Cleaning up E. coli
- Wim D'Haeze
© BioMed Central Ltd 2002
Received: 4 May 2002
Published: 24 June 2002
A new method of creating large genomic deletions has been used to make a 'clean', stable bacterial genome
Significance and context
Study of the many complete bacterial genomes now available has shown that they contain genes that are unnecessary for life under laboratory conditions and transposable elements that can cause random genome rearrangements and null mutations. This can have undesirable consequences when a bacterium is used for biotechnological purposes, as unnecessary gene products could affect the ease with which the material of interest can be purified, thereby increasing production costs. Metabolic waste products can also be a serious problem, even in small quantities, in the production of drugs and vaccines. Kolisnychenko et al. have developed a new method of deleting large stretches of DNA and tested the method on Escherichia coli to create a 'backbone-only' strain. This 'clean' strain can be used for biotechnological purposes, and to answer questions concerning the stability and evolution of the genome.
Kolisnychenko et al. deleted 12 large genomic regions from the E. coli MG1655 genome, to make E. coli MDS12. The inferred amino-acid sequence of the open reading frames (ORFs) within these deleted regions was compared with 24 bacterial proteomes, and most ORFs did not have counterparts in more than nine of these genomes. To check the precise ends of the deletions the authors sequenced across all deletion breakpoints. E. coli MDS12 contained 376,180 fewer base-pairs than its parental strain, giving an 8.1% reduction in genome size and a 9.3% reduction in gene content. The doubling times of E. coli MG1655 and MDS12 grown in rich and minimal media were nearly identical, although the final optical density of the MDS12 culture (reflecting cell numbers)was slightly, but significantly, higher than that of MG1655. There was no difference in the capacity of the two strains to be transformed by electroporation.
In the new technique of Kolisnychenko et al. the region to be deleted is first replaced by a PCR-generated DNA fragment. This contains the actual joint of the final deletion in its primer part, so that small direct repeats are created on the chromosome. Recombination then ensures that all vector DNA and the region to be deleted are cleanly removed from the genome. Because recombination between relatively short sequences occurs at low frequency, the process is stimulated by expression of an I-SceI meganuclease, a restriction enzyme that will specifically cut the DNA at two I-SceI sites present in the inserted fragment.
Additional information, an explanation of the new deletion method and step-by-step protocols are available as Supplemental material from the authors' website.
The deletion method developed by Kolisnychenko et al. provides a powerful and efficient tool to engineer microorganisms that are used for biotechnological purposes, for example to produce pharmaceuticals or antibiotics. Using for these purposes bacterial strains that are genetically 'cleaned up' would facilitate purification and diminish production costs. The method is also an efficient way of creating deletion mutants on a large scale. The E. coli MDS12 strain, constructed here in order to test the new method, could be of use to produce proteins, drugs or other compounds of interest, after determining growth kinetics and behavior in industrial-sized batch cultures. A plethora of genomes of human pathogenic bacteria, plant or animal pathogens, archaea and other microorganisms are now available for use.