生物制造
生物化学
化学
硫酸软骨素
软骨素
酶
生物过程
基质(水族馆)
跨膜蛋白
异源表达
鱼精蛋白硫酸盐
硫酸化
蛋白质工程
合成生物学
底物特异性
融合蛋白
代谢工程
组合化学
硫酸乙酰肝素
功能(生物学)
定向进化
生物过程工程
作者
Aditi Dey Tithi,Hana Zeghal,Yuefan Song,Elena E. Paskaleva,Sweta Vangaveti,Mattheos Koffas
标识
DOI:10.1021/acssynbio.5c00780
摘要
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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