D-galactonate metabolism in enteric bacteria: a molecular and physiological perspective

IF 5.9 2区 生物学 Q1 MICROBIOLOGY Current opinion in microbiology Pub Date : 2024-08-12 DOI:10.1016/j.mib.2024.102524
Swati Singh , Chetna Gola , Bhupinder Singh , Vishal Agrawal , Rachna Chaba
{"title":"D-galactonate metabolism in enteric bacteria: a molecular and physiological perspective","authors":"Swati Singh ,&nbsp;Chetna Gola ,&nbsp;Bhupinder Singh ,&nbsp;Vishal Agrawal ,&nbsp;Rachna Chaba","doi":"10.1016/j.mib.2024.102524","DOIUrl":null,"url":null,"abstract":"<div><p><span>D</span>-galactonate, a widely prevalent sugar acid, was first reported as a nutrient source for enteric bacteria in the 1970s. Since then, decades of research enabled a description of the modified Entner-Doudoroff pathway involved in its degradation and reported the structural and biochemical features of its metabolic enzymes, primarily in <em>Escherichia coli</em> K-12. However, only in the last few years, the <span>D</span>-galactonate transporter has been characterized, and the regulation of the <em>dgo</em> operon, encoding the structural genes for the transporter and enzymes of <span>D</span>-galactonate metabolism, has been detailed. Notably, in recent years, multiple evolutionary studies have identified the <em>dgo</em> operon as a dominant target for adaptation of <em>E. coli</em> in the mammalian gut. Despite considerable research on <em>dgo</em> operon, numerous fundamental questions remain to be addressed. The emerging relevance of the <em>dgo</em> operon in host–bacterial interactions further necessitates the study of <span>D</span>-galactonate metabolism in other enterobacterial strains.</p></div>","PeriodicalId":10921,"journal":{"name":"Current opinion in microbiology","volume":"81 ","pages":"Article 102524"},"PeriodicalIF":5.9000,"publicationDate":"2024-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current opinion in microbiology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1369527424001000","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

D-galactonate, a widely prevalent sugar acid, was first reported as a nutrient source for enteric bacteria in the 1970s. Since then, decades of research enabled a description of the modified Entner-Doudoroff pathway involved in its degradation and reported the structural and biochemical features of its metabolic enzymes, primarily in Escherichia coli K-12. However, only in the last few years, the D-galactonate transporter has been characterized, and the regulation of the dgo operon, encoding the structural genes for the transporter and enzymes of D-galactonate metabolism, has been detailed. Notably, in recent years, multiple evolutionary studies have identified the dgo operon as a dominant target for adaptation of E. coli in the mammalian gut. Despite considerable research on dgo operon, numerous fundamental questions remain to be addressed. The emerging relevance of the dgo operon in host–bacterial interactions further necessitates the study of D-galactonate metabolism in other enterobacterial strains.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
肠道细菌的 D-半乳糖醛酸代谢:分子和生理学视角。
D -半乳糖酸是一种广泛存在的糖酸,在 20 世纪 70 年代首次被报道为肠道细菌的营养源。此后,经过数十年的研究,人们描述了参与降解 D-半乳糖醛酸的恩特纳-杜多罗夫(Entner-Doudoroff)改良途径,并报道了其代谢酶的结构和生化特征,主要是在大肠杆菌 K-12 中。然而,直到最近几年,D-半乳糖醛酸转运体的特征才得以确定,编码 D-半乳糖醛酸转运体结构基因和 D-半乳糖醛酸代谢酶的 dgo 操作子的调控也得到了详细说明。值得注意的是,近年来,多项进化研究发现,dgo 操作子是哺乳动物肠道中大肠杆菌适应的主要目标。尽管对 dgo 操作子进行了大量研究,但仍有许多基本问题有待解决。由于 dgo 操作子在宿主与细菌相互作用中的重要性不断显现,因此有必要进一步研究其他肠道细菌菌株的 D-半乳糖醛酸代谢。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Current opinion in microbiology
Current opinion in microbiology 生物-微生物学
CiteScore
10.00
自引率
0.00%
发文量
114
审稿时长
6-12 weeks
期刊介绍: Current Opinion in Microbiology is a systematic review journal that aims to provide specialists with a unique and educational platform to keep up-to-date with the expanding volume of information published in the field of microbiology. It consists of 6 issues per year covering the following 11 sections, each of which is reviewed once a year: Host-microbe interactions: bacteria Cell regulation Environmental microbiology Host-microbe interactions: fungi/parasites/viruses Antimicrobials Microbial systems biology Growth and development: eukaryotes/prokaryotes
期刊最新文献
Temporospatial control of topoisomerases by essential cellular processes Editorial overview: Human fungal pathogens: An increasing threat It's complicated: relationships between integrative and conjugative elements and their bacterial hosts How do bacteria tune transcription termination efficiency? Temperature structuring of microbial communities on a global scale
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1