Comparative Transcriptome Analysis Reveals the Molecular Mechanisms of Acetic Acid Reduction by Adding NaHSO3 in Actinobacillus succinogenes GXAS137.

Polish journal of microbiology Pub Date : 2023-12-16 eCollection Date: 2023-12-01 DOI:10.33073/pjm-2023-036
Shiyong Li, Chaodong Song, Hongyan Zhang, Yan Qin, Mingguo Jiang, Naikun Shen
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Abstract

Acetic acid (AC) is a major by-product from fermentation processes for producing succinic acid (SA) using Actinobacillus succinogenes. Previous experiments have demonstrated that sodium bisulfate (NaHSO3) can significantly decrease AC production by A. succinogenes GXAS137 during SA fermentation. However, the mechanism of AC reduction is poorly understood. In this study, the transcriptional profiles of the strain were compared through Illumina RNA-seq to identify differentially expressed genes (DEGs). A total of 210 DEGs were identified by expression analysis: 83 and 127 genes up-regulated and down-regulated, respectively, in response to NaHSO3 treatment. The functional annotation analysis of DEGs showed that the genes were mainly involved in carbohydrates, inorganic ions, amino acid transport, metabolism, and energy production and conversion. The mechanisms of AC reduction might be related to two aspects: (i) the lipoic acid synthesis pathway (LipA, LipB) was significantly down-regulated, which blocked the pathway catalyzed by pyruvate dehydrogenase complex to synthesize acetyl-coenzyme A (acetyl-CoA) from pyruvate; (ii) the expression level of the gene encoding bifunctional acetaldehyde-alcohol dehydrogenase was significantly up-regulated, and this effect facilitated the synthesis of ethanol from acetyl-CoA. However, the reaction of NaHSO3 with the intermediate metabolite acetaldehyde blocked the production of ethanol and consumed acetyl-CoA, thereby decreasing AC production. Thus, our study provides new insights into the molecular mechanism of AC decreased underlying the treatment of NaHSO3 and will deepen the understanding of the complex regulatory mechanisms of A. succinogenes.

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琥珀酸放线杆菌GXAS137加入NaHSO3还原乙酸的分子机制
醋酸(AC)是利用琥珀酸放线菌发酵生产琥珀酸(SA)的主要副产物。先前的实验表明,硫酸氢钠(NaHSO3)可以显著降低A. succinogenes GXAS137在SA发酵过程中的AC产量。然而,人们对活性炭还原的机理了解甚少。在本研究中,通过Illumina RNA-seq比较菌株的转录谱以鉴定差异表达基因(DEGs)。通过表达分析,共鉴定出210个deg:在NaHSO3处理下,分别有83个基因上调,127个基因下调。DEGs的功能注释分析表明,这些基因主要参与碳水化合物、无机离子、氨基酸运输、代谢以及能量的产生和转化。AC还原的机制可能与两个方面有关:(1)硫辛酸合成途径(LipA、LipB)显著下调,阻断了丙酮酸脱氢酶复合物催化丙酮酸合成乙酰辅酶A (acetyl-CoA)的途径;(ii)编码双功能乙醛醇脱氢酶的基因表达水平显著上调,促进了乙酰辅酶a合成乙醇。然而,NaHSO3与中间代谢物乙醛的反应阻断了乙醇的产生并消耗了乙酰辅酶a,从而减少了AC的产生。因此,我们的研究为NaHSO3处理下AC降低的分子机制提供了新的见解,并将加深对琥珀酸草复杂调控机制的理解。
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