Abstract
Although reductive dehalogenation by anaerobic microorganisms offers great potential for the degradation of halocarbons, little is known about the biochemical mechanisms involved. It has previously been demonstrated that the dehalogenase activity involved in 3-chlorobenzoate dehalogenation by Desulfomonile tiedjei DCB-1 is present in the membrane fraction of the cell extracts. We report herein the purification of a 3-chlorobenzoate-reductive dehalogenase from the cytoplasmic membrane of D. tiedjei DCB-1. The dehalogenase activity was monitored by the conversion of 3-chlorobenzoate to benzoate with reduced methyl viologen as a reducing agent. The membrane fraction of the cell extracts was obtained by ultracentrifugation, and the membrane proteins were solubilized with either the detergent CHAPS (3-[(3-cholamidopropyl)-dimethyl-ammonio]-1-propanesulfonate) or Triton X-100 in the presence of glycerol. The solubilized dehalogenase was purified by ammonium sulfate fractionation and a combination of anion exchange, hydroxyapatite, and hydrophobic interaction chromatographies. This procedure yielded about 7% of the total dehalogenase activity with a 120-fold increase in specific activity. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis showed that the purified dehalogenase consisted of two subunits with molecular weights of 64,000 and 37,000. The enzyme converted 3-chlorobenzoate to benzoate at its highest specific activity in 10 mM potassium phosphate buffer (pH 7.2) at 38 degrees C. The enzyme was yellow and probably a heme protein. The enzyme had an adsorbance peak at 408 nm. The dithionite-reduced enzyme displayed absorbance peaks at 416, 522, and 550 nm. The dithionite-reduced enzyme was able to complex with carbon monoxide. The nature of the heme chromophore is currently unknown.
Full Text
The Full Text of this article is available as a PDF (204.3 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Ahring B. K., Christiansen N., Mathrani I., Hendriksen H. V., Macario A. J., Conway de Macario E. Introduction of a de novo bioremediation ability, aryl reductive dechlorination, into anaerobic granular sludge by inoculation of sludge with Desulfomonile tiedjei. Appl Environ Microbiol. 1992 Nov;58(11):3677–3682. doi: 10.1128/aem.58.11.3677-3682.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Balajee S., Mahadevan A. Dissimilation of 2,4-dichlorophenoxyacetic acid by Azotobacter chroococcum. Xenobiotica. 1990 Jun;20(6):607–617. doi: 10.3109/00498259009046876. [DOI] [PubMed] [Google Scholar]
- Castro C. E., Wade R. S., Belser N. O. Biodehalogenation: reactions of cytochrome P-450 with polyhalomethanes. Biochemistry. 1985 Jan 1;24(1):204–210. doi: 10.1021/bi00322a029. [DOI] [PubMed] [Google Scholar]
- DeWeerd K. A., Concannon F., Suflita J. M. Relationship between hydrogen consumption, dehalogenation, and the reduction of sulfur oxyanions by Desulfomonile tiedjei. Appl Environ Microbiol. 1991 Jul;57(7):1929–1934. doi: 10.1128/aem.57.7.1929-1934.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Deweerd K. A., Suflita J. M. Anaerobic Aryl Reductive Dehalogenation of Halobenzoates by Cell Extracts of "Desulfomonile tiedjei". Appl Environ Microbiol. 1990 Oct;56(10):2999–3005. doi: 10.1128/aem.56.10.2999-3005.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dolfing J. Reductive dechlorination of 3-chlorobenzoate is coupled to ATP production and growth in an anaerobic bacterium, strain DCB-1. Arch Microbiol. 1990;153(3):264–266. doi: 10.1007/BF00249079. [DOI] [PubMed] [Google Scholar]
- Fetzner S., Lingens F. Bacterial dehalogenases: biochemistry, genetics, and biotechnological applications. Microbiol Rev. 1994 Dec;58(4):641–685. doi: 10.1128/mr.58.4.641-685.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
- Linkfield T. G., Tiedje J. M. Characterization of the requirements and substrates for reductive dehalogenation by strain DCB-1. J Ind Microbiol. 1990 Jan;5(1):9–15. doi: 10.1007/BF01569601. [DOI] [PubMed] [Google Scholar]
