Skip to main content
Log in

Redox metabolic and molecular parameters for screening drought tolerant indigenous aromatic rice cultivars

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

Abstract

The present work makes an effort to assess and standardize some redox metabolic and molecular parameters for screening drought tolerant indigenous aromatic rice cultivars of West Bengal, India. PEG-induced dehydration stress during early germination caused disruption of redox-homeostasis and oxidative damage in four IARVs (Jamainadu, Tulaipanji, Sitabhog and Badshabhog) by enhancing the accumulation of pro-oxidants [assessed in terms of oxidation of 2′,7′-dichlorofluorescindiacetate (DCFDA), accumulation of \({\text{O}}_{2}^{ \cdot - }\) and H2O2 and in situ staining of reactive oxygen species (ROS) in germinating tissue], significant reduction of antioxidative defence (total antioxidant and radical scavenging capacity, total thiol content and activities of antioxidative defence enzymes) and aggravating protein oxidation and lipid peroxidation (assessed in terms of free carbonyl content and accumulation of thiobarbituric acid reactive substances). When compared between the indigenous aromatic rice cultivars, a clear trend in differential redox regulatory properties in which ROS-antioxidant interaction acts at metabolic interface for redox homeostasis was observed in the order Badshabhog > Tulaipanji > Sitabhog > Jamainadu. Moreover, when the efficacy of ascorbate–glutathione cycle for scavenging H2O2 generated during dehydration stress was assessed and compared between the landraces exposed to PEG-induced dehydration stress in germinating tissue, it also exhibited almost the same trend with the landrace Tulaipanji and Badsabhog exhibiting maximum and Jamainadu the minimum efficiencies of the redox cycle. The indigenous aromatic rice cultivars Tulaipanji and Badsabhog resist dehydration stress better than the other two landraces due to its early preparedness to combat oxidative stress by up-regulating expression of genes of some enzymes of ascorbate–glutathione cycle along with some other antioxidative enzymes. A model of redox homeostasis in which ROS-antioxidant (ascorbate–glutathione system) acts at metabolic interface for up-regulation of antioxidative gene expression necessary for differential drought stress tolerance among the indigenous aromatic rice varieties is suggested.

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

Similar content being viewed by others

References

  • Abbas S, Ahmed S, Sabir S, Shah A (2014) Detection of drought tolerant sugarcane genotypes (Saccharum officinarum) using lipid peroxidation, antioxidant activity, glycine betaine and proline contents. J Soil Sci Plant Nutr 14(1):233–243

    Google Scholar 

  • Anjum NA, Umar S, Iqbal M, Khan NA (2011) Cadmium causes oxidative stress in mung bean by affecting the antioxidant enzyme system and ascorbate–glutathione cycle metabolism. Russ J Plant Physiol 58:92–99

    Article  CAS  Google Scholar 

  • Basu S, Roychoudhury A, Saha PP, Sengupta DN (2010a) 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(3):551–563

    Article  CAS  Google Scholar 

  • Basu S, Roychoudhury A, Saha PP, Sengupta DN (2010b) Differential antioxidative responses of indica rice cultivars to drought stress. Plant Growth Regul 60:51–59

    Article  CAS  Google Scholar 

  • Benzie IFE, Strain JJ (1996) The ferric reducing ability of plasma (FRAP) as measure of antioxidant power: the FRAP assay. Anal Biochem 239:70–76

    Article  CAS  PubMed  Google Scholar 

  • Bhattacharjee S (2008) Calcium-dependent signaling pathway in heat-induced oxidative injury in Amaranthus lividus. Biol Plant 52:1137–1140

    Article  Google Scholar 

  • Burch-Smith TM, Schiff M, Liu Y, Dinesh-Kumar SP (2006) Efficient virus induced gene silencing in Arabidopsis. Plant Physiol 42:21–27

    Article  Google Scholar 

  • Cao BL, Ma Q, Zhao Q, Wang L, Xu K (2015) Effects of silicon on absorbed light allocation, antioxidant enzymes and ultrastructure of chloroplasts in tomato leaves under simulated drought stress. Sci Hortic 194:53–62

    Article  CAS  Google Scholar 

  • Chaitanya KSK, Naithani SC (1994) Role of superoxide, lipid peroxidation and superoxide dismutase in membrane perturbation during loss of viability of Shorea robusta Gaertn F. New Phytol 126:623–627

    Article  CAS  Google Scholar 

  • Chakraborty A, Bhattacharjee S (2015) Differential competence of redox-regulatory mechanism under extremes of temperature determines growth performances and cross tolerance in two indica rice cultivars. J Plant Physiol 176:65–77

    Article  CAS  PubMed  Google Scholar 

  • Couper A, Eley D (1984) Surface tension of polyethylene glycolsolutions. J Polym Sci 3:345–349

