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Characteristics of Parathion Hydrolase by Pseudomonas rhodesiae H5  

Yun Nam Kyung (한남대학교 이과대학 미생물학과)
Park Kyeong Ryang (한남대학교 이과대학 미생물학과)
Publication Information
Korean Journal of Microbiology / v.40, no.3, 2004 , pp. 199-204 More about this Journal
Abstract
The parathion hydrolase (OPH) produced by Pseudomonas rhodesiae H5 was purified by ammonium sulfate precipitation, DEAE-Toyopearl 650M ion exchange chromatography and Sephadex gel filtration chromatography. Parathion hydrolase from crude extracts of P. rhodesiae H5 has two components designated as OPH $I_1$ and OPH $I_2$, Optimum pH and temperature of OPH $I_1$and OPH $I_2$ were pH 7.2 and $30^{\circ}C$, and pH 7.6 and $37^{\circ}C$, respectively. The activation energy of OPH $I_1$ for the hydrolysis of parathion was 3.01 ㎉/I, II, III in the temperature range of $4^{\circ}C$ to $30^{\circ}C$, and Michaelis constant ($K_m$) for parathion was 69.2 ${\mu}M$. The activation energy of OPH $I_2$ for the hydrolysis of parathion was 4.07㎉/㏖ in the temperature range of $4^{\circ}C$ to $37^{\circ}C$, and Michaelis constant for parathion was 150.9${\mu}M$. Furthermore OPH $I_1$ was completely inhibited by 1 mM $Ca^2+$, $Cu^2+$, $Mg^2+$, $Ni^2+$, but OPH $I_2$ was less inhibited than OPH $I_1$ by the metals used in this study.
Keywords
enzyme purification; parathion hydrolase (OPH); Pseudomonas rhodesiae H5;
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1 Attaway, H., J.O. Nilson, A.M. Baya, M.J. Voll, W.E. White, D.J. Grimes, and R.R. Colwell. 1987. Bacterial detoxification of diisopropyl fluorophosphate. Appl. Environ. Microbiol. 53, 1685-1689
2 DeFrank, J.J., W.T. Beudry, T.C. Cheng, S.P. Harvey, A.N. Stroup, and I. Szafranicel.. 1993. Screening of halophilic bacteria and Alteromonas species for organophosphorus hydrolyzing enzyme activity. Chem, Biol. Interact. 87, 141-148
3 Landis, W.G., and J.J. DeFrank. 1990. Enzymatic hydrolysis of toxic organofluorophosphate compounds. Adv. Appl. Biotechnol. Ser. 4, 183-201
4 Liu, L., J. Wu, B. Wang, and D.M. Anderson. 1995. Purification and characterization of an organophosphorus acid hydrolase from Alteromonas haloplanktis C and Alteromonas sp. M. P. 12, In international workshop on biocatalytic degradation of chemical warfare related materials. U. S. Army, ERDEC, Averdeen Proving Ground, MD
5 Mazur, A. 1946. An enzyme in animal tissue capable of hydrolyzing the phosphorus-fluorine bond of alkyl fluorophosphates. J. Biol. Chem. 164, 271-289
6 Harper, L.L., C.S. McDaniel, C.E. Miller, and J.R. Wild. 1988. Dissimilar plasmid isolated from Pseudomonas diminuta MG and a Flavobacterium sp. (ATCC 27551) contain identical opd genes. Appl. Environ. Microbiol. 44, 246-249
7 Hoskin, F.C.G., and R.D. Prusch. 1983. Characterization of a DFPhydrolyzing enzyme on squid posterior salivary gland by use of Soman, DFP and manganous ion. Comp. Biochem. Physiol. 75, 17-20
8 Yun, N.K., and K.R. Park. 2004. Characteristics of the parathion degrading Pseudomonas rhodesiae H5. J. Life Sci. 14, 582-588
9 McDaniel, C.S., L.L. Harper, and J.R. Wild. 1989. Cloning and sequencing of a plasmid-borne gene(opd) encoding phospho-triesterase. J. Bacteriol. 170, 2306-2311
10 Serdar, C.M., D.T. Murdock, and M.F. Rohde. 1989. Parathion hydrolase gene from Pseudomonas diminuta MG: subcloning, compete nucleotide sequence, and expression of the mature portion of the enzyme in Escherichia coli. Bio/Technology 7, 1151- 1155
11 Munnecke, D.M., and D.P.H. Hsieh. 1976. Pathways of microbial metabolism of parathion. Appl. Environ. Microbiol. 31, 63-69
12 Dumas, D.P., H.D. Drust, W.G. Landis, F.M. Raushel, and J.R. Wild. 1990. Inactivation of orgarnophosphorus nerve agents by the phosphotriesterase from Pseudomonas diminuta. Arch. Biochem. Biophys. 277, 155-159   DOI   ScienceOn
13 Koelle. G.B. 1975. Anticholinesterase agents. The Pharmacological basic of therapeutics, 5th ed., p. 445. Macmilan, New York
14 Walter, W.M., and J.S. Karns. 1989. Purification and chracterization of three parathion hydrolases from Gram-negative bacterial strains. Appl. Environ. Microbiol. 55, 289-293
15 DeFrank, J.J., and T.C. Cheng. 1991. Purification and properties of an organophosphorus acid anhydrolase from a halophilic bacterial isolate. J. Bacteriol. 173, 1938-1943
16 Kim, S.C., and N.T. Lee. 1999. Test of degradation of soman and sarin gas by organophosphorus acid anhydrolases and applicability of the enzyme to the development of nerve agent decontaminant 한국군사 과학기술학회지 2, 140-147
17 Mounter, L.A. 1963. Metabolism of organophosphorus anticholinesterase agenets, p. 486-504. In G.B. Kolle (ed.), Hanbuch de experimentellen pharmakologie: Cholinesterases and anticholinesterase agents. Springer-Verlag, Berlin
18 Bradford, M.M. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the priciple of protein-dye binding. Anal. Biochem. 72, 248-254
19 Mulbry, W., and J.S. Karns. 1989. Parathion hydrolase specified by the Flavobacterium opd gene: relationship between the gene and protein. J. Bacteriol. 171, 6740-6746
20 Serdar, C.M., and D.T. Gibson. 1985. Enzymatic hydrolysis of organophosphates: cloning and expression of a parathion hydrolase gene from Pseudomonas diminuta. Bio/Technology 3, 567- 571
21 Mulbry, W., J.S. Karns, P.C. Kearney, J.O. Nelson, C.S. McDaniel, and J. R. Wild. 1986. Identification of a plasmid-borne parathion hydrolase gene from Flavobacterium sp. by southern hybridization with opd from Pseudomonas diminuta. Appl. Environ. Microbiol. 51, 926-930
22 Cheng, T.C., S.P .Harvey, and A.N. Stroup. 1993. Purification and properties of a highly active organophosphorus cid anhydrase from Alteromonas undina. Appl. Environ. Microbiol. 59, 3138- 3150