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Updated: Jul 16, 2026

Light-driven Enzymatic Decarboxylation
Published on: May 22, 2016
Biosynthesis of 4-Ethylphenol via an Enzyme Cascade with an Engineered Fatty Acid Photodecarboxylase
Zherui Xu1, Zhaoyang Qin1, Shuixiu Wen1
1National Key Laboratory of Agricultural Microbiology, College of Life Science and Technology, Huazhong Agricultural University, No. 1 Shizishan Street, Wuhan430070, P. R. China.
Abstract:
4-Ethylphenol (4-EP) is an important aromatic fine chemical used as a flavor compound and as an intermediate in the synthesis of polymers and pharmaceuticals. Although 4-EP occurs naturally, the decarboxylase responsible for its formation from phloretic acid has not yet been identified. To enable the biobased production of 4-EP, we designed an enzymatic cascade employing fatty acid photodecarboxylase (FAP) as the missing decarboxylase. Using structure-guided directed evolution, we engineered FAP for the decarboxylation of 3-(4-hydroxyphenyl)propanoic acid (HPPA), achieving a 3.7-fold increase in productivity. In addition, an Escherichia coli strain was engineered to produce l-tyrosine from glucose, and a whole-cell biocatalyst was developed to convert l-tyrosine into HPPA. By integrating tyrosine fermentation, multienzyme biotransformation, and photodecarboxylation, we achieved a 4-EP titer of 4.02 mM (490 mg/L)─the highest reported to date. This work demonstrates the significant potential of photoenzymes in the sustainable bioproduction of aromatic fine chemicals, particularly natural flavors and fragrances.
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