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Function Analysis of Organophosphate Pesticides Hydrolase from Pseudomonas stutzeri HS-D36

机译:斯氏假单胞菌HS-D36中有机磷农药水解酶的功能分析

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In this paper, a novel organophosphatedegrading bacterium HS-D36 belonging to Pseudomonas stutzeri was reported. This bacterium has a strong ability to hydrolyze methyl parathion and the organophosphate pesticides hydrolase gene (oph) was cloned for the organophosphate hydrolase (OPH) function analysis. The oph gene was expressed in Escherichia coli BL21 (DE3) by using pET-28 expression system. The activity of the recombinant OPH in crude extracts reached 52.5 U ·ml-1.Thermal stability experiment showed that the enzyme inactivated little for 60 minutes at temperature below 50 °C. Further, the sequence alignment and phylogenetic analysis suggested that the OPH protein from the strain HS-D36 was 99.0% similar to MPD protein from Pseudomonas sp.WBC-3 and may be originated from metallo-β-lactamases family. The protein structure prediction results suggested that the mature OPH comprise two independent subunits, each is composed of an active metal center (Zn2+ and Cd2+).
机译:本文报道了一种新型的降解斯氏假单胞菌的有机磷酸盐降解细菌HS-D36。该细菌具有很强的水解甲基对硫磷的能力,并克隆了有机磷酸酯农药水解酶基因(oph)用于有机磷酸酯水解酶(OPH)功能分析。通过使用pET-28表达系统,oph基因在大肠杆菌BL21(DE3)中表达。重组OPH在粗提物中的活性达到52.5 U·ml-1。热稳定性实验表明,在低于50℃的温度下,酶在60分钟内几乎没有失活。此外,序列比对和系统进化分析表明,HS-D36菌株的OPH蛋白与假单胞菌WBC-3的MPD蛋白有99.0%相似,可能源自金属β-内酰胺酶家族。蛋白质结构预测结果表明,成熟的OPH包含两个独立的亚基,每个亚基由活性金属中心(Zn2 +和Cd2 +)组成。

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