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Title: Catalytic mechanism of dichloromethane dehalogenase from Methylophilus sp. strain DM11.

Authors: Stourman, Nina V; Rose, James H; Vuilleumier, Stephane; Armstrong, Richard N

Published In Biochemistry, (2003 Sep 23)

Abstract: The glutathione (GSH)-dependent dichloromethane dehalogenase from Methylophilus sp. strain DM11 catalyzes the dechlorination of CH(2)Cl(2) to formaldehyde via a highly reactive, genotoxic intermediate, S-(chloromethyl)glutathione (GS-CH(2)Cl). The catalytic mechanism of the enzyme toward a series of dihalomethane and monohaloethane substrates suggests that the initial addition of GSH to the alkylhalides is fast and that the rate-limiting step in turnover is the release of either the peptide product or formaldehyde. With the exception of CH(2)ClF, which forms a relatively stable GS-CH(2)F intermediate, the turnover numbers for a series of dihalomethanes fall in a very narrow range (1-3 s(-1)). The pre-steady-state kinetics of the DM11-catalyzed addition of GSH to CH(3)CH(2)Br exhibits a burst of S-(ethyl)-glutathione (k(b) = 96 +/- 56 s(-1)) followed by a steady state with k(cat) = 0.13 +/- 0.01 s(-1). The turnover numbers for CH(3)CH(2)Cl, CH(3)CH(2)Br, and CH(3)CH(2)I are identical, indicating a common rate-limiting step. The turnover numbers of the enzyme with CH(3)CH(2)Br and CH(3)CH(2)I are dependent on viscosity and are very close to the measured off-rate of GSEt. The turnover number with CH(2)I(2) is also dependent on viscosity, suggesting that a diffusive step is rate-limiting with dihaloalkanes as well. The rate constants for solvolysis of CH(3)SCH(2)Cl, a model for GS-CH(2)Cl, range between 1 s(-1) (1:1 dioxane/water) and 64 s(-1) (1:10 dioxane/water). Solvolysis of the S-(halomethyl)glutathione intermediates may also occur in the active site of the enzyme preventing the release of the genotoxic species. Together, the results indicate that dissociation of the GS-CH(2)X or GS-CH(2)OH intermediates from the enzyme may be a relatively rare event.

PubMed ID: 12974641 Exiting the NIEHS site

MeSH Terms: Binding Sites; Catalysis; Diffusion; Dose-Response Relationship, Drug; Escherichia coli/metabolism; Formaldehyde/chemistry; Glutathione/chemistry; Glutathione/metabolism; Hydrogen-Ion Concentration; Iodides/chemistry; Kinetics; Lyases/chemistry*; Methylophilus/enzymology*; Microscopy, Fluorescence; Models, Chemical; Protein Binding; Pseudomonas putida/metabolism; Research Support, U.S. Gov't, P.H.S.; Time Factors; Viscosity

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