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Molecular Cloning and Expression of Sequence Variants of Manganese Superoxide Dismutase Genes from Wheat

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Reactive oxygen species (ROS) are very harmful to living organisms due to the potential oxidation of membrane lipids, DNA, proteins, and carbohydrates. transformed E.coli strain QC 871, superoxide dismutase (SOD) double-mutant, with three sequence variant MnSOD1, MnSOD2, and MnSOD3 manganese superoxide dismutase (MnSOD) gene isolated from wheat. Although all QC 871 transformants grown at 37 ℃ expressed mRNA of MnSOD variants, only MnSOD2 transformant had functional SOD activity. MnSOD3 expressed active protein when grown at 22℃, however, MnSOD1 did not express functional protein at any growing and induction conditions. The sequence comparison of the wheat MnSOD variants revealed that the only amino acid difference between the sequence MnSOD2 and sequences MnSOD1 and 3 is phenylalanine/serine at position 58 amino acid. We made MnSOD2S58F gene, which was made by altering the phenylalaine to serine at position 58 in MnSOD2. The expressed MnSOD2S58F protein had functional SOD activity, even at higher levels than the original MnSOD2 at all observed temperatures. These data suggest that amino acid variation can result in highly active forms of MnSOD and the MnSOD2S58F gene can be an ideal target used for transforming crops to increase tolerance to environmental stresses.

Abstract

Reactive oxygen species (ROS) are very harmful to living organisms due to the potential oxidation of membrane lipids, DNA, proteins, and carbohydrates. transformed E.coli strain QC 871, superoxide dismutase (SOD) double-mutant, with three sequence variant MnSOD1, MnSOD2, and MnSOD3 manganese superoxide dismutase (MnSOD) gene isolated from wheat. Although all QC 871 transformants grown at 37 ℃ expressed mRNA of MnSOD variants, only MnSOD2 transformant had functional SOD activity. MnSOD3 expressed active protein when grown at 22℃, however, MnSOD1 did not express functional protein at any growing and induction conditions. The sequence comparison of the wheat MnSOD variants revealed that the only amino acid difference between the sequence MnSOD2 and sequences MnSOD1 and 3 is phenylalanine/serine at position 58 amino acid. We made MnSOD2S58F gene, which was made by altering the phenylalaine to serine at position 58 in MnSOD2. The expressed MnSOD2S58F protein had functional SOD activity, even at higher levels than the original MnSOD2 at all observed temperatures. These data suggest that amino acid variation can result in highly active forms of MnSOD and the MnSOD2S58F gene can be an ideal target used for transforming crops to increase tolerance to environmental stresses.

참고문헌 (41)

