Literature DB >> 33430875

Protein over-expression in Escherichia coli triggers adaptation analogous to antimicrobial resistance.

Jack James1, Benjamin Yarnall1, Andy Koranteng1, Jane Gibson2, Tahmina Rahman3, Declan A Doyle4.   

Abstract

BACKGROUND: The E. coli pET system is the most widely used protein over-expression system worldwide. It relies on the assumption that all cells produce target protein and it is generally believed that integral membrane protein (IMP) over-expression is more toxic than their soluble counterparts.
RESULTS: Using GFP-tagged proteins, high level over-expression of either soluble or IMP targets results in > 99.9% cell loss with survival rate of only < 0.03%. Selective pressure generates three phenotypes: large green, large white and small colony variants. As a result, in overnight cultures, ~ 50% of the overall cell mass produces no protein. Genome sequencing of the phenotypes revealed genomic mutations that causes either the loss of T7 RNAP activity or its transcriptional downregulation. The over-expression process is bactericidal and is observed for both soluble and membrane proteins.
CONCLUSIONS: We demonstrate that it is the act of high-level over-expression of exogenous proteins in E. coli that sets in motion a chain of events leading to > 99.9% cell death. These results redefine our understanding of protein over-production and link it to the adaptive survival response seen in the development of antimicrobial resistance.

Entities:  

Keywords:  Antimicrobial resistance; BL21(DE3); Escherichia coli; Protein over-expression

Year:  2021        PMID: 33430875      PMCID: PMC7798265          DOI: 10.1186/s12934-020-01462-6

Source DB:  PubMed          Journal:  Microb Cell Fact        ISSN: 1475-2859            Impact factor:   5.328


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8.  Multi-omics integration accurately predicts cellular state in unexplored conditions for Escherichia coli.

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Journal:  ACS Synth Biol       Date:  2022-01-04       Impact factor: 5.110

2.  Regulating the T7 RNA polymerase expression in E. coli BL21 (DE3) to provide more host options for recombinant protein production.

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