Skip to main content
Log in

Chilling, oxidative stress and antioxidant responses inArabidopsis thaliana callus

  • Published:
Planta Aims and scope Submit manuscript

Abstract

Chilling ofArabidopsis thaliana (L.) Heynh. callus tissue to 4 °C led to conditions of oxidative stress, as indicated by increased levels of the products of peroxidative damage to cell membranes. Cellular H2O2 was also observed to increase initially upon chilling but by day 8 cellular levels had declined to below control levels. Although levels of catalase activity remained similar to those in unchilled tissue, activity of ascorbate peroxidase increased between days 4 and 8 of chilling to 4 °C. In callus held at 23 °C, levels of reduced glutathione remained static whereas they rose in callus held at 4 °C. Levels of oxidised glutathione were initially low but increased significantly by day 4 in the chilled callus. At 23 °C, however, levels of oxidised glutathione remained low. Between days 1 and 3 at 4 °C, levels of glutathione reductase activity increased but by day 8 glutathione reductase activity was similar to that in cells held at 23 °C. Exposure of callus to abscisic acid at 23 °C also led to increased activities of ascorbate peroxidase and glutathione reductase.

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.

Similar content being viewed by others

Abbreviations

ABA:

abscisic acid

GSH:

reduced glutathione

GSSG:

oxidised glutathione

TTC:

2′,3′5′-triphenyltetrazolium chloride

References

  • Aono M, Kubo A, Saji H, Natori T, Tanaka K, Kondo N (1991) Resistance to active oxygen toxicity of transgenicNicotiana tabacum that expresses the gene for glutathione reductase fromEscherichia coli. Plant Cell Physiol 32: 691–697

    Google Scholar 

  • Asada K, Takahashi M (1987) Production and scavenging of active oxygen in photosynthesis. In: Kyle DJ, Osmond CR, Arntzen CJ (eds) Photoinhibition. Elsevier Science Publishers, Amsterdam, New York, Oxford, pp 227–286

    Google Scholar 

  • Beeor-Tzahov T, Ben-Hayyim G, Holland D, Faltin Z, Eshdat Y (1995) A stress associated citrus protein is a distinct plant phospholipid hydroperoxide glutathione peroxidase. FEBS Letts 336: 151–155

    Google Scholar 

  • Boveris A, Chance B (1973) The cellular production of hydrogen peroxide. Biochem J 128: 617–630

    Google Scholar 

  • Burdon RH, Gill V, Boyd PA, O'Kane D (1994) Chilling, oxidative stress and antioxidant enzyme responses inArabidopsis thaliana. Proc R Soc Edinburgh 102B: 177–185

    Google Scholar 

  • Chen THH, Gusta LV (1983) Abscisic acid-induced freezing resistance in cultured plant cells. Plant Physiol 73: 71–75

    Google Scholar 

  • Clairborne A (1985) Catalase activity. In: Greenwald EA (ed) CRC. Handbook of methods for oxygen radical research. CRC Press, Boca Raton, pp 283–284

    Google Scholar 

  • Creissen GP, Broadbent P, Kular B, Reynolds H, Wellburn AR, Mullineaux PM (1994) Manipulation of glutathione reductase in transgenic plants: implications for plant responses to environmental stress. Proc R Soc Edinburgh 102B: 167–175

    Google Scholar 

  • del Rio LA, Sandalio LM, Palma JM, Bueno P, Corpas FJ (1992) Metabolism of oxygen radicals in peroxisomes and cellular implications. Free Rad Biol Med 13: 557–580

    Google Scholar 

  • Edwards EA, Ehard C, Creissen GP, Mullineaux PM (1994) Synthesis and properties of glutathione reductase in stressed peas. Planta 192: 137–143

    Google Scholar 

  • Gamborg OL (1970) The effect of amino acids and ammonia on the growth of plant cells in suspension culture. Plant Physiol 45: 372–377

    Google Scholar 

  • Gilmour SJ, Hajela RK, Thomashow MF (1988) Cold acclimation inArabidopsis thaliana. Plant Physiol 87: 745–750

    Google Scholar 

  • Griffith OW (1980) Determination of glutathione and glutathione disulphide using glutathione reductase and 2-vinylpyridine. Anal Biochem 106: 207–212

    Google Scholar 

  • Guy GL, Carter JV (1984) Characterisation of partially purified glutathione reductase from cold-hardened and non-hardened spinach leaf tissue. Cryobiol 21: 454–464

