Function analysis of organophosphate pesticides hydrolase from Pseudomonas stutzeri HS-D36

3rd International Conference on Bioinformatics and Biomedical Engineering, iCBBE 2009(2009)

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摘要
In this paper, a novel organophosphate-degrading 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°. 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 (Zn 2+ and Cd2+). ©2009 IEEE.
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degradation characteristics,oph protein structure,organophosphate pesticides hydrolase,sequence alignment,thermal stability,biotechnology,stability analysis,hydrolysis,molecular biophysics,strain,dna,microorganisms,protein structure,bacterium,biochemistry,production,proteins,cloning,genetic engineering,enzymes,agrochemicals,pesticides,protein structure prediction,temperature,degradation,escherichia coli,pest control,enzyme,functional analysis
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