PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2014 | 36 | 07 |

Tytuł artykułu

Effect of NaCl stress on dihaploid tobacco lines tolerant to Potato virus Y

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Salinity is an important abiotic factor that limits plant growth and development. The influence of salt stress induced by sodium chloride on plant growth, proline content, level of lipid peroxidation and activities of antioxidative enzymes was studied in F1 hybrid DH10 and four dihaploid lines (207B, 238C, 239K, 244B) of tobacco (Nicotiana tabacum L.). Dihaploids were obtained from anther-derived haploids of hybrid DH10 and were previously proved to be tolerant to Potato virus Y (PVY). In our study, plants were grown in vitro and exposed to NaCl (100 and 200 mM) for 33 days. All dihaploids and hybrid DH10 showed reduced growth after NaCl treatment. They accumulated significant amounts of sodium and proline in response to salt stress as have already been observed in tobacco and other plant species. In tobacco exposed to NaCl the lipid peroxidation level did not increase and activities of superoxide dismutase (SOD), guaiacol peroxidase (POD), ascorbate peroxidase and catalase (CAT) mostly did not change significantly. The exception was line 239K where salt induced higher activities of SOD, CAT and POD. Two (238C and 244B) out of four dihaploids appeared more susceptible to salt stress as they showed weak growth in correlation with high proline and sodium content. Therefore, it seems that salt tolerance is not associated with tolerance to PVY. Variations in malondi-aldehyde and proline content as well as in enzymes activities observed among tobacco lines imply that dihaploids have different genetic properties which might result in different sensitivity to NaCl.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

36

Numer

07

Opis fizyczny

p.1739-1747,fig.,ref.

Twórcy

autor
  • Subdepartment of Biology and Microbiology, Faculty of Food Technology Osijek, Josip Juraj Strossmayer University of Osijek, Franje Kuhaca 20, 31000 Osijek, Croatia
autor
  • Department of Biology, Faculty of Science, University of Zagreb, Rooseveltov trg 6, 10000 Zagreb, Croatia
  • Department of Biology, Faculty of Science, University of Zagreb, Rooseveltov trg 6, 10000 Zagreb, Croatia
autor
  • Department of Biology, Faculty of Science, University of Zagreb, Rooseveltov trg 6, 10000 Zagreb, Croatia
  • Department of Biology, Faculty of Science, University of Zagreb, Rooseveltov trg 6, 10000 Zagreb, Croatia

