%0 Journal Article
%T Low-mutation-rate, reduced-genome Escherichia coli: an improved host for faithful maintenance of engineered genetic constructs
%A B¨¢lint Cs£¿rg£¿
%A Tam¨¢s Feh¨¦r
%A Edit T¨ªm¨¢r
%A Frederick R Blattner
%A Gy£¿rgy P¨®sfai
%J Microbial Cell Factories
%D 2012
%I BioMed Central
%R 10.1186/1475-2859-11-11
%X By constructing low-mutation-rate variants, we reduced the evolutionary capacity of MDS42, a reduced-genome E. coli strain engineered to lack most genes irrelevant for laboratory/industrial applications. Elimination of diversity-generating, error-prone DNA polymerase enzymes involved in induced mutagenesis achieved a significant stabilization of the genome. The resulting strain, while retaining normal growth, showed a significant decrease in overall mutation rates, most notably under various stress conditions. Moreover, the error-prone polymerase-free host allowed relatively stable maintenance of a toxic methyltransferase-expressing clone. In contrast, the parental strain produced mutant clones, unable to produce functional methyltransferase, which quickly overgrew the culture to a high ratio (50% of clones in a 24-h induction period lacked functional methyltransferase activity). The surprisingly large stability-difference observed between the strains was due to the combined effects of high stress-induced mutagenesis in the parental strain, growth inhibition by expression of the toxic protein, and selection/outgrowth of mutants no longer producing an active, toxic enzyme.By eliminating stress-inducible error-prone DNA-polymerases, the genome of the mobile genetic element-free E. coli strain MDS42 was further stabilized. The resulting strain represents an improved host in various synthetic and molecular biological applications, allowing more stable production of growth-inhibiting biomolecules.Intrinsic mechanisms for generating diversity are important for survival of bacterial populations in dynamically changing environmental conditions. The ability of a population to adapt to various situations is largely dependent upon a constant fine-tuning of mutation rate [1]. However, what is beneficial in a natural environment is not necessary when conditions are relatively stable and controlled, as in laboratory and industrial settings. In fact, novel, evolved features arisin
%K Escherichia coli
%K mutation rate
%K evolvability
%K reduced genome
%K synthetic biology
%K chassis
%U http://www.microbialcellfactories.com/content/11/1/11