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首页> 外文期刊>Microbial Cell Factories >Combinatory optimization of chromosomal integrated mevalonate pathway for β-carotene production in Escherichia coli
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Combinatory optimization of chromosomal integrated mevalonate pathway for β-carotene production in Escherichia coli

机译:大肠杆菌中生产β-胡萝卜素的染色体整合甲羟戊酸途径的组合优化

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Background Plasmid expression is a popular method in studies of MVA pathway for isoprenoid production in Escherichia coli . However, heterologous gene expression with plasmid is often not stable and might burden growth of host cells, decreases cell mass and product yield. In this study, MVA pathway was divided into three modules, and two heterologous modules were integrated into the E. coli chromosome. These modules were individually modulated with regulatory parts to optimize efficiency of the pathway in terms of downstream isoprenoid production. Results MVA pathway modules Hmg1 - erg12 operon and mvaS - mvaA - mavD1 operon were integrated into E. coli chromosome followed by modulation with promoters with varied strength. Along with activation of atoB , a 26% increase of β-carotene production with no effect on cell growth was obtained. With a combinatory modulation of two key enzymes mvas and Hmg1 with degenerate RBS library, β-carotene showed a further increase of 51%. Conclusions Our study provides a novel strategy for improving production of a target compound through integration and modulation of heterologous pathways in both transcription and translation level. In addition, a genetically hard-coded chassis with both efficient MEP and MVA pathways for isoprenoid precursor supply was constructed in this work.
机译:背景质粒表达是研究MVA途径在大肠杆菌中生产类异戊二烯的一种流行方法。然而,用质粒进行的异源基因表达通常是不稳定的,并且可能加重宿主细胞的生长,降低细胞质量和产物产量。在这项研究中,MVA途径分为三个模块,两个异源模块整合到大肠杆菌染色体中。这些模块分别通过调节部分进行调节,以优化下游类异戊二烯生产的途径效率。结果将MVA途径模块Hmg1-erg12操纵子和mvaS-mvaA-mavD1操纵子整合到大肠杆菌染色体中,然后用不同强度的启动子进行调节。随着atoB的活化,β-胡萝卜素的产量增加了26%,而对细胞的生长没有影响。通过简并的RBS文库对两种关键酶mvas和Hmg1的组合调节,β-胡萝卜素进一步增加了51%。结论我们的研究提供了一种通过在转录和翻译水平上整合和调节异源途径来提高目标化合物产量的新策略。另外,在这项工作中,还构建了具有有效MEP和MVA途径的遗传硬编码底盘,用于提供类异戊二烯前体。

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