Tracing Metabolite Footsteps of Escherichia coli Along the Time Course of Recombinant Protein Expression by Two-Dimensional NMR Spectroscopy

被引:10
作者
Chae, Young Kee [1 ,2 ]
Kim, Scot Hyun [1 ,2 ]
Ellinger, James J. [3 ]
Markley, John L. [3 ]
机构
[1] Sejong Univ, Dept Chem, Seoul 143747, South Korea
[2] Sejong Univ, Inst Chem Biol, Seoul 143747, South Korea
[3] Univ Wisconsin, Dept Biochem, Madison, WI 53706 USA
基金
新加坡国家研究基金会;
关键词
Metabolite profiling; Recombinant protein; Overexpression; NMR; DISULFIDE BONDS; STRESS; OVEREXPRESSION; PURIFICATION; SOLUBILITY; CYTOPLASM; SPECTRA; DOMAIN;
D O I
10.5012/bkcs.2012.33.12.4041
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The recombinant expression of proteins has been the method of choice to meet the demands from proteomics and structural genomics studies. Despite its successful production of many heterologous proteins, Escherichia coli failed to produce many other proteins in their native forms. This may be related to the fact that the stresses resulting from the overproduction interfere with cellular processes. To better understand the physiological change during the overproduction phase, we profiled the metabolites along the time course of the recombinant protein expression. We identified 32 metabolites collected from different time points in the protein production phase. The stress induced by protein production can be characterized by (A) the increased usage of aspartic acid, choline, glycerol, and N-acetyllysine; and (B) the accumulation of adenosine, alanine, oxidized glutathione, glycine, N-acetylputrescine, and uracil. We envision that this work can be used to create a strategy for the production of usable proteins in large quantities.
引用
收藏
页码:4041 / 4046
页数:6
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