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通过代谢工程改造大肠杆菌甘油代谢途径提高 3-羟基丙酸产量。

Elevated production of 3-hydroxypropionic acid by metabolic engineering of the glycerol metabolism in Escherichia coli.

机构信息

Biomaterials Lab, SAIT, SEC, 560 Maetandong, Youngtonggu, Suwonsi, Gyunnggido 443-370, South Korea.

Biomaterials Lab, SAIT, SEC, 560 Maetandong, Youngtonggu, Suwonsi, Gyunnggido 443-370, South Korea.

出版信息

Metab Eng. 2014 May;23:116-22. doi: 10.1016/j.ymben.2014.03.001. Epub 2014 Mar 18.

Abstract

3-Hydroxypropionic acid (3-HP) is a renewable-based platform chemical which may be used to produce a wide range of chemicals including acrylic acid, 1,3-propanediol, and acrylamide. Commercialization of microbial 3-HP production from glycerol, which is produced inexpensively as a by-product of biodiesel production, could be expedited when global biodiesel production increases significantly. For enhancing 3-HP production, this study aimed to investigate metabolic engineering strategies towards eliminating by-products of 3-HP as well as optimizing the glycerol metabolism. The removal of genes involved in the generation of major by-products of 3-HP including acetate and 1,3-propanediol increased both 3-HP production level (28.1g/L) and its average yield (0.217g/g). Optimization of l-arabinose inducible expression of glycerol kinase GlpK, which catalyzes the conversion of glycerol to glycerol-3-phosphate, was also made to increase the metabolic flow from glycerol to 3-HP. To activate the whole glycerol metabolism towards 3-HP, the regulatory factor repressing the utilization of glycerol in Escherichia coli, encoded by glpR was eliminated by knocking-out in its chromosomal DNA. The resulting strain showed a significant improvement in the glycerol utilization rate as well as 3-HP titer (40.5g/L). The transcriptional analysis of glpR deletion mutant revealed the poor expression of glycerol facilitator GlpF, which is involved in glycerol transport in the cell. Additional expression of glpF in the glpR deletion mutant successfully led to an increase in 3-HP production (42.1g/L) and an average yield (0.268g/g).

摘要

3-羟基丙酸(3-HP)是一种可再生的平台化学品,可用于生产多种化学品,包括丙烯酸、1,3-丙二醇和丙烯酰胺。随着全球生物柴油产量的大幅增加,从生物柴油生产的副产品廉价甘油中微生物生产 3-HP 的商业化进程可能会加快。为了提高 3-HP 的产量,本研究旨在探讨代谢工程策略,以消除 3-HP 的主要副产物,并优化甘油代谢。去除生成 3-HP 的主要副产物(包括乙酸和 1,3-丙二醇)的相关基因,可提高 3-HP 的产量水平(28.1g/L)和平均产率(0.217g/g)。优化 l-阿拉伯糖诱导甘油激酶 GlpK 的表达,该酶可催化甘油转化为甘油-3-磷酸,也可增加甘油向 3-HP 的代谢通量。为了激活大肠杆菌中甘油代谢途径以生产 3-HP,通过敲除其染色体 DNA 中编码甘油利用抑制因子 glpR 的基因来消除该因子的抑制作用。结果表明,该突变株的甘油利用效率和 3-HP 产量(40.5g/L)均有显著提高。glpR 缺失突变株的转录分析显示,参与甘油在细胞内运输的甘油通透酶 GlpF 表达水平较低。在 glpR 缺失突变株中额外表达 glpF 可成功提高 3-HP 产量(42.1g/L)和平均产率(0.268g/g)。

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