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翻新双边围栏时是否通知隔壁和街对面的邻居:革兰氏阴性菌的生物细胞质膜为什么会显示不对称性?

Renovating a double fence with or without notifying the next door and across the street neighbors: why the biogenic cytoplasmic membrane of Gram-negative bacteria display asymmetry?

机构信息

Department of Biochemistry and Molecular Biology, University of Texas Health Science Center at Houston, McGovern Medical School, Houston, TX 77030, U.S.A.

出版信息

Emerg Top Life Sci. 2023 Mar 31;7(1):137-150. doi: 10.1042/ETLS20230042.

Abstract

The complex two-membrane organization of the envelope of Gram-negative bacteria imposes an unique biosynthetic and topological constraints that can affect translocation of lipids and proteins synthesized on the cytoplasm facing leaflet of the cytoplasmic (inner) membrane (IM), across the IM and between the IM and outer membrane (OM). Balanced growth of two membranes and continuous loss of phospholipids in the periplasmic leaflet of the IM as metabolic precursors for envelope components and for translocation to the OM requires a constant supply of phospholipids in the IM cytosolic leaflet. At present we have no explanation as to why the biogenic E. coli IM displays asymmetry. Lipid asymmetry is largely related to highly entropically disfavored, unequal headgroup and acyl group asymmetries which are usually actively maintained by active mechanisms. However, these mechanisms are largely unknown for bacteria. Alternatively, lipid asymmetry in biogenic IM could be metabolically controlled in order to maintain uniform bilayer growth and asymmetric transmembrane arrangement by balancing temporally the net rates of synthesis and flip-flop, inter IM and OM bidirectional flows and bilayer chemical and physical properties as spontaneous response. Does such flippase-less or 'lipid only", 'passive' mechanism of generation and maintenance of lipid asymmetry exists in the IM? The driving force for IM asymmetry can arise from the packing requirements imposed upon the bilayer system during cell division through disproportional distribution of two negatively curved phospholipids, phosphatidylethanolamine and cardiolipin, with consistent reciprocal tendency to increase and decrease lipid order in each membrane leaflet respectively.

摘要

革兰氏阴性细菌包膜的复杂双层组织结构带来了独特的生物合成和拓扑约束,这可能会影响在细胞质(内膜)面向细胞质的叶层上合成的脂质和蛋白质穿过内膜并在内膜和外膜之间的易位。两层膜的平衡生长和内膜周质叶层中磷脂作为包膜成分的代谢前体和向外膜的易位不断损失,这需要内膜胞质叶层中磷脂的持续供应。目前,我们还没有解释为什么生物合成的大肠杆菌内膜显示出不对称性。脂质不对称性主要与高度熵不利、不等的头部基团和酰基基团不对称性有关,这些不对称性通常通过主动机制来积极维持。然而,这些机制在细菌中很大程度上是未知的。或者,生物合成的内膜中的脂质不对称性可以通过代谢控制来维持,以通过平衡合成和翻转的净速率、内膜和外膜之间的双向流动以及双层化学和物理性质的时间来维持均匀的双层生长和不对称的跨膜排列作为自发反应。在内膜中是否存在这种没有翻转酶或“仅脂质”、“被动”的脂质不对称生成和维持机制?内膜不对称的驱动力可能来自于细胞分裂期间双层系统所施加的包装要求,通过不成比例地分配两种负曲率的磷脂,磷脂酰乙醇胺和心磷脂,分别在每个膜叶层中一致地增加和减少脂质有序性。

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