Bibliografia

  • Aebi H (1984) Catalase in vitro. Methods Enzymol 105:121–126
  • Andrianov V, Borisjuk N, Pogrebnyak N, Brinker A, Dixon J, Spitsin S, Flynn J, Matyszczuk P, Andryszak K, Laurelli M, Golovkin M, Koprowski H (2010) Tobacco as a production platform for biofuel: overexpression of Arabidopsis DGAT and LEC2 genes increases accumulation and shifts the composition of lipids in green biomass. Plant Biotech J 8:277–287
  • Ashraf M (2002) Salt tolerance of cotton: some new advances. Crit Rev Plant Sci 21:1–30
  • Azevedo-Neto AD, Ptisco JT, Eneas-Filho J, Abreu CEB, Gomez-Filho E (2006) Effect of salt stress on antioxidative enzymes and lipid peroxidation in leaves and roots of salt-tolerant and salt-sensitive maize genotypes. Environ Exp Bot 56:87–94
  • Balen B, Tkalec M, Rogić T, Šimac M, Štefanić PP, Rončević S, Krsnik-Rasol M (2013) Effects of iso-osmotic NaCl and mannitol on growth, proline content, and antioxidant defense in Mammillaria gracilis Pfeiff. in vitro-grown cultures. In Vitro Cell Dev Plant 49:21–32
  • Bameri M, Abdolshahi R, Mohammadi-Nejad G, Yousefi K, Tabatabaie SM (2012) Effect of different microelement treatment on wheat (Triticum aestivum) growth and yield. Intl Res J Appl Basic Sci 3:219–223
  • Bates LS, Waldren RP, Teare ID (1973) Rapid determination of free proline for water-stress studies. Plant Soil 39:205–207
  • Beauchamp C, Fridovich I (1971) Superoxide dismutase: improved assay and an assay applicable to PAGE. Anal Biochem 44:276–287
  • Blumwald E, Aharon GS, Apse MP (2000) Sodium transport in plant cells. Biochim Biophys Acta 1465:140–151
  • Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254
  • Bustan A, Zaccai M, Sitrity Y, Davidovici R, Pasternak D (2003) Salt-avoidance mechanisms in the halophyte Distichlis spicata as a promising source for improved salt resistance in crop plants. In: Lieth H, Mochtchenko M (eds) Cash crop halophytes. Kluwer Academic Publishers, Netherlands, pp 87–91
  • Cavalcanti FR, Oliveira JTA, Martins-Miranda AS, Viegas RA, Silveira JAG (2004) Superoxide dismutase, catalase and peroxidase activities do not confer protection against oxidative damage in salt-stressed cowpea leaves. New Phytol 163:563–571
  • Chance B, Maehly AC (1955) Assay of catalases and peroxidases. Methods Enzymol 2:764–775
  • Chen THH, Murata N (2002) Enhancement of tolerance of abiotic stress by metabolic engineering of betaines and other compatible solutes. Curr Opin Plant Biol 5:250–257
  • Chutipaijit S, Cha-Um S, Sompornpailim K (2009) Differential accumulations of proline and flavonoids in indica rice varieties against salinity. Pak J Bot 4:2497–2506
  • Claussen W (2005) Proline as a measure of stress in tomato plants. Plant Sci 168:241–248
  • Demiral T, Turkan I (2005) Comparative lipid peroxidation, antioxidant defense systems and proline content in roots of two rice cultivars differing in salt tolerance. Environ Exp Bot 53:247–257
  • El-Baky A, Hanaa H, Amal A, Hussein MM (2003) Influence of salinity on lipid peroxidation, antioxidant enzymes and electrophoretic patterns of protein and isoenzymes in leaves of some onion cultivars. Asian J Plant Sci 2:633–638
  • Esfandiari E, Fariborz Shekari F, Shekari F, Esfandiari M (2007) The effect of salt stress on antioxidant enzymes activity and lipid peroxidation on the wheat seedling. Not Bot Hort Agrobot Cluj 35:48–56
  • Fabricant DS, Farnsworth NR (2001) The value of plants used in traditional medicine for drug discovery. Environ Health Perspect 109:69–75
  • Goodin MM, Zaitlin D, Naidu RA, Lommel SA (2008) Nicotiana benthamiana: its history and future as a model for plant-pathogen interactions. Mol Plant Microbe Interact 21:1015–1026
  • Hariadi Y, Marandon K, Tian Y, Jacobsen SE, Shabala S (2010) Ionic and osmotic relations in quinoa (Chenopodium quinoa Willd.) plants grown at various salinity levels. J Exp Bot 62:185–193
  • Heath RL, Packer L (1968) Photoperoxidation in isolated chloroplasts. I. Kinetics and stoichiometry of fatty acid peroxidation. Arch Biochem Biophys 125:189–198
  • ISO 14911 International Standard Organization (1998) Water quality. Determination of dissolved Li⁺, Na⁺, NH₄⁺, K⁺, Mn²⁺, Ca²⁺, Mg²⁺, Sr²⁺ and Ba²⁺ using ion chromatography. Method for water and waste water. International Organization for Standardization, Case Postale 56, CH-1211, Geneva, Switzerland
  • Jain M, Mathur A, Koul S, Sarin NB (2001) Ameliorative effects of proline on salt stress-induced lipid peroxidation in cell lines of groundnut (Arachis hypogaea L.). Plant Cell Rep 20:463–468
  • Khan MH, Panda SK (2008) Induction of oxidative stress in roots of Oryza sativa L. in response to salt stress. Biol Plant 45:625–627