    Article  Google Scholar 

  • Cruz de Carvalho MH (2008) Drought stress and reactive oxygen species: production, scavenging and signaling. Plant Signal Behav 3(3):156–165

    Article  PubMed  PubMed Central  Google Scholar 

  • Deb D, Bhattacharya D (2005) Seeds of traditional, seeds of future: folk rice varieties of Eastern India. Research Foundation for Science, Technology, and Ecology (RFSTE)/(vrihi), New Delhi

    Google Scholar 

  • Devi S, Angrish R, Datta KS, Kumar B (2008) Antioxidant defense system in wheat seedlings under sodium chloride stress: an inductive role of sodium chloride stress. Ind J Plant Physiol 13(2):118–124

    CAS  Google Scholar 

  • Devi R, Kaur N, Gupta AK (2012) Potential antioxidant enzymes in depicting drought tolerance of wheat (Triticum aestivum L.). Indian J Biochem Biophys 49(4):257–265

    CAS  PubMed  Google Scholar 

  • Faize M, Burgos L, Faize L, Piqueras A, Nicolas E, Barba-Espin G, Clemente-Moreno MJ, Alcobendas R, Artlip T, Hernandez JA (2011) Involvement of cytosolic ascorbate peroxidase and Cu/Zn superoxide dismutase for improved tolerance against drought stress. J Exp Bot 62(8):2599–2613

    Article  CAS  PubMed  Google Scholar 

  • Fick NG, Qualset CD (1975) Genetic control of plant amylase activity. Proc Natl Acad Sci USA 72:852–862

    Article  Google Scholar 

  • Foyer CH, Noctor G (2005) Oxidant and antioxidant signalling in plants: a re-evaluation of the concept of oxidative stress in a physiological context. Plant Cell Environ 28:1056–1107

    Article  CAS  Google Scholar 

  • Foyer CH, Noctor G (2013) Redox signaling in plants. Antioxid Redox Signal 18(16):2087–2096

    Article  CAS  PubMed  Google Scholar 

  • Giannopolities CN, Ries SK (1977) Superoxide dismutases: I. Occurrence in higher plants. Plant Physiol 59:309–319

    Article  Google Scholar 

  • Gong M, Li YJ, Chan SZ (1988) ABA induced thermotolerance in maize seedlings is mediated by calcium and associated antioxidant systems. J Plant Physiol 153:488–497

    Article  Google Scholar 

  • Gossett DR, Millhollon ER, Lucas MC (1994) Antioxidant response to NaCl stress in salt tolerant and salt-sensitive cultivars of cotton. Crop Sci 34:706–714

    Article  CAS  Google Scholar 

  • Hasanuzzaman M, Nahar K, Gill SS, Gill R, Fujita M (2014) Drought stress responses in plants, oxidative stress and antioxidant defense. In: Gill SS, Tuteja N (eds) Climate change and plant abiotic stress tolerance. Blackwell, Wiley, Germany, pp 209–249

    Google Scholar 

  • He L, Gao Z, Li R (2009) Pretreatment of seed with H2O2 enhances drought tolerance of wheat (Triticum aestivum L.) seedlings. Afr J Biotechnol 08(22):6151–6157

    Article  CAS  Google Scholar 

  • Heath RL, Packer L (1968) Photoperoxidation in isolated chloroplasts. I. Kinetics and stoichiometry of fatty acid peroxidation. Arch Biochem Biophys 125:189–198

    Article  CAS  PubMed  Google Scholar 

  • Hossain MA, Ismail MR, Uddin MdK, Islam MZ and Ashrafuzzaman M (2013) Efficacy of ascorbate–glutathione cycle for scavenging H2O2 in two contrasting rice genotypes during salinity stress. Aust J Crop Sci 7(12):1801–1808

    CAS  Google Scholar 

  • Jiang M, Zhang J (2001) Effect of abscisic acid on active oxygen species, antioxidative defense system and oxidative damage in leaves of maize seedlings. Plant Cell Physiol 42:1265–1273

    Article  CAS  PubMed  Google Scholar 

  • Khush GS (2005) What it will take to feed 5.0 billion rice consumers in 2030? Plant Mol Biol 59(1):1–6

    Article  CAS  PubMed  Google Scholar 

  • Larkindale J, Huang B (2004) Thermotolerance and antioxidant system in Agrostisstolonifera: involvement of SA, ABA, Ca, H2O2 and ethylene. J Plant Physiol 161:405–413

    Article  CAS  PubMed  Google Scholar 

  • Law MY, Charles SA, Halliwell B (1983) Glutathione and ascorbic acid in spinach (Spinacia oleracea) Chloroplasts. Biochem J 210(3):899–903

