Аннотации:
© 2016, Springer Science+Business Media New York.Gram-negative bacterium Serratia marcescens is a well-known environmental microorganism and the accepted clinical pathogen causing nosocomial infections. It attracts more attention in recent years due to the emergence of strains with multiple drug resistance. Standard recombinant techniques are difficult to apply to S. marcescens due to the presence of numerous hydrolytic enzymes, in particular, extracellular nuclease and restriction endonuclease, which degrade transforming DNAs. We overcame this obstacle by utilizing restrictionless nuclease-deficient mutant strain S. marcescens TT392. As a proof of principal, in this genetic background, we generated a knockout strain with deletion of macAB locus using lambda red technology. The resulting mutation could be easily moved to a new genetic background by generalized phage transduction. This strategy provides a good tool for evaluation of S. marcescens pathogenic potential.
