Plant growth-promoting rhizobacteria for improving nodulation and nitrogen fixation in the common bean (Phaseolus vulgaris L.). World Journal of Microbiology and Biotechnology, 24, 1187–1193.

    Article  CAS  Google Scholar 

  • Fu, Q., Liu, C., Ding, N., Lin, Y., & Guo, B. (2010). Ameliorative effects of inoculation with the plant growth-promoting rhizobacterium Pseudomonas sp. DW1 on growth of eggplant (Solanum melongena L.) seedlings under salt stress. Agricultural Water Management, 97, 1994–2000.

    Article  Google Scholar 

  • Gamalero, E., Lingua, G., Berta, G., & Glick, B. R. (2009). Beneficial role of plant growth promoting bacteria and arbuscular mycorrhizal fungi on plant responses to heavy metal stress. Canadian Journal of Microbiology, 55, 501–514.

    Article  CAS  Google Scholar 

  • Geddie, J. L., & Sutherland, I. W. (1993). Uptake of metals by bacterial polysaccharides. Journal of Applied Microbiology, 74, 467–472.

    CAS  Google Scholar 

  • Glick, B. R. (1995). The enhancement of plant growth by free-living bacteria. Canadian Journal of Microbiology, 41, 109–117.

    Article  CAS  Google Scholar 

  • Glick, B. R., Penrose, D. M., & Li, J. (1998). A model for the lowering of plant ethylene concentrations by plant growth-promoting bacteria. Journal of Theoretical Biology, 190, 63–68.

    Article  CAS  Google Scholar 

  • Glick, B. R., Cheng, Z., Czarny, J., & Duan, J. (2007). Promotion of plant growth by ACC deaminase-producing soil bacteria. European Journal of Plant Pathology, 119, 329–339.

    Article  CAS  Google Scholar 

  • Gomah, H. H., Mahmoud, S. M., El-Rewainy, H. M., & Abdrabou, M. R. (2014). Soil solarization and inoculation with Sulphur oxidizing bacteria and their effects on some soil properties. Journal of Microbial Biochemistry and Technology, S3, 2.

    Google Scholar 

  • Gontia-Mishra, I., Sapre, S., & Tiwari, S. (2017). Zinc solubilizing bacteria from the rhizosphere of rice as prospective modulator of zinc biofortification in rice. Rhizosphere, 3, 185–190.

    Article  Google Scholar 

  • Goteti, P. K., Emmanuel, L. D. A., Desai, S., & Shaik, M. H. A. (2013). Prospective zinc solubilising bacteria for enhanced nutrient uptake and growth promotion in maize (Zea mays L.). International Journal of Microbiology. https://doi.org/10.1155/2013/869697.

    Article  CAS  Google Scholar 

  • Gray, E. J., & Smith, D. L. (2005). Intracellular and extracellular PGPR: Commonalities and distinctions in the plant–bacterium signaling processes. Soil Biology and Biochemistry, 37, 395–412.

    Article  CAS  Google Scholar 

  • Grichko, V. P., & Glick, B. R. (2001). Amelioration of flooding stress by ACC deaminase-containing plant growth-promoting bacteria. Plant Physiology and Biochemistry, 39, 11–17.

    Article  CAS  Google Scholar 

  • Haas, D., & Défago, G. (2005). Biological control of soil-borne pathogens by fluorescent pseudomonads. Nature Reviews. Microbiology, 3, 307–319.

    Article  CAS  Google Scholar 

  • Hadiarto, T., & Tran, L. S. P. (2011). Progress studies of drought-responsive genes in rice. Plant Cell Reports, 30, 297–310.

    Article  CAS  Google Scholar 

  • Hamdia, M. A. E. S., Shaddad, M. A. K., & Doaa, M. M. (2004). Mechanisms of salt tolerance and interactive effects of Azospirillum brasilense inoculation on maize cultivars grown under salt stress conditions. Plant Growth Regulation, 44, 165–174.

    Article  CAS  Google Scholar 

  • Han, H. S., & Lee, K. D. (2005). Phosphate and potassium solubilizing bacteria effect on mineral uptake, soil availability and growth of eggplant. Research Journal of Agriculture and Biological Sciences, 1, 176–180.

    Google Scholar 

  • Handelsman, J., & Stabb, E. V. (1996). Biocontrol of soil-borne plant pathogens. The Plant Cell, 8, 1855–1869.

    Article  CAS  Google Scholar 

  • Hariprasad, P., Divakara, S. T., & Niranjana, S. R. (2011). Isolation and characterization of chitinolytic rhizobacteria for the management of Fusarium wilt in tomato. Crop Protection, 30, 1606–1612.