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Li X, Liu F (2016) Drought stress memory and drought stress tolerance in plants: biochemical and molecular basis In: Hossain MA (ed) Drought stress tolerance in plants, vol 1. Springer, Switzerland

    Google Scholar 

  • Li XM, Zhang LH, Li YY (2012) Preconditioning alters antioxidative enzyme responses in rice seedlings to water stress. Proc Environ Sci 11:1346–1351

    Article  Google Scholar 

  • MacNevin WM, Uron PF (1953) Spectrum of hydrogen peroxide from organic hydroperox-ides. Anal Chem 25:1760–1761

    Article  CAS  Google Scholar 

  • Mensor LL, Menezes FS, Leitao GG, Reis AS, dos Santos TC, Coube CS Leitao SG (2001) Screening of Brazilian plant extracts for antioxidant activity by the use of DPPH free radical method. Phytother Res 15:127–130

    Article  CAS  PubMed  Google Scholar 

  • Mittler R (2002) Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci 7:405–441

    Article  CAS  PubMed  Google Scholar 

  • Moradi F, Ismail AAM (2007) Responses of photosynthesis, chlorophyll fluorescence and ROS-scavenging systems to salt stress during seedling and reproductive stages in rice. Ann Bot 99:1161–1173

    Article  CAS  PubMed  PubMed Central  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 

  • Noctor G, Foyer CH (1998) Ascorbate and glutathione: keeping active oxygen under control. Annu Rev Plant Physiol Plant Mol Biol 49:249–729

    Article  CAS  PubMed  Google Scholar 

  • Noctor G, Arisi ACM, Jouanin L, Kunert KJ, Rennenberg H, Foyer CH (1998) Glutathione: biosynthesis, metabolism and relationship to stress tolerance explored in transformed plants. J Exp Bot 49:623–647

    CAS  Google Scholar 

  • Palma JM, Sandalio LM, Corpas FJ, Romero-Puertas MC, Mccarthy I, Delrio LA (2002) Plant proteases, protein degradation and oxidative stress: role of peroxisomes. Plant Physiol Biochem 40:521–530

    Article  CAS  Google Scholar 

  • Pandey V, Shukla A (2015) Acclimation and tolerance strategies of rice under drought stress. Rice Sci 22(4):147–161

    Article  Google Scholar 

  • Re R, Pellegrinni N, Proteggente A, Pannala A, Yang M, Rice-Evans C (1999) Antioxidant activities applying an improved ABTS radical cation decolorization assay. Free Radic Biol Med 26:1231–1237

    Article  CAS  PubMed  Google Scholar 

  • Reddy AR, Chaitanya KV, Vivekanandan M (2004) Drought-induced responses of photosynthesis and antioxidant metabolism in higher plants. J Plant Physiol 161:1189–1202

    Article  CAS  Google Scholar 

  • RoyChoudhury A, Roy C, Sengupta DN (2007) Transgenic tobacco plants over expressing the heterologous lea gene Rab16A from rice during high salt and water deficit display enhanced tolerance to salinity stress. Plant Cell Rep 26:1839–1859

    Article  CAS  PubMed  Google Scholar 

  • Roychoudhury A, Basu S, Sarkar SN, Sengupta DN (2008) Comparative physiological and molecular responses of a common aromatic indica rice cultivar to high salinity with non-aromatic indica rice cultivars. Plant Cell Rep 27:1395–1410

    Article  CAS  PubMed  Google Scholar 

  • Rubio-Casal AE, Castillo JM, Lucue C, Fig Ureo ME (2003) Influence of salinity on germination and seed viability of two primary colonizers of Mediterranean salt plants. J Arid Environ 53:145–152

    Article  Google Scholar 

  • Schaedle M, Bassham JA (1977) Chloroplast glutathione reductase. Plant Physiol 59(5):1011–1012

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Seckin B, Aksoy M (2013) The responses of ascorbate–glutathione cycle enzymes in seedlings of Pancratium maritimum L. under Drought Treatments. J Stress Physiol Biochem 9(2):148–158

    Google Scholar 

  • Selote DS, Khanna-Chopra R (2004) Drought-induced spikelet sterility is associated with an inefficient antioxidant defence in rice panicles. Physiol Plant 121(3):462–471

    Article  CAS  Google Scholar 

  • Serraj R, McNally KL, Slamet-Loedin I, Kohli A, Haefele SM, Atlin G, Kumar A (2011) Drought resistance improvement in rice: an integrated genetic and resource management strategy. Plant Prod Sci 14(1):1–14

    Article  Google Scholar 

  • Sharma P, Dubey RS (2005) Drought induces oxidative stress and enhances the activities of antioxidant enzymes in growing rice seedlings. Plant Growth Regul 46:209–221

