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A retrospective: use of Escherichia coli as a vehicle to study phospholipid synthesis and function.一项回顾性研究:利用大肠杆菌作为载体来研究磷脂的合成与功能。
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2
Molecular genetics of membrane phospholipid synthesis.膜磷脂合成的分子遗传学
Annu Rev Genet. 1986;20:253-95. doi: 10.1146/annurev.ge.20.120186.001345.
3
Overproduction of a foreign membrane protein in Escherichia coli stimulates and depends on phospholipid synthesis.在大肠杆菌中外源膜蛋白的过量产生会刺激并依赖于磷脂合成。
Eur J Biochem. 1996 Oct 15;241(2):691-6. doi: 10.1111/j.1432-1033.1996.00691.x.
4
Involvement of the YneS/YgiH and PlsX proteins in phospholipid biosynthesis in both Bacillus subtilis and Escherichia coli.YneS/YgiH蛋白和PlsX蛋白在枯草芽孢杆菌和大肠杆菌磷脂生物合成中的作用。
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Understanding phospholipid function: Why are there so many lipids?了解磷脂的功能:为何存在如此多的脂质?
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Mutants of Escherichia coli defective in membrane phospholipid synthesis. Effects of cessation and reinitiation of phospholipid synthesis on macromolecular synthesis and phospholipid turnover.膜磷脂合成存在缺陷的大肠杆菌突变体。磷脂合成的停止和重新启动对大分子合成及磷脂周转的影响。
J Biol Chem. 1977 Jul 10;252(13):4487-93.
7
Metabolic regulations and biological functions of phospholipids in Escherichia coli.
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Anionic lipid binding to the foreign protein MGS provides a tight coupling between phospholipid synthesis and protein overexpression in Escherichia coli.阴离子脂质与外源蛋白 MGS 的结合为大肠杆菌中外源蛋白的过度表达与磷脂合成之间提供了紧密的偶联。
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9
Archaeal phospholipid biosynthetic pathway reconstructed in Escherichia coli.古菌磷脂生物合成途径在大肠杆菌中的重建。
Archaea. 2012;2012:438931. doi: 10.1155/2012/438931. Epub 2012 May 9.
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Membrane phospholipid synthesis in Escherichia coli: alteration by glycerol and physiological consequences in a pss mutant.大肠杆菌中的膜磷脂合成:甘油的改变及其在pss突变体中的生理后果
J Biochem. 1986 May;99(5):1393-400. doi: 10.1093/oxfordjournals.jbchem.a135608.

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本文引用的文献

1
Discovery of a cardiolipin synthase utilizing phosphatidylethanolamine and phosphatidylglycerol as substrates.发现一种以磷脂酰乙醇胺和磷脂酰甘油为底物的心磷脂合酶。
Proc Natl Acad Sci U S A. 2012 Oct 9;109(41):16504-9. doi: 10.1073/pnas.1212797109. Epub 2012 Sep 17.
2
Phosphatidic acid synthesis in bacteria.细菌中的磷脂酸合成
Biochim Biophys Acta. 2013 Mar;1831(3):495-502. doi: 10.1016/j.bbalip.2012.08.018. Epub 2012 Aug 30.
3
Lipid-dependent generation of dual topology for a membrane protein.脂依赖性膜蛋白的双重拓扑结构生成
J Biol Chem. 2012 Nov 2;287(45):37939-48. doi: 10.1074/jbc.M112.404103. Epub 2012 Sep 10.
4
Arrangement of the respiratory chain complexes in Saccharomyces cerevisiae supercomplex III2IV2 revealed by single particle cryo-electron microscopy.利用单颗粒冷冻电子显微镜技术揭示酿酒酵母超级复合物 III2IV2 中的呼吸链复合物排列。
J Biol Chem. 2012 Jun 29;287(27):23095-103. doi: 10.1074/jbc.M112.367888. Epub 2012 May 9.
5
An essential bacterial-type cardiolipin synthase mediates cardiolipin formation in a eukaryote.一种必需的细菌型心磷脂合酶在真核生物中介导心磷脂的形成。
Proc Natl Acad Sci U S A. 2012 Apr 17;109(16):E954-61. doi: 10.1073/pnas.1121528109. Epub 2012 Mar 26.
6
Metabolism and regulation of glycerolipids in the yeast Saccharomyces cerevisiae.酵母酿酒酵母中甘油酯的代谢和调控。
Genetics. 2012 Feb;190(2):317-49. doi: 10.1534/genetics.111.130286.
7
Exploring the relationship between lipoprotein mislocalization and activation of the Rcs signal transduction system in Escherichia coli.探讨脂蛋白定位错误与大肠杆菌 Rcs 信号转导系统激活之间的关系。
Microbiology (Reading). 2012 May;158(Pt 5):1238-1248. doi: 10.1099/mic.0.056945-0. Epub 2012 Feb 9.
8
The Raetz pathway for lipid A biosynthesis: Christian Rudolf Hubert Raetz, MD PhD, 1946–2011.脂多糖A生物合成的雷茨途径:克里斯蒂安·鲁道夫·休伯特·雷茨,医学博士、哲学博士,1946 - 2011年。
J Lipid Res. 2011 Nov;52(11):1857-1860. doi: 10.1194/jlr.e020701.
9
Chris Raetz, scientist and enduring friend.克里斯·雷茨,科学家兼挚友。
Proc Natl Acad Sci U S A. 2011 Oct 18;108(42):17255-6. doi: 10.1073/pnas.1114405108. Epub 2011 Oct 3.
10
Mitochondrial phosphatase PTPMT1 is essential for cardiolipin biosynthesis.线粒体磷酸酶 PTPMT1 对心磷脂生物合成至关重要。
Cell Metab. 2011 Jun 8;13(6):690-700. doi: 10.1016/j.cmet.2011.04.007.