    Article  Google Scholar 

  • Harman, G. E., Howell, C. R., Viterbo, A., Chet, I., & Lorito, M. (2004). Trichoderma species-opportunistic, avirulent plant symbionts. Nature Reviews Microbiology, 2, 43–56.

    Article  CAS  Google Scholar 

  • Heidari, M., Mousavinik, S. M., & Golpayegani, A. (2011). Plant growth promoting rhizobacteria (PGPR) effect on physiological parameters and mineral uptake in basil (Ocimum basilicum L.) under water stress. ARPN Journal of Agricultural Biological Science, 6, 6–11.

    Google Scholar 

  • Hernandez, M. E., Kappler, A., & Newman, D. K. (2004). Phenazines and other redox-active antibiotics promote microbial mineral reduction. Applied and Environmental Microbiology, 70, 921–928.

    Article  CAS  Google Scholar 

  • Heydari, A., & Pessarakli, M. (2010). A review on biological control of fungal plant pathogens using microbial antagonists. Journal of Biological Sciences, 10, 273–290.

    Article  Google Scholar 

  • Idris, E. E., Iglesias, D. J., Talon, M., & Borriss, R. (2007). Tryptophan-dependent production of indole-3-acetic acid (IAA) affects level of plant growth promotion by Bacillus amyloliquefaciens FZB42. Molecular Plant-Microbe Interactions, 20, 619–626.

    Article  CAS  Google Scholar 

  • Iqbal, H. M. N., Asgher, M., & Bhatti, H. N. (2011). Optimization of physical and nutritional factors for synthesis of lignin degrading enzymes by a novel strain of Trametes versicolor. BioResources, 6, 1273–1287.

    CAS  Google Scholar 

  • Jadhav, H. P., & Sayyed, R. Z. (2016). Hydrolytic enzymes of rhizospheric microbes in crop protection. MOJ Cell Science and Report, 3(5), 00070. https://doi.org/10.15406/mojcsr.2016.03.00070.

    Article  Google Scholar 

  • Jadhav, H. P., Shaikh, S. S., & Sayyed, R. Z. (2017). Role of hydrolytic enzymes of rhizoflora in biocontrol of fungal phytopathogens: An overview. In Rhizotrophs: Plant growth promotion to bioremediation (pp. 183–203). Springer.

    Google Scholar 

  • Jaleel, C. A., Manivannan, P. M., Wahid, A., Farooq, M., Al-Juburi, H. J., Somasundaram, R., & Panneerselvam, R. (2009). Drought stress in plants: A review on morphological characteristics and pigments composition. International Journal of Agriculture and Biology, 11, 100–105.

    Google Scholar 

  • Jalili, F., Khavazi, K., Pazira, E., Nejati, A., Rahmani, H. A., Sadaghiani, H. R., & Miransari, M. (2009). Isolation and characterization of ACC deaminase-producing fluorescent pseudomonads, to alleviate salinity stress on canola (Brassica napus L.) growth. Journal of Plant Physiology, 166, 667–674.

    Article  CAS  Google Scholar 

  • Jung, W. J., Kuk, J. H., Kim, K. Y., Kim, T. H., & Park, R. D. (2005). Purification and characterization of chitinase from Paenibacillus illinoisensis KJA-424. Journal of Microbiology and Biotechnology, 15, 274–280.

    CAS  Google Scholar 

  • Kamilova, F., Validov, S., Azarova, T., Mulders, I., & Lugtenberg, B. (2005). Enrichment for enhanced competitive plant root tip colonizers selects for a new class of biocontrol bacteria. Environmental Microbiology, 7, 1809–1817.

    Article  CAS  Google Scholar 

  • Kang, J. G., Shin, S. Y., Kim, M. J., Bajpai, V., Maheshwari, D. K., & Kang, S. C. (2004). Isolation and antifungal activities of 2-hydroxymethyl-chroman-4-one produced by Burkholderia sp. MSSP. The Journal of Antibiotics, 57, 726–731.

    Article  CAS  Google Scholar 

  • Kang, S. M., Joo, G. J., Hamayun, M., Na, C. I., Shin, D. H., Kim, H. Y., Hong, J. K., & Lee, I. J. (2009). Gibberellin production and phosphate solubilization by newly isolated strain of Acinetobacter calcoaceticus and its effect on plant growth. Biotechnology Letters, 31, 277–281.

    Article  CAS  Google Scholar 

  • Karnawal, A. (2009). Production of indole acetic acid by fluorescent Pseudomonas in the presence of L-tryptophan and rice root exudates. Journal of Plant Pathology, 61–63.

