Skip to main content
Log in

PGPR regulate caspase-like activity, programmed cell death, and antioxidant enzyme activity in paddy under salinity

  • Research Article
  • Published:
Physiology and Molecular Biology of Plants Aims and scope Submit manuscript

Abstract

The response of two root associated bacteria Pseudomonas pseudoalcaligenes and Bacillus pumilus were studied in the (salt-sensitive) rice GJ17 cultivar to salinity under controlled environmental growth conditions for protection of plant from adverse effect of salinity. Salinity affects the growth of salt-sensitive cultivar, but inoculation of plant growth promoting rhizobacteria (PGPR) reduces the harmful effect of salinity. The present study states that PGPR helps to reduce lipid peroxidation and superoxide dismutase activity in salt-sensitive GJ17 cultivar under salinity and play an important role in the growth regulation for positive adaptation of plants to salt stress. This study shows that inoculation of paddy (Oryza sativa) with such bacteria could provide salt-tolerant ability by reducing the toxicity of reactive oxygen species by reducing plant cell membrane index, cell caspase-like protease activity, and programmed cell death and hence resulted in increase cell viability. As these isolates remain associated with the roots, the effects of tolerance against salinity are observed here. Results also indicate that isolated PGPR strain help in alleviating up to 1.5 % salinity stress as well as improve tolerance.

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

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  • Andronis EA, Roubelakis-Angelakis KA (2010) Short-term salinity stress in tobacco plants leads to the onset of animal-like PCD hallmarks in planta in contrast to long-term stress. Planta 231:437–448

    Article  CAS  PubMed  Google Scholar 

  • Arshad M, Sharoona B, Mahmood T (2008) Inoculation with Pseudomonas spp. containing ACC-deaminase partially eliminates the effects of drought stress on growth yield and ripening of pea (Pisum sativum L). Pedosphere 18(5):611–620

    Article  Google Scholar 

  • Bashan Y, Holguin G (2002) Plant growth-promoting bacteria: a potential tool for arid mangrove reforestation. Trees 16:159–166

    Article  CAS  Google Scholar 

  • Basu S, Roychoudhury A, Saha PP, Sengupta DN (2010) Comparative analysis of some biochemical responses of three indica rice varieties during polyethylene glycol-mediated water stress exhibits distinct varietal differences. Acta Physiol Plant 32:551–563

    Article  CAS  Google Scholar 

  • Bertrand H, Nalin R, Bally R, Cleyet-Marcel JC (2001) Isolation and identification of the most efficient growth-promoting bacteria associated with canola (Brassica napus). Biol Fertil Soils 33:152–156

    Article  Google Scholar 

  • Buchanan BB, Gruissem W, Jones RL (2000) Biochemistry and Molecular Biology of Plants. American Society of Plant Physiologists, Rockville, Maryland, 1367 pp

    Google Scholar 

  • Costa MA, Pinheiro HA, Shimizu ESC, Fonseca FT, Santos Filho BGS, Moraes FKC, Figueiredo DM (2010) Lipid peroxidation chloroplastic pigments and antioxidant strategies in Carapa guianensis (Aubl) subjected to water-deficit and short-term rewetting. Trees 24:275–283

    Article  CAS  Google Scholar 

  • De Pinto MC, Locato V, De Gara L (2012) Redox regulation in plant programmed cell death. Plant Cell Environ 35:234–244

    Article  PubMed  Google Scholar 

  • Del Amor FM, Cuadra-Crespo P (2012) Plant growth-promoting bacteria as a tool to improve salinity tolerance in sweet pepper. Funct Plant Biol 39:82–90

    Article  Google Scholar 

  • Dionisiosese ML, Tobita S (1998) Antioxidant response of rice seedlings to salinity stress. Plant Sci 135:1–9

    Article  CAS  Google Scholar 

  • Dureja V (2003) Effect of salinity stress on antioxidant enzymes in salt-tolerant and salt-sensitive cultivar of rice (Oryza sativa L.) MSc Thesis. CCS Haryana Agricultural University, Hisar, India

  • Fortes AM, Costa J, Santos F, Seguí-simarro JM, Palme K, Altabell T, Tiburcio AF, Pais S (2011) Arginine decarboxylase expression polyamines biosynthesis and reactive oxygen species during organogenic nodule formation in hop. Plant Signal Behav 6:258–269

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Foyer CH, Noctor G (2005) Redox homeostasis and antioxidant signaling a metabolic interface between stress perception and physiological responses. Plant Cell 17:1866–1875

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Gill SS, Tuteja N (2010) Reactive oxygen species and antioxidant machinery in a biotic stress tolerance in crop plants. Annu Rev Plant Physiol Biochem 3:1–22

    Google Scholar 

  • Groten K, Dutilleul C, Van Heerden PDR, Vanackera H, Bernard S, Finkemeier I, Dietz KJ, Foyer CH (2006) Redox regulation of peroxiredoxin and proteinases by ascorbate and thiols during pea root nodule senescence. FEBS Lett 580:1269–1276

    Article  CAS  PubMed  Google Scholar 

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

    Google Scholar 

  • Jha Y, Subramanian RB (2012) Paddy physiology and enzymes level is regulated by rhizobacteria under saline stress. J Appl Bot Food Qual 85:168–173

    Google Scholar 

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

    Google Scholar 

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

    Article  Google Scholar 

  • Kavi Kishor PB, Sangam S, Amrutha RN, Sri Laxmi P, Naidu KR, Rao KRSS, Reddy KJ, Theriappan P, Sreenivaslu N (2005) Regulation of proline biosynthesis degradation uptake and transport in higher plants its implications in plant growth and abiotic stress tolerance. Curr Sci 88:424–438

