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Antagonistic regulation of dgkA and plsB genes of phospholipid synthesis by multiple stress responses in Escherichia coli

生物 磷脂 二酰甘油激酶 基因 大肠杆菌 生物化学 酰基转移酶 西格玛因子 细胞生物学 基因表达 发起人 蛋白激酶C
作者
Astrid Klopstad Wahl,Lætitia My,Romain Dumoulin,James N. Sturgis,Emmanuelle Bouveret
出处
期刊:Molecular Microbiology [Wiley]
卷期号:80 (5): 1260-1275 被引量:38
标识
DOI:10.1111/j.1365-2958.2011.07641.x
摘要

Summary Phospholipid homeostasis of the bacterial membrane is maintained by biochemical regulation of the synthesis enzymes depending on the environment. However, genes encoding phospholipid synthesis enzymes might also be regulated during stress responses, in order for the bacteria to adapt their growth to changing environments. While few studies have addressed this question, global analyses show that specific genes are activated by alternative Sigma factors, and that phospholipid synthesis genes are co‐ordinately regulated during stringent response. In Escherichia coli , the genes coding for glycerol‐3‐phosphate acyltransferase and diacylglycerol kinase ( plsB and dgkA ) are found next to each other in divergent orientations, suggesting a co‐ordinated regulation. We investigated their regulation and found that these two genes are inversely regulated by a diversity of stress responses. plsB activation by σE is concomitant with a reduced DgkA amount. A second proximal promoter for plsB expression is responsible for basal plsB expression and is inhibited during stringent response. Finally, dgkA is activated by the two‐component regulator BasR, linking dgkA function of phospholipid recycling to LPS modifications. In E. coli , PlsB and DgkA are key enzymes in the phospholipid synthesis pathway. Our results show that their expression is a crucial point of integration for different stress signals.

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