Aug 2026· ACS Synthetic Biology· 0 citations· 35 references
Abstract
l-arabinose, a valuable C5 pentose sugar in xylose mother liquor (a low-cost cellulose hydrolysis byproduct), remains underutilized due to costly separation requirements, resulting in significant waste of fermentable carbon resources. In this study, Escherichia coli W3110 was systematically engineered to efficiently convert l-arabinose into xylitol, a low-calorie sweetener with significant commercial value. Firstly, the l-arabinose metabolic network was reconstructed and glucose catabolic repression was alleviated through coordinated pathway modifications, enabling simultaneous utilization of both l-arabinose and glucose. Subsequently, a xylitol synthesis module consisting of l-arabinose isomerase (AraA), l-xylulose reductase (LXR), and d-psicose-3-epimerase (DPE) was systematically optimized via gene arrangement, promoter and RBS engineering. The optimized pathway was integrated into the E. coli W3110 genome at the IS5 locus using MUCICAT technology, generating a plasmid-free production strain and reducing plasmid-segregation concerns. Fed-batch fermentation in a 3 L bioreactor yielded 64.07 g/L xylitol at a productivity of 1.46 g/L/h with 90.77% l-arabinose conversion in 44 h. This achievement overcomes two critical metabolic bottlenecks: (1) glucose catabolite repression, which normally prevents pentose utilization in the presence of glucose, and (2) the successful stoichiometric balancing of three enzymatic steps (AraA, LXR, DPE). The engineered strain achieves simultaneous glucose-arabinose co-metabolism, and glucose co-utilization supports xylitol formation in a manner consistent with an endogenous reducing-power contribution, thereby eliminating the requirement for exogenous glycerol supplementation in the optimized process. This work establishes a defined-substrate engineering platform for l-arabinose-to-xylitol conversion and provides a strategic basis for future evaluation using complex industrial carbohydrate streams.
The acid-tolerant yeast Issatchenkia orientalis is a promising platform for the sustainable production of organic acids. However, the inefficient conversion of lignocellulosic biomass-derived sugars, primarily due to carbon catabolite repression (CCR), reduces overall production efficiency and limits its industrial app...
Ye-Jin Lin, Ayoung Kim, Daeun Lee et al.· Frontiers in Microbiology· 0 citations
Efficient biosynthesis of 1,3-PDO, a key bio-based chemical, depends on precise regulation of the host metabolic network. In this study, a heterologous CRISPR-Cas12a genome editing system was established and systematically optimized in Klebsiella pneumoniae, enabling efficient and stable genome editing (75-100% efficie...
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Vanillin is an important flavor compound widely used in the food, fragrance, and pharmaceutical industries. Current biotransformation processes from ferulic acid or eugenol are limited by high substrate cost and low carbon efficiency, motivating de novo biosynthesis from glucose. This study employed Escherichia coli as...
Yue Wang, Tian-Jie Han, Yan-Xiang Bao et al.· Biotechnology and applied bi...· 0 citations
The plasmid-free system constructed in this study effectively avoids the plasmid-induced metabolic burden and genetic instability and demonstrates the prominent advantages and great application potential of plasmid-free modular engineering for the efficient biosynthesis of OSH and other high-value amino acids.
Si-Min Huang, Xu-Yue He, Ruo-Nan Wang et al.· Journal of Biotechnology· 0 citations
Lacto-N-tetraose (LNT), a core component of human milk oligosaccharides (HMOs), plays essential biological roles; however, its production remains challenging due to low conversion efficiency and the accumulation of intermediates. In this study, a systematic metabolic engineering strategy was applied to Escherichia co...
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