    Article  CAS  Google Scholar 

  • Simontacchi M, Caro A, Fraga CG, Puntarulo S (1993) Oxidative stress affects α-tocopherol content in soyabean embryonic axes upon imbibitions. Plant Physiol 103:949–953

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Sinhababu A, Kar RK (2003) Comparative responses of three fuel wood yielding plants to PEG-induced water stress at seedling stage. Acta Physiol Plant 25:403–409

    Article  Google Scholar 

  • Smirnoff N (2000) Ascorbic acid: metabolism and functions of a multi-facetted molecule. Curr Opin Plant Biol 3:229–235

    Article  CAS  PubMed  Google Scholar 

  • Snell FD, Snell CT (1971) Colorimetric methods of analysis. Van Nostard Reinford Co, New York

    Google Scholar 

  • Sreenji M, Hideg E, Bebes A, Gyorgyey J (2010) Transcriptional differences in gene families of the ascorbate–glutathione cycle in wheat during mild water deficit. Plant Cell Rep 29:37–50

    Article  Google Scholar 

  • Tietze F (1969) Enzymatic method for quantitative determination of nanogram amounts of total and oxidised glutathione: application to mammalian blood and other tissues. Anal Biochem 27:502–522

    Article  CAS  PubMed  Google Scholar 

  • Turan S, Tripathy BC (2013) Salt and genotype impact on antioxidative enzymes and lipid peroxidation in two rice cultivars during de-etiolation. Protoplasma 250(1):209–222

    Article  CAS  PubMed  Google Scholar 

  • Wahid A, Parveen M, Gelani S, Basra SMA (2007) Pretreatment of seeds with H2O2 improves salt tolerance of wheat seedlings by alleviation of oxidative damage and expression of stress proteins. J Plant Physiol 164:283–294

    Article  CAS  PubMed  Google Scholar 

  • Wang JH, Geng LH, Zhang CM (2012) Research on the weak signal detecting technique for crop water stress based on wavelet denoising. Adv Mat Res 424/425:966–970

    Google Scholar 

  • Yadav M, Pal A, Bhowmick K, Adhikary B, Bhowmick MK and Santra CK (2014) Indigenous aromatic rice: quality seed production and area expansion in West Bengal. Annu Tech Issue Seed Hope Harvest 18:72–93

    Google Scholar 

  • Yang PM, Huang QC, Qin GY, Zhao SP, Zhou JG (2014) Different drought-stress responses in photosynthesis and reactive oxygen metabolism between autotetraploid and diploid rice. Photosynthetica 52(2):193–202

    Article  CAS  Google Scholar 

  • Zagorchev L, Teofanova D, Odjakova M (2016) Ascorbate–glutathione cycle: controlling the redox environment for drought tolerance. In: Hossain M, Wani S, Bhattacharjee S, Burritt D, Tran LS (eds) Drought stress tolerance in plants, vol 1. Springer, Cham, pp 187–226

  • Zhang J, Kirkham MB (1996) Antioxidant responses to drought in sunflower and sorghum seedlings. New Phytol 132:361–373

    Article  CAS  PubMed  Google Scholar 

  • Zhang LS, Lai JH, Liang ZS, Ashraf M (2014) Interactive effects of sudden and gradual drought stress and foliar applied glycinebetaine on growth, water relations, osmolyte accumulation and antioxidant defense system in two maize cultivars differing in drought tolerance. J Agron Crop Sci 200(06):425–433

    Article  CAS  Google Scholar 

Download references

Acknowledgements

ND acknowledges The University of Burdwan, West Bengal, for State Funded Research Fellowship (136/35, 31.07.31.07.2014, Government of West Bengal, India). Assistance from Anirban Bhar, Faculty Ramakrishna Mission Vivekananda Centenary College, Kolkata, for Semi-quantitative RT-PCR is thankfully acknowledged. Instrumentation facility of CAS (UGC), Govt. of India to the Department of Botany, University of Burdwan is also gratefully acknowledged.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Soumen Bhattacharjee.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Fig. 5

Effect of different magnitude of PEG induced imbibitional dehydration stress (− 0.344, − 0.851 and − 1.619 MPa) on visualization of superoxide (A) and hydrogen peroxide (B) of four indigenous aromatic rice varieties of Oryza sativa L. (Tulaipanji, Sitabhog, Badshabhog and Jamainadu) (DOC 601 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Bhattacharjee, S., Dey, N. Redox metabolic and molecular parameters for screening drought tolerant indigenous aromatic rice cultivars. Physiol Mol Biol Plants 24, 7–23 (2018). https://doi.org/10.1007/s12298-017-0484-1

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12298-017-0484-1

Keywords

Navigation