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Cloning of a rice tau class GST isozyme and characterization of its substrate specificity

Authors
Cho, Hyun-YoungYoo, Sun-YoungKong, Kwang-Hoon
Issue Date
Oct-2006
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
glutathione S-transferase; herbicide activity; Oryza sativa GST; rice; tau class GST
Citation
PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, v.86, no.2, pp 110 - 115
Pages
6
Journal Title
PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY
Volume
86
Number
2
Start Page
110
End Page
115
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/24263
DOI
10.1016/j.pestbp.2006.02.003
ISSN
0048-3575
1095-9939
Abstract
The GST cDNA was successfully cloned from an Oryza sativa cDNA library by PCR using oligonucleotide primers based on the OsGSTU5 (GenBank Accession No. AF309377) sequence. The cDNA was composed of a 687-bp open reading frame encoding for 228 amino acids. The deduced amino acid sequence of this gene shared over 60% sequence identity with the sequences of the tau class ZmGSTU6 and ZmGSTU19. This gene was expressed in Escherichia coli with the pET vector system and the gene product was purified to homogeneity by GSH-Sepharose affinity column chromatography. The expressed OsGSTU5 formed a homo-dimer composed of 25 kDa subunit and its pI value was approximately 7.5. The OsGSTU5 displays high activities towards 1-chloro-2,4-dinitrobenzene and 1,2-epoxy-3-(p-nitrophenoxy)propane. The activity of the OsGSTU5 was significantly inhibited by hematin and ethacrynic acid. The OsGSTU5 shows the highest activity towards chloro-s-triazine and acetanilide herbicides. (c) 2006 Elsevier Inc. All rights reserved.
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Kong, Kwang-Hoon
자연과학대학 (화학과)
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