Pterostilbene is a derivative of resveratrol with a higher bioavailability and biological activity, which shows antioxidant, anti-inflammatory, antitumor, and antiaging activities. Here, directed evolution and host strain engineering were used to improve the production of pterostilbene in . First, the heterologous biosynthetic pathway enzymes of pterostilbene, including tyrosine ammonia lyase, -coumarate: CoA ligase, stilbene synthase, and resveratrol O-methyltransferase, were successively directly evolved through error-prone polymerase chain reaction (PCR). Four mutant enzymes with higher activities of and were obtained. The directed evolution of the pathway enzymes increased the pterostilbene production by 13.7-fold. Then, a biosensor-guided genome shuffling strategy was used to improve the availability of the precursor L-tyrosine of the host strain TYR-30 used for the production of pterostilbene. A shuffled strain with higher L-tyrosine production was obtained. The shuffled strain harboring the evolved pathway produced 80.04 ± 5.58 mg/l pterostilbene, which is about 2.3-fold the highest titer reported in literatures.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8530161 | PMC |
http://dx.doi.org/10.3389/fmicb.2021.710405 | DOI Listing |
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