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大肠杆菌膜脂稳态的转录调控。

Transcriptional regulation of membrane lipid homeostasis in Escherichia coli.

机构信息

Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USA.

出版信息

J Biol Chem. 2009 Dec 11;284(50):34880-8. doi: 10.1074/jbc.M109.068239. Epub 2009 Oct 23.

Abstract

The biophysical properties of membrane phospholipids are controlled by the composition of their constituent fatty acids and are tightly regulated in Escherichia coli. The FabR (fatty acid biosynthesis repressor) transcriptional repressor controls the proportion of unsaturated fatty acids in the membrane by regulating the expression of the fabB (beta-ketoacyl-ACP synthase I) and fabA (beta-hydroxydecanoyl-ACP dehydratase/isomerase) genes. FabR binding to a DNA palindrome located within the promoters of the fabB and fabA genes required the presence of an unsaturated acyl-acyl carrier protein (ACP) or acyl-CoA and was antagonized by saturated acyl-ACP or acyl-CoA. The FabR-dependent repression of fabB and fabA by exogenous unsaturated fatty acids confirmed the role for FabR in responding to the acyl-CoA pool composition, and the perturbation of the unsaturated:saturated acyl-ACP ratio using a specific inhibitor of lipid A formation verified FabR-dependent regulation of fabB by the acyl-ACP composition in vivo. Thus, FabR plays a key role in controlling the membrane biophysical properties by regulating gene expression in response to the composition of the long-chain acyl-thioester pool. This mechanism ensures that a balanced composition of fatty acids is available for incorporation into the membrane via the PlsB/PlsC acyltransferases.

摘要

膜脂磷酰的生物物理性质由其组成脂肪酸的成分控制,并在大肠杆菌中受到严格调控。FabR(脂肪酸生物合成阻遏物)转录阻遏物通过调节 fabB(β-酮酰-ACP 合酶 I)和 fabA(β-羟癸酰-ACP 脱水酶/异构酶)基因的表达来控制膜中不饱和脂肪酸的比例。FabR 与位于 fabB 和 fabA 基因启动子内的 DNA 回文结构的结合需要不饱和酰基-ACP 或酰基-CoA 的存在,并且受到饱和酰基-ACP 或酰基-CoA 的拮抗。外源性不饱和脂肪酸对 fabB 和 fabA 的 FabR 依赖性抑制证实了 FabR 在响应酰基-CoA 池组成方面的作用,并且使用脂质 A 形成的特异性抑制剂扰乱不饱和:饱和酰基-ACP 比证实了 FabR 依赖性通过体内酰基-ACP 组成对 fabB 的调节。因此,FabR 通过响应长链酰基硫酯池的组成来调节基因表达,从而在控制膜生物物理性质方面发挥关键作用。该机制确保通过 PlsB/PlsC 酰基转移酶将平衡的脂肪酸组成掺入膜中。

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