Expression of heterologous non-oxidative pentose phosphate pathway from Bacillus methanolicus and phosphoglucose isomerase deletion improves methanol assimilation and metabolite production by a synthetic Escherichia coli methylotroph

被引:79
作者
Bennett, R. Kyle [1 ,2 ]
Gonzalez, Jacqueline E. [1 ]
Whitaker, W. Brian [1 ,2 ]
Antoniewicz, Maciek R. [1 ]
Papoutsakis, Eleftherios T. [1 ,2 ]
机构
[1] Univ Delaware, Dept Chem & Biomol Engn, 150 Acad St, Newark, DE 19716 USA
[2] Univ Delaware, Delaware Biotechnol Inst, Mol Biotechnol Lab, 15 Innovat Way, Newark, DE 19711 USA
关键词
Synthetic methylotrophy; Methanol; Escherichia coli; Pentose phosphate pathway; Phosphoglucose isomerase; PARALLEL LABELING EXPERIMENTS; GAS CHROMATOGRAPHY/MASS SPECTROMETRY; C-13-METABOLIC FLUX ANALYSIS; OVERFLOW METABOLISM; PROTEIN EXPRESSION; RT-QPCR; GENES; PLASMID; CONVERSION; BIOLOGY;
D O I
10.1016/j.ymben.2017.11.016
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Synthetic methylotrophy aims to develop non-native methylotrophic microorganisms to utilize methane or methanol to produce chemicals and biofuels. We report two complimentary strategies to further engineer a previously engineered methylotrophic E. coli strain for improved methanol utilization. First, we demonstrate improved methanol assimilation in the presence of small amounts of yeast extract by expressing the non-oxidative pentose phosphate pathway (PPP) from Bacillus methanolicus. Second, we demonstrate improved co-utilization of methanol and glucose by deleting the phosphoglucose isomerase gene (pgi), which rerouted glucose carbon flux through the oxidative PPP. Both strategies led to significant improvements in methanol assimilation as determined by C-13-labeling in intracellular metabolites. Introduction of an acetone-formation pathway in the pgi-deficient methylotrophic E. coli strain led to improved methanol utilization and acetone titers during glucose fed-batch fermentation.
引用
收藏
页码:75 / 85
页数:11
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