α-Bisabolol, a natural sesquiterpene alcohol with notable physiological activities, exhibits broad application prospects in the pharmaceutical, cosmetic, and flavor industries. Traditional plant extraction suffers from low efficiency and resource scarcity, while chemical synthesis faces stereoisomerism and environmental issues. In contrast, microbial synthesis overcomes these limitations by utilizing renewable agricultural feedstocks to address plant resource scarcity and enabling highly stereoselective biosynthesis to produce the more bioactive (-)-α-bisabolol. This review summarizes the physiological activities of α-bisabolol, describes its microbial biosynthetic pathway, and focuses on the key enzyme (-)-α-bisabolol synthase. Unlike previous reviews focused on pharmacological effects or chemical synthesis, this review uniquely integrates recent metabolic engineering strategies for enhancing (-)-α-bisabolol production, including chassis cell development, metabolic flux regulation, competitive pathway knockout, cofactors and global regulatory factors optimization, and fermentation scale-up. Finally, current challenges and future directions are discussed, with an emphasis on green biomanufacturing through transporter engineering, enzyme evolution, and subcellular compartmentalization.
Junsong Xiao, Zeyu Li, Jiali Zhang et al.· Journal of Agricultural and...· 0 citations
2'-Fucosyllactose (2'-FL), the most abundant human milk oligosaccharide (HMO), has attracted considerable interest for its prebiotic and immunomodulatory functions, with broad applications in infant nutrition. In this study, we report the development of a high-yield, genome-integrated 2'-FL-producing strain based on Escherichia coli MG1655 through systematic modular optimization. Starting from a single-copy BKHT strain (MGC06), we first optimized the copy number of the α-1,2-fucosyltransferase (α-1,2-FT) gene BKHT. Subsequently, the GDP-L-fucose supply was enhanced through coordinated genomic integration of the gene clusters cpsG-cpsB and gmd-fcl, while the multidrug efflux transporter gene mdfA was integrated to improve product export and strain robustness. BKHT copy number was then re-evaluated in the optimized background, with four copies yielding the highest production. The final engineered strain, harboring all genetic modifications stably integrated into the chromosome, produced 17.18 g/L 2'-FL in shake-flask culture. In fed-batch fermentation using a 5-L bioreactor, this strain achieved a titer of 154.12 g/L after 60 h, with a productivity of 2.57 g/L/h. Notably, throughout the entire fermentation process, no antibiotics or inducers were supplemented, underscoring the genetic stability and regulatory compliance of this plasmid-free system. To our knowledge, this represents the highest 2'-FL titer reported to date, positioning our engineered strain as a promising candidate for commercial 2'-FL production.
Roulin Chen, Longhao Yang, Hao Wang et al.· Enzyme and Microbial Technol...· 0 citations