| Literature DB >> 25164030 |
Toshiki Furuya1, Misa Miura, Kuniki Kino.
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.Entities:
Keywords: biocatalysis; cascade reaction; decarboxylation; oxidation; sustainable chemistry
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Year: 2014 PMID: 25164030 DOI: 10.1002/cbic.201402215
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164