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Fermentation study of metabolically engineered Escherichia coli strains for high-level 1-propanol production

机译:代谢工程化大肠杆菌菌株用于高水平1-丙醇生产的发酵研究

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摘要

As the current global energy requirements are mainly met through the combustion of petroleum, coal, and natural gas, concerns over the global warming and the sustainability of the future exploitation of fossil fuels are growing. 1-propanol of which carbon chain is longer than the ethanol could be a better biofuel for blending with gasoline. Previously in our lab, a novel alternative 1-propanol biosynthesis pathway was constructed by introducing the sleeping beauty mutase (Sbm) operon into the native E.coli. During the anaerobic cultivation of a metabolically engineered E.coli strain in a shake flask, approximately 150 mg/L of 1-propanol was produced using glucose as the main carbon source. In this study, we demonstrated high-level production of both 1-propanol and ethanol by fermenting our novel metabolically engineered E. coli strains anaerobically with glycerol/glucose as the main carbon source. In a batch fermentation of a wild type E. coli stain harboring a low copy number plasmid with an active Sbm operon, low concentration of 1-propanol was detected in the culture media. By knocking out the gene involved in the major carbon flux competing pathway (ldhA), the titer of 1-propanol was increased by four-fold. Due to glucose’s limited NADH-generating capacity, glycerol, which is a more reduced compound, was used as the main carbon source, and the 1-propanol titer reached 2.15 g/L and 4.12 g/L from 30 g/L and 87 g/L of glycerol, respectively. Further enhancement in the 1-propanol production was achieved by constructing a plasmid-free propanogenic E. coli strain that had a faster glycerol dissimilation rate and higher 1-propanol yield. In summary, 7.52 g/L and 35.66 g/L of 1-propanol and ethanol, respectively, was produced from 116 g/L of glycerol in a fed-batch cultivation of the plasmid-free propanogenic E. coli strain.
机译:由于当前全球能源需求主要通过石油,煤炭和天然气的燃烧来满足,因此人们对全球变暖和未来化石燃料开采的可持续性的担忧日益增加。碳链长于乙醇的1-丙醇可能是与汽油混合的更好的生物燃料。以前在我们的实验室中,通过将睡眠美容变异酶(Sbm)操纵子引入天然大肠杆菌中,构建了一种新型的1-丙醇替代合成途径。在摇瓶中厌氧培养代谢工程大肠杆菌的过程中,使用葡萄糖作为主要碳源,产生了约150 mg / L的1-丙醇。在这项研究中,我们证明了通过以甘油/葡萄糖为主要碳源厌氧发酵我们的新型代谢工程化大肠杆菌菌株,可以高水平生产1-丙醇和乙醇。在带有低拷贝数质粒和活性Sbm操纵子的野生型大肠杆菌染色的分批发酵中,在培养基中检测到低浓度的1-丙醇。通过敲除参与主要碳通量竞争途径(ldhA)的基因,1-丙醇的效价提高了四倍。由于葡萄糖有限的NADH生成能力,甘油(一种还原程度更高的化合物)被用作主要的碳源,1-丙醇滴度分别从30 g / L和87 g分别达到2.15 g / L和4.12 g / L。 / L的甘油分别。通过构建无质粒的丙三醇异化速率更快和1-丙醇产率更高的无丙酸大肠杆菌菌株,可以进一步提高1-丙醇的产量。总之,在无质粒促生大肠杆菌菌株的分批分批培养中,由116 g / L甘油分别生产了7.52 g / L和35.66 g / L 1-丙醇和乙醇。

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    Liu Xuejia;

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  • 年度 2015
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  • 原文格式 PDF
  • 正文语种 en
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