Depending on the growth substrate, different O-demethylases are induced in Acetobacterium dehalogenans. A vanillate- and a veratrol-O-demethylase of this organism have been described earlier. The methyltransferase I (MT I), a component of this enzyme system, catalyzes the ether cleavage and the transfer of the methyl group to a super-reduced corrinoid bound to a protein. GKT137831 manufacturer The MT I of the vanillate- and veratrol-O-demethylase (MT Ivan and MT Iver) were found to be zinc-containing enzymes. By site-directed mutagenesis, putative zinc ligands were identified, from which the following unique zinc-binding motifs were derived: E-X14-E-X20-H for MT Ivan and D-X27-C-X39-C for MT Iver. Phenyl

methyl ethers are natural components of lignin and are formed upon lignin degradation by fungi. The methyl groups of the phenyl methyl ethers can be utilized as growth this website substrates by different acetogenic bacteria such as Acetobacterium dehalogenans, Acetobacterium woodii, Holophaga foetida, Moorella thermoacetica and Sporomusa ovata (Bache & Pfennig, 1981; Daniel et al., 1991; Traunecker

et al., 1991; Kasmi et al., 1994; Stupperich et al., 1996; Kaufmann et al., 1997; Kreft & Schink, 1997). The cleavage of the ether bond and the transfer of the methyl group to tetrahydrofolate are catalyzed by the O-demethylase enzyme system (Kaufmann et al., 1997; Engelmann et al., 2001; Naidu & Ragsdale, 2001). For A. dehalogenans, two O-demethylases have been described. They consist of two

methyltransferases (MT I and MT II), a corrinoid protein (CP) and an activating enzyme (AE) per enzyme system (Kaufmann et al., 1997; Engelmann et al., 2001). MT I mediates the cleavage of the ether bond and the transfer of the methyl group to the super-reduced corrinoid cofactor of CP. CP is subsequently demethylated by the second methyltransferase MT II and the methyl group is transferred to tetrahydrofolate. The methyl group of methyltetrahyrofolate is further oxidized to CO2 or converted to the methyl group of acetate (Drake et al., 2006). For the methylation of CP, the cobalamin cofactor has to be in its super-reduced form. Because Quisqualic acid of the negative redox potential of the cob(II)alamin/cob(I)alamin couple in CP ([CoI]/[CoII]≤550 mV; Siebert et al., 2005), inadvertent oxidation of the cofactor may occur, which leads to the formation of the inactive cob(II)alamin. Therefore, an AE (RACE protein; Schilhabel et al., 2009) is required that reduces the cob(II)alamin cofactor of CP to the super-reduced form in an ATP-dependent reaction. During the course of the activation, AE increases the redox potential of the corrinoid (Schilhabel et al., 2009). Acetobacterium dehalogenans induces different O-demethylase systems depending on the growth substrate of the organism (Kaufmann et al., 1997; Kaufmann et al., 1998; Engelmann et al., 2001). Two O-demethylase systems have been characterized so far, designated vanillate- and veratrol-O-demethylase (Kaufmann et al.