    Google Scholar 

  • Kaur, R., Macleod, J., Foley, W., & Nayudu, M. (2006). Gluconic acid: An antifungal agent produced by Pseudomonas species in biological control of take-all. Phytochemistry, 67, 595–604.

    Article  CAS  Google Scholar 

  • Kaymak, H. C., Guvenc, I., & Gurol, A. (2010). Elemental analysis of different radish (Raphanus sativus L.) cultivars by using wavelength-dispersive x-ray fluorescence spectrometry (wdxrf). Bulgaraian Journal of Agricultural Science, 16, 769–774.

    Google Scholar 

  • Khalid, A., Arshad, M., & Zahir, Z. A. (2004). Screening plant growth-promoting rhizobacteria for improving growth and yield of wheat. Journal of Applied Microbiology, 96, 473–480.

    Article  CAS  Google Scholar 

  • Khan, M. S., Zaidi, A., Ahemad, M., Oves, M., & Wani, P. A. (2010). Plant growth promotion by phosphate solubilizing fungi-current perspective. Archieves in Agronomy Soil Science, 56, 73–98.

    Article  CAS  Google Scholar 

  • Khodair, T. A., Galal, G. F., & El-Tayeb, T. S. (2008). Effect of inoculating wheat seedlings with exopolysaccharide-producing bacteria in saline soil. Journal of Applied Sciences Research, 4, 2065–2070.

    Google Scholar 

  • Kloepper, J. W., & Schroth, M. N. (1978). Plant growth-promoting rhizobacteria on radishes. In Proceedings of the 4th international conference on plant pathogenic bacteria (Vol. 2, pp. 879–882).

    Google Scholar 

  • Kotan, R., Cakir, A., Dadasoglu, F., Aydin, T., Cakmakci, R., Ozer, H., Kordali, S., Mete, E., & Dikbas, N. (2010). Antibacterial activities of essential oils and extracts of turkish achillea, satureja and thymus species against plant pathogenic bacteria. Journal of the Science of Food and Agriculture, 90, 145–160.

    Article  CAS  Google Scholar 

  • Labuschagne, N., Pretorius, T., & Idris, A. H. (2010). Plant growth promoting rhizobacteria as biocontrol agents against soil-borne plant diseases. In Plant growth and health promoting bacteria (pp. 211–230). Berlin, Heidelberg: Springer.

    Chapter  Google Scholar 

  • Lanteigne, C., Gadkar, V. J., Wallon, T., Novinscak, A., & Filion, M. (2012). Production of DAPG and HCN by Pseudomonas sp. LBUM300 contributes to the biological control of bacterial canker of tomato. Phytopathology, 102, 967–973.

    Article  CAS  Google Scholar 

  • Laville, J., Blumer, C., Von Schroetter, C., Gaia, V., Défago, G., Keel, C., & Haas, D. (1998). Characterization of the hcn ABC gene cluster encoding hydrogen cyanide synthase and anaerobic regulation by ANR in the strictly aerobic biocontrol agent Pseudomonas fluorescens CHA0. Journal of Bacteriology, 180, 3187–3196.

    CAS  Google Scholar 

  • Loper, J. E., & Gross, H. (2007). Genomic analysis of antifungal metabolite production by Pseudomonas fluorescens Pf-5. European Journal of Plant Pathology, 119, 265–278.

    Article  CAS  Google Scholar 

  • Lorck, H. (1948). Production of hydrocyanic acid by bacteria. Physiologia Plantarum, 1, 142–146.

    Article  CAS  Google Scholar 

  • Lugtenberg, B., & Kamilova, F. (2009). Plant-growth-promoting rhizobacteria. Annual Review of Microbiology, 63, 541–556.

    Article  CAS  Google Scholar 

  • Lugtenberg, B. J., Dekkers, L., & Bloemberg, G. V. (2001). Molecular determinants of rhizosphere colonization by Pseudomonas. Annual Review of Phytology, 39, 461–490.

    Article  CAS  Google Scholar 

  • Mabood, F., Zhou, X., & Smith, D. L. (2014). Microbial signaling and plant growth promotion. Canadian Journal of Plant Science, 94, 1051–1063.

    Article  CAS  Google Scholar 

  • Maggio, A., Barbieri, G., Raimondi, G., & De Pascale, S. (2010). Contrasting effects of GA3 treatments on tomato plants exposed to increasing salinity. Journal of Plant Growth Regulation, 29, 63–72.

