A Eukaryote-Featured Membrane Phospholipid Enhances Bacterial Formaldehyde Tolerance and Assimilation of One-Carbon Feedstocks.

IF 3.7 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
MengKun Li, Wenjie Sun, Xin Wang, Kequan Chen, Yan Feng, Zaigao Tan
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Abstract

Efficient bioassimilation of one-carbon (C1) feedstocks is often hindered by the toxicity of C1 substrates and/or intermediates. We compared the toxicity of several common C1 substrates/intermediates and found that formaldehyde imposes the highest toxicity on the representative bacterium Escherichia coli. Besides causing chromosomal DNA and protein damage effects, here, we revealed that formaldehyde greatly impairs cell membranes. To this end, here, we sought to remodel the cell membrane of E. coli by introducing a non-native, eukaryote-featured membrane phospholipid composition, phosphatidylcholine (PC). This engineered E. coli strain exhibited significantly increased membrane integrity, resulting in enhanced formaldehyde tolerance. When applied to C1 assimilation, the PC-harboring E. coli consumed up to 4.7 g/L methanol, which is 23-fold higher than that of the control strain (0.2 g/L). In summary, the present study highlights the detrimental impact of formaldehyde-induced membrane damage and thus underscores the significance of membrane remodeling in enhancing formaldehyde tolerance and facilitating the assimilation of C1 substrates.

真核生物膜磷脂可增强细菌耐受甲醛和吸收一碳原料的能力
单碳(C1)原料的高效生物同化作用往往受到 C1 底物和/或中间体毒性的阻碍。我们比较了几种常见 C1 底物/中间体的毒性,发现甲醛对代表性细菌大肠杆菌的毒性最高。除了造成染色体 DNA 和蛋白质损伤效应外,我们还发现甲醛会极大地损害细胞膜。为此,我们试图通过引入一种非原生的、具有真核细胞特征的膜磷脂成分--磷脂酰胆碱(PC)来重塑大肠杆菌的细胞膜。这种改造后的大肠杆菌菌株的膜完整性明显增强,从而提高了甲醛耐受性。当应用于 C1 同化时,含 PC 的大肠杆菌消耗的甲醇高达 4.7 克/升,是对照菌株(0.2 克/升)的 23 倍。总之,本研究强调了甲醛诱导的膜损伤的有害影响,从而突出了膜重塑在增强甲醛耐受性和促进 C1 底物同化方面的重要意义。
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来源期刊
CiteScore
8.00
自引率
10.60%
发文量
380
审稿时长
6-12 weeks
期刊介绍: The journal is particularly interested in studies on the design and synthesis of new genetic circuits and gene products; computational methods in the design of systems; and integrative applied approaches to understanding disease and metabolism. Topics may include, but are not limited to: Design and optimization of genetic systems Genetic circuit design and their principles for their organization into programs Computational methods to aid the design of genetic systems Experimental methods to quantify genetic parts, circuits, and metabolic fluxes Genetic parts libraries: their creation, analysis, and ontological representation Protein engineering including computational design Metabolic engineering and cellular manufacturing, including biomass conversion Natural product access, engineering, and production Creative and innovative applications of cellular programming Medical applications, tissue engineering, and the programming of therapeutic cells Minimal cell design and construction Genomics and genome replacement strategies Viral engineering Automated and robotic assembly platforms for synthetic biology DNA synthesis methodologies Metagenomics and synthetic metagenomic analysis Bioinformatics applied to gene discovery, chemoinformatics, and pathway construction Gene optimization Methods for genome-scale measurements of transcription and metabolomics Systems biology and methods to integrate multiple data sources in vitro and cell-free synthetic biology and molecular programming Nucleic acid engineering.
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