De Novo Synthesis of Tyrosol and Hydroxytyrosol through Temperature-Inducible Systems and Metabolic Engineering.

Abstract

Hydroxytyrosol (HT) has various biological and pharmacological activities, including potent antioxidant activity. The efficient synthesis of HT and tyrosol has been achieved by microbial synthesis. However, more strategies are needed to enhance its yield and meet the demands of industrialization. In this study, SceARO10 and EcoyahK were used for the de novo synthesis of tyrosol in Escherichia coli using a temperature-inducible system. Different sources of phenolic acid decarboxylase and alcohol reductase were investigated, with YliARO10 and YliPAR4 from Yarrowia lipolytica showing the best catalytic performance, yielding 4.05 g/L of tyrosol at 60 h in shake flasks, the highest yield reported. Next, EblHpaBC from E. coli BL21 (DE3) was introduced for HT biosynthesis, and the HT-related degradation gene mhpB was functionally characterized in E. coli. Subsequently, by enhancing precursor supply, eliminating competing metabolic pathways, and knocking out mhpB, the HT yield reached 1.28 g/L after 60 h. Finally, in a 5 L bioreactor, titers of 6.18 and 4.97 g/L of tyrosol and HT were achieved for the first time using a temperature-induced strategy. This study presents a method for the modification of microbial chassis for the efficient synthesis of tyrosol and HT.