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携带有经改造的外源性全局调控因子 IrrE 的大肠杆菌菌株的转录组和蛋白质组的显著重编。

Significant rewiring of the transcriptome and proteome of an Escherichia coli strain harboring a tailored exogenous global regulator IrrE.

机构信息

Department of Chemical Engineering, Tsinghua University, Beijing, China.

出版信息

PLoS One. 2012;7(7):e37126. doi: 10.1371/journal.pone.0037126. Epub 2012 Jul 5.

Abstract

Cell reprogramming for microorganisms via engineered or artificial transcription factors and RNA polymerase mutants has presented a powerful tool for eliciting complex traits that are practically useful particularly for industrial strains, and for understanding at the global level the regulatory network of gene transcription. We previously further showed that an exogenous global regulator IrrE (derived from the extreme radiation-resistant bacterium Deinococcus radiodurans) can be tailored to confer Escherichia coli (E. coli) with significantly enhanced tolerances to different stresses. In this work, based on comparative transcriptomic and proteomic analyses of the representative strains E1 and E0, harboring the ethanol-tolerant IrrE mutant E1 and the ethanol-intolerant wild type IrrE, respectively, we found that the transcriptome and proteome of E. coli were extensively rewired by the tailored IrrE protein. Overall, 1196 genes (or approximately 27% of E. coli genes) were significantly altered at the transcriptomic level, including notably genes in the nitrate-nitrite-nitric oxide (NO) pathway, and genes for non-coding RNAs. The proteomic profile revealed significant up- or downregulation of several proteins associated with syntheses of the cell membrane and cell wall. Analyses of the intracellular NO level and cell growth under reduced temperature supported a close correlation between NO and ethanol tolerance, and also suggests a role for membrane fluidity. The significantly different omic profiles of strain E1 indicate that IrrE functions as a global regulator in E. coli, and that IrrE may be evolved for other cellular tolerances. In this sense, it will provide synthetic biology with a practical and evolvable regulatory "part" that operates at a higher level of complexity than local regulators. This work also suggests a possibility of introducing and engineering other exogenous global regulators to rewire the genomes of microorganism cells.

摘要

通过工程或人工转录因子和 RNA 聚合酶突变体对微生物进行细胞重编程,为获得具有实际用途的复杂特性提供了一种强大的工具,特别是对于工业菌株,并且可以在全球范围内了解基因转录的调控网络。我们之前进一步表明,一种外源性全局调节剂 IrrE(源自极端抗辐射细菌 Deinococcus radiodurans)可以被定制,以使大肠杆菌(E. coli)对不同压力具有显着增强的耐受性。在这项工作中,基于分别携带耐受乙醇的 IrrE 突变体 E1 和不耐受乙醇的野生型 IrrE 的代表菌株 E1 和 E0 的比较转录组学和蛋白质组学分析,我们发现定制的 IrrE 蛋白广泛地重新连接了大肠杆菌的转录组和蛋白质组。总体而言,1196 个基因(或约占大肠杆菌基因的 27%)在转录组水平上发生了显着改变,包括硝酸盐-亚硝酸盐-一氧化氮(NO)途径中的基因和非编码 RNA 基因。蛋白质组谱显示与细胞膜和细胞壁合成相关的几种蛋白质的表达水平显著上调或下调。在低温下分析细胞内 NO 水平和细胞生长情况,支持了 NO 与乙醇耐受性之间的密切相关性,并表明膜流动性的作用。菌株 E1 的显着不同的组学图谱表明,IrrE 在大肠杆菌中作为全局调节剂发挥作用,并且 IrrE 可能是为其他细胞耐受性而进化的。从这个意义上讲,它将为合成生物学提供一种实用且可进化的调节“部件”,其作用在比局部调节剂更高的复杂水平上。这项工作还表明,有可能引入和工程化其他外源性全局调节剂来重新布线微生物细胞的基因组。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/943a/3390347/08e34acbdd7e/pone.0037126.g001.jpg

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