  1. Allen, S. P., "Two novel heat shock genes encoding proteins produced in response to heterologous protein expression", E. coli, J. Bacteriol., 174, pp.6938~6947 (1992)
  2. Allen, R. D., "Dissection of oxidative stress tolerance using transgenic plants", Plant Physiol, 107, pp.1049~1054 (1995)
  3. Baek, K. -H., "Alteration of antioxidant enzyme gene expression during cold acclimation of near-isogenic wheat lines", Plant Sci., 165, pp.1221~1227 (2003)
  4. Baek,K. -H., "Differential expression of manganese superoxide dismutase sequence variants in near isogenic lines of wheat during cold acclimation", Plant Cell Rep., 25, pp.223~230 (2006)
  5. Basu, U., "Transgenic Brassica napus plants overexpressing aluminuminduced mitochondrial manganese superoxide dismutase cDNA are resistant to aluminum", Plant, Cell, and Environ, 24, pp.1269~1278 (2001)
  6. Beauchamp, C. O., "Superoxide dismutase: improved assays and an assay applicable to acrylamide gels", Anal. Biochem, 44, pp.267~287 (1971)
  7. Borgstahl G. E. O., "Human mitochondrial manganese superoxide dismutase polymorphic variant Ile58Thr reduces activity by destabilizing the tetrameric interface", Biochemistry, 35, pp.4287~4297 (1996)
  8. Bowler, C., "Manganese superoxide dismutase can reduce cellular damage mediated by oxygen radicals in transgenic plants", EMBO J., 10, pp.1723~1732 (1991)
  9. Bowler, C., "Superoxide dismutase and stress tolerance", Annu. Rev. Plant Physiol. Plant Mol. Biol., 43, pp.83~116 (1992)
  10. Breusegem, F., "Effects of overproduction of tobacco MnSOD in maize chloroplasts on foliar tolerance to cold and oxidative stress", J. Exp. Bot., 50, pp.71~78 (1999)
  11. Carlioz, A., "Isolation of superoxide dismutase mutants in Escherichia coli: Is superoxide dismutase necessary for aerobic life?", EMBO J., 5, pp.623~630 (1986)
  12. Chen,C. -N., "Assay of superoxide dismutase activity by combining electrophoresis and densitometry", Bot. Bull.Acad. Sin., 37, pp.107~111 (1996)
  13. Fischer, B., "Isolation, renaturation, and formation of disulfide bonds of eukaryotic proteins expressed in Escherichia coli as inclusion bodies", Biotechnol. Bioeng., 41, pp.3~13 (1993)
  14. Fucci, L., "Inactivation of metabolic enzymes by mixed-function oxidation reaction: possible implication in protein turnover and ageing", Proc. Natl. Acad. Sci. U.S.A., 80, pp.1521~1525 (1983)
  15. Giannopolitis, C. N., "Superoxide dismutase I. Occurrence in higher plants", Plant Physiol, 59, pp.309~314 (1977)
  16. Greenleaf, W. B., "Role of hydrogen bonding in the active site of human manganesesuperoxide dismutase", Biochemistry, 43, pp.7038~7045 (2004)
  17. Halliwell, B., "Free radicals in biology and medicine, Fourth ed.", pp.262~282 (2007), Oxford Unizversity Press
  18. Houot, V., "Hydrogen peroxide induces programmed cell death features in cultured tobacco BY-2 cells, in a dose-dependent manner", J. Exp. Bot., 52, pp.1721~1730 (2001)
  19. Kendall, E. J., "Free radical and freezing injury to cell membranes of winter wheat", Physiol. Plant, 76, pp.86~94 (1989)
  20. Kim, A., "Enhanced expression of mitochondrial superoxide dismutase leads to prolonged in vivo cell cycle progression and up-regulation of mitochondrial thioredoxin, Free", Radic. Biol. Med. (2010)
  21. Laemmli, U. K., "Cleavage of structural proteins during the assembly of the head of bacteriophage T4", Nature, 227, pp.680~685 (1970)
  22. Larkin, M. A., "ClustalW and ClustalX version 2", Bioinformatics, 23, pp.2947~2948 (2007)
  23. Lee, N., "Molecular aspects of ara regulation. in: The Operon, Cold Spring Harbor", Cold Spring Harbor Laboratory, pp.389~410 (1980)
  24. Lee, N., "Arabinose- Induced Binding of AraC Protein to aria Activates the araBAD Operon Promoter", Proc. Natl. Acad. Sci. U.S.A., 84, pp.8814~8818 (1987)
  25. McCord, J. M., "Superoxide dismutase, an enzymic function for Erythrocuprein (Hemocuprein)", J. Biol. Chem., 244, pp.6019~6055 (1969)
  26. McKersie, B. D., "Superoxide dismutase enhances tolerance of freezing stress in transgenic alfalfa (Medicago sativa L.)", Plant Physiol, 103, pp.1155~1163 (1993)
  27. Miao, Z., "Molecular cloning, characterization and expression of Mn-superoxide dismutase from the rubber tree (Hevea brasiliensis)", Plant Mol. Biol., 23, pp.267~277 (1993)
  28. Rubio, M. C., "Expression studies of superoxide dismutases in nodules and leaves of transgenic alfalfa reveal abundance of iron-containing isozymes, posttranslational regulation, and compensation of isozyme activities", Mol. Plant Microbe, 14, pp.1178~1188 (2001)
  29. Rudolph, R., "In vitro folding of inclusion body proteins", FASEB J., 10, pp.49~56 (1996)
  30. Sambrook, J., "Molecular cloning: A laboratory manual, third ed.", Cold Spring Laboratory
  31. Sato, I., "Depolymerization of hyaluronic acid by D-fructose 6-phosphate", Biosci. Biotechnol. Biochem., 57, pp.2005~2009 (1993)
  32. Schrank, I. S., "Functional expression of the yeast Mn-superoxide dismutase gene in Escherichia coli requires deletion of the signal peptide sequence", Gene, 73, pp.121~130 (1988)
  33. Storlie, E. W., "Effect of the Vrn1-Fr1 interval on cold hardiness levels in near isogenic wheat lines", Crop Sci., 38, pp.483~488 (1998)
  34. Streller, S., "Isolation and purification of mitochondrial Mn-superoxide dismutase from the gymnosperm Pinus sylvestris L", Plant Cell Physiol, 35, pp.859~867 (1994)
  35. Wang, Y. C., "Enhanced salt tolerance of transgenic poplar plants expressing a manganese superoxide dismutase from Tamarix androssowii", Mol. Biol. Rep., 37, pp.1119~1124 (2010)
  36. Wilder, M. S., "Composition for preventing or alleviating skin irritation by formulations containing superoxide dismutase", U.S. Patent, 4957(740), pp.1~12 (1990)
  37. Wu, G., "Activation of host defense mechanisms by elevated production of H2O2 in transgenic plants", Plant Physiol, 115, pp.427~435 (1997)
  38. Wu, G., "Isolation, chromosome localization, and differential expression of mitochondrial manganese superoxide dismutase and chloroplastic copper", Zinc superoxide dismutase genes in wheat, 1999, pp.120, 513~520
  39. Xie, Y., "Isolation and identification of a super strong plant promoter from cotton leaf curl Multan virus", Plant Mol. Biol., 53, pp.1~14 (2003)
  40. Zelko, I. N., "Superoxide dismutase multigene family: A comparison of CuZn-SOD (SOD1), Mn-SOD (SOD2), and EC-SOD (SOD3) gene structures, evolution, and expression", Free Radic. Biol. Med., 33, pp.337~349 (2002)
  41. Zhu, D., "Maize mitochondrial manganese superoxide dismutases are encoded by a differentially expressed multigene family", Proc. Natl. Acad. Sci. U.S.A., 90, pp.9310~9314 (1993)

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