    Article  CAS  Google Scholar 

  • Maksimov, I. V., Abizgil’Dina, R. R., & Pusenkova, L. I. (2011). Plant growth promoting rhizobacteria as alternative to chemical crop protectors from pathogens. Applied Biochemistry and Microbiology, 47(4), 333–345.

    Article  CAS  Google Scholar 

  • Mansour, F., Aldesuquy, H., & Hamedo, H. (1994). Studies on plant growth regulators and enzymes production by some bacteria. Qatar University Science Journal, 14, 281–288.

    CAS  Google Scholar 

  • Markovich, N. A., & Kononova, G. L. (2003). Lytic enzymes of Trichoderma and their role in plant defense from fungal diseases: A review. Applied Biochemistry Microbiology, 39, 341–351.

    Article  CAS  Google Scholar 

  • Mattoo, A., & Suttle, J. C. (1991). The plant hormone ethylene (pp. 352–361). Boca Raton: CRC Press.

    Google Scholar 

  • Mayak, S., Tirosh, T., & Glick, B. R. (2004). Plant growth-promoting bacteria confer resistance in tomato plants to salt stress. Plant Physiology and Biochemistry, 42, 565–572.

    Article  CAS  Google Scholar 

  • Merchan, F., de Lorenzo, L., González-Rizzo, S., Niebel, A., Megías, M., Frugier, F., Sousa, C., & Crespi, M. (2007). Analysis of regulatory pathways involved in the reacquisition of root growth after salt stress in Medicago truncatula. The Plant Journal, 51, 1–17.

    Article  CAS  Google Scholar 

  • Minuto, A., Spadaro, D., Garibaldi, A., & Gullino, M. L. (2006). Control of soil borne pathogens of tomato using a commercial formulation of Streptomyces griseoviridis and solarization. Crop Protection, 25, 468–475.

    Article  Google Scholar 

  • Nadeem, S. M., Zahir, Z. A., Naveed, M., Arshad, M., & Shahzad, S. M. (2006a). Variation in growth and ion uptake of maize due to inoculation with plant growth promoting rhizobacteria under salt stress. Soil & Environment, 25, 78–84.

    Google Scholar 

  • Nadeem, S. M., Hussain, I., Naveed, M., Asghar, H. N., Zahir, Z. A., & Arshad, M. (2006b). Performance of plant growth promoting rhizobacteria containing ACC-deaminase activity for improving growth of maize under salt-stressed conditions. Pakistan Journal of Agricultural Sciences, 43, 114–121.

    Google Scholar 

  • Nadeem, S. M., Zahir, Z. A., Naveed, M., & Arshad, M. (2007). Preliminary investigations on inducing salt tolerance in maize through inoculation with rhizobacteria containing ACC deaminase activity. Canadian Journal of Microbiology, 53, 1141–1149.

    Article  CAS  Google Scholar 

  • Nayani, S., Mayak, S., & Glick, B. R. (1998). Effect of plant growth-promoting rhizobacteria on senescence of flower petals. Indian Journal Experimental Biology, 36, 836–839.

    Google Scholar 

  • Nihorimbere, V., Ongena, M., Smargiassi, M., & Thonart, P. (2011). Beneficial effect of the rhizosphere microbial community for plant growth and health. Biotechnology, Agronomy Society and Environment, 15, 327.

    Google Scholar 

  • Noumavo, P. A., Agbodjato, N. A., Baba-Moussa, F., Adjanohoun, A., & Baba-Moussa, L. (2016). Plant growth promoting rhizobacteria: Beneficial effects for healthy and sustainable agriculture. African Journal of Biotechnology, 15, 1452–1463.

    Article  CAS  Google Scholar 

  • O’sullivan, D. J., & O’Gara, F. (1992). Traits of fluorescent Pseudomonas spp. involved in suppression of plant root pathogens. Microbiological Reviews, 56, 662–676.

    Google Scholar 

  • Palumbo, J. D., Yuen, G. Y., Jochum, C. C., Tatum, K., & Kobayashi, D. Y. (2005). Mutagenesis of β-1,3-glucanase genes in Lysobacter enzymogenes strain C3 results in reduced biological control activity toward bipolaris leaf spot of tall fescue and pythium damping-off of sugar beet. Phytopathology, 95, 701–707.

    Article  CAS  Google Scholar 

  • Patel, S., Sayyed, R., & Saraf, M. (2016). Bacterial determinants and plant defense induction: Their role as bio-control agent in agriculture. In K. Hakeem (Ed.), Plant soil-microbes (pp. 187–204). Cham: Springer.

    Google Scholar 

  • Patten, C. L., & Glick, B. R. (1996). Bacterial biosynthesis of indole-3-acetic acid. Canadian Journal of Microbiology, 42, 207–220.

