• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

法德R,代谢便利性的转录协调。

FadR, transcriptional co-ordination of metabolic expediency.

作者信息

Cronan J E, Subrahmanyam S

机构信息

Department of Microbiology, University of Illinois, Urbana 61801, USA.

出版信息

Mol Microbiol. 1998 Aug;29(4):937-43. doi: 10.1046/j.1365-2958.1998.00917.x.

DOI:10.1046/j.1365-2958.1998.00917.x
PMID:9767562
Abstract

FadR is an Escherichia coli transcriptional regulator that optimizes fatty acid metabolism in response to exogenously added fatty acids. Many bacteria grow well on long-chain fatty acids as sole carbon source, but at the expense of consuming a useful structural material. Exogenous fatty acids are readily incorporated into membrane phospholipids in place of the acyl chains synthesized by the organism, and phospholipids composed of any of a large variety of exogenously derived acyl chains make biologically functional membranes. It would be wasteful for bacteria to degrade fatty acids to acetyl-CoA and then use this acetyl-CoA to synthesize the same (or functionally equivalent) fatty acids for phospholipid synthesis. This line of reasoning suggests that bacteria might shut down endogenous fatty acid synthesis on the addition of long-chain fatty acids to the growth medium. Moreover, this shutdown could be closely coupled to fatty acid degradation, such that a bacterial cell would use a portion of the exogenous fatty acid for phospholipid synthesis while degrading the remainder to acetyl-CoA. To a degree, the bacterium could both have its cake (the acyl chains for phospholipid synthesis) and eat it (to form acetyl-CoA). This scenario turns out to be true in E. coli. The key player in this regulatory gambit is FadR, a transcription factor that acts both as a repressor of the fatty acid degradation and as an activator of fatty acid biosynthesis.

摘要

FadR是一种大肠杆菌转录调节因子,它能响应外源添加的脂肪酸来优化脂肪酸代谢。许多细菌能以长链脂肪酸作为唯一碳源良好生长,但这是以消耗一种有用的结构材料为代价的。外源脂肪酸很容易取代生物体合成的酰基链掺入膜磷脂中,由多种外源衍生的酰基链中的任何一种组成的磷脂都能形成具有生物学功能的膜。细菌将脂肪酸降解为乙酰辅酶A,然后再用这种乙酰辅酶A合成相同(或功能等效)的脂肪酸用于磷脂合成,这将是一种浪费。这种推理表明,在向生长培养基中添加长链脂肪酸时,细菌可能会关闭内源性脂肪酸合成。此外,这种关闭可能与脂肪酸降解紧密相关,这样细菌细胞会将一部分外源脂肪酸用于磷脂合成,同时将其余部分降解为乙酰辅酶A。在一定程度上,细菌既能得到它的蛋糕(用于磷脂合成的酰基链)又能吃掉它(形成乙酰辅酶A)。事实证明,在大肠杆菌中就是这种情况。这一调节策略中的关键角色是FadR,它是一种转录因子,既作为脂肪酸降解的阻遏物,又作为脂肪酸生物合成的激活剂。

相似文献

1
FadR, transcriptional co-ordination of metabolic expediency.法德R,代谢便利性的转录协调。
Mol Microbiol. 1998 Aug;29(4):937-43. doi: 10.1046/j.1365-2958.1998.00917.x.
2
The Escherichia coli FadR transcription factor: Too much of a good thing?大肠杆菌 FadR 转录因子:过犹不及?
Mol Microbiol. 2021 Jun;115(6):1080-1085. doi: 10.1111/mmi.14663. Epub 2020 Dec 19.
3
Regulation of transcription of genes required for fatty acid transport and unsaturated fatty acid biosynthesis in Escherichia coli by FadR.FadR对大肠杆菌中脂肪酸转运及不饱和脂肪酸生物合成所需基因转录的调控
Mol Microbiol. 1993 Jan;7(2):311-22. doi: 10.1111/j.1365-2958.1993.tb01122.x.
4
Analysis of acyl coenzyme A binding to the transcription factor FadR and identification of amino acid residues in the carboxyl terminus required for ligand binding.酰基辅酶A与转录因子FadR结合的分析以及鉴定配体结合所需羧基末端的氨基酸残基。
J Biol Chem. 1995 Jan 20;270(3):1092-7. doi: 10.1074/jbc.270.3.1092.
5
A new glimpse of FadR-DNA crosstalk revealed by deep dissection of the E. coli FadR regulatory protein.通过对大肠杆菌FadR调节蛋白的深入剖析揭示了FadR与DNA相互作用的新视角。
Protein Cell. 2014 Dec;5(12):928-39. doi: 10.1007/s13238-014-0107-3. Epub 2014 Oct 15.
6
The Vibrio cholerae fatty acid regulatory protein, FadR, represses transcription of plsB, the gene encoding the first enzyme of membrane phospholipid biosynthesis.霍乱弧菌脂肪酸调节蛋白 FadR 抑制编码膜磷脂生物合成第一步酶的 plsB 基因的转录。
Mol Microbiol. 2011 Aug;81(4):1020-33. doi: 10.1111/j.1365-2958.2011.07748.x. Epub 2011 Jul 19.
7
Modulation of FadR binding capacity for acyl-CoA fatty acids through structure-guided mutagenesis.通过结构引导诱变对FadR与酰基辅酶A脂肪酸结合能力的调节。
Protein J. 2015 Oct;34(5):359-66. doi: 10.1007/s10930-015-9630-1.
8
Reassessment of the Genetic Regulation of Fatty Acid Synthesis in Escherichia coli: Global Positive Control by the Dual Functional Regulator FadR.大肠杆菌中脂肪酸合成的遗传调控的重新评估:双功能调节因子FadR的全局正调控
J Bacteriol. 2015 Jun;197(11):1862-72. doi: 10.1128/JB.00064-15. Epub 2015 Mar 23.
9
Unexpected functional diversity among FadR fatty acid transcriptional regulatory proteins.FadR脂肪酸转录调节蛋白之间意想不到的功能多样性。
J Biol Chem. 2005 Sep 16;280(37):32148-56. doi: 10.1074/jbc.M504054200. Epub 2005 Jul 15.
10
Binding of Shewanella FadR to the fabA fatty acid biosynthetic gene: implications for contraction of the fad regulon.希瓦氏菌FadR与fabA脂肪酸生物合成基因的结合:对fad操纵子收缩的影响
Protein Cell. 2015 Sep;6(9):667-679. doi: 10.1007/s13238-015-0172-2. Epub 2015 Jun 7.

