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Label-free and redox proteomic analyses of the triacylglycerol-accumulating Rhodococcus jostii RHA1

机译:无基酰基甘油积累rhodococcus jostii rha1的无标记和氧化还原蛋白质组学分析

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The bacterium Rhodococcus jostii RHA1 synthesizes large amounts of triacylglycerols (TAGs) under conditions of nitrogen starvation. To better understand the molecular mechanisms behind this process, we performed proteomic studies in this oleaginous bacterium. Upon nitrogen starvation, we observed a re-routing of the carbon flux towards the formation of TAGs. Under these conditions, the cellular lipid content made up more than half of the cell’s dry weight. On the proteome level, this coincided with a shift towards non-glycolytic carbohydrate-metabolizing pathways. These pathways (Entner–Doudoroff and pentose-phosphate shunt) contribute NADPH and precursors of glycerol 3-phosphate and acetyl-CoA to lipogenesis. The expression of proteins involved in the degradation of branched-chain amino acids and the methylmalonyl-CoA pathway probably provided propionyl-CoA for the biosynthesis of odd-numbered fatty acids, which make up almost 30?% of RHA1 fatty acid composition. Additionally, lipolytic and glycerol-degrading enzymes increased in abundance, suggesting a dynamic cycling of cellular lipids. Conversely, abundance of proteins involved in consuming intermediates of lipogenesis decreased. Furthermore, we identified another level of lipogenesis regulation through redox-mediated thiol modification in R. jostii. Enzymes affected included acetyl-CoA carboxylase and a β-ketoacyl-[acyl-carrier protein] synthase II (FabF). An integrative metabolic model for the oleaginous RHA1 strain is proposed on the basis of our results.
机译:细菌rhodococcus jostii rha1在氮饥饿条件下合成大量的三酰基甘油(标签)。为了更好地了解该过程背后的分子机制,我们在这种含油细菌中进行了蛋白质组学研究。在氮饥饿后,我们观察到碳通量朝向形成标签的重新路由。在这些条件下,细胞脂质含量构成细胞的干重的一半以上。在蛋白质组水平上,这与朝向非甘露糖碳水化合物代谢途径的转变一致。这些途径(Entner-doudoroff和pentose-磷酸分流)有助于NADPH和甘油3-磷酸盐和乙酰-COA的前体对脂肪生成。参与分支链氨基酸降解的蛋白质的表达和甲基马隆-CoA途径可能为奇数脂肪酸的生物合成提供了丙酰基-CoA,其占rhA1脂肪酸组合物的近30?%。另外,脂溶解和甘油降解的酶在丰度中增加,表明细胞脂质的动态循环。相反,参与消耗脂肪生成中间体的丰富蛋白质降低了。此外,我们通过R.Jostii中的氧化还原介导的硫醇改性鉴定了另一种脂肪生成调节水平。受影响的酶包括乙酰基 - COA羧化酶和β-酮酰基 - α-乙基载体蛋白]合成酶II(Fabf)。在我们的结果的基础上提出了of抗性Rha1菌株的一体化代谢模型。

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