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Cloning and characterization of a pyrethroid pesticide decomposing esterase gene, Est3385, from Rhodopseudomonas palustris PSB-S

文献类型： 外文期刊

作者： Luo, Xiangwen 1 ; Zhang, Deyong 1 ; Zhou, Xuguo 2 ; Du, Jiao 1 ; Zhang, Songhai 1 ; Liu, Yong 1 ;

作者机构： 1.Hunan Acad Agr Sci, Hunan Plant Protect Inst, Key Lab Pest Management Hort Crop Hunan Prov, Changsha 410125, Hunan, Peoples R China

2.Univ Kentucky, Dept Entomol, Lexington, KY 40546 USA

期刊名称：SCIENTIFIC REPORTS （ 影响因子：4.379； 五年影响因子：5.133 ）

ISSN： 2045-2322

年卷期： 2018 年 8 卷

页码：

收录情况： SCI

摘要： Full length open reading frame of pyrethroid detoxification gene, Est3385, contains 963 nucleotides. This gene was identified and cloned based on the genome sequence of Rhodopseudomonas palustris PSB-S available at the GneBank. The predicted amino acid sequence of Est3385 shared moderate identities (30-46%) with the known homologous esterases. Phylogenetic analysis revealed that Est3385 was a member in the esterase family I. Recombinant Est3385 was heterologous expressed in E. coli, purified and characterized for its substrate specificity, kinetics and stability under various conditions. The optimal temperature and pH for Est3385 were 35 degrees C and 6.0, respectively. This enzyme could detoxify various pyrethroid pesticides and degrade the optimal substrate fenpropathrin with a Km and Vmax value of 0.734 +/- 0.013 mmol.l(-1) and 0.918 +/- 0.025 U.mu g(-1), respectively. No cofactor was found to affect Est3385 activity but substantial reduction of enzymatic activity was observed when metal ions were applied. Taken together, a new pyrethroid degradation esterase was identified and characterized. Modification of Est3385 with protein engineering toolsets should enhance its potential for field application to reduce the pesticide residue from agroecosystems.

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