H-NS involved in positive regulation of glycerol dehydratase gene expression in Klebsiella pneumoniae 2e.

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Applied and Environmental Microbiology Pub Date : 2024-08-21 Epub Date: 2024-07-12 DOI:10.1128/aem.00075-24
Le Li, Qiang Li, Yuting Xiao, Jiangshan Ma, Gao-Qiang Liu
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Abstract

Glycerol dehydratase is the key and rate-limiting enzyme in the 1,3-propanediol synthesis pathway of Klebsiella pneumoniae, which determined the producing rate and yield of 1,3-propanediol. However, the expression regulation mechanism of glycerol dehydratase gene dhaB remains poorly unknown. In this study, a histone-like nucleoid-structuring (H-NS) protein was identified and characterized as the positive transcription regulator for dhaB expression in K. pneumoniae 2e, which exhibited high tolerance against crude glycerol in our previous study. Deletion of hns gene significantly decreased the transcription level of dhaB in K. pneumoniae 2e, which led to a remarkable defect on strain growth, glycerol dehydratase activity, and 3-hydroxypropanal production during glycerol fermentation. The transcription level of dhaB was significantly up-regulated in crude glycerol relative to pure glycerol, while the inactivation of H-NS resulted in more negative effect for transcription level of dhaB in the former. Though the H-NS expression level was almost comparable in both substrates, its multimer state was reduced in crude glycerol relative to pure glycerol, suggesting that the oligomerization state of H-NS might have contributed for positive regulation of dhaB expression. Furthermore, electrophoretic mobility shift and DNase I footprinting assays showed that H-NS could directly bind to the upstream promoter region of dhaB by recognizing the AT-rich region. These findings provided new insight into the transcriptional regulation mechanism of H-NS for glycerol dehydratase expression in K. pneumoniae, which might offer new target for engineering bacteria to industrially produce 1,3-propanediol.IMPORTANCEThe biological production of 1,3-propanediol from glycerol by microbial fermentation shows great promising prospect on industrial application. Glycerol dehydratase catalyzes the penultimate step in glycerol metabolism and is regarded as one of the key and rate-limiting enzymes for 1,3-propanediol production. H-NS was reported as a pleiotropic modulator with negative effects on gene expression in most studies. Here, we reported for the first time that the expression of glycerol dehydratase gene is positively regulated by the H-NS. The results provide insight into a novel molecular mechanism of H-NS for positive regulation of glycerol dehydratase gene expression in K. pneumoniae, which holds promising potential for facilitating construction of engineering highly efficient 1,3-propanediol-producing strains.

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H-NS 参与正向调节肺炎克雷伯氏菌 2e 中甘油脱水酶基因的表达。
甘油脱水酶是肺炎克雷伯氏菌 1,3-丙二醇合成途径中的关键酶和限速酶,决定着 1,3-丙二醇的产生速率和产量。然而,甘油脱水酶基因 dhaB 的表达调控机制仍然鲜为人知。本研究发现了一种组蛋白样核结构蛋白(H-NS),并将其表征为肺炎双球菌 2e 中 dhaB 表达的正转录调节因子。删除 hns 基因会显著降低肺炎双球菌 2e 中 dhaB 的转录水平,从而导致菌株生长、甘油脱水酶活性和甘油发酵过程中 3-羟基丙醛产量的显著缺陷。与纯甘油相比,粗甘油中 dhaB 的转录水平明显上调,而 H-NS 失活则对前者中 dhaB 的转录水平产生了更大的负面影响。虽然 H-NS 在两种底物中的表达水平几乎相当,但其多聚体状态在粗甘油中相对于纯甘油有所降低,这表明 H-NS 的寡聚化状态可能对 dhaB 的表达有正向调节作用。此外,电泳迁移和DNase I足迹分析表明,H-NS可通过识别富含AT的区域直接与dhaB上游启动子区域结合。这些发现为了解 H-NS 在肺炎双球菌中对甘油脱水酶表达的转录调控机制提供了新的视角,可能为工业化生产 1,3-丙二醇的细菌工程提供新的靶标。重要意义通过微生物发酵以甘油为原料生产 1,3-丙二醇具有广阔的工业应用前景。甘油脱水酶催化甘油代谢的倒数第二步,被认为是生产 1,3-丙二醇的关键和限速酶之一。据报道,在大多数研究中,H-NS 是一种多效调节剂,对基因表达有负面影响。在此,我们首次报道了甘油脱水酶基因的表达受 H-NS 的正向调节。该研究结果提供了一种新的 H-NS 正向调控肺炎双球菌甘油脱水酶基因表达的分子机制,有望促进构建高效的 1,3 丙二醇生产菌株。
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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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