Departamento de Microbiología Molecular, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Cuernavaca, Morelos, México.
Centro de Ciencias Genómicas, Universidad Nacional Autónoma de México, Cuernavaca, Morelos, México.
Microbiol Res. 2021 Aug;249:126775. doi: 10.1016/j.micres.2021.126775. Epub 2021 Apr 29.
In Pseudomonas spp. PsrA, a transcriptional activator of the rpoS gene, regulates fatty acid catabolism by repressing the fadBA5 β-oxidation operon. In Azotobacter vinelandii, a soil bacterium closely related to Pseudomonas species, PsrA is also an activator of rpoS expression, although its participation in the regulation of lipid metabolism has not been analyzed. In this work we found that inactivation of psrA had no effect on the expression of β-oxidation genes in this bacterium, but instead decreased expression of the unsaturated fatty acid biosynthetic operon fabAB (3-hydroxydecanoyl-ACP dehydratase/isomerase and 3-ketoacyl-ACP synthase I). This inactivation also reduced the unsaturated fatty acid content, as revealed by the thin-layer chromatographic analysis, and confirmed by gas chromatography; notably, there was also a lower content of cyclopropane fatty acids, which are synthesized from unsaturated fatty acids. The absence of PsrA has no effect on the growth rate, but showed loss of cell viability during long-term growth, in accordance with the role of these unsaturated and cyclopropane fatty acids in the protection of membranes. Finally, an electrophoretic mobility shift assay revealed specific binding of PsrA to the fabA promoter region, where a putative binding site for this regulator was located. Taken together, our data show that PsrA plays an important role in the regulation of unsaturated fatty acids metabolism in A. vinelandii by positively regulating fabAB.
在假单胞菌属 spp. 中,PsrA 是 rpoS 基因的转录激活因子,通过抑制 fadBA5β-氧化操纵子来调节脂肪酸代谢。在与假单胞菌属密切相关的土壤细菌固氮菌中,PsrA 也是 rpoS 表达的激活因子,尽管其参与脂质代谢的调节尚未被分析。在这项工作中,我们发现 psrA 的失活对该细菌中β-氧化基因的表达没有影响,但反而降低了不饱和脂肪酸生物合成操纵子 fabAB(3-羟癸酰-ACP 脱水酶/异构酶和 3-酮酰-ACP 合酶 I)的表达。这种失活还降低了不饱和脂肪酸的含量,如薄层色谱分析所揭示的,并通过气相色谱法得到证实;值得注意的是,环丙烷脂肪酸的含量也较低,这些脂肪酸是从不饱和脂肪酸合成的。PsrA 的缺失对生长速率没有影响,但在长期生长过程中显示出细胞活力的丧失,这与这些不饱和和环丙烷脂肪酸在保护膜中的作用一致。最后,电泳迁移率变动分析显示 PsrA 与 fabA 启动子区域特异性结合,该区域存在该调节剂的一个假定结合位点。总之,我们的数据表明,PsrA 通过正向调节 fabAB 在固氮菌不饱和脂肪酸代谢的调节中发挥重要作用。