    Article  CAS  Google Scholar 

  • Patten, C. L., & Glick, B. R. (2002). Role of Pseudomonas putida indole acetic acid in development of the host plant root system. Applied and Environmental Microbiology, 68, 3795–3801.

    Article  CAS  Google Scholar 

  • Perneel, M., D'hondt, L., De Maeyer, K., Adiobo, A., Rabaey, K., & Höfte, M. (2008). Phenazines and biosurfactants interact in the biological control of soil-borne diseases caused by Pythium spp. Environmental Microbiology, 10, 778–788.

    Article  Google Scholar 

  • Pierik, R., Tholen, D., Poorter, H., Visser, E. J., & Voesenek, L. A. (2006). The janus face of ethylene: Growth inhibition and stimulation. Trends in Plant Science, 11, 176–183.

    Article  CAS  Google Scholar 

  • Pieterse, C. M., Zamioudis, C., Berendsen, R. L., Weller, D. M., Van Wees, S. C., & Bakker, P. A. (2014). Induced systemic resistance by beneficial microbes. Annual Review of Phytology, 52, 347–375.

    Article  CAS  Google Scholar 

  • Pospíšilová, J. (2003). Interaction of cytokinins and abscisic acid during regulation of stomatal opening in bean leaves. Photosynthetica, 41, 49–56.

    Article  Google Scholar 

  • Prapagdee, B., Kuekulvong, C., & Mongkolsuk, S. (2008). Antifungal potential of extracellular metabolites produced by Streptomyces hygroscopicus against phytopathogenic fungi. International Journal of Biological Sciences, 4, 330.

    Article  CAS  Google Scholar 

  • Qualhato, T. F., Lopes, F. A. C., Steindorff, A. S., Brandao, R. S., Jesuino, R. S. A., & Ulhoa, C. J. (2013). Mycoparasitism studies of Trichoderma species against three phytopathogenic fungi: Evaluation of antagonism and hydrolytic enzyme production. Biotechnology Letters, 35(9), 1461–1468.

    Article  CAS  Google Scholar 

  • Qurashi, A. W., & Sabri, A. N. (2012). Bacterial exopolysaccharide and biofilm formation stimulate chickpea growth and soil aggregation under salt stress. Brazilian Journal of Microbiology, 43, 1183–1191.

    Article  CAS  Google Scholar 

  • Radi, A. E., Acero Sánchez, J. L., Baldrich, E., & O’Sullivan, C. K. (2006). Reagentless, reusable, ultrasensitive electrochemical molecular beacon aptasensor. Journal of the American Chemical Society, 28, 117–124.

    Article  CAS  Google Scholar 

  • Raghavendra, M. P., Nayaka, S. C., & Nuthan, B. R. (2016). Role of Rhizosphere microflora in potassium solubilization. In Potassium solubilizing microorganisms for sustainable agriculture (pp. 43–59). New Delhi: Springer.

    Chapter  Google Scholar 

  • Ramos Solano, B., Barriuso Maicas, J., Pereyra De La Iglesia, M. T., Domenech, J., & Gutiérrez Mañero, F. J. (2008). Systemic disease protection elicited by plant growth promoting rhizobacteria strains: Relationship between metabolic responses, systemic disease protection, and biotic elicitors. Phytopathology, 98, 451–457.

    Article  CAS  Google Scholar 

  • Reshma, P., Naik, M. K., Aiyaz, M., Niranjana, S. R., Chennappa, G., Shaikh, S. S., & Sayyed, R. Z. (2018). Induced systemic resistance by 2, 4-diacetylphloroglucinol positive fluorescent pseudomonas strains against rice sheath blight. Indian Journal of Experimental Biology, 56, 207–212.

    CAS  Google Scholar 

  • Romero, D., de Vicente, A., Rakotoaly, R. H., Dufour, S. E., Veening, J. W., Arrebola, E., Cazorla, F. M., Kuipers, O. P., Paquot, M., & Pérez-García, A. (2007). The iturin and fengycin families of lipopeptides are key factors in antagonism of Bacillus subtilis toward Podosphaera fusca. Molecular Plant-Microbe Interactions, 20, 430–440.

    Article  CAS  Google Scholar 

  • Ryals, J. A., Neuenschwander, U. H., Willits, M. G., Molina, A., Steiner, H. Y., & Hunt, M. D. (1996). Systemic acquired resistance. Plant Cell, 8, 1809.

