Physiological characterization of SUB1 trait in rice under subsequent submergence and re-aeration with interaction of chemical elicitors

Authors

  • Bipul Sarkar University of Kalyani
  • Arnab Kumar De University of Kalyani
  • M K Adak Plant Physiology and Plant Molecular Biology Research Unit, Department of Botany, University of Kalyani, Nadia, West Bengal

DOI:

https://doi.org/10.14719/pst.2017.4.4.351

Keywords:

rice, antioxidative enzymes, polyamine, salicylic acid, submergence, ROS

Abstract

In the present study, the sensitivity of two chemical elicitors: polyamine (PA) and salicylic (SA) acid were exercised for submergence sensitivity in Swarna Sub1A rice variety. Under 5 days of submergence, the antioxidation responses were more distinguished in plants against control. Along with the anti-oxidation modules, significant changes in biomolecule loss were registered through lipid and protein oxidation by 1.91 and 1.46 -fold respectively. PA and SA treated plants were the reliever to recover the membrane potential. Total carbohydrate and reducing sugars were varied under submergence by down regulation of 36.66 and 44.44% as compared to control. This was also supported by regulation of ?-amylase activity under submergence that also recovered significantly with PA and SA treatments against submergence. In association with carbohydrate metabolism, Under submergence Swarna Sub1A recorded to be prone with oxidative stress through O2.- (1.55 fold) and peroxide (1.70-fold) over-accumulation but recovered as PA and SA applied. In both cases, sustenance of non-enzymatic anti-oxidant like total carotenoid and lycopene content were also contributory through down-regulation. The enzymatic anti-oxidation paths like SOD, GPX, CAT and GR were regulated by 11.11, 19.54, 13.65, 10.03% declined respectively and thoroughly discussed with reference to PA and SA interactions.

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Author Biographies

Bipul Sarkar, University of Kalyani

University Research Scholar,

Department of Botany,

University of Kalyani,

Kalyani- 741235

Arnab Kumar De, University of Kalyani

Research Scholar,

Department of Botany,

University of Kalyani,

Kalyani- 741235

References

1. Jones HG. Monitoring plant and soil water status: established and novel methods revisited and their relevance to studies of drought tolerance. Journal of experimental botany. 2006 Sep 15;58(2):119-30. https://doi.org/10.1093/jxb/erl118

2. Smith RD, Pregnall AM, Alberte RS. Effects of anaerobiosis on root metabolism of Zostera marina (eelgrass): implications for survival in reducing sediments. Marine Biology. 1988 May 1;98(1):131-41. https://doi.org/10.1007/BF00392668

3. Das K, Roychoudhury A. Reactive oxygen species (ROS) and response of antioxidants as ROS-scavengers during environmental stress in plants. Frontiers in Environmental Science. 2014 Dec 2;2:53. https://doi.org/10.3389/fenvs.2014.00053

4. Chaves MM, Flexas J, Pinheiro C. Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell. Annals of botany. 2009 Feb 1;103(4):551-60. https://doi.org/10.1093/aob/mcn125

5. Garrity GM, Bell JA, Lilburn T. Family IV. Halomonadaceae Franzmann, Wehmeyer and Stackebrandt 1989, 205VP emend. Dobson and Franzmann 1996, 558. Bergey's Manual® of Systematic Bacteriology: Volume 2: The Proteobacteria, Part B: The Gammaproteobacteria. 2007 Dec 14;2:300.