一项回顾性研究:利用大肠杆菌作为载体来研究磷脂的合成与功能。

A retrospective: use of Escherichia coli as a vehicle to study phospholipid synthesis and function.

作者信息

Dowhan William

机构信息

Department of Biochemistry and Molecular Biology, University of Texas Medical School-Houston, Houston, TX 77030, USA.

出版信息

Biochim Biophys Acta. 2013 Mar;1831(3):471-94. doi: 10.1016/j.bbalip.2012.08.007. Epub 2012 Aug 14.

DOI:10.1016/j.bbalip.2012.08.007
PMID:22925633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3513495/
Abstract

Although the study of individual phospholipids and their synthesis began in the 1920s first in plants and then mammals, it was not until the early 1960s that Eugene Kennedy using Escherichia coli initiated studies of bacterial phospholipid metabolism. With the base of information already available from studies of mammalian tissue, the basic blueprint of phospholipid biosynthesis in E. coli was worked out by the late 1960s. In 1970s and 1980s most of the enzymes responsible for phospholipid biosynthesis were purified and many of the genes encoding these enzymes were identified. By the late 1990s conditional and null mutants were available along with clones of the genes for every step of phospholipid biosynthesis. Most of these genes had been sequenced before the complete E. coli genome sequence was available. Strains of E. coli were developed in which phospholipid composition could be changed in a systematic manner while maintaining cell viability. Null mutants, strains in which phospholipid metabolism was artificially regulated, and strains synthesizing foreign lipids not found in E. coli have been used to this day to define specific roles for individual phospholipid. This review will trace the findings that have led to the development of E. coli as an excellent model system to study mechanisms underlying the synthesis and function of phospholipids that are widely applicable to other prokaryotic and eukaryotic systems. This article is part of a Special Issue entitled Phospholipids and Phospholipid Metabolism.

摘要

尽管对单个磷脂及其合成的研究始于20世纪20年代,最初是在植物中,然后是在哺乳动物中,但直到20世纪60年代初,尤金·肯尼迪利用大肠杆菌才开始了对细菌磷脂代谢的研究。基于对哺乳动物组织研究已有的信息基础,到20世纪60年代末,大肠杆菌中磷脂生物合成的基本蓝图已被绘制出来。在20世纪70年代和80年代,大多数负责磷脂生物合成的酶被纯化,并且许多编码这些酶的基因被鉴定出来。到20世纪90年代末,条件突变体和无效突变体已可获得,同时磷脂生物合成每一步的基因克隆也已具备。在完整的大肠杆菌基因组序列可用之前,这些基因中的大多数已经被测序。已开发出大肠杆菌菌株,在这些菌株中,磷脂组成可以以系统的方式改变,同时保持细胞活力。至今,无效突变体、磷脂代谢被人工调控的菌株以及合成大肠杆菌中不存在的外源脂质的菌株,都被用于确定单个磷脂的特定作用。本综述将追溯那些使大肠杆菌成为研究磷脂合成和功能机制的优秀模型系统的研究成果,这些机制广泛适用于其他原核和真核系统。本文是名为“磷脂与磷脂代谢”的特刊的一部分。