    Article  CAS  Google Scholar 

  • Saber, H. F., Torang, A., Mobaleghi, M., Dehpouri, A., & Saber, H. Z. (2013). Study of nitrogen and potash fertilizers on crop yield, soluble and non soluble sugar in stevia plant (Stevia Rebaudiana Bertoni). New Findings In Agriculture, 7(2), 127–135.

    Google Scholar 

  • Sacherer, P., Défago, G., & Haas, D. (1994). Extracellular protease and phospholipase C are controlled by the global regulatory gene gacA in the biocontrol strain Pseudomonas fluorescens CHA0. FEMS Microbiology Letters, 116, 155–160.

    Article  CAS  Google Scholar 

  • Saharan, B. S., & Nehra, V. (2011). Plant growth promoting rhizobacteria: A critical review. Life Sciences and Medicine Research, 21, 1–30.

    Google Scholar 

  • Saravanakumar, D., Vijayakumar, C., Kumar, N., & Samiyappan, R. (2007). PGPR-induced defense responses in the tea plant against blister blight disease. Crop Protection, 26, 556–565.

    Article  Google Scholar 

  • Sayyed, R. Z., & Chincholkar, S. B. (2006). Purification of siderophores of Alcaligenes feacalis on XAD. Bioresource Technology, 97, 1026–1029.

    Article  CAS  Google Scholar 

  • Sayyed, R. Z., Patel, D. C., & Patel, P. R. (2007). Plant growth promoting potential of P solubilizing Pseudomonas sp. occurring in acidic soil of Jalgaon. Asian Journal of Microbiology, Biotechnology and Environment Science, 4, 925–928.

    Google Scholar 

  • Sayyed, R. Z., Naphade, B. S., Joshi, S. A., Gangurde, N. S., Bhamare, H. M., & Chincholkar, S. B. (2009). Consortium of a. Feacalis and P. fluorescens promoted the growth of Arachis hypogea (groundnut). Asian Journal of Microbiology, Biotechnology and Environment Science, 1, 48–51.

    Google Scholar 

  • Sayyed, R. Z., & Chincholkar, S. B. (2010). Growth and siderophore production in A. faecalis is influenced by metal ions. Indian Journal of Microbiology, 50, 179–182.

    Article  CAS  Google Scholar 

  • Sayyed, R. Z., & Patel, P. R. (2011). Soil microbes & environmental health. International Journal of Biotechnology & Bioscience, 1, 41–66.

    Google Scholar 

  • Sayyed, R. Z., Naphade, B. S., & Chincholkar, S. B. (2004). Ecologically competent rhizobacteria for plant growth promotion and disease management. In M. K. Rai, N. J. Chikhale, P. V. Thakare, P. A. Wadegaonkar, & A. P. Ramteke (Eds.), Recent trends in biotechnology (pp. 1–16). Jodhpur: Scientific Publisher.

    Google Scholar 

  • Sayyed, R. Z., Chincholkar, S. B., Meyer, J. M., & Kale, S. P. (2011). Chemical characterization, crossfeeding and uptake studies on hydroxamate siderophore of Alcaligenes faecalis. Indian Journal of Microbiology, 51, 176–181.

    Article  CAS  Google Scholar 

  • Sayyed, R. Z., Reddy, M. S., Deshmukh, A. M., Pate, A. S., & Gangurde, N. S. (2012). Potential of plant growth promoting rhizobacteria for sustainable agriculture bacteria. In D. K. Maheshwari (Ed.), Agrobiology: Plant probiotics (pp. 287–314). Berlin: Springer.

    Chapter  Google Scholar 

  • Sayyed, R. Z., Chincholkar, S. B., Reddy, M. S., Gangurde, N. S., & Patel, P. R. (2013). Siderophore producing PGPR for crop nutrition and phytopathogen suppression bacteria. In D. K. Maheshwari (Ed.), Agrobiology: Disease management (pp. 449–471). Dordrecht: Springer.

    Chapter  Google Scholar 

  • Sayyed, R. Z., Patel, P. R., & Shaikh, S. S. (2015). Plant growth promotion and root colonization by EPS producing Enterobacter sp. RZS5 under heavy metal contaminated soil. Indian Journal of Experimental Biology, 53, 116–123.

    CAS  Google Scholar 

  • Shaikh, S. S., & Sayyed, R. Z. (2015). Role of plant growth-promoting rhizobacteria and their formulation in biocontrol of plant diseases. In N. K. Arora (Ed.), Plant microbes symbiosis: Applied facets (pp. 337–351). New Delhi: Springer.