  • Lin CC, Kao KH (2001) Cell wall peroxidase activity, hydrogen peroxide level and NaCl-inhibited root growth of rice seedlings. Plant Soil 230:135–143
  • Liu CW, Lin KH, Kuo YM (2003) Application of factor analysis in the assessment of groundwater quality in a blackfoot disease area in Taiwan. Sci Total Environ 313:77–89
  • McNeil SD, Nuccio ML, Hanson AD (1999) Betaines and related osmoprotectants: targets for metabolic engineering of stress resistance. Plant Physiol 120:945–949
  • Meloni DA, Marco A, Carlos A (2003) Photosynthesis and activity of superoxide dismutase, peroxidase and glutathione reductase in cotton under salt stress. Environ Exp Bot 49:69–76
  • Mittler R (2002) Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci 7:405–410
  • Munns R (2002) Comparative physiology of salt and water stress. Plant Cell Environ 25:239–250
  • Munns R, Tester M (2008) Mechanisms of salinity tolerance. Annu Rev Plant Biol 59:651–681
  • Murashige T, Skoog F (1962) A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol Plant 15:473–497
  • Nakano Y, Asada K (1981) Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant Cell Physiol 22:867–880
  • Niknam V, Bagherzadeh M, Ebraahimzadeh H, Sokhansanj A (2004) Effect of NaCl on biomass and contents of sugar, proline and proteins in seedlings and leaf explants of Nicotiana tabacum grown in vitro. Biol Plant 48:613–615
  • Parida AK, Das AB (2005) Salt tolerance and salinity effects on plants: a review. Ecotoxicol Environ Saf 60:324–349
  • Parvanova D, Ivanov S, Konstantinova T, Karanov E, Atanassov A, Tsvetkov T, Alexieva V, Djilianov D (2004) Transgenic tobacco plants accumulating osmolytes show reduced oxidative damage under freezing stress. Plant Physiol Biochem 42:57–63
  • Pitzschke A, Forzani C, Hirt H (2006) Reactive oxygen species signalling in plants. Antioxid Redox Sign 8:1757–1764
  • Rahnama H, Ebrahimzadeh H (2006) Antioxidant isozymes activities in Potato plants (Solanum tuberosum L.) under salt stress. J Sci Islam Repub Iran 17:225–230
  • Razavizadeh R, Ehsanpour AA, Ahsan N, Komatsu S (2009) Proteome analysis of tobacco leaves under salt stress. Peptides 30:1651–1659
  • Rout GR, Senapati SK, Panda JJ (2008) Selection of salt tolerant plants of Nicotiana tabacum L. through in vitro and its biochemical characterization. Acta Biol Hung 59:77–92
  • Sairam RK, Tyagi A (2004) Physiology and molecular biology of salinity stress tolerance in plants. Curr Sci 86:407–421
  • Saitanis CJ, Karandinos MG (2002) Effects of ozone on tobacco (Nicotiana tabacum L.) varieties. J Agron Crop Sci 188:51–58
  • Savouré A, Thorin D, Davey M, Xue-Jun H, Maniro S, Van Montagu M, Inzé D, Verbruggen N (1999) NaCl and CuSO₄ treatments trigger distinct oxidative defence mechanisms in Nicotiana plumbaginifolia L. Plant Cell Environ 22:387–396
  • Scholthof K-BG, Adkins S, Czosnek H, Palukaitis P, Jacquot E, Hohn T, Hohn B, Saunders K, Candresse T, Ahlquist P, Hemenway C, Foster GD (2011) Top 10 plant viruses in molecular plant pathology. Mol Plant Pathol 12:938–954
  • Shabala S, Cuin TA (2007) Potassium transport and plant salt tolerance. Physiol Plant 133:651–669
  • Šmalcelj B, Ćurković-Perica M (2000) Development of anther-derived flue-cured tobacco dihaploids from PVY resistant DH10 hybrid. Die Bodenkultur 51:11–17
  • Sreenivasulu N, Grimm B, Wobus U, Weschke W (2000) Differential response of antioxidant compounds to salinity stress in salt-tolerant and salt sensitive seedlings of foxtail millet (Setaria italica). Physiol Plant 109:435–442
  • Sudhakar C, Lakshmi A, Giridarakumar S (2001) Changes in the antioxidant enzyme efficacy in two high yielding genotypes of mulberry (Morus alba L.) under NaCl salinity. Plant Sci 161:613–619
  • Sudhir P, Murthy SDS (2004) Effects of salt stress on basic processes of photosynthesis. Photosynthetica 42:481–486
  • Szabados L, Savoure A (2009) Proline: a multifunctional amino acid. Trends Plant Sci 15:89–97
  • Szabolcs I (1994) Soils and salinisation. In: Pessarakali M (ed) Handbook of plant and crop stress. Marcel Dekker, New York, pp 3–11
  • Tavallali V, Rahemi M, Eshghi S, Kholdebarin B, Ramezanian A (2010) Zinc alleviates salt stress and increases antioxidant enzyme activity in the leaves of pistachio (Pistacia vera L. ‘Badami’) seedlings. Turk J Agric For 34:349–359
  • Verbruggen N, Hermans C (2008) Proline accumulation in plants: a review. Amino Acids 35:753–759

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-1379eff2-2d92-42ec-ac2e-4bed59b5f132
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.