Metabolic Engineering of <i>Yarrowia lipolytica</i> for Enhanced Production of Naringenin-Derived Flavonoids: Apigenin and Acacetin
Nahye Park, Yangsub Ham, Seungwoo Cha, Byeongseon Jang, Gyeongmin Kim, Seung-Ho Baek, Ji‐Sook Hahn
Abstract
Apigenin and acacetin are flavonoids with potent antioxidant, anti-inflammatory, and anticancer activities, making them attractive for pharmaceutical and nutraceutical applications. However, their low natural abundance presents a challenge to large-scale production. In this study, we engineered Yarrowia lipolytica for the de novo biosynthesis of apigenin and acacetin from naringenin. To enhance naringenin production from l -tyrosine, we introduced four heterologous genes, optimized the flux through the l -tyrosine pathway, and eliminated the competing homogentisate pathway. Malonyl-CoA availability was increased by downregulating FAS1 (fatty acid synthase 1), while erythrose-4-phosphate levels were elevated through overexpression of TKL1 (transketolase 1). Additionally, genes encoding flavone synthase and flavonoid 4′-O-methyltransferase were integrated to convert naringenin into apigenin, and subsequently apigenin into acacetin. Under fed-batch fermentation with an optimized carbon-to-nitrogen ratio, acacetin production reached 1.10 g/L─the highest titer reported to date in a microbial system. These results highlight Y. lipolytica as a promising chassis for scalable flavonoid biosynthesis.