    Google Scholar 

  • Shaikh, S. S., Patel, P. R., Patel, S. S., Nikam, S. D., Rane, T. U., & Sayyed, R. Z. (2014). Production of biocontrol traits by banana field fluorescent Pseudomonads and comparison with chemical fungicide. Indian Journal of Experimental Biology, 52, 917–920.

    CAS  Google Scholar 

  • Shaikh, S. S., Reddy, M. S., & Sayyed, R. Z. (2016). Plant growth promoting rhizobacteria: An eco-friendly approach for sustainable agroecosystem. In K. Hakeem (Ed.), Plant soil-microbes (pp. 182–201). Cham: Springer.

    Google Scholar 

  • Shaikh, S. S., & Saraf, M. S. (2017). Optimization of growth conditions for zinc solubilizing plant growth associated Bacteria and Fungi. Journal of Advanced Research in Biotechnology, 2(1), 9.

    Article  Google Scholar 

  • Sharma, A., Shankhdhar, D., & Shankhdhar, S. C. (2013). Enhancing grain iron content of rice by the application of plant growth promoting rhizobacteria. Plant Soil Environment, 59(2), 89–94.

    Article  CAS  Google Scholar 

  • Shobha, G., & Kumudini, B. S. (2012). Antagonistic effect of the newly isolated PGPR Bacillus spp. on Fusarium oxysporum. International Journal of Applied Science and Engineering Research, 1, 463–474.

    Article  Google Scholar 

  • Shuhegger, R., Ihring, A., Gantner, S., Bahnweg, G., Knappe, C., Vogg, G., Hutzler, P., Schmid, M., Van Breusegem, F., Eberl, L., Hartmann, A., & Langebartels, C. (2006). Induction of systemic resistance in tomato by N-acyl-L-homoserine lactone-producing rhizosphere bacteria. Plant, Cell & Environment, 29, 909–918.

    Article  CAS  Google Scholar 

  • Siddikee, M. A., Chauhan, P. S., & Sa, T. (2012). Regulation of ethylene biosynthesis under salt stress in red pepper (Capsicum annuum L.) by 1-aminocyclopropane-1-carboxylic acid (ACC) deaminase-producing halotolerant bacteria. Journal of Plant Growth Regulation, 31, 265–272.

    Article  CAS  Google Scholar 

  • Singh, B. B., Mai-Kodomi, Y., & Terao, T. (1999). A simple screening method for drought tolerance in cowpea. The Indian Journal of Genetics and Plant and Breeding, 59, 211–220.

    Google Scholar 

  • Soltani, A., Khodarahmpour, Z., Jafari, A. A., & Nakhjavan, S. (2012). Selection of alfalfa (Medicago sativa L.) cultivars for salt stress tolerance using germination indices. African Journal of Biotechnology, 11, 7899–7905.

    CAS  Google Scholar 

  • Tank, N., & Saraf, M. (2010). Salinity-resistant plant growth promoting rhizobacteria ameliorates sodium chloride stress on tomato plants. Journal of Plant Interactions, 5, 51–58.

    Article  CAS  Google Scholar 

  • Ten Hoopen, G. M., & Krauss, U. (2006). Biology and control of Rosellinia bunodes, Rosellinia necatrix and Rosellinia pepo: A review. Crop Protection, 25, 89–107.

    Article  Google Scholar 

  • Tewari, S., & Arora, N. K. (2018). Role of salicylic acid from Pseudomonas aeruginosa PF23EPS+ in growth promotion of sunflower in saline soils infested with phytopathogen Macrophomina phaseolina. Environmental Sustainability, 1(1), 49–59.

    Article  Google Scholar 

  • Upadhyaya, C. P., Akula, N., Kim, H. S., Jeon, J. H., Ho, O. M., Chun, S. C., Kim, D. H., & Park, S. W. (2011). Biochemical analysis of enhanced tolerance in transgenic potato plants overexpressing d-galacturonic acid reductase gene in response to various abiotic stresses. Molecular Breeding, 28, 105–115.

    Article  CAS  Google Scholar 

  • Van Loon, L. C. (2007). Plant responses to plant growth-promoting rhizobacteria. European Journal of Plant Pathology, 119, 243–254.

    Article  CAS  Google Scholar 

  • Vettakkorumakankav, N. N., Falk, D., Saxena, P., & Fletcher, R. A. (1999). A crucial role for gibberellins in stress protection of plants. Plant & Cell Physiology, 40, 542–548.

    Article  CAS  Google Scholar 

  • Vinay, J. U., Naik, M. K., Rangeshwaran, R., Chennappa, G., Sohel, S. S., & Sayyed, R. Z. (2016). Detection of antimicrobial traits in fluorescent pseudomonads and molecular characterization of an antibiotic pyoluteorin. 3 Biotech, 6, 1–11.

