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Regulation of Plant Physiology and Antioxidant Enzymes for Alleviating Salinity Stress by Potassium-Mobilizing Bacteria

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Potassium Solubilizing Microorganisms for Sustainable Agriculture

Abstract

Potassium (K) is among the most important essential macronutrients for plant growth. About 98 % of the potassium in the earth’s crust exists in insoluble forms as rocks and silicate minerals, resulting in very low concentrations of soluble potassium in the soil for plant growth and development. Rhizosphere bacteria are a group of metal-mobilizing, plant growth–promoting bacteria having the ability to solubilize potassium from insoluble potassium rocks. KSM (a potassium-solubilizing microorganism) is a metal-mobilizing, plant growth–promoting bacterium living symbiotically in/on the root surface and helps directly or indirectly in promoting plant growth via solubilization of insoluble minerals (K and P), assisting in resource acquisition (macro- and micronutrients), production of phytohormones and secretion of different regulatory chemicals in the purlieu of the rhizosphere of the plant root. KSM such as Bacillus spp. and Pseudomonas spp. are the most dominant plant growth–promoting bacteria (PGPB) of rhizospheric soils. Inoculation of KSM is found to be promising to induce growth of plants under 2.3–3.5 dSm−1 salinity levels and low availability of P and K, protecting the plants from salinity injury by enhancing their growth-related physiology and lipid peroxidation. These KSM help in the decrement of lipid peroxidation and enhance the stability of the plant cell membrane for the survival of the plant under salt stress. Inoculation of plants with such beneficial root-associated bacteria could provide salt tolerance to plants as these isolates also reside within the root, which is the plant part first directly in contact with saline soil. Hence it serves as a useful tool for alleviating salinity stress as well as in uptake of important mineral nutrients. The diversity of potassium-solubilizing microbes (KSM) and ability to mobilize important macronutrients from insoluble to soluble forms through biological conversion make them a good choice for agricultural use. Application of such efficient KSM aims to develop future prospects to provide a sustainable environmental system in different crop fields under both normal and stress conditions.

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References

  • Akatsuka T, Nelson OE (1966) Starch granule-bound adenosine diphosphate glucose starch glucosyltransferases of maize seeds. J Biol Chem 241:2280–2286

    CAS  PubMed  Google Scholar 

  • Aseri GK, Jain N, Panwar J, Rao AV, Meghwal PR (2008) Biofertilizers improve plant growth, fruit yield, nutrition, metabolism and rhizosphere enzyme activities of pomegranate (Punica granatum L.) in Indian Thar desert. Sci Horticult 117:130–135

    Article  Google Scholar 

  • Ashraf M, Foolad MR (2007) Role of glycine betaine and proline in improving plant abiotic stress resistance. Environ Exp Bot 59:206–216

    Article  CAS  Google Scholar 

  • Bais HP, Weir TL, Perry LG, Gilroy S, Vivanco JM (2006) The role of root exudates in rhizosphere interactions with plants and other organisms. Annu Rev Plant Biol 57:233–266

    Article  CAS  PubMed  Google Scholar 

  • Barea JM, Azcon-Aguilar C, Azcon R (1997) Interactions between mycorrhizal fungi and rhizosphere microorganisms within the context of sustainable soil–plant systems. In: Gange AC, Brown VK (eds) Multitrophic interactions in terrestrial systems. Blackwell Science, Cambridge, pp 65–77

    Google Scholar 

  • Bashan Y, Holguin G, de-Bashan LE (2004) Azospirillum-plant relationships: physiological, molecular, agricultural, and environmental advances (1997–2003). Can J Microbiol 50:521–577

    Article  CAS  PubMed  Google Scholar 

  • Bhattacharyya PN, Jha D (2012) Plant growth–promoting rhizobacteria (PGPR): emergence in agriculture. World J Microbiol Biotechnol 28:1327–1350

    Article  CAS  PubMed  Google Scholar 

  • Casano LM, Gomez LD, Lascano HR, Gonzalez C, Trippi VS (1997) Inactivation and degradation of CuZn – SOD by active oxygen species in wheat chloroplasts exposed to photo-oxidative stress. Plant Cell Physiol 38:433–440

    Article  CAS  PubMed  Google Scholar 

  • Chakraborty U, Swarnendu R, Chakraborty AP, Dey P, Chakraborty B (2011) Plant growth promotion and amelioration of salinity stress in crop plants by a salt-tolerant bacterium. Recent Res Sci Technol 3(11):61–70

    CAS  Google Scholar 

  • Cheesman JM (1988) Mechanisms of salinity tolerance in plant. Plant Physiol 87:547–550

    Google Scholar 

  • Edreva A (2005) Generation and scavenging of reactive oxygen species in chloroplasts: a submolecular approach. Agric Ecosyst Environ 106:119–133

