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Chilling tolerance in Nicotiana tabacum induced by seed priming with putrescine

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Abstract

Chilling stress is one of primary constraints to tobacco production in many parts of the world. The present study was conducted to induce chilling tolerance in tobacco by seed priming with putrescine (Put) in relation to physiological changes, using seeds from two tobacco varieties, MSk326 (chilling sensitive variety) and Honghuadajinyuan (HHDJY, chilling tolerant variety). Seed germination, seedling antioxidant enzyme activities and malondialdehyde (MDA) concentration, as well as polyamine concentration were determined under low temperature. During chilling stress at 11°C, seed priming with 0.01 mM Put for 48 h (Put0.01mM48 h) and seed priming with 0.1 mM Put for 48 h (Put0.1mM48 h) significantly increased germination percentage, germination index, seedling length and dry weight of both varieties compared to the controls without Put treatment. When seedlings of 4-leaf stage suffered a short chilling stress (5°C), Put 0.1 mM 48 h improved the activities of antioxidant enzymes including superoxide dismutase (SOD), peroxidase (POD), catalase (CAT) and ascorbate peroxidase (APX), increased endogenous Put, Spd and Spm concentration and decreased the MDA concentration. The results showed that Put priming treatments were available to enhance the chilling tolerance of tobacco seedlings. The optimal treatment of Put was Put0.1 mM48 h.

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Abbreviations

APX:

Ascorbate peroxidase

CAT:

Catalase

EDTA:

Ethylenediamine tetra-acetic acid

MDA:

Malondialdehyde

NBT:

Nitroblue tetrazolium

PA:

Polyamine

POD:

Peroxidase

Put:

Putrescine

SOD:

Superoxide dismutase

Spd:

Spermidine

Spm:

Spermine

TBA:

2-Thiobarbituric acid

TCA:

Trichloroacetic acid

References

  • Afzal I, Munir F, Ayub CM, Basra SMA, Hameed A, Nawaz A (2009) Changes in antioxidant enzymes, germination capacity and vigour of tomato seeds in response of priming with polyamines. Seed Sci Technol 37(3):765–770

    Google Scholar 

  • Alcazar R, Altabella T, Marco F, Bortolotti C, Reymond M, Koncz C, Carrasco P, Tiburcio A (2010) Polyamines: molecules with regulatory functions in plant abiotic stress tolerance. Planta 231:1237–1249

    Article  PubMed  CAS  Google Scholar 

  • Altman A (2006) Polyamines and wounded storage tissues–inhibition of RNase activity and solute leakage. Physiol Plant 54(2):194–198

    Article  Google Scholar 

  • An LZ, Liu GX, Zhang MX, Chen T, Liu YH, Feng HY, Xu SJ, Qiang WY, Wang XL (2004) Effect of enhanced UV-B radiation on polyamine content and membrane permeability in cucumber leaves. Russ J Plant Physiol 51:658–662

    Article  CAS  Google Scholar 

  • Besford RT, Richardson CM, Campos JL, Tiburcio AF (1993) Effect of polyamines on stabilization of molecular complexes in thylakoid membranes of osmotically stressed oat leaves. Planta 189:201–206

    Article  CAS  Google Scholar 

  • Bolkhina O, Virolainen E, Fagerstedt K (2003) Antioxidants, oxidative damage and oxygen deprivation stress: a review. Ann Bot 91:179–194

    Article  Google Scholar 

  • Bowler C, Van Montagu M, Inze D (1992) Superoxide dismutase and stress tolerance. Annu Rev Plant Physiol Plant Mol Biol 43:83–116

    Article  CAS  Google Scholar 

  • Cakmak I, Marschner H (1992) Magnesium deficiency and high light intensity enhance activities of superoxide dismutase, ascorbate peroxidase, and glutathione reductase in bean leaves. Plant Physiol 98:1222–1227

    Article  PubMed  CAS  Google Scholar 

  • Cao DD, Hu J, Gao CH, Guan YJ, Zhang S, Xiao JF (2008) Chilling tolerance of maize (Zea mays L.) can be improved by seed soaking in putrescine. Seed Sci Technol 36:191–197

