Catalytic mechanism of the haloalkane dehalogenase LinB from Sphingomonas paucimobilis UT26

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Authors

PROKOP Zbyněk MONINCOVÁ Marta CHALOUPKOVÁ Radka KLVAŇA Martin NAGATA Yuji JANSSEN Dick B. DAMBORSKÝ Jiří

Year of publication 2003
Type Article in Periodical
Magazine / Source Journal of Biological Chemistry
MU Faculty or unit

Faculty of Science

Citation
Web http://ncbr.chemi.muni.cz/~jiri/abstracts/jbc03b.html
Field Biochemistry
Keywords ENZYME; KINETICS; MECHANISM; LINB; HALOALKANE DEHALOGENASE
Description Haloalkane dehalogenases are bacterial enzymes capable of carbon-halogen bond cleavage in halogenated compounds. To obtain insight in the mechanism of the haloalkane dehalogenase from Sphingomonas paucimobilis UT26 (LinB), we studied the steady-state and pre-steady-state kinetics of the conversion of the substrates 1-chlorohexane, chlorocyclohexane and bromocyclohexane. The results lead to a proposal of a minimal kinetic mechanism consisting of three main steps: (i) substrate binding, (ii) cleavage of the carbon-halogen bond with simultaneous formation of an alkyl-enzyme intermediate and (iii) hydrolysis of the alkyl-enzyme intermediate. Release of both products, halide and alcohol, is a fast process that was not included in reaction mechanism as a distinct step. Comparison of the kinetic mechanism of LinB with that of haloalkane dehalogenase DhlA from Xantobacter autotrophicus GJ10 and the haloalkane dehalogenase DhaA from Rhodococcus rhodochrous NCIMB 13064 shows that the overall mechanisms are similar. The main difference is in the rate-limiting step, which is hydrolysis of the alkyl-enzyme intermediate in LinB, halide release in DhlA, and liberation of an alcohol in DhaA. The occurrence of different rate-limiting steps for three enzymes that belong to the same protein family indicates that extrapolation of this important catalytic property from one enzyme to another can be misleading even for evolutionary closely related proteins. The differences in the rate-limiting step were related to: (i) a number and size of the entrance tunnels, (ii) protein flexibility and (iii) composition of the halide-stabilizing active site residues based on comparison of protein structures.
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