    Article  CAS  Google Scholar 

  • El Kramany MF, Bahr AA, Mohamed MF, Kabesh MO (2007) Utilization of bio-fertilisers in field crops production 16-groundnut yield, its components and seeds content as affected by partial replacement of chemical fertilizers by bio-organic fertilizers. J Appl Sci Res 3(1):25–29

    Google Scholar 

  • Fallik E, Sarig S, Okon Y (1994) Morphology and physiology of plant roots associated with Azospirillum. In: Okon Y (ed) Azospirillum/plant associations. CRC Press, Florida, pp 77–85

    Google Scholar 

  • Hossein H, Daliri MS, Mobaser HR, Moosavi AA (2011) Effect of different nitrogen and potassium fertilizer levels on quality and quantity yield of flue-cured tobacco (Coker 347). World Appl Sci J 15(7):941–946

    Google Scholar 

  • Han HS, Lee KD (2005) Physiological responses of soybean – inoculation of Bradyrhizobiumjaponicum with PGPB in saline soil conditions. Res J Agric Biol Sci 1(3):216–221

    Google Scholar 

  • Han HS, Supanjani E, Lee KD (2006) Effect of co-inoculation with phosphate and potassium solubilizing bacteria on mineral uptake and growth of pepper and cucumber. Plant Soil Environ 52(3):130–136

    CAS  Google Scholar 

  • Hettema EH, Ruigrok CC, Koerkamp MG, van den Berg M, Tabak HF, Distel B, Braakman I (1998) The cytosolic DnaJ-like protein djp1p is involved specifically in peroxisomal protein import. J Cell Biol 142(2):421–434

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Hinsinger P, Bengough AG, Vetterlein D, Young IM (2009) Rhizosphere: biophysics, biogeochemistry and ecological relevance. Plant Soil. doi:10.1007/S11104-008-9885-9

    Google Scholar 

  • Jha Y, Subramanian RB (2011) Endophytic Pseudomonas pseudoalcaligenes shows better response against the Magnaporthegrisea than a rhizospheric Bacillus pumilus in Oryzasativa (Rice). Arch Phytopathol Plant Protect 44(6):592–604

    Article  Google Scholar 

  • Jha Y, Subramanian RB (2013a) Rhizobacteria regulates physiology and enzyme levels in paddy under salinity. J Appl Bot Food Qual 85:168–173

    Google Scholar 

  • Jha Y, Subramanian RB (2013b) Root associated bacteria from the rice antagonizes the growth of Magnaporthe grisea. J Plant Pathol Microb 4:164. doi:10.4172/2157-7471.1000164

    Google Scholar 

  • Jha Y, Subramanian RB (2013c) Paddy inoculated with PGPR show better growth physiology and nutrient content under salinity. Chil J Agric Res 73(1):213–219

    Article  Google Scholar 

  • Jha Y, Subramanian RB (2014a) PGPR regulate caspase-like activity, programmed cell death, and antioxidant enzyme activity in paddy under salinity. Physiol Mol Biol Plants 20(2):201–207

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Jha Y, Subramanian RB (2014b) Characterization of root-associated bacteria from paddy and its growth-promotion efficacy.3. Biotech 4(3):325–330

    Google Scholar 

  • Jha Y, Subramanian RB (2015) Reduced apoptosis like cell death and improved cell membrane integrity in paddy under salinity by root associate bacteria. Theor Exp Plant Physiol 27:227–235

    Article  Google Scholar 

  • Jha Y, Subramanian RB, Patel S (2011) Combination of endophytic and rhizospheric plant growth promoting rhizobacteria in Oryzasativa shows higher accumulation of osmoprotectant against saline stress. Acta Physiol Plant 33:797–802

    Article  Google Scholar 

  • Jha Y, Sablok G, Naidu Subbarao N, Sudhakar R, TurabeFazil MHU, Subramanian RB, Squartini, Kumar S (2014a) Bacterial-induced expression of RAB18 protein in Orzyasativa salinity stress and insights into molecular interaction with GTP ligand. J Mol Recognit 27:521–527

    Article  CAS  PubMed  Google Scholar 

  • Jha Y, Subramanian RB, Jethwa R, Patel N (2014b) Isolation and identification of PGPR from rhizobacteria from Suaedanudiflora plant and its effect on maize (pioneer 30 v92). Indian J Plant Prot 42(4):422–429

    Google Scholar 

  • Kaymak HC, Yarali F, Guvenc I, Donmez MF (2008) The effect of inoculation cuttings with plant growth Rhizobacteria (PGPR) on root formation of mint (MenthapiperitaL). Afr J Biotechnol 7:4479–4483

    CAS  Google Scholar 

  • Keren R (2000) Salinity. In: Sumner ME (ed) Handbook of soil science. CRC Press, Boca Raton, pp G3–G25

