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从头合成途径和 GDP-岩藻糖补救合成途径之间的相互作用。

Interplay between de novo and salvage pathways of GDP-fucose synthesis.

机构信息

Department of Biochemistry, Faculty of Biotechnology, University of Wroclaw, Wroclaw, Poland.

出版信息

PLoS One. 2024 Oct 24;19(10):e0309450. doi: 10.1371/journal.pone.0309450. eCollection 2024.

Abstract

GDP-fucose is synthesised via two pathways: de novo and salvage. The first uses GDP-mannose as a substrate, and the second uses free fucose. To date, these pathways have been considered to work separately and not to have an influence on each other. We report the mutual response of the de novo and salvage pathways to the lack of enzymes from a particular route of GDP-fucose synthesis. We detected different efficiencies of GDP-fucose and fucosylated structure synthesis after a single inactivation of enzymes of the de novo pathway. Our study demonstrated the unequal influence of the salvage enzymes on the production of GDP-fucose by enzymes of the de novo biosynthesis pathway. Simultaneously, we detected an elevated level of one of the enzymes of the de novo pathway in the cell line lacking the enzyme of the salvage biosynthesis pathway. Additionally, we identified dissimilarities in fucose uptake between cells lacking TSTA3 and GMDS proteins.

摘要

GDP-岩藻糖通过两条途径合成:从头合成和补救合成。第一条途径使用 GDP-甘露糖作为底物,第二条途径使用游离岩藻糖。迄今为止,这些途径被认为是独立工作的,彼此之间没有影响。我们报告了从头合成途径和补救合成途径对缺乏 GDP-岩藻糖合成特定途径的酶的相互反应。在单个失活从头途径的酶后,我们检测到 GDP-岩藻糖和岩藻糖基化结构合成的不同效率。我们的研究表明,补救途径的酶对从头生物合成途径的酶产生 GDP-岩藻糖的影响是不平等的。同时,我们在缺乏补救生物合成途径酶的细胞系中检测到一种从头途径的酶水平升高。此外,我们在缺乏 TSTA3 和 GMDS 蛋白的细胞之间鉴定到了岩藻糖摄取的差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d51b/11501016/7ccfb157a708/pone.0309450.g001.jpg

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