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肠道细菌硫酸盐还原代谢途径的最新研究进展。

Recent Advances in Metabolic Pathways of Sulfate Reduction in Intestinal Bacteria.

机构信息

Department of Experimental Biology, Faculty of Science, Masaryk University, Kamenice 753/5, 62500 Brno, Czech Republic.

Department of Molecular Biology and Pharmaceutical Biotechnology, University of Veterinary and Pharmaceutical Sciences Brno, 61242 Brno, Czech Republic.

出版信息

Cells. 2020 Mar 12;9(3):698. doi: 10.3390/cells9030698.

Abstract

Sulfate is present in foods, beverages, and drinking water. Its reduction and concentration in the gut depend on the intestinal microbiome activity, especially sulfate-reducing bacteria (SRB), which can be involved in inflammatory bowel disease (IBD). Assimilatory sulfate reduction (ASR) is present in all living organisms. In this process, sulfate is reduced to hydrogen sulfide and then included in cysteine and methionine biosynthesis. In contrast to assimilatory sulfate reduction, the dissimilatory process is typical for SRB. A terminal product of this metabolism pathway is hydrogen sulfide, which can be involved in gut inflammation and also causes problems in industries (due to corrosion effects). The aim of the review was to compare assimilatory and dissimilatory sulfate reduction (DSR). These processes occur in some species of intestinal bacteria (e.g., and genera). The main attention was focused on the description of genes and their location in selected strains. Their coding expression of the enzymes is associated with anabolic processes in various intestinal bacteria. These analyzed recent advances can be important factors for proposing possibilities of metabolic pathway extension from hydrogen sulfide to cysteine in intestinal SRB. The switch from the DSR metabolic pathway to the ASR metabolic pathway is important since toxic sulfide is not produced as a final product.

摘要

硫酸盐存在于食物、饮料和饮用水中。其在肠道中的还原和浓缩取决于肠道微生物组的活性,特别是硫酸盐还原菌(SRB),它可能与炎症性肠病(IBD)有关。同化硫酸盐还原(ASR)存在于所有生物体中。在这个过程中,硫酸盐被还原为硫化氢,然后被纳入半胱氨酸和蛋氨酸的生物合成中。与同化硫酸盐还原相反,异化过程是 SRB 的典型特征。这种代谢途径的末端产物是硫化氢,它可能参与肠道炎症,也会给工业带来问题(由于腐蚀作用)。本综述的目的是比较同化和异化硫酸盐还原(DSR)。这些过程发生在一些肠道细菌物种中(例如, 和 属)。主要关注的是描述基因及其在选定菌株中的位置。它们编码的酶与各种肠道细菌中的合成代谢过程有关。这些分析的最新进展可能是提出从硫化氢到肠道 SRB 中的半胱氨酸扩展代谢途径的可能性的重要因素。从 DSR 代谢途径到 ASR 代谢途径的转变很重要,因为最终产物不会产生有毒的硫化物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24d9/7140700/a45e1554464f/cells-09-00698-g001.jpg

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