    Google Scholar 

  • Khan MS, Zaidi A, Wani PA (2006) Role of phosphatesolubilizing microorganisms in sustainable agriculture – a review. Agron Sustain Dev 27:29–43

    Article  Google Scholar 

  • Kumar SG, Reddy AM, Sudhakar C (2003) Nacl effects on proline metabolism in two high yielding genotypes of mulberry (Morusalba L.) with contrasting salt tolerance. Plant Sci 165:1245–1251

    Article  CAS  Google Scholar 

  • Kumar A, Bahadur I, Maurya BR, Raghuwanshi R, Meena VS, Singh DK, Dixit J (2015a) Dose a plant growth promoting rhizobacteria enhance agricultural sustainability. J Pure Appl Microbiol 9(1):715–724

    Google Scholar 

  • Kumar A, Maurya BR, Raghuwanshi R (2015b) Characterization of bacterial strains and their impact on plant growth promotion and yield of wheat and microbial populations of soil. Afr J Agric Res 10(12):1367–1375. doi:10.5897/AJAR2014.8894

    Google Scholar 

  • Lack AJ, Evans DE (2005) Instant notes in plant biology, 1st edn, vol 7. Bios Scientific Publishers, Oxford, pp 68–71

    Google Scholar 

  • Laemmli UK (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227(259):680–685

    Article  CAS  PubMed  Google Scholar 

  • Landon JR (1991) Booker tropical soil manual. A handbook for soil survey and agricultural land evaluation in the tropics and subtropics. Booker Tate Essex: Longman Scientific & Technical Publishers, Harlow

    Google Scholar 

  • Lee GJ, Vierling E (2000) A small heat shock protein cooperates with heat shock protein 70 systems to reactivate a heat- denatured protein. Plant Physiol 1:189–198

    Article  Google Scholar 

  • Lian B, Fu P, Mo DM, Liu CQ (2002) A comprehensive review of the mechanism of potassium release by silicate bacteria. Acta Mineral Sin 22:179–183

    CAS  Google Scholar 

  • Maliha R, Samina K, Najma A, Sadia A, Farooq L (2004) Organic acids production and phosphate solubilization by phosphate solubilizing microorganisms under in vitro conditions. Pak J Biol Sci 7:187–196

    Article  Google Scholar 

  • Mandhania S, Madan S, Sawhney V (2006) Antioxidant defense mechanism under salt stress in wheat seedling. Biol Plant 50:227–231

    Article  CAS  Google Scholar 

  • Maurya BR, Meena VS, Meena OP (2014) Influence of Inceptisol and Alfisol’s potassium solubilizing bacteria (KSB) isolates on release of K from waste mica. Vegetos 27(1):181–187

    Google Scholar 

  • McCue KF, Hanson AD (1990) Drought and salt tolerance: towards understanding and application. Trends Biotechnol 8:358–362

    Article  CAS  Google Scholar 

  • Meena OP, Maurya BR, Meena VS (2013) Influence of K-solubilizing bacteria isolates on release of K from waste mica. Agric Sustain Dev 1(1):53–56

    Google Scholar 

  • Meena VS, Maurya BR, Bahadur I (2014a) Potassium solubilisation by bacteria strain in waste mica. Bangladesh J Bot 43(2):235–237

    Google Scholar 

  • Meena VS, Maurya BR, Verma JP (2014b) Does a rhizospheric microorganism enhance K+ availability in agricultural soil? Microbiol Res 169:337–347

    Article  CAS  PubMed  Google Scholar 

  • Meena RK, Singh RK, Singh NP, Meena SK, Meena VS (2015a) Isolation of low temperature surviving plant growth promoting bacteria (PGPR) from pea (PisumSativum L) and demonstration of their plant growth promoting trait. Biocatal Agric Biotechnol. doi:10.1016/j.bcab.2015.08.006

    Google Scholar 

  • Meena VS, Maurya BR, Verma JP, Arora A, Kumar A, Kim K, Bajpai VK (2015b) Potassium solubilizing rhizobactera (KSR): isolation, identification and K-release dynamics from waste mica. Ecol Eng 81:340–347

    Article  Google Scholar 

  • Pessarakli M, Szabolcs I (1999) Soil salinity and sodicity as particular plant/crop stress factors. In: Pessarakli M (ed) Handbook of plant and crop stress, 2nd edn. Marcel Dekker, New York, pp 1–15

    Chapter  Google Scholar 

  • Pradhan N, Sukla LB (2005) Solubilization of inorganic phosphate by fungi isolated from agriculture soil. Afr J Biotechnol 5:850–854

    Google Scholar 

  • Rajan SSS, Watkinson JH, Sinclair AG (1996) Phosphate rock of for direct application to soils. Adv Agron 57:77–159