6. Ellis RH, Hong TD. Temperature sensitivity of the low-moisture-content limit to negative seed longevity–moisture content relationships in hermetic storage. Annals of botany. 2006 Feb 22;97(5):785-91. https://doi.org/10.1093/aob/mcl035

7. Tirani MM, Nasibi F, Kalantari KM. Interaction of salicylic acid and ethylene and their effects on some physiological and biochemical parameters in canola plants (Brassica napus L.). Photosynthetica. 2013 Sep 1;51(3):411-8. https://doi.org/10.1007/s11099-013-0041-2

8. Ghosh N, Adak MK. Effects of Putrescine on Anti-Oxidative Enzymes in Two Rice Cultivars Subjected to Salinity. Advances in Crop Science and Technology. 2016 Feb 17,4:210. https://doi.org/10.4172/2329-8863.1000210

9. Hedge JE, Hofreiter BT. Determination of reducing sugars and carbohydrates: anthrone colorimetric method. Methods in carbohydrate chemistry. 1962;1:389-90.

10. Miller GL. Estimation of reducing sugar by dinitrosalicylic acid method. Anal Chem. 1972;31:426-8.

11. Kruger JE. Changes in the amylases of hard red spring wheat during grwoth and maturation. Cereal chemistry. 1972.

12. Zakaria M, Simpson K, Brown PR, Krstulovic A. Use of reversed-phase high-performance liquid chromatographic analysis for the determination of provitamin A carotenes in tomatoes. Journal of Chromatography A. 1979 Aug 1;176(1):109-17. https://doi.org/10.1016/S0021-9673(00)92091-0

13. Heath RL, Packer L. Photoperoxidation in isolated chloroplasts: I. Kinetics and stoichiometry of fatty acid peroxidation. Archives of biochemistry and biophysics. 1968 Apr 1;125(1):189-98. https://doi.org/10.1016/0003-9861(68)90654-1

14. Foyer CH, Noctor G. Oxidant and antioxidant signalling in plants: a re?evaluation of the concept of oxidative stress in a physiological context. Plant, Cell & Environment. 2005 Aug 1;28(8):1056-71. https://doi.org/10.1111/j.1365-3040.2005.01327.x

15. Elstner EF, Heupel A. Inhibition of nitrite formation from hydroxylammoniumchloride: a simple assay for superoxide dismutase. Analytical biochemistry. 1976 Feb 1;70(2):616-20. https://doi.org/10.1016/0003-2697(76)90488-7

16. Ghosh N, Adak MK, Ghosh PD, Gupta S, Gupta DS, Mandal C. Differential responses of two rice varieties to salt stress. Plant Biotechnology Reports. 2011 Jan 1;5(1):89-103. https://doi.org/10.1007/s11816-010-0163-y

17. Cakmak I, Marschner H. Magnesium deficiency and high light intensity enhance activities of superoxide dismutase, ascorbate peroxidase, and glutathione reductase in bean leaves. Plant physiology. 1992 Apr 1;98(4):1222-7. https://doi.org/0032-0889/92/98/1 222/06/$01.00/0

18. Verma S, Dubey RS. Lead toxicity induces lipid peroxidation and alters the activities of antioxidant enzymes in growing rice plants. Plant Science. 2003 Apr 30;164(4):645-55. https://doi.org/10.1016/S0168-9452(03)00022-0

19. Barclay AM, Crawford RM. Plant growth and survival under strict anaerobiosis. Journal of Experimental Botany. 1982 Jun 1;33(3):541-9. https://doi.org/10.1093/jxb/33.3.541

20. Sarkar RK, Reddy JN, Sharma SG, Ismail AM. Physiological basis of submergence tolerance in rice and implications for crop improvement. Current Science. 2006 Oct 10:899-906. http://www.jstor.org/stable/24094287

21. Barar J. Cellular trafficking and subcellular interactions of cationic gene delivery nanomaterials. Journal of Pharmacy and Nutrition Sciences. 2011;1(1). http://dx.doi.org/10.6000/1927-5951.2011.01.01.12

22. Kathuria H, Giri J, Tyagi H, Tyagi AK. Advances in transgenic rice biotechnology. Critical Reviews in Plant Sciences. 2007 Mar 19;26(2):65-103. http://dx.doi.org/10.1080/07352680701252809

23. Barding Jr GA, Fukao T, Béni S, Bailey-Serres J, Larive CK. Differential metabolic regulation governed by the rice SUB1A gene during submergence stress and identification of alanylglycine by 1H NMR spectroscopy. Journal of proteome research. 2011 Nov 11;11(1):320-30. https://doi.org/10.1021/pr200919b

24. Neale PJ, Cullen JJ, Lesser MP, Melis A. Physiological bases for detecting and predicting photoinhibition of aquatic photosynthesis by PAR and UV radiation. Photosynthetic responses to the environment. 1993 Jun;33:61-77.

