Arbuscular Mycorrhizal Fungi Encourage Drought Tolerance Of Chlorophytum Borivilianum By Enhancing Antioxidant Enzyme System

Authors

  • Sushma Dave Central Arid Zone Research Institute, Jodhpur 342 003, Rajasthan, India
  • J C Tarafdar Central Arid Zone Research Institute, Jodhpur 342 003, Rajasthan, India

DOI:

https://doi.org/10.48165/

Keywords:

Antioxidant enzymes, arbuscular mycorrhiza, Chlorophytum borivilianum, drought stress, Glomus species

Abstract

Chlorophytum borivilianum, due to the presence of high valued  industrially important steroidal saponins in its roots, has attracted  pharmacological societies worldwide and motivated the farmers of arid  and semi-arid zones to cultivate this medicinal herb on commercial scale.  However, drought stress is a major abiotic constraint in the successful  cultivation of this crop in these areas. One possible way to enhance its  production is to improve its drought tolerance through arbuscular  mycorrhizal symbiosis. The mechanism by which mycorrhizal symbiosis  protects the plants against reactive oxygen species, induced by drought  stress, is investigated by evaluating the activity of a set of antioxidant  enzymes in relation to different mycorrhizal inocula at various growth  stages. The influence of three mycorrhizal inocula viz., Glomus  fasciculatum, G. intraradices and G. mosseae on superoxide dismutase,  catalase, glutathione reductase, glutathione-s-transferase, polyphenol  oxidase and peroxidase enzyme activities were evaluated in well-watered  and drought stressed conditions. The result revealed that the entire mycorrhizal plant materials showed higher drought tolerance effect than  non-mycorrhizal ones by enhancing antioxidant enzyme activities.  Antioxidant activities were more at 180 days of crop harvest. Therefore,  it is recommended to harvest C. borivilianum roots at 180 days crop age.  Mycorrhizal drought-stressed roots showed significantly higher anti oxidant activities than the well-watered conditions. Thus, it can be  assumed that higher antioxidant activities in roots of mycorrhizal plants  might have contributed to alleviate the oxidative damage to biomolecules.  The cultivation of C. borivilianum with arbuscular mycorrhizae in arid zone, therefore, can be a value addition against drought stress. 

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References

Abo-Ghalia, H.H. and Khalafallah, A.A. 2008. Responses of wheat plants associated with arbuscular mycorrhizal fungi to short-term water mycorrhizal and nonmycorrhizal rose exposed to drought stress. Plant Physiology, 82: 765-770.

Arines, J., Quintela, M., Vilarino, A. and Palma, J.M. 1994. Protein pattern and superoxide dismutase activity in non-mycorrhizal and arbuscular mycorrhizal Pisum sativum L. plants. Plant and Soil, 166: 37-45.

Auge, R.M. 2001. Water relations, drought and vesicular-arbuscular mycorrhizal symbiosis. Mycorrhizae, 11: 3-42.

Auge, R.M., Foster, J.G., Loescher, W.H. and Stodola, A.W. 1992. Symplastic sugar and free amino acid molality of Rosa roots with regard to mycorrhizal colonization and drought. Symbiosis, 12: 1-17

Auge, R.M., Toler, H.D., Moore, J.L., Cho, K. and Saxton, A.M. 2007. Comparing contributions of soil versus root colonization to variations in stomatal behavior and soil drying in mycorrhizal Sorghum bicolor and Cucurbita pepo. Journal of Plant Physiology, 164: 1289-1299.

Beak, K.H. and Skinner, D.Z. 2003. Alteration of antioxidant enzyme gene expression during cold acclimation of near-isogenic wheat lines. Plant Science, 165: 1221-1227.

Becana, M., Aparicio-Tejo, P., Irigoyan, J.J. and Sanchez-Diaz, M. 1986. Some enzymes of hydrogen peroxide metabolism in leaves and root nodules of Medicago sativa. Plant Physiology, 82: 1169- 1171.

Chance, B. and Maehly, A.C. 1955. Assay of catalase and peroxidases. Methods of Enzymology, 2: 764- 765.

Fitter, A.H. 2005. Darkness visible: Reflections on underground ecology. Journal of Ecology, 93: 231- 243.