    Google Scholar 

  • Chattopadhayay MK, Tiwari BS, Chattopadhayay G, Bose A, Sengupta DN, Ghosh B (2002) Protective role of exogenous polyamines on salinity-stressed rice (Oriza sativa) plants. Physiol Plantarum 116:192–199

    Article  CAS  Google Scholar 

  • Cuevas JC, Lopez-Cobollo R, Alcazar R, Zarza X, Koncz C, Altabella T, Salinas J, Tiburcio AF, Ferrando A (2008) Putrescine is involved in Arabidopsis freezing tolerance and cold acclimation by regulating abscisic acid levels in response to low temperature. Plant Physiol 148:1094–1105

    Article  PubMed  CAS  Google Scholar 

  • Dadlani M (1992) Seed coating to improve stand establishment in rice. Seed Sci Technol 20:307–313

    Google Scholar 

  • Farooq M, Wahid A, Lee DJ (2009) Exogenously applied polyamines increase drought tolerance of rice by improving leaf water status, photosynthesis and membrane properties. Acta Physiol Plant 31:937–945

    Article  CAS  Google Scholar 

  • Flores HE, Galston WA (1982) Analysis of polyamine in higher plants by high performance liquid chromatography. Plant Physiol 69:701–706

    Article  PubMed  CAS  Google Scholar 

  • Gao CH, Hu J, Zhang S (2009) Association of polyamines in governing the chilling sensitivity of maize genotypes. Plant Growth Regul 57:31–38

    Article  CAS  Google Scholar 

  • Gechev T, Willekens H, Van Montagu M, Inzé D, Van Camp W, Toneva V, Minkov I (2003) Different responses of tobacco antioxidant enzymes to light and chilling stress. Plant Physiol 160:509–515

    Article  CAS  Google Scholar 

  • Guo Z, Ou W, Lu S, Zhong Q (2006) Differential responses of antioxidative system to chilling and drought in four rice cultivars differing in sensitivity. Plant Physiol Biochem 44:828–836

    Article  PubMed  CAS  Google Scholar 

  • Ha HC, Sirisoma NS, Kuppusamy P, Zweier JL, Woster PM, Casero RA (1998) The natural polamine spermie functions directly as a free radical scavenger. Biochemistry 95:11140–11145

    CAS  Google Scholar 

  • Han JF, Zhu DH, Lin XW, Han W (1992) Effects of polyamines on tobacco root growth and development. Plant Physiol Commun 28(2):124–126

    CAS  Google Scholar 

  • Kasinathan V, Wingler A (2004) Effect of reduced arginine decarboxylase activity on salt tolerance and on polyamine formation during salt stress in Arabidopsis thaliana. Physiol Plantarum 121:101–107

    Article  CAS  Google Scholar 

  • Kim TE, Kim SK, Han TJ, Lee JS, Chang SC (2002) ABA and polyamines act independently in primary leaves of cold-stressed tomato (Lycopersicon esculentum). Physiol Plantarum 115:370–376

    Article  CAS  Google Scholar 

  • Kovacs Z, Simon-Sarkadi L, Szucs A, Kocsy G (2010) Differential effects of cold, osmotic stress and abscisic acid on polyamine accumulation in wheat. Amino Acids 38:623–631

    Article  PubMed  CAS  Google Scholar 

  • Kubiś J (2006) Exogenous spermidine alters in different way membrane permeability and lipid peroxidation in water stressed barley leaves. Acta Physiologiae Plantarum 28:27–33

    Article  Google Scholar 

  • Li YP, Xu SC, Ma WG, Zheng YY, Hu J (2009) Identification of chilling-tolerance in tobacco cultivars at germination and seedling growth stages. Bull Sci Technol 25(6):807–811

    CAS  Google Scholar 

  • Lin JM, Sung JM (2001) Pre-sowing treatments for improving emergence of bitter gourd seedlings under optimal and sub-optimal temperatures. Seed Sci Technol 29(1):39–50

    Google Scholar 

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

    CAS  Google Scholar 

  • Nayyar H (2005) Putrescine increases floral retention, pod set and seed yield in cold stressed chickpea. J Agron Crop Sci 191(5):340–345

