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乙醇胺在细菌中的利用。

Ethanolamine Utilization in Bacteria.

机构信息

Department of Microbiology and Molecular Genetics and The UT Center for Antimicrobial Resistance and Microbial Genomics, McGovern Medical School, The University of Texas Health Science Center at Houston, Texas, USA.

Department of Microbiology and Molecular Genetics and The UT Center for Antimicrobial Resistance and Microbial Genomics, McGovern Medical School, The University of Texas Health Science Center at Houston, Texas, USA

出版信息

mBio. 2018 Feb 20;9(1):e00066-18. doi: 10.1128/mBio.00066-18.

Abstract

Ethanolamine (EA) is a valuable source of carbon and/or nitrogen for bacteria capable of its catabolism. Because it is derived from the membrane phospholipid phosphatidylethanolamine, it is particularly prevalent in the gastrointestinal tract, which is membrane rich due to turnover of the intestinal epithelium and the resident microbiota. Intriguingly, many gut pathogens carry the (ethanolamine utilization) genes. EA utilization has been studied for about 50 years, with most of the early work occurring in just a couple of species of Once the metabolic pathways and enzymes were characterized by biochemical approaches, genetic screens were used to map the various activities to the genes. With the rise of genomics, the diversity of bacteria containing the genes and surprising differences in gene content were recognized. Some species contain nearly 20 genes and encode many accessory proteins, while others contain only the core catabolic enzyme. Moreover, the genes are regulated by very different mechanisms, depending on the organism and the regulator encoded. In the last several years, exciting progress has been made in elucidating the complex regulatory mechanisms that govern gene expression. Furthermore, a new appreciation for how EA contributes to infection and colonization in the host is emerging. In addition to providing an overview of EA-related biology, this minireview will give special attention to these recent advances.

摘要

乙醇胺 (EA) 是能够代谢它的细菌的有价值的碳源和/或氮源。因为它来源于膜磷脂磷脂酰乙醇胺,所以它在富含膜的胃肠道中特别普遍,这是由于肠上皮细胞和常驻微生物群的周转。有趣的是,许多肠道病原体都带有 (乙醇胺利用) 基因。EA 利用已经研究了大约 50 年,早期的大部分工作只在少数几种 中进行。一旦通过生化方法对代谢途径和酶进行了表征,就使用遗传筛选将各种活性映射到 基因上。随着基因组学的兴起,人们认识到含有 基因的细菌的多样性和 基因含量的惊人差异。一些物种包含近 20 个基因,并编码许多辅助蛋白,而另一些物种只包含核心代谢酶。此外, 基因的调控机制因生物体和编码的 调节剂而异。在过去几年中,在阐明控制 基因表达的复杂调控机制方面取得了令人兴奋的进展。此外,人们对 EA 如何促进宿主感染和定植的认识也在不断提高。除了概述与 EA 相关的生物学外,这篇迷你评论还将特别关注这些最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6460/5821096/f67f2ba6533e/mbo0011837310001.jpg

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