    Google Scholar 

  • Keyster M, Klein A, Ludidi N (2012) Caspase-like enzymatic activity and the ascorbate-glutathione cycle participate in salt stress tolerance of maize conferred by exogenously applied nitric oxide. Plant Signal Behav 7(3):1–12

    Article  Google Scholar 

  • Kohler J, Caravaca F, Alguacil MM, Roldán A (2009) Elevated CO2 increases the effect of an arbuscular mycorrhizal fungus and a plant-growth-promoting rhizobacterium on structural stability of a semiarid agricultural soil under drought conditions. Soil Biol Biochem 41:1710–1716

    Article  CAS  Google Scholar 

  • Li JY, Jiang AL, Zhang W (2007) Salt stress-induced programmed cell death in rice root tip cells. J Integr Plant Biol 49:481–486

    Article  CAS  Google Scholar 

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

    Article  CAS  PubMed  Google Scholar 

  • Mahajan S, Tuteja N (2005) Cold salinity and drought stresses an overview. Arch Biochem Biophys 444:139–158

    Article  CAS  PubMed  Google Scholar 

  • María Rodríguez-Serrano, Ivett Bárány, Deepak Prem, María-José, Coronado María C, Risueño, Pilar S, Testillano (2011) NO ROS and cell death associated with caspase-like activity increase in stress-induced microspore embryogenesis of barley. J Exp Bot. doi: 10.1093/jxb/err400

  • Miller G, Suzuki N, Ciftci-Yilmazi N, Mittler R (2010) Reactive oxygen species homeostasis and signaling during drought and salinity stresses. Plant Cell Environ 33:453–467

    Article  CAS  PubMed  Google Scholar 

  • Mittler R (2002) Oxidative stress antioxidants and stress tolerance. Trends Plant Sci 7:405–410

    Article  CAS  PubMed  Google Scholar 

  • Mittler R, Vanderauwera S, Suzuki N, Miller G, Tognetti VB, Vandepoele K, Gollery M, Shulaev V, Breusegem FV (2011) ROS signalling the new wave. Trends Plant Sci 16:300–309

    Article  CAS  PubMed  Google Scholar 

  • Nakano Y, Asada K (1981) Hydrogen peroxide is scavenged by ascorbate specific peroxidase in spinach chloroplasts. Plant Cell Physiol 22:867–880

    CAS  Google Scholar 

  • Oztürk L, Demir Y (2002) In vivo and in vitro protective role of proline. Plant Growth Regul 38:259–264

    Article  Google Scholar 

  • Parida AK, Das AB (2005) Salt tolerance and salinity effects on plants—a review. Ecotoxicol Environ Saf 60:324–349

    Article  CAS  PubMed  Google Scholar 

  • Rojas-Tapias D, Moreno-Galván A, Pardo-Díaz S, Obando M, Rivera D, Bonilla R (2012) Effect of inoculation with plant growth-promoting bacteria (PGPB) on amelioration of saline stress in maize (Zea mays). Appl Soil Ecol 61:264–272

    Article  Google Scholar 

  • Sairam RK, Srivastava GC (2001) Water stress tolerance of wheat (Triticum aestivum L) variations in hydrogen peroxide accumulation and antioxidant activity in tolerant and susceptible genotypes. J Agron Crop Sci 186:63–70

    Article  CAS  Google Scholar 

  • Sairam RK, Deshmukh PS, Shukla DS (1997) Increased antioxidant enzyme activity in response to drought and temperature stress related with stress tolerance in wheat genotypes. Abstract National Seminar (ISSP) IARI New Delhi pp 69

  • Sanevas N, Sunohara Y, Matsumoto H (2007) Characterization of reactive oxygen species-involved oxidative damage in Hapalosiphon species crude extract-treated wheat and onion roots. Weed Biol Mana 7:172–177

    Article  CAS  Google Scholar 

  • Shao HB, Liang ZS, Shao MA, Wang BC (2005) Impacts of PEG-6000 pretreatment for barley (Hordeum vulgare L) seeds on the effect of their mature embryo in vitro culture and primary investigation on its physiological mechanism. Colloids Surf B Biointerfaces 41(2–3):73–77

    CAS  Google Scholar 

  • Thapa G, Dey M, Sahoo L, Panda SK (2011) An insight into the osmotic stress induced alterations in plants. Biol Plant 55:603–613

    Article  CAS  Google Scholar 

  • Vessey JK (2003) Plant growth promoting rhizobacteria as biofertilizers. Plant Soil 255:571–586

    Article  CAS  Google Scholar 

  • Wang J, Li X, Liu Y, Zhao X (2010) Salt stress induces programmed cell death in Thellungiella halophila suspension-cultured cells. J Plant Physiol 167:1145–1151

    Article  CAS  PubMed  Google Scholar 

  • Zhu J, Fu X, Koo YD, Zhu JK (2007) An enhancer mutant of Arabidopsis salt overly sensitive 3 mediates both ion homeostasis and the oxidative stress response. Mol Cell Biol 27:5214–5224

    Article  CAS  PubMed Central  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Yachana Jha.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Jha, Y., Subramanian, R.B. PGPR regulate caspase-like activity, programmed cell death, and antioxidant enzyme activity in paddy under salinity. Physiol Mol Biol Plants 20, 201–207 (2014). https://doi.org/10.1007/s12298-014-0224-8

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12298-014-0224-8

Keywords

Navigation