    Article  CAS  Google Scholar 

  • Nayyar H, Chander S (2004) Protective effects of polyamines against oxidative stress induced by water and cold stress in chickpea. J Agron Crop Sci 190:355–365

    Article  CAS  Google Scholar 

  • Ndayiragije A, Lutts S (2006) Do exogenous polyamines have an impact on the response of a salt-sensitive rice cultivar to NaCl? J Plant Physiol 163:506–516

    Article  PubMed  CAS  Google Scholar 

  • Qiu J, Wang R, Yan J, Hu J (2005) Seed film coating with uniconazole improves rape seedling growth in relation to physiological changes under waterlogging stress. Plant Growth Regul 47:75–81

    Article  CAS  Google Scholar 

  • Rao KVM, Sresty TVS (2000) Antioxidant parameters in the seedlings of pigeon pea (Cajanus cajan (L.) Millspaugh) in response to Zn and Ni stresses. Plant Sci 157:113–128

    Article  Google Scholar 

  • Rodríguez-Kessler M, Alpuche-Solís AG, Ruiz OA, Jiménez-Bremont JF (2006) Effect of salt stress on the regulation of maize (Zea mays L.) genes involved in polyamine biosynthesis. Plant Growth Regul 48:175–185

    Article  Google Scholar 

  • Sanchez DH, Cuevas JC, Chiesa MA, Oscar RA (2005) Free spermidine and spermine content in Lotus glaber under long-term salt stress. Plant Sci 168:541–546

    Article  CAS  Google Scholar 

  • Simon EW, Minchin A, McMenamin MM, Smith JM (1976) The low temperature limit for seed germination. New Phytol 77:301–311

    Article  Google Scholar 

  • Urano K, Yoshiba Y, Nanjo T, Igarashi Y, Seki M, Sekiguchi F, Yamaguchi-Shinozaki K, Shinozaki K (2003) Characterization of Arabidopsis genes involved in biosynthesis of polyamines in abiotic stress responses and developmental stages. Plant Cell Environ 26:1917–1926

    Article  CAS  Google Scholar 

  • Wallace MH, Fraser VA, Hughes A (2003) A perspective of polyamine metabolism. Biochem J 376:1–14

    Article  PubMed  CAS  Google Scholar 

  • Wu QS, Zou YN, He XH (2010) Exogenous putrescine, not spermine or spermidine, enhances root mycorrhizal development and plant growth of trifoliate orange (Poncirus trifoliata) seedlings. Int J Agri Biol 12:576–580

    Google Scholar 

  • Zhang XZ (1992) The measurement and mechanism of lipid peroxidation and SOD, POD and CAT activities in biological system. In: Zhang XZ (ed) Research methodology of crop physiology. Agriculture Press, Beijing, pp 208–211

    Google Scholar 

  • Zhang S, Hu J, Zhang Y, Xie XJ, Knapp A (2007) Seed priming with brassinolide improves lucerne (Medicago sativa L.) seed germination and seedling growth in relation to physiological changes under salinity stress. Aust J Agr Res 58:811–815

    Article  CAS  Google Scholar 

  • Zhao ZF, Guo AH, Feng ZW (2003) Amelioration of chilling stress by triadimefon in cucumber seedlings. Plant Growth Regul 39(3):277–283

    Article  Google Scholar 

Download references

Acknowledgments

The research was supported by the Yunnan Province Tobacco Company (No. 07A02, 09YN008), Major Science and Technology Special Project (priority subject) of Zhejiang Province (No. 2008C12005-1) and Major special project of Ministry of Agriculture (No. 2008ZX08005-005), China. The authors are grateful to the editor and anonymous reviewers for comments that improved the presentation of the paper.

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Correspondence to Jin Hu.

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Xu, S., Hu, J., Li, Y. et al. Chilling tolerance in Nicotiana tabacum induced by seed priming with putrescine. Plant Growth Regul 63, 279–290 (2011). https://doi.org/10.1007/s10725-010-9528-z

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  • DOI: https://doi.org/10.1007/s10725-010-9528-z

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