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      A coenzyme-independent decarboxylase/oxygenase cascade for the efficient synthesis of vanillin.

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          Abstract

          Vanillin is one of the most widely used flavor compounds in the world as well as a promising versatile building block. The biotechnological production of vanillin from plant-derived ferulic acid has attracted much attention as a new alternative to chemical synthesis. One limitation of the known metabolic pathway to vanillin is its requirement for expensive coenzymes. Here, we developed a novel route to vanillin from ferulic acid that does not require any coenzymes. This artificial pathway consists of a coenzyme-independent decarboxylase and a coenzyme-independent oxygenase. When Escherichia coli cells harboring the decarboxylase/oxygenase cascade were incubated with ferulic acid, the cells efficiently synthesized vanillin (8.0 mM, 1.2 g L(-1) ) via 4-vinylguaiacol in one pot, without the generation of any detectable aromatic by-products. The efficient method described here might be applicable to the synthesis of other high-value chemicals from plant-derived aromatics.

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          Author and article information

          Journal
          Chembiochem
          Chembiochem : a European journal of chemical biology
          Wiley
          1439-7633
          1439-4227
          Oct 13 2014
          : 15
          : 15
          Affiliations
          [1 ] Department of Applied Chemistry, Faculty of Science and Engineering, Waseda University, 3-4-1 Ohkubo, Shinjuku-ku, 169-8555 Tokyo (Japan). tfuruya@fuji.waseda.jp.
          Article
          10.1002/cbic.201402215
          25164030
          a0eae081-e640-41b5-bfad-566c9a247ff1
          History

          cascade reaction,biocatalysis,decarboxylation,oxidation,sustainable chemistry

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