Abstract
Resveratrol is a plant phenolic secondary metabolite derived from phenylpropane metabolic pathway. It is a phytoalexin of high pharmaceutical interest produced in the defense response of plants. To produce resveratrol in Chlamydomonas reinhardtii, 4-coumaroyl-CoA ligase (4CL) and stilbene synthase (STS), two enzymes in the last two steps of resveratrol synthesis in higher plants, were fused together by a glycine–serine–glycine (GSG) tripeptide linker after codon adaptation according to the genome of C. reinhardtii. The fusion protein 4CL-GSG-STS was overexpressed in a wild-type (CC125) and a wall-deficient C. reinhardtii (CC 425). A high level of resveratrol accumulation (22.8 μg g−1, dry weight) was obtained in CC125 transformed with codon-adapted 4CL-GSG-STS after supplementary of cinnamic acid in the culture medium.
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This study was supported by the National Natural Science Foundation of China (grant no. 31370674).
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Xiang, C., Liu, J., Ma, L. et al. Overexpressing codon-adapted fusion proteins of 4-coumaroyl-CoA ligase (4CL) and stilbene synthase (STS) for resveratrol production in Chlamydomonas reinhardtii. J Appl Phycol 32, 1669–1676 (2020). https://doi.org/10.1007/s10811-020-02123-2
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DOI: https://doi.org/10.1007/s10811-020-02123-2