Abstract

This review covers the main transcriptional mechanisms that control membrane phospholipid synthesis in bacteria. The fatty acid components are the most energetically expensive modules to produce; thus, the regulation of fatty acid production is very tightly controlled to match the growth rate of cells. Gram-negative and Gram-positive bacteria have evolved different structural classes of regulators to control the genes required for fatty acid biosynthesis. Also, there are other transcriptional regulators that allow the cells to alter the structure of fatty acids in existing phospholipid molecules or to modify the structures of exogenous fatty acids prior to their incorporation into the bilayer. A major thrust for future research in this area is the identification of the ligands or effectors that control the DNA binding activity of the transcriptional regulators of fatty acid biosynthesis. With the exception of malonyl-CoA regulation of FapR from Bacillus subtilis and long-chain acyl-CoA regulation of FadR from Escherichia coli and DesT from Pseudomonas aeruginosa, the identity of these intracellular regulators remains unknown.

Highlights

  • This review covers the main transcriptional mechanisms that control membrane phospholipid synthesis in bacteria

  • Coordination of fatty acid synthesis and degradation by FadR in Escherichia coli The fatty acid degradative and biosynthetic pathways are coordinated in E. coli to take advantage of the changing availability of fatty acids in their environment through a bifunctional transcription factor, FadR [2]

  • Genetic data had demonstrated that the fatty acid degradative enzymes encoded by the fad genes are inducible, and it was subsequently shown that FadR controls the transcription of the entire fad regulon that consists of all enzymes required to completely degrade fatty acids to acetyl-CoA plus the enzymes of the glyoxylate bypass

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Summary

Introduction

This review covers the main transcriptional mechanisms that control membrane phospholipid synthesis in bacteria. The 240 region is typically associated with transcriptional activators, and this finding suggested that DNA-bound FadR functions as a repressor of b-oxidation regulon, and is an activator of the fabA gene of fatty acid biosynthesis (Table 1). FadR was demonstrated to regulate the fabB gene expression [10], a second protein that is essential for unsaturated fatty acid synthesis in E. coli.

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