    Google Scholar 

  • Jahnke LS, Hull MR, Long SP (1991) Chilling stress and oxygen metabolising enzymes inZea mays andZea diploperennis. Plant Cell Environ 14: 97–104

    Google Scholar 

  • Jarillo JA, Leyva A, Salinas J, Martinez-Zapater JM (1993) Low temperature induces the accumulation of alcohol dehydrogenase mRNA inArabidopsis thaliana a chilling-tolerant plant. Plant Physiol 101: 833–837

    Google Scholar 

  • Kubo A, Sano T, Saji H, Tanaka K, Kondo N, Tanaka K (1993) Primary structure and properties of glutathione reductase fromArabidopsis thaliana. Plant Cell Physiol 34: 1259–1266

    Google Scholar 

  • Levitt J (1980) Responses of plants to environment stress: chilling, freezing and high temperature stress (2nd edn). Academic Press, New York

    Google Scholar 

  • Loschen G, Azzi A, Flohe L (1973) Mitochondrial H2O2 formation at site II. Hoppe-Seyler Zeit Physiol Chem 354: 791–794

    Google Scholar 

  • Murashige T, Skoog F (1962) A revised medium for rapid growth and bioassays with tobacco cultures. Physiol Plant 15: 473–497

    Google Scholar 

  • May MJ, Leaver CJ (1993) Oxidative stimulation of glutathione synthesis inArabidopsis thaliana suspension cultures. Plant Physiol 103: 621–627

    Google Scholar 

  • Miguel M, James D, Dooner H, Browse J (1993)Arabidopsis requires polyunsaturated lipids for low-temperature survival. Proc Natl Acad Sci USA 90: 6208–6212

    Google Scholar 

  • Melhorn H (1990) Ethylene-promoted ascorbate peroxidase activity protects plants against hydrogen peroxide, ozone and paraquat. Plant Cell Environ 13: 971–976

    Google Scholar 

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

    Google Scholar 

  • Nohl H, Heger D (1978) Do mitochondria produce oxygen radicals in vivo. Eur J Biochem 82: 563–567

    Google Scholar 

  • Okuda T, Masuda Y, Yamanaka A, Sagisaka S (1991) Abrupt increase in the level of hydrogen peroxide in leaves of winter wheat is caused by cold treatment. Plant Physiol 97: 1265–1267

    Google Scholar 

  • Omran RG (1980) Peroxide levels and activities of catalase, peroxidase and indoleacetic acid oxidase during and after chilling cucumber seedlings. Plant Physiol 65: 407–408

    Google Scholar 

  • Peng M, Kuo J (1992) Peroxidase-generated hydrogen peroxide as a source of antifungal activity in vitro and on tobacco leaf discs. Phytopathology 82: 696–699

    Google Scholar 

  • Prasad TK, Anderson MD, Martin BA, Steward CR (1994) Evidence for chilling-induced oxidative stress in maize seedlings and a regulatory role for hydrogen peroxide. Plant Cell 6: 65–74

    Google Scholar 

  • Quinn PJ (1988) Effects of temperature on cell membranes. Symp Soc Expt Biol 42: 237–258

    Google Scholar 

  • Sandalio LM, Palma JM, del Rio LA (1987) Localisation of Mnsuperoxide dismutase in peroxisomes fromPisum sativum L. Plant Sci 51: 1–8

    Google Scholar 

  • Sen Gupta A, Webb RP, Holaday AS, Allen RD (1993) Overexpression of superoxide dismutase protects plants from oxidative stress. Plant Physiol 103: 1067–1074

    Google Scholar 

  • Taylor AO, Slack CR, McPherson HG (1974) Plants under climatic stress VI chilling and light effect on photosynthetic enzymes of sorghum and maize. Plant Physiol 54: 696–701

    Google Scholar 

  • Towill LE, Mazur P (1975) Studies on the reduction of 2′,3′,5′triphenyltetrazolium chloride as a viability assay for plant tissue culture. Can J Bot 53: 1097–1102

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

This work is supported by a grant from the Biotechnology and Biological Sciences Research Council.

Rights and permissions

Reprints and permissions

About this article

Cite this article

O'Kane, D., Gill, V., Boyd, P. et al. Chilling, oxidative stress and antioxidant responses inArabidopsis thaliana callus. Planta 198, 371–377 (1996). https://doi.org/10.1007/BF00620053

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00620053

Key words

Navigation