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Interactive Regulation of Formate Dehydrogenase during CO 2 Fixation in Gas-Fermenting Bacteria

机译:含有CO 2 固定期间甲酸脱氢酶的互动调节液体发酵细菌

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Protein lysine acetylation, a prevalent posttranslational modification, regulates numerous crucial biological processes in cells. Nevertheless, how lysine acetylation interacts with other types of regulation to coordinate metabolism remains largely unknown owing to the complexity of the process. Here, using a representative gas-fermenting bacterium, Clostridium ljungdahlii , we revealed a novel regulatory mechanism that employs both the lysine acetylation and transcriptional regulation systems to interactively control CO _(2) fixation, a key biological process for utilizing this one-carbon gas. A dominant lysine acetyltransferase/deacetylase system, At2/Dat1, was identified and found to regulate FDH1 (formate dehydrogenase responsible for CO _(2) fixation) activity via a crucial acetylation site (lysine-29). Notably, the global transcription factor CcpA was also shown to be regulated by At2/Dat1; in turn, CcpA could directly control At2 expression, thus indicating an unreported interaction mode between the acetylation system and transcription factors. Moreover, CcpA was observed to negatively regulate FDH1 expression, which, when combined with At2/Dat1, leads to the collaborative regulation of this enzyme. Based on this concept, we reconstructed the regulatory network related to FDH1, realizing significantly increased CO _(2) utilization by C. ljungdahlii .
机译:蛋白质赖氨酸乙酰化,普遍的后期改性,调节细胞中许多关键的生物过程。然而,由于该方法的复杂性,赖氨酸乙酰化与其他类型的调节相互作用以坐标的调节仍然在很大程度上是未知的。在这里,使用代表性气体发酵细菌,Ljungdahlii,我们揭示了一种新的调节机制,该调节机制采用赖氨酸乙酰化和转录调节系统以交互控制CO _(2)固定,是利用该单碳气体的关键生物学方法。鉴定了一种主要的赖氨酸乙酰转移酶/脱乙酰酶系统,AT2 / DAT1,并发现通过关键的乙酰化位点(Lysine-29)调节FDH1(甲醛负责的脱氢酶,负责CO _(2)固定)活性。值得注意的是,还显示全局转录因子CCPA由AT2 / DAT1调节;反过来,CCPA可以直接控制AT2表达,从而指示乙酰化系统和转录因子之间的未报告的相互作用模式。此外,观察到CCPA对抗FDH1表达,当与AT2 / DAT1结合时,该表达导致该酶的协同调节。基于这一概念,我们重建了与FDH1相关的监管网络,实现了C.Ljungdahlii的C. Ljungdahlii的显着增加了Co _(2)利用。

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