Amino acid stabilization for cell-free protein synthesis by modification of the Escherichia coli genome

被引:79
作者
Michel-Reydellet, N [1 ]
Calhoun, K [1 ]
Swartz, J [1 ]
机构
[1] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
基金
美国国家科学基金会;
关键词
cell-free biology; cell-free protein synthesis; amino acid stabilization; Escherichia coli; cell extract;
D O I
10.1016/j.ymben.2004.01.003
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
Cell-free biology provides a unique opportunity to assess and to manipulate microbial systems by inverse metabolic engineering. We have applied this approach to amino acid metabolism, one of the systems in cell-free biology that limits protein synthesis reactions. Four amino acids (arginine, tryptophan, serine and cysteine) are depleted during a 3-h batch cell-free protein synthesis reaction under various conditions. By modifying the genome of the Escherichia coli strain used to make the cell extract, we see significant stabilization of arginine, tryptophan and serine. Cysteine, however, continues to be degraded. Cell-free protein synthesis with the modified cell extract produces increased yields of the cysteine-free protein Outer Membrane Protein T (OmpT). (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:197 / 203
页数:7
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