Biosynthesis of plant-speciWc phenylpropanoids by construction of an artiWcial biosynthetic pathway in Escherichia coli

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Abstract

Biological synthesis of plant secondary metabolites has attracted increasing attention due to their proven or assumed beneWcial properties and health-promoting eVects. Phenylpropanoids are the precursors to a range of important plant metabolites such as the secondary metabolites belonging to the Xavonoid/stilbenoid class of compounds. In this study, engineered Escherichia coli containing artiWcial phenylpropanoid biosynthetic pathways utilizing tyrosine as the initial precursor were established for production of plant-speciWc metabolites such as ferulic acid, naringenin, and resveratrol. The construction of the artiWcial pathway utilized tyrosine ammonia lyase and 4-coumarate 3-hydroxylase from Saccharothrix espanaensis, cinnamate/4-coumarate: coenzyme A ligase from Streptomyces coelicolor, caVeic acid O-methyltransferase and chalcone synthase from Arabidopsis thaliana, and stilbene synthase from Arachis hypogaea. © Society for Industrial Microbiology 2011.

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APA

Choi, O., Wu, C. Z., Kang, S. Y., Ahn, J. S., Uhm, T. B., & Hong, Y. S. (2011). Biosynthesis of plant-speciWc phenylpropanoids by construction of an artiWcial biosynthetic pathway in Escherichia coli. Journal of Industrial Microbiology and Biotechnology, 38(10), 1657–1665. https://doi.org/10.1007/s10295-011-0954-3

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