Abstract

Two glutathione S-transferase (GST) cDNAs, GSTD2 and GSTS2, were cloned from the silkworm Bombyx mori. The B. mori GSTD2 (BmGSTD2) gene spans 4371 bp and consists of four introns and five exons that encode 222 amino acid residues. The deduced amino acid sequence of BmGSTD2 showed 58% protein sequence identity to the Delta-class GST of Maduca sexta. The B. mori GSTS2 (BmGSTS2) gene spans 3470 bp and consists of three introns and four exons that encode 206 amino acid residues. The deduced amino acid sequence of BmGSTS2 revealed 67%, 63%, and 61% protein sequence identities to the Sigma-class GSTs from B. mori, Platynota idaeusalis, and M. sexta, respectively. The BmGSTD2 and BmGSTS2 cDNAs were expressed as 25 kDa and 23 kDa polypeptides, respectively, in baculovirus-infected insect Sf9 cells. Northern blot and Western blot analyses showed that BmGSTD2 and BmGSTS2 were specifically expressed in three gut regions, indicating that the gut is the prime site for BmGSTD2 and BmGSTS2 synthesis in B. mori larvae.

Highlights

  • Glutathione S-transferases (GSTs, EC 2.5.1.18) are detoxification enzymes that catalyze the conjugation of electrophilic compounds with the thiol group of reduced glutathione (GSH)

  • This paper describes the cloning of two novel genes encoding a Delta-class glutathione S-transferase (GST) (BmGSTD2) and a Sigma-class GST (BmGSTS2) from B. mori

  • The clone containing the cDNA insert was selected from expressed sequence tags (ESTs), which were generated from a cDNA library constructed using whole bodies of B. mori larvae (Kim et al, 2003)

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Summary

Introduction

Glutathione S-transferases (GSTs, EC 2.5.1.18) are detoxification enzymes that catalyze the conjugation of electrophilic compounds with the thiol group of reduced glutathione (GSH). This paper describes the cloning of two novel genes encoding a Delta-class GST (BmGSTD2) and a Sigma-class GST (BmGSTS2) from B. mori. We cloned and sequenced the cDNAs and genomic DNAs of two novel GSTs of B. mori larvae, and expressed the recombinant GSTs in baculovirus-infected insect cells.

Results
Conclusion

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