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Isolation and Characterization of a Theta Glutathione S-transferase Gene from Panax ginseng Meyer

  • Kim, Yu-Jin (Department of Oriental Medicinal Materials and Processing, College of Life Science, Kyung Hee University) ;
  • Lee, Ok-Ran (Department of Oriental Medicinal Materials and Processing, College of Life Science, Kyung Hee University) ;
  • Lee, Sung-Young (Department of Computer Engineering, Kyung Hee University) ;
  • Kim, Kyung-Tack (Processing Technology Research Group, Korea Food Research Institute) ;
  • Yang, Deok-Chun (Department of Oriental Medicinal Materials and Processing, College of Life Science, Kyung Hee University)
  • Received : 2012.06.10
  • Accepted : 2012.08.11
  • Published : 2012.10.15

Abstract

Plants have versatile detoxification systems to encounter the phytotoxicity of the wide range of natural and synthetic compounds present in the environment. Glutathione S-transferase (GST) is an enzyme that detoxifies natural and exogenous toxic compounds by conjugation with glutathione (GSH). Recently, several roles of GST giving stress tolerance in plants have demonstrated, but little is known about the role of ginseng GSTs. Therefore, this work aimed to provide further information on the GST gene present in Panax ginseng genome as well as its expression and function. A GST cDNA (PgGST) was isolated from P. ginseng cDNA library, and it showed the amino acid sequence similarity with theta type of GSTs. PgGST in ginseng plant was induced by exposure to metals, plant hormone, heavy metals, and high light irradiance. To improve the resistance against environmental stresses, full-length cDNA of PgGST was introduced into Nicotiana tabacum. Overexpression of PgGST led to twofold increase in GST-specific activity compared to the non-transgenic plants, and the GST overexpressed plant showed resistance against herbicide phosphinothricin. The results suggested that the PgGST isolated from ginseng might have a role in the protection mechanism against toxic materials such as heavy metals and herbicides.

