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Enhanced bacterial expression of several mammalian cytochrome P450s by codon optimization and chaperone coexpression.

Wu ZL, Qiao J, Zhang ZG, Guengerich FP, Liu Y, Pei XQ
Biotechnol Lett. 2009 31 (10): 1589-93

PMID: 19557307 · PMCID: PMC4188451 · DOI:10.1007/s10529-009-0059-5

To elucidate the effects of codon optimization and chaperone coexpression on the heterologous expression of mammalian cytochrome P450s (P450) in Escherichia coli, the expression of P450s 2B1, 2S1, 2U1, 2W1, and 27C1 were investigated. With codon optimization for N-terminus or the entire gene, the expression levels of P450 27C1, 2U1 and 2W1 increased 22-fold, 3.6-fold and 2.1-fold, respectively, while those for P450s 2B1 and 2S1 remained unchanged. With coexpression of E. coli molecular chaperones GroEL/ES, the expression level increased up to 14-fold for P450 27C1, and 3- to 5-fold for P450s 2B1, 2S1, and 2W1. Simultaneous application of these two techniques resulted in synergetic effects.

MeSH Terms (8)

Animals Codon Cytochrome P-450 Enzyme System Escherichia coli Gene Expression Mammals Molecular Chaperones Recombinant Proteins

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