Skip to main content
Log in

Purification, regulation and cloning of a glutathione transferase (GST) from maize resembling the auxin-inducible type-III GSTs

  • Published:
Plant Molecular Biology Aims and scope Submit manuscript

Abstract

The glutathione transferases (GSTs) from maize (Zea mays L.) with activities toward the chloroacetanilide herbicide metolachlor and the diphenyl ether herbicide fluorodifen were fractionated into two pools based on binding to affinity columns. Pool 1 GSTs were retained on Orange A agarose and were identified as isoenzymes Zea mays (Zm) GST I-I, Zm GST I-II and Zm GST I-III, which have been described previously. Pool 2 GSTs selectively bound to S-hexyl-glutathione-Sepharose and were distinct from the pool 1 GSTs, being composed of a homodimer of 28.5 kDa subunits, termed Zm GST V-V, and a heterodimer of the 28.5 kDa polypeptide and a 27.5 kDa subunit, termed Zm GST V-VI. Using an antibody raised to Zm GST V-VI, a cDNA expression library was screened and a Zm GST V clone identified showing sequence similarity to the type-III auxin-inducible GSTs previously identified in tobacco and other dicotyledenous species. Recombinant Zm GST V-V showed high GST activity towards the diphenyl ether herbicide fluorodifen, detoxified toxic alkenal derivatives and reduced organic hydroperoxides. Antibodies raised to Zm GST I-II and Zm GST V-VI were used to monitor the expression of GST subunits in maize seedlings. Over a 24 h period the Zm GST I subunit was unresponsive to chemical treatment, while expression of Zm GST II was enhanced by auxins, herbicides, the herbicide safener dichlormid and glutathione. The Zm GST V subunit was more selective in its induction, only accumulating significantly in response to dichlormid treatment. During development Zm GST I and Zm GST V were expressed more in roots than in shoots, with Zm GST II expression limited to the roots.

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

References

  1. Bollag DM, Edelstein SJ: Protein Methods. Wiley-Liss, New York (1991).

    Google Scholar 

  2. Cleveland DW, Fischer SG, Kirschner MW, Laemmli UK: Peptide mapping by limited proteolysis in sodium dodecyl sulfate and analysis by gel electrophoresis. J Biol Chem 252: 1102–1106 (1977).

    PubMed  Google Scholar 

  3. Dean JV, Devarenne TP: Peroxidase-mediated conjugation of glutathione to unsaturated phenylpropanoids. Evidence against glutathione S-transferase involvement. Physiol Plant 99: 271–278 (1997).

    Google Scholar 

  4. Dean JV, Devarenne TP, Lee I-S, Orlofsky LE: Properties of a maize glutathione S-transferase that conjugates coumaric acid and other phenylpropanoids. Plant Physiol 108: 985–994 (1995).

    PubMed  Google Scholar 

  5. Dixon D, Cole DJ, Edwards R: Characterisation of multiple glutathione transferases containing the GST I subunit with activities toward herbicide substrates in maize (Zea mays). Pestic Sci 50: 72–82 (1997).

    Google Scholar 

  6. Droog F: Plant glutathione S-transferases, a tale of theta and tau. J Plant Growth Regul 16: 95–107 (1997).

    Google Scholar 

  7. Droog FNJ, Hooykaas PJJ, Libbenga KR, van der Zaal, EJ: Proteins encoded by an auxin-regulated gene family of tobacco share limited but significant homology with glutathione Stransferases and one member indeed shows in vitro GST activity. Plant Mol Biol 21: 965–972 (1993).

    Article  PubMed  Google Scholar 

  8. Droog FNJ, Hooykaas PJJ, van der Zaal BJ: 2,4-Dichlorophenoxyacetic acid and related chlorinated compounds inhibit two auxin-regulated type-III tobacco glutathione S-transferases. Plant Physiol 107: 1139–1146 (1995).

    PubMed  Google Scholar 

  9. Edwards R: Characterization of glutathione transferases and glutathione peroxidases in pea (Pisum sativum). Physiol Plant 98: 594–604 (1996).

    Google Scholar 

  10. Farago S, Brunold C, Kreuz K: Herbicide safeners and glutathione metabolism. Physiol Plant 91: 537–542 (1994).

    Google Scholar 

  11. Fuerst EP, Irzyk GP, Miller KD: Partial characterization of glutathione S-transferase isozymes induced by the herbicide safener benoxacor in maize. Plant Physiol 102: 795–802 (1993).