Keywords

References

  1. Droog F, Hooykaas P, Van Der Zaal BJ. 2,4-Dichlorophenoxyacetic acid and related chlorinated compounds inhibit two auxin-regulated type-III tobacco glutathione S-transferases. Plant Physiol 1995;107:1139-1146. https://doi.org/10.1104/pp.107.4.1139
  2. Dixon DP, Lapthorn A, Edwards R. Plant glutathione transferases. Genome Biol 2002;3:REVIEWS3004.
  3. Droog F. Plant glutathione S-transferases, a tale of theta and tau. J Plant Growth Regul 1997;16:95-107. https://doi.org/10.1007/PL00006984
  4. Wilce MC, Parker MW. Structure and function of glutathione S-transferases. Biochim Biophys Acta 1994;1205:1-18. https://doi.org/10.1016/0167-4838(94)90086-8
  5. Park MS, Cho EJ, Lee SK, Lee EJ, Lee DS, Lee KH, Jeon BH. Korean red ginseng protects oxidative injury caused by lead poisoning. J Ginseng Res 2010;34:132-137. https://doi.org/10.5142/jgr.2010.34.2.132
  6. Dudler R, Hertig C, Rebmann G, Bull J, Mauch F. A pathogen-induced wheat gene encodes a protein homologous to glutathione-S-transferases. Mol Plant Microbe Interact 1991;4:14-18. https://doi.org/10.1094/MPMI-4-014
  7. Marrs KA. The functions and regulation of glutathione Stransferases in plants. Annu Rev Plant Physiol Plant Mol Biol 1996;47:127-158. https://doi.org/10.1146/annurev.arplant.47.1.127
  8. Lee OR, Sathiyaraj G, Kim YJ, In JG, Kwon WS, Kim JH, Yang DC. Defense genes induced by pathogens and abiotic stresses in Panax ginseng C.A. Meyer. J Ginseng Res 2011;35:1-11. https://doi.org/10.5142/jgr.2011.35.1.001
  9. Kim MK, Lee BS, In JG, Sun H, Yoon JH, Yang DC. Comparative analysis of expressed sequence tags (ESTs) of ginseng leaf. Plant Cell Rep 2006;25:599-606. https://doi.org/10.1007/s00299-005-0095-0
  10. Gasteiger E, Hoogland C, Gattiker A, Duvaud S, Wilkins MR, Appel RD, Bairoch A. Protein identification and analysis tools on the ExPASy server. In: Walker JM, ed. The proteomics protocols handbook. Totowa: Humana Press, 2005. p.571-607.
  11. Kim YJ, Shim JS, Krishna PR, Kim SY, In JG, Kim MK, Yang DC. Isolation and characterization of a glutaredoxin gene from Panax ginseng C. A. Meyer. Plant Mol Biol Report 2008;26:335-349. https://doi.org/10.1007/s11105-008-0053-4
  12. Ditta G, Stanfi eld S, Corbin D, Helinski DR. Broad host range DNA cloning system for gram-negative bacteria: construction of a gene bank of Rhizobium meliloti. Proc Natl Acad Sci U S A 1980;77:7347-7351. https://doi.org/10.1073/pnas.77.12.7347
  13. Dean JV, Gronwald JW, Eberlein CV. Induction of glutathione s-transferase isozymes in sorghum by herbicide antidotes. Plant Physiol 1990;92:467-473. https://doi.org/10.1104/pp.92.2.467
  14. Lichtenthaler HK. Chlorophylls and carotenoids: pigments of photosynthetic biomembranes. Methods Enzymol 1987;34:350-382.
  15. Kyte J, Doolittle RF. A simple method for displaying the hydropathic character of a protein. J Mol Biol 1982;157:105-132. https://doi.org/10.1016/0022-2836(82)90515-0
  16. Rhee JS, Lee YM, Hwang DS, Won EJ, Raisuddin S, Shin KH, Lee JS. Molecular cloning, expression, biochemical characteristics, and biomarker potential of theta class glutathione S-transferase (GST-T) from the polychaete Neanthes succinea. Aquat Toxicol 2007;83:104-115. https://doi.org/10.1016/j.aquatox.2007.03.015
  17. Choi CY, An KW, An MI. Molecular characterization and mRNA expression of glutathione peroxidase and glutathione S-transferase during osmotic stress in olive fl ounder (Paralichthys olivaceus). Comp Biochem Physiol A Mol Integr Physiol 2008;149:330-337. https://doi.org/10.1016/j.cbpa.2008.01.013
  18. Moons A. Regulatory and functional interactions of plant growth regulators and plant glutathione S-transferases (GSTs). Vitam Horm 2005;72:155-202. https://doi.org/10.1016/S0083-6729(05)72005-7
  19. Loyall L, Uchida K, Braun S, Furuya M, Frohnmeyer H. Glutathione and a UV light-induced glutathione Stransferase are involved in signaling to chalcone synthase in cell cultures. Plant Cell 2000;12:1939-1950. https://doi.org/10.1105/tpc.12.10.1939
  20. Chen W, Singh KB. The auxin, hydrogen peroxide and salicylic acid induced expression of the Arabidopsis GST6 promoter is mediated in part by an ocs element. Plant J 1999;19:667-677. https://doi.org/10.1046/j.1365-313x.1999.00560.x
  21. Roxas VP, Smith RK Jr, Allen ER, Allen RD. Overexpression of glutathione S-transferase/glutathione peroxidase enhances the growth of transgenic tobacco seedlings during stress. Nat Biotechnol 1997;15:988-991. https://doi.org/10.1038/nbt1097-988
  22. Jouve L, Hoffmann L, Hausman JF. Polyamine, carbohydrate, and proline content changes during salt stress exposure of aspen (Populus tremula L.): involvement of oxidation and osmoregulation metabolism. Plant Biol (Stuttg) 2004;6:74-80. https://doi.org/10.1055/s-2003-44687
  23. Wendler C, Barniske M, Wild A. Effect of phosphinothricin (glufosinate) on photosynthesis and photorespiration of C3 and C4 plants. Photosynth Res 1990;24:55-61. https://doi.org/10.1007/BF00032644
  24. Pascual MB. Expresio'n de glutamina sintetasa e isocitrato deshidrogenasa en a'rboles transge'nicos: papel en el desarrollo [dissertation]. Malaga: Universidad de Malaga, 2007.

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