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通过黄素单核苷酸介导的细胞外电子转移发电以上调上皮I型胶原蛋白表达,从而促进微生物对肠道的黏附。

Generate Electricity through Flavin Mononucleotide-Mediated Extracellular Electron Transfer to Upregulate Epithelial Type I Collagen Expression and Thereby Promote Microbial Adhesion to Intestine.

作者信息

Ganzorig Binderiya, Zayabaatar Enkhbat, Pham Minh Tan, Marito Shinta, Huang Chun-Ming, Lee Yu-Hsiang

机构信息

Department of Biomedical Sciences and Engineering, National Central University, Taoyuan City 320317, Taiwan.

Faculty of Applied Sciences, Ton Duc Thang University, Ho Chi Minh City 700000, Vietnam.

出版信息

Biomedicines. 2023 Feb 23;11(3):677. doi: 10.3390/biomedicines11030677.

Abstract

The mechanism behind how flavin mononucleotide (FMN)-producing bacteria attach to a host intestine remains unclear. In order to address this issue, this study isolated the Gram-positive bacteria from Mongolian fermented Airag, named . MA. These bacteria were further employed as the model microbes, and their electrogenic properties were first identified by their significant expression of type II NADH-quinone oxidoreductase. This study also demonstrated that the electrical activity of MA can be conducted through flavin mononucleotide (FMN)-based extracellular electron transfer, which is highly dependent on the presence of a carbon source in the medium. Our data show that approximately 15 µM of FMN, one of the key electron donors for the generation of electricity, can be produced from MA, as they were cultured in the presence of lactulose for 24 h. We further demonstrated that the electrical activity of MA can promote microbial adhesion and can thus enhance the colonization effectiveness of Caco-2 cells and mouse cecum. Such enhanced adhesiveness was attributed to the increased expression of type I collagens in the intestinal epithelium after treatment with MA. This study reveals the mechanism behind the electrogenic activity of MA and shows how the bacteria utilize electricity to modulate the protein expression of gut tissue for an enhanced adhesion process.

摘要

产生黄素单核苷酸(FMN)的细菌附着于宿主肠道的背后机制仍不清楚。为了解决这个问题,本研究从蒙古发酵马奶酒中分离出革兰氏阳性菌,命名为MA。这些细菌被进一步用作模型微生物,其产电特性首先通过II型NADH-醌氧化还原酶的显著表达得以确定。本研究还表明,MA的电活性可通过基于黄素单核苷酸(FMN)的细胞外电子传递来传导,这高度依赖于培养基中碳源的存在。我们的数据显示,当MA在乳果糖存在下培养24小时时,可产生约15µM的FMN,FMN是发电的关键电子供体之一。我们进一步证明,MA的电活性可促进微生物粘附,从而增强Caco-2细胞和小鼠盲肠的定殖效果。这种增强的粘附性归因于用MA处理后肠道上皮中I型胶原蛋白表达的增加。本研究揭示了MA产电活性背后的机制,并展示了细菌如何利用电来调节肠道组织的蛋白质表达以促进粘附过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60b7/10045142/a92b67135a9d/biomedicines-11-00677-g001.jpg

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