Foyer, C.H., Descourvieres, P. and Kunert, K.J. 1994. Protection against oxygen radicals: An important defence mechanism studied in transgenic plants. Plant Cell Environment, 76: 507-523. Foyer, C.H., Lelandais, M., Galap, C. and Kunert, K.J. 1991. Effects of elevated cytosolic glutathione reductase activity on the cellular glutathione pool and photosynthesis in leaves under normal and stress conditions. Plant Physiology, 97: 863-872.

Foyer, C.H., Souriau, N., Perret, S., Lelandais. M. and Junert, K.J. 1995. Over expression of glutathione reductase but not glutathione synthetase leads to increases in antioxidant capacity and resistance to photoinhibition in poplar trees. Plant Physiology, 109: 1047-1057.

Gaur, A. and Adholeya, A. 1994. Estimation of VAMF spores in soil: A modified method. Mycorrhiza News, 6: 10-11.

Gerdemann, J.W. and Nicolson, T. H. 1963. Spores of mycorrhizal Endogone species extracted from soil by wet sieving and decanting. Transactions of British Mycological Society, 46: 235-244. Graham, J.H., Drouillard, D.L. and Hodge, N.C. 1996. Carbon economy of sour orange in response to different Glomus spp. Tree Physiology, 16: 1023-1029.

Hardie, K. 1985. The effect to removal of extraradical hyphae on water uptake by vesicular-arbuscular mycorrhizal plants. New Phytologist, 101: 667-684.

Jackson, M.L. 1967. Soil Chemical Analysis. Prentice-Hall of India, New Delhi, India. Klironomos, J.N. 2002. Feedback with soil biota contributes to plant rarity and invasiveness in communities. Nature, 417: 67-70.

Drought tolerance of Chlorophytum borivilianum through arbuscular mycorrhiza 69

Kramer, P.J. and Boyer, J.S. 1997. Water Relations of Plants and Soils. Academic Press, San Diego, USA.

Maiti, S. and Geetha, K.A. 2005. Characterization, genetic diversity and cultivation of Chlorophytum borivilianum - an important medicinal plant of India. Plant Genetic Resources: Characterization and Utilization, 3: 264-272.

Mannervik, B. and Guthenberg, C. 1981. Glutathione transferase (human placenta). Methods of Enzymology, 77: 231-235.

Martinez, C.A., Loureiro, M.E., Oliva, M.A. and Maestri, M. 2001. Differential responses of superoxide dismutase in freezing resistant Solanum tuberosum subjected to oxidative and water stress. Plant Science, 160: 505-515.

Mimaki, Y., Kanmoto, T., Sashida, Y., Nishino, A., Satomi, Y. and Nishino, H. 1996. Steroidal saponins from the underground parts of Chlorophytum comosum and their inhibitory activity on tumor promoter-induced phospholipid metabolism of HeLa cells. Phytochemistry, 41: 1405-1410.

Mittler, R. 2002. Oxidative stress, antioxidants and stress tolerance. Trends in Plant Science, 7: 405- 410.

Noctor, G. and Foyer, C.H. 1998. Ascorbate and glutathione: Keeping active oxygen under control. Annual Review of Plant Physiology, 49: 249-279.

Passardi, F., Penel, C. and Dunand, C. 2004. Performing the paradoxical: How plant peroxidases modify the cell wall. Trends in Plant Science, 9: 534-540.

Philips, J.M. and Hayman, D.S. 1970. Improved procedures for clearing roots and staining parasitic and vesicular-arbuscular mycorrhizal fungi for rapid assessment of infection. Transactions of British Mycological Society, 55: 158-161.

Porcel, R., Barea, J.M. and Ruiz-Lozano, J.M. 2003. Antioxidant activities in mycorrhizal soybean plants under drought stress and their possible relationship to the process of nodule senescence. New Phytologist, 157: 135-143.

Puri, H.S. 2003. Rasayana-Ayurvedic Herbs for Longevity and Rejuvenation. Taylor and Francis, London, UK.

Requena, N., Perez-Solis, E., Azcon-Aguilar, C., Jeffries, P. and Barea, J.M. 2001. Management of indigenous plant-microbe symbioses aids restoration of desertified ecosystems. Applied Environmental Microbiology, 67: 495-498.

Roldan, A., Diaz-Vivancos, P., Hernandez, J.A., Carrosco, L. and Caravaca, F. 2008. Superoxide dismutase and total peroxidase activities in relation to drought recovery performance of mycorrhizal shrub seedlings grown in an amended semiarid soil. Journal of Plant Physiology, 165: 715-722.

