Expanding the landscape of recombinant protein production in Escherichia coli

被引:21
作者
Hochkoeppler, Alejandro [1 ,2 ]
机构
[1] Univ Bologna, Dept Pharm & Biotechnol, I-40136 Bologna, Italy
[2] Univ Florence, CSGI, I-50019 Florence, Italy
关键词
Co-expression; Compatible plasmids; Escherichia coli; Post-translational modifications; Protein complexes; Protein production; Unnatural amino acids; HIGH-LEVEL EXPRESSION; HIV-1; REVERSE-TRANSCRIPTASE; DNA-POLYMERASE III; EXTRACELLULAR SECRETION; ERWINIA-CHRYSANTHEMI; CAMPYLOBACTER-JEJUNI; COEXPRESSION SYSTEM; THYMOSIN ALPHA-1; GENETIC-CODE; COPY NUMBER;
D O I
10.1007/s10529-013-1396-y
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
Over the years, several vectors and host strains have been constructed to improve the overexpression of recombinant proteins in Escherichia coli. More recently, attention has focused on the co-expression of genes in E. coli, either by means of a single vector or by cotransformation with multiple compatible plasmids. Co-expression was initially designed to generate protein complexes in vivo, and later served to extend the use of E. coli as a platform for the production of heterologous proteins. This review shows how the co-expression of genes in E. coli is challenging the production of protein complexes and proteins bearing post-translational modifications or unnatural amino acids. In addition, the importance of co-expression to achieve efficient secretion of recombinant proteins in E. coli is discussed, with recent insights into the use of co-expression to overproduce membrane proteins.
引用
收藏
页码:1971 / 1981
页数:11
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