引用本文的文献

1
Characterizing the fatty acid degradation operon.对脂肪酸降解操纵子进行表征。
J Bacteriol. 2025 Jul 17:e0008925. doi: 10.1128/jb.00089-25.
2
PlsX and PlsY: Additional roles beyond glycerophospholipid synthesis in Gram-negative bacteria.PlsX和PlsY:革兰氏阴性菌中甘油磷脂合成之外的其他作用。
mBio. 2024 Dec 11;15(12):e0296924. doi: 10.1128/mbio.02969-24. Epub 2024 Oct 30.
3
Regulation of fadR on the ROS defense mechanism in Shewanalla oneidensis.调控 Shewanalla oneidensis 活性氧防御机制中的 fadR。
Biotechnol Lett. 2024 Aug;46(4):691-698. doi: 10.1007/s10529-024-03487-y. Epub 2024 May 6.
4
A guide to virulence capabilities, as we currently understand them.一份关于我们目前所理解的毒力能力的指南。
Front Cell Infect Microbiol. 2024 Jan 11;13:1322853. doi: 10.3389/fcimb.2023.1322853. eCollection 2023.
5
Unsaturated fatty acid synthesis in bacteria: Mechanisms and regulation of canonical and remarkably noncanonical pathways.细菌中不饱和脂肪酸的合成:典型和显著非典型途径的机制和调控。
Biochimie. 2024 Mar;218:137-151. doi: 10.1016/j.biochi.2023.09.007. Epub 2023 Sep 6.
6
Transient Antibiotic Tolerance Triggered by Nutrient Shifts From Gluconeogenic Carbon Sources to Fatty Acid.由糖异生碳源向脂肪酸的营养物质转变引发的短暂抗生素耐受性
Front Microbiol. 2022 Mar 11;13:854272. doi: 10.3389/fmicb.2022.854272. eCollection 2022.
7
Checkpoints That Regulate Balanced Biosynthesis of Lipopolysaccharide and Its Essentiality in .调控脂多糖平衡生物合成的检查点及其在 …… 中的必要性
Int J Mol Sci. 2021 Dec 24;23(1):189. doi: 10.3390/ijms23010189.
8
Cellular Self-Digestion and Persistence in Bacteria.细菌中的细胞自我消化与持续性
Microorganisms. 2021 Oct 31;9(11):2269. doi: 10.3390/microorganisms9112269.
9
The Classical, Yet Controversial, First Enzyme of Lipid Synthesis: Escherichia coli Acetyl-CoA Carboxylase.经典但颇具争议的脂质合成第一酶:大肠杆菌乙酰辅酶 A 羧化酶。
Microbiol Mol Biol Rev. 2021 Aug 18;85(3):e0003221. doi: 10.1128/MMBR.00032-21. Epub 2021 Jun 16.
10
Mycobacterial fatty acid catabolism is repressed by FdmR to sustain lipogenesis and virulence.分枝杆菌的脂肪酸分解代谢受到 FdmR 的抑制,以维持脂生成和毒力。
Proc Natl Acad Sci U S A. 2021 Apr 20;118(16). doi: 10.1073/pnas.2019305118.