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首页> 外文期刊>Biotechnology Journal: Healthcare,Nutrition,Technology >Efficient 3-Hydroxybutyrate Production by Quiescent Escherichia coli Microbial Cell Factories is Facilitated by Indole-Induced Proteomic and Metabolomic Changes
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Efficient 3-Hydroxybutyrate Production by Quiescent Escherichia coli Microbial Cell Factories is Facilitated by Indole-Induced Proteomic and Metabolomic Changes

机译:通过吲哚诱导的蛋白质组学和代谢组变化,促进了静态大肠杆菌微生物细胞工厂的高效3-羟基丁酸盐生产

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The authors show that quiescent (Q-Cell) Escherichia coli cultures can maintain metabolic activity in the absence of growth for up to 24h, leading to four times greater specific productivity of a model metabolite, 3-hydroxybutyrate (3HB), than a control. Q-cells can be created by using the proton ionophore indole to halt cell division of an hns mutant strain. This uncouples metabolism from cell growth and allows for more efficient use of carbon feedstocks because less metabolic effort is diverted to surplus biomass production. However, the reason for the increased productivity of cells in the quiescent state was previously unknown. In this study, proteome expression patterns between wild-type and Q-cell cultures show that Q-cells overexpress stress response proteins, which prime them to tolerate the metabolic imbalances incurred through indole addition. Metabolomic data reveal the accumulation of acetyl-coenzyme A and phosphoenolpyruvate: excellent starting points for high-value chemical production. We demonstrate the exploitation of these accumulated metabolites by engineering a simple pathway for 3HB production from acetyl-coenzyme A. Quiescent cultures produced half the cell biomass of control cultures lacking indole, but were still able to produce 39.4gL(-1) of 3HB compared to 18.6gL(-1) in the control. Q-cells therefore have great potential as a platform technology for the efficient production of a wide range of commodity and high value chemicals.
机译:作者表明,静止(Q细胞)大肠杆菌培养物可以在没有增长的情况下维持代谢活性最多24小时,导致模型代谢物,3-羟基丁酸酯(3HB)的比例较高的四倍。可以通过使用质子离子载体吲哚来创建Q细胞,以阻止HNS突变菌株的细胞分裂。这种脱位来自细胞生长的代谢并允许更有效地使用碳原料,因为代谢努力减少到过剩的生物质生产。然而,静态状态下细胞生产率提高的原因先前是未知的。在该研究中,野生型和Q细胞培养物之间的蛋白酶组表达模式表明Q-Cells过表达应激响应蛋白,其使它们赋予通过吲哚加入产生的代谢性失调。代谢物数据揭示了乙酰辅酶A和磷酸丙酯的积累:高价值化学生产的优异出发点。我们通过工程证明了这些积累了代谢物的剥削了一种简单的途径,从乙酰辅酶A.静止培养物产生了一半的对照培养物缺乏吲哚的细胞生物质,但相比仍然能够产生39.4g1(-1)3hb在控制中到18.6gl(-1)。因此,Q-Cells具有巨大的潜力作为高效生产各种商品和高价值化学品的平台技术。

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