Roxas, V.P., Lodhi, S.A., Garrett, D.K., Mahan, J.R. and Allen, R.D. 2000. Stress tolerance in transgenic tobacco seedlings that over express glutathione-s-transferase/guaiacol peroxidase. Plant Cell Physiology, 41: 1229-1234.

Ruiz-Lozano, J.M., Azcon, R. and Palma, J.M. 1996. Superoxide dismutase activity in arbuscular mycorrhizal Lactuca sativa plants subjected to drought stress. New Phytologist, 134: 327-333. Ruiz-Lozano, J.M., Collados, C., Barea, J.M. and Azcon, R. 2001. Arbuscular mycorrhizal symbiosis can alleviate drought-induced nodule senescence in soybean plants. New Phytologist, 151: 493- 502.

Ruiz-Lozano, J.M., Porcel, R. and Aroca, R. 2008. Evaluation of the possible participation of drought induced genes in the enhanced tolerance of arbuscular mycorrhizal plants to water deficit. pp. 185–205. In: Mycorrhiza: State of the Art, Genetics and Molecular Biology, Eco-function, Biotechnology, Eco-physiology, Structure and Systematics (ed. A. Varma), Springer-Verlag, Germany.

Sushma Dave and J.C. Tarafdar

Sakihama, Y., Cohen, M.F., Grace, S.C. and Yamasaki, H. 2002. Plant phenolic antioxidant and prooxidant activities: Phenolics-induced oxidative damage mediated by metals in plants. Toxicology, 177: 67-80.

Scandalios, J.G. 1993. Oxygen stress and superoxide dismutases. Plant Physiology, 101: 7-12. Shaedle, M. and Bassham, J.A. 1977. Chloroplast glutathione reductase. Plant Physiology, 59: 1011- 1012.

Sinsabaugh, R.L., Saiya-Cork, K., Long, T., Osgoodc, M.P., Neher, D.A., Zakd, D.R. and Norby, R.J. 2003. Soil microbial activity in a Liquidambar plantation unresponsive to CO2-driven increases in primary production. Applied Soil Ecology, 24: 263-271.

Smith, S.E., Facelli, E., Pope, S. and Smith, F.A. 2010. Plant performance in stressful environments: Interpreting new and established knowledge of the roles of arbuscular mycorrhizas. Plant and Soil, 326: 3-20.

Smith, S.E. and Read, D.J. 1997. Mycorrhizal Symbiosis. Academic Press, San Diego, USA. Stampe, E.D. and Daehler, C.C. 2003. Mycorrhizal species identity affects plant community structure and invasion: A microcosm study. Oikos, 100: 362-372.

Toro, M., Azcon, R. and Barea, J.M. 1997. Improvement of arbuscular mycorrhiza development by inoculation of soil phosphate solubilizing rhizobacteria to improve rock phosphate bioavailability (32P) and nutrient cycling. Applied Environmental Microbiology, 63: 4408-4412.

Vallino, M., Greppi, D., Novero, M., Bonfante, P. and Lupotto, E. 2009. Rice root colonization by mycorrhizal and endophytic fungi in aerobic soil. Annals of Applied Biology, 154: 195-204. Vander-Heijden, M.G.A. 2004. Arbuscular mycorrhizal fungi as support systems for seedling establishment in grassland. Ecology Letter, 7: 293-303.

Wu, Q.S., Xia, R.X. and Hu, Z. 2006a. Effect of arbuscular mycorrhizae on the drought tolerance of Poncirus trifoliata seedlings. Frontiers of Forestry in China, 1: 100-104.

Wu, Q.S., Xia, R.X. and Zou, Y.N. 2008. Improved soil structure and citrus growth after inoculation with three arbuscular mycorrhizal fungi under drought stress. European Journal of Soil Biology, 44: 122-128.

Wu, Q.S., Zou, Y.N. and Xia, R.X. 2006b. Effect of water stress and arbuscular mycorrhizal fungi on reactive oxygen metabolism and antioxidant production by citrus (Citrus tangerine) roots. European Journal of Soil Biology, 42: 166-172.

Published

2012-03-21

How to Cite

Arbuscular Mycorrhizal Fungi Encourage Drought Tolerance Of Chlorophytum Borivilianum By Enhancing Antioxidant Enzyme System . (2012). Applied Biological Research, 14(1), 60–70. https://doi.org/10.48165/