    Article  Google Scholar 

  • Voisard, C., Keel, C., Haas, D., & Dèfago, G. (1989). Cyanide production by Pseudomonas fluorescens helps suppress black root rot of tobacco under gnotobiotic conditions. The EMBO Journal, 8, 351–358.

    Article  CAS  Google Scholar 

  • Walsh, U. F., Morrissey, J. P., & O'Gara, F. (2001). Pseudomonas for biocontrol of phytopathogens: From functional genomics to commercial exploitation. Current Opinion in Biotechnology, 12, 289–295.

    Article  CAS  Google Scholar 

  • Weller, D. M. (2007). Pseudomonas biocontrol agents of soil borne pathogens: Looking back over 30 years. Phytopathology, 97, 250–256.

    Article  Google Scholar 

  • Weller, D. M., & Thomashow, L. S. (1993). Use of rhizobacteria for biocontrol. Current Opinion in Biotechnology, 4, 306–311.

    Article  Google Scholar 

  • Whipps, J. M. (1990). Carbon utilization. In J. M. Lynch (Ed.), The rhizosphere (pp. 59–97). Chichester: Wiley Interscience.

    Google Scholar 

  • Whipps, J. M. (2001). Microbial interactions and biocontrol in the rhizosphere. Journal of Experimental Botany, 52, 487–511.

    Article  CAS  Google Scholar 

  • Yamaguchi, S. (2008). Gibberellin metabolism and its regulation. Annual Review of Plant Biology, 59, 225–251.

    Article  CAS  Google Scholar 

  • Yaxley, J. R., Ross, J. J., Sherriff, L. J., & Reid, J. B. (2001). Gibberellin biosynthesis mutations and root development in pea. Plant Physiology, 125, 627–633.

    Article  CAS  Google Scholar 

  • Yue, H., Mo, W., Li, C., Zheng, Y., & Li, H. (2007). The salt stress relief and growth promotion effect of Rs-5 on cotton. Plant and Soil, 297, 139–145.

    Article  CAS  Google Scholar 

  • Zahedi, H. (2016). Growth-promoting effect of potassium-solubilizing microorganisms on some crop species. In Potassium solubilizing microorganisms for sustainable agriculture (pp. 31–42). New Delhi: Springer.

    Chapter  Google Scholar 

  • Zahir, Z. A., Munir, A., Asghar, H. N., Shaharoona, B., & Arshad, M. (2008). Effectiveness of rhizobacteria containing ACC deaminase for growth promotion of peas (Pisum sativum) under drought conditions. Journal of Microbiology and Biotechnology, 18, 958–963.

    CAS  Google Scholar 

  • Zahir, Z. A., Ghani, U., Naveed, M., Nadeem, S. M., & Asghar, H. N. (2009). Comparative effectiveness of Pseudomonas and Serratia sp. containing ACC-deaminase for improving growth and yield of wheat (Triticum aestivum L.) under salt-stressed conditions. Archives of Microbiology, 191, 415–424.

    Article  CAS  Google Scholar 

  • Zahir, Z. A., Shah, M. K., Naveed, M., & Akhter, M. J. (2010). Substrate-dependent auxin production by Rhizobium phaseoli improves the growth and yield of Vigna radiata L. under salt stress conditions. Journal of Microbiology and Biotechnology, 20, 1288–1294.

    Article  CAS  Google Scholar 

  • Zapata, P. J., Serrano, M., Pretel, M. T., Amoros, A., & Botella, M. A. (2004). Polyamines and ethylene changes during germination of different plant species under salinity. Plant Science, 167, 781–788.

    Article  CAS  Google Scholar 

  • Zehnder, G. W., Murphy, J. F., Sikora, E. J., & Kloepper, J. W. (2001). Application of rhizobacteria for induced resistance. European Journal of Plant Pathology, 107, 39–50.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to R. Z. Sayyed .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2019 Springer Nature Singapore Pte Ltd.

About this chapter

Check for updates. Verify currency and authenticity via CrossMark

Cite this chapter

Sayyed, R.Z., Ilyas, N., Tabassum, B., Hashem, A., Abd_Allah, E.F., Jadhav, H.P. (2019). Plausible Role of Plant Growth-Promoting Rhizobacteria in Future Climatic Scenario. In: Sobti, R., Arora, N., Kothari, R. (eds) Environmental Biotechnology: For Sustainable Future. Springer, Singapore. https://doi.org/10.1007/978-981-10-7284-0_7

Download citation

Publish with us

Policies and ethics