1. Ether cleaving methyltransferases of the strict anaerobe Acetobacterium dehalogenans: controlling the substrate spectrum by genetic engineering of the N-terminus.
- Author
-
Kreher S, Studenik S, and Diekert G
- Subjects
- Acetobacterium genetics, Anisoles metabolism, Bacterial Proteins genetics, Bacterial Proteins metabolism, Cloning, Molecular, Gene Deletion, Methyltransferases genetics, Oxidoreductases, O-Demethylating genetics, Recombinant Proteins genetics, Recombinant Proteins metabolism, Substrate Specificity, Vanillic Acid metabolism, Acetobacterium enzymology, Methyltransferases metabolism, Oxidoreductases, O-Demethylating metabolism
- Abstract
The anaerobic cleavage of ether bonds of methoxylated substrates such as vanillate or veratrol in acetogenic bacteria is mediated by multi-component enzyme systems, the O-demethylases. Acetobacterium dehalogenans harbours different inducible O-demethylases with various substrate spectra. Two of these enzyme systems, the vanillate- and the veratrol-O-demethylases, have been characterized so far. One component of this enzyme system, the methyltransferase I (MT I), catalyses the cleavage of the substrate ether bond and the subsequent transfer of the methyl group to a corrinoid protein. For the C-termini of the methyltransferases I of the vanillate- and the veratrol-O-demethylases, a TIM barrel structure of the enzymes was predicted, whereas the N-termini are not part of this conserved structure. The deletion of the N-terminal regions led to a significant increase of activity (up to 20-fold) and an extended substrate spectrum of the mutants, which also comprised non-aromatic compounds such as the thioether methionine and diethylether. The exchange of the N-termini of the two methyltransferases I resulted in chimeric enzymes whose substrate specificities were those of the enzymes from which the N-termini were derived. This demonstrated the crucial role of the N-termini for the substrate specificity of the methyltransferases., (© 2010 Blackwell Publishing Ltd.)
- Published
- 2010
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