    Article  CAS  Google Scholar 

  • Rao MKV, Sresty TVS (2000) Antioxidative parameters in the seedlings of pigeonpea (Cajanuscajan L. Millspaugh) in response to Zn and Ni stresses. Plant Sci 157:113–128

    Article  Google Scholar 

  • Raven JA, Edwards D (2001) Roots: evolutionary origins and biogeochemical significance. J Exp Bot 52:381–401

    Article  CAS  PubMed  Google Scholar 

  • Rhodes D, Hanson AD (1993) Quaternary ammonium and tertiary sulfonium compounds in higher-plants. Annu Rev Plant Phys 44:357–384

    Article  CAS  Google Scholar 

  • Selvakumar G, Joshi P, Nazim S, Mishra PK, Bisht JK, Gupta HS (2009) Phosphate solubilization and growth promotion by Pseudomonas fragi CS11RH1 (MTCC 8984) a psychrotolerant bacterium isolated from a high altitude Himalayan rhizosphere. Biologia 64:239–245

    Article  CAS  Google Scholar 

  • Shannon MC (1984) Breeding, selection, and the genetics of salt tolerance. In: Wiley J (ed) Salinity tolerance in plants strategies for crop improvement. Wiley, New York, pp 231–254

    Google Scholar 

  • Sheng XF, Huang WY (2002) Mechanism of potassium release from feldspar affected by the strain NBT of silicate bacterium. Acta Pedol Sin 39:863–871

    CAS  Google Scholar 

  • Simonsson M, Andersson S, Andrist-angel Y, Hillier S, Mattsson l, Oborn I (2007) Potassium release and fixation as a function of fertilizer application rate and soil parent material. Geoderma 140:188–198

    Article  CAS  Google Scholar 

  • Singh NP, Singh RK, Meena VS, Meena RK (2015) Can we use maize (Zea mays) rhizobacteria as plant growth promoter? Vegetos 28(1):86–99

    Google Scholar 

  • Skovsen E, Snyder JW, Lambert JD, Ogilby PR (2005) Lifetime and diffusion of singlet oxygen in a cell. J Phys Chem B 109:8570–8573

    Article  CAS  PubMed  Google Scholar 

  • Sudhakar C, Lakshmi A, Giridarakumar S (2001) Changes in the antioxidant enzyme efficacy in two high yielding genotypes of mulberry (Morusalba L.) under NaCl salinity. Plant Sci 161:613–619

    Article  CAS  Google Scholar 

  • Sugumaran P, Janartham B (2007) Solubilization of potassium containing minerals by bacteria and their effect on plant growth. World J Agric Sci 3(3):350–355

    Google Scholar 

  • Supanjani Han HS, Jung SJ, Lee KD (2006) Rock phosphate potassium and rock solubilizing bacteria as alternative sustainable fertilizers. Agron Sustain Dev 26:233–240

    Article  Google Scholar 

  • Syers JK (1998) Soil and plant potassium in agriculture. Proceedings no. 411, The International Fertiliser Society York, UK: 32 pp

    Google Scholar 

  • Tao GC, Tian SJ, Cai MY, Xie GH (2008) Phosphate solubilizing and -mineralizing abilities of bacteria isolated from. Pedosphere 18:515–523

    Article  CAS  Google Scholar 

  • Vranova E, Inze D, Van Breusegem F (2002) Signal transduction during oxidative stress. J Exp Bot 53:1227–1236

    Article  CAS  PubMed  Google Scholar 

  • Welcher FJ (1958) The analytical uses of ethylene diamine tetraacetic acid (EDTA). D. Van Nostrandcompany, Princeton

    Google Scholar 

  • Whitelaw MA, Harden TJ, Helyar KR (1999) Phosphate solubilisation in solution culture by the soil fungus Penicilliumradicum. Soil Biol Biochem 31:655–665

    Article  CAS  Google Scholar 

  • Yancy PH, Clark ME, Hand SC, Bowlus RD, Somero GN (1982) Living with water stress, evolution of osmolytes systems. Science 217:1214–1223

    Article  Google Scholar 

  • Zaidi A, Khan MS, Ahemad M, Oves M (2009) Plant growth promotion by phosphate solubilizing bacteria. Acta Microbiol Immunol Hung 56:263–284

    Article  CAS  PubMed  Google Scholar 

  • Zapata F, Roy RN (2004) Use of phosphate rock for sustainable agriculture. FAO and IAEA, Rome

    Google Scholar 

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Jha, Y., Subramanian, R.B. (2016). Regulation of Plant Physiology and Antioxidant Enzymes for Alleviating Salinity Stress by Potassium-Mobilizing Bacteria. In: Meena, V., Maurya, B., Verma, J., Meena, R. (eds) Potassium Solubilizing Microorganisms for Sustainable Agriculture. Springer, New Delhi. https://doi.org/10.1007/978-81-322-2776-2_11

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