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携带α-氨基己二酸转氨酶基因的“护盾”武装可编程益生菌调节色氨酸代谢和肠道微生物群以缓解炎症性肠病

"Shield" Armed Programmable Probiotics Harboring α-Aminoadipate Aminotransferase Gene Regulate Tryptophan Metabolism and Gut Microbiota to Alleviate the Inflammatory Bowel Disease.

作者信息

Liu Aijiang, Ma Jun, Liu Zengguang, Qiu Tianyuan, Zhao Qixuan, Li Guangquan, Liang Xiao, Li Quanshun

机构信息

Jilin Provincial Key Laboratory on Molecular and Chemical Genetics, The Second Hospital of Jilin University, Changchun 130012, China.

Key Laboratory for Molecular Enzymology and Engineering of Ministry of Education, School of Life Sciences, Jilin University, Changchun 130012, China.

出版信息

J Agric Food Chem. 2025 Apr 2;73(13):7920-7932. doi: 10.1021/acs.jafc.4c13017. Epub 2025 Mar 21.

Abstract

Current treatment of inflammatory bowel disease (IBD) relies on anti-inflammatory and immunosuppressive agents. However, this concept is considered outdated due to its restricted efficacy and unavoidable side effects. Herein, a polynorepinephrine-coated programmable probiotic expressing α-aminoadipate aminotransferase (NE-EcN-pA) was constructed to improve the levels of kynurenic acid and xanthurenic acid in the intestine by modulating the endogenous tryptophan metabolism. The NE layer could protect EcN-pA against the harsh environment of the gastrointestinal tract, enhancing its survival and colonization. In UC mice, oral administration of NE-EcN-pA effectively alleviated intestinal inflammation and restored the intestinal epithelial barrier owing to the activation of the aryl hydrocarbon receptor pathway. Furthermore, NE-EcN-pA promoted the diversity of intestinal flora, improved the imbalance of flora, and enhanced the content of short-chain fatty acids in the colon. Overall, NE-EcN-pA can regulate endogenous tryptophan metabolism and gut microbiota, showing promise in the treatment of gastrointestinal disorders.

摘要

炎症性肠病(IBD)的当前治疗依赖于抗炎和免疫抑制药物。然而,由于其疗效有限和不可避免的副作用,这一概念被认为已过时。在此,构建了一种表达α-氨基己二酸转氨酶的聚去甲肾上腺素包被的可编程益生菌(NE-EcN-pA),以通过调节内源性色氨酸代谢来提高肠道中犬尿酸和黄尿酸的水平。NE层可以保护EcN-pA免受胃肠道恶劣环境的影响,提高其存活率和定殖能力。在UC小鼠中,口服NE-EcN-pA可有效减轻肠道炎症并恢复肠道上皮屏障,这是由于芳烃受体途径的激活。此外,NE-EcN-pA促进了肠道菌群的多样性,改善了菌群失衡,并提高了结肠中短链脂肪酸的含量。总体而言,NE-EcN-pA可以调节内源性色氨酸代谢和肠道微生物群,在治疗胃肠道疾病方面显示出前景。

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