- Madsen T., Licht D. Isolation and characterization of an anaerobic chlorophenol-transforming bacterium. Appl Environ Microbiol. 1992 Sep;58(9):2874–2878. doi: 10.1128/aem.58.9.2874-2878.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Miller T. L., Wolin M. J. A serum bottle modification of the Hungate technique for cultivating obligate anaerobes. Appl Microbiol. 1974 May;27(5):985–987. doi: 10.1128/am.27.5.985-987.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mohn W. W., Kennedy K. J. Reductive dehalogenation of chlorophenols by Desulfomonile tiedjei DCB-1. Appl Environ Microbiol. 1992 Apr;58(4):1367–1370. doi: 10.1128/aem.58.4.1367-1370.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mohn W. W., Tiedje J. M. Catabolic thiosulfate disproportionation and carbon dioxide reduction in strain DCB-1, a reductively dechlorinating anaerobe. J Bacteriol. 1990 Apr;172(4):2065–2070. doi: 10.1128/jb.172.4.2065-2070.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mohn W. W., Tiedje J. M. Microbial reductive dehalogenation. Microbiol Rev. 1992 Sep;56(3):482–507. doi: 10.1128/mr.56.3.482-507.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mohn W. W., Tiedje J. M. Strain DCB-1 conserves energy for growth from reductive dechlorination coupled to formate oxidation. Arch Microbiol. 1990;153(3):267–271. doi: 10.1007/BF00249080. [DOI] [PubMed] [Google Scholar]
- Neumann A., Scholz-Muramatsu H., Diekert G. Tetrachloroethene metabolism of Dehalospirillum multivorans. Arch Microbiol. 1994;162(4):295–301. doi: 10.1007/BF00301854. [DOI] [PubMed] [Google Scholar]
- Picardal F. W., Arnold R. G., Couch H., Little A. M., Smith M. E. Involvement of cytochromes in the anaerobic biotransformation of tetrachloromethane by Shewanella putrefaciens 200. Appl Environ Microbiol. 1993 Nov;59(11):3763–3770. doi: 10.1128/aem.59.11.3763-3770.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shelton D. R., Tiedje J. M. Isolation and partial characterization of bacteria in an anaerobic consortium that mineralizes 3-chlorobenzoic Acid. Appl Environ Microbiol. 1984 Oct;48(4):840–848. doi: 10.1128/aem.48.4.840-848.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stevens T. O., Linkfield T. G., Tiedje J. M. Physiological characterization of strain DCB-1, a unique dehalogenating sulfidogenic bacterium. Appl Environ Microbiol. 1988 Dec;54(12):2938–2943. doi: 10.1128/aem.54.12.2938-2943.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Suflita J. M., Horowitz A., Shelton D. R., Tiedje J. M. Dehalogenation: a novel pathway for the anaerobic biodegradation of haloaromatic compounds. Science. 1982 Dec 10;218(4577):1115–1117. doi: 10.1126/science.218.4577.1115. [DOI] [PubMed] [Google Scholar]
- Utkin I., Woese C., Wiegel J. Isolation and characterization of Desulfitobacterium dehalogenans gen. nov., sp. nov., an anaerobic bacterium which reductively dechlorinates chlorophenolic compounds. Int J Syst Bacteriol. 1994 Oct;44(4):612–619. doi: 10.1099/00207713-44-4-612. [DOI] [PubMed] [Google Scholar]
- Xun L., Orser C. S. Purification and properties of pentachlorophenol hydroxylase, a flavoprotein from Flavobacterium sp. strain ATCC 39723. J Bacteriol. 1991 Jul;173(14):4447–4453. doi: 10.1128/jb.173.14.4447-4453.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Xun L., Topp E., Orser C. S. Purification and characterization of a tetrachloro-p-hydroquinone reductive dehalogenase from a Flavobacterium sp. J Bacteriol. 1992 Dec;174(24):8003–8007. doi: 10.1128/jb.174.24.8003-8007.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zehnder A. J., Wuhrmann K. Titanium (III) citrate as a nontoxic oxidation-reduction buffering system for the culture of obligate anaerobes. Science. 1976 Dec 10;194(4270):1165–1166. doi: 10.1126/science.793008. [DOI] [PubMed] [Google Scholar]
- van den Tweel W. J., Kok J. B., de Bont J. A. Reductive dechlorination of 2,4-dichlorobenzoate to 4-chlorobenzoate and hydrolytic dehalogenation of 4-chloro-, 4-bromo-, and 4-iodobenzoate by Alcaligenes denitrificans NTB-1. Appl Environ Microbiol. 1987 Apr;53(4):810–815. doi: 10.1128/aem.53.4.810-815.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]