Weiming Lai, Lingrong Wen, Yueming Jiang, Bao Yang
Journal: Journal of agricultural and food chemistry 2026;74(34):26885-26906
PMID: 42690779
Prenylated stilbenoids are valuable nutraceutical candidates found in dietary plants. Compared to their nonprenylated counterparts, they often exhibit enhanced bioactivities, which are attributed to the increased lipophilicity conferred by the prenyl groups, facilitating their partitioning into cell membranes and interaction with lipid-associated targets. This review systematically examines prenylated stilbenoid biosynthesis via three core aspects: the structural diversity and structure-activity relationships of prenylated stilbenoids, focusing on how prenyl chain length, linkage, and substitution position modulate bioactivities; catalytic mechanisms and regioselectivity of prenyltransferases that transfer from prenyl donors to stilbenoid backbones; and metabolic engineering strategies for microbial heterologous production, emphasizing precursor flux optimization, enzyme and host engineering such as peroxisomal compartmentalization, and strain mating. Finally, we outline key challenges─poor prenyltransferase expression, precursor competition, and product cytotoxicity─and discuss future AI-guided enzyme engineering and autonomous dynamic control systems, providing a roadmap for the sustainable industrial production of these high-value nutraceuticals.
© 2026 American Chemical Society.
© Copyright 2026, Nutrition Evidence
We use cookies to improve your experience and analyze site traffic with Google Analytics. By continuing to use our site, you agree to our use of cookies. Learn more.