Evolution of the Catalytic Activity of<i>Arabidopsis thaliana</i>Glutathione Transferase Zeta Class-1 by Saturation Mutagenesis
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- CHEN Defu
- Laboratory of Molecular Genetics, College of Life Sciences, Nankai University
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- LIU Jia
- Department of Chemistry and Biochemistry, University of Maryland
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- LIU Jian
- Laboratory of Molecular Genetics, College of Life Sciences, Nankai University
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- CHEN Xiwen
- Laboratory of Molecular Genetics, College of Life Sciences, Nankai University
書誌事項
- タイトル別名
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- Evolution of the Catalytic Activity of Arabidopsis thaliana Glutathione Transferase Zeta Class-1 by Saturation Mutagenesis
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Saturation mutagenesis was performed on three non-catalytic residues, Asn71, Leu108, and Gly177, in and near the active site of Arabidopsis thaliana GSTZ-1 (AtGSTZ-1). Forty unique mutants with more than 10% activity increases, were obtained. Of these, 12 resulted in large activity improvement and were purified for further characterization. Remarkably, 11 of them contained mutations at Leu108, suggesting that Leu108 plays an important role in dichloroacetic acid-dechlorinating (DCA-DC) activity. Kinetic analysis revealed that multiple mutations at these residues increased kcat/Km toward DCA and GSH by as much as 2.2- and 5.8-fold, respectively. Since the catalytic residues were not involved in mutagenesis, the activity enhancements were presumably due to structural change in the active site rather than to a change in catalysis. Our results also suggest that the specific shape of the active site in AtGSTZ-1 is essential to its unique DCA-DC activity.
収録刊行物
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- Bioscience, Biotechnology, and Biochemistry
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Bioscience, Biotechnology, and Biochemistry 74 (7), 1458-1461, 2010
公益社団法人 日本農芸化学会
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詳細情報 詳細情報について
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- CRID
- 1390282681456228864
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- NII論文ID
- 10027557461
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- NII書誌ID
- AA10824164
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- ISSN
- 13476947
- 09168451
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- NDL書誌ID
- 10766704
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
- Crossref
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- 抄録ライセンスフラグ
- 使用不可