25. Hérouart D, Baudouin E, Frendo P, Harrison J, Santos R, Jamet A, Van de Sype G, Touati D, Puppo A. Reactive oxygen species, nitric oxide and glutathione: a key role in the establishment of the legume–Rhizobium symbiosis. Plant Physiology and Biochemistry. 2002 Aug 31;40(6):619-24. https://doi.org/10.1016/S0981-9428(02)01415-8

26. Maheswari M, Yadav SK, Shanker AK, Kumar MA, Venkateswarlu B. Overview of plant stresses: Mechanisms, adaptations and research pursuit. InCrop Stress and its Management: Perspectives and Strategies 2012 (pp. 1-18). Springer Netherlands. https://doi.org/10.1007/978-94-007-2220-0_1

27. Higuchi Y. Glutathione depletion?induced chromosomal DNA fragmentation associated with apoptosis and necrosis. Journal of cellular and molecular medicine. 2004 Oct 1;8(4):455-64. https://doi.org/10.1111/j.1582-4934.2004.tb00470.x

28. Guo W, Ngo HH, Li J. A mini-review on membrane fouling. Bioresource technology. 2012 Oct 31;122:27-34. https://doi.org/10.1016/j.biortech.2012.04.089

29. Choi D. Ethylene-induced stem growth of deep water rice is correlated with expression of gibberellin-and abscisic acid-biosynthetic genes. Journal of Plant Biology. 2007 Oct 1;50(5):595-9. https://doi.org/10.1007/BF03030714

30. Jackson MB, Ram PC. Physiological and molecular basis of susceptibility and tolerance of rice plants to complete submergence. Annals of botany. 2003 Jan 2;91(2):227-41. https://doi.org/10.1093/aob/mcf242

31. Sakai N, Gerard D, Matile S. Electrostatics of cell membrane recognition: Structure and activity of neutral and cationic rigid push-pull rods in isoelectric, anionic, and polarized lipid bilayer membranes. Journal of the American Chemical Society. 2001 Mar 21;123(11):2517-24. https://doi.org/10.1021/ja003141

32. Tamanti F. Phytoremediation by poplar: polyphenols polyamines and oxidative damage in the response to heavy metals in in vitro and in hydroponic cultures (Doctoral dissertation, alma). https://doi.org/10.6092/unibo/amsdottorato/4374.

33. Gharbi E, Martínez JP, Benahmed H, Fauconnier ML, Lutts S, Quinet M. Salicylic acid differently impacts ethylene and polyamine synthesis in the glycophyte Solanum lycopersicum and the wild?related halophyte Solanum chilense exposed to mild salt stress. Physiologia plantarum. 2016 Oct 1;158(2):152-67. https://doi.org/10.1111/ppl.12458

34. Poór P, Kovács J, Szopkó D, Tari I. Ethylene signaling in salt stress-and salicylic acid-induced programmed cell death in tomato suspension cells. Protoplasma. 2013 Feb 1;250(1):273-84. https://doi.org/10.1007/s00709-012-0408-4

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Published

27-11-2017

How to Cite

1.
Sarkar B, De AK, Adak MK. Physiological characterization of SUB1 trait in rice under subsequent submergence and re-aeration with interaction of chemical elicitors. Plant Sci. Today [Internet]. 2017 Nov. 27 [cited 2024 Nov. 4];4(4):177-90. Available from: https://horizonepublishing.com/journals/index.php/PST/article/view/351

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Research Articles