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在基因工程. 中高效生产功能性人乳寡糖 3'-唾液酸乳糖

Efficient Production of a Functional Human Milk Oligosaccharide 3'-Sialyllactose in Genetically Engineered .

机构信息

State Key Laboratory of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu 214122, People's Republic of China.

International Joint Laboratory on Food Safety, Jiangnan University, Wuxi 214122, People's Republic of China.

出版信息

ACS Synth Biol. 2022 Aug 19;11(8):2837-2845. doi: 10.1021/acssynbio.2c00243. Epub 2022 Jul 8.

DOI:10.1021/acssynbio.2c00243
Abstract

3'-Sialyllactose (3'-SL) is one of the most important and simplest sialylated human milk oligosaccharides. In this study, a plasmid-based pathway optimization along with chromosomal integration strategies was applied for 3'-SL production. Specifically, the precursor CMP-Neu5Ac synthesis pathway genes and α2,3-sialyltransferase-encoding gene were introduced into BL21(DE3)Δ to realize 3'-SL synthesis. Genes and involved in Neu5Ac catabolism were further deleted to reduce the metabolic flux of competitive pathway. Several α2,3-sialyltransferases from different species were selected to evaluate the sialylation effect. The precursor pools were balanced and improved by optimizing key enzyme expression involved in the UDP-GlcNAc and CMP-Neu5Ac synthesis pathway. Finally, an additional α2,3-sialyltransferase expression cassette was integrated into chromosome to maximize 3'-SL synthesis, and 4.5 g/L extracellular 3'-SL was produced at a shake-flask level. The extracellular 3'-SL concentration was raised to 23.1 g/L in a 5 L bioreactor fermentation, which represents the highest extracellular value ever reported.

摘要

3'-唾液乳糖(3'-SL)是最重要和最简单的人乳寡糖之一。在本研究中,应用基于质粒的途径优化和染色体整合策略来生产 3'-SL。具体而言,将前体 CMP-Neu5Ac 合成途径基因和编码 α2,3-唾液酸转移酶的基因引入 BL21(DE3)Δ 中以实现 3'-SL 合成。进一步删除参与 Neu5Ac 分解代谢的基因 和 ,以减少竞争途径的代谢通量。选择来自不同物种的几种 α2,3-唾液酸转移酶来评估唾液酸化效果。通过优化涉及 UDP-GlcNAc 和 CMP-Neu5Ac 合成途径的关键酶表达来平衡和改进前体库。最后,将额外的 α2,3-唾液酸转移酶表达盒整合到染色体中,以最大限度地提高 3'-SL 的合成量,在摇瓶水平下可产生 4.5 g/L 的细胞外 3'-SL。在 5 L 生物反应器发酵中,细胞外 3'-SL 的浓度提高到 23.1 g/L,这是迄今为止报道的最高细胞外值。

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