Dowhan William
Department of Biochemistry and Molecular Biology, University of Texas Medical School-Houston, Houston, TX 77030, USA.
Biochim Biophys Acta. 2013 Mar;1831(3):471-94. doi: 10.1016/j.bbalip.2012.08.007. Epub 2012 Aug 14.
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.
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。