    PubMed  Google Scholar 

  12. Graff G, Anderson LA, Jaques LW: Preparation and purification of soybean lipoxygenase-derived unsaturated hydroperoxy and hydroxy fatty acids and determination of molar absorptivities of hydroxy fatty acids. Anal Biochem 188: 38–47 (1990).

    Google Scholar 

  13. Guddewar MB, Dauterman WC: Purification and properties of a glutathione S-transferase from corn which conjugates striazine herbicides. Phytochemistry 18: 735–740 (1979).

    Google Scholar 

  14. Harlow E, Lane D: Antibodies: A Laboratory Manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY (1988).

    Google Scholar 

  15. Hatton PJ, Dixon D, Cole DJ, Edwards R: Glutathione transferase activities and herbicide selectivity in maize and associated weed species. Pestic Sci 46: 267–275 (1996).

    Google Scholar 

  16. Holt DC, Lay VJ, Clarke ED, Dinsmore A, Jepson, I, Bright SWJ, Greenland AJ: Characterization of the safener-induced glutathione S-transferase isoform II from maize. Planta 196: 295–302 (1995).

    PubMed  Google Scholar 

  17. Irzyk G, Potter S, Ward E, Fuerst EP: A cDNA clone encoding the 27-kilodalton subunits of glutathione S-transferase IV from Zea mays. Plant Physiol 107: 311–312 (1995).

    PubMed  Google Scholar 

  18. Irzyk GP, Fuerst EP: Purification and characterization of a glutathione S-transferase from benoxacor-treated maize (Zea mays). Plant Physiol 102: 803–810 (1993).

    PubMed  Google Scholar 

  19. Jakoby WB, Ketterer B, Mannervik B: Glutathione transferases: nomenclature. Biochem Pharmacol 33: 2539–2540 (1984).

    PubMed  Google Scholar 

  20. Jepson I, Lay VJ, Holt DC, Bright SWJ, Greenland AJ: Cloning and characterization of maize herbicide safener-induced cDNAs encoding subunits of glutathione S-transferase isoforms I, II and IV. Plant Mol Biol 26: 1855–1866 (1994).

    PubMed  Google Scholar 

  21. Kolm RH, Danielson UH, Zhang Y, Talalay P, Mannervik B: Isothiocyanates as substrates for human glutathione transferases: structure-activity studies. Biochem J 311: 453–459 (1995).

    PubMed  Google Scholar 

  22. Laemmli UK: Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227: 680–685 (1970).

    PubMed  Google Scholar 

  23. Marrs KA: The functions and regulation of glutathione Stransferases in plants. Annu Rev Plant Physiol Plant Mol Biol 47: 127–158 (1996).

    PubMed  Google Scholar 

  24. Marrs KA, Alfenito MR, Lloyd AM, Walbot V: A glutathione S-transferase involved in vacuolar transfer encoded by the maize gene Bronze-2. Nature 375: 397–400 (1995).

    Article  PubMed  Google Scholar 

  25. O'Connell KM, Breaux EJ, Fraley RT: Different rates of metabolism of two chloroacetanilide herbicides in Pioneer 3320 corn. Plant Physiol 86: 359–363 (1988).

    Google Scholar 

  26. Rossini L, Jepson I, Greenland AJ, Sari Gorla M: Characterization of glutathione S-transferase isoforms in three maize inbred lines exhibiting differential sensitivity to alachlor. Plant Physiol 112: 1595–1600 (1996).

    PubMed  Google Scholar 

  27. Rossini L, Pé ME, Frova C, Hein K, Sari-Gorla M: Molecular analysis andmapping of two genes encoding maize glutathione S-transferases (GST I and GST II). Mol Gen Genet 248: 535–539 (1995).

    PubMed  Google Scholar 

  28. Sambrook J, Fritch EF, Maniatis T: Molecular Cloning: A Laboratory Manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY (1989).

    Google Scholar 

  29. Takahashi Y, Nagata T: parB: An auxin-regulated gene encoding glutathione S-transferase. Proc Natl Acad Sci USA 89: 56–59 (1992).

    PubMed  Google Scholar 

  30. Timmerman KP: Molecular characterization of corn glutathione S-transferase isozymes involved in herbicide detoxication. Physiol Plant 77: 465–471 (1989).

    Google Scholar 

  31. Wendel A: Glutathione peroxidase. Meth Enzymol 77: 325–333 (1981).

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Dixon, D.P., Cole, D.J. & Edwards, R. Purification, regulation and cloning of a glutathione transferase (GST) from maize resembling the auxin-inducible type-III GSTs. Plant Mol Biol 36, 75–87 (1998). https://doi.org/10.1023/A:1005958711207

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1005958711207

Navigation