Biomanufacturing shows 67% sulfation of chondroitin in engineered E. coli, indicating a sustainable method for producing chondroitin sulfate C.
Chondroitin sulfate C (CS-C) is a biologically significant glycosaminoglycan in which a precise 6-O-sulfation pattern confers critical structural and signaling functions in connective and neural tissues. Here, we report the first functional expression of human chondroitin 6-O-sulfotransferase-1 (C6ST-1) in Escherichia coli, enabling cell-free biosynthesis of CS-C. By applying structure-guided protein engineering combining transmembrane truncation, His₆ -MBP fusion, and PROSS-directed stabilizing mutations, we generated a soluble and catalytically active variant in E. coli Origami B (DE3) and modified Shuffle T7 Express. Under optimized reaction conditions (MES buffer pH 5.5, 30 °C, Mg²⁺/Ca²⁺/Mn²⁺ with protamine sulfate), the engineered enzyme catalyzed up to 67% sulfation of chondroitin (CS-O) to CS-C, verified via SAX-HPLC. Kinetic and molecular dynamics analyses revealed enhanced substrate affinity and catalytic efficiency for the M9 Δ131 mutant. This study establishes a sustainable, animal-free platform for high-purity CS-C biomanufacturing and provides a generalizable strategy for engineering eukaryotic sulfotransferases for functional expression in bacterial hosts.
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Tithi et al. (2026) studied this question.
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