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18.3 Conclusion and Outlook  417

               acids into the corresponding methyl esters [71] which are the main constituents of
               biofuel. Another promising candidate is CypM, an NMT isolated from Streptomyces
               sp., which might be a useful tool in the post-translational modification of the
               α-amino group of peptides [104]. The most relevant preparative applications were,
               and in the near future likely will be, those of OMTs. They are usually more
               promiscuous than their C-and N-affine relatives, and access and application by
               nonexperts is easier.
                Overall, MTs have great potential for applications in biotechnology. The require-
               ments for ‘‘Green Chemistry’’ and the hazardous properties of alkylating agents in
               general make the substitution of existing methods and processes inevitable. MTs
               can provide excellent chemo- and regioselectivity, sometimes contrasting those of
               chemical methylation processes. The enzymes are well behaved in biocatalysis and
               usually not very sensitive. Nevertheless, only very few applications of selected MTs
               seem to be mature [28, 57a, 90], with most of the work done still in infancy. Thus
               there is a huge potential for improvements and new developments, such as SAM
               regeneration, its substitution by simple alkyl donors, design of more active variants,
               expansion of substrate, and cofactor scope, to name just a few. This by no means
               exhaustive list of future tasks for research and development in the field of MTs will
               soon become shorter considering the importance of methylation processes in the
               bio-based productions of high-value products and in influencing cellular processes.

               Abbreviations

               MT   methyltransferase
               NMT N-methyltransferase
               OMT O-methyltransferase
               SAH  S-adenosyl-l-homocysteine
               SAM S-adenosyl-l-methionine
               Met  methionine
               THF  tetrahydrofolate


               Acknowledgement

               This work has been partially supported by the Federal Ministry of Economy, Family
               and Youth (BMWFJ), the Federal Ministry of Traffic, Innovation and Technology
               (bmvit), the Styrian Business Promotion Agency SFG, the Standortagentur Tirol
               and ZIT – Technology Agency of the City of Vienna through the COMET-
               Funding Program managed by the Austrian Research Promotion Agency FFG.
               MGK acknowledge financial support from the Austrian Science Foundation (FWF)
               through project P24135-N17 and Innovative Medicines Initiative (IMI) project
                ◦
               n 115360.
                It was also partially supported by EU COST actions FA 1006 (PlantEngine) and FA
               0907 (Bioflavour), FP7 KBBE-Project BioNexGen (no 266025, Developing the Next
               Generation of Biocatalysts for Industrial Chemical Synthesis), Science Campus
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